Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 7103 |
|---|---|
| ensemblid | ENSG00000127324.9 |
| hgncid | 11855 |
| symbol | TSPAN8 |
| name | tetraspanin 8 |
| refseq_nuc | NM_004616.3 |
| refseq_prot | NP_004607.1 |
| ensembl_nuc | ENST00000247829.8 |
| ensembl_prot | ENSP00000247829.3 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 71125096 |
| end | 71157999 |
| strand | - |
| ver | v1.2 |
| region | chr12:71125096-71157999 |
| region5000 | chr12:71120096-71162999 |
| regionname0 | TSPAN8_chr12_71125096_71157999 |
| regionname5000 | TSPAN8_chr12_71120096_71162999 |
| 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 | 237 | 274 | 85 | 44 | 104 | 11 | 28 | 74 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | copy fasta | chr12 | 71120096 | 71162999 |
| a0002 | 0/0 | 237 | 89 | 3 | 15 | 53 | 5 | 13 | 42 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | copy fasta | chr12 | 71120096 | 71162999 |
| a0003 | 0/0 | 237 | 36 | 1 | 5 | 28 | 0 | 2 | 23 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | copy fasta | chr12 | 71120096 | 71162999 |
| a0004 | 0/0 | 237 | 9 | 9 | 0 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | copy fasta | chr12 | 71120096 | 71162999 |
| a0005 | 0/0 | 237 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | copy fasta | chr12 | 71120096 | 71162999 |
| a0006 | 0/0 | 237 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | copy fasta | chr12 | 71120096 | 71162999 |
| a0007 | 0/0 | 237 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | copy fasta | chr12 | 71120096 | 71162999 |
| a0008 | 0/0 | 237 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | copy fasta | chr12 | 71120096 | 71162999 |
| 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 | 714 | 178 | 80 | 27 | 41 | 11 | 17 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | copy fasta | chr12 | 71120096 | 71162999 |
| c0002 | 0/0 | 714 | 89 | 3 | 15 | 53 | 5 | 13 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | copy fasta | chr12 | 71120096 | 71162999 |
| c0003 | 0/0 | 714 | 87 | 5 | 17 | 54 | 0 | 11 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | copy fasta | chr12 | 71120096 | 71162999 |
| c0004 | 0/0 | 714 | 36 | 1 | 5 | 28 | 0 | 2 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | copy fasta | chr12 | 71120096 | 71162999 |
| c0005 | 0/0 | 714 | 9 | 9 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | copy fasta | chr12 | 71120096 | 71162999 |
| c0006 | 0/0 | 714 | 9 | 0 | 0 | 9 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | copy fasta | chr12 | 71120096 | 71162999 |
| c0007 | 0/0 | 714 | 2 | 0 | 0 | 0 | 0 | 2 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | copy fasta | chr12 | 71120096 | 71162999 |
| c0008 | 0/0 | 714 | 2 | 2 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | copy fasta | chr12 | 71120096 | 71162999 |
| c0009 | 0/0 | 714 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | copy fasta | chr12 | 71120096 | 71162999 |
| c0010 | 0/0 | 714 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | copy fasta | chr12 | 71120096 | 71162999 |
| 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 | 418 | 300 | 78 | 48 | 132 | 9 | 31 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | copy fasta | chr12 | 71120096 | 71162999 |
| t0002 | 0/0 | 418 | 102 | 13 | 14 | 53 | 7 | 15 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | copy fasta | chr12 | 71120096 | 71162999 |
| t0003 | 0/0 | 418 | 8 | 7 | 1 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | copy fasta | chr12 | 71120096 | 71162999 |
| t0004 | 0/0 | 418 | 2 | 1 | 1 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | copy fasta | chr12 | 71120096 | 71162999 |
| t0005 | 0/0 | 418 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | copy fasta | chr12 | 71120096 | 71162999 |
| t0006 | 0/0 | 418 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | copy fasta | chr12 | 71120096 | 71162999 |
| 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 | 11 | 0 | 3 | 1 | 5 | 2 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0002 | 0/0 | 10 | 0 | 0 | 9 | 0 | 1 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0003 | 0/0 | 9 | 1 | 0 | 7 | 0 | 1 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0004 | 0/0 | 8 | 0 | 3 | 4 | 0 | 1 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0005 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0006 | 1/0 | 5 | 0 | 3 | 0 | 1 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0007 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0008 | 0/0 | 5 | 0 | 4 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0009 | 0/0 | 5 | 2 | 2 | 0 | 0 | 1 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0010 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0011 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0012 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0013 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0014 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0017 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0018 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0020 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0021 | 0/0 | 3 | 0 | 0 | 1 | 2 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0022 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0023 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0025 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0026 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0032 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0035 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0036 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0049 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0050 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0051 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0052 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0053 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0054 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0055 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0056 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0057 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0176 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0252 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| 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 | 714 | 178 | 80 | 27 | 41 | 11 | 17 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | copy fasta | chr12 | 71120096 | 71162999 |
| a0001c0003 | 0/0 | 714 | 87 | 5 | 17 | 54 | 0 | 11 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | copy fasta | chr12 | 71120096 | 71162999 |
| a0001c0006 | 0/0 | 714 | 9 | 0 | 0 | 9 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | copy fasta | chr12 | 71120096 | 71162999 |
| a0002c0002 | 0/0 | 714 | 89 | 3 | 15 | 53 | 5 | 13 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | copy fasta | chr12 | 71120096 | 71162999 |
| a0003c0004 | 0/0 | 714 | 36 | 1 | 5 | 28 | 0 | 2 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | copy fasta | chr12 | 71120096 | 71162999 |
| a0004c0005 | 0/0 | 714 | 9 | 9 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | copy fasta | chr12 | 71120096 | 71162999 |
| a0005c0007 | 0/0 | 714 | 2 | 0 | 0 | 0 | 0 | 2 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | copy fasta | chr12 | 71120096 | 71162999 |
| a0006c0008 | 0/0 | 714 | 2 | 2 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | copy fasta | chr12 | 71120096 | 71162999 |
| a0007c0010 | 0/0 | 714 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | copy fasta | chr12 | 71120096 | 71162999 |
| a0008c0009 | 0/0 | 714 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | copy fasta | chr12 | 71120096 | 71162999 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 1131 | 164 | 71 | 25 | 40 | 9 | 17 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | copy fasta | chr12 | 71120096 | 71162999 |
| a0001c0001t0002 | 0/0 | 1131 | 5 | 2 | 0 | 1 | 2 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | copy fasta | chr12 | 71120096 | 71162999 |
| a0001c0001t0003 | 0/0 | 1131 | 7 | 6 | 1 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | copy fasta | chr12 | 71120096 | 71162999 |
| a0001c0001t0004 | 0/0 | 1131 | 2 | 1 | 1 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | copy fasta | chr12 | 71120096 | 71162999 |
| a0001c0003t0001 | 0/0 | 1131 | 86 | 4 | 17 | 54 | 0 | 11 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | copy fasta | chr12 | 71120096 | 71162999 |
| a0001c0003t0003 | 0/0 | 1131 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | copy fasta | chr12 | 71120096 | 71162999 |
| a0001c0006t0001 | 0/0 | 1131 | 9 | 0 | 0 | 9 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | copy fasta | chr12 | 71120096 | 71162999 |
| a0002c0002t0001 | 0/0 | 1131 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | copy fasta | chr12 | 71120096 | 71162999 |
| a0002c0002t0002 | 0/0 | 1131 | 87 | 3 | 14 | 52 | 5 | 13 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | copy fasta | chr12 | 71120096 | 71162999 |
| a0002c0002t0006 | 0/0 | 1131 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | copy fasta | chr12 | 71120096 | 71162999 |
| a0003c0004t0001 | 0/0 | 1131 | 36 | 1 | 5 | 28 | 0 | 2 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | copy fasta | chr12 | 71120096 | 71162999 |
| a0004c0005t0002 | 0/0 | 1131 | 8 | 8 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | copy fasta | chr12 | 71120096 | 71162999 |
| a0004c0005t0005 | 0/0 | 1131 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | copy fasta | chr12 | 71120096 | 71162999 |
| a0005c0007t0002 | 0/0 | 1131 | 2 | 0 | 0 | 0 | 0 | 2 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | copy fasta | chr12 | 71120096 | 71162999 |
| a0006c0008t0001 | 0/0 | 1131 | 2 | 2 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | copy fasta | chr12 | 71120096 | 71162999 |
| a0007c0010t0001 | 0/0 | 1131 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | copy fasta | chr12 | 71120096 | 71162999 |
| a0008c0009t0001 | 0/0 | 1131 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | copy fasta | chr12 | 71120096 | 71162999 |
