Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 928 |
|---|---|
| ensemblid | ENSG00000010278.15 |
| hgncid | 1709 |
| symbol | CD9 |
| name | CD9 molecule |
| refseq_nuc | NM_001769.4 |
| refseq_prot | NP_001760.1 |
| ensembl_nuc | ENST00000009180.10 |
| ensembl_prot | ENSP00000009180.4 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 6200400 |
| end | 6238266 |
| strand | + |
| ver | v1.2 |
| region | chr12:6200400-6238266 |
| region5000 | chr12:6195400-6243266 |
| regionname0 | CD9_chr12_6200400_6238266 |
| regionname5000 | CD9_chr12_6195400_6243266 |
| 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 | 228 | 375 | 92 | 62 | 171 | 8 | 40 | 135 | CD9_chr12_6195400_6243266 | CD9 | copy fasta | chr12 | 6195400 | 6243266 |
| a0002 | 0/0 | 228 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | CD9_chr12_6195400_6243266 | CD9 | copy fasta | chr12 | 6195400 | 6243266 |
| a0003 | 0/0 | 110 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CD9_chr12_6195400_6243266 | CD9 | copy fasta | chr12 | 6195400 | 6243266 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 687 | 370 | 90 | 62 | 169 | 8 | 39 | CD9_chr12_6195400_6243266 | CD9 | copy fasta | chr12 | 6195400 | 6243266 |
| c0002 | 0/0 | 687 | 2 | 0 | 0 | 2 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | copy fasta | chr12 | 6195400 | 6243266 |
| c0003 | 0/0 | 687 | 2 | 0 | 0 | 2 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | copy fasta | chr12 | 6195400 | 6243266 |
| c0004 | 0/0 | 712 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | copy fasta | chr12 | 6195400 | 6243266 |
| c0005 | 0/0 | 687 | 1 | 0 | 0 | 0 | 0 | 1 | CD9_chr12_6195400_6243266 | CD9 | copy fasta | chr12 | 6195400 | 6243266 |
| c0006 | 0/0 | 687 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | copy fasta | chr12 | 6195400 | 6243266 |
| c0007 | 0/0 | 687 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | copy fasta | chr12 | 6195400 | 6243266 |
| 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 | 1/1 | 539 | 329 | 56 | 57 | 170 | 7 | 37 | CD9_chr12_6195400_6243266 | CD9 | copy fasta | chr12 | 6195400 | 6243266 |
| t0002 | 0/0 | 539 | 48 | 35 | 5 | 4 | 1 | 3 | CD9_chr12_6195400_6243266 | CD9 | copy fasta | chr12 | 6195400 | 6243266 |
| t0003 | 0/0 | 539 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | copy fasta | chr12 | 6195400 | 6243266 |
| 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 | 7 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0002 | 0/0 | 7 | 0 | 1 | 6 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0003 | 0/0 | 7 | 0 | 2 | 3 | 0 | 2 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0004 | 0/0 | 7 | 2 | 1 | 3 | 1 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0005 | 0/0 | 6 | 0 | 2 | 1 | 0 | 3 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0006 | 0/0 | 4 | 0 | 1 | 0 | 1 | 2 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0011 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0012 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0013 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0016 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0017 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0018 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0022 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0024 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0025 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0026 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0027 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0028 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0029 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0035 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0040 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0220 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0262 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0300 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 687 | 370 | 90 | 62 | 169 | 8 | 39 | CD9_chr12_6195400_6243266 | CD9 | copy fasta | chr12 | 6195400 | 6243266 |
| a0001c0002 | 0/0 | 687 | 2 | 0 | 0 | 2 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | copy fasta | chr12 | 6195400 | 6243266 |
| a0001c0005 | 0/0 | 687 | 1 | 0 | 0 | 0 | 0 | 1 | CD9_chr12_6195400_6243266 | CD9 | copy fasta | chr12 | 6195400 | 6243266 |
| a0001c0006 | 0/0 | 687 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | copy fasta | chr12 | 6195400 | 6243266 |
| a0001c0007 | 0/0 | 687 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | copy fasta | chr12 | 6195400 | 6243266 |
| a0002c0003 | 0/0 | 687 | 2 | 0 | 0 | 2 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | copy fasta | chr12 | 6195400 | 6243266 |
| a0003c0004 | 0/0 | 712 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | copy fasta | chr12 | 6195400 | 6243266 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 1225 | 321 | 54 | 57 | 165 | 7 | 36 | CD9_chr12_6195400_6243266 | CD9 | copy fasta | chr12 | 6195400 | 6243266 |
| a0001c0001t0002 | 0/0 | 1225 | 48 | 35 | 5 | 4 | 1 | 3 | CD9_chr12_6195400_6243266 | CD9 | copy fasta | chr12 | 6195400 | 6243266 |
| a0001c0001t0003 | 0/0 | 1225 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | copy fasta | chr12 | 6195400 | 6243266 |
| a0001c0002t0001 | 0/0 | 1225 | 2 | 0 | 0 | 2 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | copy fasta | chr12 | 6195400 | 6243266 |
| a0001c0005t0001 | 0/0 | 1225 | 1 | 0 | 0 | 0 | 0 | 1 | CD9_chr12_6195400_6243266 | CD9 | copy fasta | chr12 | 6195400 | 6243266 |
| a0001c0006t0001 | 0/0 | 1225 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | copy fasta | chr12 | 6195400 | 6243266 |
| a0001c0007t0001 | 0/0 | 1225 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | copy fasta | chr12 | 6195400 | 6243266 |
| a0002c0003t0001 | 0/0 | 1225 | 2 | 0 | 0 | 2 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | copy fasta | chr12 | 6195400 | 6243266 |
| a0003c0004t0001 | 0/0 | 1250 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | copy fasta | chr12 | 6195400 | 6243266 |
| 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 | 7 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0002 | 0/0 | 6 | 0 | 1 | 5 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0003 | 0/0 | 6 | 0 | 2 | 2 | 0 | 2 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0004 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0005 | 0/0 | 6 | 0 | 2 | 1 | 0 | 3 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0006 | 0/0 | 4 | 0 | 1 | 0 | 1 | 2 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0011 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0220 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0262 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0002g0004 | 0/0 | 6 | 2 | 1 | 3 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0002g0012 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0002g0035 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0002g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0002g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0002g0040 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0002g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0002g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0002g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0002g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0002g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0002g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0002g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0002g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0002g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0002g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0002g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0002g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0002g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0002g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0002g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0002g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0002g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0002g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0002g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0002g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0002g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0002g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0002g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0002g0300 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0002g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0002g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0002g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0002g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0002g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0002g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0001t0003g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0002t0001g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0002t0001g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0005t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0006t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0001c0007t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0002c0003t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0002c0003t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| a0003c0004t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | CHS | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | CHS | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | CHS | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | CHS | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | CHS | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | CHS | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | CHS | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | CHS | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | CHS | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | CHS | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | CHS | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | CHS | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0227 | AMR | PUR | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | CHS | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | CHS | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG00733 | hp1 | a0001 | c0001 | t0002 | g0299 | AMR | PUR | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0109 | AMR | PUR | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0133 | AMR | PUR | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | PUR | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0177 | AMR | PUR | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0222 | AMR | PUR | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0072 | AMR | PUR | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0066 | AMR | PUR | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0094 | AMR | PUR | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0112 | AMR | PUR | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0095 | AMR | PUR | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0213 | AMR | PUR | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0291 | AMR | PUR | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0239 | AMR | CLM | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0099 | AMR | CLM | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0135 | AMR | CLM | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0219 | AMR | CLM | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0196 | AMR | CLM | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0275 | AMR | CLM | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0236 | AMR | CLM | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0120 | AMR | CLM | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0151 | AMR | CLM | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0121 | AMR | CLM | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0139 | AMR | CLM | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0129 | EUR | IBS | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0027 | EUR | IBS | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0006 | EUR | IBS | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG01516 | hp2 | a0001 | c0001 | t0002 | g0300 | EUR | IBS | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG01884 | hp1 | a0001 | c0001 | t0002 | g0295 | AFR | ACB | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG01884 | hp2 | a0001 | c0001 | t0002 | g0282 | AFR | ACB | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG01891 | hp1 | a0001 | c0001 | t0002 | g0285 | AFR | ACB | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0297 | AFR | ACB | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0172 | AMR | PEL | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0154 | AMR | PEL | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | PEL | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0029 | AMR | PEL | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0171 | AMR | PEL | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0035 | AMR | PEL | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0076 | AMR | PEL | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0169 | AMR | PEL | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | PEL | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0061 | AMR | PEL | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0070 | AMR | PEL | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PEL | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | KHV | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | KHV | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | KHV | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0305 | EAS | KHV | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | ACB | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | KHV | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | KHV | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | KHV | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | KHV | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | KHV | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | KHV | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | KHV | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | KHV | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0085 | AFR | ACB | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG02145 | hp2 | a0001 | c0001 | t0002 | g0272 | AFR | ACB | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | PEL | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG02148 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | PEL | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | CDX | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | CDX | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | CDX | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | CDX | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0207 | AFR | ACB | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0304 | AFR | ACB | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0244 | AFR | ACB | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0287 | AFR | ACB | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | PEL | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0060 | AFR | ACB | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0277 | AFR | ACB | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PEL | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0189 | AMR | PEL | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG02451 | hp1 | a0001 | c0001 | t0002 | g0273 | AFR | ACB | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | ACB | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0274 | AFR | GWD | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0253 | AFR | GWD | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0105 | SAS | PJL | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0053 | SAS | PJL | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0251 | AFR | GWD | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0289 | AFR | GWD | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG02622 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | GWD | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0245 | AFR | GWD | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0290 | AFR | GWD | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG02630 | hp2 | a0001 | c0001 | t0002 | g0150 | AFR | GWD | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0178 | AFR | GWD | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | GWD | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0217 | SAS | PJL | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0098 | SAS | PJL | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG02717 | hp1 | a0001 | c0001 | t0002 | g0286 | AFR | GWD | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0267 | AFR | GWD | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0266 | AFR | GWD | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG02735 | hp2 | a0001 | c0005 | t0001 | g0228 | SAS | PJL | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG02809 | hp1 | a0001 | c0001 | t0002 | g0298 | AFR | GWD | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | GWD | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0303 | AFR | GWD | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG02818 | hp2 | a0001 | c0001 | t0002 | g0296 | AFR | GWD | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0036 | AFR | GWD | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | GWD | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG02895 | hp2 | a0001 | c0001 | t0002 | g0037 | AFR | GWD | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG02896 | hp1 | a0001 | c0001 | t0002 | g0037 | AFR | GWD | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0164 | AFR | GWD | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0163 | AFR | GWD | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG02897 | hp2 | a0001 | c0001 | t0002 | g0281 | AFR | GWD | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG02922 | hp1 | a0001 | c0001 | t0002 | g0284 | AFR | ESN | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG02922 | hp2 | a0001 | c0001 | t0003 | g0288 | AFR | ESN | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0153 | AFR | ESN | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG02965 | hp2 | a0001 | c0001 | t0002 | g0036 | AFR | ESN | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | ESN | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG02976 | hp2 | a0001 | c0007 | t0001 | g0161 | AFR | ESN | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0062 | SAS | PJL | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0041 | SAS | PJL | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0254 | AFR | MSL | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG03098 | hp2 | a0001 | c0001 | t0002 | g0276 | AFR | MSL | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG03130 | hp1 | a0001 | c0001 | t0002 | g0152 | AFR | ESN | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | ESN | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0087 | AFR | ESN | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | ESN | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG03195 | hp1 | a0001 | c0001 | t0002 | g0012 | AFR | ESN | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0248 | AFR | ESN | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0035 | AFR | MSL | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | MSL | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG03225 | hp1 | a0001 | c0006 | t0001 | g0188 | AFR | MSL | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0269 | AFR | MSL | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0101 | SAS | PJL | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0200 | SAS | PJL | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0024 | SAS | PJL | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0013 | SAS | PJL | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0197 | SAS | PJL | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0043 | SAS | PJL | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0013 | SAS | PJL | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0042 | SAS | PJL | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | ESN | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | ESN | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0249 | AFR | GWD | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0280 | AFR | GWD | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0306 | AFR | MSL | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | MSL | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0215 | SAS | PJL | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0199 | SAS | PJL | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0108 | SAS | PJL | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0025 | SAS | STU | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0040 | SAS | STU | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0216 | SAS | PJL | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | BEB | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0301 | SAS | BEB | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0026 | SAS | BEB | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0106 | SAS | BEB | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0116 | SAS | STU | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0097 | SAS | STU | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0029 | SAS | STU | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0218 | SAS | STU | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0223 | SAS | STU | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | STU | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0017 | SAS | STU | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0040 | SAS | STU | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| NA18522 | hp1 | a0001 | c0001 | t0002 | g0278 | AFR | YRI | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| NA18522 | hp2 | a0001 | c0001 | t0002 | g0012 | AFR | YRI | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | CHB | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| NA18612 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | CHB | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | CHB | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | CHB | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | YRI | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0279 | AFR | YRI | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| NA18951 | hp1 | a0002 | c0003 | t0001 | g0007 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| NA18974 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| NA18986 | hp1 | a0002 | c0003 | t0001 | g0051 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| NA19012 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0065 | AFR | LWK | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0292 | AFR | LWK | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0243 | AFR | LWK | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | LWK | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| NA19075 | hp2 | a0003 | c0004 | t0001 | g0146 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | YRI | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0149 | AFR | YRI | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0268 | AFR | ASW | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | ASW | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0028 | EUR | TSI | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0018 | EUR | TSI | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0202 | EUR | TSI | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0004 | EUR | TSI | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0203 | SAS | GIH | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0022 | SAS | GIH | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0125 | AMR | CLM | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0179 | AMR | CLM | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0293 | AFR | ACB | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG02109 | hp2 | a0001 | c0001 | t0002 | g0012 | AFR | ACB | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0250 | AFR | ACB | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0124 | AFR | ACB | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0294 | AFR | ACB | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | ACB | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0252 | AFR | MSL | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | MSL | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | USA | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| HG06807 | hp2 | a0001 | c0001 | t0002 | g0302 | AFR | USA | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0283 | AFR | USA | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0073 | AFR | USA | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | LWK | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| NA21309 | hp2 | a0001 | c0001 | t0002 | g0271 | AFR | LWK | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0220 | REF | REF | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0262 | REF | REF | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
| chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:6233438
|
C | CGCCATTG others(18): Show |
1 | a0003 | 1 | NA19075.hp2 | frameshift_variant&stop_gained | HIGH | c.302_326dupCCATTGAA others(17): Show |
p.Trp109fs | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 4/8 | 427/1225 | 327/687 | 109/228 | INFO_REALIGN_3_PRIME | chr12 | 6233438 | |
| chr12:6237784
|
A | G | 1 | a0002 | 2 | NA18951.hp1 NA18986.hp1 |
missense_variant | MODERATE | c.643A>G | p.Met215Val | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 8/8 | 743/1225 | 643/687 | 215/228 | chr12 | 6237784 |
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:6232684
|
G | A | 1 | a0001c0002 | 2 | NA18612.hp2 NA18974.hp2 |
synonymous_variant | LOW | c.228G>A | p.Leu76Leu | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 3/8 | 328/1225 | 228/687 | 76/228 | chr12 | 6232684 | ||
| chr12:6235306
|
G | A | 1 | a0001c0005 | 1 | HG02735.hp2 | synonymous_variant | LOW | c.426G>A | p.Thr142Thr | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 5/8 | 526/1225 | 426/687 | 142/228 | chr12 | 6235306 | ||
| chr12:6235559
|
C | T | 1 | a0001c0007 | 1 | HG02976.hp2 | synonymous_variant | LOW | c.531C>T | p.Thr177Thr | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 6/8 | 631/1225 | 531/687 | 177/228 | chr12 | 6235559 | ||
| chr12:6236206
|
C | T | 1 | a0001c0006 | 1 | HG03225.hp1 | synonymous_variant | LOW | c.552C>T | p.Ala184Ala | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 7/8 | 652/1225 | 552/687 | 184/228 | chr12 | 6236206 |
| chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:6200432
|
C | T | 1 | a0001c0001t0002 | 48 | HG00733.hp1 HG01346.hp1 HG01358.hp2 others(45): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-68C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/8 | chr12 | 6200432 | ||||||
| chr12:6238039
|
T | G | 1 | a0001c0001t0003 | 1 | HG02922.hp2 | 3_prime_UTR_variant | MODIFIER | c.*211T>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 8/8 | 211 | chr12 | 6238039 |
| chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:6200615
|
G | C | 4 | a0001c0001t0001g0013a0001c0001t0001g0041a0001c0001t0001g0042others(1): Show | 5 | HG03017.hp2 HG03490.hp2 HG03491.hp2 others(2): Show |
intron_variant | MODIFIER | c.66+50G>C | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6200615 | ||||||
| chr12:6200630
|
G | A | 2 | a0001c0001t0001g0044a0001c0001t0001g0045 | 2 | HG02055.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.66+65G>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6200630 | ||||||
| chr12:6200729
|
G | A | 112 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(109): Show | 138 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(135): Show |
intron_variant | MODIFIER | c.66+164G>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6200729 | ||||||
| chr12:6200729
|
G | C | 9 | a0001c0001t0001g0140a0001c0001t0001g0141a0001c0001t0001g0142others(6): Show | 9 | HG02129.hp1 HG02165.hp2 NA18966.hp2 others(6): Show |
intron_variant | MODIFIER | c.66+164G>C | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6200729 | ||||||
| chr12:6200885
|
G | C | 3 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048 | 3 | NA18962.hp1 NA18969.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.66+320G>C | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6200885 | ||||||
| chr12:6201007
|
C | A | 1 | a0001c0001t0001g0049 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.66+442C>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6201007 | ||||||
| chr12:6201044
|
G | A | 5 | a0001c0001t0001g0007a0001c0001t0001g0050a0001c0001t0001g0052others(2): Show | 6 | HG00609.hp2 NA18951.hp1 NA18954.hp1 others(3): Show |
intron_variant | MODIFIER | c.66+479G>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6201044 | ||||||
| chr12:6201091
|
C | T | 15 | a0001c0001t0001g0004a0001c0001t0002g0004a0001c0001t0002g0040others(12): Show | 21 | HG00733.hp1 HG01516.hp2 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.66+526C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6201091 | ||||||
| chr12:6201103
|
C | T | 4 | a0001c0001t0001g0039a0001c0001t0001g0292a0001c0001t0001g0293others(1): Show | 5 | HG02109.hp1 HG02559.hp1 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.66+538C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6201103 | ||||||
| chr12:6201275
|
A | T | 1 | a0001c0001t0001g0291 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.66+710A>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6201275 | ||||||
| chr12:6201306
|
C | CA | 117 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(114): Show | 143 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(140): Show |
intron_variant | MODIFIER | c.66+742dupA | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 6201306 | |||||
| chr12:6201377
|
C | T | 2 | a0001c0001t0001g0039a0001c0001t0001g0294 | 3 | HG02559.hp1 HG03579.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.66+812C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6201377 | ||||||
| chr12:6201455
|
C | T | 1 | a0001c0001t0001g0139 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.66+890C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6201455 | ||||||
| chr12:6201477
|
G | A | 2 | a0001c0001t0001g0292a0001c0001t0001g0293 | 2 | HG02109.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.66+912G>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6201477 | ||||||
| chr12:6201555
|
C | T | 5 | a0001c0001t0001g0038a0001c0001t0001g0287a0001c0001t0001g0289others(2): Show | 6 | HG02258.hp2 HG02451.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.66+990C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6201555 | ||||||
| chr12:6201684
|
A | G | 35 | a0001c0001t0001g0004a0001c0001t0002g0004a0001c0001t0002g0012others(32): Show | 46 | HG00733.hp1 HG01346.hp1 HG01516.hp2 others(43): Show |
intron_variant | MODIFIER | c.66+1119A>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6201684 | ||||||
| chr12:6201898
|
C | T | 4 | a0001c0001t0002g0012a0001c0001t0002g0284a0001c0001t0002g0285others(1): Show | 6 | HG01891.hp1 HG02109.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.66+1333C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6201898 | ||||||
| chr12:6201939
|
G | T | 1 | a0001c0001t0001g0138 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.66+1374G>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6201939 | ||||||
| chr12:6201994
|
C | T | 117 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(114): Show | 142 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(139): Show |
intron_variant | MODIFIER | c.66+1429C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6201994 | ||||||
| chr12:6202066
|
A | C | 3 | a0001c0001t0001g0011a0001c0001t0001g0269a0001c0001t0001g0291 | 5 | HG01192.hp2 HG02055.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.66+1501A>C | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6202066 | ||||||
| chr12:6202404
|
G | A | 1 | a0001c0001t0001g0154 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.66+1839G>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6202404 | ||||||
| chr12:6202595
|
C | G | 3 | a0001c0001t0001g0266a0001c0001t0001g0267a0001c0001t0001g0268 | 3 | HG02717.hp2 HG02723.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.66+2030C>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6202595 | ||||||
| chr12:6202856
|
C | T | 3 | a0001c0001t0001g0263a0001c0001t0001g0264a0001c0001t0001g0265 | 3 | NA18950.hp1 NA19060.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.66+2291C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6202856 | ||||||
| chr12:6203001
|
G | A | 309 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(306): Show | 377 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(374): Show |
intron_variant | MODIFIER | c.66+2436G>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6203001 | ||||||
| chr12:6203149
|
T | C | 35 | a0001c0001t0001g0004a0001c0001t0002g0004a0001c0001t0002g0012others(32): Show | 46 | HG00733.hp1 HG01346.hp1 HG01516.hp2 others(43): Show |
intron_variant | MODIFIER | c.66+2584T>C | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6203149 | ||||||
| chr12:6203191
|
T | C | 2 | a0001c0001t0001g0266a0001c0001t0001g0267 | 2 | HG02717.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.66+2626T>C | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6203191 | ||||||
| chr12:6203341
|
