Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 3732 |
|---|---|
| ensemblid | ENSG00000085117.12 |
| hgncid | 6210 |
| symbol | CD82 |
| name | CD82 molecule |
| refseq_nuc | NM_002231.4 |
| refseq_prot | NP_002222.1 |
| ensembl_nuc | ENST00000227155.9 |
| ensembl_prot | ENSP00000227155.4 |
| mane_status | MANE Select |
| chr | chr11 |
| start | 44565663 |
| end | 44620358 |
| strand | + |
| ver | v1.2 |
| region | chr11:44565663-44620358 |
| region5000 | chr11:44560663-44625358 |
| regionname0 | CD82_chr11_44565663_44620358 |
| regionname5000 | CD82_chr11_44560663_44625358 |
| 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 | 267 | 190 | 60 | 28 | 80 | 9 | 11 | 56 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| a0002 | 0/0 | 267 | 181 | 32 | 52 | 59 | 7 | 31 | 43 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| a0003 | 0/0 | 267 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/0 | 804 | 105 | 41 | 24 | 24 | 6 | 9 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| c0002 | 0/0 | 804 | 62 | 1 | 15 | 32 | 1 | 13 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| c0003 | 0/0 | 804 | 47 | 21 | 17 | 3 | 1 | 5 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| c0004 | 0/0 | 804 | 28 | 1 | 8 | 7 | 2 | 10 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| c0005 | 0/0 | 804 | 19 | 1 | 0 | 18 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| c0006 | 0/1 | 804 | 15 | 0 | 1 | 10 | 2 | 1 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| c0007 | 0/0 | 804 | 14 | 3 | 9 | 1 | 0 | 1 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| c0008 | 0/0 | 804 | 13 | 0 | 0 | 11 | 0 | 2 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| c0009 | 0/0 | 804 | 13 | 4 | 0 | 8 | 1 | 0 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| c0010 | 0/0 | 804 | 12 | 4 | 3 | 5 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| c0011 | 0/0 | 804 | 11 | 0 | 0 | 11 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| c0012 | 0/0 | 804 | 5 | 5 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| c0013 | 0/0 | 804 | 4 | 0 | 1 | 0 | 3 | 0 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| c0014 | 0/0 | 804 | 4 | 0 | 0 | 3 | 0 | 1 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| c0015 | 0/0 | 804 | 4 | 3 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| c0016 | 0/0 | 804 | 3 | 3 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| c0017 | 0/0 | 804 | 3 | 0 | 0 | 3 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| c0018 | 0/0 | 804 | 2 | 2 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| c0019 | 0/0 | 804 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| c0020 | 0/0 | 804 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| c0021 | 0/0 | 804 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| c0022 | 0/0 | 804 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| c0023 | 0/0 | 804 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| c0024 | 0/0 | 804 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| c0025 | 0/0 | 804 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| c0026 | 0/0 | 804 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| 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 | 0/1 | 1408 | 109 | 8 | 32 | 44 | 8 | 16 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| t0002 | 0/0 | 1407 | 65 | 5 | 15 | 40 | 1 | 4 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| t0003 | 0/0 | 1409 | 56 | 7 | 17 | 19 | 4 | 9 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| t0004 | 0/0 | 1410 | 34 | 26 | 0 | 7 | 0 | 1 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| t0005 | 0/0 | 1409 | 12 | 1 | 1 | 9 | 1 | 0 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| t0006 | 0/0 | 1409 | 8 | 0 | 7 | 0 | 1 | 0 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| t0007 | 0/0 | 1411 | 7 | 5 | 0 | 2 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| t0008 | 0/0 | 1408 | 6 | 6 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| t0009 | 0/0 | 1408 | 5 | 0 | 1 | 0 | 0 | 4 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| t0010 | 0/0 | 1406 | 5 | 0 | 0 | 4 | 0 | 1 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| t0011 | 0/0 | 1410 | 5 | 5 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| t0012 | 1/0 | 1409 | 5 | 4 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| t0013 | 0/0 | 1408 | 4 | 0 | 1 | 3 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| t0014 | 0/0 | 1409 | 4 | 3 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| t0015 | 0/0 | 1407 | 4 | 4 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| t0016 | 0/0 | 1407 | 3 | 2 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| t0017 | 0/0 | 1410 | 3 | 3 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| t0018 | 0/0 | 1410 | 2 | 0 | 0 | 0 | 1 | 1 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| t0019 | 0/0 | 1408 | 2 | 0 | 1 | 0 | 0 | 1 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| t0020 | 0/0 | 1409 | 2 | 0 | 0 | 2 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| t0021 | 0/0 | 1409 | 1 | 0 | 0 | 0 | 0 | 1 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| t0022 | 0/0 | 1408 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| t0023 | 0/0 | 1409 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| t0024 | 0/0 | 1409 | 1 | 0 | 0 | 0 | 0 | 1 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| t0025 | 0/0 | 1408 | 1 | 0 | 0 | 0 | 0 | 1 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| t0026 | 0/0 | 1408 | 1 | 0 | 0 | 0 | 0 | 1 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| t0027 | 0/0 | 1408 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| t0028 | 0/0 | 1410 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| t0029 | 0/0 | 1410 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| t0030 | 0/0 | 1408 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| t0031 | 0/0 | 1410 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| t0032 | 0/0 | 1410 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| t0033 | 0/0 | 1410 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| t0034 | 0/0 | 1407 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| t0035 | 0/0 | 1407 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| t0036 | 0/0 | 1408 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| t0037 | 0/0 | 1409 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| t0038 | 0/0 | 1409 | 1 | 0 | 0 | 0 | 0 | 1 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| t0039 | 0/0 | 1410 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| t0040 | 0/0 | 1409 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| t0041 | 0/0 | 1410 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| t0042 | 0/0 | 1409 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| t0043 | 0/0 | 1410 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| t0044 | 0/0 | 1408 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| t0045 | 0/0 | 1411 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| t0046 | 0/0 | 1408 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| t0047 | 0/0 | 1407 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| t0048 | 0/0 | 1411 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| t0049 | 0/0 | 1409 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| t0050 | 0/0 | 1408 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| t0051 | 0/0 | 1408 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| 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 | 7 | 0 | 1 | 6 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0002 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0004 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0009 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0015 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0089 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0177 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0242 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0243 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0267 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0274 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0296 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 804 | 105 | 41 | 24 | 24 | 6 | 9 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| a0001c0005 | 0/0 | 804 | 19 | 1 | 0 | 18 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| a0001c0006 | 0/1 | 804 | 15 | 0 | 1 | 10 | 2 | 1 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| a0001c0009 | 0/0 | 804 | 13 | 4 | 0 | 8 | 1 | 0 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| a0001c0010 | 0/0 | 804 | 12 | 4 | 3 | 5 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| a0001c0011 | 0/0 | 804 | 11 | 0 | 0 | 11 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| a0001c0012 | 0/0 | 804 | 5 | 5 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| a0001c0014 | 0/0 | 804 | 4 | 0 | 0 | 3 | 0 | 1 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| a0001c0016 | 0/0 | 804 | 3 | 3 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| a0001c0018 | 0/0 | 804 | 2 | 2 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| a0001c0023 | 0/0 | 804 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| a0002c0002 | 0/0 | 804 | 62 | 1 | 15 | 32 | 1 | 13 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| a0002c0003 | 0/0 | 804 | 47 | 21 | 17 | 3 | 1 | 5 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| a0002c0004 | 0/0 | 804 | 28 | 1 | 8 | 7 | 2 | 10 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| a0002c0007 | 0/0 | 804 | 14 | 3 | 9 | 1 | 0 | 1 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| a0002c0008 | 0/0 | 804 | 13 | 0 | 0 | 11 | 0 | 2 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| a0002c0013 | 0/0 | 804 | 4 | 0 | 1 | 0 | 3 | 0 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| a0002c0015 | 0/0 | 804 | 4 | 3 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| a0002c0017 | 0/0 | 804 | 3 | 0 | 0 | 3 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| a0002c0019 | 0/0 | 804 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| a0002c0020 | 0/0 | 804 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| a0002c0021 | 0/0 | 804 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| a0002c0024 | 0/0 | 804 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| a0002c0025 | 0/0 | 804 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| a0002c0026 | 0/0 | 804 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| a0003c0022 | 0/0 | 804 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 2211 | 36 | 5 | 9 | 13 | 4 | 5 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| a0001c0001t0002 | 0/0 | 2210 | 8 | 2 | 0 | 5 | 1 | 0 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| a0001c0001t0003 | 0/0 | 2212 | 13 | 3 | 8 | 1 | 0 | 1 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| a0001c0001t0004 | 0/0 | 2213 | 12 | 12 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| a0001c0001t0005 | 0/0 | 2212 | 3 | 0 | 1 | 2 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| a0001c0001t0006 | 0/0 | 2212 | 4 | 0 | 3 | 0 | 1 | 0 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| a0001c0001t0007 | 0/0 | 2214 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| a0001c0001t0008 | 0/0 | 2211 | 4 | 4 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| a0001c0001t0011 | 0/0 | 2213 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| a0001c0001t0012 | 1/0 | 2212 | 3 | 2 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| a0001c0001t0013 | 0/0 | 2211 | 4 | 0 | 1 | 3 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| a0001c0001t0014 | 0/0 | 2212 | 2 | 1 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| a0001c0001t0015 | 0/0 | 2210 | 3 | 3 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| a0001c0001t0016 | 0/0 | 2210 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| a0001c0001t0017 | 0/0 | 2213 | 2 | 2 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| a0001c0001t0018 | 0/0 | 2213 | 1 | 0 | 0 | 0 | 0 | 1 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| a0001c0001t0025 | 0/0 | 2211 | 1 | 0 | 0 | 0 | 0 | 1 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| a0001c0001t0026 | 0/0 | 2211 | 1 | 0 | 0 | 0 | 0 | 1 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| a0001c0001t0027 | 0/0 | 2211 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| a0001c0001t0046 | 0/0 | 2211 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| a0001c0001t0049 | 0/0 | 2212 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| a0001c0001t0050 | 0/0 | 2211 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| a0001c0001t0051 | 0/0 | 2211 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| a0001c0005t0001 | 0/0 | 2211 | 4 | 1 | 0 | 3 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| a0001c0005t0002 | 0/0 | 2210 | 8 | 0 | 0 | 8 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| a0001c0005t0003 | 0/0 | 2212 | 2 | 0 | 0 | 2 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| a0001c0005t0004 | 0/0 | 2213 | 3 | 0 | 0 | 3 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| a0001c0005t0034 | 0/0 | 2210 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| a0001c0005t0037 | 0/0 | 2212 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| a0001c0006t0001 | 0/1 | 2211 | 4 | 0 | 0 | 3 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| a0001c0006t0002 | 0/0 | 2210 | 5 | 0 | 0 | 5 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| a0001c0006t0003 | 0/0 | 2212 | 4 | 0 | 1 | 2 | 1 | 0 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| a0001c0006t0005 | 0/0 | 2212 | 1 | 0 | 0 | 0 | 1 | 0 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| a0001c0006t0024 | 0/0 | 2212 | 1 | 0 | 0 | 0 | 0 | 1 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| a0001c0009t0001 | 0/0 | 2211 | 3 | 1 | 0 | 1 | 1 | 0 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| a0001c0009t0002 | 0/0 | 2210 | 3 | 0 | 0 | 3 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| a0001c0009t0003 | 0/0 | 2212 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| a0001c0009t0004 | 0/0 | 2213 | 2 | 1 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| a0001c0009t0010 | 0/0 | 2209 | 2 | 0 | 0 | 2 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| a0001c0009t0011 | 0/0 | 2213 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| a0001c0009t0015 | 0/0 | 2210 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| a0001c0010t0001 | 0/0 | 2211 | 3 | 0 | 2 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| a0001c0010t0002 | 0/0 | 2210 | 2 | 0 | 1 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| a0001c0010t0003 | 0/0 | 2212 | 2 | 0 | 0 | 2 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| a0001c0010t0004 | 0/0 | 2213 | 2 | 2 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| a0001c0010t0007 | 0/0 | 2214 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| a0001c0010t0008 | 0/0 | 2211 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| a0001c0010t0040 | 0/0 | 2212 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| a0001c0011t0001 | 0/0 | 2211 | 3 | 0 | 0 | 3 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| a0001c0011t0005 | 0/0 | 2212 | 7 | 0 | 0 | 7 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| a0001c0011t0033 | 0/0 | 2213 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| a0001c0012t0003 | 0/0 | 2212 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| a0001c0012t0004 | 0/0 | 2213 | 3 | 3 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| a0001c0012t0016 | 0/0 | 2210 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| a0001c0014t0001 | 0/0 | 2211 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| a0001c0014t0002 | 0/0 | 2210 | 2 | 0 | 0 | 2 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| a0001c0014t0003 | 0/0 | 2212 | 1 | 0 | 0 | 0 | 0 | 1 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| a0001c0016t0004 | 0/0 | 2213 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| a0001c0016t0017 | 0/0 | 2213 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| a0001c0016t0048 | 0/0 | 2214 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| a0001c0018t0012 | 0/0 | 2212 | 2 | 2 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| a0001c0023t0002 | 0/0 | 2210 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| a0002c0002t0001 | 0/0 | 2211 | 26 | 0 | 11 | 8 | 1 | 6 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| a0002c0002t0002 | 0/0 | 2210 | 9 | 0 | 0 | 6 | 0 | 3 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| a0002c0002t0003 | 0/0 | 2212 | 17 | 0 | 3 | 10 | 0 | 4 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| a0002c0002t0004 | 0/0 | 2213 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| a0002c0002t0006 | 0/0 | 2212 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| a0002c0002t0007 | 0/0 | 2214 | 2 | 0 | 0 | 2 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| a0002c0002t0020 | 0/0 | 2212 | 2 | 0 | 0 | 2 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| a0002c0002t0022 | 0/0 | 2211 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| a0002c0002t0023 | 0/0 | 2212 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| a0002c0002t0032 | 0/0 | 2213 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| a0002c0002t0036 | 0/0 | 2211 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| a0002c0003t0001 | 0/0 | 2211 | 14 | 1 | 7 | 3 | 0 | 3 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| a0002c0003t0002 | 0/0 | 2210 | 4 | 2 | 2 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| a0002c0003t0003 | 0/0 | 2212 | 5 | 1 | 2 | 0 | 1 | 1 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| a0002c0003t0004 | 0/0 | 2213 | 5 | 5 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| a0002c0003t0005 | 0/0 | 2212 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| a0002c0003t0006 | 0/0 | 2212 | 3 | 0 | 3 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| a0002c0003t0007 | 0/0 | 2214 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| a0002c0003t0008 | 0/0 | 2211 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| a0002c0003t0011 | 0/0 | 2213 | 2 | 2 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| a0002c0003t0014 | 0/0 | 2212 | 2 | 2 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| a0002c0003t0028 | 0/0 | 2213 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| a0002c0003t0029 | 0/0 | 2213 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| a0002c0003t0030 | 0/0 | 2211 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| a0002c0003t0038 | 0/0 | 2212 | 1 | 0 | 0 | 0 | 0 | 1 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| a0002c0003t0041 | 0/0 | 2213 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| a0002c0003t0042 | 0/0 | 2212 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| a0002c0003t0043 | 0/0 | 2213 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| a0002c0003t0044 | 0/0 | 2211 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| a0002c0003t0045 | 0/0 | 2214 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| a0002c0004t0001 | 0/0 | 2211 | 8 | 0 | 3 | 2 | 1 | 2 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| a0002c0004t0002 | 0/0 | 2210 | 4 | 0 | 2 | 2 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| a0002c0004t0003 | 0/0 | 2212 | 4 | 0 | 1 | 1 | 0 | 2 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| a0002c0004t0009 | 0/0 | 2211 | 5 | 0 | 1 | 0 | 0 | 4 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| a0002c0004t0016 | 0/0 | 2210 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| a0002c0004t0018 | 0/0 | 2213 | 1 | 0 | 0 | 0 | 1 | 0 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| a0002c0004t0019 | 0/0 | 2211 | 2 | 0 | 1 | 0 | 0 | 1 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| a0002c0004t0021 | 0/0 | 2212 | 1 | 0 | 0 | 0 | 0 | 1 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| a0002c0004t0035 | 0/0 | 2210 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| a0002c0004t0039 | 0/0 | 2213 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| a0002c0007t0002 | 0/0 | 2210 | 12 | 1 | 9 | 1 | 0 | 1 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| a0002c0007t0003 | 0/0 | 2212 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| a0002c0007t0004 | 0/0 | 2213 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| a0002c0008t0001 | 0/0 | 2211 | 5 | 0 | 0 | 5 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| a0002c0008t0002 | 0/0 | 2210 | 4 | 0 | 0 | 4 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| a0002c0008t0004 | 0/0 | 2213 | 2 | 0 | 0 | 1 | 0 | 1 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| a0002c0008t0010 | 0/0 | 2209 | 2 | 0 | 0 | 1 | 0 | 1 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| a0002c0013t0001 | 0/0 | 2211 | 1 | 0 | 0 | 0 | 1 | 0 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| a0002c0013t0003 | 0/0 | 2212 | 3 | 0 | 1 | 0 | 2 | 0 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| a0002c0015t0003 | 0/0 | 2212 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| a0002c0015t0007 | 0/0 | 2214 | 2 | 2 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| a0002c0015t0031 | 0/0 | 2213 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| a0002c0017t0001 | 0/0 | 2211 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| a0002c0017t0002 | 0/0 | 2210 | 2 | 0 | 0 | 2 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| a0002c0019t0011 | 0/0 | 2213 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| a0002c0020t0010 | 0/0 | 2209 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| a0002c0021t0003 | 0/0 | 2212 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| a0002c0024t0047 | 0/0 | 2210 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| a0002c0025t0004 | 0/0 | 2213 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| a0002c0026t0002 | 0/0 | 2210 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| a0003c0022t0004 | 0/0 | 2213 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | copy fasta | chr11 | 44560663 | 44625358 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 7 | 0 | 1 | 6 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0001c0001t0001g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0001c0001t0001g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0001c0001t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0001c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0001c0001t0001g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0001c0001t0001g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0001c0001t0001g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0001c0001t0001g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0001c0001t0002g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0001c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0001c0001t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0001c0001t0002g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0001c0001t0002g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0001c0001t0003g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0001c0001t0003g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0001c0001t0003g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0001c0001t0003g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0001c0001t0003g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0001c0001t0003g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0001c0001t0003g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0001c0001t0003g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0001c0001t0003g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0001c0001t0003g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0001c0001t0003g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0001c0001t0003g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0001c0001t0003g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0001c0001t0004g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0001c0001t0004g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0001c0001t0004g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0001c0001t0004g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0001c0001t0004g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0001c0001t0004g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0001c0001t0004g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0001c0001t0004g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0001c0001t0004g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0001c0001t0004g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0001c0001t0004g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0001c0001t0004g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0001c0001t0005g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0001c0001t0005g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0001c0001t0005g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0001c0001t0006g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0001c0001t0006g0015 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0001c0001t0006g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0001c0001t0007g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0001c0001t0008g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0001c0001t0008g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0001c0001t0008g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0001c0001t0008g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0001c0001t0011g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0001c0001t0012g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0001c0001t0012g0089 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0001c0001t0012g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0001c0001t0013g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0001c0001t0013g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0001c0001t0013g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0001c0001t0013g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0001c0001t0014g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0001c0001t0014g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0001c0001t0015g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0001c0001t0015g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0001c0001t0015g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0001c0001t0016g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0001c0001t0017g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0001c0001t0017g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0001c0001t0018g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0001c0001t0025g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0001c0001t0026g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0001c0001t0027g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0001c0001t0046g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0001c0001t0049g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0001c0001t0050g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0001c0001t0051g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0001c0005t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0001c0005t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0001c0005t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0001c0005t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0001c0005t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0001c0005t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0001c0005t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0001c0005t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0001c0005t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0001c0005t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0001c0005t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0001c0005t0002g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0001c0005t0003g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0001c0005t0003g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0001c0005t0004g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0001c0005t0004g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0001c0005t0004g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0001c0005t0034g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0001c0005t0037g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0001c0006t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0001c0006t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0001c0006t0001g0177 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0001c0006t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0001c0006t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0001c0006t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0001c0006t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0001c0006t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0001c0006t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0001c0006t0003g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0001c0006t0003g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0001c0006t0003g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0001c0006t0003g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0001c0006t0005g0274 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0001c0006t0024g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0001c0009t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0001c0009t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0001c0009t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0001c0009t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0001c0009t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0001c0009t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0001c0009t0003g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0001c0009t0004g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0001c0009t0004g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0001c0009t0010g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0001c0009t0010g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0001c0009t0011g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0001c0009t0015g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0001c0010t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0001c0010t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0001c0010t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0001c0010t0002g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0001c0010t0002g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0001c0010t0003g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0001c0010t0003g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0001c0010t0004g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0001c0010t0004g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0001c0010t0007g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0001c0010t0008g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0001c0010t0040g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0001c0011t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0001c0011t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0001c0011t0001g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0001c0011t0005g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0001c0011t0005g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0001c0011t0005g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0001c0011t0005g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0001c0011t0005g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0001c0011t0005g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0001c0011t0005g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0001c0011t0033g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0001c0012t0003g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0001c0012t0004g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0001c0012t0004g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0001c0012t0004g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0001c0012t0016g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0001c0014t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0001c0014t0002g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0001c0014t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0001c0014t0003g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0001c0016t0004g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0001c0016t0017g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0001c0016t0048g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0001c0018t0012g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0001c0018t0012g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0001c0023t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0002c0002t0001g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0002c0002t0001g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0002c0002t0001g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0002c0002t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0002c0002t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0002c0002t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0002c0002t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0002c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0002c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0002c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0002c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0002c0002t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0002c0002t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0002c0002t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0002c0002t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0002c0002t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0002c0002t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0002c0002t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0002c0002t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0002c0002t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0002c0002t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0002c0002t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0002c0002t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0002c0002t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0002c0002t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0002c0002t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0002c0002t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0002c0002t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0002c0002t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0002c0002t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0002c0002t0002g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0002c0002t0002g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0002c0002t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0002c0002t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0002c0002t0002g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0002c0002t0003g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0002c0002t0003g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0002c0002t0003g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0002c0002t0003g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0002c0002t0003g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0002c0002t0003g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0002c0002t0003g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0002c0002t0003g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0002c0002t0003g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0002c0002t0003g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0002c0002t0003g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0002c0002t0003g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0002c0002t0003g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0002c0002t0003g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0002c0002t0003g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0002c0002t0003g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0002c0002t0003g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0002c0002t0004g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0002c0002t0006g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0002c0002t0007g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0002c0002t0007g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0002c0002t0020g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0002c0002t0020g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0002c0002t0022g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0002c0002t0023g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0002c0002t0032g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0002c0002t0036g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0002c0003t0001g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0002c0003t0001g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0002c0003t0001g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0002c0003t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0002c0003t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0002c0003t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0002c0003t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0002c0003t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0002c0003t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0002c0003t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0002c0003t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0002c0003t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0002c0003t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0002c0003t0001g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0002c0003t0002g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0002c0003t0002g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0002c0003t0002g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0002c0003t0002g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0002c0003t0003g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0002c0003t0003g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0002c0003t0003g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0002c0003t0003g0296 