| 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 | 11 | 0 | 3 | 1 | 5 | 2 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0005 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0006 | 1/0 | 5 | 0 | 3 | 0 | 1 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0009 | 0/0 | 5 | 2 | 2 | 0 | 0 | 1 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0011 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0012 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0020 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0022 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0023 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0026 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0050 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0052 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0053 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0054 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0055 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0056 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0057 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0176 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0002g0021 | 0/0 | 3 | 0 | 0 | 1 | 2 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0002g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0002g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0003g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0003g0025 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0003g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0003g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0003g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0004g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0004g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0003t0001g0003 | 0/0 | 9 | 1 | 0 | 7 | 0 | 1 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0003t0001g0013 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0003t0001g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0003t0001g0018 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0003t0001g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0003t0001g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0003t0001g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0003t0001g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0003t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0003t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0003t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0003t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0003t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0003t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0003t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0003t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0003t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0003t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0003t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0003t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0003t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0003t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0003t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0003t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0003t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0003t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0003t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0003t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0003t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0003t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0003t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0003t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0003t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0003t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0003t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0003t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0003t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0003t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0003t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0003t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0003t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0003t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0003t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0003t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0003t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0003t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0003t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0003t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0003t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0003t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0003t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0003t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0003t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0003t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0003t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0003t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0003t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0003t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0003t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0003t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0003t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0003t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0003t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0003t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0003t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0003t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0003t0003g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0006t0001g0007 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0006t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0006t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0006t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0002c0002t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0002c0002t0002g0004 | 0/0 | 8 | 0 | 3 | 4 | 0 | 1 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0002c0002t0002g0010 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0002c0002t0002g0014 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0002c0002t0002g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0002c0002t0002g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0002c0002t0002g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0002c0002t0002g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0002c0002t0002g0032 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0002c0002t0002g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0002c0002t0002g0035 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0002c0002t0002g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0002c0002t0002g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0002c0002t0002g0049 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0002c0002t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0002c0002t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0002c0002t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0002c0002t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0002c0002t0002g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0002c0002t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0002c0002t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0002c0002t0002g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0002c0002t0002g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0002c0002t0002g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0002c0002t0002g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0002c0002t0002g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0002c0002t0002g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0002c0002t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0002c0002t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0002c0002t0002g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0002c0002t0002g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0002c0002t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0002c0002t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0002c0002t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0002c0002t0002g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0002c0002t0002g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0002c0002t0002g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0002c0002t0002g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0002c0002t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0002c0002t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0002c0002t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0002c0002t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0002c0002t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0002c0002t0002g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0002c0002t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0002c0002t0002g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0002c0002t0002g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0002c0002t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0002c0002t0002g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0002c0002t0002g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0002c0002t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0002c0002t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0002c0002t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0002c0002t0002g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0002c0002t0002g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0002c0002t0002g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0002c0002t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0002c0002t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0002c0002t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0002c0002t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0002c0002t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0002c0002t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0002c0002t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0002c0002t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0002c0002t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0002c0002t0002g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0002c0002t0006g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0003c0004t0001g0002 | 0/0 | 10 | 0 | 0 | 9 | 0 | 1 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0003c0004t0001g0008 | 0/0 | 5 | 0 | 4 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0003c0004t0001g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0003c0004t0001g0017 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0003c0004t0001g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0003c0004t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0003c0004t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0003c0004t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0003c0004t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0003c0004t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0003c0004t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0003c0004t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0003c0004t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0003c0004t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0003c0004t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0003c0004t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0003c0004t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0003c0004t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0004c0005t0002g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0004c0005t0002g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0004c0005t0002g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0004c0005t0002g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0004c0005t0002g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0004c0005t0002g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0004c0005t0002g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0004c0005t0005g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0005c0007t0002g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0005c0007t0002g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0006c0008t0001g0051 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0007c0010t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0008c0009t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0002 | t0002 | g0089 | EUR | GBR | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0177 | EUR | GBR | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0006 | EUR | FIN | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG00280 | hp2 | a0002 | c0002 | t0002 | g0112 | EUR | FIN | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | CHS | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG00423 | hp2 | a0001 | c0003 | t0001 | g0205 | EAS | CHS | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG00438 | hp1 | a0002 | c0002 | t0002 | g0049 | EAS | CHS | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG00438 | hp2 | a0002 | c0002 | t0002 | g0098 | EAS | CHS | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG00544 | hp1 | a0001 | c0003 | t0001 | g0216 | EAS | CHS | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG00544 | hp2 | a0002 | c0002 | t0002 | g0040 | EAS | CHS | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG00558 | hp1 | a0001 | c0003 | t0001 | g0182 | EAS | CHS | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | CHS | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG00609 | hp1 | a0002 | c0002 | t0002 | g0004 | EAS | CHS | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG00609 | hp2 | a0002 | c0002 | t0002 | g0144 | EAS | CHS | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | CHS | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG00621 | hp2 | a0002 | c0002 | t0002 | g0004 | EAS | CHS | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0254 | AMR | PUR | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG00639 | hp2 | a0001 | c0003 | t0001 | g0179 | AMR | PUR | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG00642 | hp2 | a0002 | c0002 | t0002 | g0035 | AMR | PUR | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | CHS | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG00673 | hp2 | a0002 | c0002 | t0002 | g0004 | EAS | CHS | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG00735 | hp2 | a0002 | c0002 | t0002 | g0110 | AMR | PUR | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0233 | AMR | PUR | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG00738 | hp2 | a0002 | c0002 | t0002 | g0095 | AMR | PUR | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0255 | AMR | PUR | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0262 | AMR | PUR | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG01071 | hp1 | a0002 | c0002 | t0002 | g0004 | AMR | PUR | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG01106 | hp2 | a0002 | c0002 | t0002 | g0118 | AMR | PUR | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0062 | AMR | PUR | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG01167 | hp1 | a0001 | c0003 | t0001 | g0197 | AMR | PUR | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG01167 | hp2 | a0001 | c0001 | t0003 | g0025 | AMR | PUR | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG01168 | hp2 | a0002 | c0002 | t0002 | g0028 | AMR | PUR | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG01169 | hp1 | a0002 | c0002 | t0002 | g0028 | AMR | PUR | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG01169 | hp2 | a0001 | c0003 | t0001 | g0198 | AMR | PUR | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG01175 | hp1 | a0001 | c0003 | t0001 | g0218 | AMR | PUR | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG01175 | hp2 | a0002 | c0002 | t0001 | g0239 | AMR | PUR | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG01192 | hp1 | a0001 | c0003 | t0001 | g0212 | AMR | PUR | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG01192 | hp2 | a0002 | c0002 | t0002 | g0032 | AMR | PUR | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG01243 | hp1 | a0002 | c0002 | t0002 | g0035 | AMR | PUR | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG01255 | hp1 | a0001 | c0003 | t0001 | g0206 | AMR | CLM | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0247 | AMR | CLM | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG01257 | hp1 | a0003 | c0004 | t0001 | g0008 | AMR | CLM | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG01257 | hp2 | a0002 | c0002 | t0002 | g0096 | AMR | CLM | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG01261 | hp1 | a0001 | c0003 | t0001 | g0146 | AMR | CLM | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG01346 | hp1 | a0002 | c0002 | t0002 | g0004 | AMR | CLM | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0052 | AMR | CLM | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG01358 | hp1 | a0001 | c0003 | t0001 | g0227 | AMR | CLM | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG01358 | hp2 | a0002 | c0002 | t0002 | g0004 | AMR | CLM | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0269 | AMR | CLM | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | CLM | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | CLM | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0052 | AMR | CLM | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG01496 | hp1 | a0003 | c0004 | t0001 | g0008 | AMR | CLM | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG01496 | hp2 | a0001 | c0001 | t0004 | g0059 | AMR | CLM | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG01515 | hp1 | a0002 | c0002 | t0002 | g0092 | EUR | IBS | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0021 | EUR | IBS | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0036 | EUR | IBS | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0021 | EUR | IBS | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG01884 | hp1 | a0002 | c0002 | t0002 | g0085 | AFR | ACB | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0276 | AFR | ACB | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG01891 | hp1 | a0001 | c0001 | t0002 | g0260 | AFR | ACB | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0168 | AFR | ACB | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG01934 | hp1 | a0003 | c0004 | t0001 | g0008 | AMR | PEL | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG01934 | hp2 | a0001 | c0003 | t0001 | g0185 | AMR | PEL | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG01943 | hp1 | a0001 | c0003 | t0001 | g0013 | AMR | PEL | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG01943 | hp2 | a0003 | c0004 | t0001 | g0008 | AMR | PEL | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | PEL | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG01952 | hp2 | a0002 | c0002 | t0002 | g0125 | AMR | PEL | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG01978 | hp1 | a0001 | c0003 | t0001 | g0219 | AMR | PEL | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | PEL | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG01981 | hp1 | a0001 | c0003 | t0001 | g0013 | AMR | PEL | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG01981 | hp2 | a0001 | c0003 | t0001 | g0192 | AMR | PEL | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0070 | AMR | PEL | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02004 | hp1 | a0003 | c0004 | t0001 | g0163 | AMR | PEL | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | PEL | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02015 | hp1 | a0003 | c0004 | t0001 | g0002 | EAS | KHV | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02015 | hp2 | a0001 | c0003 | t0001 | g0188 | EAS | KHV | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | KHV | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02027 | hp2 | a0002 | c0002 | t0006 | g0292 | EAS | KHV | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02040 | hp1 | a0001 | c0003 | t0001 | g0046 | EAS | KHV | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02040 | hp2 | a0001 | c0003 | t0001 | g0195 | EAS | KHV | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0173 | AFR | ACB | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0248 | AFR | ACB | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02056 | hp1 | a0001 | c0003 | t0001 | g0213 | EAS | KHV | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02056 | hp2 | a0001 | c0003 | t0001 | g0225 | EAS | KHV | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02071 | hp1 | a0003 | c0004 | t0001 | g0016 | EAS | KHV | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02071 | hp2 | a0001 | c0003 | t0001 | g0224 | EAS | KHV | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02074 | hp1 | a0002 | c0002 | t0002 | g0077 | EAS | KHV | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | KHV | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02080 | hp1 | a0001 | c0003 | t0001 | g0226 | EAS | KHV | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02080 | hp2 | a0001 | c0003 | t0001 | g0138 | EAS | KHV | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | KHV | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | KHV | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02129 | hp1 | a0001 | c0003 | t0001 | g0152 | EAS | KHV | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02129 | hp2 | a0003 | c0004 | t0001 | g0016 | EAS | KHV | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | KHV | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | KHV | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02135 | hp1 | a0002 | c0002 | t0002 | g0104 | EAS | KHV | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0021 | EAS | KHV | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0053 | AFR | ACB | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02145 | hp2 | a0004 | c0005 | t0002 | g0238 | AFR | ACB | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02148 | hp1 | a0001 | c0003 | t0001 | g0013 | AMR | PEL | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02148 | hp2 | a0001 | c0003 | t0001 | g0214 | AMR | PEL | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02155 | hp1 | a0001 | c0003 | t0001 | g0202 | EAS | CDX | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02155 | hp2 | a0002 | c0002 | t0002 | g0040 | EAS | CDX | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02165 | hp1 | a0003 | c0004 | t0001 | g0149 | EAS | CDX | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | CDX | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02257 | hp1 | a0001 | c0003 | t0001 | g0187 | AFR | ACB | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0278 | AFR | ACB | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0286 | AFR | ACB | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02258 | hp2 | a0002 | c0002 | t0002 | g0116 | AFR | ACB | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0057 | AFR | ACB | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02280 | hp2 | a0004 | c0005 | t0002 | g0037 | AFR | ACB | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02300 | hp1 | a0002 | c0002 | t0002 | g0014 | AMR | PEL | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02300 | hp2 | a0001 | c0003 | t0001 | g0203 | AMR | PEL | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0288 | AFR | ACB | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | KHV | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02523 | hp2 | a0001 | c0003 | t0001 | g0204 | EAS | KHV | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0279 | AFR | GWD | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0289 | AFR | GWD | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02602 | hp1 | a0001 | c0003 | t0001 | g0209 | SAS | PJL | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0253 | SAS | PJL | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02615 | hp1 | a0002 | c0002 | t0002 | g0084 | AFR | GWD | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02615 | hp2 | a0001 | c0003 | t0001 | g0210 | AFR | GWD | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0268 | AFR | GWD | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0290 | AFR | GWD | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0231 | AFR | GWD | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0164 | AFR | GWD | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0175 | AFR | GWD | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02683 | hp2 | a0005 | c0007 | t0002 | g0141 | SAS | PJL | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02698 | hp1 | a0003 | c0004 | t0001 | g0002 | SAS | PJL | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0020 | SAS | PJL | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0284 | AFR | GWD | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | GWD | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0072 | AFR | GWD | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0166 | AFR | GWD | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02735 | hp1 | a0002 | c0002 | t0002 | g0081 | SAS | PJL | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0064 | AFR | GWD | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0267 | AFR | GWD | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0230 | AFR | GWD | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0249 | AFR | GWD | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0056 | AFR | GWD | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0130 | AFR | GWD | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02896 | hp1 | a0001 | c0001 | t0003 | g0068 | AFR | GWD | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02896 | hp2 | a0004 | c0005 | t0005 | g0234 | AFR | GWD | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0056 | AFR | GWD | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02897 | hp2 | a0001 | c0001 | t0003 | g0025 | AFR | GWD | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0174 | AFR | ESN | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | ESN | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0165 | AFR | ESN | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | ESN | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0283 | AFR | ESN | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0236 | AFR | ESN | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0061 | AFR | ESN | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | ESN | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG03017 | hp1 | a0001 | c0003 | t0001 | g0018 | SAS | PJL | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0270 | SAS | PJL | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0282 | AFR | GWD | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0245 | AFR | MSL | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG03098 | hp2 | a0001 | c0001 | t0003 | g0066 | AFR | MSL | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0167 | AFR | ESN | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG03130 | hp2 | a0006 | c0008 | t0001 | g0051 | AFR | ESN | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0277 | AFR | ESN | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0071 | AFR | ESN | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0264 | AFR | ESN | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0055 | AFR | ESN | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0235 | AFR | MSL | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG03209 | hp2 | a0004 | c0005 | t0002 | g0037 | AFR | MSL | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG03225 | hp1 | a0004 | c0005 | t0002 | g0291 | AFR | MSL | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0057 | AFR | MSL | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG03239 | hp1 | a0002 | c0002 | t0002 | g0014 | SAS | PJL | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0256 | SAS | PJL | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0054 | AFR | MSL | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0285 | AFR | MSL | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0054 | AFR | MSL | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0053 | AFR | MSL | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0265 | SAS | PJL | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG03490 | hp2 | a0002 | c0002 | t0002 | g0091 | SAS | PJL | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG03491 | hp1 | a0002 | c0002 | t0002 | g0090 | SAS | PJL | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG03491 | hp2 | a0001 | c0003 | t0001 | g0018 | SAS | PJL | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0063 | AFR | ESN | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG03516 | hp2 | a0001 | c0001 | t0003 | g0024 | AFR | ESN | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG03540 | hp1 | a0001 | c0001 | t0004 | g0058 | AFR | GWD | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0171 | AFR | GWD | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG03579 | hp1 | a0001 | c0003 | t0001 | g0193 | AFR | MSL | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG03579 | hp2 | a0001 | c0001 | t0003 | g0024 | AFR | MSL | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG03654 | hp1 | a0003 | c0004 | t0001 | g0017 | SAS | PJL | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG03654 | hp2 | a0002 | c0002 | t0002 | g0004 | SAS | PJL | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0076 | SAS | PJL | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0244 | SAS | PJL | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG03688 | hp1 | a0001 | c0003 | t0001 | g0183 | SAS | STU | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0036 | SAS | STU | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG03704 | hp1 | a0001 | c0003 | t0001 | g0250 | SAS | PJL | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG03704 | hp2 | a0008 | c0009 | t0001 | g0273 | SAS | PJL | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG03710 | hp1 | a0002 | c0002 | t0002 | g0103 | SAS | PJL | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0023 | SAS | PJL | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG03831 | hp1 | a0001 | c0003 | t0001 | g0086 | SAS | BEB | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG03831 | hp2 | a0002 | c0002 | t0002 | g0102 | SAS | BEB | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG03834 | hp1 | a0001 | c0003 | t0001 | g0251 | SAS | BEB | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG03834 | hp2 | a0002 | c0002 | t0002 | g0294 | SAS | BEB | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0261 | SAS | BEB | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG03927 | hp2 | a0002 | c0002 | t0002 | g0123 | SAS | BEB | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG03942 | hp1 | a0002 | c0002 | t0002 | g0101 | SAS | BEB | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG03942 | hp2 | a0001 | c0003 | t0001 | g0003 | SAS | BEB | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG04115 | hp1 | a0002 | c0002 | t0002 | g0032 | SAS | STU | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG04115 | hp2 | a0001 | c0003 | t0001 | g0139 | SAS | STU | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0115 | SAS | BEB | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG04184 | hp2 | a0002 | c0002 | t0002 | g0119 | SAS | BEB | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG04199 | hp1 | a0001 | c0003 | t0001 | g0018 | SAS | STU | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG04199 | hp2 | a0002 | c0002 | t0002 | g0100 | SAS | STU | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG04204 | hp1 | a0005 | c0007 | t0002 | g0140 | SAS | STU | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | STU | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0266 | SAS | STU | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG04228 | hp2 | a0001 | c0003 | t0001 | g0184 | SAS | STU | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | YRI | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0246 | AFR | YRI | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA18612 | hp1 | a0001 | c0003 | t0001 | g0003 | EAS | CHB | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0275 | EAS | CHB | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA18747 | hp1 | a0001 | c0003 | t0001 | g0046 | EAS | CHB | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA18747 | hp2 | a0003 | c0004 | t0001 | g0151 | EAS | CHB | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | YRI | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA18906 | hp2 | a0004 | c0005 | t0002 | g0237 | AFR | YRI | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA18942 | hp1 | a0001 | c0003 | t0001 | g0003 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA18942 | hp2 | a0002 | c0002 | t0002 | g0029 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA18943 | hp1 | a0003 | c0004 | t0001 | g0161 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA18943 | hp2 | a0001 | c0003 | t0001 | g0228 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA18944 | hp1 | a0001 | c0003 | t0001 | g0148 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA18944 | hp2 | a0003 | c0004 | t0001 | g0002 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA18946 | hp1 | a0002 | c0002 | t0002 | g0031 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA18947 | hp1 | a0001 | c0003 | t0001 | g0019 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA18947 | hp2 | a0003 | c0004 | t0001 | g0002 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA18948 | hp1 | a0002 | c0002 | t0002 | g0094 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA18948 | hp2 | a0003 | c0004 | t0001 | g0154 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA18949 | hp1 | a0002 | c0002 | t0002 | g0033 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA18951 | hp1 | a0003 | c0004 | t0001 | g0041 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA18951 | hp2 | a0002 | c0002 | t0002 | g0031 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA18952 | hp2 | a0001 | c0003 | t0001 | g0229 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA18957 | hp1 | a0003 | c0004 | t0001 | g0143 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA18957 | hp2 | a0002 | c0002 | t0002 | g0121 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA18960 | hp1 | a0002 | c0002 | t0002 | g0111 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA18960 | hp2 | a0001 | c0003 | t0001 | g0003 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA18962 | hp1 | a0001 | c0003 | t0001 | g0190 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA18962 | hp2 | a0002 | c0002 | t0002 | g0082 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA18963 | hp1 | a0002 | c0002 | t0002 | g0201 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA18964 | hp1 | a0001 | c0006 | t0001 | g0038 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA18964 | hp2 | a0002 | c0002 | t0002 | g0117 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA18965 | hp1 | a0002 | c0002 | t0002 | g0033 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA18965 | hp2 | a0001 | c0003 | t0001 | g0136 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA18966 | hp1 | a0002 | c0002 | t0002 | g0097 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA18966 | hp2 | a0001 | c0006 | t0001 | g0137 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA18968 | hp1 | a0002 | c0002 | t0002 | g0030 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA18968 | hp2 | a0001 | c0003 | t0001 | g0211 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA18969 | hp1 | a0002 | c0002 | t0002 | g0107 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA18969 | hp2 | a0001 | c0003 | t0001 | g0207 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA18970 | hp1 | a0001 | c0006 | t0001 | g0007 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA18970 | hp2 | a0003 | c0004 | t0001 | g0008 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA18971 | hp1 | a0003 | c0004 | t0001 | g0142 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA18974 | hp1 | a0002 | c0002 | t0002 | g0105 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA18974 | hp2 | a0001 | c0003 | t0001 | g0135 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA18975 | hp1 | a0001 | c0003 | t0001 | g0015 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA18975 | hp2 | a0002 | c0002 | t0002 | g0120 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA18977 | hp1 | a0003 | c0004 | t0001 | g0002 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA18977 | hp2 | a0002 | c0002 | t0002 | g0126 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA18978 | hp1 | a0001 | c0003 | t0001 | g0019 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA18978 | hp2 | a0002 | c0002 | t0002 | g0200 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA18979 | hp1 | a0001 | c0003 | t0001 | g0191 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA18980 | hp1 | a0001 | c0003 | t0001 | g0015 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA18981 | hp1 | a0001 | c0003 | t0001 | g0215 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA18981 | hp2 | a0002 | c0002 | t0002 | g0049 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA18982 | hp1 | a0002 | c0002 | t0002 | g0078 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA18983 | hp1 | a0001 | c0003 | t0001 | g0003 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA18984 | hp1 | a0003 | c0004 | t0001 | g0002 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA18984 | hp2 | a0001 | c0003 | t0001 | g0186 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA18985 | hp1 | a0002 | c0002 | t0002 | g0196 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA18985 | hp2 | a0001 | c0006 | t0001 | g0038 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA18986 | hp1 | a0001 | c0003 | t0001 | g0189 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA18986 | hp2 | a0002 | c0002 | t0002 | g0122 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA18990 | hp2 | a0003 | c0004 | t0001 | g0157 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA18991 | hp1 | a0001 | c0006 | t0001 | g0156 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA18991 | hp2 | a0002 | c0002 | t0002 | g0010 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA18992 | hp1 | a0001 | c0006 | t0001 | g0007 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA18994 | hp1 | a0001 | c0003 | t0001 | g0220 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA18995 | hp1 | a0002 | c0002 | t0002 | g0108 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA18998 | hp2 | a0003 | c0004 | t0001 | g0016 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA19000 | hp2 | a0001 | c0003 | t0001 | g0048 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA19002 | hp1 | a0002 | c0002 | t0002 | g0010 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA19002 | hp2 | a0007 | c0010 | t0001 | g0258 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA19007 | hp2 | a0002 | c0002 | t0002 | g0045 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA19009 | hp1 | a0001 | c0003 | t0001 | g0019 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA19009 | hp2 | a0003 | c0004 | t0001 | g0145 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA19010 | hp1 | a0002 | c0002 | t0002 | g0127 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA19010 | hp2 | a0003 | c0004 | t0001 | g0002 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA19011 | hp1 | a0001 | c0006 | t0001 | g0007 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA19030 | hp1 | a0001 | c0003 | t0003 | g0065 | AFR | LWK | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA19030 | hp2 | a0003 | c0004 | t0001 | g0131 | AFR | LWK | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0073 | AFR | LWK | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0263 | AFR | LWK | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA19054 | hp1 | a0003 | c0004 | t0001 | g0002 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA19055 | hp1 | a0003 | c0004 | t0001 | g0041 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA19055 | hp2 | a0001 | c0003 | t0001 | g0217 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA19056 | hp2 | a0002 | c0002 | t0002 | g0045 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA19058 | hp1 | a0001 | c0003 | t0001 | g0048 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA19058 | hp2 | a0002 | c0002 | t0002 | g0010 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA19063 | hp1 | a0003 | c0004 | t0001 | g0017 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA19063 | hp2 | a0002 | c0002 | t0002 | g0030 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA19064 | hp1 | a0002 | c0002 | t0002 | g0079 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA19064 | hp2 | a0001 | c0003 | t0001 | g0162 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA19066 | hp1 | a0002 | c0002 | t0002 | g0004 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA19066 | hp2 | a0002 | c0002 | t0002 | g0222 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA19068 | hp1 | a0001 | c0006 | t0001 | g0007 