G | A | 2 | a0001c0001t0001g0155a0001c0001t0001g0156 | 2 | NA18946.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.66+2776G>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6203341 | ||||||
| chr12:6203474
|
G | A | 3 | a0001c0001t0001g0020a0001c0001t0001g0157a0001c0001t0001g0158 | 4 | NA18945.hp1 NA18946.hp2 NA18956.hp2 others(1): Show |
intron_variant | MODIFIER | c.66+2909G>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6203474 | ||||||
| chr12:6203497
|
G | A | 118 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(115): Show | 144 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(141): Show |
intron_variant | MODIFIER | c.66+2932G>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6203497 | ||||||
| chr12:6203529
|
T | C | 4 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0001t0001g0164others(1): Show | 4 | HG02896.hp2 HG02897.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.66+2964T>C | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6203529 | ||||||
| chr12:6203945
|
T | A | 1 | a0001c0001t0001g0053 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.66+3380T>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6203945 | ||||||
| chr12:6204095
|
C | T | 60 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(57): Show | 76 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(73): Show |
intron_variant | MODIFIER | c.66+3530C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6204095 | ||||||
| chr12:6204193
|
G | T | 14 | a0001c0001t0002g0012a0001c0001t0002g0036a0001c0001t0002g0037others(11): Show | 18 | HG01884.hp2 HG01891.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.66+3628G>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6204193 | ||||||
| chr12:6204233
|
A | G | 9 | a0001c0001t0001g0010a0001c0001t0001g0034a0001c0001t0001g0255others(6): Show | 12 | HG02155.hp2 NA18944.hp1 NA18959.hp1 others(9): Show |
intron_variant | MODIFIER | c.66+3668A>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6204233 | ||||||
| chr12:6204245
|
A | G | 179 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(176): Show | 222 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(219): Show |
intron_variant | MODIFIER | c.66+3680A>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6204245 | ||||||
| chr12:6204282
|
A | C | 9 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0248others(6): Show | 11 | HG02486.hp1 HG02572.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.66+3717A>C | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6204282 | ||||||
| chr12:6204299
|
A | G | 123 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(120): Show | 149 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(146): Show |
intron_variant | MODIFIER | c.66+3734A>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6204299 | ||||||
| chr12:6204407
|
A | C | 1 | a0001c0001t0001g0093 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.66+3842A>C | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6204407 | ||||||
| chr12:6204518
|
T | C | 3 | a0001c0001t0001g0011a0001c0001t0001g0149a0001c0001t0001g0269 | 5 | HG02055.hp2 HG02723.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.66+3953T>C | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6204518 | ||||||
| chr12:6204765
|
G | A | 26 | a0001c0001t0001g0032a0001c0001t0001g0094a0001c0001t0001g0095others(23): Show | 32 | HG01167.hp2 HG01169.hp2 HG01884.hp2 others(29): Show |
intron_variant | MODIFIER | c.66+4200G>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6204765 | ||||||
| chr12:6204879
|
C | T | 181 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(178): Show | 224 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(221): Show |
intron_variant | MODIFIER | c.66+4314C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6204879 | ||||||
| chr12:6204988
|
T | C | 2 | a0001c0001t0001g0246a0001c0001t0001g0247 | 2 | NA18941.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.66+4423T>C | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6204988 | ||||||
| chr12:6205022
|
C | T | 2 | a0001c0001t0001g0246a0001c0001t0001g0247 | 2 | NA18941.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.66+4457C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6205022 | ||||||
| chr12:6205023
|
G | A | 3 | a0001c0001t0001g0033a0001c0001t0001g0253a0001c0001t0001g0254 | 4 | HG02572.hp2 HG03098.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.66+4458G>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6205023 | ||||||
| chr12:6205077
|
T | C | 181 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(178): Show | 224 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(221): Show |
intron_variant | MODIFIER | c.66+4512T>C | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6205077 | ||||||
| chr12:6205144
|
C | T | 1 | a0001c0001t0001g0240 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.66+4579C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6205144 | ||||||
| chr12:6205160
|
T | C | 2 | a0001c0001t0001g0246a0001c0001t0001g0247 | 2 | NA18941.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.66+4595T>C | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6205160 | ||||||
| chr12:6205174
|
C | G | 1 | a0001c0001t0002g0282 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.66+4609C>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6205174 | ||||||
| chr12:6205354
|
C | T | 2 | a0001c0001t0001g0246a0001c0001t0001g0247 | 2 | NA18941.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.66+4789C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6205354 | ||||||
| chr12:6205501
|
G | T | 6 | a0001c0001t0001g0149a0001c0001t0001g0153a0001c0001t0001g0162others(3): Show | 6 | HG02896.hp2 HG02897.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.66+4936G>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6205501 | ||||||
| chr12:6205753
|
A | G | 2 | a0001c0001t0001g0246a0001c0001t0001g0247 | 2 | NA18941.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.66+5188A>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6205753 | ||||||
| chr12:6205788
|
C | T | 1 | a0001c0001t0001g0136 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.66+5223C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6205788 | ||||||
| chr12:6205971
|
G | A | 2 | a0001c0001t0001g0094a0001c0001t0001g0095 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.66+5406G>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6205971 | ||||||
| chr12:6206013
|
C | A | 9 | a0001c0001t0001g0032a0001c0001t0001g0045a0001c0001t0001g0248others(6): Show | 11 | HG01346.hp1 HG01952.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.66+5448C>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6206013 | ||||||
| chr12:6206158
|
C | CA | 18 | a0001c0001t0001g0038a0001c0001t0001g0055a0001c0001t0001g0137others(15): Show | 19 | HG00673.hp2 HG01928.hp1 HG01928.hp2 others(16): Show |
intron_variant | MODIFIER | c.66+5608dupA | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 6206158 | |||||
| chr12:6206158
|
CA | C | 139 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(136): Show | 174 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(171): Show |
intron_variant | MODIFIER | c.66+5608delA | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 6206158 | |||||
| chr12:6206158
|
CAA | C | 24 | a0001c0001t0001g0032a0001c0001t0001g0045a0001c0001t0001g0248others(21): Show | 30 | HG01346.hp1 HG01884.hp2 HG01891.hp1 others(27): Show |
intron_variant | MODIFIER | c.66+5607_66+5608del others(2): Show |
CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 6206158 | |||||
| chr12:6206186
|
G | C | 1 | a0001c0001t0002g0283 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.66+5621G>C | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6206186 | ||||||
| chr12:6206321
|
C | G | 121 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(118): Show | 147 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(144): Show |
intron_variant | MODIFIER | c.66+5756C>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6206321 | ||||||
| chr12:6206361
|
T | A | 1 | a0001c0001t0001g0174 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.66+5796T>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6206361 | ||||||
| chr12:6206454
|
G | C | 2 | a0001c0001t0001g0047a0001c0001t0001g0048 | 2 | NA18969.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.66+5889G>C | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6206454 | ||||||
| chr12:6206527
|
A | C | 1 | a0001c0001t0001g0031 | 2 | HG01934.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.66+5962A>C | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6206527 | ||||||
| chr12:6206900
|
A | AT | 16 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0134others(13): Show | 16 | HG00673.hp2 HG01258.hp2 HG01928.hp1 others(13): Show |
intron_variant | MODIFIER | c.66+6349dupT | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 6206900 | |||||
| chr12:6206900
|
AT | A | 8 | a0001c0001t0001g0021a0001c0001t0001g0038a0001c0001t0001g0175others(5): Show | 10 | HG02258.hp2 HG02451.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.66+6349delT | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 6206900 | |||||
| chr12:6207059
|
T | G | 1 | a0001c0001t0001g0253 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.66+6494T>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6207059 | ||||||
| chr12:6207165
|
A | C | 6 | a0001c0001t0001g0244a0001c0001t0001g0245a0001c0001t0002g0035others(3): Show | 7 | HG01346.hp1 HG01952.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.66+6600A>C | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6207165 | ||||||
| chr12:6207172
|
A | G | 1 | a0001c0001t0001g0237 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.66+6607A>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6207172 | ||||||
| chr12:6207277
|
G | A | 1 | a0001c0001t0001g0022 | 2 | HG01175.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.66+6712G>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6207277 | ||||||
| chr12:6207295
|
C | T | 4 | a0001c0001t0001g0038a0001c0001t0001g0287a0001c0001t0001g0289others(1): Show | 5 | HG02258.hp2 HG02451.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.66+6730C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6207295 | ||||||
| chr12:6207432
|
G | A | 1 | a0001c0001t0002g0283 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.66+6867G>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6207432 | ||||||
| chr12:6207453
|
C | T | 1 | a0001c0001t0001g0253 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.66+6888C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6207453 | ||||||
| chr12:6207494
|
A | G | 1 | a0001c0001t0002g0283 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.66+6929A>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6207494 | ||||||
| chr12:6207596
|
C | G | 3 | a0001c0001t0001g0020a0001c0001t0001g0157a0001c0001t0001g0158 | 4 | NA18945.hp1 NA18946.hp2 NA18956.hp2 others(1): Show |
intron_variant | MODIFIER | c.66+7031C>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6207596 | ||||||
| chr12:6207807
|
T | C | 1 | a0001c0001t0001g0044 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.66+7242T>C | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6207807 | ||||||
| chr12:6207825
|
G | T | 3 | a0001c0001t0001g0038a0001c0001t0001g0289a0001c0001t0003g0288 | 4 | HG02451.hp2 HG02615.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.66+7260G>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6207825 | ||||||
| chr12:6207842
|
C | T | 130 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(127): Show | 157 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(154): Show |
intron_variant | MODIFIER | c.66+7277C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6207842 | ||||||
| chr12:6207951
|
G | A | 1 | a0001c0001t0002g0272 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.66+7386G>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6207951 | ||||||
| chr12:6208020
|
T | A | 3 | a0001c0001t0001g0039a0001c0001t0001g0291a0001c0001t0001g0294 | 4 | HG01192.hp2 HG02559.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.66+7455T>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6208020 | ||||||
| chr12:6208148
|
T | C | 51 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0032others(48): Show | 67 | HG00733.hp1 HG01192.hp2 HG01346.hp1 others(64): Show |
intron_variant | MODIFIER | c.66+7583T>C | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6208148 | ||||||
| chr12:6208178
|
C | G | 9 | a0001c0001t0001g0030a0001c0001t0001g0229a0001c0001t0001g0230others(6): Show | 10 | NA18941.hp1 NA18967.hp2 NA18969.hp2 others(7): Show |
intron_variant | MODIFIER | c.66+7613C>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6208178 | ||||||
| chr12:6208202
|
C | G | 6 | a0001c0001t0001g0251a0001c0001t0001g0266a0001c0001t0001g0268others(3): Show | 6 | HG02109.hp1 HG02615.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.66+7637C>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6208202 | ||||||
| chr12:6208236
|
A | AG | 9 | a0001c0001t0001g0030a0001c0001t0001g0229a0001c0001t0001g0230others(6): Show | 10 | NA18941.hp1 NA18967.hp2 NA18969.hp2 others(7): Show |
intron_variant | MODIFIER | c.66+7671_66+7672ins others(1): Show |
CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6208236 | ||||||
| chr12:6208264
|
G | C | 2 | a0001c0001t0001g0099a0001c0001t0001g0100 | 2 | HG01074.hp1 HG01255.hp2 |
intron_variant | MODIFIER | c.66+7699G>C | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6208264 | ||||||
| chr12:6208306
|
C | T | 3 | a0001c0001t0001g0011a0001c0001t0001g0269a0001c0001t0001g0287 | 5 | HG02055.hp2 HG02258.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.66+7741C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6208306 | ||||||
| chr12:6208419
|
A | T | 1 | a0001c0005t0001g0228 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.66+7854A>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6208419 | ||||||
| chr12:6208557
|
G | T | 1 | a0001c0001t0002g0283 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.66+7992G>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6208557 | ||||||
| chr12:6208575
|
G | A | 1 | a0001c0001t0001g0253 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.66+8010G>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6208575 | ||||||
| chr12:6208686
|
C | T | 1 | a0001c0001t0001g0253 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.66+8121C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6208686 | ||||||
| chr12:6208692
|
C | T | 1 | a0001c0001t0002g0275 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.66+8127C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6208692 | ||||||
| chr12:6208730
|
C | T | 1 | a0001c0001t0001g0098 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.66+8165C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6208730 | ||||||
| chr12:6208974
|
T | C | 1 | a0001c0001t0002g0275 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.66+8409T>C | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6208974 | ||||||
| chr12:6209078
|
C | G | 1 | a0001c0001t0002g0274 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.66+8513C>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6209078 | ||||||
| chr12:6209374
|
A | G | 1 | a0001c0001t0002g0040 | 2 | HG03688.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.66+8809A>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6209374 | ||||||
| chr12:6209463
|
A | G | 1 | a0001c0001t0002g0274 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.66+8898A>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6209463 | ||||||
| chr12:6209497
|
A | C | 9 | a0001c0001t0001g0030a0001c0001t0001g0229a0001c0001t0001g0230others(6): Show | 10 | NA18941.hp1 NA18967.hp2 NA18969.hp2 others(7): Show |
intron_variant | MODIFIER | c.66+8932A>C | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6209497 | ||||||
| chr12:6209599
|
C | T | 1 | a0001c0001t0001g0133 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.66+9034C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6209599 | ||||||
| chr12:6209604
|
C | G | 1 | a0001c0001t0001g0173 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.66+9039C>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6209604 | ||||||
| chr12:6209679
|
CT | C | 15 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0045others(12): Show | 17 | HG01074.hp2 HG01934.hp1 HG01981.hp2 others(14): Show |
intron_variant | MODIFIER | c.66+9135delT | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 6209679 | |||||
| chr12:6209679
|
CTTTTTTT | C | 130 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(127): Show | 157 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(154): Show |
intron_variant | MODIFIER | c.66+9129_66+9135del others(7): Show |
CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 6209679 | |||||
| chr12:6209977
|