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0002c0003t0003g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0002c0003t0004g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0002c0003t0004g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0002c0003t0004g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0002c0003t0004g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0002c0003t0004g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0002c0003t0005g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0002c0003t0006g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0002c0003t0006g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0002c0003t0006g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0002c0003t0007g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0002c0003t0008g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0002c0003t0011g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0002c0003t0011g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0002c0003t0014g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0002c0003t0014g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0002c0003t0028g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0002c0003t0029g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0002c0003t0030g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0002c0003t0038g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0002c0003t0041g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0002c0003t0042g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0002c0003t0043g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0002c0003t0044g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0002c0003t0045g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0002c0004t0001g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0002c0004t0001g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0002c0004t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0002c0004t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0002c0004t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0002c0004t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0002c0004t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0002c0004t0001g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0002c0004t0002g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0002c0004t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0002c0004t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0002c0004t0002g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0002c0004t0003g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0002c0004t0003g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0002c0004t0003g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0002c0004t0003g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0002c0004t0009g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0002c0004t0009g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0002c0004t0009g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0002c0004t0009g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0002c0004t0009g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0002c0004t0016g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0002c0004t0018g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0002c0004t0019g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0002c0004t0019g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0002c0004t0021g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0002c0004t0035g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0002c0004t0039g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0002c0007t0002g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0002c0007t0002g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0002c0007t0002g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0002c0007t0002g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0002c0007t0002g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0002c0007t0002g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0002c0007t0002g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0002c0007t0002g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0002c0007t0002g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0002c0007t0002g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0002c0007t0002g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0002c0007t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0002c0007t0003g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0002c0007t0004g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0002c0008t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0002c0008t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0002c0008t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0002c0008t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0002c0008t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0002c0008t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0002c0008t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0002c0008t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0002c0008t0002g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0002c0008t0004g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0002c0008t0004g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0002c0008t0010g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0002c0008t0010g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0002c0013t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0002c0013t0003g0004 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0002c0013t0003g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0002c0015t0003g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0002c0015t0007g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0002c0015t0007g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0002c0015t0031g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0002c0017t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0002c0017t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0002c0017t0002g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0002c0019t0011g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0002c0020t0010g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0002c0021t0003g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0002c0024t0047g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0002c0025t0004g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0002c0026t0002g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| a0003c0022t0004g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0004 | t0018 | g0230 | EUR | GBR | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0267 | EUR | GBR | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG00140 | hp1 | a0002 | c0013 | t0001 | g0110 | EUR | GBR | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG00140 | hp2 | a0002 | c0003 | t0003 | g0296 | EUR | GBR | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG00323 | hp1 | a0002 | c0004 | t0001 | g0061 | EUR | FIN | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG00323 | hp2 | a0002 | c0002 | t0001 | g0233 | EUR | FIN | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG00408 | hp1 | a0001 | c0006 | t0002 | g0141 | EAS | CHS | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG00408 | hp2 | a0001 | c0005 | t0002 | g0206 | EAS | CHS | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG00423 | hp2 | a0002 | c0002 | t0001 | g0167 | EAS | CHS | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG00438 | hp1 | a0001 | c0010 | t0001 | g0117 | EAS | CHS | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG00438 | hp2 | a0002 | c0002 | t0003 | g0107 | EAS | CHS | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG00544 | hp1 | a0001 | c0009 | t0002 | g0129 | EAS | CHS | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG00544 | hp2 | a0001 | c0005 | t0002 | g0048 | EAS | CHS | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG00558 | hp1 | a0001 | c0010 | t0003 | g0238 | EAS | CHS | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0118 | EAS | CHS | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG00597 | hp1 | a0001 | c0005 | t0004 | g0072 | EAS | CHS | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG00597 | hp2 | a0002 | c0008 | t0002 | g0298 | EAS | CHS | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG00609 | hp1 | a0002 | c0002 | t0002 | g0188 | EAS | CHS | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG00609 | hp2 | a0001 | c0009 | t0004 | g0239 | EAS | CHS | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG00621 | hp1 | a0001 | c0001 | t0005 | g0019 | EAS | CHS | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG00621 | hp2 | a0001 | c0001 | t0013 | g0216 | EAS | CHS | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG00639 | hp1 | a0001 | c0010 | t0001 | g0212 | AMR | PUR | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG00639 | hp2 | a0001 | c0006 | t0003 | g0344 | AMR | PUR | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG00642 | hp1 | a0001 | c0001 | t0003 | g0304 | AMR | PUR | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG00642 | hp2 | a0002 | c0026 | t0002 | g0054 | AMR | PUR | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG00673 | hp1 | a0002 | c0008 | t0004 | g0088 | EAS | CHS | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG00673 | hp2 | a0001 | c0023 | t0002 | g0200 | EAS | CHS | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG00733 | hp2 | a0002 | c0002 | t0001 | g0005 | AMR | PUR | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG00735 | hp1 | a0002 | c0004 | t0019 | g0057 | AMR | PUR | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG00735 | hp2 | a0002 | c0021 | t0003 | g0005 | AMR | PUR | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG00738 | hp1 | a0002 | c0002 | t0003 | g0231 | AMR | PUR | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG00738 | hp2 | a0002 | c0007 | t0002 | g0049 | AMR | PUR | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG00741 | hp1 | a0002 | c0004 | t0001 | g0059 | AMR | PUR | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG00741 | hp2 | a0002 | c0003 | t0006 | g0132 | AMR | PUR | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG01070 | hp1 | a0002 | c0004 | t0001 | g0008 | AMR | PUR | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG01070 | hp2 | a0002 | c0007 | t0002 | g0012 | AMR | PUR | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG01071 | hp1 | a0002 | c0003 | t0001 | g0112 | AMR | PUR | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG01071 | hp2 | a0002 | c0007 | t0002 | g0013 | AMR | PUR | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG01074 | hp1 | a0002 | c0002 | t0001 | g0135 | AMR | PUR | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG01074 | hp2 | a0002 | c0003 | t0003 | g0320 | AMR | PUR | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG01081 | hp1 | a0002 | c0004 | t0002 | g0008 | AMR | PUR | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG01081 | hp2 | a0002 | c0002 | t0006 | g0161 | AMR | PUR | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG01099 | hp1 | a0002 | c0007 | t0002 | g0040 | AMR | PUR | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG01099 | hp2 | a0002 | c0002 | t0003 | g0246 | AMR | PUR | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG01106 | hp1 | a0002 | c0007 | t0002 | g0041 | AMR | PUR | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG01106 | hp2 | a0001 | c0010 | t0001 | g0211 | AMR | PUR | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG01109 | hp1 | a0002 | c0003 | t0002 | g0325 | AMR | PUR | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG01109 | hp2 | a0001 | c0001 | t0014 | g0280 | AMR | PUR | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG01167 | hp1 | a0002 | c0004 | t0002 | g0228 | AMR | PUR | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG01167 | hp2 | a0002 | c0007 | t0002 | g0126 | AMR | PUR | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG01168 | hp1 | a0002 | c0003 | t0003 | g0007 | AMR | PUR | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG01168 | hp2 | a0001 | c0001 | t0003 | g0108 | AMR | PUR | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG01169 | hp1 | a0002 | c0003 | t0001 | g0007 | AMR | PUR | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG01169 | hp2 | a0002 | c0007 | t0002 | g0125 | AMR | PUR | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG01175 | hp1 | a0001 | c0001 | t0005 | g0214 | AMR | PUR | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG01175 | hp2 | a0002 | c0002 | t0003 | g0134 | AMR | PUR | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG01192 | hp1 | a0002 | c0002 | t0001 | g0149 | AMR | PUR | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG01192 | hp2 | a0001 | c0010 | t0002 | g0014 | AMR | PUR | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG01243 | hp1 | a0002 | c0003 | t0043 | g0276 | AMR | PUR | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG01243 | hp2 | a0001 | c0001 | t0016 | g0120 | AMR | PUR | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG01255 | hp1 | a0002 | c0002 | t0001 | g0046 | AMR | CLM | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG01255 | hp2 | a0001 | c0001 | t0013 | g0071 | AMR | CLM | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | CLM | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0051 | AMR | CLM | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG01257 | hp2 | a0001 | c0001 | t0006 | g0010 | AMR | CLM | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG01258 | hp2 | a0001 | c0001 | t0006 | g0010 | AMR | CLM | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG01261 | hp1 | a0002 | c0007 | t0002 | g0055 | AMR | CLM | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG01261 | hp2 | a0001 | c0001 | t0003 | g0002 | AMR | CLM | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG01346 | hp2 | a0002 | c0003 | t0002 | g0306 | AMR | CLM | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0315 | AMR | CLM | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG01358 | hp2 | a0002 | c0003 | t0001 | g0002 | AMR | CLM | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG01496 | hp1 | a0002 | c0003 | t0029 | g0275 | AMR | CLM | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG01496 | hp2 | a0002 | c0002 | t0001 | g0136 | AMR | CLM | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0058 | EUR | IBS | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG01515 | hp2 | a0002 | c0013 | t0003 | g0004 | EUR | IBS | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0243 | EUR | IBS | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG01516 | hp2 | a0001 | c0009 | t0001 | g0166 | EUR | IBS | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0242 | EUR | IBS | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG01517 | hp2 | a0002 | c0013 | t0003 | g0004 | EUR | IBS | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG01884 | hp1 | a0001 | c0018 | t0012 | g0269 | AFR | ACB | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG01884 | hp2 | a0002 | c0003 | t0014 | g0328 | AFR | ACB | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG01891 | hp1 | a0002 | c0007 | t0002 | g0123 | AFR | ACB | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG01891 | hp2 | a0001 | c0001 | t0004 | g0270 | AFR | ACB | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG01928 | hp1 | a0002 | c0002 | t0001 | g0042 | AMR | PEL | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG01928 | hp2 | a0001 | c0001 | t0003 | g0295 | AMR | PEL | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG01943 | hp1 | a0002 | c0002 | t0001 | g0045 | AMR | PEL | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG01943 | hp2 | a0002 | c0003 | t0001 | g0218 | AMR | PEL | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0044 | AMR | PEL | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG01952 | hp2 | a0002 | c0003 | t0001 | g0043 | AMR | PEL | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG01975 | hp1 | a0002 | c0002 | t0001 | g0138 | AMR | PEL | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG01975 | hp2 | a0001 | c0001 | t0003 | g0299 | AMR | PEL | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG01978 | hp1 | a0002 | c0003 | t0006 | g0217 | AMR | PEL | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG01978 | hp2 | a0001 | c0001 | t0003 | g0303 | AMR | PEL | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG01981 | hp1 | a0002 | c0013 | t0003 | g0053 | AMR | PEL | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG01981 | hp2 | a0001 | c0001 | t0003 | g0096 | AMR | PEL | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG01993 | hp1 | a0002 | c0002 | t0001 | g0016 | AMR | PEL | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG01993 | hp2 | a0002 | c0002 | t0001 | g0139 | AMR | PEL | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG02004 | hp1 | a0002 | c0003 | t0030 | g0305 | AMR | PEL | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG02004 | hp2 | a0002 | c0004 | t0001 | g0056 | AMR | PEL | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG02015 | hp1 | a0002 | c0002 | t0036 | g0114 | EAS | KHV | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0308 | EAS | KHV | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG02055 | hp1 | a0002 | c0002 | t0022 | g0273 | AFR | ACB | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG02055 | hp2 | a0001 | c0016 | t0004 | g0351 | AFR | ACB | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG02056 | hp1 | a0001 | c0006 | t0001 | g0036 | EAS | KHV | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0278 | EAS | KHV | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG02071 | hp1 | a0002 | c0002 | t0023 | g0106 | EAS | KHV | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG02071 | hp2 | a0002 | c0002 | t0003 | g0156 | EAS | KHV | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG02074 | hp1 | a0002 | c0002 | t0001 | g0127 | EAS | KHV | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG02074 | hp2 | a0001 | c0001 | t0003 | g0104 | EAS | KHV | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0356 | EAS | KHV | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | KHV | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG02129 | hp1 | a0002 | c0002 | t0020 | g0143 | EAS | KHV | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG02129 | hp2 | a0001 | c0005 | t0001 | g0204 | EAS | KHV | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG02132 | hp1 | a0001 | c0006 | t0003 | g0077 | EAS | KHV | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG02132 | hp2 | a0001 | c0010 | t0003 | g0158 | EAS | KHV | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG02135 | hp1 | a0001 | c0006 | t0001 | g0115 | EAS | KHV | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG02135 | hp2 | a0002 | c0004 | t0035 | g0236 | EAS | KHV | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG02145 | hp1 | a0002 | c0003 | t0044 | g0268 | AFR | ACB | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG02145 | hp2 | a0002 | c0003 | t0042 | g0311 | AFR | ACB | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG02148 | hp1 | a0002 | c0003 | t0006 | g0221 | AMR | PEL | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0047 | AMR | PEL | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG02257 | hp1 | a0001 | c0001 | t0008 | g0181 | AFR | ACB | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG02257 | hp2 | a0001 | c0010 | t0007 | g0095 | AFR | ACB | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG02258 | hp1 | a0001 | c0001 | t0051 | g0223 | AFR | ACB | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG02258 | hp2 | a0001 | c0016 | t0017 | g0030 | AFR | ACB | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG02273 | hp1 | a0002 | c0002 | t0001 | g0137 | AMR | PEL | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG02273 | hp2 | a0002 | c0003 | t0001 | g0176 | AMR | PEL | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG02280 | hp1 | a0002 | c0003 | t0011 | g0326 | AFR | ACB | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG02280 | hp2 | a0002 | c0003 | t0004 | g0252 | AFR | ACB | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG02293 | hp1 | a0001 | c0001 | t0006 | g0215 | AMR | PEL | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG02293 | hp2 | a0002 | c0004 | t0009 | g0241 | AMR | PEL | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG02300 | hp1 | a0002 | c0003 | t0001 | g0026 | AMR | PEL | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG02300 | hp2 | a0002 | c0007 | t0002 | g0111 | AMR | PEL | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG02451 | hp1 | a0001 | c0012 | t0004 | g0258 | AFR | ACB | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG02451 | hp2 | a0001 | c0001 | t0012 | g0083 | AFR | ACB | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG02523 | hp1 | a0002 | c0008 | t0010 | g0157 | EAS | KHV | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG02523 | hp2 | a0002 | c0002 | t0007 | g0076 | EAS | KHV | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG02572 | hp1 | a0001 | c0001 | t0004 | g0094 | AFR | GWD | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG02572 | hp2 | a0001 | c0001 | t0002 | g0317 | AFR | GWD | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG02602 | hp1 | a0002 | c0004 | t0001 | g0009 | SAS | PJL | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0288 | SAS | PJL | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG02615 | hp1 | a0001 | c0001 | t0015 | g0263 | AFR | GWD | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG02615 | hp2 | a0002 | c0003 | t0005 | g0150 | AFR | GWD | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG02622 | hp1 | a0001 | c0009 | t0015 | g0224 | AFR | GWD | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG02622 | hp2 | a0001 | c0001 | t0049 | g0343 | AFR | GWD | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG02630 | hp1 | a0002 | c0003 | t0008 | g0350 | AFR | GWD | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG02630 | hp2 | a0001 | c0009 | t0004 | g0084 | AFR | GWD | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG02683 | hp1 | a0002 | c0002 | t0001 | g0197 | SAS | PJL | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG02683 | hp2 | a0001 | c0001 | t0018 | g0182 | SAS | PJL | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG02698 | hp1 | a0002 | c0003 | t0001 | g0289 | SAS | PJL | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG02698 | hp2 | a0002 | c0004 | t0019 | g0039 | SAS | PJL | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG02717 | hp1 | a0002 | c0015 | t0003 | g0339 | AFR | GWD | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG02717 | hp2 | a0001 | c0012 | t0016 | g0313 | AFR | GWD | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG02735 | hp1 | a0002 | c0003 | t0001 | g0011 | SAS | PJL | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG02735 | hp2 | a0002 | c0003 | t0003 | g0152 | SAS | PJL | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG02738 | hp1 | a0001 | c0001 | t0003 | g0310 | SAS | PJL | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG02738 | hp2 | a0002 | c0002 | t0002 | g0192 | SAS | PJL | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG02809 | hp1 | a0001 | c0010 | t0004 | g0093 | AFR | GWD | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG02809 | hp2 | a0002 | c0003 | t0004 | g0271 | AFR | GWD | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG02818 | hp1 | a0002 | c0003 | t0011 | g0261 | AFR | GWD | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG02818 | hp2 | a0001 | c0010 | t0008 | g0248 | AFR | GWD | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG02886 | hp1 | a0001 | c0009 | t0001 | g0086 | AFR | GWD | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG02886 | hp2 | a0001 | c0001 | t0004 | g0321 | AFR | GWD | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG02895 | hp1 | a0001 | c0001 | t0004 | g0164 | AFR | GWD | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG02895 | hp2 | a0001 | c0001 | t0004 | g0254 | AFR | GWD | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG02896 | hp1 | a0002 | c0003 | t0004 | g0255 | AFR | GWD | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG02896 | hp2 | a0001 | c0001 | t0004 | g0037 | AFR | GWD | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG02897 | hp1 | a0002 | c0003 | t0003 | g0256 | AFR | GWD | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG02897 | hp2 | a0001 | c0001 | t0004 | g0165 | AFR | GWD | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG02922 | hp1 | a0001 | c0001 | t0003 | g0163 | AFR | ESN | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG02922 | hp2 | a0001 | c0001 | t0008 | g0266 | AFR | ESN | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG02965 | hp1 | a0002 | c0003 | t0004 | g0346 | AFR | ESN | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG02965 | hp2 | a0002 | c0003 | t0004 | g0253 | AFR | ESN | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG02970 | hp1 | a0001 | c0001 | t0003 | g0006 | AFR | ESN | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG02970 | hp2 | a0001 | c0012 | t0004 | g0257 | AFR | ESN | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG02976 | hp1 | a0001 | c0018 | t0012 | g0341 | AFR | ESN | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG02976 | hp2 | a0002 | c0025 | t0004 | g0349 | AFR | ESN | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG03017 | hp1 | a0001 | c0001 | t0026 | g0190 | SAS | PJL | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG03017 | hp2 | a0002 | c0002 | t0003 | g0113 | SAS | PJL | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG03041 | hp1 | a0001 | c0005 | t0001 | g0265 | AFR | GWD | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG03041 | hp2 | a0002 | c0007 | t0003 | g0331 | AFR | GWD | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG03098 | hp1 | a0001 | c0001 | t0004 | g0323 | AFR | MSL | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG03098 | hp2 | a0002 | c0015 | t0007 | g0078 | AFR | MSL | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG03130 | hp1 | a0001 | c0001 | t0015 | g0260 | AFR | ESN | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0250 | AFR | ESN | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG03139 | hp2 | a0002 | c0003 | t0041 | g0312 | AFR | ESN | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG03195 | hp1 | a0002 | c0003 | t0014 | g0259 | AFR | ESN | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG03195 | hp2 | a0001 | c0016 | t0048 | g0031 | AFR | ESN | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG03209 | hp1 | a0001 | c0001 | t0004 | g0249 | AFR | MSL | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG03209 | hp2 | a0001 | c0001 | t0002 | g0147 | AFR | MSL | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG03239 | hp1 | a0002 | c0002 | t0002 | g0225 | SAS | PJL | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0060 | SAS | PJL | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG03453 | hp1 | a0002 | c0024 | t0047 | g0283 | AFR | MSL | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG03453 | hp2 | a0001 | c0001 | t0004 | g0281 | AFR | MSL | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG03486 | hp1 | a0002 | c0003 | t0045 | g0065 | AFR | MSL | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG03486 | hp2 | a0001 | c0012 | t0004 | g0179 | AFR | MSL | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG03492 | hp1 | a0002 | c0004 | t0009 | g0009 | SAS | PJL | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG03492 | hp2 | a0002 | c0002 | t0001 | g0148 | SAS | PJL | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG03516 | hp1 | a0001 | c0012 | t0003 | g0340 | AFR | ESN | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG03516 | hp2 | a0001 | c0001 | t0004 | g0333 | AFR | ESN | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0332 | AFR | GWD | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG03540 | hp2 | a0001 | c0001 | t0003 | g0017 | AFR | GWD | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG03579 | hp1 | a0001 | c0010 | t0004 | g0174 | AFR | MSL | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG03579 | hp2 | a0001 | c0001 | t0050 | g0277 | AFR | MSL | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG03654 | hp1 | a0002 | c0004 | t0021 | g0201 | SAS | PJL | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG03654 | hp2 | a0002 | c0002 | t0001 | g0018 | SAS | PJL | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG03669 | hp1 | a0002 | c0004 | t0009 | g0245 | SAS | PJL | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG03669 | hp2 | a0002 | c0004 | t0001 | g0307 | SAS | PJL | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG03688 | hp1 | a0002 | c0002 | t0003 | g0052 | SAS | STU | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG03688 | hp2 | a0002 | c0003 | t0038 | g0279 | SAS | STU | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG03704 | hp1 | a0002 | c0002 | t0003 | g0187 | SAS | PJL | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG03704 | hp2 | a0002 | c0002 | t0002 | g0195 | SAS | PJL | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG03710 | hp1 | a0001 | c0001 | t0025 | g0285 | SAS | PJL | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG03710 | hp2 | a0002 | c0004 | t0003 | g0234 | SAS | PJL | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG03831 | hp1 | a0002 | c0008 | t0010 | g0153 | SAS | BEB | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG03831 | hp2 | a0001 | c0014 | t0003 | g0128 | SAS | BEB | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG03834 | hp1 | a0002 | c0002 | t0003 | g0162 | SAS | BEB | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG03834 | hp2 | a0002 | c0002 | t0001 | g0244 | SAS | BEB | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0319 | SAS | BEB | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG03927 | hp2 | a0002 | c0007 | t0002 | g0063 | SAS | BEB | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG04115 | hp1 | a0001 | c0006 | t0024 | g0297 | SAS | STU | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG04115 | hp2 | a0002 | c0004 | t0009 | g0237 | SAS | STU | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0287 | SAS | BEB | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG04184 | hp2 | a0002 | c0003 | t0001 | g0240 | SAS | BEB | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG04204 | hp1 | a0002 | c0008 | t0004 | g0232 | SAS | STU | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0229 | SAS | STU | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG04228 | hp1 | a0002 | c0002 | t0001 | g0282 | SAS | STU | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG04228 | hp2 | a0002 | c0002 | t0001 | g0066 | SAS | STU | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| NA18522 | hp1 | a0001 | c0001 | t0015 | g0352 | AFR | YRI | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| NA18522 | hp2 | a0002 | c0003 | t0002 | g0324 | AFR | YRI | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| NA18612 | hp1 | a0001 | c0005 | t0002 | g0169 | EAS | CHB | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| NA18612 | hp2 | a0002 | c0002 | t0002 | g0196 | EAS | CHB | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| NA18747 | hp1 | a0002 | c0002 | t0002 | g0189 | EAS | CHB | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| NA18747 | hp2 | a0002 | c0003 | t0001 | g0067 | EAS | CHB | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| NA18906 | hp1 | a0002 | c0003 | t0028 | g0262 | AFR | YRI | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| NA18906 | hp2 | a0001 | c0001 | t0008 | g0272 | AFR | YRI | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| NA18939 | hp1 | a0001 | c0005 | t0002 | g0292 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| NA18939 | hp2 | a0002 | c0002 | t0032 | g0131 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| NA18941 | hp1 | a0001 | c0006 | t0002 | g0116 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| NA18941 | hp2 | a0001 | c0005 | t0002 | g0291 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| NA18942 | hp1 | a0001 | c0005 | t0037 | g0082 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| NA18942 | hp2 | a0002 | c0002 | t0001 | g0034 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| NA18945 | hp2 | a0002 | c0002 | t0001 | g0121 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| NA18947 | hp1 | a0003 | c0022 | t0004 | g0207 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| NA18948 | hp1 | a0001 | c0009 | t0010 | g0080 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| NA18948 | hp2 | a0002 | c0003 | t0001 | g0085 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| NA18949 | hp1 | a0001 | c0011 | t0033 | g0294 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| NA18949 | hp2 | a0001 | c0005 | t0003 | g0097 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0355 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| NA18950 | hp2 | a0001 | c0011 | t0005 | g0140 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| NA18951 | hp1 | a0002 | c0004 | t0001 | g0198 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| NA18951 | hp2 | a0001 | c0005 | t0004 | g0103 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| NA18954 | hp1 | a0002 | c0015 | t0031 | g0220 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| NA18954 | hp2 | a0002 | c0004 | t0002 | g0226 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| NA18957 | hp1 | a0001 | c0010 | t0002 | g0022 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| NA18957 | hp2 | a0002 | c0008 | t0002 | g0109 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| NA18959 | hp1 | a0001 | c0006 | t0002 | g0151 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| NA18959 | hp2 | a0001 | c0009 | t0010 | g0081 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0160 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0353 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| NA18963 | hp1 | a0002 | c0004 | t0002 | g0227 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| NA18963 | hp2 | a0001 | c0011 | t0005 | g0300 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| NA18965 | hp1 | a0002 | c0002 | t0003 | g0101 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| NA18965 | hp2 | a0001 | c0011 | t0001 | g0336 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| NA18967 | hp1 | a0002 | c0008 | t0001 | g0124 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| NA18967 | hp2 | a0001 | c0001 | t0005 | g0293 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| NA18970 | hp2 | a0002 | c0002 | t0002 | g0130 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| NA18973 | hp1 | a0001 | c0011 | t0005 | g0301 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| NA18973 | hp2 | a0001 | c0011 | t0001 | g0334 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| NA18975 | hp2 | a0002 | c0002 | t0002 | g0203 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| NA18979 | hp1 | a0002 | c0008 | t0001 | g0208 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| NA18979 | hp2 | a0002 | c0004 | t0003 | g0186 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| NA18980 | hp1 | a0002 | c0004 | t0001 | g0073 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| NA18980 | hp2 | a0002 | c0002 | t0007 | g0028 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| NA18984 | hp1 | a0002 | c0007 | t0002 | g0235 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| NA18984 | hp2 | a0002 | c0002 | t0003 | g0035 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| NA18985 | hp1 | a0001 | c0005 | t0001 | g0087 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| NA18985 | hp2 | a0002 | c0002 | t0002 | g0102 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| NA18988 | hp1 | a0001 | c0011 | t0005 | g0302 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| NA18988 | hp2 | a0002 | c0002 | t0001 | g0159 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| NA18994 | hp1 | a0002 | c0002 | t0004 | g0122 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| NA18994 | hp2 | a0002 | c0003 | t0001 | g0075 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| NA18995 | hp1 | a0002 | c0002 | t0003 | g0050 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| NA18995 | hp2 | a0001 | c0005 | t0004 | g0074 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| NA18998 | hp1 | a0001 | c0005 | t0003 | g0210 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| NA18998 | hp2 | a0001 | c0001 | t0013 | g0222 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| NA18999 | hp1 | a0001 | c0009 | t0002 | g0172 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| NA18999 | hp2 | a0001 | c0005 | t0034 | g0173 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| NA19000 | hp1 | a0001 | c0011 | t0005 | g0318 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| NA19000 | hp2 | a0002 | c0004 | t0039 | g0168 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| NA19003 | hp1 | a0002 | c0002 | t0020 | g0194 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| NA19003 | hp2 | a0002 | c0008 | t0001 | g0286 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| NA19004 | hp1 | a0002 | c0017 | t0002 | g0193 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| NA19004 | hp2 | a0001 | c0009 | t0001 | g0032 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| NA19005 | hp1 | a0002 | c0002 | t0003 | g0105 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| NA19005 | hp2 | a0001 | c0001 | t0013 | g0024 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| NA19007 | hp1 | a0001 | c0005 | t0002 | g0175 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| NA19009 | hp1 | a0002 | c0020 | t0010 | g0155 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| NA19009 | hp2 | a0001 | c0009 | t0003 | g0171 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| NA19011 | hp1 | a0001 | c0005 | t0002 | g0209 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| NA19011 | hp2 | a0002 | c0002 | t0001 | g0098 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| NA19012 | hp1 | a0001 | c0006 | t0002 | g0142 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| NA19012 | hp2 | a0001 | c0014 | t0002 | g0183 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| NA19030 | hp1 | a0002 | c0007 | t0004 | g0347 | AFR | LWK | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| NA19030 | hp2 | a0001 | c0001 | t0017 | g0090 | AFR | LWK | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| NA19043 | hp1 | a0002 | c0003 | t0007 | g0021 | AFR | LWK | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| NA19043 | hp2 | a0001 | c0001 | t0014 | g0213 | AFR | LWK | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| NA19054 | hp1 | a0002 | c0017 | t0002 | g0335 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| NA19054 | hp2 | a0001 | c0011 | t0005 | g0314 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| NA19057 | hp1 | a0002 | c0008 | t0001 | g0191 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| NA19057 | hp2 | a0001 | c0011 | t0005 | g0338 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| NA19067 | hp1 | a0002 | c0002 | t0001 | g0070 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| NA19067 | hp2 | a0002 | c0017 | t0001 | g0202 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| NA19070 | hp1 | a0001 | c0011 | t0001 | g0337 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| NA19070 | hp2 | a0001 | c0014 | t0002 | g0025 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| NA19074 | hp1 | a0001 | c0009 | t0002 | g0170 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| NA19074 | hp2 | a0002 | c0002 | t0003 | g0100 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| NA19076 | hp1 | a0001 | c0010 | t0040 | g0029 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| NA19076 | hp2 | a0002 | c0002 | t0003 | g0154 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| NA19081 | hp1 | a0001 | c0006 | t0001 | g0199 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| NA19081 | hp2 | a0001 | c0001 | t0002 | g0184 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| NA19082 | hp1 | a0001 | c0006 | t0002 | g0146 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| NA19085 | hp1 | a0002 | c0008 | t0002 | g0145 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0354 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| NA19086 | hp1 | a0002 | c0008 | t0001 | g0023 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| NA19086 | hp2 | a0001 | c0006 | t0003 | g0185 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| NA19087 | hp1 | a0002 | c0008 | t0002 | g0068 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| NA19087 | hp2 | a0001 | c0005 | t0002 | g0079 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| NA19088 | hp1 | a0002 | c0002 | t0001 | g0290 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| NA19088 | hp2 | a0001 | c0005 | t0001 | g0205 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| NA19090 | hp1 | a0001 | c0014 | t0001 | g0180 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| NA19090 | hp2 | a0002 | c0002 | t0003 | g0099 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| NA19091 | hp2 | a0002 | c0002 | t0003 | g0348 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| NA19240 | hp1 | a0001 | c0001 | t0027 | g0322 | AFR | YRI | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| NA19240 | hp2 | a0002 | c0003 | t0002 | g0038 | AFR | YRI | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| NA20752 | hp1 | a0001 | c0006 | t0003 | g0178 | EUR | TSI | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0144 | EUR | TSI | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| NA20805 | hp1 | a0001 | c0001 | t0006 | g0015 | EUR | TSI | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| NA20805 | hp2 | a0001 | c0006 | t0005 | g0274 | EUR | TSI | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| NA20905 | hp1 | a0002 | c0004 | t0003 | g0219 | SAS | GIH | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| NA20905 | hp2 | a0002 | c0004 | t0009 | g0062 | SAS | GIH | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG01123 | hp1 | a0001 | c0001 | t0003 | g0316 | AMR | CLM | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG01123 | hp2 | a0002 | c0004 | t0003 | g0069 | AMR | CLM | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG02109 | hp1 | a0002 | c0003 | t0001 | g0091 | AFR | ACB | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0064 | AFR | ACB | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG02486 | hp1 | a0001 | c0009 | t0011 | g0264 | AFR | ACB | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0251 | AFR | ACB | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG02559 | hp1 | a0001 | c0001 | t0017 | g0284 | AFR | ACB | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG02559 | hp2 | a0002 | c0019 | t0011 | g0345 | AFR | ACB | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG03471 | hp1 | a0001 | c0001 | t0008 | g0330 | AFR | MSL | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG03471 | hp2 | a0002 | c0015 | t0007 | g0247 | AFR | MSL | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG06807 | hp1 | a0001 | c0001 | t0011 | g0329 | AFR | USA | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| HG06807 | hp2 | a0001 | c0001 | t0007 | g0327 | AFR | USA | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| NA20300 | hp1 | a0002 | c0004 | t0016 | g0119 | AFR | USA | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| NA20300 | hp2 | a0001 | c0001 | t0046 | g0092 | AFR | USA | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| NA21309 | hp1 | a0001 | c0001 | t0012 | g0342 | AFR | LWK | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| NA21309 | hp2 | a0001 | c0001 | t0004 | g0309 | AFR | LWK | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0006 | t0001 | g0177 | REF | REF | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0012 | g0089 | REF | REF | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
| chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:44615330
|
G | T | 1 | a0003 | 1 | NA18947.hp1 | missense_variant | MODERATE | c.395G>T | p.Arg132Leu | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 7/10 | 571/2212 | 395/804 | 132/267 | chr11 | 44615330 | ||
| chr11:44618718
|
A | G | 1 | a0002 | 181 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(178): Show |
missense_variant | MODERATE | c.721A>G | p.Ile241Val | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 9/10 | 897/2212 | 721/804 | 241/267 | chr11 | 44618718 |
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:44600202
|
C | T | 1 | a0002c0026 | 1 | HG00642.hp2 | synonymous_variant | LOW | c.108C>T | p.Ala36Ala | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 4/10 | 284/2212 | 108/804 | 36/267 | chr11 | 44600202 | ||
| chr11:44605107
|
G | A | 2 | a0001c0016a0002c0019 | 4 | HG02055.hp2 HG02258.hp2 HG02559.hp2 others(1): Show |
synonymous_variant | LOW | c.186G>A | p.Val62Val | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 5/10 | 362/2212 | 186/804 | 62/267 | chr11 | 44605107 | ||
| chr11:44605179
|
G | T | 1 | a0001c0018 | 2 | HG01884.hp1 HG02976.hp1 |
synonymous_variant | LOW | c.258G>T | p.Gly86Gly | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 5/10 | 434/2212 | 258/804 | 86/267 | chr11 | 44605179 | ||
| chr11:44615283
|
G | A | 8 | a0001c0006a0001c0014a0002c0002others(5): Show | 101 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(98): Show |
synonymous_variant | LOW | c.348G>A | p.Glu116Glu | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 7/10 | 524/2212 | 348/804 | 116/267 | chr11 | 44615283 | ||
| chr11:44615289
|
C | T | 6 | a0001c0005a0001c0009a0002c0004others(3): Show | 76 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(73): Show |
synonymous_variant | LOW | c.354C>T | p.Gly118Gly | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 7/10 | 530/2212 | 354/804 | 118/267 | chr11 | 44615289 | ||
| chr11:44615298
|
G | A | 3 | a0001c0011a0001c0023a0002c0017 | 15 | HG00673.hp2 NA18949.hp1 NA18950.hp2 others(12): Show |
synonymous_variant | LOW | c.363G>A | p.Val121Val | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 7/10 | 539/2212 | 363/804 | 121/267 | chr11 | 44615298 | ||
| chr11:44618675
|
G | A | 1 | a0002c0013 | 4 | HG00140.hp1 HG01515.hp2 HG01517.hp2 others(1): Show |
synonymous_variant | LOW | c.678G>A | p.Glu226Glu | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 9/10 | 854/2212 | 678/804 | 226/267 | chr11 | 44618675 | ||
| chr11:44618696
|
C | T | 1 | a0002c0025 | 1 | HG02976.hp2 | synonymous_variant | LOW | c.699C>T | p.Gly233Gly | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 9/10 | 875/2212 | 699/804 | 233/267 | chr11 | 44618696 | ||
| chr11:44618702
|
C | T | 1 | a0002c0021 | 1 | HG00735.hp2 | synonymous_variant | LOW | c.705C>T | p.Gly235Gly | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 9/10 | 881/2212 | 705/804 | 235/267 | chr11 | 44618702 | ||
| chr11:44619066
|
G | C | 2 | a0001c0012a0002c0024 | 6 | HG02451.hp1 HG02717.hp2 HG02970.hp2 others(3): Show |
synonymous_variant | LOW | c.744G>C | p.Leu248Leu | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 10/10 | 920/2212 | 744/804 | 248/267 | chr11 | 44619066 | ||
| chr11:44619090
|
C | G | 9 | a0001c0005a0001c0010a0001c0014others(6): Show | 69 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(66): Show |
synonymous_variant | LOW | c.768C>G | p.Val256Val | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 10/10 | 944/2212 | 768/804 | 256/267 | chr11 | 44619090 | ||
| chr11:44619096
|
C | T | 1 | a0002c0020 | 1 | NA19009.hp1 | synonymous_variant | LOW | c.774C>T | p.Ser258Ser | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 10/10 | 950/2212 | 774/804 | 258/267 | chr11 | 44619096 |
| chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:44587498
|
C | T | 1 | a0001c0001t0051 | 1 | HG02258.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-79C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/10 | chr11 | 44587498 | ||||||
| chr11:44619242
|
T | C | 116 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(113): Show | 361 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(358): Show |
3_prime_UTR_variant | MODIFIER | c.*116T>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 10/10 | 116 | chr11 | 44619242 | |||||
| chr11:44619243
|
C | G | 16 | a0001c0001t0008a0001c0001t0011a0001c0001t0014others(13): Show | 24 | HG01109.hp2 HG01243.hp1 HG01884.hp2 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*117C>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 10/10 | 117 | chr11 | 44619243 | |||||
| chr11:44619373
|
A | C | 2 | a0002c0003t0041a0002c0003t0042 | 2 | HG02145.hp2 HG03139.hp2 |
3_prime_UTR_variant | MODIFIER | c.*247A>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 10/10 | 247 | chr11 | 44619373 | |||||
| chr11:44619475
|
G | A | 10 | a0001c0001t0006a0001c0001t0013a0001c0001t0018others(7): Show | 23 | HG00099.hp1 HG00621.hp2 HG00735.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*349G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 10/10 | 349 | chr11 | 44619475 | |||||
| chr11:44619484
|
C | G | 1 | a0001c0010t0040 | 1 | NA19076.hp1 | 3_prime_UTR_variant | MODIFIER | c.*358C>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 10/10 | 358 | chr11 | 44619484 | |||||
| chr11:44619485
|
G | A | 1 | a0002c0002t0023 | 1 | HG02071.hp1 | 3_prime_UTR_variant | MODIFIER | c.*359G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 10/10 | 359 | chr11 | 44619485 | |||||
| chr11:44619489
|
G | A | 3 | a0001c0001t0025a0001c0001t0026a0001c0006t0024 | 3 | HG03017.hp1 HG03710.hp1 HG04115.hp1 |
3_prime_UTR_variant | MODIFIER | c.*363G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 10/10 | 363 | chr11 | 44619489 | |||||
| chr11:44619508
|
A | G | 1 | a0002c0004t0039 | 1 | NA19000.hp2 | 3_prime_UTR_variant | MODIFIER | c.*382A>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 10/10 | 382 | chr11 | 44619508 | |||||
| chr11:44619529
|
G | A | 1 | a0001c0001t0027 | 1 | NA19240.hp1 | 3_prime_UTR_variant | MODIFIER | c.*403G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 10/10 | 403 | chr11 | 44619529 | |||||
| chr11:44619540
|
A | G | 1 | a0002c0003t0038 | 1 | HG03688.hp2 | 3_prime_UTR_variant | MODIFIER | c.*414A>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 10/10 | 414 | chr11 | 44619540 | |||||
| chr11:44619558
|
C | T | 1 | a0001c0005t0037 | 1 | NA18942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*432C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 10/10 | 432 | chr11 | 44619558 | |||||
| chr11:44619578
|
T | C | 1 | a0002c0003t0043 | 1 | HG01243.hp1 | 3_prime_UTR_variant | MODIFIER | c.*452T>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 10/10 | 452 | chr11 | 44619578 | |||||
| chr11:44619590
|
G | A | 2 | a0002c0003t0028a0002c0003t0044 | 2 | HG02145.hp1 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*464G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 10/10 | 464 | chr11 | 44619590 | |||||
| chr11:44619622
|
G | A | 3 | a0002c0003t0029a0002c0003t0030a0002c0004t0009 | 7 | HG01496.hp1 HG02004.hp1 HG02293.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*496G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 10/10 | 496 | chr11 | 44619622 | |||||
| chr11:44619695
|
C | T | 2 | a0002c0002t0020a0002c0002t0036 | 3 | HG02015.hp1 HG02129.hp1 NA19003.hp1 |
3_prime_UTR_variant | MODIFIER | c.*569C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 10/10 | 569 | chr11 | 44619695 | |||||
| chr11:44619724
|
AC | A | 4 | a0001c0009t0010a0002c0004t0035a0002c0008t0010others(1): Show | 6 | HG02135.hp2 HG02523.hp1 HG03831.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*599delC | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 10/10 | 599 | chr11 | 44619724 | |||||
| chr11:44619763
|
C | CA | 28 | a0001c0001t0004a0001c0001t0011a0001c0001t0017others(25): Show | 52 | HG00099.hp1 HG00597.hp1 HG00609.hp2 others(49): Show |
3_prime_UTR_variant | MODIFIER | c.*663dupA | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 10/10 | 664 | INFO_REALIGN_3_PRIME | chr11 | 44619763 | ||||
| chr11:44619763
|
C | CAA | 7 | a0001c0001t0007a0001c0010t0007a0001c0016t0048others(4): Show | 9 | HG02257.hp2 HG02523.hp2 HG03098.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*662_*663dupAA | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 10/10 | 664 | INFO_REALIGN_3_PRIME | chr11 | 44619763 | ||||
| chr11:44619763
|
CA | C | 30 | a0001c0001t0001a0001c0001t0008a0001c0001t0013others(27): Show | 137 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(134): Show |
3_prime_UTR_variant | MODIFIER | c.*663delA | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 10/10 | 663 | INFO_REALIGN_3_PRIME | chr11 | 44619763 | ||||
| chr11:44619763
|
CAA | C | 24 | a0001c0001t0002a0001c0001t0015a0001c0001t0016others(21): Show | 79 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(76): Show |
3_prime_UTR_variant | MODIFIER | c.*662_*663delAA | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 10/10 | 662 | INFO_REALIGN_3_PRIME | chr11 | 44619763 | ||||
| chr11:44619806
|
G | A | 1 | a0002c0015t0031 | 1 | NA18954.hp1 | 3_prime_UTR_variant | MODIFIER | c.*680G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 10/10 | 680 | chr11 | 44619806 | |||||
| chr11:44619872
|
G | A | 1 | a0001c0010t0040 | 1 | NA19076.hp1 | 3_prime_UTR_variant | MODIFIER | c.*746G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 10/10 | 746 | chr11 | 44619872 | |||||
| chr11:44619873
|
A | C | 1 | a0001c0010t0040 | 1 | NA19076.hp1 | 3_prime_UTR_variant | MODIFIER | c.*747A>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 10/10 | 747 | chr11 | 44619873 | |||||
| chr11:44619935
|
T | C | 1 | a0002c0002t0032 | 1 | NA18939.hp2 | 3_prime_UTR_variant | MODIFIER | c.*809T>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 10/10 | 809 | chr11 | 44619935 | |||||
| chr11:44620029
|
G | A | 2 | a0001c0001t0025a0001c0001t0049 | 2 | HG02622.hp2 HG03710.hp1 |
3_prime_UTR_variant | MODIFIER | c.*903G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 10/10 | 903 | chr11 | 44620029 | |||||
| chr11:44620034
|
A | G | 7 | a0001c0001t0015a0001c0001t0016a0001c0001t0046others(4): Show | 9 | HG01243.hp2 HG02145.hp2 HG02615.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*908A>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 10/10 | 908 | chr11 | 44620034 | |||||
| chr11:44620101
|
A | G | 3 | a0001c0001t0018a0002c0002t0022a0002c0004t0018 | 3 | HG00099.hp1 HG02055.hp1 HG02683.hp2 |
3_prime_UTR_variant | MODIFIER | c.*975A>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 10/10 | 975 | chr11 | 44620101 | |||||
| chr11:44620181
|
G | A | 1 | a0001c0005t0034 | 1 | NA18999.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1055G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 10/10 | 1055 | chr11 | 44620181 | |||||
| chr11:44620198
|
G | A | 1 | a0002c0024t0047 | 1 | HG03453.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1072G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 10/10 | 1072 | chr11 | 44620198 | |||||
| chr11:44620279
|
G | T | 10 | a0001c0001t0005a0001c0001t0006a0001c0001t0013others(7): Show | 26 | HG00621.hp1 HG00621.hp2 HG00741.hp2 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*1153G>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 10/10 | 1153 | chr11 | 44620279 | |||||
| chr11:44620353
|
A | T | 1 | a0001c0010t0040 | 1 | NA19076.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1227A>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 10/10 | 1227 | chr11 | 44620353 |
| chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:44565814
|
G | A | 5 | a0001c0001t0006g0015a0001c0010t0002g0014a0002c0003t0001g0011others(2): Show | 5 | HG01070.hp2 HG01071.hp2 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.-103+78G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44565814 | ||||||
| chr11:44565856
|
G | A | 15 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0027others(12): Show | 21 | HG00423.hp1 HG00621.hp1 HG00733.hp1 others(18): Show |
intron_variant | MODIFIER | c.-103+120G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44565856 | ||||||
| chr11:44565924
|
C | T | 4 | a0001c0001t0001g0353a0001c0001t0001g0354a0001c0001t0001g0356others(1): Show | 4 | HG02083.hp1 NA18950.hp1 NA18962.hp2 others(1): Show |
intron_variant | MODIFIER | c.-103+188C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44565924 | ||||||
| chr11:44566042
|
C | T | 17 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0027others(14): Show | 23 | HG00423.hp1 HG00621.hp1 HG00733.hp1 others(20): Show |
intron_variant | MODIFIER | c.-103+306C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44566042 | ||||||
| chr11:44566044
|
GA | G | 5 | a0001c0001t0006g0015a0001c0010t0002g0014a0002c0003t0001g0011others(2): Show | 5 | HG01070.hp2 HG01071.hp2 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.-103+310delA | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr11 | 44566044 | |||||
| chr11:44566198
|
C | G | 157 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0027others(154): Show | 164 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(161): Show |
intron_variant | MODIFIER | c.-103+462C>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44566198 | ||||||
| chr11:44566290
|
C | T | 1 | a0002c0003t0008g0350 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-103+554C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44566290 | ||||||
| chr11:44566337
|
T | G | 1 | a0002c0002t0002g0225 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-103+601T>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44566337 | ||||||
| chr11:44566449
|
G | A | 35 | a0001c0001t0001g0229a0001c0001t0001g0242a0001c0001t0001g0243others(32): Show | 35 | HG00099.hp1 HG00323.hp2 HG00558.hp1 others(32): Show |
intron_variant | MODIFIER | c.-103+713G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44566449 | ||||||
| chr11:44566473
|
A | G | 1 | a0002c0025t0004g0349 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-103+737A>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44566473 | ||||||
| chr11:44566706
|
T | C | 26 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0027others(23): Show | 32 | HG00423.hp1 HG00621.hp1 HG00733.hp1 others(29): Show |
intron_variant | MODIFIER | c.-103+970T>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44566706 | ||||||
| chr11:44566707
|
G | A | 5 | a0001c0001t0015g0260a0001c0012t0004g0257a0001c0012t0004g0258others(2): Show | 5 | HG02451.hp1 HG02818.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.-103+971G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44566707 | ||||||
| chr11:44566740
|
G | A | 62 | a0001c0001t0001g0287a0001c0001t0001g0288a0001c0001t0001g0308others(59): Show | 63 | HG00099.hp2 HG00140.hp2 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.-103+1004G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44566740 | ||||||
| chr11:44566794
|
C | CT | 8 | a0001c0001t0001g0315a0001c0001t0001g0319a0001c0001t0002g0317others(5): Show | 8 | HG01074.hp2 HG01123.hp1 HG01358.hp1 others(5): Show |
intron_variant | MODIFIER | c.-103+1068dupT | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr11 | 44566794 | |||||
| chr11:44566971
|
A | C | 15 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0027others(12): Show | 21 | HG00423.hp1 HG00621.hp1 HG00733.hp1 others(18): Show |
intron_variant | MODIFIER | c.-103+1235A>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44566971 | ||||||
| chr11:44567204
|
G | A | 141 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0027others(138): Show | 148 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(145): Show |
intron_variant | MODIFIER | c.-103+1468G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44567204 | ||||||
| chr11:44567603
|
G | C | 1 | a0001c0001t0002g0267 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-103+1867G>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44567603 | ||||||
| chr11:44567703
|
C | G | 16 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0027others(13): Show | 22 | HG00423.hp1 HG00621.hp1 HG00733.hp1 others(19): Show |
intron_variant | MODIFIER | c.-103+1967C>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44567703 | ||||||
| chr11:44567714
|
C | T | 15 | a0001c0001t0005g0214a0001c0001t0006g0215a0001c0001t0013g0216others(12): Show | 15 | HG00621.hp2 HG01175.hp1 HG01943.hp2 others(12): Show |
intron_variant | MODIFIER | c.-103+1978C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44567714 | ||||||
| chr11:44567729
|
G | A | 10 | a0001c0001t0012g0342a0001c0001t0049g0343a0001c0006t0003g0344others(7): Show | 10 | HG00639.hp2 HG02559.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.-103+1993G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44567729 | ||||||
| chr11:44567753
|
G | A | 2 | a0001c0016t0017g0030a0001c0016t0048g0031 | 2 | HG02258.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-103+2017G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44567753 | ||||||
| chr11:44567884
|
A | G | 17 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0027others(14): Show | 23 | HG00423.hp1 HG00621.hp1 HG00733.hp1 others(20): Show |
intron_variant | MODIFIER | c.-103+2148A>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44567884 | ||||||
| chr11:44568182
|
C | T | 1 | a0001c0001t0004g0333 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-103+2446C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44568182 | ||||||
| chr11:44568291
|
G | T | 172 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0027others(169): Show | 179 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.-103+2555G>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44568291 | ||||||
| chr11:44568353
|
C | G | 6 | a0001c0001t0001g0332a0001c0001t0007g0327a0001c0001t0008g0330others(3): Show | 6 | HG01884.hp2 HG03041.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.-103+2617C>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44568353 | ||||||
| chr11:44568512
|
T | A | 1 | a0001c0009t0001g0032 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.-103+2776T>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44568512 | ||||||
| chr11:44568531
|
A | G | 17 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0027others(14): Show | 23 | HG00423.hp1 HG00621.hp1 HG00733.hp1 others(20): Show |
intron_variant | MODIFIER | c.-103+2795A>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44568531 | ||||||
| chr11:44568655
|
T | C | 1 | a0001c0001t0027g0322 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-103+2919T>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44568655 | ||||||
| chr11:44568683
|
C | T | 17 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0027others(14): Show | 23 | HG00423.hp1 HG00621.hp1 HG00733.hp1 others(20): Show |
intron_variant | MODIFIER | c.-103+2947C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44568683 | ||||||
| chr11:44568706
|
G | A | 5 | a0001c0001t0001g0033a0001c0016t0017g0030a0001c0016t0048g0031others(2): Show | 5 | HG02258.hp2 HG03195.hp2 NA18942.hp2 others(2): Show |
intron_variant | MODIFIER | c.-103+2970G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44568706 | ||||||
| chr11:44568737
|
G | A | 1 | a0001c0006t0001g0036 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-103+3001G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44568737 | ||||||
| chr11:44568776
|
G | A | 1 | a0001c0001t0004g0037 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-103+3040G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44568776 | ||||||
| chr11:44568805
|
C | A | 17 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0027others(14): Show | 23 | HG00423.hp1 HG00621.hp1 HG00733.hp1 others(20): Show |
intron_variant | MODIFIER | c.-103+3069C>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44568805 | ||||||
| chr11:44568884
|
G | A | 1 | a0001c0001t0004g0333 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-103+3148G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44568884 | ||||||
| chr11:44569023
|
C | T | 1 | a0001c0001t0013g0222 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.-103+3287C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44569023 | ||||||
| chr11:44569045
|