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA19068 | hp2 | a0002 | c0002 | t0002 | g0106 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA19072 | hp1 | a0002 | c0002 | t0002 | g0080 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA19072 | hp2 | a0001 | c0003 | t0001 | g0180 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA19074 | hp1 | a0001 | c0003 | t0001 | g0013 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA19074 | hp2 | a0002 | c0002 | t0002 | g0083 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA19077 | hp2 | a0001 | c0003 | t0001 | g0047 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA19079 | hp1 | a0002 | c0002 | t0002 | g0093 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA19079 | hp2 | a0003 | c0004 | t0001 | g0017 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA19080 | hp1 | a0002 | c0002 | t0002 | g0010 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA19080 | hp2 | a0001 | c0003 | t0001 | g0003 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA19081 | hp1 | a0003 | c0004 | t0001 | g0150 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA19082 | hp1 | a0001 | c0003 | t0001 | g0109 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA19082 | hp2 | a0003 | c0004 | t0001 | g0293 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA19083 | hp1 | a0002 | c0002 | t0002 | g0128 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA19083 | hp2 | a0001 | c0003 | t0001 | g0221 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA19084 | hp2 | a0002 | c0002 | t0002 | g0199 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA19085 | hp2 | a0001 | c0003 | t0001 | g0075 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA19086 | hp1 | a0002 | c0002 | t0002 | g0029 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA19086 | hp2 | a0001 | c0003 | t0001 | g0003 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA19088 | hp1 | a0001 | c0006 | t0001 | g0007 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA19088 | hp2 | a0003 | c0004 | t0001 | g0002 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA19089 | hp1 | a0002 | c0002 | t0002 | g0099 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA19089 | hp2 | a0001 | c0003 | t0001 | g0003 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA19090 | hp1 | a0001 | c0003 | t0001 | g0147 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA19090 | hp2 | a0001 | c0003 | t0001 | g0047 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA19091 | hp1 | a0003 | c0004 | t0001 | g0002 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA19091 | hp2 | a0001 | c0003 | t0001 | g0015 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0287 | AFR | YRI | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA19240 | hp2 | a0004 | c0005 | t0002 | g0129 | AFR | YRI | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA20129 | hp1 | a0004 | c0005 | t0002 | g0069 | AFR | ASW | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA20129 | hp2 | a0001 | c0003 | t0001 | g0003 | AFR | ASW | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA20752 | hp2 | a0002 | c0002 | t0002 | g0014 | EUR | TSI | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0252 | EUR | TSI | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA20805 | hp2 | a0002 | c0002 | t0002 | g0124 | EUR | TSI | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0026 | SAS | GIH | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0242 | SAS | GIH | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG01123 | hp1 | a0001 | c0003 | t0001 | g0153 | AMR | CLM | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0259 | AMR | CLM | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | ACB | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02109 | hp2 | a0001 | c0001 | t0002 | g0172 | AFR | ACB | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0281 | AFR | ACB | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02486 | hp2 | a0006 | c0008 | t0001 | g0051 | AFR | ACB | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0232 | AFR | ACB | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02559 | hp2 | a0004 | c0005 | t0002 | g0134 | AFR | ACB | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0170 | AFR | MSL | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG03471 | hp2 | a0001 | c0001 | t0003 | g0067 | AFR | MSL | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0060 | AFR | USA | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | USA | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA18955 | hp1 | a0003 | c0004 | t0001 | g0280 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA18955 | hp2 | a0001 | c0003 | t0001 | g0208 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0178 | AFR | USA | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | USA | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0169 | AFR | LWK | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0274 | AFR | LWK | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0176 | REF | REF | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0006 | REF | REF | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:71129354
|
A | C | 3 | a0002a0004a0005 | 100 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(97): Show |
missense_variant | MODERATE | c.637T>G | p.Ser213Ala | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 8/9 | 816/1131 | 637/714 | 213/237 | chr12 | 71129354 | ||
| chr12:71132802
|
T | C | 1 | a0008 | 1 | HG03704.hp2 | missense_variant | MODERATE | c.467A>G | p.Asn156Ser | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 7/9 | 646/1131 | 467/714 | 156/237 | chr12 | 71132802 | ||
| chr12:71138054
|
G | A | 1 | a0007 | 1 | NA19002.hp2 | missense_variant | MODERATE | c.343C>T | p.Arg115Cys | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/9 | 522/1131 | 343/714 | 115/237 | chr12 | 71138054 | ||
| chr12:71139754
|
C | G | 2 | a0002a0005 | 91 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(88): Show |
missense_variant | MODERATE | c.218G>C | p.Gly73Ala | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 4/9 | 397/1131 | 218/714 | 73/237 | chr12 | 71139754 | ||
| chr12:71139812
|
C | T | 1 | a0006 | 2 | HG02486.hp2 HG03130.hp2 |
missense_variant | MODERATE | c.160G>A | p.Val54Ile | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 4/9 | 339/1131 | 160/714 | 54/237 | chr12 | 71139812 | ||
| chr12:71139842
|
C | T | 1 | a0003 | 36 | HG01257.hp1 HG01496.hp1 HG01934.hp1 others(33): Show |
missense_variant | MODERATE | c.130G>A | p.Gly44Ser | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 4/9 | 309/1131 | 130/714 | 44/237 | chr12 | 71139842 | ||
| chr12:71144171
|
C | T | 1 | a0005 | 2 | HG02683.hp2 HG04204.hp1 |
missense_variant | MODERATE | c.103G>A | p.Val35Ile | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 3/9 | 282/1131 | 103/714 | 35/237 | chr12 | 71144171 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:71132813
|
G | A | 1 | a0001c0003 | 87 | HG00423.hp2 HG00544.hp1 HG00558.hp1 others(84): Show |
synonymous_variant | LOW | c.456C>T | p.Cys152Cys | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 7/9 | 635/1131 | 456/714 | 152/237 | chr12 | 71132813 | ||
| chr12:71139714
|
C | T | 1 | a0001c0006 | 9 | NA18964.hp1 NA18966.hp2 NA18970.hp1 others(6): Show |
synonymous_variant | LOW | c.258G>A | p.Leu86Leu | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 4/9 | 437/1131 | 258/714 | 86/237 | chr12 | 71139714 | ||
| chr12:71139801
|
G | A | 1 | a0001c0006 | 9 | NA18964.hp1 NA18966.hp2 NA18970.hp1 others(6): Show |
synonymous_variant | LOW | c.171C>T | p.Asp57Asp | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 4/9 | 350/1131 | 171/714 | 57/237 | chr12 | 71139801 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:71125220
|
A | G | 1 | a0004c0005t0005 | 1 | HG02896.hp2 | 3_prime_UTR_variant | MODIFIER | c.*114T>C | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 9/9 | 114 | chr12 | 71125220 | |||||
| chr12:71125316
|
G | C | 6 | a0001c0001t0002a0002c0002t0002a0002c0002t0006others(3): Show | 104 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(101): Show |
3_prime_UTR_variant | MODIFIER | c.*18C>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 9/9 | 18 | chr12 | 71125316 | |||||
| chr12:71157681
|
C | T | 2 | a0001c0001t0003a0001c0003t0003 | 8 | HG01167.hp2 HG02896.hp1 HG02897.hp2 others(5): Show |
5_prime_UTR_variant | MODIFIER | c.-3G>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/9 | 3 | chr12 | 71157681 | |||||
| chr12:71157769
|
G | A | 1 | a0002c0002t0006 | 1 | HG02027.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-91C>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/9 | chr12 | 71157769 | ||||||
| chr12:71157996
|
C | G | 1 | a0001c0001t0004 | 2 | HG01496.hp2 HG03540.hp1 |
5_prime_UTR_variant | MODIFIER | c.-176G>C | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 1/9 | 318 | chr12 | 71157996 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:71125393
|
G | A | 6 | a0001c0001t0003g0025a0001c0001t0003g0068a0001c0006t0001g0007others(3): Show | 12 | HG01167.hp2 HG02896.hp1 HG02897.hp2 others(9): Show |
splice_region_variant&intron_variant | LOW | c.661-6C>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 8/8 | chr12 | 71125393 | ||||||
| chr12:71125614
|
A | G | 1 | a0001c0001t0001g0160 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.661-227T>C | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 8/8 | chr12 | 71125614 | ||||||
| chr12:71125710
|
G | A | 1 | a0002c0002t0002g0144 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.661-323C>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 8/8 | chr12 | 71125710 | ||||||
| chr12:71125713
|
C | T | 79 | a0001c0001t0002g0021a0001c0001t0002g0172a0001c0001t0002g0260others(76): Show | 104 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.661-326G>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 8/8 | chr12 | 71125713 | ||||||
| chr12:71125766
|
A | C | 239 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0012others(236): Show | 332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.661-379T>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 8/8 | chr12 | 71125766 | ||||||
| chr12:71125768
|