G | A | 1 | a0001c0001t0001g0060 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.66+9412G>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6209977 | ||||||
| chr12:6210022
|
T | C | 9 | a0001c0001t0001g0030a0001c0001t0001g0229a0001c0001t0001g0230others(6): Show | 10 | NA18941.hp1 NA18967.hp2 NA18969.hp2 others(7): Show |
intron_variant | MODIFIER | c.66+9457T>C | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6210022 | ||||||
| chr12:6210144
|
G | A | 17 | a0001c0001t0001g0250a0001c0001t0001g0252a0001c0001t0002g0012others(14): Show | 21 | HG01346.hp1 HG01884.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.66+9579G>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6210144 | ||||||
| chr12:6210152
|
G | GTTC | 141 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(138): Show | 169 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(166): Show |
intron_variant | MODIFIER | c.66+9589_66+9591dup others(3): Show |
CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 6210152 | |||||
| chr12:6210199
|
C | T | 1 | a0001c0001t0001g0227 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.66+9634C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6210199 | ||||||
| chr12:6210333
|
G | A | 1 | a0001c0001t0001g0141 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.66+9768G>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6210333 | ||||||
| chr12:6210361
|
G | A | 1 | a0001c0001t0001g0041 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.66+9796G>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6210361 | ||||||
| chr12:6210467
|
C | G | 21 | a0001c0001t0001g0032a0001c0001t0001g0045a0001c0001t0001g0248others(18): Show | 26 | HG01346.hp1 HG01884.hp2 HG01891.hp1 others(23): Show |
intron_variant | MODIFIER | c.66+9902C>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6210467 | ||||||
| chr12:6210473
|
G | A | 1 | a0001c0001t0001g0178 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.66+9908G>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6210473 | ||||||
| chr12:6210578
|
C | T | 3 | a0001c0001t0001g0011a0001c0001t0001g0269a0001c0001t0001g0287 | 5 | HG02055.hp2 HG02258.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.66+10013C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6210578 | ||||||
| chr12:6210671
|
G | A | 131 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(128): Show | 158 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(155): Show |
intron_variant | MODIFIER | c.66+10106G>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6210671 | ||||||
| chr12:6210722
|
A | G | 1 | a0001c0001t0001g0130 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.66+10157A>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6210722 | ||||||
| chr12:6210835
|
CT | C | 18 | a0001c0001t0001g0030a0001c0001t0001g0091a0001c0001t0001g0099others(15): Show | 19 | HG01074.hp1 HG01255.hp2 HG02083.hp2 others(16): Show |
intron_variant | MODIFIER | c.66+10290delT | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 6210835 | |||||
| chr12:6210835
|
CTT | C | 124 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(121): Show | 151 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(148): Show |
intron_variant | MODIFIER | c.66+10289_66+10290d others(4): Show |
CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 6210835 | |||||
| chr12:6210897
|
C | T | 5 | a0001c0001t0001g0088a0001c0001t0001g0089a0001c0001t0001g0090others(2): Show | 5 | HG00544.hp2 HG00673.hp1 HG02040.hp2 others(2): Show |
intron_variant | MODIFIER | c.66+10332C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6210897 | ||||||
| chr12:6210917
|
A | G | 9 | a0001c0001t0001g0030a0001c0001t0001g0229a0001c0001t0001g0230others(6): Show | 10 | NA18941.hp1 NA18967.hp2 NA18969.hp2 others(7): Show |
intron_variant | MODIFIER | c.66+10352A>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6210917 | ||||||
| chr12:6210925
|
C | A | 10 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0155others(7): Show | 12 | HG00621.hp1 HG03490.hp1 NA18944.hp2 others(9): Show |
intron_variant | MODIFIER | c.66+10360C>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6210925 | ||||||
| chr12:6211037
|
C | T | 1 | a0001c0001t0001g0261 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.66+10472C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6211037 | ||||||
| chr12:6211038
|
A | G | 1 | a0001c0001t0001g0261 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.66+10473A>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6211038 | ||||||
| chr12:6211043
|
G | A | 1 | a0001c0001t0001g0261 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.66+10478G>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6211043 | ||||||
| chr12:6211050
|
C | A | 1 | a0001c0001t0001g0261 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.66+10485C>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6211050 | ||||||
| chr12:6211087
|
T | C | 1 | a0001c0001t0001g0061 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.66+10522T>C | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6211087 | ||||||
| chr12:6211125
|
C | T | 1 | a0001c0001t0002g0271 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.66+10560C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6211125 | ||||||
| chr12:6211220
|
C | T | 141 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(138): Show | 171 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(168): Show |
intron_variant | MODIFIER | c.66+10655C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6211220 | ||||||
| chr12:6211226
|
A | T | 2 | a0001c0001t0001g0011a0001c0001t0001g0287 | 4 | HG02055.hp2 HG02258.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.66+10661A>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6211226 | ||||||
| chr12:6211232
|
G | A | 3 | a0001c0001t0001g0039a0001c0001t0001g0291a0001c0001t0001g0294 | 4 | HG01192.hp2 HG02559.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.66+10667G>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6211232 | ||||||
| chr12:6211558
|
G | A | 3 | a0001c0001t0001g0290a0001c0001t0001g0292a0001c0001t0001g0293 | 3 | HG02109.hp1 HG02630.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.66+10993G>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6211558 | ||||||
| chr12:6211588
|
C | T | 4 | a0001c0001t0001g0251a0001c0001t0001g0266a0001c0001t0001g0268others(1): Show | 4 | HG02615.hp1 HG02723.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.66+11023C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6211588 | ||||||
| chr12:6211663
|
C | T | 4 | a0001c0001t0001g0224a0001c0001t0001g0225a0001c0001t0001g0226others(1): Show | 4 | NA18962.hp2 NA18992.hp2 NA19000.hp2 others(1): Show |
intron_variant | MODIFIER | c.66+11098C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6211663 | ||||||
| chr12:6211703
|
C | T | 1 | a0001c0001t0002g0280 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.66+11138C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6211703 | ||||||
| chr12:6211895
|
A | T | 1 | a0001c0001t0001g0223 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.66+11330A>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6211895 | ||||||
| chr12:6211910
|
C | T | 1 | a0001c0001t0002g0283 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.66+11345C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6211910 | ||||||
| chr12:6212415
|
A | G | 3 | a0001c0001t0001g0290a0001c0001t0001g0292a0001c0001t0001g0293 | 3 | HG02109.hp1 HG02630.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.66+11850A>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6212415 | ||||||
| chr12:6212696
|
C | G | 132 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(129): Show | 159 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(156): Show |
intron_variant | MODIFIER | c.66+12131C>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6212696 | ||||||
| chr12:6212826
|
A | G | 1 | a0001c0001t0001g0222 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.66+12261A>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6212826 | ||||||
| chr12:6212838
|
A | G | 1 | a0001c0001t0001g0221 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.66+12273A>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6212838 | ||||||
| chr12:6212864
|
G | A | 1 | a0001c0001t0001g0269 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.66+12299G>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6212864 | ||||||
| chr12:6212909
|
A | G | 7 | a0001c0001t0001g0149a0001c0001t0001g0153a0001c0001t0001g0162others(4): Show | 7 | HG02896.hp2 HG02897.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.66+12344A>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6212909 | ||||||
| chr12:6212958
|
G | A | 1 | a0001c0001t0001g0175 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.66+12393G>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6212958 | ||||||
| chr12:6212987
|
G | C | 1 | a0001c0001t0001g0178 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.66+12422G>C | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6212987 | ||||||
| chr12:6213028
|
C | A | 1 | a0001c0001t0001g0065 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.67-12398C>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6213028 | ||||||
| chr12:6213091
|
G | A | 1 | a0001c0001t0002g0283 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.67-12335G>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6213091 | ||||||
| chr12:6213119
|
A | G | 1 | a0001c0001t0001g0126 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.67-12307A>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6213119 | ||||||
| chr12:6213149
|
T | C | 3 | a0001c0001t0001g0038a0001c0001t0001g0289a0001c0001t0003g0288 | 4 | HG02451.hp2 HG02615.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.67-12277T>C | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6213149 | ||||||
| chr12:6213335
|
A | G | 2 | a0001c0001t0001g0011a0001c0001t0001g0287 | 4 | HG02055.hp2 HG02258.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.67-12091A>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6213335 | ||||||
| chr12:6213540
|
T | C | 3 | a0001c0001t0001g0185a0001c0001t0001g0186a0001c0001t0001g0187 | 3 | HG00408.hp2 HG02132.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.67-11886T>C | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6213540 | ||||||
| chr12:6213584
|
A | C | 1 | a0001c0001t0001g0125 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.67-11842A>C | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6213584 | ||||||
| chr12:6213618
|
C | T | 1 | a0001c0001t0001g0128 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.67-11808C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6213618 | ||||||
| chr12:6213651
|
T | C | 196 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(193): Show | 240 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(237): Show |
intron_variant | MODIFIER | c.67-11775T>C | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6213651 | ||||||
| chr12:6213692
|
T | C | 1 | a0001c0001t0001g0128 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.67-11734T>C | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6213692 | ||||||
| chr12:6213706
|
G | A | 1 | a0001c0001t0002g0303 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.67-11720G>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6213706 | ||||||
| chr12:6213788
|
A | G | 1 | a0001c0001t0002g0275 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.67-11638A>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6213788 | ||||||
| chr12:6213826
|
C | T | 11 | a0001c0001t0001g0030a0001c0001t0001g0033a0001c0001t0001g0229others(8): Show | 13 | HG03098.hp1 HG03130.hp2 HG03516.hp2 others(10): Show |
intron_variant | MODIFIER | c.67-11600C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6213826 | ||||||
| chr12:6213828
|
A | C | 11 | a0001c0001t0001g0030a0001c0001t0001g0033a0001c0001t0001g0229others(8): Show | 13 | HG03098.hp1 HG03130.hp2 HG03516.hp2 others(10): Show |
intron_variant | MODIFIER | c.67-11598A>C | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6213828 | ||||||
| chr12:6213864
|
G | T | 1 | a0001c0001t0002g0282 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.67-11562G>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6213864 | ||||||
| chr12:6213882
|
A | C | 1 | a0001c0001t0001g0064 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.67-11544A>C | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6213882 | ||||||
| chr12:6213974
|
G | A | 1 | a0001c0001t0001g0189 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.67-11452G>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6213974 | ||||||
| chr12:6213998
|
A | C | 1 | a0001c0001t0001g0065 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.67-11428A>C | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6213998 | ||||||
| chr12:6214003
|
A | G | 1 | a0001c0001t0002g0282 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.67-11423A>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6214003 | ||||||
| chr12:6214015
|
A | T | 2 | a0001c0001t0001g0063a0001c0001t0001g0064 | 2 | NA19085.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.67-11411A>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6214015 | ||||||
| chr12:6214035
|
C | A | 21 | a0001c0001t0001g0032a0001c0001t0001g0045a0001c0001t0001g0244others(18): Show | 26 | HG01346.hp1 HG01891.hp1 HG01952.hp2 others(23): Show |
intron_variant | MODIFIER | c.67-11391C>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6214035 | ||||||
| chr12:6214058
|
C | T | 1 | a0001c0001t0002g0283 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.67-11368C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6214058 | ||||||
| chr12:6214134
|
T | A | 16 | a0001c0001t0001g0004a0001c0001t0001g0039a0001c0001t0001g0054others(13): Show | 23 | HG00733.hp1 HG01192.hp2 HG01516.hp2 others(20): Show |
intron_variant | MODIFIER | c.67-11292T>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6214134 | ||||||
| chr12:6214227
|
C | A | 49 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0016others(46): Show | 57 | HG00423.hp2 HG00544.hp2 HG00673.hp1 others(54): Show |
intron_variant | MODIFIER | c.67-11199C>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6214227 | ||||||
| chr12:6214344
|
C | CT | 37 | a0001c0001t0001g0004a0001c0001t0001g0032a0001c0001t0001g0039others(34): Show | 47 | HG00733.hp1 HG01192.hp2 HG01261.hp1 others(44): Show |
intron_variant | MODIFIER | c.67-11058dupT | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 6214344 | |||||
| chr12:6214344
|
C | CTT | 10 | a0001c0001t0001g0030a0001c0001t0001g0033a0001c0001t0001g0229others(7): Show | 12 | HG02451.hp1 HG03130.hp2 HG03516.hp2 others(9): Show |
intron_variant | MODIFIER | c.67-11059_67-11058d others(4): Show |
CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 6214344 | |||||
| chr12:6214344
|
C | CTTT | 6 | a0001c0001t0001g0011a0001c0001t0001g0234a0001c0001t0001g0254others(3): Show | 8 | HG01346.hp1 HG01884.hp2 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.67-11060_67-11058d others(5): Show |
CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 6214344 | |||||
| chr12:6214344
|
C | CTTTT | 7 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0103others(4): Show | 9 | HG02257.hp2 HG02922.hp1 HG03471.hp2 others(6): Show |
intron_variant | MODIFIER | c.67-11061_67-11058d others(6): Show |
CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 6214344 | |||||
| chr12:6214344
|
C | CTTTTT | 90 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(87): Show | 114 | HG00408.hp1 HG00544.hp2 HG00558.hp1 others(111): Show |
intron_variant | MODIFIER | c.67-11062_67-11058d others(7): Show |
CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 6214344 | |||||
| chr12:6214344
|
C | CTTTTTT | 34 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0019others(31): Show | 37 | HG00423.hp2 HG00438.hp2 HG00639.hp2 others(34): Show |
intron_variant | MODIFIER | c.67-11063_67-11058d others(8): Show |
CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 6214344 | |||||
| chr12:6214344
|
C | CTTTTTTT | 5 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0001g0124others(2): Show | 6 | HG02486.hp2 HG02895.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.67-11064_67-11058d others(9): Show |
CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 6214344 | |||||
| chr12:6214344
|
CT | C | 6 | a0001c0001t0001g0174a0001c0001t0001g0185a0001c0001t0001g0257others(3): Show | 6 | HG00408.hp2 HG02735.hp2 NA18951.hp2 others(3): Show |
intron_variant | MODIFIER | c.67-11058delT | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 6214344 | |||||
| chr12:6214344
|
CTTTTTTT others(2): Show |
C | 6 | a0001c0001t0001g0162a0001c0001t0001g0251a0001c0001t0001g0266others(3): Show | 6 | HG02615.hp1 HG02723.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.67-11066_67-11058d others(11): Show |
CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 6214344 | |||||
| chr12:6214361
|
T | C | 3 | a0001c0001t0001g0290a0001c0001t0001g0292a0001c0001t0001g0293 | 3 | HG02109.hp1 HG02630.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.67-11065T>C | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6214361 | ||||||
| chr12:6214439
|
T | C | 3 | a0001c0001t0001g0165a0001c0001t0001g0190a0001c0001t0001g0191 | 3 | NA18612.hp1 NA18960.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.67-10987T>C | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6214439 | ||||||
| chr12:6214524
|
T | C | 2 | a0001c0001t0001g0143a0001c0001t0001g0144 | 2 | NA18968.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.67-10902T>C | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6214524 | ||||||
| chr12:6214639
|
C | T | 2 | a0001c0001t0001g0217a0001c0001t0001g0222 | 2 | HG01081.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.67-10787C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6214639 | ||||||
| chr12:6214766
|
G | C | 1 | a0001c0001t0001g0066 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.67-10660G>C | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6214766 | ||||||
| chr12:6214766
|
G | T | 1 | a0001c0001t0001g0216 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.67-10660G>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6214766 | ||||||
| chr12:6215100
|
G | A | 1 | a0001c0001t0001g0220 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.67-10326G>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6215100 | ||||||
| chr12:6215236
|
C | T | 1 | a0001c0001t0001g0215 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.67-10190C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6215236 | ||||||
| chr12:6215272
|
A | G | 1 | a0001c0001t0001g0253 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.67-10154A>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6215272 | ||||||
| chr12:6215435
|
C | T | 1 | a0001c0001t0002g0283 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.67-9991C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6215435 | ||||||
| chr12:6215539
|
A | G | 1 | a0001c0001t0001g0178 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.67-9887A>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6215539 | ||||||
| chr12:6215597
|
G | A | 2 | a0001c0001t0001g0143a0001c0001t0001g0144 | 2 | NA18968.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.67-9829G>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6215597 | ||||||
| chr12:6215709
|
A | G | 9 | a0001c0001t0001g0030a0001c0001t0001g0229a0001c0001t0001g0230others(6): Show | 10 | NA18941.hp1 NA18967.hp2 NA18969.hp2 others(7): Show |
intron_variant | MODIFIER | c.67-9717A>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6215709 | ||||||
| chr12:6215757
|
G | A | 1 | a0001c0001t0001g0031 | 2 | HG01934.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.67-9669G>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6215757 | ||||||
| chr12:6215805
|
C | T | 12 | a0001c0001t0001g0060a0001c0001t0001g0085a0001c0001t0001g0087others(9): Show | 15 | HG01891.hp1 HG02109.hp2 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.67-9621C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6215805 | ||||||
| chr12:6215806
|
G | A | 1 | a0001c0001t0002g0283 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.67-9620G>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6215806 | ||||||
| chr12:6215855
|
C | T | 1 | a0001c0001t0001g0184 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.67-9571C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6215855 | ||||||
| chr12:6215862
|
A | G | 22 | a0001c0001t0001g0004a0001c0001t0001g0039a0001c0001t0001g0054others(19): Show | 29 | HG00733.hp1 HG01192.hp2 HG01516.hp2 others(26): Show |
intron_variant | MODIFIER | c.67-9564A>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6215862 | ||||||
| chr12:6215957
|
T | A | 14 | a0001c0001t0001g0010a0001c0001t0001g0020a0001c0001t0001g0034others(11): Show | 18 | HG00558.hp2 NA18944.hp1 NA18945.hp1 others(15): Show |
intron_variant | MODIFIER | c.67-9469T>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6215957 | ||||||
| chr12:6216256
|
C | T | 9 | a0001c0001t0001g0030a0001c0001t0001g0229a0001c0001t0001g0230others(6): Show | 10 | NA18941.hp1 NA18967.hp2 NA18969.hp2 others(7): Show |
intron_variant | MODIFIER | c.67-9170C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6216256 | ||||||
| chr12:6216416
|
C | G | 137 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(134): Show | 167 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(164): Show |
intron_variant | MODIFIER | c.67-9010C>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6216416 | ||||||
| chr12:6216497
|
C | T | 9 | a0001c0001t0001g0030a0001c0001t0001g0229a0001c0001t0001g0230others(6): Show | 10 | NA18941.hp1 NA18967.hp2 NA18969.hp2 others(7): Show |
intron_variant | MODIFIER | c.67-8929C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6216497 | ||||||
| chr12:6216522
|
T | C | 16 | a0001c0001t0001g0004a0001c0001t0001g0039a0001c0001t0001g0054others(13): Show | 23 | HG00733.hp1 HG01192.hp2 HG01516.hp2 others(20): Show |
intron_variant | MODIFIER | c.67-8904T>C | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6216522 | ||||||
| chr12:6216700
|
A | G | 7 | a0001c0001t0001g0030a0001c0001t0001g0229a0001c0001t0001g0230others(4): Show | 8 | NA18941.hp1 NA18967.hp2 NA18969.hp2 others(5): Show |
intron_variant | MODIFIER | c.67-8726A>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6216700 | ||||||
| chr12:6216701
|
G | A | 7 | a0001c0001t0001g0030a0001c0001t0001g0229a0001c0001t0001g0230others(4): Show | 8 | NA18941.hp1 NA18967.hp2 NA18969.hp2 others(5): Show |
intron_variant | MODIFIER | c.67-8725G>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6216701 | ||||||
| chr12:6216748
|
C | G | 177 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(174): Show | 219 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(216): Show |
intron_variant | MODIFIER | c.67-8678C>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6216748 | ||||||
| chr12:6216909
|
T | C | 1 | a0001c0001t0001g0194 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.67-8517T>C | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6216909 | ||||||
| chr12:6216918
|
A | G | 8 | a0001c0001t0001g0030a0001c0001t0001g0229a0001c0001t0001g0230others(5): Show | 9 | NA18941.hp1 NA18967.hp2 NA18969.hp2 others(6): Show |
intron_variant | MODIFIER | c.67-8508A>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6216918 | ||||||
| chr12:6217078
|
T | A | 8 | a0001c0001t0001g0030a0001c0001t0001g0229a0001c0001t0001g0230others(5): Show | 9 | NA18941.hp1 NA18967.hp2 NA18969.hp2 others(6): Show |
intron_variant | MODIFIER | c.67-8348T>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6217078 | ||||||
| chr12:6217167
|
A | G | 1 | a0001c0001t0002g0306 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.67-8259A>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6217167 | ||||||
| chr12:6217358
|
C | CA | 4 | a0001c0001t0001g0038a0001c0001t0001g0050a0001c0001t0001g0289others(1): Show | 5 | HG02451.hp2 HG02615.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.67-8060dupA | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 6217358 | |||||
| chr12:6217461
|
G | A | 3 | a0001c0001t0001g0038a0001c0001t0001g0289a0001c0001t0003g0288 | 4 | HG02451.hp2 HG02615.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.67-7965G>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6217461 | ||||||
| chr12:6217621
|
A | G | 1 | a0001c0001t0001g0060 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.67-7805A>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6217621 | ||||||
| chr12:6217638
|
A | T | 3 | a0001c0001t0001g0038a0001c0001t0001g0289a0001c0001t0003g0288 | 4 | HG02451.hp2 HG02615.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.67-7788A>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6217638 | ||||||
| chr12:6217734
|
G | A | 1 | a0001c0001t0001g0145 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.67-7692G>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6217734 | ||||||
| chr12:6217842
|
A | G | 178 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(175): Show | 216 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(213): Show |
intron_variant | MODIFIER | c.67-7584A>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6217842 | ||||||
| chr12:6217872
|
C | T | 2 | a0001c0001t0001g0011a0001c0001t0001g0287 | 4 | HG02055.hp2 HG02258.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.67-7554C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6217872 | ||||||
| chr12:6217901
|
A | G | 1 | a0001c0001t0001g0033 | 2 | HG03130.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.67-7525A>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6217901 | ||||||
| chr12:6218001
|
G | T | 1 | a0001c0001t0002g0279 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.67-7425G>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6218001 | ||||||
| chr12:6218083
|
T | C | 7 | a0001c0001t0001g0039a0001c0001t0001g0054a0001c0001t0001g0291others(4): Show | 8 | HG01192.hp2 HG01884.hp1 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.67-7343T>C | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6218083 | ||||||
| chr12:6218087
|
C | T | 1 | a0001c0001t0001g0171 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.67-7339C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6218087 | ||||||
| chr12:6218227
|
C | CA | 134 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(131): Show | 164 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(161): Show |
intron_variant | MODIFIER | c.67-7187dupA | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 6218227 | |||||
| chr12:6218227
|
CA | C | 9 | a0001c0001t0001g0030a0001c0001t0001g0158a0001c0001t0001g0229others(6): Show | 10 | NA18941.hp1 NA18946.hp2 NA18967.hp2 others(7): Show |
intron_variant | MODIFIER | c.67-7187delA | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 6218227 | |||||
| chr12:6218271
|
A | G | 1 | a0001c0001t0001g0062 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.67-7155A>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6218271 | ||||||
| chr12:6218299
|
G | A | 1 | a0001c0001t0001g0215 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.67-7127G>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6218299 | ||||||
| chr12:6218605
|
C | T | 1 | a0001c0001t0001g0176 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.67-6821C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6218605 | ||||||
| chr12:6218651
|
A | G | 1 | a0001c0001t0001g0235 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.67-6775A>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6218651 | ||||||
| chr12:6218752
|
G | A | 2 | a0001c0001t0001g0008a0001c0001t0001g0127 | 4 | NA18939.hp1 NA18990.hp1 NA18994.hp1 others(1): Show |
intron_variant | MODIFIER | c.67-6674G>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6218752 | ||||||
| chr12:6218754
|
G | T | 1 | a0001c0001t0001g0084 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.67-6672G>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6218754 | ||||||
| chr12:6218823
|
T | C | 179 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(176): Show | 217 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(214): Show |
intron_variant | MODIFIER | c.67-6603T>C | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6218823 | ||||||
| chr12:6218841
|
G | T | 3 | a0001c0001t0001g0039a0001c0001t0001g0291a0001c0001t0001g0294 | 4 | HG01192.hp2 HG02559.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.67-6585G>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6218841 | ||||||
| chr12:6218892
|
C | T | 1 | a0001c0001t0001g0250 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.67-6534C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6218892 | ||||||
| chr12:6218947
|
T | C | 8 | a0001c0001t0001g0004a0001c0001t0001g0101a0001c0001t0002g0004others(5): Show | 14 | HG00733.hp1 HG01891.hp2 HG02148.hp2 others(11): Show |
intron_variant | MODIFIER | c.67-6479T>C | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6218947 | ||||||
| chr12:6219154
|
C | T | 147 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(144): Show | 181 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(178): Show |
intron_variant | MODIFIER | c.67-6272C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6219154 | ||||||
| chr12:6219163
|
G | A | 1 | a0001c0001t0001g0013 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.67-6263G>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6219163 | ||||||
| chr12:6219166
|
C | T | 2 | a0001c0001t0001g0054a0001c0001t0002g0295 | 2 | HG01884.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.67-6260C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6219166 | ||||||
| chr12:6219524
|
C | T | 2 | a0001c0001t0001g0155a0001c0001t0001g0156 | 2 | NA18946.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.67-5902C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6219524 | ||||||
| chr12:6219540
|
C | G | 1 | a0001c0001t0001g0084 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.67-5886C>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6219540 | ||||||
| chr12:6219564
|
C | T | 2 | a0001c0001t0001g0211a0001c0001t0001g0212 | 2 | NA18956.hp1 NA18965.hp1 |
intron_variant | MODIFIER | c.67-5862C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6219564 | ||||||
| chr12:6219631
|
A | G | 1 | a0001c0001t0001g0090 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.67-5795A>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6219631 | ||||||
| chr12:6219635
|
G | A | 1 | a0001c0001t0001g0195 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.67-5791G>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6219635 | ||||||
| chr12:6219977
|
A | T | 15 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0047others(12): Show | 22 | HG00544.hp2 HG00673.hp1 HG01069.hp2 others(19): Show |
intron_variant | MODIFIER | c.67-5449A>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6219977 | ||||||
| chr12:6220082
|
G | A | 12 | a0001c0001t0001g0060a0001c0001t0001g0085a0001c0001t0001g0087others(9): Show | 15 | HG01891.hp1 HG02109.hp2 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.67-5344G>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6220082 | ||||||
| chr12:6220125
|
T | C | 1 | a0001c0001t0001g0107 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.67-5301T>C | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6220125 | ||||||
| chr12:6220446
|
G | T | 1 | a0001c0001t0002g0152 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.67-4980G>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6220446 | ||||||
| chr12:6220450
|
T | C | 4 | a0001c0001t0001g0014a0001c0001t0001g0290a0001c0001t0001g0292others(1): Show | 5 | HG02109.hp1 HG02630.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.67-4976T>C | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6220450 | ||||||
| chr12:6220466
|
G | A | 1 | a0001c0001t0002g0283 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.67-4960G>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6220466 | ||||||
| chr12:6220568
|
G | A | 1 | a0001c0001t0001g0196 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.67-4858G>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6220568 | ||||||
| chr12:6220629
|
T | C | 7 | a0001c0001t0001g0039a0001c0001t0001g0054a0001c0001t0001g0291others(4): Show | 8 | HG01192.hp2 HG01884.hp1 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.67-4797T>C | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6220629 | ||||||
| chr12:6220758
|
A | C | 1 | a0001c0001t0001g0174 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.67-4668A>C | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6220758 | ||||||
| chr12:6220845
|
C | T | 1 | a0001c0001t0002g0151 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.67-4581C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6220845 | ||||||
| chr12:6221204
|
C | T | 3 | a0001c0001t0001g0174a0001c0001t0001g0209a0001c0001t0001g0210 | 3 | HG00438.hp1 HG00621.hp2 NA18951.hp2 |
intron_variant | MODIFIER | c.67-4222C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6221204 | ||||||
| chr12:6221306
|
G | A | 21 | a0001c0001t0001g0010a0001c0001t0001g0020a0001c0001t0001g0034others(18): Show | 25 | HG00558.hp2 HG03017.hp1 HG03669.hp2 others(22): Show |
intron_variant | MODIFIER | c.67-4120G>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6221306 | ||||||
| chr12:6221434
|
G | A | 2 | a0001c0001t0001g0011a0001c0001t0001g0287 | 4 | HG02055.hp2 HG02258.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.67-3992G>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6221434 | ||||||
| chr12:6221446
|
C | T | 4 | a0001c0001t0001g0014a0001c0001t0001g0290a0001c0001t0001g0292others(1): Show | 5 | HG02109.hp1 HG02630.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.67-3980C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6221446 | ||||||