G | A | 2 | a0001c0001t0051g0223a0001c0009t0015g0224 | 2 | HG02258.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.-103+3309G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44569045 | ||||||
| chr11:44569152
|
A | G | 1 | a0001c0011t0005g0314 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.-103+3416A>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44569152 | ||||||
| chr11:44569161
|
G | A | 7 | a0001c0001t0006g0015a0001c0010t0001g0211a0001c0010t0001g0212others(4): Show | 7 | HG00639.hp1 HG01070.hp2 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.-103+3425G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44569161 | ||||||
| chr11:44569168
|
A | T | 2 | a0001c0001t0051g0223a0001c0009t0015g0224 | 2 | HG02258.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.-103+3432A>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44569168 | ||||||
| chr11:44569179
|
G | A | 146 | a0001c0001t0001g0229a0001c0001t0001g0242a0001c0001t0001g0243others(143): Show | 147 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(144): Show |
intron_variant | MODIFIER | c.-103+3443G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44569179 | ||||||
| chr11:44569310
|
C | T | 2 | a0001c0005t0002g0209a0001c0005t0003g0210 | 2 | NA18998.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.-103+3574C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44569310 | ||||||
| chr11:44569323
|
G | A | 3 | a0001c0018t0012g0269a0002c0003t0008g0350a0002c0003t0044g0268 | 3 | HG01884.hp1 HG02145.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.-103+3587G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44569323 | ||||||
| chr11:44569340
|
G | A | 1 | a0002c0004t0019g0039 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-103+3604G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44569340 | ||||||
| chr11:44569466
|
T | C | 2 | a0002c0007t0002g0040a0002c0007t0002g0041 | 2 | HG01099.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.-103+3730T>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44569466 | ||||||
| chr11:44569703
|
T | G | 1 | a0002c0002t0003g0348 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.-103+3967T>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44569703 | ||||||
| chr11:44569748
|
C | T | 1 | a0001c0001t0004g0037 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-103+4012C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44569748 | ||||||
| chr11:44569807
|
G | C | 2 | a0002c0004t0002g0226a0002c0004t0002g0227 | 2 | NA18954.hp2 NA18963.hp1 |
intron_variant | MODIFIER | c.-103+4071G>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44569807 | ||||||
| chr11:44569818
|
G | A | 6 | a0001c0001t0012g0342a0001c0001t0049g0343a0001c0012t0003g0340others(3): Show | 6 | HG02622.hp2 HG02717.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.-103+4082G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44569818 | ||||||
| chr11:44569882
|
A | T | 68 | a0001c0001t0001g0287a0001c0001t0001g0288a0001c0001t0001g0308others(65): Show | 69 | HG00099.hp2 HG00140.hp2 HG00597.hp2 others(66): Show |
intron_variant | MODIFIER | c.-103+4146A>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44569882 | ||||||
| chr11:44569954
|
A | T | 1 | a0003c0022t0004g0207 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.-103+4218A>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44569954 | ||||||
| chr11:44570189
|
C | T | 3 | a0001c0005t0001g0204a0001c0005t0001g0205a0001c0005t0002g0206 | 3 | HG00408.hp2 HG02129.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.-103+4453C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44570189 | ||||||
| chr11:44570232
|
CTGGCTGC others(43): Show |
C | 1 | a0001c0001t0004g0321 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-103+4549_-103+459 others(54): Show |
CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr11 | 44570232 | |||||
| chr11:44570273
|
C | T | 20 | a0001c0001t0026g0190a0001c0006t0001g0036a0001c0006t0001g0199others(17): Show | 20 | HG00609.hp1 HG00673.hp2 HG01168.hp1 others(17): Show |
intron_variant | MODIFIER | c.-103+4537C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44570273 | ||||||
| chr11:44570469
|
C | T | 1 | a0002c0004t0003g0186 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.-103+4733C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44570469 | ||||||
| chr11:44570624
|
G | C | 167 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0027others(164): Show | 174 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(171): Show |
intron_variant | MODIFIER | c.-103+4888G>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44570624 | ||||||
| chr11:44570691
|
GCTT | G | 7 | a0001c0001t0001g0044a0001c0001t0001g0047a0002c0002t0001g0042others(4): Show | 7 | HG01255.hp1 HG01928.hp1 HG01943.hp1 others(4): Show |
intron_variant | MODIFIER | c.-103+4958_-103+496 others(7): Show |
CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr11 | 44570691 | |||||
| chr11:44570707
|
C | T | 3 | a0001c0012t0016g0313a0002c0003t0041g0312a0002c0003t0042g0311 | 3 | HG02145.hp2 HG02717.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-103+4971C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44570707 | ||||||
| chr11:44570719
|
TTTA | T | 220 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0020others(217): Show | 228 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(225): Show |
intron_variant | MODIFIER | c.-103+4987_-103+498 others(7): Show |
CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr11 | 44570719 | |||||
| chr11:44570728
|
C | T | 1 | a0002c0002t0007g0028 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.-103+4992C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44570728 | ||||||
| chr11:44570813
|
G | C | 1 | a0002c0002t0003g0187 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-103+5077G>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44570813 | ||||||
| chr11:44571052
|
T | C | 6 | a0001c0001t0001g0332a0001c0001t0007g0327a0001c0001t0008g0330others(3): Show | 6 | HG01884.hp2 HG03041.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.-103+5316T>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44571052 | ||||||
| chr11:44571125
|
G | A | 2 | a0001c0001t0004g0323a0001c0001t0015g0352 | 2 | HG03098.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-103+5389G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44571125 | ||||||
| chr11:44571158
|
G | A | 39 | a0001c0001t0001g0229a0001c0001t0001g0242a0001c0001t0001g0243others(36): Show | 39 | HG00099.hp1 HG00323.hp2 HG00558.hp1 others(36): Show |
intron_variant | MODIFIER | c.-103+5422G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44571158 | ||||||
| chr11:44571189
|
G | A | 1 | a0002c0008t0004g0088 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.-103+5453G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44571189 | ||||||
| chr11:44571278
|
C | G | 2 | a0001c0016t0004g0351a0002c0003t0002g0038 | 2 | HG02055.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-103+5542C>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44571278 | ||||||
| chr11:44571384
|
A | G | 356 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(353): Show | 365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.-103+5648A>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44571384 | ||||||
| chr11:44571405
|
C | T | 7 | a0001c0001t0015g0260a0001c0012t0004g0257a0001c0012t0004g0258others(4): Show | 7 | HG02055.hp2 HG02451.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.-103+5669C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44571405 | ||||||
| chr11:44571479
|
T | C | 2 | a0001c0001t0008g0266a0001c0005t0001g0265 | 2 | HG02922.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.-103+5743T>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44571479 | ||||||
| chr11:44571543
|
A | G | 22 | a0001c0001t0005g0214a0001c0001t0006g0015a0001c0001t0006g0215others(19): Show | 22 | HG00621.hp2 HG00639.hp1 HG01070.hp2 others(19): Show |
intron_variant | MODIFIER | c.-103+5807A>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44571543 | ||||||
| chr11:44571655
|
A | C | 2 | a0002c0003t0003g0256a0002c0003t0004g0255 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-103+5919A>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44571655 | ||||||
| chr11:44571866
|
G | A | 1 | a0001c0001t0003g0017 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-103+6130G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44571866 | ||||||
| chr11:44571954
|
C | A | 1 | a0001c0001t0003g0096 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.-103+6218C>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44571954 | ||||||
| chr11:44572116
|
G | A | 2 | a0001c0001t0008g0266a0001c0005t0001g0265 | 2 | HG02922.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.-103+6380G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44572116 | ||||||
| chr11:44572238
|
C | T | 3 | a0001c0018t0012g0269a0002c0003t0008g0350a0002c0003t0044g0268 | 3 | HG01884.hp1 HG02145.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.-103+6502C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44572238 | ||||||
| chr11:44572256
|
C | T | 167 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0027others(164): Show | 174 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(171): Show |
intron_variant | MODIFIER | c.-103+6520C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44572256 | ||||||
| chr11:44572280
|
G | A | 22 | a0001c0001t0005g0214a0001c0001t0006g0015a0001c0001t0006g0215others(19): Show | 22 | HG00621.hp2 HG00639.hp1 HG01070.hp2 others(19): Show |
intron_variant | MODIFIER | c.-103+6544G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44572280 | ||||||
| chr11:44572283
|
A | G | 2 | a0001c0001t0004g0323a0001c0001t0015g0352 | 2 | HG03098.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-103+6547A>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44572283 | ||||||
| chr11:44572334
|
T | A | 39 | a0001c0001t0001g0229a0001c0001t0001g0242a0001c0001t0001g0243others(36): Show | 39 | HG00099.hp1 HG00323.hp2 HG00558.hp1 others(36): Show |
intron_variant | MODIFIER | c.-103+6598T>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44572334 | ||||||
| chr11:44572620
|
CAA | C | 80 | a0001c0001t0001g0287a0001c0001t0001g0288a0001c0001t0001g0308others(77): Show | 81 | HG00099.hp2 HG00140.hp2 HG00597.hp2 others(78): Show |
intron_variant | MODIFIER | c.-103+6885_-103+688 others(6): Show |
CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44572620 | ||||||
| chr11:44572810
|
T | C | 167 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0027others(164): Show | 174 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(171): Show |
intron_variant | MODIFIER | c.-103+7074T>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44572810 | ||||||
| chr11:44572817
|
T | TATGG | 59 | a0001c0001t0001g0287a0001c0001t0001g0288a0001c0001t0001g0308others(56): Show | 60 | HG00099.hp2 HG00140.hp2 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.-103+7083_-103+708 others(8): Show |
CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr11 | 44572817 | |||||
| chr11:44572837
|
C | A | 2 | a0001c0001t0008g0266a0001c0005t0001g0265 | 2 | HG02922.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.-103+7101C>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44572837 | ||||||
| chr11:44572841
|
T | C | 169 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0027others(166): Show | 176 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(173): Show |
intron_variant | MODIFIER | c.-103+7105T>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44572841 | ||||||
| chr11:44572905
|
CAG | C | 70 | a0001c0001t0001g0287a0001c0001t0001g0288a0001c0001t0001g0308others(67): Show | 71 | HG00099.hp2 HG00140.hp2 HG00597.hp2 others(68): Show |
intron_variant | MODIFIER | c.-103+7172_-103+717 others(6): Show |
CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr11 | 44572905 | |||||
| chr11:44573004
|
G | T | 3 | a0001c0001t0002g0184a0001c0006t0003g0185a0001c0014t0002g0183 | 3 | NA19012.hp2 NA19081.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.-103+7268G>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44573004 | ||||||
| chr11:44573029
|
C | T | 1 | a0002c0002t0003g0187 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-103+7293C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44573029 | ||||||
| chr11:44573061
|
T | A | 106 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0027others(103): Show | 113 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(110): Show |
intron_variant | MODIFIER | c.-103+7325T>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44573061 | ||||||
| chr11:44573090
|
G | A | 39 | a0001c0001t0001g0229a0001c0001t0001g0242a0001c0001t0001g0243others(36): Show | 39 | HG00099.hp1 HG00323.hp2 HG00558.hp1 others(36): Show |
intron_variant | MODIFIER | c.-103+7354G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44573090 | ||||||
| chr11:44573127
|
A | G | 1 | a0001c0001t0018g0182 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-103+7391A>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44573127 | ||||||
| chr11:44573145
|
T | A | 8 | a0001c0001t0001g0315a0001c0001t0002g0267a0001c0001t0003g0316others(5): Show | 9 | HG00099.hp2 HG01123.hp1 HG01257.hp2 others(6): Show |
intron_variant | MODIFIER | c.-103+7409T>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44573145 | ||||||
| chr11:44573187
|
G | C | 6 | a0001c0001t0001g0332a0001c0001t0007g0327a0001c0001t0008g0330others(3): Show | 6 | HG01884.hp2 HG03041.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.-103+7451G>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44573187 | ||||||
| chr11:44573190
|
TATGTGTT others(17): Show |
T | 65 | a0001c0001t0001g0229a0001c0001t0001g0242a0001c0001t0001g0243others(62): Show | 65 | HG00099.hp1 HG00323.hp2 HG00558.hp1 others(62): Show |
intron_variant | MODIFIER | c.-103+7456_-103+747 others(28): Show |
CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr11 | 44573190 | |||||
| chr11:44573241
|
C | T | 2 | a0001c0001t0051g0223a0001c0009t0015g0224 | 2 | HG02258.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.-103+7505C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44573241 | ||||||
| chr11:44573300
|
T | C | 15 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0027others(12): Show | 21 | HG00423.hp1 HG00621.hp1 HG00733.hp1 others(18): Show |
intron_variant | MODIFIER | c.-103+7564T>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44573300 | ||||||
| chr11:44573384
|
C | T | 13 | a0001c0001t0001g0250a0001c0001t0001g0251a0001c0001t0004g0249others(10): Show | 13 | HG02280.hp2 HG02486.hp1 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.-103+7648C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44573384 | ||||||
| chr11:44573555
|
T | A | 2 | a0001c0001t0008g0266a0001c0005t0001g0265 | 2 | HG02922.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.-103+7819T>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44573555 | ||||||
| chr11:44573556
|
C | T | 2 | a0001c0001t0008g0266a0001c0005t0001g0265 | 2 | HG02922.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.-103+7820C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44573556 | ||||||
| chr11:44573590
|
G | A | 12 | a0001c0001t0003g0104a0001c0005t0002g0209a0001c0005t0003g0097others(9): Show | 12 | HG02074.hp2 NA18949.hp2 NA18951.hp2 others(9): Show |
intron_variant | MODIFIER | c.-103+7854G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44573590 | ||||||
| chr11:44573674
|
T | C | 88 | a0001c0001t0001g0287a0001c0001t0001g0288a0001c0001t0001g0308others(85): Show | 89 | HG00099.hp2 HG00140.hp2 HG00597.hp2 others(86): Show |
intron_variant | MODIFIER | c.-103+7938T>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44573674 | ||||||
| chr11:44573899
|
G | A | 6 | a0001c0001t0001g0332a0001c0001t0007g0327a0001c0001t0008g0330others(3): Show | 6 | HG01884.hp2 HG03041.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.-103+8163G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44573899 | ||||||
| chr11:44574091
|
T | TG | 7 | a0001c0001t0015g0260a0001c0012t0004g0257a0001c0012t0004g0258others(4): Show | 7 | HG02055.hp2 HG02451.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.-103+8361dupG | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr11 | 44574091 | |||||
| chr11:44574144
|
T | C | 1 | a0001c0001t0004g0333 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-103+8408T>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44574144 | ||||||
| chr11:44574159
|
G | C | 92 | a0001c0001t0001g0287a0001c0001t0001g0288a0001c0001t0001g0308others(89): Show | 93 | HG00099.hp2 HG00140.hp2 HG00597.hp2 others(90): Show |
intron_variant | MODIFIER | c.-103+8423G>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44574159 | ||||||
| chr11:44574173
|
G | C | 1 | a0002c0003t0028g0262 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-103+8437G>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44574173 | ||||||
| chr11:44574212
|
G | A | 2 | a0001c0001t0008g0266a0001c0005t0001g0265 | 2 | HG02922.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.-103+8476G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44574212 | ||||||
| chr11:44574306
|
G | A | 1 | a0001c0005t0002g0048 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.-103+8570G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44574306 | ||||||
| chr11:44574319
|
C | T | 91 | a0001c0001t0001g0287a0001c0001t0001g0288a0001c0001t0001g0308others(88): Show | 92 | HG00099.hp2 HG00140.hp2 HG00597.hp2 others(89): Show |
intron_variant | MODIFIER | c.-103+8583C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44574319 | ||||||
| chr11:44574416
|
T | G | 91 | a0001c0001t0001g0287a0001c0001t0001g0288a0001c0001t0001g0308others(88): Show | 92 | HG00099.hp2 HG00140.hp2 HG00597.hp2 others(89): Show |
intron_variant | MODIFIER | c.-103+8680T>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44574416 | ||||||
| chr11:44574486
|
C | A | 7 | a0001c0001t0006g0015a0001c0010t0001g0211a0001c0010t0001g0212others(4): Show | 7 | HG00639.hp1 HG01070.hp2 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.-103+8750C>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44574486 | ||||||
| chr11:44574606
|
G | GT | 15 | a0001c0001t0001g0027a0001c0001t0003g0310a0001c0001t0004g0254others(12): Show | 15 | HG01099.hp2 HG02055.hp1 HG02148.hp1 others(12): Show |
intron_variant | MODIFIER | c.-103+8878dupT | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr11 | 44574606 | |||||
| chr11:44574636
|
C | T | 1 | a0001c0009t0011g0264 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-103+8900C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44574636 | ||||||
| chr11:44574836
|
C | G | 2 | a0001c0001t0008g0266a0001c0005t0001g0265 | 2 | HG02922.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.-103+9100C>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44574836 | ||||||
| chr11:44574878
|
G | A | 8 | a0001c0001t0001g0229a0002c0002t0001g0233a0002c0002t0003g0231others(5): Show | 8 | HG00099.hp1 HG00323.hp2 HG00738.hp1 others(5): Show |
intron_variant | MODIFIER | c.-103+9142G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44574878 | ||||||
| chr11:44574952
|
G | A | 1 | a0001c0001t0007g0327 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-103+9216G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44574952 | ||||||
| chr11:44574974
|
G | A | 15 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0027others(12): Show | 21 | HG00423.hp1 HG00621.hp1 HG00733.hp1 others(18): Show |
intron_variant | MODIFIER | c.-103+9238G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44574974 | ||||||
| chr11:44575035
|
G | A | 3 | a0001c0012t0004g0257a0001c0012t0004g0258a0002c0003t0014g0259 | 3 | HG02451.hp1 HG02970.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.-103+9299G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44575035 | ||||||
| chr11:44575267
|
A | G | 36 | a0001c0001t0001g0229a0001c0001t0001g0242a0001c0001t0001g0243others(33): Show | 36 | HG00099.hp1 HG00323.hp2 HG00558.hp1 others(33): Show |
intron_variant | MODIFIER | c.-103+9531A>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44575267 | ||||||
| chr11:44575358
|
C | T | 1 | a0001c0001t0008g0266 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-103+9622C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44575358 | ||||||
| chr11:44575407
|
G | A | 1 | a0002c0002t0023g0106 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.-103+9671G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44575407 | ||||||
| chr11:44575452
|
ACT | A | 9 | a0001c0001t0008g0266a0001c0001t0051g0223a0001c0005t0001g0265others(6): Show | 9 | HG01884.hp1 HG02055.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.-103+9719_-103+972 others(6): Show |
CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr11 | 44575452 | |||||
| chr11:44575601
|
G | A | 15 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0027others(12): Show | 21 | HG00423.hp1 HG00621.hp1 HG00733.hp1 others(18): Show |
intron_variant | MODIFIER | c.-103+9865G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44575601 | ||||||
| chr11:44575746
|
T | C | 1 | a0001c0009t0001g0086 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-103+10010T>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44575746 | ||||||
| chr11:44575998
|
A | C | 3 | a0001c0018t0012g0269a0002c0003t0008g0350a0002c0003t0044g0268 | 3 | HG01884.hp1 HG02145.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.-103+10262A>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44575998 | ||||||
| chr11:44576028
|
G | A | 3 | a0001c0018t0012g0269a0002c0003t0008g0350a0002c0003t0044g0268 | 3 | HG01884.hp1 HG02145.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.-103+10292G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44576028 | ||||||
| chr11:44576335
|
G | C | 1 | a0002c0002t0003g0107 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-103+10599G>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44576335 | ||||||
| chr11:44576397
|
C | T | 3 | a0001c0018t0012g0269a0002c0003t0008g0350a0002c0003t0044g0268 | 3 | HG01884.hp1 HG02145.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.-103+10661C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44576397 | ||||||
| chr11:44576530
|
C | T | 3 | a0001c0018t0012g0269a0002c0003t0008g0350a0002c0003t0044g0268 | 3 | HG01884.hp1 HG02145.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.-103+10794C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44576530 | ||||||
| chr11:44576532
|
G | A | 24 | a0001c0001t0001g0033a0001c0001t0003g0108a0001c0001t0005g0214others(21): Show | 24 | HG00621.hp2 HG00639.hp1 HG01070.hp2 others(21): Show |
intron_variant | MODIFIER | c.-103+10796G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44576532 | ||||||
| chr11:44576553
|
A | G | 1 | a0001c0012t0004g0179 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-103+10817A>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44576553 | ||||||
| chr11:44576602
|
G | A | 4 | a0001c0001t0004g0333a0001c0001t0015g0260a0001c0001t0015g0263others(1): Show | 4 | HG02615.hp1 HG02818.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.-103+10866G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44576602 | ||||||
| chr11:44576685
|
A | G | 175 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0027others(172): Show | 182 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(179): Show |
intron_variant | MODIFIER | c.-102-10790A>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44576685 | ||||||
| chr11:44576753
|
A | G | 2 | a0001c0006t0001g0177a0001c0006t0003g0178 | 2 | NA20752.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.-102-10722A>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44576753 | ||||||
| chr11:44576773
|
T | C | 175 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0027others(172): Show | 182 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(179): Show |
intron_variant | MODIFIER | c.-102-10702T>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44576773 | ||||||
| chr11:44576845
|
T | G | 4 | a0001c0012t0004g0257a0001c0012t0004g0258a0002c0003t0014g0259others(1): Show | 4 | HG02451.hp1 HG02970.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.-102-10630T>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44576845 | ||||||
| chr11:44576868
|
G | A | 35 | a0001c0001t0001g0229a0001c0001t0001g0242a0001c0001t0001g0243others(32): Show | 35 | HG00099.hp1 HG00323.hp2 HG00558.hp1 others(32): Show |
intron_variant | MODIFIER | c.-102-10607G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44576868 | ||||||
| chr11:44576886
|
A | G | 277 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(274): Show | 285 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(282): Show |
intron_variant | MODIFIER | c.-102-10589A>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44576886 | ||||||
| chr11:44576887
|
G | A | 202 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(199): Show | 204 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(201): Show |
intron_variant | MODIFIER | c.-102-10588G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44576887 | ||||||
| chr11:44576963
|
G | T | 1 | a0002c0007t0004g0347 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-102-10512G>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44576963 | ||||||
| chr11:44577083
|
C | T | 1 | a0001c0001t0001g0308 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-102-10392C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44577083 | ||||||
| chr11:44577084
|
G | T | 1 | a0001c0001t0001g0308 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-102-10391G>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44577084 | ||||||
| chr11:44577100
|
C | A | 2 | a0001c0001t0004g0323a0001c0001t0015g0352 | 2 | HG03098.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-102-10375C>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44577100 | ||||||
| chr11:44577206
|
A | G | 1 | a0002c0003t0001g0085 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.-102-10269A>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44577206 | ||||||
| chr11:44577224
|
G | A | 2 | a0001c0016t0017g0030a0001c0016t0048g0031 | 2 | HG02258.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-102-10251G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44577224 | ||||||
| chr11:44577464
|
C | T | 3 | a0001c0016t0004g0351a0002c0003t0002g0038a0002c0017t0001g0202 | 3 | HG02055.hp2 NA19067.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-102-10011C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44577464 | ||||||
| chr11:44577525
|
C | T | 2 | a0001c0001t0046g0092a0002c0003t0001g0091 | 2 | HG02109.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-102-9950C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44577525 | ||||||
| chr11:44577658
|
G | A | 1 | a0002c0003t0044g0268 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-102-9817G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44577658 | ||||||
| chr11:44577676
|
T | C | 12 | a0001c0001t0003g0108a0001c0001t0006g0015a0001c0010t0001g0211others(9): Show | 12 | HG00639.hp1 HG01070.hp2 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.-102-9799T>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44577676 | ||||||
| chr11:44577818
|
A | G | 1 | a0001c0001t0018g0182 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-102-9657A>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44577818 | ||||||
| chr11:44577828
|
G | A | 1 | a0002c0007t0002g0049 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-102-9647G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44577828 | ||||||
| chr11:44577894
|
G | A | 1 | a0001c0001t0007g0327 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-102-9581G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44577894 | ||||||
| chr11:44577993
|
C | T | 23 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0027others(20): Show | 29 | HG00423.hp1 HG00621.hp1 HG00733.hp1 others(26): Show |
intron_variant | MODIFIER | c.-102-9482C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44577993 | ||||||
| chr11:44578110
|
G | A | 1 | a0002c0008t0002g0109 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.-102-9365G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44578110 | ||||||
| chr11:44578213
|
AC | A | 12 | a0001c0001t0003g0108a0001c0001t0006g0015a0001c0010t0001g0211others(9): Show | 12 | HG00639.hp1 HG01070.hp2 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.-102-9259delC | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr11 | 44578213 | |||||
| chr11:44578285
|
G | A | 1 | a0002c0002t0003g0050 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.-102-9190G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44578285 | ||||||
| chr11:44578560
|
A | G | 9 | a0001c0001t0004g0094a0001c0001t0004g0323a0001c0001t0015g0352others(6): Show | 9 | HG01109.hp1 HG02257.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.-102-8915A>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44578560 | ||||||
| chr11:44578660
|
C | T | 3 | a0001c0012t0016g0313a0002c0003t0041g0312a0002c0003t0042g0311 | 3 | HG02145.hp2 HG02717.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-102-8815C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44578660 | ||||||
| chr11:44578742
|
C | T | 8 | a0001c0001t0001g0033a0001c0011t0001g0334a0001c0011t0001g0336others(5): Show | 8 | NA18942.hp2 NA18965.hp2 NA18970.hp1 others(5): Show |
intron_variant | MODIFIER | c.-102-8733C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44578742 | ||||||
| chr11:44578858
|
A | G | 362 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(359): Show | 371 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(368): Show |
intron_variant | MODIFIER | c.-102-8617A>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44578858 | ||||||
| chr11:44578900
|
T | C | 2 | a0002c0015t0003g0339a0002c0025t0004g0349 | 2 | HG02717.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.-102-8575T>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44578900 | ||||||
| chr11:44579053
|
A | G | 1 | a0002c0015t0003g0339 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-102-8422A>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44579053 | ||||||
| chr11:44579104
|
A | G | 8 | a0001c0001t0003g0108a0001c0001t0006g0015a0001c0010t0001g0211others(5): Show | 8 | HG00639.hp1 HG01070.hp2 HG01071.hp2 others(5): Show |
intron_variant | MODIFIER | c.-102-8371A>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44579104 | ||||||
| chr11:44579147
|
T | A | 1 | a0002c0003t0001g0085 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.-102-8328T>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44579147 | ||||||
| chr11:44579168
|
A | G | 12 | a0001c0001t0003g0108a0001c0001t0006g0015a0001c0010t0001g0211others(9): Show | 12 | HG00639.hp1 HG01070.hp2 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.-102-8307A>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44579168 | ||||||
| chr11:44579183
|
G | A | 12 | a0001c0001t0003g0108a0001c0001t0006g0015a0001c0010t0001g0211others(9): Show | 12 | HG00639.hp1 HG01070.hp2 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.-102-8292G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44579183 | ||||||
| chr11:44579240
|
A | G | 172 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0027others(169): Show | 179 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.-102-8235A>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44579240 | ||||||
| chr11:44579256
|
G | T | 1 | a0002c0002t0001g0046 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-102-8219G>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44579256 | ||||||
| chr11:44579285
|
G | A | 8 | a0001c0001t0003g0108a0001c0001t0006g0015a0001c0010t0001g0211others(5): Show | 8 | HG00639.hp1 HG01070.hp2 HG01071.hp2 others(5): Show |
intron_variant | MODIFIER | c.-102-8190G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44579285 | ||||||
| chr11:44579290
|
T | C | 12 | a0001c0001t0003g0108a0001c0001t0006g0015a0001c0010t0001g0211others(9): Show | 12 | HG00639.hp1 HG01070.hp2 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.-102-8185T>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44579290 | ||||||
| chr11:44579426
|
G | A | 1 | a0001c0001t0027g0322 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-102-8049G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44579426 | ||||||
| chr11:44579433
|
C | A | 2 | a0001c0001t0001g0229a0002c0004t0002g0228 | 2 | HG01167.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.-102-8042C>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44579433 | ||||||
| chr11:44579493
|
G | A | 36 | a0001c0001t0001g0229a0001c0001t0001g0242a0001c0001t0001g0243others(33): Show | 36 | HG00099.hp1 HG00323.hp2 HG00558.hp1 others(33): Show |
intron_variant | MODIFIER | c.-102-7982G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44579493 | ||||||
| chr11:44579564
|
C | T | 185 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(182): Show | 187 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(184): Show |
intron_variant | MODIFIER | c.-102-7911C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44579564 | ||||||
| chr11:44579619
|
G | A | 1 | a0001c0001t0014g0213 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-102-7856G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44579619 | ||||||
| chr11:44579638
|
C | T | 1 | a0002c0003t0004g0346 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-102-7837C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44579638 | ||||||
| chr11:44579710
|
G | A | 32 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0027others(29): Show | 38 | HG00423.hp1 HG00621.hp1 HG00621.hp2 others(35): Show |
intron_variant | MODIFIER | c.-102-7765G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44579710 | ||||||
| chr11:44579713
|
G | A | 3 | a0001c0006t0001g0036a0002c0002t0002g0188a0002c0002t0002g0189 | 3 | HG00609.hp1 HG02056.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.-102-7762G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44579713 | ||||||
| chr11:44579736
|