G | A | 79 | a0001c0001t0002g0021a0001c0001t0002g0172a0001c0001t0002g0260others(76): Show | 104 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.661-381C>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 8/8 | chr12 | 71125768 | ||||||
| chr12:71125820
|
A | C | 144 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0012others(141): Show | 206 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(203): Show |
intron_variant | MODIFIER | c.661-433T>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 8/8 | chr12 | 71125820 | ||||||
| chr12:71125870
|
T | TA | 79 | a0001c0001t0002g0021a0001c0001t0002g0172a0001c0001t0002g0260others(76): Show | 104 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.661-484dupT | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 8/8 | chr12 | 71125870 | ||||||
| chr12:71125887
|
C | CT | 79 | a0001c0001t0002g0021a0001c0001t0002g0172a0001c0001t0002g0260others(76): Show | 104 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.661-501dupA | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 8/8 | chr12 | 71125887 | ||||||
| chr12:71125978
|
A | C | 4 | a0001c0006t0001g0007a0001c0006t0001g0038a0001c0006t0001g0137others(1): Show | 9 | NA18964.hp1 NA18966.hp2 NA18970.hp1 others(6): Show |
intron_variant | MODIFIER | c.661-591T>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 8/8 | chr12 | 71125978 | ||||||
| chr12:71126139
|
T | C | 1 | a0001c0001t0004g0058 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.661-752A>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 8/8 | chr12 | 71126139 | ||||||
| chr12:71126157
|
A | G | 238 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0012others(235): Show | 331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): Show |
intron_variant | MODIFIER | c.661-770T>C | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 8/8 | chr12 | 71126157 | ||||||
| chr12:71126173
|
A | G | 1 | a0001c0001t0004g0058 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.661-786T>C | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 8/8 | chr12 | 71126173 | ||||||
| chr12:71126272
|
C | A | 1 | a0001c0001t0003g0066 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.661-885G>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 8/8 | chr12 | 71126272 | ||||||
| chr12:71126487
|
G | C | 79 | a0001c0001t0002g0021a0001c0001t0002g0172a0001c0001t0002g0260others(76): Show | 104 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.661-1100C>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 8/8 | chr12 | 71126487 | ||||||
| chr12:71126488
|
T | A | 238 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0012others(235): Show | 331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): Show |
intron_variant | MODIFIER | c.661-1101A>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 8/8 | chr12 | 71126488 | ||||||
| chr12:71126561
|
G | C | 77 | a0001c0001t0002g0172a0002c0002t0002g0004a0002c0002t0002g0010others(74): Show | 100 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.661-1174C>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 8/8 | chr12 | 71126561 | ||||||
| chr12:71126647
|
T | A | 2 | a0001c0001t0003g0025a0001c0001t0003g0068 | 3 | HG01167.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.661-1260A>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 8/8 | chr12 | 71126647 | ||||||
| chr12:71126697
|
A | C | 6 | a0001c0001t0003g0025a0001c0001t0003g0068a0001c0006t0001g0007others(3): Show | 12 | HG01167.hp2 HG02896.hp1 HG02897.hp2 others(9): Show |
intron_variant | MODIFIER | c.661-1310T>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 8/8 | chr12 | 71126697 | ||||||
| chr12:71126761
|
CT | C | 79 | a0001c0001t0001g0115a0001c0001t0002g0172a0001c0003t0001g0189others(76): Show | 102 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.661-1375delA | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 8/8 | chr12 | 71126761 | ||||||
| chr12:71126820
|
T | C | 78 | a0001c0001t0002g0172a0002c0002t0001g0239a0002c0002t0002g0004others(75): Show | 101 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.661-1433A>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 8/8 | chr12 | 71126820 | ||||||
| chr12:71126866
|
G | T | 2 | a0001c0001t0003g0025a0001c0001t0003g0068 | 3 | HG01167.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.661-1479C>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 8/8 | chr12 | 71126866 | ||||||
| chr12:71126970
|
T | G | 1 | a0001c0001t0001g0164 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.661-1583A>C | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 8/8 | chr12 | 71126970 | ||||||
| chr12:71126981
|
T | G | 84 | a0001c0001t0002g0172a0001c0001t0003g0025a0001c0001t0003g0068others(81): Show | 113 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.661-1594A>C | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 8/8 | chr12 | 71126981 | ||||||
| chr12:71127057
|
G | A | 78 | a0001c0001t0002g0172a0002c0002t0001g0239a0002c0002t0002g0004others(75): Show | 101 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.661-1670C>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 8/8 | chr12 | 71127057 | ||||||
| chr12:71127092
|
T | A | 1 | a0001c0001t0001g0052 | 2 | HG01346.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.661-1705A>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 8/8 | chr12 | 71127092 | ||||||
| chr12:71127284
|
C | CT | 233 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0012others(230): Show | 326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
intron_variant | MODIFIER | c.661-1898dupA | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 8/8 | chr12 | 71127284 | ||||||
| chr12:71127288
|
G | T | 236 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0012others(233): Show | 329 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(326): Show |
intron_variant | MODIFIER | c.661-1901C>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 8/8 | chr12 | 71127288 | ||||||
| chr12:71127465
|
A | G | 77 | a0002c0002t0001g0239a0002c0002t0002g0004a0002c0002t0002g0010others(74): Show | 100 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.660+1866T>C | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 8/8 | chr12 | 71127465 | ||||||
| chr12:71127618
|
G | A | 1 | a0004c0005t0002g0069 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.660+1713C>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 8/8 | chr12 | 71127618 | ||||||
| chr12:71127656
|
T | C | 2 | a0001c0001t0001g0073a0001c0001t0001g0074 | 2 | HG02922.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.660+1675A>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 8/8 | chr12 | 71127656 | ||||||
| chr12:71128003
|
A | C | 1 | a0003c0004t0001g0293 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.660+1328T>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 8/8 | chr12 | 71128003 | ||||||
| chr12:71128051
|
T | C | 77 | a0002c0002t0001g0239a0002c0002t0002g0004a0002c0002t0002g0010others(74): Show | 100 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.660+1280A>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 8/8 | chr12 | 71128051 | ||||||
| chr12:71128176
|
T | A | 7 | a0001c0001t0001g0012a0001c0001t0001g0056a0001c0001t0001g0168others(4): Show | 11 | HG01361.hp1 HG01891.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.660+1155A>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 8/8 | chr12 | 71128176 | ||||||
| chr12:71128247
|
C | G | 3 | a0001c0003t0001g0188a0001c0003t0001g0208a0001c0003t0001g0220 | 3 | HG02015.hp2 NA18955.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.660+1084G>C | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 8/8 | chr12 | 71128247 | ||||||
| chr12:71128270
|
A | T | 3 | a0001c0003t0001g0188a0001c0003t0001g0208a0001c0003t0001g0220 | 3 | HG02015.hp2 NA18955.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.660+1061T>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 8/8 | chr12 | 71128270 | ||||||
| chr12:71128279
|
A | T | 1 | a0002c0002t0002g0093 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.660+1052T>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 8/8 | chr12 | 71128279 | ||||||
| chr12:71128342
|
C | T | 5 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0062others(2): Show | 5 | HG01109.hp2 HG02818.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.660+989G>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 8/8 | chr12 | 71128342 | ||||||
| chr12:71128377
|
C | A | 1 | a0001c0003t0001g0109 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.660+954G>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 8/8 | chr12 | 71128377 | ||||||
| chr12:71128555
|
G | T | 7 | a0001c0001t0001g0012a0001c0001t0001g0056a0001c0001t0001g0168others(4): Show | 11 | HG01361.hp1 HG01891.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.660+776C>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 8/8 | chr12 | 71128555 | ||||||
| chr12:71128617
|
G | C | 28 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0052others(25): Show | 45 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.660+714C>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 8/8 | chr12 | 71128617 | ||||||
| chr12:71128641
|
G | GT | 68 | a0001c0003t0001g0109a0001c0003t0001g0204a0002c0002t0001g0239others(65): Show | 88 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(85): Show |
intron_variant | MODIFIER | c.660+689dupA | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 8/8 | chr12 | 71128641 | ||||||
| chr12:71128641
|
G | GTT | 5 | a0002c0002t0002g0014a0002c0002t0002g0081a0002c0002t0002g0118others(2): Show | 7 | HG01106.hp2 HG01952.hp2 HG02300.hp1 others(4): Show |
intron_variant | MODIFIER | c.660+688_660+689dup others(2): Show |
TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 8/8 | chr12 | 71128641 | ||||||
| chr12:71128655
|
T | A | 9 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0062others(6): Show | 9 | HG01109.hp2 HG01123.hp1 HG01261.hp1 others(6): Show |
intron_variant | MODIFIER | c.660+676A>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 8/8 | chr12 | 71128655 | ||||||
| chr12:71128655
|
TA | T | 21 | a0001c0001t0001g0132a0001c0001t0001g0255a0001c0006t0001g0137others(18): Show | 39 | HG01069.hp1 HG01257.hp1 HG01496.hp1 others(36): Show |
intron_variant | MODIFIER | c.660+675delT | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 8/8 | chr12 | 71128655 | ||||||