| chr12:6221526
|
A | G | 1 | a0001c0001t0001g0218 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.67-3900A>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6221526 | ||||||
| chr12:6221556
|
G | A | 3 | a0001c0001t0001g0185a0001c0001t0001g0186a0001c0001t0001g0187 | 3 | HG00408.hp2 HG02132.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.67-3870G>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6221556 | ||||||
| chr12:6221813
|
C | A | 4 | a0001c0001t0001g0006a0001c0001t0001g0197a0001c0001t0001g0213others(1): Show | 7 | HG00733.hp2 HG01175.hp2 HG01516.hp1 others(4): Show |
intron_variant | MODIFIER | c.67-3613C>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6221813 | ||||||
| chr12:6221813
|
C | CA | 19 | a0001c0001t0001g0062a0001c0001t0001g0077a0001c0001t0001g0087others(16): Show | 19 | HG00621.hp2 HG01358.hp2 HG02056.hp1 others(16): Show |
intron_variant | MODIFIER | c.67-3593dupA | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 6221813 | |||||
| chr12:6221813
|
CA | C | 41 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(38): Show | 46 | HG00408.hp2 HG00423.hp1 HG00558.hp2 others(43): Show |
intron_variant | MODIFIER | c.67-3593delA | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 6221813 | |||||
| chr12:6221861
|
G | A | 2 | a0001c0001t0001g0011a0001c0001t0001g0287 | 4 | HG02055.hp2 HG02258.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.67-3565G>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6221861 | ||||||
| chr12:6221878
|
C | G | 2 | a0001c0001t0001g0011a0001c0001t0001g0287 | 4 | HG02055.hp2 HG02258.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.67-3548C>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6221878 | ||||||
| chr12:6221926
|
C | A | 5 | a0001c0001t0001g0031a0001c0001t0001g0196a0001c0001t0001g0198others(2): Show | 6 | HG00609.hp1 HG01255.hp1 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.67-3500C>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6221926 | ||||||
| chr12:6222042
|
C | T | 1 | a0001c0001t0001g0026 | 2 | HG00735.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.67-3384C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6222042 | ||||||
| chr12:6222085
|
T | G | 1 | a0001c0001t0002g0304 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.67-3341T>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6222085 | ||||||
| chr12:6222103
|
C | T | 5 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0113others(2): Show | 5 | NA18939.hp2 NA18982.hp2 NA18995.hp2 others(2): Show |
intron_variant | MODIFIER | c.67-3323C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6222103 | ||||||
| chr12:6222262
|
G | A | 1 | a0001c0001t0001g0252 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.67-3164G>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6222262 | ||||||
| chr12:6222321
|
C | T | 2 | a0001c0001t0001g0029a0001c0001t0001g0220 | 3 | HG01934.hp2 HG04199.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.67-3105C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6222321 | ||||||
| chr12:6222323
|
A | T | 2 | a0001c0001t0001g0029a0001c0001t0001g0220 | 3 | HG01934.hp2 HG04199.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.67-3103A>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6222323 | ||||||
| chr12:6222355
|
T | C | 1 | a0001c0001t0001g0250 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.67-3071T>C | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6222355 | ||||||
| chr12:6222415
|
C | G | 4 | a0001c0001t0001g0014a0001c0001t0001g0290a0001c0001t0001g0292others(1): Show | 5 | HG02109.hp1 HG02630.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.67-3011C>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6222415 | ||||||
| chr12:6222428
|
A | G | 8 | a0001c0001t0001g0039a0001c0001t0001g0054a0001c0001t0001g0162others(5): Show | 9 | HG01192.hp2 HG01884.hp1 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.67-2998A>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6222428 | ||||||
| chr12:6222506
|
G | A | 1 | a0001c0001t0001g0101 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.67-2920G>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6222506 | ||||||
| chr12:6222525
|
G | A | 4 | a0001c0001t0001g0014a0001c0001t0001g0290a0001c0001t0001g0292others(1): Show | 5 | HG02109.hp1 HG02630.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.67-2901G>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6222525 | ||||||
| chr12:6222584
|
AAG | A | 8 | a0001c0001t0001g0039a0001c0001t0001g0054a0001c0001t0001g0162others(5): Show | 9 | HG01192.hp2 HG01884.hp1 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.67-2838_67-2837del others(2): Show |
CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 6222584 | |||||
| chr12:6222724
|
A | C | 1 | a0001c0001t0002g0283 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.67-2702A>C | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6222724 | ||||||
| chr12:6222778
|
T | C | 1 | a0001c0001t0001g0014 | 2 | HG03471.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.67-2648T>C | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6222778 | ||||||
| chr12:6223017
|
A | G | 1 | a0001c0001t0002g0273 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.67-2409A>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6223017 | ||||||
| chr12:6223032
|
C | G | 8 | a0001c0001t0001g0039a0001c0001t0001g0054a0001c0001t0001g0162others(5): Show | 9 | HG01192.hp2 HG01884.hp1 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.67-2394C>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6223032 | ||||||
| chr12:6223144
|
G | C | 131 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(128): Show | 158 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(155): Show |
intron_variant | MODIFIER | c.67-2282G>C | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6223144 | ||||||
| chr12:6223261
|
CT | C | 178 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(175): Show | 214 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(211): Show |
intron_variant | MODIFIER | c.67-2147delT | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 6223261 | |||||
| chr12:6223354
|
C | T | 16 | a0001c0001t0001g0030a0001c0001t0001g0039a0001c0001t0001g0054others(13): Show | 18 | HG01192.hp2 HG01884.hp1 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.67-2072C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6223354 | ||||||
| chr12:6223409
|
C | T | 2 | a0001c0001t0001g0149a0001c0001t0001g0256 | 2 | HG02155.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.67-2017C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6223409 | ||||||
| chr12:6223564
|
C | G | 2 | a0001c0001t0001g0094a0001c0001t0001g0095 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.67-1862C>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6223564 | ||||||
| chr12:6223590
|
TG | T | 18 | a0001c0001t0001g0032a0001c0001t0001g0044a0001c0001t0001g0045others(15): Show | 21 | HG01346.hp1 HG01952.hp2 HG02055.hp1 others(18): Show |
intron_variant | MODIFIER | c.67-1828delG | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 6223590 | |||||
| chr12:6223596
|
G | A | 3 | a0001c0001t0001g0039a0001c0001t0001g0291a0001c0001t0001g0294 | 4 | HG01192.hp2 HG02559.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.67-1830G>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6223596 | ||||||
| chr12:6223597
|
G | T | 7 | a0001c0001t0001g0010a0001c0001t0001g0034a0001c0001t0001g0257others(4): Show | 10 | NA18944.hp1 NA18959.hp1 NA18963.hp2 others(7): Show |
intron_variant | MODIFIER | c.67-1829G>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6223597 | ||||||
| chr12:6223598
|
G | A | 5 | a0001c0001t0001g0044a0001c0001t0002g0035a0001c0001t0002g0271others(2): Show | 6 | HG01346.hp1 HG01952.hp2 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.67-1828G>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6223598 | ||||||
| chr12:6223660
|
C | G | 1 | a0001c0001t0001g0059 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.67-1766C>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6223660 | ||||||
| chr12:6223672
|
A | G | 243 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(240): Show | 296 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(293): Show |
intron_variant | MODIFIER | c.67-1754A>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6223672 | ||||||
| chr12:6223721
|
G | A | 18 | a0001c0001t0001g0032a0001c0001t0001g0044a0001c0001t0001g0045others(15): Show | 21 | HG01346.hp1 HG01952.hp2 HG02055.hp1 others(18): Show |
intron_variant | MODIFIER | c.67-1705G>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6223721 | ||||||
| chr12:6223744
|
A | G | 141 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(138): Show | 170 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(167): Show |
intron_variant | MODIFIER | c.67-1682A>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6223744 | ||||||
| chr12:6223760
|
G | A | 1 | a0001c0001t0001g0018 | 2 | HG00639.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.67-1666G>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6223760 | ||||||
| chr12:6223778
|
C | T | 1 | a0001c0001t0002g0304 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.67-1648C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6223778 | ||||||
| chr12:6223870
|
C | G | 1 | a0001c0001t0001g0065 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.67-1556C>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6223870 | ||||||
| chr12:6224014
|
G | A | 1 | a0001c0001t0001g0138 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.67-1412G>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6224014 | ||||||
| chr12:6224039
|
C | T | 20 | a0001c0001t0001g0011a0001c0001t0001g0032a0001c0001t0001g0044others(17): Show | 25 | HG01346.hp1 HG01952.hp2 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.67-1387C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6224039 | ||||||
| chr12:6224353
|
A | T | 1 | a0001c0001t0002g0283 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.67-1073A>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6224353 | ||||||
| chr12:6224418
|
A | G | 1 | a0001c0001t0001g0254 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.67-1008A>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6224418 | ||||||
| chr12:6224422
|
C | A | 1 | a0001c0001t0001g0254 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.67-1004C>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6224422 | ||||||
| chr12:6224442
|
A | G | 1 | a0001c0001t0001g0112 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.67-984A>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6224442 | ||||||
| chr12:6224546
|
G | A | 3 | a0001c0001t0001g0268a0001c0001t0002g0302a0001c0007t0001g0161 | 3 | HG02976.hp2 HG06807.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.67-880G>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6224546 | ||||||
| chr12:6224562
|
G | C | 4 | a0001c0001t0001g0014a0001c0001t0001g0290a0001c0001t0001g0292others(1): Show | 5 | HG02109.hp1 HG02630.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.67-864G>C | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6224562 | ||||||
| chr12:6224705
|
C | T | 8 | a0001c0001t0001g0039a0001c0001t0001g0054a0001c0001t0001g0162others(5): Show | 9 | HG01192.hp2 HG01884.hp1 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.67-721C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6224705 | ||||||
| chr12:6224724
|
C | T | 1 | a0001c0001t0001g0129 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.67-702C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6224724 | ||||||
| chr12:6224729
|
G | A | 1 | a0003c0004t0001g0146 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.67-697G>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6224729 | ||||||
| chr12:6224759
|
T | C | 1 | a0001c0001t0001g0194 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.67-667T>C | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6224759 | ||||||
| chr12:6224808
|
A | G | 1 | a0001c0001t0001g0111 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.67-618A>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6224808 | ||||||
| chr12:6225019
|
C | T | 1 | a0001c0001t0001g0256 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.67-407C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6225019 | ||||||
| chr12:6225208
|
C | T | 1 | a0001c0001t0001g0213 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.67-218C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6225208 | ||||||
| chr12:6225247
|
T | A | 2 | a0001c0001t0001g0033a0001c0001t0001g0254 | 3 | HG03098.hp1 HG03130.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.67-179T>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6225247 | ||||||
| chr12:6225322
|
C | T | 1 | a0001c0001t0001g0208 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.67-104C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6225322 | ||||||
| chr12:6225363
|
C | T | 1 | a0001c0001t0001g0201 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.67-63C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6225363 | ||||||
| chr12:6225563
|
C | G | 1 | a0001c0001t0001g0194 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.175+29C>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | chr12 | 6225563 | ||||||
| chr12:6225563
|
C | T | 2 | a0001c0001t0001g0246a0001c0001t0001g0247 | 2 | NA18941.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.175+29C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | chr12 | 6225563 | ||||||
| chr12:6225706
|
G | A | 1 | a0001c0001t0001g0032 | 2 | HG02809.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.175+172G>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | chr12 | 6225706 | ||||||
| chr12:6225719
|
C | T | 3 | a0001c0001t0001g0268a0001c0001t0002g0302a0001c0007t0001g0161 | 3 | HG02976.hp2 HG06807.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.175+185C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | chr12 | 6225719 | ||||||
| chr12:6226312
|
G | A | 8 | a0001c0001t0001g0030a0001c0001t0001g0229a0001c0001t0001g0230others(5): Show | 9 | NA18941.hp1 NA18967.hp2 NA18969.hp2 others(6): Show |
intron_variant | MODIFIER | c.175+778G>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | chr12 | 6226312 | ||||||
| chr12:6226384
|
G | A | 5 | a0001c0001t0001g0019a0001c0001t0001g0102a0001c0001t0001g0122others(2): Show | 6 | NA18957.hp1 NA18968.hp1 NA18983.hp2 others(3): Show |
intron_variant | MODIFIER | c.175+850G>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | chr12 | 6226384 | ||||||
| chr12:6226581
|
G | T | 1 | a0001c0001t0001g0075 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.175+1047G>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | chr12 | 6226581 | ||||||
| chr12:6226633
|
G | A | 2 | a0001c0001t0001g0011a0001c0001t0001g0287 | 4 | HG02055.hp2 HG02258.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.175+1099G>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | chr12 | 6226633 | ||||||
| chr12:6226733
|
A | G | 2 | a0001c0001t0002g0036a0001c0001t0002g0279 | 3 | HG02886.hp2 HG02965.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.175+1199A>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | chr12 | 6226733 | ||||||
| chr12:6226741
|
A | G | 2 | a0001c0001t0001g0011a0001c0001t0001g0287 | 4 | HG02055.hp2 HG02258.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.175+1207A>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | chr12 | 6226741 | ||||||
| chr12:6226818
|
A | G | 16 | a0001c0001t0001g0030a0001c0001t0001g0039a0001c0001t0001g0054others(13): Show | 18 | HG01192.hp2 HG01884.hp1 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.175+1284A>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | chr12 | 6226818 | ||||||
| chr12:6226872
|
G | A | 1 | a0001c0001t0001g0186 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.175+1338G>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | chr12 | 6226872 | ||||||
| chr12:6226971
|
C | G | 1 | a0001c0001t0002g0272 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.175+1437C>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | chr12 | 6226971 | ||||||
| chr12:6226978
|
A | G | 1 | a0001c0001t0002g0272 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.175+1444A>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | chr12 | 6226978 | ||||||
| chr12:6227019
|
T | A | 1 | a0003c0004t0001g0146 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.175+1485T>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | chr12 | 6227019 | ||||||
| chr12:6227053
|
T | C | 23 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0047others(20): Show | 30 | HG00544.hp2 HG00673.hp1 HG01069.hp2 others(27): Show |
intron_variant | MODIFIER | c.175+1519T>C | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | chr12 | 6227053 | ||||||