G | A | 22 | a0001c0001t0001g0003a0001c0001t0001g0051a0001c0001t0001g0058others(19): Show | 24 | HG00140.hp1 HG00323.hp1 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.-102-7739G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44579736 | ||||||
| chr11:44579949
|
A | T | 185 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(182): Show | 187 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(184): Show |
intron_variant | MODIFIER | c.-102-7526A>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44579949 | ||||||
| chr11:44580406
|
G | T | 186 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(183): Show | 188 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(185): Show |
intron_variant | MODIFIER | c.-102-7069G>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44580406 | ||||||
| chr11:44580457
|
G | C | 1 | a0001c0005t0003g0097 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.-102-7018G>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44580457 | ||||||
| chr11:44580542
|
G | A | 1 | a0001c0005t0003g0097 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.-102-6933G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44580542 | ||||||
| chr11:44580788
|
G | A | 16 | a0001c0001t0001g0033a0001c0001t0005g0214a0001c0001t0006g0215others(13): Show | 16 | HG00621.hp2 HG01175.hp1 HG01943.hp2 others(13): Show |
intron_variant | MODIFIER | c.-102-6687G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44580788 | ||||||
| chr11:44580885
|
C | T | 1 | a0001c0001t0027g0322 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-102-6590C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44580885 | ||||||
| chr11:44580891
|
G | C | 357 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(354): Show | 366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.-102-6584G>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44580891 | ||||||
| chr11:44580928
|
G | T | 1 | a0001c0001t0007g0327 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-102-6547G>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44580928 | ||||||
| chr11:44581066
|
T | C | 1 | a0002c0002t0001g0042 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.-102-6409T>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44581066 | ||||||
| chr11:44581157
|
G | C | 1 | a0002c0004t0009g0237 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-102-6318G>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44581157 | ||||||
| chr11:44581231
|
G | A | 16 | a0001c0001t0001g0033a0001c0001t0005g0214a0001c0001t0006g0215others(13): Show | 16 | HG00621.hp2 HG01175.hp1 HG01943.hp2 others(13): Show |
intron_variant | MODIFIER | c.-102-6244G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44581231 | ||||||
| chr11:44581378
|
A | C | 2 | a0001c0016t0004g0351a0002c0003t0002g0038 | 2 | HG02055.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-102-6097A>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44581378 | ||||||
| chr11:44581425
|
T | C | 2 | a0001c0016t0004g0351a0002c0003t0002g0038 | 2 | HG02055.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-102-6050T>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44581425 | ||||||
| chr11:44581704
|
C | T | 2 | a0001c0009t0004g0084a0002c0004t0003g0186 | 2 | HG02630.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.-102-5771C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44581704 | ||||||
| chr11:44581730
|
T | A | 1 | a0001c0001t0027g0322 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-102-5745T>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44581730 | ||||||
| chr11:44581778
|
A | G | 258 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0044others(255): Show | 259 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(256): Show |
intron_variant | MODIFIER | c.-102-5697A>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44581778 | ||||||
| chr11:44581796
|
C | G | 1 | a0001c0005t0002g0175 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.-102-5679C>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44581796 | ||||||
| chr11:44581913
|
G | A | 3 | a0001c0006t0001g0115a0001c0006t0002g0116a0001c0010t0001g0117 | 3 | HG00438.hp1 HG02135.hp1 NA18941.hp1 |
intron_variant | MODIFIER | c.-102-5562G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44581913 | ||||||
| chr11:44582047
|
T | C | 255 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(252): Show | 257 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(254): Show |
intron_variant | MODIFIER | c.-102-5428T>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44582047 | ||||||
| chr11:44582059
|
G | T | 31 | a0001c0001t0001g0332a0001c0001t0004g0094a0001c0001t0004g0323others(28): Show | 31 | HG00639.hp2 HG01109.hp1 HG01884.hp1 others(28): Show |
intron_variant | MODIFIER | c.-102-5416G>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44582059 | ||||||
| chr11:44582073
|
G | A | 5 | a0001c0010t0008g0248a0002c0003t0003g0256a0002c0003t0004g0252others(2): Show | 5 | HG02280.hp2 HG02818.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.-102-5402G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44582073 | ||||||
| chr11:44582088
|
A | G | 4 | a0001c0012t0004g0257a0001c0012t0004g0258a0002c0003t0014g0259others(1): Show | 4 | HG02451.hp1 HG02970.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.-102-5387A>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44582088 | ||||||
| chr11:44582157
|
G | A | 2 | a0002c0003t0001g0007a0002c0003t0003g0007 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.-102-5318G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44582157 | ||||||
| chr11:44582194
|
T | TG | 351 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(348): Show | 354 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(351): Show |
intron_variant | MODIFIER | c.-102-5277dupG | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr11 | 44582194 | |||||
| chr11:44582231
|
C | T | 2 | a0001c0005t0001g0205a0001c0005t0002g0206 | 2 | HG00408.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.-102-5244C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44582231 | ||||||
| chr11:44582271
|
G | A | 7 | a0001c0001t0004g0094a0001c0010t0004g0093a0001c0010t0007g0095others(4): Show | 7 | HG01109.hp1 HG02257.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.-102-5204G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44582271 | ||||||
| chr11:44582341
|
C | T | 235 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(232): Show | 237 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(234): Show |
intron_variant | MODIFIER | c.-102-5134C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44582341 | ||||||
| chr11:44582345
|
G | A | 1 | a0002c0003t0001g0067 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-102-5130G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44582345 | ||||||
| chr11:44582462
|
G | T | 1 | a0001c0009t0002g0172 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.-102-5013G>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44582462 | ||||||
| chr11:44582490
|
C | G | 117 | a0001c0001t0001g0003a0001c0001t0001g0033a0001c0001t0001g0051others(114): Show | 119 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(116): Show |
intron_variant | MODIFIER | c.-102-4985C>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44582490 | ||||||
| chr11:44582590
|
A | G | 5 | a0001c0001t0001g0319a0002c0003t0002g0306a0002c0003t0003g0320others(2): Show | 5 | HG01074.hp2 HG01346.hp2 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.-102-4885A>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44582590 | ||||||
| chr11:44582606
|
G | A | 350 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(347): Show | 353 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(350): Show |
intron_variant | MODIFIER | c.-102-4869G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44582606 | ||||||
| chr11:44582614
|
A | G | 1 | a0001c0001t0003g0096 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.-102-4861A>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44582614 | ||||||
| chr11:44582631
|
A | G | 320 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(317): Show | 323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.-102-4844A>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44582631 | ||||||
| chr11:44582750
|
C | G | 1 | a0001c0010t0007g0095 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-102-4725C>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44582750 | ||||||
| chr11:44582801
|
G | A | 24 | a0001c0001t0001g0033a0001c0001t0003g0108a0001c0001t0005g0214others(21): Show | 24 | HG00621.hp2 HG00639.hp1 HG01070.hp2 others(21): Show |
intron_variant | MODIFIER | c.-102-4674G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44582801 | ||||||
| chr11:44582997
|
A | G | 1 | a0002c0003t0011g0261 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-102-4478A>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44582997 | ||||||
| chr11:44583096
|
C | T | 1 | a0002c0003t0001g0112 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.-102-4379C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44583096 | ||||||
| chr11:44583186
|
A | C | 5 | a0001c0001t0001g0332a0001c0001t0008g0272a0001c0001t0008g0330others(2): Show | 5 | HG03041.hp2 HG03471.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.-102-4289A>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44583186 | ||||||
| chr11:44583250
|
G | C | 1 | a0001c0005t0001g0265 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-102-4225G>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44583250 | ||||||
| chr11:44583473
|
C | A | 3 | a0001c0005t0003g0097a0002c0002t0001g0098a0002c0002t0003g0099 | 3 | NA18949.hp2 NA19011.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.-102-4002C>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44583473 | ||||||
| chr11:44583666
|
C | T | 1 | a0001c0014t0002g0025 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.-102-3809C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44583666 | ||||||
| chr11:44583722
|
T | C | 3 | a0001c0012t0004g0257a0001c0012t0004g0258a0002c0015t0007g0247 | 3 | HG02451.hp1 HG02970.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.-102-3753T>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44583722 | ||||||
| chr11:44583751
|
A | G | 1 | a0001c0005t0003g0210 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.-102-3724A>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44583751 | ||||||
| chr11:44583762
|
G | A | 3 | a0001c0001t0016g0120a0001c0012t0004g0179a0002c0004t0016g0119 | 3 | HG01243.hp2 HG03486.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-102-3713G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44583762 | ||||||
| chr11:44583785
|
A | G | 226 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0044others(223): Show | 227 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(224): Show |
intron_variant | MODIFIER | c.-102-3690A>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44583785 | ||||||
| chr11:44583912
|
A | G | 93 | a0001c0001t0001g0003a0001c0001t0001g0051a0001c0001t0001g0064others(90): Show | 95 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.-102-3563A>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44583912 | ||||||
| chr11:44583917
|
G | A | 24 | a0001c0001t0001g0033a0001c0001t0003g0108a0001c0001t0005g0214others(21): Show | 24 | HG00621.hp2 HG00639.hp1 HG01070.hp2 others(21): Show |
intron_variant | MODIFIER | c.-102-3558G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44583917 | ||||||
| chr11:44583955
|
G | A | 1 | a0001c0001t0003g0017 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-102-3520G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44583955 | ||||||
| chr11:44583967
|
A | G | 1 | a0002c0004t0002g0228 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-102-3508A>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44583967 | ||||||
| chr11:44583981
|
C | T | 27 | a0001c0001t0001g0033a0001c0001t0001g0064a0001c0001t0003g0108others(24): Show | 27 | HG00621.hp2 HG00639.hp1 HG01070.hp2 others(24): Show |
intron_variant | MODIFIER | c.-102-3494C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44583981 | ||||||
| chr11:44584030
|
A | G | 1 | a0001c0005t0001g0265 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-102-3445A>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44584030 | ||||||
| chr11:44584076
|
A | T | 6 | a0001c0005t0001g0087a0001c0005t0002g0079a0001c0005t0037g0082others(3): Show | 6 | NA18942.hp1 NA18948.hp1 NA18959.hp2 others(3): Show |
intron_variant | MODIFIER | c.-102-3399A>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44584076 | ||||||
| chr11:44584223
|
T | A | 347 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(344): Show | 350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.-102-3252T>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44584223 | ||||||
| chr11:44584405
|
G | A | 2 | a0001c0001t0001g0003a0001c0001t0001g0051 | 3 | HG01256.hp2 HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.-102-3070G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44584405 | ||||||
| chr11:44584438
|
C | T | 3 | a0001c0001t0004g0333a0001c0001t0012g0083a0002c0007t0004g0347 | 3 | HG02451.hp2 HG03516.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-102-3037C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44584438 | ||||||
| chr11:44584668
|
A | T | 1 | a0001c0009t0002g0170 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.-102-2807A>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44584668 | ||||||
| chr11:44584668
|
AT | A | 25 | a0001c0001t0001g0033a0001c0001t0003g0108a0001c0001t0005g0214others(22): Show | 25 | HG00621.hp2 HG00639.hp1 HG01070.hp2 others(22): Show |
intron_variant | MODIFIER | c.-102-2796delT | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr11 | 44584668 | |||||
| chr11:44584999
|
G | A | 3 | a0001c0005t0002g0291a0001c0005t0002g0292a0001c0009t0011g0264 | 3 | HG02486.hp1 NA18939.hp1 NA18941.hp2 |
intron_variant | MODIFIER | c.-102-2476G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44584999 | ||||||
| chr11:44585387
|
A | G | 1 | a0001c0001t0046g0092 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-102-2088A>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44585387 | ||||||
| chr11:44585555
|
G | A | 3 | a0001c0001t0004g0333a0001c0001t0012g0083a0002c0007t0004g0347 | 3 | HG02451.hp2 HG03516.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-102-1920G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44585555 | ||||||
| chr11:44585652
|
C | T | 1 | a0002c0002t0036g0114 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-102-1823C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44585652 | ||||||
| chr11:44585731
|
C | T | 36 | a0001c0001t0001g0064a0001c0001t0001g0242a0001c0001t0001g0243others(33): Show | 36 | HG00099.hp1 HG00558.hp1 HG00609.hp2 others(33): Show |
intron_variant | MODIFIER | c.-102-1744C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44585731 | ||||||
| chr11:44585781
|
G | A | 1 | a0002c0002t0001g0121 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.-102-1694G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44585781 | ||||||
| chr11:44585782
|
T | G | 170 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0044others(167): Show | 172 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(169): Show |
intron_variant | MODIFIER | c.-102-1693T>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44585782 | ||||||
| chr11:44585856
|
C | T | 4 | a0001c0001t0004g0333a0001c0001t0012g0083a0001c0009t0001g0086others(1): Show | 4 | HG02451.hp2 HG02886.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.-102-1619C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44585856 | ||||||
| chr11:44585860
|
G | A | 1 | a0002c0003t0001g0026 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.-102-1615G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44585860 | ||||||
| chr11:44585881
|
T | C | 1 | a0002c0003t0014g0259 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-102-1594T>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44585881 | ||||||
| chr11:44585921
|
G | A | 350 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(347): Show | 353 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(350): Show |
intron_variant | MODIFIER | c.-102-1554G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44585921 | ||||||
| chr11:44585981
|
C | T | 3 | a0001c0012t0004g0257a0001c0012t0004g0258a0002c0015t0007g0247 | 3 | HG02451.hp1 HG02970.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.-102-1494C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44585981 | ||||||
| chr11:44585982
|
G | A | 1 | a0002c0002t0004g0122 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.-102-1493G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44585982 | ||||||
| chr11:44586277
|
C | T | 1 | a0001c0005t0001g0265 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-102-1198C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44586277 | ||||||
| chr11:44586288
|
T | TGGG | 350 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(347): Show | 353 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(350): Show |
intron_variant | MODIFIER | c.-102-1185_-102-118 others(7): Show |
CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr11 | 44586288 | |||||
| chr11:44586299
|
A | T | 23 | a0001c0001t0001g0033a0001c0001t0003g0108a0001c0001t0005g0214others(20): Show | 23 | HG00621.hp2 HG00639.hp1 HG01070.hp2 others(20): Show |
intron_variant | MODIFIER | c.-102-1176A>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44586299 | ||||||
| chr11:44586340
|
T | C | 41 | a0001c0001t0001g0064a0001c0001t0001g0242a0001c0001t0001g0243others(38): Show | 41 | HG00099.hp1 HG00558.hp1 HG00609.hp2 others(38): Show |
intron_variant | MODIFIER | c.-102-1135T>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44586340 | ||||||
| chr11:44586357
|
A | G | 1 | a0001c0001t0003g0108 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.-102-1118A>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44586357 | ||||||
| chr11:44586417
|
C | G | 1 | a0001c0001t0003g0017 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-102-1058C>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44586417 | ||||||
| chr11:44586482
|
G | A | 41 | a0001c0001t0001g0064a0001c0001t0001g0242a0001c0001t0001g0243others(38): Show | 41 | HG00099.hp1 HG00558.hp1 HG00609.hp2 others(38): Show |
intron_variant | MODIFIER | c.-102-993G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44586482 | ||||||
| chr11:44586525
|
G | A | 3 | a0001c0001t0004g0333a0001c0001t0012g0083a0002c0007t0004g0347 | 3 | HG02451.hp2 HG03516.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-102-950G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44586525 | ||||||
| chr11:44586728
|
G | A | 2 | a0001c0001t0001g0315a0001c0001t0003g0316 | 2 | HG01123.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.-102-747G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44586728 | ||||||
| chr11:44586885
|
C | G | 1 | a0001c0001t0006g0015 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-102-590C>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44586885 | ||||||
| chr11:44586936
|
G | C | 1 | a0001c0001t0017g0284 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-102-539G>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44586936 | ||||||
| chr11:44587013
|
C | T | 38 | a0001c0001t0001g0242a0001c0001t0001g0243a0001c0001t0001g0287others(35): Show | 38 | HG00099.hp1 HG00558.hp1 HG00609.hp2 others(35): Show |
intron_variant | MODIFIER | c.-102-462C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44587013 | ||||||
| chr11:44587055
|
C | G | 273 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(270): Show | 276 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(273): Show |
intron_variant | MODIFIER | c.-102-420C>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44587055 | ||||||
| chr11:44587180
|
G | A | 2 | a0001c0009t0001g0166a0002c0004t0003g0069 | 2 | HG01123.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.-102-295G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44587180 | ||||||
| chr11:44587217
|
C | T | 350 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(347): Show | 353 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(350): Show |
intron_variant | MODIFIER | c.-102-258C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44587217 | ||||||
| chr11:44587272
|
A | G | 10 | a0001c0001t0004g0094a0001c0010t0004g0093a0001c0010t0007g0095others(7): Show | 10 | HG01109.hp1 HG02257.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.-102-203A>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44587272 | ||||||
| chr11:44587286
|
C | T | 3 | a0001c0001t0004g0333a0001c0001t0012g0083a0002c0007t0004g0347 | 3 | HG02451.hp2 HG03516.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-102-189C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44587286 | ||||||
| chr11:44587316
|
T | C | 350 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(347): Show | 353 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(350): Show |
intron_variant | MODIFIER | c.-102-159T>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44587316 | ||||||
| chr11:44587330
|
G | A | 8 | a0001c0001t0004g0323a0001c0010t0008g0248a0002c0003t0003g0256others(5): Show | 8 | HG02280.hp2 HG02818.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.-102-145G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44587330 | ||||||
| chr11:44587385
|
G | A | 1 | a0001c0001t0004g0309 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-102-90G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44587385 | ||||||
| chr11:44587579
|
T | A | 173 | a0001c0001t0001g0002a0001c0001t0001g0044a0001c0001t0001g0133others(170): Show | 173 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(170): Show |
intron_variant | MODIFIER | c.-21+23T>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | chr11 | 44587579 | ||||||
| chr11:44587595
|
A | G | 1 | a0002c0002t0003g0162 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-21+39A>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | chr11 | 44587595 | ||||||
| chr11:44587631
|
G | A | 1 | a0001c0005t0002g0209 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.-21+75G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | chr11 | 44587631 | ||||||
| chr11:44587648
|
G | A | 263 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0044others(260): Show | 266 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(263): Show |
intron_variant | MODIFIER | c.-21+92G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | chr11 | 44587648 | ||||||
| chr11:44587799
|
C | G | 26 | a0001c0001t0001g0033a0001c0001t0003g0108a0001c0001t0004g0333others(23): Show | 26 | HG00621.hp2 HG00639.hp1 HG01070.hp2 others(23): Show |
intron_variant | MODIFIER | c.-21+243C>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | chr11 | 44587799 | ||||||
| chr11:44587851
|
C | T | 9 | a0001c0001t0004g0094a0001c0010t0004g0093a0001c0010t0007g0095others(6): Show | 9 | HG01109.hp1 HG02257.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.-21+295C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | chr11 | 44587851 | ||||||
| chr11:44588000
|
G | T | 350 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(347): Show | 353 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(350): Show |
intron_variant | MODIFIER | c.-21+444G>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | chr11 | 44588000 | ||||||
| chr11:44588007
|
T | C | 350 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(347): Show | 353 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(350): Show |
intron_variant | MODIFIER | c.-21+451T>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | chr11 | 44588007 | ||||||
| chr11:44588033
|
C | T | 2 | a0001c0005t0002g0209a0001c0005t0003g0210 | 2 | NA18998.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.-21+477C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | chr11 | 44588033 | ||||||
| chr11:44588034
|
G | A | 1 | a0002c0003t0042g0311 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-21+478G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | chr11 | 44588034 | ||||||
| chr11:44588124
|
A | G | 37 | a0001c0001t0001g0242a0001c0001t0001g0243a0001c0001t0001g0287others(34): Show | 37 | HG00099.hp1 HG00558.hp1 HG00609.hp2 others(34): Show |
intron_variant | MODIFIER | c.-21+568A>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | chr11 | 44588124 | ||||||
| chr11:44588205
|
T | TG | 131 | a0001c0001t0001g0002a0001c0001t0001g0044a0001c0001t0001g0133others(128): Show | 131 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(128): Show |
intron_variant | MODIFIER | c.-21+653dupG | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr11 | 44588205 | |||||
| chr11:44588209
|
G | GT | 190 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0047others(187): Show | 193 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(190): Show |
intron_variant | MODIFIER | c.-21+663dupT | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr11 | 44588209 | |||||
| chr11:44588220
|
G | T | 1 | a0002c0003t0004g0271 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-21+664G>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | chr11 | 44588220 | ||||||
| chr11:44588222
|
T | G | 1 | a0002c0003t0004g0271 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-21+666T>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | chr11 | 44588222 | ||||||
| chr11:44588234
|
G | GT | 279 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(276): Show | 282 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(279): Show |
intron_variant | MODIFIER | c.-21+686dupT | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr11 | 44588234 | |||||
| chr11:44588254
|
C | T | 3 | a0001c0001t0004g0333a0001c0001t0012g0083a0002c0007t0004g0347 | 3 | HG02451.hp2 HG03516.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-21+698C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | chr11 | 44588254 | ||||||
| chr11:44588287
|
G | A | 8 | a0001c0001t0004g0094a0001c0010t0004g0093a0001c0016t0017g0030others(5): Show | 8 | HG01109.hp1 HG02258.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.-21+731G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | chr11 | 44588287 | ||||||
| chr11:44588465
|
G | A | 1 | a0002c0024t0047g0283 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-21+909G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | chr11 | 44588465 | ||||||
| chr11:44588514
|
A | T | 37 | a0001c0001t0001g0242a0001c0001t0001g0243a0001c0001t0001g0287others(34): Show | 37 | HG00099.hp1 HG00558.hp1 HG00609.hp2 others(34): Show |
intron_variant | MODIFIER | c.-21+958A>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | chr11 | 44588514 | ||||||
| chr11:44588738
|
G | A | 1 | a0002c0008t0001g0191 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.-21+1182G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | chr11 | 44588738 | ||||||
| chr11:44588809
|
T | C | 350 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(347): Show | 353 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(350): Show |
intron_variant | MODIFIER | c.-21+1253T>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | chr11 | 44588809 | ||||||
| chr11:44588870
|
T | C | 12 | a0001c0001t0001g0064a0001c0001t0004g0094a0001c0010t0004g0093others(9): Show | 12 | HG01109.hp1 HG02109.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.-21+1314T>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | chr11 | 44588870 | ||||||
| chr11:44588902
|
C | G | 1 | a0002c0003t0001g0218 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.-21+1346C>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | chr11 | 44588902 | ||||||
| chr11:44588904
|
T | A | 1 | a0002c0003t0001g0218 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.-21+1348T>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | chr11 | 44588904 | ||||||
| chr11:44588994
|
C | T | 9 | a0001c0001t0004g0094a0001c0010t0004g0093a0001c0010t0007g0095others(6): Show | 9 | HG01109.hp1 HG02257.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.-21+1438C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | chr11 | 44588994 | ||||||
| chr11:44589049
|
G | C | 23 | a0001c0001t0001g0033a0001c0001t0003g0108a0001c0001t0005g0214others(20): Show | 23 | HG00621.hp2 HG00639.hp1 HG01070.hp2 others(20): Show |
intron_variant | MODIFIER | c.-21+1493G>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | chr11 | 44589049 | ||||||
| chr11:44589112
|
C | T | 275 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(272): Show | 278 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(275): Show |
intron_variant | MODIFIER | c.-21+1556C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | chr11 | 44589112 | ||||||
| chr11:44589117
|
A | G | 3 | a0001c0001t0001g0064a0002c0003t0001g0091a0002c0015t0007g0247 | 3 | HG02109.hp1 HG02109.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.-21+1561A>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | chr11 | 44589117 | ||||||
| chr11:44589227
|
G | C | 23 | a0001c0001t0001g0033a0001c0001t0003g0108a0001c0001t0005g0214others(20): Show | 23 | HG00621.hp2 HG00639.hp1 HG01070.hp2 others(20): Show |
intron_variant | MODIFIER | c.-21+1671G>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | chr11 | 44589227 | ||||||
| chr11:44589241
|
G | A | 275 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(272): Show | 278 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(275): Show |
intron_variant | MODIFIER | c.-21+1685G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | chr11 | 44589241 | ||||||
| chr11:44589277
|
CA | C | 5 | a0001c0001t0001g0250a0001c0001t0001g0251a0001c0001t0004g0249others(2): Show | 5 | HG02486.hp2 HG02895.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.-21+1722delA | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | chr11 | 44589277 | ||||||
| chr11:44589449
|
A | C | 1 | a0001c0001t0014g0213 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-21+1893A>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | chr11 | 44589449 | ||||||
| chr11:44589517
|
C | T | 1 | a0001c0001t0049g0343 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-21+1961C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | chr11 | 44589517 | ||||||
| chr11:44589629
|
G | A | 1 | a0002c0015t0007g0247 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-21+2073G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | chr11 | 44589629 | ||||||
| chr11:44589697
|
G | A | 5 | a0001c0001t0001g0250a0001c0001t0001g0251a0001c0001t0004g0249others(2): Show | 5 | HG02486.hp2 HG02895.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.-21+2141G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | chr11 | 44589697 | ||||||
| chr11:44589818
|
G | C | 3 | a0001c0001t0004g0333a0001c0001t0012g0083a0002c0007t0004g0347 | 3 | HG02451.hp2 HG03516.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-21+2262G>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | chr11 | 44589818 | ||||||
| chr11:44589887
|
G | A | 2 | a0001c0016t0017g0030a0001c0016t0048g0031 | 2 | HG02258.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-21+2331G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | chr11 | 44589887 | ||||||
| chr11:44589896
|
C | T | 1 | a0001c0001t0003g0304 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-21+2340C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | chr11 | 44589896 | ||||||
| chr11:44589942
|
T | C | 9 | a0001c0001t0004g0094a0001c0010t0004g0093a0001c0010t0007g0095others(6): Show | 9 | HG01109.hp1 HG02257.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.-21+2386T>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | chr11 | 44589942 | ||||||
| chr11:44589994
|
T | C | 284 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(281): Show | 287 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(284): Show |
intron_variant | MODIFIER | c.-21+2438T>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | chr11 | 44589994 | ||||||
| chr11:44590034
|
C | T | 9 | a0001c0001t0004g0094a0001c0010t0004g0093a0001c0010t0007g0095others(6): Show | 9 | HG01109.hp1 HG02257.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.-21+2478C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | chr11 | 44590034 | ||||||
| chr11:44590063
|
C | G | 26 | a0001c0001t0001g0033a0001c0001t0003g0108a0001c0001t0004g0333others(23): Show | 26 | HG00621.hp2 HG00639.hp1 HG01070.hp2 others(23): Show |
intron_variant | MODIFIER | c.-21+2507C>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | chr11 | 44590063 | ||||||
| chr11:44590119
|
C | T | 347 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(344): Show | 350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.-21+2563C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | chr11 | 44590119 | ||||||
| chr11:44590183
|
C | T | 1 | a0001c0010t0008g0248 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-21+2627C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | chr11 | 44590183 | ||||||
| chr11:44590191
|
G | A | 3 | a0001c0001t0004g0333a0001c0001t0012g0083a0002c0007t0004g0347 | 3 | HG02451.hp2 HG03516.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-21+2635G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | chr11 | 44590191 | ||||||
| chr11:44590230
|
A | AG | 324 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(321): Show | 327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
intron_variant | MODIFIER | c.-21+2676dupG | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr11 | 44590230 | |||||
| chr11:44590475
|
G | C | 3 | a0001c0001t0001g0064a0002c0003t0001g0091a0002c0015t0007g0247 | 3 | HG02109.hp1 HG02109.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.-21+2919G>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | chr11 | 44590475 | ||||||
| chr11:44590543
|
G | A | 2 | a0001c0012t0004g0257a0001c0012t0004g0258 | 2 | HG02451.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.-21+2987G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | chr11 | 44590543 | ||||||
| chr11:44590610
|
C | CAAAAA | 14 | a0001c0001t0003g0163a0001c0001t0004g0164a0001c0001t0004g0165others(11): Show | 14 | HG00639.hp2 HG01243.hp1 HG01496.hp1 others(11): Show |
intron_variant | MODIFIER | c.-21+3070_-21+3074d others(7): Show |
CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr11 | 44590610 | |||||
| chr11:44590610
|
C | CAAAAAA | 12 | a0001c0001t0001g0250a0001c0001t0001g0251a0001c0001t0004g0254others(9): Show | 12 | HG01884.hp1 HG02486.hp2 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.-21+3069_-21+3074d others(8): Show |
CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr11 | 44590610 | |||||
| chr11:44590610
|
C | CAAAAAAA | 60 | a0001c0001t0001g0047a0001c0001t0001g0058a0001c0001t0001g0060others(57): Show | 61 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(58): Show |
intron_variant | MODIFIER | c.-21+3068_-21+3074d others(9): Show |
CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr11 | 44590610 | |||||
| chr11:44590610
|
C | CAAAAAAA others(1): Show |
17 | a0001c0001t0001g0006a0001c0001t0001g0315a0001c0001t0001g0319others(14): Show | 17 | HG00735.hp1 HG01243.hp2 HG01358.hp1 others(14): Show |
intron_variant | MODIFIER | c.-21+3067_-21+3074d others(10): Show |
CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr11 | 44590610 | |||||
| chr11:44590610
|
C | CAAAAAAA others(2): Show |
12 | a0001c0001t0002g0160a0001c0001t0004g0094a0001c0005t0037g0082others(9): Show | 12 | HG02132.hp1 HG02257.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.-21+3066_-21+3074d others(11): Show |
CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr11 | 44590610 | |||||
| chr11:44590610
|
C | CAAAAAAA others(3): Show |
52 | a0001c0001t0002g0184a0001c0001t0013g0071a0001c0005t0001g0204others(49): Show | 53 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(50): Show |
intron_variant | MODIFIER | c.-21+3065_-21+3074d others(12): Show |
CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr11 | 44590610 | |||||
| chr11:44590610
|
C | CAAAAAAA others(4): Show |
98 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0044others(95): Show | 99 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.-21+3064_-21+3074d others(13): Show |
CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr11 | 44590610 | |||||
| chr11:44590610
|
C | CAAAAAAA others(5): Show |
32 | a0001c0001t0001g0242a0001c0001t0001g0243a0001c0001t0001g0308others(29): Show | 32 | HG00099.hp1 HG00544.hp1 HG00733.hp2 others(29): Show |
intron_variant | MODIFIER | c.-21+3063_-21+3074d others(14): Show |
CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr11 | 44590610 | |||||
| chr11:44590610
|
C | CAAAAAAA others(6): Show |
13 | a0001c0001t0001g0287a0001c0001t0001g0288a0002c0002t0003g0187others(10): Show | 13 | HG01167.hp2 HG01169.hp2 HG02071.hp1 others(10): Show |
intron_variant | MODIFIER | c.-21+3062_-21+3074d others(15): Show |
CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr11 | 44590610 | |||||
| chr11:44590610
|
C | CAAAAAAA others(7): Show |
4 | a0001c0009t0004g0239a0002c0004t0002g0226a0002c0004t0002g0227others(1): Show | 4 | HG00609.hp2 HG01891.hp1 NA18954.hp2 others(1): Show |
intron_variant | MODIFIER | c.-21+3061_-21+3074d others(16): Show |
CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr11 | 44590610 | |||||
| chr11:44590610
|
C | CAAAAAAA others(8): Show |
2 | a0001c0005t0002g0169a0001c0010t0003g0238 | 2 | HG00558.hp1 NA18612.hp1 |
intron_variant | MODIFIER | c.-21+3060_-21+3074d others(17): Show |
CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr11 | 44590610 | |||||
| chr11:44590610
|
C | CAAAAAAA others(13): Show |
7 | a0001c0001t0001g0064a0001c0001t0013g0216a0001c0001t0013g0222others(4): Show | 7 | HG00621.hp2 HG01978.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.-21+3055_-21+3074d others(22): Show |
CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr11 | 44590610 | |||||
| chr11:44590610
|
C | CAAAAAAA others(14): Show |
10 | a0001c0001t0006g0215a0001c0010t0001g0212a0001c0010t0002g0014others(7): Show | 10 | HG00639.hp1 HG01192.hp2 HG02148.hp1 others(7): Show |
intron_variant | MODIFIER | c.-21+3074_-21+3075i others(23): Show |
CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr11 | 44590610 | |||||
| chr11:44590610
|
C | CAAAAAAA others(15): Show |
3 | a0001c0001t0001g0033a0001c0010t0001g0211a0001c0011t0001g0334 | 3 | HG01106.hp2 NA18970.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.-21+3074_-21+3075i others(24): Show |
CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr11 | 44590610 | |||||
| chr11:44590610
|
C | CAAAAAAA others(16): Show |
2 | a0002c0007t0002g0012a0002c0007t0002g0013 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.-21+3074_-21+3075i others(25): Show |
CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr11 | 44590610 | |||||
| chr11:44590610
|
C | CAAAAAAA others(17): Show |
3 | a0001c0001t0005g0214a0001c0001t0006g0015a0002c0003t0001g0011 | 3 | HG01175.hp1 HG02735.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.-21+3074_-21+3075i others(26): Show |
CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr11 | 44590610 | |||||
| chr11:44590610
|
C | CAAAAAAA others(18): Show |
1 | a0001c0001t0003g0108 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.-21+3074_-21+3075i others(27): Show |
CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr11 | 44590610 | |||||
| chr11:44590642
|
T | TTCTTAGC others(139): Show |
3 | a0001c0005t0002g0169a0001c0009t0004g0239a0001c0010t0003g0238 | 3 | HG00558.hp1 HG00609.hp2 NA18612.hp1 |
intron_variant | MODIFIER | c.-21+3087_-21+3232d others(148): Show |
CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr11 | 44590642 | |||||
| chr11:44590732
|
T | C | 1 | a0001c0016t0004g0351 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-21+3176T>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | chr11 | 44590732 | ||||||
| chr11:44590803
|
C | G | 47 | a0001c0001t0001g0047a0001c0001t0001g0058a0001c0001t0001g0060others(44): Show | 48 | HG00099.hp2 HG00323.hp1 HG00558.hp2 others(45): Show |
intron_variant | MODIFIER | c.-21+3247C>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | chr11 | 44590803 | ||||||
| chr11:44590909
|
G | A | 1 | a0001c0001t0014g0280 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-21+3353G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | chr11 | 44590909 | ||||||
| chr11:44590957
|
C | T | 350 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(347): Show | 353 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(350): Show |
intron_variant | MODIFIER | c.-21+3401C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | chr11 | 44590957 | ||||||
| chr11:44590984
|
C | T | 73 | a0001c0001t0001g0006a0001c0001t0001g0047a0001c0001t0001g0058others(70): Show | 74 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(71): Show |
intron_variant | MODIFIER | c.-21+3428C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | chr11 | 44590984 | ||||||
| chr11:44591098
|
C | T | 1 | a0002c0003t0005g0150 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-21+3542C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | chr11 | 44591098 | ||||||
| chr11:44591125
|
T | A | 3 | a0001c0006t0002g0151a0001c0006t0003g0185a0001c0014t0002g0183 | 3 | NA18959.hp1 NA19012.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.-20-3518T>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | chr11 | 44591125 | ||||||
| chr11:44591164
|
C | G | 172 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0044others(169): Show | 174 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(171): Show |
intron_variant | MODIFIER | c.-20-3479C>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | chr11 | 44591164 | ||||||
| chr11:44591186
|
G | A | 3 | a0001c0001t0006g0010a0002c0003t0045g0065a0002c0015t0003g0339 | 4 | HG01257.hp2 HG01258.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.-20-3457G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | chr11 | 44591186 | ||||||
| chr11:44591243
|
G | A | 9 | a0001c0001t0004g0094a0001c0010t0004g0093a0001c0010t0007g0095others(6): Show | 9 | HG01109.hp1 HG02257.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.-20-3400G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | chr11 | 44591243 | ||||||
| chr11:44591260
|
C | T | 2 | a0002c0004t0001g0008a0002c0004t0002g0008 | 2 | HG01070.hp1 HG01081.hp1 |
intron_variant | MODIFIER | c.-20-3383C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | chr11 | 44591260 | ||||||
| chr11:44591425
|
C | A | 1 | a0001c0005t0002g0048 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.-20-3218C>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | chr11 | 44591425 | ||||||
| chr11:44591833
|
A | AT | 307 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(304): Show | 310 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(307): Show |
intron_variant | MODIFIER | c.-20-2802dupT | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr11 | 44591833 | |||||
| chr11:44591842
|
G | C | 2 | a0001c0012t0004g0257a0001c0012t0004g0258 | 2 | HG02451.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.-20-2801G>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | chr11 | 44591842 | ||||||
| chr11:44591850
|
G | T | 1 | a0002c0002t0001g0159 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.-20-2793G>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | chr11 | 44591850 | ||||||
| chr11:44591893
|
C | T | 5 | a0001c0001t0001g0250a0001c0001t0001g0251a0001c0001t0004g0249others(2): Show | 5 | HG02486.hp2 HG02895.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.-20-2750C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | chr11 | 44591893 | ||||||
| chr11:44592121
|
T | C | 60 | a0001c0001t0001g0033a0001c0001t0001g0242a0001c0001t0001g0243others(57): Show | 60 | HG00099.hp1 HG00558.hp1 HG00609.hp2 others(57): Show |
intron_variant | MODIFIER | c.-20-2522T>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | chr11 | 44592121 | ||||||
| chr11:44592170
|
G | A | 106 | a0001c0001t0001g0002a0001c0001t0001g0044a0001c0001t0001g0133others(103): Show | 106 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(103): Show |
intron_variant | MODIFIER | c.-20-2473G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | chr11 | 44592170 | ||||||
| chr11:44592239
|
C | T | 1 | a0001c0005t0002g0175 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.-20-2404C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | chr11 | 44592239 | ||||||
| chr11:44592430
|
C | T | 2 | a0001c0001t0008g0266a0001c0001t0015g0352 | 2 | HG02922.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-20-2213C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | chr11 | 44592430 | ||||||
| chr11:44592455
|
G | C | 1 | a0002c0002t0003g0154 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.-20-2188G>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | chr11 | 44592455 | ||||||
| chr11:44592480
|
G | T | 3 | a0001c0001t0004g0333a0001c0001t0012g0083a0002c0007t0004g0347 | 3 | HG02451.hp2 HG03516.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-20-2163G>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | chr11 | 44592480 | ||||||
| chr11:44592607
|
G | A | 1 | a0001c0001t0001g0058 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.-20-2036G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | chr11 | 44592607 | ||||||
| chr11:44592908
|
G | A | 72 | a0001c0001t0001g0003a0001c0001t0001g0051a0001c0001t0001g0332others(69): Show | 74 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(71): Show |
intron_variant | MODIFIER | c.-20-1735G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | chr11 | 44592908 | ||||||
| chr11:44593033
|
T | C | 216 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0044others(213): Show | 217 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(214): Show |
intron_variant | MODIFIER | c.-20-1610T>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | chr11 | 44593033 | ||||||
| chr11:44593259
|
G | A | 7 | a0001c0001t0004g0037a0001c0001t0004g0323a0001c0010t0008g0248others(4): Show | 7 | HG02818.hp2 HG02896.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.-20-1384G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | chr11 | 44593259 | ||||||
| chr11:44593343
|
G | A | 2 | a0001c0001t0027g0322a0001c0010t0004g0174 | 2 | HG03579.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-20-1300G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | chr11 | 44593343 | ||||||
| chr11:44593354
|
C | A | 1 | a0002c0002t0001g0127 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-20-1289C>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | chr11 | 44593354 | ||||||
| chr11:44593357
|
C | G | 2 | a0001c0016t0017g0030a0001c0016t0048g0031 | 2 | HG02258.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-20-1286C>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | chr11 | 44593357 | ||||||
| chr11:44593363
|
C | T | 1 | a0001c0016t0048g0031 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-20-1280C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | chr11 | 44593363 | ||||||
| chr11:44593546
|
C | T | 61 | a0001c0001t0001g0003a0001c0001t0001g0051a0001c0001t0002g0160others(58): Show | 63 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(60): Show |
intron_variant | MODIFIER | c.-20-1097C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | chr11 | 44593546 | ||||||
| chr11:44593547
|
A | G | 228 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0033others(225): Show | 230 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(227): Show |
intron_variant | MODIFIER | c.-20-1096A>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | chr11 | 44593547 | ||||||
| chr11:44593628
|
G | A | 33 | a0001c0001t0001g0242a0001c0001t0001g0243a0001c0001t0001g0287others(30): Show | 33 | HG00099.hp1 HG00558.hp1 HG00609.hp2 others(30): Show |
intron_variant | MODIFIER | c.-20-1015G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | chr11 | 44593628 | ||||||
| chr11:44593639
|
G | GAA | 19 | a0001c0001t0001g0033a0001c0001t0005g0214a0001c0001t0006g0215others(16): Show | 19 | HG00621.hp2 HG00639.hp1 HG01106.hp2 others(16): Show |
intron_variant | MODIFIER | c.-20-1001_-20-1000d others(4): Show |
CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr11 | 44593639 | |||||
| chr11:44593718
|
T | G | 4 | a0002c0002t0002g0130a0002c0002t0032g0131a0002c0008t0001g0023others(1): Show | 4 | NA18939.hp2 NA18967.hp1 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.-20-925T>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | chr11 | 44593718 | ||||||
| chr11:44593742
|
G | C | 35 | a0001c0001t0001g0242a0001c0001t0001g0243a0001c0001t0001g0287others(32): Show | 35 | HG00099.hp1 HG00558.hp1 HG00609.hp2 others(32): Show |
intron_variant | MODIFIER | c.-20-901G>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | chr11 | 44593742 | ||||||
| chr11:44593880
|
G | A | 82 | a0001c0001t0001g0006a0001c0001t0001g0047a0001c0001t0001g0058others(79): Show | 83 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(80): Show |
intron_variant | MODIFIER | c.-20-763G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | chr11 | 44593880 | ||||||
| chr11:44593977
|
A | T | 350 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(347): Show | 353 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(350): Show |
intron_variant | MODIFIER | c.-20-666A>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | chr11 | 44593977 | ||||||
| chr11:44593994
|
TAC | T | 20 | a0001c0001t0001g0033a0001c0001t0005g0214a0001c0001t0006g0215others(17): Show | 20 | HG00621.hp2 HG00639.hp1 HG01106.hp2 others(17): Show |
intron_variant | MODIFIER | c.-20-628_-20-627del others(2): Show |
CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr11 | 44593994 | |||||
| chr11:44593994
|
TACAC | T | 329 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(326): Show | 332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.-20-630_-20-627del others(4): Show |
CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr11 | 44593994 | |||||
| chr11:44594009
|
A | G | 2 | a0001c0001t0004g0037a0001c0001t0007g0327 | 2 | HG02896.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.-20-634A>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | chr11 | 44594009 | ||||||
| chr11:44594149
|
C | T | 96 | a0001c0001t0001g0003a0001c0001t0001g0051a0001c0001t0001g0250others(93): Show | 98 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(95): Show |
intron_variant | MODIFIER | c.-20-494C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | chr11 | 44594149 | ||||||
| chr11:44594159
|
A | G | 225 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0044others(222): Show | 226 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(223): Show |
intron_variant | MODIFIER | c.-20-484A>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | chr11 | 44594159 | ||||||
| chr11:44594265
|
G | T | 41 | a0001c0001t0001g0064a0001c0001t0001g0242a0001c0001t0001g0243others(38): Show | 41 | HG00099.hp1 HG00558.hp1 HG00609.hp2 others(38): Show |
intron_variant | MODIFIER | c.-20-378G>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | chr11 | 44594265 | ||||||
| chr11:44594295
|
C | A | 1 | a0002c0003t0029g0275 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-20-348C>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | chr11 | 44594295 | ||||||
| chr11:44594303
|
C | G | 2 | a0001c0005t0002g0291a0001c0005t0002g0292 | 2 | NA18939.hp1 NA18941.hp2 |
intron_variant | MODIFIER | c.-20-340C>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | chr11 | 44594303 | ||||||
| chr11:44594388
|
A | ACCAGCC | 111 | a0001c0001t0001g0006a0001c0001t0001g0047a0001c0001t0001g0058others(108): Show | 112 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(109): Show |
intron_variant | MODIFIER | c.-20-232_-20-227dup others(6): Show |
CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr11 | 44594388 | |||||
| chr11:44594388
|
A | ACCAGCCC others(5): Show |
2 | a0001c0016t0004g0351a0002c0025t0004g0349 | 2 | HG02055.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.-20-238_-20-227dup others(12): Show |
CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr11 | 44594388 | |||||
| chr11:44594490
|
T | A | 34 | a0001c0001t0001g0242a0001c0001t0001g0243a0001c0001t0001g0287others(31): Show | 34 | HG00099.hp1 HG00558.hp1 HG00609.hp2 others(31): Show |
intron_variant | MODIFIER | c.-20-153T>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | chr11 | 44594490 | ||||||
| chr11:44594775
|
C | T | 1 | a0002c0003t0001g0091 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.63+50C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 3/9 | chr11 | 44594775 | ||||||
| chr11:44594813
|
G | A | 1 | a0002c0003t0044g0268 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.63+88G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 3/9 | chr11 | 44594813 | ||||||
| chr11:44594859
|
A | C | 2 | a0001c0001t0001g0319a0002c0003t0003g0320 | 2 | HG01074.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.63+134A>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 3/9 | chr11 | 44594859 | ||||||
| chr11:44594984
|
C | T | 85 | a0001c0001t0001g0006a0001c0001t0001g0047a0001c0001t0001g0058others(82): Show | 86 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(83): Show |
intron_variant | MODIFIER | c.63+259C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 3/9 | chr11 | 44594984 | ||||||
| chr11:44594992
|
A | G | 105 | a0001c0001t0001g0003a0001c0001t0001g0051a0001c0001t0001g0250others(102): Show | 107 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(104): Show |
intron_variant | MODIFIER | c.63+267A>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 3/9 | chr11 | 44594992 | ||||||
| chr11:44595070
|
C | A | 2 | a0001c0001t0004g0037a0001c0001t0007g0327 | 2 | HG02896.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.63+345C>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 3/9 | chr11 | 44595070 | ||||||
| chr11:44595091
|
C | A | 1 | a0002c0002t0001g0070 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.63+366C>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 3/9 | chr11 | 44595091 | ||||||
| chr11:44595108
|
G | A | 3 | a0002c0007t0002g0123a0002c0007t0002g0125a0002c0007t0002g0126 | 3 | HG01167.hp2 HG01169.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.63+383G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 3/9 | chr11 | 44595108 | ||||||
| chr11:44595118
|
G | A | 1 | a0002c0004t0001g0056 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.63+393G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 3/9 | chr11 | 44595118 | ||||||
| chr11:44595242
|
C | T | 1 | a0001c0005t0004g0103 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.63+517C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 3/9 | chr11 | 44595242 | ||||||
| chr11:44595279
|
G | A | 330 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(327): Show | 333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.63+554G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 3/9 | chr11 | 44595279 | ||||||
| chr11:44595362
|
C | T | 2 | a0001c0012t0004g0257a0001c0012t0004g0258 | 2 | HG02451.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.63+637C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 3/9 | chr11 | 44595362 | ||||||
| chr11:44595489
|
TA | T | 226 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0033others(223): Show | 228 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(225): Show |
intron_variant | MODIFIER | c.63+766delA | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 44595489 | |||||
| chr11:44595523
|
C | T | 30 | a0001c0001t0001g0242a0001c0001t0001g0243a0001c0001t0001g0287others(27): Show | 30 | HG00099.hp1 HG00558.hp1 HG00609.hp2 others(27): Show |
intron_variant | MODIFIER | c.63+798C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 3/9 | chr11 | 44595523 | ||||||
| chr11:44595530
|
A | T | 310 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(307): Show | 313 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(310): Show |
intron_variant | MODIFIER | c.63+805A>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 3/9 | chr11 | 44595530 | ||||||
| chr11:44595562
|
G | A | 22 | a0001c0001t0001g0033a0001c0001t0001g0133a0001c0001t0005g0214others(19): Show | 22 | HG00621.hp2 HG00639.hp1 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.63+837G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 3/9 | chr11 | 44595562 | ||||||
| chr11:44595592
|
G | A | 101 | a0001c0001t0001g0002a0001c0001t0001g0044a0001c0001t0001g0133others(98): Show | 101 | HG00408.hp1 HG00438.hp2 HG00609.hp1 others(98): Show |
intron_variant | MODIFIER | c.63+867G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 3/9 | chr11 | 44595592 | ||||||
| chr11:44595908
|
C | CA | 73 | a0001c0001t0001g0044a0001c0001t0001g0064a0001c0001t0001g0250others(70): Show | 73 | HG00621.hp1 HG00621.hp2 HG00642.hp1 others(70): Show |
intron_variant | MODIFIER | c.63+1206dupA | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 44595908 | |||||
| chr11:44595908
|
C | CAA | 23 | a0001c0001t0001g0033a0001c0001t0005g0214a0001c0001t0013g0071others(20): Show | 23 | HG00639.hp1 HG01106.hp2 HG01109.hp1 others(20): Show |
intron_variant | MODIFIER | c.63+1205_63+1206dup others(2): Show |
CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 44595908 | |||||
| chr11:44595908
|
C | CAAAAA | 8 | a0001c0001t0001g0315a0001c0006t0003g0344a0001c0016t0017g0030others(5): Show | 8 | HG00639.hp2 HG00741.hp2 HG01358.hp1 others(5): Show |
intron_variant | MODIFIER | c.63+1202_63+1206dup others(5): Show |
CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 44595908 | |||||
| chr11:44595908
|
C | CAAAAAAA others(3): Show |
3 | a0001c0001t0002g0317a0001c0001t0004g0281a0001c0001t0004g0321 | 3 | HG02572.hp2 HG02886.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.63+1197_63+1206dup others(10): Show |
CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 44595908 | |||||
| chr11:44595908
|
CAAAAA | C | 50 | a0001c0001t0001g0003a0001c0001t0001g0051a0001c0005t0001g0087others(47): Show | 52 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(49): Show |
intron_variant | MODIFIER | c.63+1202_63+1206del others(5): Show |
CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 44595908 | |||||
| chr11:44596014
|
T | G | 46 | a0001c0001t0001g0033a0001c0001t0002g0160a0001c0001t0008g0266others(43): Show | 46 | HG00639.hp1 HG00673.hp1 HG01106.hp2 others(43): Show |
intron_variant | MODIFIER | c.63+1289T>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 3/9 | chr11 | 44596014 | ||||||
| chr11:44596118
|
C | T | 1 | a0002c0007t0002g0111 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.63+1393C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 3/9 | chr11 | 44596118 | ||||||
| chr11:44596199
|
G | A | 92 | a0001c0001t0001g0144a0001c0001t0001g0242a0001c0001t0001g0243others(89): Show | 92 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.63+1474G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 3/9 | chr11 | 44596199 | ||||||
| chr11:44596377
|
G | A | 1 | a0002c0003t0005g0150 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.63+1652G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 3/9 | chr11 | 44596377 | ||||||
| chr11:44596453
|
A | T | 2 | a0001c0001t0002g0160a0001c0001t0002g0184 | 2 | NA18962.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.63+1728A>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 3/9 | chr11 | 44596453 | ||||||
| chr11:44596619
|
G | A | 2 | a0001c0009t0001g0086a0002c0003t0014g0328 | 2 | HG01884.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.63+1894G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 3/9 | chr11 | 44596619 | ||||||
| chr11:44596641
|
C | T | 6 | a0001c0010t0004g0093a0001c0010t0007g0095a0002c0003t0002g0324others(3): Show | 6 | HG01109.hp1 HG02257.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.63+1916C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 3/9 | chr11 | 44596641 | ||||||
| chr11:44596685
|
G | C | 131 | a0001c0001t0001g0133a0001c0001t0001g0319a0001c0001t0002g0147others(128): Show | 132 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(129): Show |
intron_variant | MODIFIER | c.63+1960G>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 3/9 | chr11 | 44596685 | ||||||
| chr11:44596685
|
G | T | 3 | a0001c0009t0004g0084a0002c0003t0004g0271a0002c0015t0007g0078 | 3 | HG02630.hp2 HG02809.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.63+1960G>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 3/9 | chr11 | 44596685 | ||||||
| chr11:44596800
|
G | A | 1 | a0002c0003t0003g0296 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.63+2075G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 3/9 | chr11 | 44596800 | ||||||
| chr11:44596816
|
C | T | 1 | a0002c0002t0001g0197 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.63+2091C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 3/9 | chr11 | 44596816 | ||||||
| chr11:44596935
|
G | A | 3 | a0002c0003t0001g0007a0002c0003t0001g0289a0002c0003t0003g0007 | 3 | HG01168.hp1 HG01169.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.63+2210G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 3/9 | chr11 | 44596935 | ||||||
| chr11:44596951
|
T | A | 1 | a0001c0001t0001g0356 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.63+2226T>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 3/9 | chr11 | 44596951 | ||||||
| chr11:44597148
|
G | A | 6 | a0001c0010t0004g0093a0001c0010t0007g0095a0002c0003t0002g0324others(3): Show | 6 | HG01109.hp1 HG02257.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.63+2423G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 3/9 | chr11 | 44597148 | ||||||
| chr11:44597169
|
G | A | 10 | a0001c0001t0002g0147a0001c0001t0004g0164a0001c0001t0004g0165others(7): Show | 10 | HG01243.hp1 HG01496.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.63+2444G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 3/9 | chr11 | 44597169 | ||||||
| chr11:44597213
|
T | C | 267 | a0001c0001t0001g0006a0001c0001t0001g0064a0001c0001t0001g0133others(264): Show | 268 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(265): Show |
intron_variant | MODIFIER | c.63+2488T>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 3/9 | chr11 | 44597213 | ||||||
| chr11:44597214
|
G | A | 1 | a0001c0001t0008g0266 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.63+2489G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 3/9 | chr11 | 44597214 | ||||||
| chr11:44597232
|
C | T | 1 | a0001c0001t0001g0319 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.63+2507C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 3/9 | chr11 | 44597232 | ||||||
| chr11:44597361
|
TG | T | 120 | a0001c0001t0001g0133a0001c0001t0001g0319a0001c0001t0002g0147others(117): Show | 121 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(118): Show |
intron_variant | MODIFIER | c.63+2641delG | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 44597361 | |||||
| chr11:44597397
|
C | G | 1 | a0001c0005t0001g0265 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.63+2672C>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 3/9 | chr11 | 44597397 | ||||||
| chr11:44597490
|
G | A | 100 | a0001c0001t0001g0144a0001c0001t0001g0242a0001c0001t0001g0243others(97): Show | 100 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(97): Show |
intron_variant | MODIFIER | c.64-2668G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 3/9 | chr11 | 44597490 | ||||||
| chr11:44597702
|
T | C | 1 | a0001c0009t0011g0264 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.64-2456T>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 3/9 | chr11 | 44597702 | ||||||
| chr11:44597727
|
T | C | 137 | a0001c0001t0001g0133a0001c0001t0001g0250a0001c0001t0001g0251others(134): Show | 138 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(135): Show |
intron_variant | MODIFIER | c.64-2431T>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 3/9 | chr11 | 44597727 | ||||||
| chr11:44597733
|
G | A | 5 | a0001c0001t0001g0332a0001c0001t0008g0272a0001c0001t0008g0330others(2): Show | 5 | HG03041.hp2 HG03471.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.64-2425G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 3/9 | chr11 | 44597733 | ||||||
| chr11:44597809
|
C | A | 8 | a0001c0005t0001g0087a0001c0005t0002g0079a0001c0005t0037g0082others(5): Show | 8 | NA18942.hp1 NA18948.hp1 NA18959.hp2 others(5): Show |
intron_variant | MODIFIER | c.64-2349C>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 3/9 | chr11 | 44597809 | ||||||
| chr11:44598142
|
G | A | 1 | a0001c0001t0011g0329 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.64-2016G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 3/9 | chr11 | 44598142 | ||||||
| chr11:44598400
|
A | ATTTT | 33 | a0001c0001t0001g0242a0001c0001t0001g0332a0001c0001t0002g0160others(30): Show | 33 | HG00140.hp2 HG00408.hp1 HG00733.hp2 others(30): Show |
intron_variant | MODIFIER | c.64-1732_64-1729dup others(4): Show |
CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 44598400 | |||||
| chr11:44598400
|
A | ATTTTT | 43 | a0001c0001t0001g0006a0001c0001t0001g0144a0001c0001t0001g0243others(40): Show | 43 | HG00140.hp1 HG00323.hp2 HG00597.hp2 others(40): Show |
intron_variant | MODIFIER | c.64-1733_64-1729dup others(5): Show |
CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 44598400 | |||||
| chr11:44598400
|
A | ATTTTTT | 40 | a0001c0001t0001g0064a0001c0001t0001g0251a0001c0001t0002g0118others(37): Show | 40 | HG00438.hp2 HG00544.hp1 HG00558.hp2 others(37): Show |
intron_variant | MODIFIER | c.64-1734_64-1729dup others(6): Show |
CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 44598400 | |||||
| chr11:44598400
|
A | ATTTTTTT | 69 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0044others(66): Show | 70 | HG00099.hp2 HG00323.hp1 HG00558.hp1 others(67): Show |
intron_variant | MODIFIER | c.64-1735_64-1729dup others(7): Show |
CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 44598400 | |||||
| chr11:44598400
|
A | ATTTTTTT others(1): Show |
29 | a0001c0001t0001g0047a0001c0001t0001g0229a0001c0001t0001g0287others(26): Show | 30 | HG00423.hp2 HG00642.hp1 HG01106.hp2 others(27): Show |
intron_variant | MODIFIER | c.64-1736_64-1729dup others(8): Show |
CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 44598400 | |||||
| chr11:44598400
|
A | ATTTTTTT others(2): Show |
14 | a0001c0001t0001g0308a0001c0001t0002g0355a0001c0001t0003g0017others(11): Show | 14 | HG00673.hp1 HG00735.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.64-1737_64-1729dup others(9): Show |
CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 44598400 | |||||
| chr11:44598400
|
A | ATTTTTTT others(3): Show |
5 | a0001c0001t0003g0104a0001c0009t0001g0032a0002c0003t0002g0325others(2): Show | 5 | HG00099.hp1 HG01109.hp1 HG02074.hp2 others(2): Show |
intron_variant | MODIFIER | c.64-1738_64-1729dup others(10): Show |
CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 44598400 | |||||
| chr11:44598400
|
A | ATTTTTTT others(4): Show |
3 | a0001c0010t0007g0095a0002c0003t0014g0328a0002c0003t0028g0262 | 3 | HG01884.hp2 HG02257.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.64-1739_64-1729dup others(11): Show |
CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 44598400 | |||||
| chr11:44598400
|
A | ATTTTTTT others(5): Show |
1 | a0001c0009t0011g0264 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.64-1740_64-1729dup others(12): Show |
CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 44598400 | |||||
| chr11:44598400
|
A | ATTTTTTT others(6): Show |
1 | a0001c0010t0004g0174 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.64-1741_64-1729dup others(13): Show |
CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 44598400 | |||||
| chr11:44598400
|
A | ATTTTTTT others(12): Show |
1 | a0001c0009t0001g0086 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.64-1747_64-1729dup others(19): Show |
CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 44598400 | |||||
| chr11:44598400
|
ATT | A | 11 | a0001c0005t0001g0265a0001c0011t0001g0334a0001c0011t0001g0336others(8): Show | 11 | HG03041.hp1 NA18942.hp2 NA18950.hp2 others(8): Show |
intron_variant | MODIFIER | c.64-1730_64-1729del others(2): Show |
CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 44598400 | |||||
| chr11:44598400
|
ATTT | A | 15 | a0001c0001t0005g0214a0001c0001t0006g0215a0001c0001t0013g0024others(12): Show | 15 | HG00621.hp2 HG00741.hp2 HG01071.hp2 others(12): Show |