| chr12:6227138
|
A | G | 1 | a0001c0001t0002g0272 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.175+1604A>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | chr12 | 6227138 | ||||||
| chr12:6227181
|
A | G | 1 | a0001c0001t0001g0213 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.175+1647A>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | chr12 | 6227181 | ||||||
| chr12:6227195
|
T | TTTTTTTT others(331): Show |
4 | a0001c0001t0001g0014a0001c0001t0001g0290a0001c0001t0001g0292others(1): Show | 5 | HG02109.hp1 HG02630.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.175+1661_175+1662i others(340): Show |
CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | chr12 | 6227195 | ||||||
| chr12:6227196
|
A | T | 4 | a0001c0001t0001g0014a0001c0001t0001g0290a0001c0001t0001g0292others(1): Show | 5 | HG02109.hp1 HG02630.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.175+1662A>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | chr12 | 6227196 | ||||||
| chr12:6227205
|
A | AT | 16 | a0001c0001t0001g0030a0001c0001t0001g0039a0001c0001t0001g0054others(13): Show | 18 | HG01192.hp2 HG01884.hp1 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.175+1681dupT | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 6227205 | |||||
| chr12:6227377
|
T | C | 4 | a0001c0001t0001g0014a0001c0001t0001g0290a0001c0001t0001g0292others(1): Show | 5 | HG02109.hp1 HG02630.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.175+1843T>C | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | chr12 | 6227377 | ||||||
| chr12:6227386
|
C | T | 1 | a0001c0001t0001g0038 | 2 | HG02451.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.175+1852C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | chr12 | 6227386 | ||||||
| chr12:6227639
|
C | G | 1 | a0001c0001t0001g0216 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.175+2105C>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | chr12 | 6227639 | ||||||
| chr12:6227707
|
G | C | 2 | a0001c0001t0001g0167a0001c0001t0001g0168 | 2 | NA18963.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.175+2173G>C | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | chr12 | 6227707 | ||||||
| chr12:6227846
|
G | T | 1 | a0001c0001t0001g0216 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.175+2312G>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | chr12 | 6227846 | ||||||
| chr12:6227875
|
C | T | 3 | a0001c0001t0001g0006a0001c0001t0001g0197a0001c0001t0001g0213 | 6 | HG00733.hp2 HG01175.hp2 HG01516.hp1 others(3): Show |
intron_variant | MODIFIER | c.175+2341C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | chr12 | 6227875 | ||||||
| chr12:6227910
|
G | A | 4 | a0001c0001t0001g0017a0001c0001t0001g0053a0001c0001t0001g0116others(1): Show | 5 | HG01346.hp2 HG02004.hp2 HG02602.hp2 others(2): Show |
intron_variant | MODIFIER | c.175+2376G>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | chr12 | 6227910 | ||||||
| chr12:6228014
|
G | C | 16 | a0001c0001t0001g0030a0001c0001t0001g0039a0001c0001t0001g0054others(13): Show | 18 | HG01192.hp2 HG01884.hp1 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.175+2480G>C | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | chr12 | 6228014 | ||||||
| chr12:6228017
|
G | T | 1 | a0001c0001t0001g0207 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.175+2483G>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | chr12 | 6228017 | ||||||
| chr12:6228088
|
G | T | 132 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(129): Show | 160 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(157): Show |
intron_variant | MODIFIER | c.175+2554G>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | chr12 | 6228088 | ||||||
| chr12:6228121
|
G | A | 3 | a0001c0001t0001g0038a0001c0001t0001g0289a0001c0001t0003g0288 | 4 | HG02451.hp2 HG02615.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.175+2587G>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | chr12 | 6228121 | ||||||
| chr12:6228132
|
T | A | 1 | a0001c0001t0002g0303 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.175+2598T>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | chr12 | 6228132 | ||||||
| chr12:6228163
|
G | T | 8 | a0001c0001t0001g0030a0001c0001t0001g0229a0001c0001t0001g0230others(5): Show | 9 | NA18941.hp1 NA18967.hp2 NA18969.hp2 others(6): Show |
intron_variant | MODIFIER | c.175+2629G>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | chr12 | 6228163 | ||||||
| chr12:6228183
|
C | T | 1 | a0001c0001t0001g0265 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.175+2649C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | chr12 | 6228183 | ||||||
| chr12:6228228
|
A | G | 16 | a0001c0001t0001g0030a0001c0001t0001g0039a0001c0001t0001g0054others(13): Show | 18 | HG01192.hp2 HG01884.hp1 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.175+2694A>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | chr12 | 6228228 | ||||||
| chr12:6228265
|
A | C | 16 | a0001c0001t0001g0030a0001c0001t0001g0039a0001c0001t0001g0054others(13): Show | 18 | HG01192.hp2 HG01884.hp1 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.175+2731A>C | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | chr12 | 6228265 | ||||||
| chr12:6228336
|
G | A | 15 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0047others(12): Show | 22 | HG00544.hp2 HG00673.hp1 HG01069.hp2 others(19): Show |
intron_variant | MODIFIER | c.175+2802G>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | chr12 | 6228336 | ||||||
| chr12:6228558
|
C | CA | 22 | a0001c0001t0001g0050a0001c0001t0001g0077a0001c0001t0001g0079others(19): Show | 22 | HG00438.hp2 HG00621.hp2 HG00735.hp1 others(19): Show |
intron_variant | MODIFIER | c.175+3047dupA | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 6228558 | |||||
| chr12:6228558
|
CA | C | 146 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(143): Show | 181 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(178): Show |
intron_variant | MODIFIER | c.175+3047delA | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 6228558 | |||||
| chr12:6228558
|
CAA | C | 24 | a0001c0001t0001g0011a0001c0001t0001g0032a0001c0001t0001g0044others(21): Show | 29 | HG01346.hp1 HG01884.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.175+3046_175+3047d others(4): Show |
CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 6228558 | |||||
| chr12:6228558
|
CAAA | C | 6 | a0001c0001t0001g0014a0001c0001t0001g0287a0001c0001t0001g0290others(3): Show | 7 | HG02109.hp1 HG02258.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.175+3045_175+3047d others(5): Show |
CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 6228558 | |||||
| chr12:6228576
|
A | C | 3 | a0001c0001t0001g0268a0001c0001t0002g0302a0001c0007t0001g0161 | 3 | HG02976.hp2 HG06807.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.175+3042A>C | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | chr12 | 6228576 | ||||||
| chr12:6228655
|
A | G | 1 | a0001c0001t0001g0109 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.175+3121A>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | chr12 | 6228655 | ||||||
| chr12:6228690
|
G | A | 1 | a0001c0001t0001g0267 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.175+3156G>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | chr12 | 6228690 | ||||||
| chr12:6228709
|
C | T | 3 | a0001c0001t0001g0054a0001c0001t0001g0162a0001c0001t0002g0295 | 3 | HG01884.hp1 HG02647.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.175+3175C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | chr12 | 6228709 | ||||||
| chr12:6228743
|
C | T | 1 | a0001c0001t0001g0289 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.175+3209C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | chr12 | 6228743 | ||||||
| chr12:6228758
|
C | T | 3 | a0001c0001t0001g0038a0001c0001t0001g0289a0001c0001t0003g0288 | 4 | HG02451.hp2 HG02615.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.175+3224C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | chr12 | 6228758 | ||||||
| chr12:6228773
|
G | A | 1 | a0001c0001t0002g0283 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.175+3239G>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | chr12 | 6228773 | ||||||
| chr12:6228808
|
A | G | 172 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(169): Show | 208 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(205): Show |
intron_variant | MODIFIER | c.175+3274A>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | chr12 | 6228808 | ||||||
| chr12:6229252
|
C | A | 13 | a0001c0001t0001g0015a0001c0001t0001g0041a0001c0001t0001g0042others(10): Show | 14 | HG01109.hp1 HG01358.hp2 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.176-3380C>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | chr12 | 6229252 | ||||||
| chr12:6229460
|
A | G | 8 | a0001c0001t0001g0030a0001c0001t0001g0229a0001c0001t0001g0230others(5): Show | 9 | NA18941.hp1 NA18967.hp2 NA18969.hp2 others(6): Show |
intron_variant | MODIFIER | c.176-3172A>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | chr12 | 6229460 | ||||||
| chr12:6229471
|
C | T | 173 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(170): Show | 208 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(205): Show |
intron_variant | MODIFIER | c.176-3161C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | chr12 | 6229471 | ||||||
| chr12:6229492
|
T | C | 1 | a0001c0001t0001g0013 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.176-3140T>C | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | chr12 | 6229492 | ||||||
| chr12:6229500
|
C | G | 8 | a0001c0001t0001g0039a0001c0001t0001g0054a0001c0001t0001g0162others(5): Show | 9 | HG01192.hp2 HG01884.hp1 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.176-3132C>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | chr12 | 6229500 | ||||||
| chr12:6229546
|
C | T | 8 | a0001c0001t0001g0030a0001c0001t0001g0229a0001c0001t0001g0230others(5): Show | 9 | NA18941.hp1 NA18967.hp2 NA18969.hp2 others(6): Show |
intron_variant | MODIFIER | c.176-3086C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | chr12 | 6229546 | ||||||
| chr12:6229679
|
A | G | 4 | a0001c0001t0001g0014a0001c0001t0001g0290a0001c0001t0001g0292others(1): Show | 5 | HG02109.hp1 HG02630.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.176-2953A>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | chr12 | 6229679 | ||||||
| chr12:6229711
|
G | GTCC | 14 | a0001c0001t0001g0060a0001c0001t0001g0085a0001c0001t0001g0087others(11): Show | 17 | HG01891.hp1 HG02109.hp2 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.176-2918_176-2916d others(5): Show |
CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 6229711 | |||||
| chr12:6229724
|
G | C | 16 | a0001c0001t0001g0030a0001c0001t0001g0039a0001c0001t0001g0054others(13): Show | 18 | HG01192.hp2 HG01884.hp1 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.176-2908G>C | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | chr12 | 6229724 | ||||||
| chr12:6229779
|
A | G | 4 | a0001c0001t0001g0148a0001c0001t0001g0224a0001c0001t0001g0225others(1): Show | 4 | NA18962.hp2 NA18970.hp2 NA18992.hp2 others(1): Show |
intron_variant | MODIFIER | c.176-2853A>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | chr12 | 6229779 | ||||||
| chr12:6229820
|
C | CT | 6 | a0001c0001t0001g0029a0001c0001t0001g0050a0001c0001t0001g0097others(3): Show | 7 | HG01934.hp2 HG02698.hp2 HG04115.hp2 others(4): Show |
intron_variant | MODIFIER | c.176-2796dupT | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 6229820 | |||||
| chr12:6229963
|
G | A | 16 | a0001c0001t0001g0030a0001c0001t0001g0039a0001c0001t0001g0054others(13): Show | 18 | HG01192.hp2 HG01884.hp1 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.176-2669G>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | chr12 | 6229963 | ||||||
| chr12:6230245
|
G | A | 6 | a0001c0001t0001g0030a0001c0001t0001g0229a0001c0001t0001g0230others(3): Show | 7 | NA18967.hp2 NA18969.hp2 NA18979.hp2 others(4): Show |
intron_variant | MODIFIER | c.176-2387G>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | chr12 | 6230245 | ||||||
| chr12:6230282
|
G | A | 2 | a0001c0001t0001g0021a0001c0001t0001g0175 | 3 | NA18747.hp2 NA19074.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.176-2350G>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | chr12 | 6230282 | ||||||
| chr12:6230420
|
C | T | 1 | a0003c0004t0001g0146 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.176-2212C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | chr12 | 6230420 | ||||||
| chr12:6230422
|
T | G | 1 | a0003c0004t0001g0146 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.176-2210T>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | chr12 | 6230422 | ||||||
| chr12:6230447
|
C | G | 2 | a0001c0001t0001g0030a0001c0001t0001g0229 | 3 | NA18999.hp1 NA19088.hp2 NA19089.hp2 |
intron_variant | MODIFIER | c.176-2185C>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | chr12 | 6230447 | ||||||
| chr12:6230491
|
G | A | 8 | a0001c0001t0001g0030a0001c0001t0001g0229a0001c0001t0001g0230others(5): Show | 9 | NA18941.hp1 NA18967.hp2 NA18969.hp2 others(6): Show |
intron_variant | MODIFIER | c.176-2141G>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | chr12 | 6230491 | ||||||
| chr12:6230555
|
T | A | 1 | a0003c0004t0001g0146 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.176-2077T>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | chr12 | 6230555 | ||||||
| chr12:6230690
|
T | C | 178 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(175): Show | 214 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(211): Show |
intron_variant | MODIFIER | c.176-1942T>C | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | chr12 | 6230690 | ||||||
| chr12:6230697
|
A | G | 276 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(273): Show | 336 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(333): Show |
intron_variant | MODIFIER | c.176-1935A>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | chr12 | 6230697 | ||||||
| chr12:6230743
|
G | A | 1 | a0001c0001t0001g0074 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.176-1889G>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | chr12 | 6230743 | ||||||
| chr12:6230803
|
C | A | 1 | a0003c0004t0001g0146 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.176-1829C>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | chr12 | 6230803 | ||||||
| chr12:6230804
|
A | G | 1 | a0003c0004t0001g0146 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.176-1828A>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | chr12 | 6230804 | ||||||
| chr12:6230873
|
G | A | 1 | a0001c0001t0002g0152 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.176-1759G>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | chr12 | 6230873 | ||||||
| chr12:6231072
|
G | A | 1 | a0001c0001t0001g0071 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.176-1560G>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | chr12 | 6231072 | ||||||
| chr12:6231073
|
T | A | 1 | a0001c0001t0001g0071 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.176-1559T>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | chr12 | 6231073 | ||||||
| chr12:6231079
|
TGTGTATT others(9): Show |
T | 1 | a0001c0001t0001g0071 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.176-1552_176-1537d others(18): Show |
CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | chr12 | 6231079 | ||||||
| chr12:6231121
|
C | T | 2 | a0001c0001t0001g0011a0001c0001t0001g0287 | 4 | HG02055.hp2 HG02258.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.176-1511C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | chr12 | 6231121 | ||||||
| chr12:6231169
|
G | A | 1 | a0001c0001t0001g0175 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.176-1463G>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | chr12 | 6231169 | ||||||
| chr12:6231222
|
T | C | 129 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(126): Show | 156 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(153): Show |
intron_variant | MODIFIER | c.176-1410T>C | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | chr12 | 6231222 | ||||||
| chr12:6231230
|
C | T | 1 | a0001c0001t0001g0096 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.176-1402C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | chr12 | 6231230 | ||||||
| chr12:6231276
|
A | C | 1 | a0001c0001t0001g0170 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.176-1356A>C | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | chr12 | 6231276 | ||||||
| chr12:6231345
|
C | T | 1 | a0001c0001t0001g0205 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.176-1287C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | chr12 | 6231345 | ||||||
| chr12:6231397
|
A | T | 1 | a0001c0001t0002g0273 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.176-1235A>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | chr12 | 6231397 | ||||||