intron_variant | MODIFIER | c.64-1731_64-1729del others(3): Show |
CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 44598400 | |||||
| chr11:44598400
|
ATTTT | A | 55 | a0001c0001t0001g0133a0001c0001t0002g0147a0001c0001t0003g0163others(52): Show | 55 | HG00408.hp2 HG00544.hp2 HG00597.hp1 others(52): Show |
intron_variant | MODIFIER | c.64-1732_64-1729del others(4): Show |
CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 44598400 | |||||
| chr11:44598400
|
ATTTTT | A | 5 | a0001c0001t0004g0164a0001c0005t0002g0079a0001c0005t0002g0291others(2): Show | 6 | HG01515.hp2 HG01517.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.64-1733_64-1729del others(5): Show |
CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 44598400 | |||||
| chr11:44598400
|
ATTTTTTT others(5): Show |
A | 14 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0027others(11): Show | 20 | HG00423.hp1 HG00438.hp1 HG00621.hp1 others(17): Show |
intron_variant | MODIFIER | c.64-1740_64-1729del others(12): Show |
CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 44598400 | |||||
| chr11:44598400
|
ATTTTTTT others(6): Show |
A | 1 | a0001c0001t0004g0254 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.64-1741_64-1729del others(13): Show |
CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 44598400 | |||||
| chr11:44598400
|
ATTTTTTT others(8): Show |
A | 1 | a0002c0003t0007g0021 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.64-1743_64-1729del others(15): Show |
CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 44598400 | |||||
| chr11:44598449
|
G | C | 30 | a0001c0001t0001g0319a0001c0001t0002g0317a0001c0001t0003g0108others(27): Show | 30 | HG00140.hp2 HG01074.hp2 HG01109.hp2 others(27): Show |
intron_variant | MODIFIER | c.64-1709G>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 3/9 | chr11 | 44598449 | ||||||
| chr11:44598496
|
G | A | 9 | a0001c0001t0002g0317a0001c0001t0003g0108a0001c0001t0004g0270others(6): Show | 9 | HG01109.hp2 HG01168.hp2 HG01243.hp2 others(6): Show |
intron_variant | MODIFIER | c.64-1662G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 3/9 | chr11 | 44598496 | ||||||
| chr11:44598553
|
C | T | 2 | a0001c0001t0002g0267a0001c0001t0006g0010 | 3 | HG00099.hp2 HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.64-1605C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 3/9 | chr11 | 44598553 | ||||||
| chr11:44598657
|
G | A | 1 | a0001c0005t0001g0265 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.64-1501G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 3/9 | chr11 | 44598657 | ||||||
| chr11:44598706
|
C | T | 26 | a0001c0001t0004g0323a0001c0001t0004g0333a0001c0001t0008g0266others(23): Show | 26 | HG01109.hp1 HG01884.hp2 HG02055.hp2 others(23): Show |
intron_variant | MODIFIER | c.64-1452C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 3/9 | chr11 | 44598706 | ||||||
| chr11:44598775
|
C | T | 1 | a0001c0001t0012g0342 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.64-1383C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 3/9 | chr11 | 44598775 | ||||||
| chr11:44598792
|
C | T | 1 | a0002c0003t0006g0217 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.64-1366C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 3/9 | chr11 | 44598792 | ||||||
| chr11:44598793
|
G | A | 7 | a0001c0010t0004g0093a0001c0010t0004g0174a0001c0010t0007g0095others(4): Show | 7 | HG01109.hp1 HG02257.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.64-1365G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 3/9 | chr11 | 44598793 | ||||||
| chr11:44598852
|
G | A | 8 | a0001c0001t0001g0003a0001c0001t0001g0051a0001c0001t0001g0058others(5): Show | 9 | HG00741.hp1 HG01256.hp2 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.64-1306G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 3/9 | chr11 | 44598852 | ||||||
| chr11:44598889
|
G | A | 1 | a0001c0005t0001g0265 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.64-1269G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 3/9 | chr11 | 44598889 | ||||||
| chr11:44598992
|
C | A | 1 | a0002c0003t0006g0132 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.64-1166C>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 3/9 | chr11 | 44598992 | ||||||
| chr11:44599069
|
G | A | 7 | a0001c0010t0004g0093a0001c0010t0004g0174a0001c0010t0007g0095others(4): Show | 7 | HG01109.hp1 HG02257.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.64-1089G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 3/9 | chr11 | 44599069 | ||||||
| chr11:44599407
|
G | A | 100 | a0001c0001t0001g0144a0001c0001t0001g0242a0001c0001t0001g0243others(97): Show | 100 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(97): Show |
intron_variant | MODIFIER | c.64-751G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 3/9 | chr11 | 44599407 | ||||||
| chr11:44599565
|
G | A | 1 | a0001c0010t0001g0117 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.64-593G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 3/9 | chr11 | 44599565 | ||||||
| chr11:44599567
|
C | A | 1 | a0001c0009t0001g0086 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.64-591C>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 3/9 | chr11 | 44599567 | ||||||
| chr11:44599592
|
G | C | 1 | a0002c0025t0004g0349 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.64-566G>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 3/9 | chr11 | 44599592 | ||||||
| chr11:44599622
|
G | A | 87 | a0001c0001t0001g0133a0001c0001t0002g0147a0001c0001t0003g0163others(84): Show | 88 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(85): Show |
intron_variant | MODIFIER | c.64-536G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 3/9 | chr11 | 44599622 | ||||||
| chr11:44599646
|
A | G | 1 | a0002c0003t0014g0328 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.64-512A>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 3/9 | chr11 | 44599646 | ||||||
| chr11:44599732
|
C | T | 2 | a0002c0002t0001g0233a0002c0002t0022g0273 | 2 | HG00323.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.64-426C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 3/9 | chr11 | 44599732 | ||||||
| chr11:44600114
|
T | C | 4 | a0002c0003t0029g0275a0002c0003t0043g0276a0002c0003t0045g0065others(1): Show | 4 | HG01243.hp1 HG01496.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.64-44T>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 3/9 | chr11 | 44600114 | ||||||
| chr11:44600357
|
G | T | 1 | a0001c0001t0002g0118 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.136+127G>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 4/9 | chr11 | 44600357 | ||||||
| chr11:44600495
|
T | C | 2 | a0002c0003t0041g0312a0002c0003t0042g0311 | 2 | HG02145.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.136+265T>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 4/9 | chr11 | 44600495 | ||||||
| chr11:44600607
|
G | A | 62 | a0001c0001t0001g0133a0001c0001t0002g0147a0001c0001t0003g0163others(59): Show | 63 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(60): Show |
intron_variant | MODIFIER | c.136+377G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 4/9 | chr11 | 44600607 | ||||||
| chr11:44600676
|
C | G | 88 | a0001c0001t0001g0133a0001c0001t0002g0147a0001c0001t0003g0163others(85): Show | 89 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(86): Show |
intron_variant | MODIFIER | c.136+446C>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 4/9 | chr11 | 44600676 | ||||||
| chr11:44600762
|
G | A | 53 | a0001c0001t0001g0133a0001c0001t0003g0163a0001c0005t0001g0087others(50): Show | 54 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(51): Show |
intron_variant | MODIFIER | c.136+532G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 4/9 | chr11 | 44600762 | ||||||
| chr11:44600859
|
C | T | 1 | a0002c0003t0011g0326 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.136+629C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 4/9 | chr11 | 44600859 | ||||||
| chr11:44600898
|
GACTCGA | G | 2 | a0001c0001t0001g0003a0001c0001t0001g0051 | 3 | HG01256.hp2 HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.136+673_136+678del others(6): Show |
CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr11 | 44600898 | |||||
| chr11:44600994
|
G | T | 1 | a0002c0002t0001g0045 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.136+764G>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 4/9 | chr11 | 44600994 | ||||||
| chr11:44601031
|
C | T | 1 | a0002c0003t0014g0259 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.136+801C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 4/9 | chr11 | 44601031 | ||||||
| chr11:44601032
|
G | A | 6 | a0001c0005t0001g0087a0001c0005t0002g0079a0001c0005t0037g0082others(3): Show | 6 | NA18942.hp1 NA18948.hp1 NA18959.hp2 others(3): Show |
intron_variant | MODIFIER | c.136+802G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 4/9 | chr11 | 44601032 | ||||||
| chr11:44601039
|
C | T | 8 | a0001c0001t0001g0133a0001c0005t0001g0204a0001c0005t0002g0175others(5): Show | 8 | HG00673.hp2 HG02083.hp2 HG02129.hp2 others(5): Show |
intron_variant | MODIFIER | c.136+809C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 4/9 | chr11 | 44601039 | ||||||
| chr11:44601101
|
GGA | G | 362 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(359): Show | 371 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(368): Show |
intron_variant | MODIFIER | c.136+875_136+876del others(2): Show |
CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr11 | 44601101 | |||||
| chr11:44601161
|
T | C | 259 | a0001c0001t0001g0006a0001c0001t0001g0064a0001c0001t0001g0133others(256): Show | 260 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(257): Show |
intron_variant | MODIFIER | c.136+931T>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 4/9 | chr11 | 44601161 | ||||||
| chr11:44601179
|
C | T | 62 | a0001c0001t0001g0133a0001c0001t0002g0147a0001c0001t0003g0163others(59): Show | 63 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(60): Show |
intron_variant | MODIFIER | c.136+949C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 4/9 | chr11 | 44601179 | ||||||
| chr11:44601183
|
G | A | 28 | a0001c0001t0001g0319a0001c0001t0002g0317a0001c0001t0003g0108others(25): Show | 28 | HG00140.hp2 HG01074.hp2 HG01109.hp2 others(25): Show |
intron_variant | MODIFIER | c.136+953G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 4/9 | chr11 | 44601183 | ||||||
| chr11:44601489
|
C | G | 9 | a0001c0001t0004g0323a0001c0012t0016g0313a0002c0003t0002g0038others(6): Show | 9 | HG02280.hp2 HG02717.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.136+1259C>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 4/9 | chr11 | 44601489 | ||||||
| chr11:44601585
|
C | T | 8 | a0001c0001t0001g0353a0001c0001t0001g0354a0001c0001t0001g0356others(5): Show | 8 | HG00558.hp1 HG00558.hp2 HG02056.hp2 others(5): Show |
intron_variant | MODIFIER | c.136+1355C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 4/9 | chr11 | 44601585 | ||||||
| chr11:44601637
|
C | T | 1 | a0001c0001t0007g0327 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.136+1407C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 4/9 | chr11 | 44601637 | ||||||
| chr11:44601707
|
T | G | 1 | a0001c0001t0051g0223 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.136+1477T>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 4/9 | chr11 | 44601707 | ||||||
| chr11:44601750
|
G | A | 31 | a0001c0001t0001g0319a0001c0001t0002g0317a0001c0001t0003g0108others(28): Show | 31 | HG00140.hp2 HG01074.hp2 HG01109.hp2 others(28): Show |
intron_variant | MODIFIER | c.136+1520G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 4/9 | chr11 | 44601750 | ||||||
| chr11:44601780
|
G | A | 7 | a0001c0010t0004g0093a0001c0010t0004g0174a0001c0010t0007g0095others(4): Show | 7 | HG01109.hp1 HG02257.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.136+1550G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 4/9 | chr11 | 44601780 | ||||||
| chr11:44601963
|
C | T | 2 | a0001c0001t0002g0147a0002c0003t0044g0268 | 2 | HG02145.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.136+1733C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 4/9 | chr11 | 44601963 | ||||||
| chr11:44602029
|
T | A | 1 | a0001c0001t0004g0333 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.136+1799T>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 4/9 | chr11 | 44602029 | ||||||
| chr11:44602108
|
G | T | 52 | a0001c0001t0001g0133a0001c0001t0003g0163a0001c0005t0001g0087others(49): Show | 53 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(50): Show |
intron_variant | MODIFIER | c.136+1878G>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 4/9 | chr11 | 44602108 | ||||||
| chr11:44602122
|
T | C | 88 | a0001c0001t0001g0133a0001c0001t0002g0147a0001c0001t0003g0163others(85): Show | 89 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(86): Show |
intron_variant | MODIFIER | c.136+1892T>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 4/9 | chr11 | 44602122 | ||||||
| chr11:44602145
|
C | T | 1 | a0002c0019t0011g0345 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.136+1915C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 4/9 | chr11 | 44602145 | ||||||
| chr11:44602270
|
G | A | 9 | a0001c0001t0001g0044a0001c0001t0001g0047a0001c0001t0003g0096others(6): Show | 9 | HG00642.hp1 HG01192.hp1 HG01928.hp2 others(6): Show |
intron_variant | MODIFIER | c.136+2040G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 4/9 | chr11 | 44602270 | ||||||
| chr11:44602347
|
G | A | 44 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0044others(41): Show | 45 | HG00558.hp1 HG00558.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.136+2117G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 4/9 | chr11 | 44602347 | ||||||
| chr11:44602599
|
T | C | 14 | a0001c0001t0005g0214a0001c0001t0006g0215a0001c0001t0013g0024others(11): Show | 14 | HG00621.hp2 HG00741.hp2 HG01070.hp2 others(11): Show |
intron_variant | MODIFIER | c.136+2369T>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 4/9 | chr11 | 44602599 | ||||||
| chr11:44602605
|
A | G | 1 | a0001c0009t0004g0239 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.136+2375A>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 4/9 | chr11 | 44602605 | ||||||
| chr11:44602627
|
G | A | 1 | a0001c0001t0002g0267 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.136+2397G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 4/9 | chr11 | 44602627 | ||||||
| chr11:44602630
|
C | T | 1 | a0001c0001t0004g0254 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.136+2400C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 4/9 | chr11 | 44602630 | ||||||
| chr11:44602672
|
GA | G | 62 | a0001c0001t0001g0133a0001c0001t0002g0147a0001c0001t0003g0163others(59): Show | 63 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(60): Show |
intron_variant | MODIFIER | c.137-2377delA | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr11 | 44602672 | |||||
| chr11:44602681
|
A | T | 89 | a0001c0001t0001g0064a0001c0001t0001g0250a0001c0001t0001g0251others(86): Show | 89 | HG00140.hp2 HG00621.hp2 HG00741.hp2 others(86): Show |
intron_variant | MODIFIER | c.137-2377A>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 4/9 | chr11 | 44602681 | ||||||
| chr11:44602734
|
C | T | 1 | a0002c0003t0001g0067 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.137-2324C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 4/9 | chr11 | 44602734 | ||||||
| chr11:44602891
|
C | T | 1 | a0001c0012t0016g0313 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.137-2167C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 4/9 | chr11 | 44602891 | ||||||
| chr11:44602901
|
C | G | 89 | a0001c0001t0001g0133a0001c0001t0002g0147a0001c0001t0003g0163others(86): Show | 90 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(87): Show |
intron_variant | MODIFIER | c.137-2157C>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 4/9 | chr11 | 44602901 | ||||||
| chr11:44602901
|
C | T | 1 | a0001c0010t0001g0117 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.137-2157C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 4/9 | chr11 | 44602901 | ||||||
| chr11:44602930
|
C | T | 31 | a0001c0001t0001g0319a0001c0001t0002g0317a0001c0001t0003g0108others(28): Show | 31 | HG00140.hp2 HG01074.hp2 HG01109.hp2 others(28): Show |
intron_variant | MODIFIER | c.137-2128C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 4/9 | chr11 | 44602930 | ||||||
| chr11:44602960
|
G | A | 31 | a0001c0001t0001g0319a0001c0001t0002g0317a0001c0001t0003g0108others(28): Show | 31 | HG00140.hp2 HG01074.hp2 HG01109.hp2 others(28): Show |
intron_variant | MODIFIER | c.137-2098G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 4/9 | chr11 | 44602960 | ||||||
| chr11:44603255
|
T | C | 89 | a0001c0001t0001g0133a0001c0001t0002g0147a0001c0001t0003g0163others(86): Show | 90 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(87): Show |
intron_variant | MODIFIER | c.137-1803T>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 4/9 | chr11 | 44603255 | ||||||
| chr11:44603264
|
G | A | 1 | a0002c0002t0001g0034 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.137-1794G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 4/9 | chr11 | 44603264 | ||||||
| chr11:44603373
|
C | G | 1 | a0001c0005t0001g0265 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.137-1685C>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 4/9 | chr11 | 44603373 | ||||||
| chr11:44603408
|
C | T | 4 | a0001c0016t0004g0351a0001c0016t0017g0030a0001c0016t0048g0031others(1): Show | 4 | HG02055.hp2 HG02258.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.137-1650C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 4/9 | chr11 | 44603408 | ||||||
| chr11:44603449
|
C | G | 1 | a0002c0008t0004g0088 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.137-1609C>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 4/9 | chr11 | 44603449 | ||||||
| chr11:44603516
|
G | A | 2 | a0001c0009t0001g0086a0002c0003t0014g0328 | 2 | HG01884.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.137-1542G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 4/9 | chr11 | 44603516 | ||||||
| chr11:44603551
|
C | T | 2 | a0002c0003t0002g0038a0002c0003t0011g0261 | 2 | HG02818.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.137-1507C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 4/9 | chr11 | 44603551 | ||||||
| chr11:44603592
|
C | T | 1 | a0001c0005t0001g0265 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.137-1466C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 4/9 | chr11 | 44603592 | ||||||
| chr11:44603629
|
C | T | 5 | a0001c0001t0001g0064a0001c0001t0008g0181a0002c0003t0001g0091others(2): Show | 5 | HG02109.hp1 HG02109.hp2 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.137-1429C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 4/9 | chr11 | 44603629 | ||||||
| chr11:44603632
|
G | A | 1 | a0001c0016t0004g0351 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.137-1426G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 4/9 | chr11 | 44603632 | ||||||
| chr11:44603762
|
T | C | 1 | a0001c0001t0004g0281 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.137-1296T>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 4/9 | chr11 | 44603762 | ||||||
| chr11:44603792
|
T | A | 1 | a0002c0008t0002g0109 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.137-1266T>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 4/9 | chr11 | 44603792 | ||||||
| chr11:44603799
|
G | A | 1 | a0002c0002t0002g0196 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.137-1259G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 4/9 | chr11 | 44603799 | ||||||
| chr11:44603810
|
G | A | 17 | a0001c0001t0004g0323a0001c0001t0008g0266a0001c0010t0004g0093others(14): Show | 17 | HG01109.hp1 HG02257.hp2 HG02280.hp1 others(14): Show |
intron_variant | MODIFIER | c.137-1248G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 4/9 | chr11 | 44603810 | ||||||
| chr11:44603842
|
T | C | 90 | a0001c0001t0001g0133a0001c0001t0002g0147a0001c0001t0003g0163others(87): Show | 91 | HG00323.hp1 HG00408.hp2 HG00544.hp1 others(88): Show |
intron_variant | MODIFIER | c.137-1216T>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 4/9 | chr11 | 44603842 | ||||||
| chr11:44603898
|
C | T | 2 | a0001c0001t0051g0223a0002c0003t0004g0346 | 2 | HG02258.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.137-1160C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 4/9 | chr11 | 44603898 | ||||||
| chr11:44603899
|
G | A | 1 | a0002c0004t0003g0186 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.137-1159G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 4/9 | chr11 | 44603899 | ||||||
| chr11:44603943
|
T | C | 91 | a0001c0001t0001g0133a0001c0001t0002g0147a0001c0001t0003g0163others(88): Show | 92 | HG00323.hp1 HG00408.hp2 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.137-1115T>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 4/9 | chr11 | 44603943 | ||||||
| chr11:44603961
|
C | A | 3 | a0002c0002t0001g0233a0002c0002t0003g0052a0002c0002t0022g0273 | 3 | HG00323.hp2 HG02055.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.137-1097C>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 4/9 | chr11 | 44603961 | ||||||
| chr11:44604062
|
C | T | 1 | a0002c0002t0001g0137 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.137-996C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 4/9 | chr11 | 44604062 | ||||||
| chr11:44604065
|
C | T | 1 | a0001c0006t0001g0199 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.137-993C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 4/9 | chr11 | 44604065 | ||||||
| chr11:44604321
|
C | T | 3 | a0001c0009t0015g0224a0001c0012t0004g0257a0001c0012t0004g0258 | 3 | HG02451.hp1 HG02622.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.137-737C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 4/9 | chr11 | 44604321 | ||||||
| chr11:44604350
|
G | A | 4 | a0002c0002t0001g0016a0002c0002t0001g0042a0002c0002t0001g0045others(1): Show | 4 | HG01255.hp1 HG01928.hp1 HG01943.hp1 others(1): Show |
intron_variant | MODIFIER | c.137-708G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 4/9 | chr11 | 44604350 | ||||||
| chr11:44604430
|
G | A | 3 | a0001c0001t0001g0006a0001c0001t0003g0006a0001c0001t0046g0092 | 3 | HG02970.hp1 HG03139.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.137-628G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 4/9 | chr11 | 44604430 | ||||||
| chr11:44604529
|
GTTA | G | 10 | a0001c0011t0001g0334a0001c0011t0001g0336a0001c0011t0001g0337others(7): Show | 10 | NA18942.hp2 NA18950.hp2 NA18965.hp2 others(7): Show |
intron_variant | MODIFIER | c.137-524_137-522del others(3): Show |
CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr11 | 44604529 | |||||
| chr11:44604706
|
C | T | 1 | a0001c0001t0002g0317 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.137-352C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 4/9 | chr11 | 44604706 | ||||||
| chr11:44604732
|
TTGG | T | 10 | a0001c0011t0001g0334a0001c0011t0001g0336a0001c0011t0001g0337others(7): Show | 10 | NA18942.hp2 NA18950.hp2 NA18965.hp2 others(7): Show |
intron_variant | MODIFIER | c.137-322_137-320del others(3): Show |
CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr11 | 44604732 | |||||
| chr11:44604826
|
G | A | 1 | a0001c0016t0004g0351 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.137-232G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 4/9 | chr11 | 44604826 | ||||||
| chr11:44604834
|
G | A | 1 | a0001c0009t0011g0264 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.137-224G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 4/9 | chr11 | 44604834 | ||||||
| chr11:44604847
|
G | A | 98 | a0001c0001t0001g0064a0001c0001t0001g0133a0001c0001t0001g0250others(95): Show | 99 | HG00323.hp1 HG00408.hp2 HG00544.hp1 others(96): Show |
intron_variant | MODIFIER | c.137-211G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 4/9 | chr11 | 44604847 | ||||||
| chr11:44604911
|
C | G | 100 | a0001c0001t0001g0144a0001c0001t0001g0242a0001c0001t0001g0243others(97): Show | 100 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(97): Show |
intron_variant | MODIFIER | c.137-147C>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 4/9 | chr11 | 44604911 | ||||||
| chr11:44604930
|
C | A | 8 | a0001c0006t0001g0177a0001c0006t0003g0178a0001c0006t0003g0344others(5): Show | 8 | HG00140.hp1 HG00639.hp2 HG00738.hp1 others(5): Show |
intron_variant | MODIFIER | c.137-128C>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 4/9 | chr11 | 44604930 | ||||||
| chr11:44605043
|
T | A | 3 | a0002c0003t0001g0007a0002c0003t0001g0289a0002c0003t0003g0007 | 3 | HG01168.hp1 HG01169.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.137-15T>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 4/9 | chr11 | 44605043 | ||||||
| chr11:44605562
|
G | A | 1 | a0002c0007t0002g0111 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.336+133G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44605562 | ||||||
| chr11:44605618
|
G | A | 88 | a0001c0001t0001g0133a0001c0001t0002g0147a0001c0001t0003g0163others(85): Show | 89 | HG00323.hp1 HG00408.hp2 HG00544.hp1 others(86): Show |
intron_variant | MODIFIER | c.336+189G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44605618 | ||||||
| chr11:44605720
|
T | C | 1 | a0001c0009t0011g0264 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.336+291T>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44605720 | ||||||
| chr11:44605842
|
A | G | 63 | a0001c0001t0001g0133a0001c0001t0002g0147a0001c0001t0003g0163others(60): Show | 64 | HG00323.hp1 HG00408.hp2 HG00544.hp1 others(61): Show |
intron_variant | MODIFIER | c.336+413A>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44605842 | ||||||
| chr11:44605857
|
C | T | 1 | a0002c0008t0002g0109 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.336+428C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44605857 | ||||||
| chr11:44606162
|
T | G | 87 | a0001c0001t0002g0147a0001c0001t0003g0163a0001c0001t0004g0164others(84): Show | 88 | HG00323.hp1 HG00408.hp2 HG00544.hp1 others(85): Show |
intron_variant | MODIFIER | c.336+733T>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44606162 | ||||||
| chr11:44606234
|
G | A | 1 | a0001c0005t0001g0265 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.336+805G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44606234 | ||||||
| chr11:44606298
|
G | A | 1 | a0001c0001t0001g0064 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.336+869G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44606298 | ||||||
| chr11:44606467
|
C | CA | 188 | a0001c0001t0001g0006a0001c0001t0001g0064a0001c0001t0001g0133others(185): Show | 188 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(185): Show |
intron_variant | MODIFIER | c.336+1058dupA | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr11 | 44606467 | |||||
| chr11:44606467
|
C | CAA | 78 | a0001c0001t0002g0147a0001c0001t0002g0317a0001c0001t0003g0163others(75): Show | 79 | HG00323.hp1 HG00408.hp2 HG00544.hp1 others(76): Show |
intron_variant | MODIFIER | c.336+1057_336+1058d others(4): Show |
CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr11 | 44606467 | |||||
| chr11:44606467
|
C | CAAA | 15 | a0001c0001t0013g0071a0001c0005t0002g0291a0001c0009t0011g0264others(12): Show | 15 | HG01167.hp2 HG01169.hp2 HG01255.hp2 others(12): Show |
intron_variant | MODIFIER | c.336+1056_336+1058d others(5): Show |
CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr11 | 44606467 | |||||
| chr11:44606543
|
A | G | 1 | a0002c0007t0003g0331 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.336+1114A>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44606543 | ||||||
| chr11:44606680
|
G | T | 1 | a0001c0001t0003g0163 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.336+1251G>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44606680 | ||||||
| chr11:44606817
|
A | G | 6 | a0001c0001t0001g0064a0001c0001t0008g0181a0002c0003t0001g0091others(3): Show | 6 | HG02109.hp1 HG02109.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.336+1388A>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44606817 | ||||||
| chr11:44606852
|
C | T | 13 | a0001c0001t0004g0323a0001c0001t0008g0266a0001c0009t0015g0224others(10): Show | 13 | HG02280.hp2 HG02451.hp1 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.336+1423C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44606852 | ||||||
| chr11:44606871
|
C | T | 1 | a0002c0003t0038g0279 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.336+1442C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44606871 | ||||||
| chr11:44606917
|
C | T | 1 | a0002c0003t0003g0296 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.336+1488C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44606917 | ||||||
| chr11:44606929
|
C | T | 137 | a0001c0001t0001g0133a0001c0001t0001g0250a0001c0001t0001g0251others(134): Show | 138 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(135): Show |
intron_variant | MODIFIER | c.336+1500C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44606929 | ||||||
| chr11:44607525
|
C | G | 11 | a0001c0001t0013g0071a0001c0011t0001g0334a0001c0011t0001g0336others(8): Show | 11 | HG01255.hp2 NA18942.hp2 NA18950.hp2 others(8): Show |
intron_variant | MODIFIER | c.336+2096C>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44607525 | ||||||
| chr11:44607681
|
T | C | 1 | a0002c0003t0003g0296 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.336+2252T>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44607681 | ||||||
| chr11:44607793
|
T | C | 1 | a0001c0005t0004g0103 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.336+2364T>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44607793 | ||||||
| chr11:44607914
|
G | A | 86 | a0001c0001t0002g0147a0001c0001t0003g0163a0001c0001t0004g0164others(83): Show | 87 | HG00323.hp1 HG00408.hp2 HG00544.hp1 others(84): Show |
intron_variant | MODIFIER | c.336+2485G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44607914 | ||||||
| chr11:44608084
|
C | T | 1 | a0002c0002t0003g0156 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.336+2655C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44608084 | ||||||
| chr11:44608252
|
G | A | 5 | a0001c0001t0001g0332a0001c0001t0008g0272a0001c0001t0008g0330others(2): Show | 5 | HG03041.hp2 HG03471.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.336+2823G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44608252 | ||||||
| chr11:44608303
|
C | T | 7 | a0001c0001t0001g0353a0001c0001t0001g0354a0001c0001t0001g0356others(4): Show | 7 | HG00558.hp1 HG00558.hp2 HG02083.hp1 others(4): Show |
intron_variant | MODIFIER | c.336+2874C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44608303 | ||||||
| chr11:44608361
|
G | A | 1 | a0002c0008t0001g0023 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.336+2932G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44608361 | ||||||
| chr11:44608405
|
C | T | 1 | a0002c0015t0003g0339 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.336+2976C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44608405 | ||||||
| chr11:44608434
|
C | A | 1 | a0002c0002t0002g0203 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.336+3005C>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44608434 | ||||||
| chr11:44608499
|
A | G | 258 | a0001c0001t0001g0006a0001c0001t0001g0064a0001c0001t0001g0133others(255): Show | 259 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(256): Show |
intron_variant | MODIFIER | c.336+3070A>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44608499 | ||||||
| chr11:44608509
|
A | G | 87 | a0001c0001t0002g0147a0001c0001t0003g0163a0001c0001t0004g0164others(84): Show | 88 | HG00323.hp1 HG00408.hp2 HG00544.hp1 others(85): Show |
intron_variant | MODIFIER | c.336+3080A>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44608509 | ||||||
| chr11:44608515
|
T | C | 5 | a0001c0001t0001g0250a0001c0001t0001g0251a0001c0001t0004g0249others(2): Show | 5 | HG02486.hp2 HG02895.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.336+3086T>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44608515 | ||||||
| chr11:44608642
|
A | G | 36 | a0001c0005t0001g0087a0001c0005t0001g0204a0001c0005t0001g0205others(33): Show | 36 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(33): Show |
intron_variant | MODIFIER | c.336+3213A>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44608642 | ||||||
| chr11:44608755
|
A | G | 247 | a0001c0001t0001g0064a0001c0001t0001g0133a0001c0001t0001g0144others(244): Show | 248 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(245): Show |
intron_variant | MODIFIER | c.336+3326A>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44608755 | ||||||
| chr11:44608770
|
A | G | 3 | a0001c0009t0015g0224a0001c0012t0004g0257a0001c0012t0004g0258 | 3 | HG02451.hp1 HG02622.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.336+3341A>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44608770 | ||||||
| chr11:44608847
|
C | A | 1 | a0002c0003t0001g0011 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.336+3418C>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44608847 | ||||||
| chr11:44608854
|
C | T | 13 | a0001c0001t0013g0071a0001c0009t0001g0086a0001c0011t0001g0334others(10): Show | 13 | HG01255.hp2 HG01884.hp2 HG02886.hp1 others(10): Show |
intron_variant | MODIFIER | c.336+3425C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44608854 | ||||||
| chr11:44608860
|
G | A | 5 | a0001c0001t0001g0332a0001c0001t0008g0272a0001c0001t0008g0330others(2): Show | 5 | HG03041.hp2 HG03471.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.336+3431G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44608860 | ||||||
| chr11:44608913
|
C | T | 2 | a0001c0001t0001g0287a0001c0001t0001g0288 | 2 | HG02602.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.336+3484C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44608913 | ||||||
| chr11:44608914
|
G | T | 5 | a0001c0001t0001g0250a0001c0001t0001g0251a0001c0001t0004g0249others(2): Show | 5 | HG02486.hp2 HG02895.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.336+3485G>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44608914 | ||||||
| chr11:44609003
|
A | G | 11 | a0001c0001t0013g0071a0001c0011t0001g0334a0001c0011t0001g0336others(8): Show | 11 | HG01255.hp2 NA18942.hp2 NA18950.hp2 others(8): Show |
intron_variant | MODIFIER | c.336+3574A>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44609003 | ||||||
| chr11:44609095
|
C | A | 4 | a0002c0002t0001g0016a0002c0002t0001g0042a0002c0002t0001g0045others(1): Show | 4 | HG01255.hp1 HG01928.hp1 HG01943.hp1 others(1): Show |
intron_variant | MODIFIER | c.336+3666C>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44609095 | ||||||
| chr11:44609120
|
T | C | 1 | a0001c0001t0013g0071 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.336+3691T>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44609120 | ||||||
| chr11:44609129
|
C | T | 2 | a0001c0001t0001g0006a0001c0001t0003g0006 | 2 | HG02970.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.336+3700C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44609129 | ||||||
| chr11:44609137
|
G | A | 9 | a0001c0001t0004g0323a0001c0012t0016g0313a0002c0003t0002g0038others(6): Show | 9 | HG02280.hp2 HG02717.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.336+3708G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44609137 | ||||||
| chr11:44609191
|
C | T | 3 | a0002c0003t0001g0007a0002c0003t0001g0289a0002c0003t0003g0007 | 3 | HG01168.hp1 HG01169.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.336+3762C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44609191 | ||||||
| chr11:44609535
|
C | A | 2 | a0002c0004t0009g0062a0002c0004t0019g0057 | 2 | HG00735.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.336+4106C>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44609535 | ||||||
| chr11:44609652
|
G | A | 118 | a0001c0001t0001g0064a0001c0001t0001g0133a0001c0001t0001g0319others(115): Show | 119 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(116): Show |
intron_variant | MODIFIER | c.336+4223G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44609652 | ||||||
| chr11:44609809
|
G | A | 1 | a0002c0003t0001g0218 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.336+4380G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44609809 | ||||||
| chr11:44609983
|
G | A | 1 | a0002c0025t0004g0349 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.336+4554G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44609983 | ||||||
| chr11:44609995
|
G | A | 1 | a0001c0001t0008g0266 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.336+4566G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44609995 | ||||||
| chr11:44610105
|
T | C | 142 | a0001c0001t0001g0064a0001c0001t0001g0133a0001c0001t0001g0250others(139): Show | 143 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(140): Show |
intron_variant | MODIFIER | c.336+4676T>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44610105 | ||||||
| chr11:44610295
|
A | G | 353 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(350): Show | 362 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(359): Show |
intron_variant | MODIFIER | c.336+4866A>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44610295 | ||||||
| chr11:44610319
|
T | C | 1 | a0001c0009t0011g0264 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.336+4890T>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44610319 | ||||||
| chr11:44610415
|
G | A | 7 | a0001c0010t0004g0093a0001c0010t0004g0174a0001c0010t0007g0095others(4): Show | 7 | HG01109.hp1 HG02257.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.337-4857G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44610415 | ||||||
| chr11:44610611
|
C | T | 4 | a0001c0001t0001g0064a0001c0001t0008g0181a0002c0003t0001g0091others(1): Show | 4 | HG02109.hp1 HG02109.hp2 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.337-4661C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44610611 | ||||||
| chr11:44610635
|
G | C | 1 | a0002c0003t0001g0067 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.337-4637G>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44610635 | ||||||
| chr11:44610792
|
C | T | 4 | a0001c0001t0001g0250a0001c0001t0001g0251a0001c0001t0004g0249others(1): Show | 4 | HG02486.hp2 HG03130.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.337-4480C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44610792 | ||||||
| chr11:44610831
|
C | CT | 7 | a0001c0001t0001g0064a0001c0001t0008g0181a0001c0009t0011g0264others(4): Show | 7 | HG02109.hp1 HG02109.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.337-4431dupT | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr11 | 44610831 | |||||
| chr11:44610904
|
G | A | 1 | a0001c0001t0002g0184 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.337-4368G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44610904 | ||||||
| chr11:44611055
|
G | A | 1 | a0001c0001t0002g0147 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.337-4217G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44611055 | ||||||
| chr11:44611301
|
G | A | 8 | a0001c0001t0001g0006a0001c0001t0003g0006a0001c0001t0004g0037others(5): Show | 8 | HG02818.hp2 HG02896.hp2 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.337-3971G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44611301 | ||||||
| chr11:44611348
|
C | T | 52 | a0001c0001t0003g0163a0001c0005t0001g0087a0001c0005t0001g0204others(49): Show | 53 | HG00323.hp1 HG00408.hp2 HG00544.hp1 others(50): Show |
intron_variant | MODIFIER | c.337-3924C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44611348 | ||||||
| chr11:44611404
|
T | C | 104 | a0001c0001t0001g0144a0001c0001t0001g0242a0001c0001t0001g0243others(101): Show | 104 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.337-3868T>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44611404 | ||||||
| chr11:44611510
|
G | A | 33 | a0001c0001t0001g0133a0001c0001t0001g0319a0001c0001t0002g0147others(30): Show | 33 | HG00140.hp2 HG01074.hp2 HG01109.hp2 others(30): Show |
intron_variant | MODIFIER | c.337-3762G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44611510 | ||||||
| chr11:44611518
|
C | T | 33 | a0001c0001t0001g0133a0001c0001t0001g0319a0001c0001t0002g0147others(30): Show | 33 | HG00140.hp2 HG01074.hp2 HG01109.hp2 others(30): Show |
intron_variant | MODIFIER | c.337-3754C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44611518 | ||||||
| chr11:44611618
|
C | T | 46 | a0001c0001t0001g0133a0001c0001t0001g0250a0001c0001t0001g0251others(43): Show | 46 | HG00140.hp2 HG01074.hp2 HG01109.hp2 others(43): Show |
intron_variant | MODIFIER | c.337-3654C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44611618 | ||||||
| chr11:44611636
|
A | G | 1 | a0001c0009t0011g0264 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.337-3636A>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44611636 | ||||||
| chr11:44611842
|
ATGGAAAC others(12): Show |
A | 24 | a0001c0001t0005g0214a0001c0001t0006g0215a0001c0001t0013g0024others(21): Show | 24 | HG00621.hp2 HG00741.hp2 HG01070.hp2 others(21): Show |
intron_variant | MODIFIER | c.337-3416_337-3398d others(21): Show |
CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr11 | 44611842 | |||||
| chr11:44611845
|
G | C | 2 | a0001c0001t0008g0272a0001c0001t0008g0330 | 2 | HG03471.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.337-3427G>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44611845 | ||||||
| chr11:44611881
|
A | G | 1 | a0002c0002t0001g0127 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.337-3391A>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44611881 | ||||||
| chr11:44612092
|
G | C | 1 | a0001c0001t0008g0266 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.337-3180G>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44612092 | ||||||
| chr11:44612175
|
C | T | 1 | a0001c0010t0004g0093 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.337-3097C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44612175 | ||||||
| chr11:44612197
|
G | A | 1 | a0002c0008t0002g0145 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.337-3075G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44612197 | ||||||
| chr11:44612510
|
T | C | 2 | a0002c0004t0002g0226a0002c0004t0002g0227 | 2 | NA18954.hp2 NA18963.hp1 |
intron_variant | MODIFIER | c.337-2762T>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44612510 | ||||||
| chr11:44612535
|
C | CT | 32 | a0001c0001t0004g0323a0001c0001t0008g0266a0001c0009t0004g0239others(29): Show | 32 | HG00099.hp1 HG00609.hp2 HG00735.hp1 others(29): Show |
intron_variant | MODIFIER | c.337-2720dupT | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr11 | 44612535 | |||||
| chr11:44612535
|
CT | C | 113 | a0001c0001t0001g0020a0001c0001t0001g0051a0001c0001t0001g0064others(110): Show | 115 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(112): Show |
intron_variant | MODIFIER | c.337-2720delT | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr11 | 44612535 | |||||
| chr11:44612595
|
G | A | 24 | a0001c0001t0005g0214a0001c0001t0006g0215a0001c0001t0013g0024others(21): Show | 24 | HG00621.hp2 HG00741.hp2 HG01070.hp2 others(21): Show |
intron_variant | MODIFIER | c.337-2677G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44612595 | ||||||
| chr11:44612623
|
A | AT | 112 | a0001c0001t0001g0006a0001c0001t0001g0144a0001c0001t0001g0242others(109): Show | 112 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.337-2622dupT | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr11 | 44612623 | |||||
| chr11:44612623
|
A | ATT | 35 | a0001c0001t0001g0064a0001c0001t0003g0163a0001c0001t0015g0352others(32): Show | 35 | HG00140.hp1 HG00673.hp1 HG01074.hp1 others(32): Show |
intron_variant | MODIFIER | c.337-2623_337-2622d others(4): Show |
CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr11 | 44612623 | |||||
| chr11:44612623
|
A | ATTT | 47 | a0001c0001t0005g0214a0001c0001t0006g0215a0001c0001t0008g0181others(44): Show | 48 | HG00323.hp1 HG00408.hp2 HG00544.hp1 others(45): Show |
intron_variant | MODIFIER | c.337-2624_337-2622d others(5): Show |
CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr11 | 44612623 | |||||
| chr11:44612623
|
A | ATTTT | 18 | a0001c0001t0002g0184a0001c0001t0003g0108a0001c0001t0013g0024others(15): Show | 18 | HG00621.hp2 HG00741.hp2 HG01168.hp2 others(15): Show |
intron_variant | MODIFIER | c.337-2625_337-2622d others(6): Show |
CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr11 | 44612623 | |||||
| chr11:44612623
|
A | ATTTTT | 20 | a0001c0001t0001g0133a0001c0001t0001g0319a0001c0001t0002g0160others(17): Show | 20 | HG01074.hp2 HG01109.hp2 HG01243.hp2 others(17): Show |
intron_variant | MODIFIER | c.337-2626_337-2622d others(7): Show |
CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr11 | 44612623 | |||||
| chr11:44612623
|
A | ATTTTTT | 8 | a0001c0001t0002g0317a0001c0001t0008g0266a0001c0009t0011g0264others(5): Show | 8 | HG00140.hp2 HG01346.hp2 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.337-2627_337-2622d others(8): Show |
CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr11 | 44612623 | |||||
| chr11:44612623
|
A | ATTTTTTT others(3): Show |
2 | a0001c0001t0001g0251a0001c0001t0004g0249 | 2 | HG02486.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.337-2631_337-2622d others(12): Show |
CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr11 | 44612623 | |||||
| chr11:44612623
|
A | ATTTTTTT others(4): Show |
1 | a0002c0003t0011g0261 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.337-2632_337-2622d others(13): Show |
CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr11 | 44612623 | |||||
| chr11:44612623
|
AT | A | 11 | a0001c0001t0001g0020a0001c0001t0001g0027a0001c0001t0001g0051others(8): Show | 11 | HG01168.hp1 HG01169.hp1 HG01256.hp1 others(8): Show |
intron_variant | MODIFIER | c.337-2622delT | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr11 | 44612623 | |||||
| chr11:44612623
|
ATTTTTTT others(3): Show |
A | 3 | a0001c0009t0015g0224a0001c0012t0004g0257a0001c0012t0004g0258 | 3 | HG02451.hp1 HG02622.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.337-2631_337-2622d others(12): Show |
CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr11 | 44612623 | |||||
| chr11:44612779
|
C | G | 1 | a0001c0009t0002g0172 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.337-2493C>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44612779 | ||||||
| chr11:44612907
|
A | G | 1 | a0001c0010t0040g0029 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.337-2365A>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44612907 | ||||||
| chr11:44613017
|
A | G | 3 | a0001c0001t0004g0037a0001c0001t0007g0327a0001c0010t0008g0248 | 3 | HG02818.hp2 HG02896.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.337-2255A>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44613017 | ||||||
| chr11:44613171
|
C | T | 1 | a0002c0003t0004g0346 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.337-2101C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44613171 | ||||||
| chr11:44613176
|
T | C | 10 | a0001c0010t0004g0093a0001c0010t0004g0174a0001c0010t0007g0095others(7): Show | 10 | HG01109.hp1 HG02257.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.337-2096T>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44613176 | ||||||
| chr11:44613215
|
T | A | 287 | a0001c0001t0001g0006a0001c0001t0001g0064a0001c0001t0001g0133others(284): Show | 288 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(285): Show |
intron_variant | MODIFIER | c.337-2057T>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44613215 | ||||||
| chr11:44613233
|
CATTTGCC others(9): Show |
C | 1 | a0001c0006t0002g0151 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.337-2038_337-2023d others(18): Show |
CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44613233 | ||||||
| chr11:44613308
|
G | A | 1 | a0001c0006t0002g0151 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.337-1964G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44613308 | ||||||
| chr11:44613324
|
A | G | 1 | a0001c0006t0002g0151 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.337-1948A>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44613324 | ||||||
| chr11:44613331
|
C | G | 1 | a0001c0006t0002g0151 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.337-1941C>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44613331 | ||||||
| chr11:44613332
|
T | G | 1 | a0001c0006t0002g0151 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.337-1940T>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44613332 | ||||||
| chr11:44613360
|
C | T | 29 | a0001c0001t0001g0064a0001c0001t0001g0319a0001c0001t0002g0317others(26): Show | 29 | HG00140.hp2 HG01074.hp2 HG01109.hp2 others(26): Show |
intron_variant | MODIFIER | c.337-1912C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44613360 | ||||||
| chr11:44613403
|
A | G | 1 | a0001c0006t0002g0151 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.337-1869A>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44613403 | ||||||
| chr11:44613406
|
C | A | 1 | a0001c0006t0002g0151 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.337-1866C>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44613406 | ||||||
| chr11:44613415
|
T | C | 10 | a0001c0001t0001g0006a0001c0001t0003g0006a0001c0001t0046g0092others(7): Show | 10 | HG02451.hp1 HG02622.hp1 HG02970.hp1 others(7): Show |
intron_variant | MODIFIER | c.337-1857T>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44613415 | ||||||
| chr11:44613445
|
T | C | 34 | a0001c0001t0001g0064a0001c0001t0001g0133a0001c0001t0001g0319others(31): Show | 34 | HG00140.hp2 HG01074.hp2 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.337-1827T>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44613445 | ||||||
| chr11:44613448
|
G | A | 1 | a0002c0008t0002g0145 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.337-1824G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44613448 | ||||||
| chr11:44613465
|
T | G | 1 | a0001c0006t0002g0151 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.337-1807T>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44613465 | ||||||
| chr11:44613468
|
T | G | 1 | a0001c0006t0002g0151 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.337-1804T>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44613468 | ||||||
| chr11:44613469
|
G | T | 1 | a0001c0006t0002g0151 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.337-1803G>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44613469 | ||||||
| chr11:44613470
|
C | G | 1 | a0001c0006t0002g0151 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.337-1802C>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44613470 | ||||||
| chr11:44613471
|
T | G | 1 | a0001c0006t0002g0151 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.337-1801T>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44613471 | ||||||
| chr11:44613475
|
C | T | 1 | a0001c0006t0002g0151 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.337-1797C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44613475 | ||||||
| chr11:44613477
|
C | G | 1 | a0001c0006t0002g0151 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.337-1795C>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44613477 | ||||||
| chr11:44613535
|
G | A | 1 | a0001c0006t0002g0151 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.337-1737G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44613535 | ||||||
| chr11:44613536
|
A | T | 1 | a0001c0006t0002g0151 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.337-1736A>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44613536 | ||||||
| chr11:44613537
|
T | C | 34 | a0001c0001t0001g0064a0001c0001t0001g0133a0001c0001t0001g0319others(31): Show | 34 | HG00140.hp2 HG01074.hp2 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.337-1735T>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44613537 | ||||||
| chr11:44613539
|
T | G | 1 | a0001c0006t0002g0151 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.337-1733T>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44613539 | ||||||
| chr11:44613545
|
A | T | 1 | a0001c0006t0002g0151 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.337-1727A>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44613545 | ||||||
| chr11:44613553
|
T | C | 1 | a0002c0008t0001g0208 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.337-1719T>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44613553 | ||||||
| chr11:44613555
|
T | G | 1 | a0001c0006t0002g0151 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.337-1717T>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44613555 | ||||||
| chr11:44613561
|
G | T | 1 | a0001c0006t0002g0151 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.337-1711G>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44613561 | ||||||
| chr11:44613658
|
G | A | 183 | a0001c0001t0001g0006a0001c0001t0001g0064a0001c0001t0001g0319others(180): Show | 183 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(180): Show |
intron_variant | MODIFIER | c.337-1614G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44613658 | ||||||
| chr11:44613695
|
T | C | 1 | a0001c0001t0013g0071 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.337-1577T>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44613695 | ||||||
| chr11:44613715
|
T | C | 17 | a0001c0001t0004g0323a0001c0001t0008g0266a0001c0010t0004g0093others(14): Show | 17 | HG01109.hp1 HG02257.hp2 HG02280.hp1 others(14): Show |
intron_variant | MODIFIER | c.337-1557T>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44613715 | ||||||
| chr11:44613812
|
C | T | 2 | a0001c0016t0017g0030a0001c0016t0048g0031 | 2 | HG02258.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.337-1460C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44613812 | ||||||
| chr11:44613843
|
CA | C | 228 | a0001c0001t0001g0006a0001c0001t0003g0006a0001c0001t0003g0108others(225): Show | 229 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(226): Show |
intron_variant | MODIFIER | c.337-1417delA | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr11 | 44613843 | |||||
| chr11:44613990
|
GTTGTTGT others(5): Show |
G | 99 | a0001c0006t0001g0036a0001c0006t0001g0115a0001c0006t0001g0177others(96): Show | 100 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(97): Show |
intron_variant | MODIFIER | c.337-1264_337-1253d others(14): Show |
CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr11 | 44613990 | |||||
| chr11:44614010
|
TG | T | 15 | a0001c0001t0003g0108a0001c0001t0005g0214a0001c0001t0006g0015others(12): Show | 15 | HG00621.hp2 HG00741.hp2 HG01168.hp2 others(12): Show |
intron_variant | MODIFIER | c.337-1261delG | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44614010 | ||||||
| chr11:44614020
|
T | C | 212 | a0001c0001t0001g0006a0001c0001t0003g0006a0001c0001t0003g0108others(209): Show | 213 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(210): Show |
intron_variant | MODIFIER | c.337-1252T>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44614020 | ||||||
| chr11:44614076
|
G | A | 9 | a0001c0001t0004g0323a0001c0012t0016g0313a0002c0003t0002g0038others(6): Show | 9 | HG02280.hp2 HG02717.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.337-1196G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44614076 | ||||||
| chr11:44614272
|
G | T | 2 | a0001c0018t0012g0269a0001c0018t0012g0341 | 2 | HG01884.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.337-1000G>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44614272 | ||||||
| chr11:44614420
|
A | G | 1 | a0001c0001t0004g0254 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.337-852A>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44614420 | ||||||
| chr11:44614525
|
T | G | 1 | a0002c0008t0002g0298 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.337-747T>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44614525 | ||||||
| chr11:44614598
|
A | G | 9 | a0001c0001t0004g0323a0001c0012t0016g0313a0002c0003t0002g0038others(6): Show | 9 | HG02280.hp2 HG02717.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.337-674A>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44614598 | ||||||
| chr11:44614641
|
G | A | 1 | a0001c0001t0006g0010 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.337-631G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44614641 | ||||||
| chr11:44614693
|
G | A | 1 | a0002c0008t0001g0191 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.337-579G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44614693 | ||||||
| chr11:44614982
|
G | A | 1 | a0002c0008t0002g0145 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.337-290G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44614982 | ||||||
| chr11:44614997
|
G | A | 101 | a0001c0006t0001g0036a0001c0006t0001g0115a0001c0006t0001g0177others(98): Show | 102 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(99): Show |
intron_variant | MODIFIER | c.337-275G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44614997 | ||||||
| chr11:44615088
|
T | G | 1 | a0001c0006t0002g0151 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.337-184T>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44615088 | ||||||
| chr11:44615121
|
G | C | 1 | a0001c0006t0002g0151 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.337-151G>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44615121 | ||||||
| chr11:44615122
|
C | A | 1 | a0001c0006t0002g0151 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.337-150C>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44615122 | ||||||
| chr11:44615123
|
A | C | 1 | a0001c0006t0002g0151 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.337-149A>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44615123 | ||||||
| chr11:44615130
|
G | C | 1 | a0002c0008t0004g0232 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.337-142G>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44615130 | ||||||
| chr11:44615134
|
G | T | 71 | a0001c0005t0001g0087a0001c0005t0001g0204a0001c0005t0001g0205others(68): Show | 71 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(68): Show |
intron_variant | MODIFIER | c.337-138G>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44615134 | ||||||
| chr11:44615203
|
G | A | 1 | a0001c0001t0017g0090 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.337-69G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44615203 | ||||||
| chr11:44615764
|
T | C | 1 | a0001c0001t0008g0266 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.438+391T>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 7/9 | chr11 | 44615764 | ||||||
| chr11:44615810
|
T | C | 1 | a0002c0003t0045g0065 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.438+437T>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 7/9 | chr11 | 44615810 | ||||||
| chr11:44615834
|
A | G | 10 | a0001c0001t0004g0323a0001c0001t0008g0266a0001c0012t0016g0313others(7): Show | 10 | HG02280.hp2 HG02717.hp2 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.438+461A>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 7/9 | chr11 | 44615834 | ||||||
| chr11:44615890
|
T | C | 15 | a0001c0011t0001g0334a0001c0011t0001g0336a0001c0011t0001g0337others(12): Show | 15 | HG00673.hp2 NA18949.hp1 NA18950.hp2 others(12): Show |
intron_variant | MODIFIER | c.438+517T>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 7/9 | chr11 | 44615890 | ||||||
| chr11:44615929
|
C | T | 6 | a0001c0001t0001g0250a0001c0001t0001g0251a0001c0001t0004g0249others(3): Show | 6 | HG02451.hp1 HG02486.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.438+556C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 7/9 | chr11 | 44615929 | ||||||
| chr11:44615930
|
A | G | 352 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(349): Show | 361 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(358): Show |
intron_variant | MODIFIER | c.438+557A>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 7/9 | chr11 | 44615930 | ||||||
| chr11:44616021
|
C | T | 10 | a0001c0001t0004g0323a0001c0001t0008g0266a0001c0012t0016g0313others(7): Show | 10 | HG02280.hp2 HG02717.hp2 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.438+648C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 7/9 | chr11 | 44616021 | ||||||
| chr11:44616096
|
C | T | 1 | a0002c0002t0003g0134 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.438+723C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 7/9 | chr11 | 44616096 | ||||||
| chr11:44616507
|
A | G | 1 | a0002c0004t0001g0056 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.438+1134A>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 7/9 | chr11 | 44616507 | ||||||
| chr11:44616558
|
C | T | 8 | a0001c0001t0001g0006a0001c0001t0003g0006a0001c0001t0004g0037others(5): Show | 8 | HG02818.hp2 HG02896.hp2 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.438+1185C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 7/9 | chr11 | 44616558 | ||||||
| chr11:44616666
|
G | A | 1 | a0001c0001t0004g0094 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.438+1293G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 7/9 | chr11 | 44616666 | ||||||
| chr11:44616849
|
A | G | 3 | a0001c0001t0008g0266a0002c0003t0002g0038a0002c0003t0011g0261 | 3 | HG02818.hp1 HG02922.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.439-1313A>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 7/9 | chr11 | 44616849 | ||||||
| chr11:44616850
|
C | T | 1 | a0002c0025t0004g0349 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.439-1312C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 7/9 | chr11 | 44616850 | ||||||
| chr11:44617019
|
C | T | 3 | a0001c0001t0001g0006a0001c0001t0003g0006a0001c0001t0046g0092 | 3 | HG02970.hp1 HG03139.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.439-1143C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 7/9 | chr11 | 44617019 | ||||||
| chr11:44617034
|
T | C | 5 | a0001c0001t0001g0319a0002c0003t0002g0306a0002c0003t0003g0296others(2): Show | 5 | HG00140.hp2 HG01074.hp2 HG01346.hp2 others(2): Show |
intron_variant | MODIFIER | c.439-1128T>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 7/9 | chr11 | 44617034 | ||||||
| chr11:44617105
|
G | A | 45 | a0001c0001t0001g0064a0001c0001t0001g0319a0001c0001t0003g0163others(42): Show | 45 | HG00140.hp2 HG01074.hp2 HG01109.hp1 others(42): Show |
intron_variant | MODIFIER | c.439-1057G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 7/9 | chr11 | 44617105 | ||||||
| chr11:44617222
|
G | T | 2 | a0001c0001t0001g0242a0001c0001t0001g0243 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.439-940G>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 7/9 | chr11 | 44617222 | ||||||
| chr11:44617354
|
G | T | 4 | a0001c0001t0008g0266a0002c0003t0002g0038a0002c0003t0011g0261others(1): Show | 4 | HG02818.hp1 HG02922.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.439-808G>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 7/9 | chr11 | 44617354 | ||||||
| chr11:44617508
|
A | G | 1 | a0001c0009t0015g0224 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.439-654A>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 7/9 | chr11 | 44617508 | ||||||
| chr11:44617560
|
G | GA | 14 | a0001c0001t0001g0044a0001c0001t0001g0047a0001c0001t0001g0287others(11): Show | 14 | HG01952.hp1 HG02015.hp2 HG02056.hp2 others(11): Show |
intron_variant | MODIFIER | c.439-580dupA | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr11 | 44617560 | |||||
| chr11:44617560
|
GA | G | 199 | a0001c0001t0001g0058a0001c0001t0001g0064a0001c0001t0001g0250others(196): Show | 200 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(197): Show |
intron_variant | MODIFIER | c.439-580delA | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr11 | 44617560 | |||||
| chr11:44617560
|
GAA | G | 35 | a0001c0001t0003g0108a0001c0001t0006g0015a0001c0001t0013g0071others(32): Show | 35 | HG00099.hp1 HG00735.hp1 HG00741.hp1 others(32): Show |
intron_variant | MODIFIER | c.439-581_439-580del others(2): Show |
CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr11 | 44617560 | |||||
| chr11:44617618
|
CT | C | 11 | a0001c0001t0001g0250a0001c0001t0001g0251a0001c0001t0001g0332others(8): Show | 11 | HG02451.hp1 HG02486.hp2 HG02970.hp2 others(8): Show |
intron_variant | MODIFIER | c.439-537delT | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr11 | 44617618 | |||||
| chr11:44617635
|
C | G | 21 | a0001c0001t0001g0064a0001c0001t0001g0319a0001c0001t0004g0270others(18): Show | 21 | HG00140.hp2 HG01074.hp2 HG01109.hp2 others(18): Show |
intron_variant | MODIFIER | c.439-527C>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 7/9 | chr11 | 44617635 | ||||||
| chr11:44617706
|
C | A | 1 | a0001c0011t0001g0336 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.439-456C>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 7/9 | chr11 | 44617706 | ||||||
| chr11:44617836
|
C | G | 2 | a0001c0001t0015g0352a0002c0025t0004g0349 | 2 | HG02976.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.439-326C>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 7/9 | chr11 | 44617836 | ||||||
| chr11:44618001
|
T | C | 65 | a0001c0001t0001g0064a0001c0001t0001g0319a0001c0001t0003g0163others(62): Show | 65 | HG00099.hp1 HG00140.hp2 HG00609.hp2 others(62): Show |
intron_variant | MODIFIER | c.439-161T>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 7/9 | chr11 | 44618001 | ||||||
| chr11:44618048
|
G | A | 1 | a0002c0002t0002g0192 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.439-114G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 7/9 | chr11 | 44618048 | ||||||
| chr11:44618371
|
C | G | 1 | a0001c0011t0005g0318 | 1 | NA19000.hp1 | splice_region_variant&intron_variant | LOW | c.642+6C>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 8/9 | chr11 | 44618371 | ||||||
| chr11:44618371
|
C | T | 171 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(168): Show | 179 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(176): Show |
splice_region_variant&intron_variant | LOW | c.642+6C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 8/9 | chr11 | 44618371 | ||||||
| chr11:44618382
|
G | A | 81 | a0001c0001t0003g0310a0001c0006t0001g0036a0001c0006t0001g0115others(78): Show | 81 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.642+17G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 8/9 | chr11 | 44618382 | ||||||
| chr11:44618466
|
A | G | 282 | a0001c0001t0001g0006a0001c0001t0001g0044a0001c0001t0001g0064others(279): Show | 283 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(280): Show |
intron_variant | MODIFIER | c.642+101A>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 8/9 | chr11 | 44618466 | ||||||
| chr11:44618494
|
A | G | 9 | a0001c0001t0004g0309a0001c0001t0015g0263a0001c0009t0001g0086others(6): Show | 9 | HG01884.hp2 HG02145.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.642+129A>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 8/9 | chr11 | 44618494 | ||||||
| chr11:44618550
|
C | T | 28 | a0001c0001t0001g0044a0001c0001t0001g0250a0001c0001t0001g0251others(25): Show | 28 | HG00621.hp2 HG00639.hp2 HG00741.hp2 others(25): Show |
intron_variant | MODIFIER | c.643-90C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 8/9 | chr11 | 44618550 | ||||||
| chr11:44618909
|
C | T | 1 | a0001c0001t0015g0263 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.727-140C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 9/9 | chr11 | 44618909 | ||||||
| chr11:44618927
|
A | G | 20 | a0001c0001t0001g0044a0001c0001t0002g0317a0001c0001t0003g0108others(17): Show | 20 | HG00099.hp1 HG00621.hp2 HG00639.hp2 others(17): Show |
intron_variant | MODIFIER | c.727-122A>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 9/9 | chr11 | 44618927 | ||||||
| chr11:44618969
|
A | G | 4 | a0001c0001t0001g0332a0001c0001t0008g0272a0001c0001t0008g0330others(1): Show | 4 | HG03471.hp1 HG03540.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.727-80A>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 9/9 | chr11 | 44618969 | ||||||
| chr11:44619035
|
G | A | 1 | a0001c0006t0002g0142 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.727-14G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 9/9 | chr11 | 44619035 |