| chr12:6231901
|
T | C | 2 | a0001c0001t0001g0094a0001c0001t0001g0095 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.176-731T>C | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | chr12 | 6231901 | ||||||
| chr12:6231966
|
C | A | 1 | a0003c0004t0001g0146 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.176-666C>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | chr12 | 6231966 | ||||||
| chr12:6232032
|
C | G | 4 | a0001c0001t0001g0014a0001c0001t0001g0290a0001c0001t0001g0292others(1): Show | 5 | HG02109.hp1 HG02630.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.176-600C>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | chr12 | 6232032 | ||||||
| chr12:6232050
|
T | C | 1 | a0001c0001t0001g0072 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.176-582T>C | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | chr12 | 6232050 | ||||||
| chr12:6232327
|
A | T | 1 | a0001c0001t0001g0100 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.176-305A>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | chr12 | 6232327 | ||||||
| chr12:6232333
|
G | A | 162 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(159): Show | 195 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(192): Show |
intron_variant | MODIFIER | c.176-299G>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | chr12 | 6232333 | ||||||
| chr12:6232336
|
G | A | 1 | a0001c0001t0001g0189 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.176-296G>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | chr12 | 6232336 | ||||||
| chr12:6232394
|
G | C | 2 | a0001c0001t0001g0174a0001c0001t0001g0209 | 2 | HG00621.hp2 NA18951.hp2 |
intron_variant | MODIFIER | c.176-238G>C | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | chr12 | 6232394 | ||||||
| chr12:6232602
|
C | T | 5 | a0001c0001t0001g0137a0001c0001t0001g0268a0001c0001t0002g0152others(2): Show | 5 | HG02976.hp2 HG03130.hp1 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.176-30C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | chr12 | 6232602 | ||||||
| chr12:6232899
|
C | T | 2 | a0001c0001t0001g0166a0001c0001t0001g0208 | 2 | HG02132.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.273+170C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 3/7 | chr12 | 6232899 | ||||||
| chr12:6232902
|
T | C | 1 | a0001c0001t0002g0273 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.273+173T>C | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 3/7 | chr12 | 6232902 | ||||||
| chr12:6233075
|
G | A | 4 | a0001c0001t0001g0054a0001c0001t0001g0162a0001c0001t0002g0282others(1): Show | 4 | HG01884.hp1 HG01884.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.274-337G>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 3/7 | chr12 | 6233075 | ||||||
| chr12:6233111
|
A | G | 2 | a0001c0001t0001g0011a0001c0001t0001g0287 | 4 | HG02055.hp2 HG02258.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.274-301A>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 3/7 | chr12 | 6233111 | ||||||
| chr12:6233391
|
C | T | 1 | a0001c0001t0001g0191 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.274-21C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 3/7 | chr12 | 6233391 | ||||||
| chr12:6233614
|
C | T | 1 | a0001c0001t0001g0215 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.348+128C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 4/7 | chr12 | 6233614 | ||||||
| chr12:6233755
|
G | T | 122 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(119): Show | 149 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(146): Show |
intron_variant | MODIFIER | c.348+269G>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 4/7 | chr12 | 6233755 | ||||||
| chr12:6233841
|
C | A | 1 | a0001c0001t0001g0178 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.348+355C>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 4/7 | chr12 | 6233841 | ||||||
| chr12:6233890
|
C | T | 1 | a0001c0001t0002g0273 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.348+404C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 4/7 | chr12 | 6233890 | ||||||
| chr12:6233909
|
C | G | 11 | a0001c0001t0001g0140a0001c0001t0001g0141a0001c0001t0001g0142others(8): Show | 11 | HG02155.hp2 HG02165.hp2 HG03491.hp1 others(8): Show |
intron_variant | MODIFIER | c.348+423C>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 4/7 | chr12 | 6233909 | ||||||
| chr12:6233957
|
C | T | 26 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0044others(23): Show | 30 | HG00609.hp1 HG01255.hp1 HG01261.hp2 others(27): Show |
intron_variant | MODIFIER | c.348+471C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 4/7 | chr12 | 6233957 | ||||||
| chr12:6233985
|
A | G | 2 | a0001c0001t0001g0289a0001c0001t0003g0288 | 2 | HG02615.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.348+499A>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 4/7 | chr12 | 6233985 | ||||||
| chr12:6234258
|
G | C | 3 | a0001c0001t0001g0082a0001c0001t0001g0104a0001c0001t0001g0113 | 3 | NA18952.hp1 NA18981.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.348+772G>C | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 4/7 | chr12 | 6234258 | ||||||
| chr12:6234284
|
G | A | 2 | a0001c0001t0002g0150a0001c0001t0002g0151 | 2 | HG01358.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.348+798G>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 4/7 | chr12 | 6234284 | ||||||
| chr12:6234414
|
G | A | 1 | a0001c0001t0002g0277 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.349-815G>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 4/7 | chr12 | 6234414 | ||||||
| chr12:6234470
|
T | TA | 21 | a0001c0001t0001g0011a0001c0001t0001g0014a0001c0001t0001g0023others(18): Show | 25 | HG00621.hp1 HG01358.hp1 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.349-743dupA | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr12 | 6234470 | |||||
| chr12:6234470
|
TA | T | 30 | a0001c0001t0001g0004a0001c0001t0001g0046a0001c0001t0001g0050others(27): Show | 36 | HG00423.hp2 HG00733.hp1 HG01169.hp2 others(33): Show |
intron_variant | MODIFIER | c.349-743delA | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr12 | 6234470 | |||||
| chr12:6234489
|
T | C | 1 | a0001c0001t0001g0199 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.349-740T>C | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 4/7 | chr12 | 6234489 | ||||||
| chr12:6234648
|
G | A | 1 | a0001c0001t0002g0299 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.349-581G>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 4/7 | chr12 | 6234648 | ||||||
| chr12:6234684
|
C | T | 1 | a0001c0001t0001g0160 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.349-545C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 4/7 | chr12 | 6234684 | ||||||
| chr12:6235008
|
A | G | 197 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(194): Show | 240 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(237): Show |
intron_variant | MODIFIER | c.349-221A>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 4/7 | chr12 | 6235008 | ||||||
| chr12:6235013
|
G | A | 9 | a0001c0001t0001g0039a0001c0001t0001g0268a0001c0001t0001g0291others(6): Show | 11 | HG01192.hp2 HG01884.hp2 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.349-216G>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 4/7 | chr12 | 6235013 | ||||||
| chr12:6235038
|
G | A | 2 | a0001c0001t0001g0094a0001c0001t0001g0095 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.349-191G>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 4/7 | chr12 | 6235038 | ||||||
| chr12:6235186
|
G | T | 1 | a0001c0001t0001g0065 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.349-43G>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 4/7 | chr12 | 6235186 | ||||||
| chr12:6235203
|
G | A | 5 | a0001c0001t0001g0061a0001c0001t0001g0070a0001c0001t0001g0076others(2): Show | 5 | HG00735.hp1 HG01928.hp1 HG01978.hp1 others(2): Show |
intron_variant | MODIFIER | c.349-26G>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 4/7 | chr12 | 6235203 | ||||||
| chr12:6235209
|
C | T | 1 | a0001c0001t0001g0239 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.349-20C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 4/7 | chr12 | 6235209 | ||||||
| chr12:6235220
|
C | G | 2 | a0001c0001t0001g0289a0001c0001t0003g0288 | 2 | HG02615.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.349-9C>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 4/7 | chr12 | 6235220 | ||||||
| chr12:6235335
|
G | A | 2 | a0001c0001t0001g0009a0001c0001t0002g0273 | 4 | HG02451.hp1 NA18959.hp2 NA18983.hp1 others(1): Show |
splice_region_variant&intron_variant | LOW | c.447+8G>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 5/7 | chr12 | 6235335 | ||||||
| chr12:6235361
|
T | C | 1 | a0001c0001t0001g0217 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.447+34T>C | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 5/7 | chr12 | 6235361 | ||||||
| chr12:6235434
|
C | A | 171 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(168): Show | 206 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(203): Show |
intron_variant | MODIFIER | c.448-42C>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 5/7 | chr12 | 6235434 | ||||||
| chr12:6235437
|
T | A | 1 | a0001c0001t0001g0255 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.448-39T>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 5/7 | chr12 | 6235437 | ||||||
| chr12:6235454
|
C | A | 1 | a0001c0001t0001g0255 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.448-22C>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 5/7 | chr12 | 6235454 | ||||||
| chr12:6235455
|
A | T | 1 | a0001c0001t0001g0255 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.448-21A>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 5/7 | chr12 | 6235455 | ||||||
| chr12:6235456
|
T | C | 1 | a0001c0001t0001g0255 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.448-20T>C | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 5/7 | chr12 | 6235456 | ||||||
| chr12:6235659
|
C | A | 14 | a0001c0001t0001g0014a0001c0001t0001g0030a0001c0001t0001g0229others(11): Show | 16 | HG02109.hp1 HG02451.hp1 HG02630.hp1 others(13): Show |
intron_variant | MODIFIER | c.537+94C>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 6/7 | chr12 | 6235659 | ||||||
| chr12:6235914
|
G | A | 175 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(172): Show | 212 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(209): Show |
intron_variant | MODIFIER | c.538-278G>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 6/7 | chr12 | 6235914 | ||||||
| chr12:6235977
|
A | G | 4 | a0001c0001t0001g0011a0001c0001t0001g0287a0001c0001t0001g0289others(1): Show | 6 | HG02055.hp2 HG02258.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.538-215A>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 6/7 | chr12 | 6235977 | ||||||
| chr12:6236033
|
C | T | 145 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(142): Show | 177 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(174): Show |
intron_variant | MODIFIER | c.538-159C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 6/7 | chr12 | 6236033 | ||||||
| chr12:6236292
|
C | T | 9 | a0001c0001t0001g0030a0001c0001t0001g0204a0001c0001t0001g0229others(6): Show | 10 | NA18941.hp1 NA18967.hp2 NA18969.hp2 others(7): Show |
intron_variant | MODIFIER | c.621+17C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 7/7 | chr12 | 6236292 | ||||||
| chr12:6236365
|
C | G | 1 | a0001c0001t0002g0278 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.621+90C>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 7/7 | chr12 | 6236365 | ||||||
| chr12:6236440
|
C | T | 1 | a0001c0001t0002g0305 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.621+165C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 7/7 | chr12 | 6236440 | ||||||
| chr12:6236577
|
A | G | 1 | a0001c0001t0001g0293 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.621+302A>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 7/7 | chr12 | 6236577 | ||||||
| chr12:6236578
|
T | C | 2 | a0001c0001t0001g0011a0001c0001t0001g0287 | 4 | HG02055.hp2 HG02258.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.621+303T>C | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 7/7 | chr12 | 6236578 | ||||||
| chr12:6236590
|
C | T | 2 | a0001c0001t0001g0011a0001c0001t0001g0287 | 4 | HG02055.hp2 HG02258.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.621+315C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 7/7 | chr12 | 6236590 | ||||||
| chr12:6236618
|
C | A | 130 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(127): Show | 160 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(157): Show |
intron_variant | MODIFIER | c.621+343C>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 7/7 | chr12 | 6236618 | ||||||
| chr12:6236783
|
C | T | 1 | a0001c0001t0001g0260 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.621+508C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 7/7 | chr12 | 6236783 | ||||||
| chr12:6236807
|
G | A | 29 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0047others(26): Show | 36 | HG00544.hp2 HG00673.hp1 HG01069.hp2 others(33): Show |
intron_variant | MODIFIER | c.621+532G>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 7/7 | chr12 | 6236807 | ||||||
| chr12:6236826
|
TC | T | 2 | a0001c0001t0001g0011a0001c0001t0001g0287 | 4 | HG02055.hp2 HG02258.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.621+556delC | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr12 | 6236826 | |||||
| chr12:6236906
|
C | T | 5 | a0001c0001t0001g0244a0001c0001t0001g0289a0001c0001t0002g0276others(2): Show | 5 | HG02258.hp1 HG02615.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.621+631C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 7/7 | chr12 | 6236906 | ||||||
| chr12:6236926
|
A | G | 15 | a0001c0001t0001g0032a0001c0001t0001g0044a0001c0001t0001g0045others(12): Show | 18 | HG01346.hp1 HG01952.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.621+651A>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 7/7 | chr12 | 6236926 | ||||||
| chr12:6236949
|
G | A | 2 | a0001c0001t0001g0246a0001c0001t0001g0247 | 2 | NA18941.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.621+674G>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 7/7 | chr12 | 6236949 | ||||||
| chr12:6237221
|
T | C | 172 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(169): Show | 209 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(206): Show |
intron_variant | MODIFIER | c.622-542T>C | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 7/7 | chr12 | 6237221 | ||||||
| chr12:6237263
|
C | T | 1 | a0001c0001t0001g0045 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.622-500C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 7/7 | chr12 | 6237263 | ||||||
| chr12:6237289
|
C | T | 1 | a0001c0001t0002g0152 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.622-474C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 7/7 | chr12 | 6237289 | ||||||
| chr12:6237312
|
T | C | 175 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(172): Show | 212 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(209): Show |
intron_variant | MODIFIER | c.622-451T>C | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 7/7 | chr12 | 6237312 | ||||||
| chr12:6237314
|
T | C | 9 | a0001c0001t0001g0039a0001c0001t0001g0268a0001c0001t0001g0291others(6): Show | 11 | HG01192.hp2 HG01884.hp2 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.622-449T>C | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 7/7 | chr12 | 6237314 | ||||||
| chr12:6237387
|
G | GA | 6 | a0001c0001t0001g0031a0001c0001t0001g0196a0001c0001t0001g0198others(3): Show | 7 | HG00609.hp1 HG01255.hp1 HG01261.hp2 others(4): Show |
intron_variant | MODIFIER | c.622-366dupA | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr12 | 6237387 | |||||
| chr12:6237505
|
A | G | 1 | a0001c0001t0001g0245 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.622-258A>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 7/7 | chr12 | 6237505 | ||||||
| chr12:6237635
|
C | T | 8 | a0001c0001t0001g0030a0001c0001t0001g0229a0001c0001t0001g0230others(5): Show | 9 | NA18941.hp1 NA18967.hp2 NA18969.hp2 others(6): Show |
intron_variant | MODIFIER | c.622-128C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 7/7 | chr12 | 6237635 | ||||||
| chr12:6237700
|
C | T | 2 | a0001c0001t0001g0011a0001c0001t0001g0287 | 4 | HG02055.hp2 HG02258.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.622-63C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 7/7 | chr12 | 6237700 | ||||||
| chr12:6237721
|
G | C | 3 | a0001c0001t0001g0054a0001c0001t0001g0162a0001c0001t0002g0295 | 3 | HG01884.hp1 HG02647.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.622-42G>C | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 7/7 | chr12 | 6237721 |