| chr12:71128656
|
A | T | 69 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0012others(66): Show | 103 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(100): Show |
intron_variant | MODIFIER | c.660+675T>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 8/8 | chr12 | 71128656 | ||||||
| chr12:71128657
|
A | T | 21 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0052others(18): Show | 37 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(34): Show |
intron_variant | MODIFIER | c.660+674T>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 8/8 | chr12 | 71128657 | ||||||
| chr12:71128658
|
A | T | 1 | a0001c0001t0001g0130 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.660+673T>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 8/8 | chr12 | 71128658 | ||||||
| chr12:71128772
|
T | C | 6 | a0001c0001t0003g0025a0001c0001t0003g0068a0001c0006t0001g0007others(3): Show | 12 | HG01167.hp2 HG02896.hp1 HG02897.hp2 others(9): Show |
intron_variant | MODIFIER | c.660+559A>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 8/8 | chr12 | 71128772 | ||||||
| chr12:71129008
|
CT | C | 53 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0012others(50): Show | 79 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(76): Show |
intron_variant | MODIFIER | c.660+322delA | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 8/8 | chr12 | 71129008 | ||||||
| chr12:71129027
|
G | C | 77 | a0002c0002t0001g0239a0002c0002t0002g0004a0002c0002t0002g0010others(74): Show | 100 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.660+304C>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 8/8 | chr12 | 71129027 | ||||||
| chr12:71129068
|
C | A | 6 | a0001c0003t0001g0013a0001c0003t0001g0182a0001c0003t0001g0203others(3): Show | 9 | HG00558.hp1 HG01255.hp1 HG01358.hp1 others(6): Show |
intron_variant | MODIFIER | c.660+263G>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 8/8 | chr12 | 71129068 | ||||||
| chr12:71129080
|
C | G | 1 | a0001c0003t0001g0109 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.660+251G>C | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 8/8 | chr12 | 71129080 | ||||||
| chr12:71129107
|
A | G | 228 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0012others(225): Show | 321 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(318): Show |
intron_variant | MODIFIER | c.660+224T>C | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 8/8 | chr12 | 71129107 | ||||||
| chr12:71129173
|
G | C | 117 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0012others(114): Show | 163 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(160): Show |
intron_variant | MODIFIER | c.660+158C>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 8/8 | chr12 | 71129173 | ||||||
| chr12:71129232
|
GT | G | 6 | a0001c0001t0003g0025a0001c0001t0003g0068a0001c0006t0001g0007others(3): Show | 12 | HG01167.hp2 HG02896.hp1 HG02897.hp2 others(9): Show |
intron_variant | MODIFIER | c.660+98delA | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 8/8 | chr12 | 71129232 | ||||||
| chr12:71129263
|
C | A | 144 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0012others(141): Show | 208 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(205): Show |
intron_variant | MODIFIER | c.660+68G>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 8/8 | chr12 | 71129263 | ||||||
| chr12:71129307
|
C | T | 1 | a0002c0002t0002g0097 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.660+24G>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 8/8 | chr12 | 71129307 | ||||||
| chr12:71129419
|
TA | T | 18 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0169others(15): Show | 19 | HG00423.hp2 HG01884.hp2 HG02040.hp1 others(16): Show |
splice_region_variant&intron_variant | LOW | c.577-6delT | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 7/8 | chr12 | 71129419 | ||||||
| chr12:71129419
|
TAA | T | 77 | a0002c0002t0001g0239a0002c0002t0002g0004a0002c0002t0002g0010others(74): Show | 100 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(97): Show |
splice_region_variant&intron_variant | LOW | c.577-7_577-6delTT | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 7/8 | chr12 | 71129419 | ||||||
| chr12:71129429
|
A | C | 6 | a0001c0001t0003g0025a0001c0001t0003g0068a0001c0006t0001g0007others(3): Show | 12 | HG01167.hp2 HG02896.hp1 HG02897.hp2 others(9): Show |
intron_variant | MODIFIER | c.577-15T>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 7/8 | chr12 | 71129429 | ||||||
| chr12:71129692
|
T | C | 1 | a0001c0003t0001g0193 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.577-278A>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 7/8 | chr12 | 71129692 | ||||||
| chr12:71129746
|
T | C | 4 | a0001c0001t0001g0050a0001c0001t0001g0240a0001c0001t0001g0243others(1): Show | 5 | HG00621.hp1 NA18612.hp2 NA18982.hp2 others(2): Show |
intron_variant | MODIFIER | c.577-332A>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 7/8 | chr12 | 71129746 | ||||||
| chr12:71129761
|
T | C | 77 | a0002c0002t0001g0239a0002c0002t0002g0004a0002c0002t0002g0010others(74): Show | 100 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.577-347A>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 7/8 | chr12 | 71129761 | ||||||
| chr12:71129783
|
T | C | 2 | a0001c0001t0003g0025a0001c0001t0003g0068 | 3 | HG01167.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.577-369A>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 7/8 | chr12 | 71129783 | ||||||
| chr12:71129854
|
T | A | 76 | a0002c0002t0001g0239a0002c0002t0002g0004a0002c0002t0002g0010others(73): Show | 99 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.577-440A>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 7/8 | chr12 | 71129854 | ||||||
| chr12:71129951
|
C | CT | 11 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0062others(8): Show | 12 | HG01109.hp2 HG01167.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.577-538dupA | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 7/8 | chr12 | 71129951 | ||||||
| chr12:71129951
|
CT | C | 5 | a0001c0003t0001g0190a0004c0005t0002g0037a0004c0005t0002g0129others(2): Show | 6 | HG02280.hp2 HG02559.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.577-538delA | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 7/8 | chr12 | 71129951 | ||||||
| chr12:71129951
|
CTT | C | 68 | a0002c0002t0001g0239a0002c0002t0002g0004a0002c0002t0002g0010others(65): Show | 88 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(85): Show |
intron_variant | MODIFIER | c.577-539_577-538del others(2): Show |
TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 7/8 | chr12 | 71129951 | ||||||
| chr12:71129951
|
CTTT | C | 5 | a0002c0002t0002g0014a0002c0002t0002g0081a0002c0002t0002g0118others(2): Show | 7 | HG01106.hp2 HG01952.hp2 HG02300.hp1 others(4): Show |
intron_variant | MODIFIER | c.577-540_577-538del others(3): Show |
TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 7/8 | chr12 | 71129951 | ||||||
| chr12:71129991
|
C | T | 1 | a0001c0001t0001g0171 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.577-577G>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 7/8 | chr12 | 71129991 | ||||||
| chr12:71130008
|
A | G | 2 | a0001c0001t0003g0025a0001c0001t0003g0068 | 3 | HG01167.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.577-594T>C | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 7/8 | chr12 | 71130008 | ||||||
| chr12:71130161
|
C | T | 77 | a0002c0002t0001g0239a0002c0002t0002g0004a0002c0002t0002g0010others(74): Show | 100 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.577-747G>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 7/8 | chr12 | 71130161 | ||||||
| chr12:71130262
|
C | G | 83 | a0001c0001t0003g0025a0001c0001t0003g0068a0001c0006t0001g0007others(80): Show | 112 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(109): Show |
intron_variant | MODIFIER | c.577-848G>C | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 7/8 | chr12 | 71130262 | ||||||
| chr12:71130511
|
G | A | 151 | a0001c0001t0003g0025a0001c0001t0003g0068a0001c0001t0004g0058others(148): Show | 200 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(197): Show |
intron_variant | MODIFIER | c.577-1097C>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 7/8 | chr12 | 71130511 | ||||||
| chr12:71130556
|
T | C | 1 | a0004c0005t0002g0069 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.577-1142A>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 7/8 | chr12 | 71130556 | ||||||
| chr12:71130639
|
C | CT | 145 | a0001c0001t0004g0058a0001c0003t0001g0003a0001c0003t0001g0013others(142): Show | 188 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(185): Show |
intron_variant | MODIFIER | c.577-1226dupA | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 7/8 | chr12 | 71130639 | ||||||
| chr12:71130693
|
G | A | 69 | a0002c0002t0001g0239a0002c0002t0002g0004a0002c0002t0002g0010others(66): Show | 91 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.577-1279C>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 7/8 | chr12 | 71130693 | ||||||
| chr12:71130802
|
T | C | 145 | a0001c0001t0004g0058a0001c0003t0001g0003a0001c0003t0001g0013others(142): Show | 188 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(185): Show |
intron_variant | MODIFIER | c.577-1388A>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 7/8 | chr12 | 71130802 | ||||||
| chr12:71130873
|
T | C | 4 | a0001c0006t0001g0007a0001c0006t0001g0038a0001c0006t0001g0137others(1): Show | 9 | NA18964.hp1 NA18966.hp2 NA18970.hp1 others(6): Show |
intron_variant | MODIFIER | c.577-1459A>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 7/8 | chr12 | 71130873 | ||||||
| chr12:71131030
|
A | G | 151 | a0001c0001t0003g0025a0001c0001t0003g0068a0001c0001t0004g0058others(148): Show | 200 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(197): Show |
intron_variant | MODIFIER | c.577-1616T>C | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 7/8 | chr12 | 71131030 | ||||||
| chr12:71131078
|
C | G | 145 | a0001c0001t0004g0058a0001c0003t0001g0003a0001c0003t0001g0013others(142): Show | 188 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(185): Show |
intron_variant | MODIFIER | c.576+1615G>C | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 7/8 | chr12 | 71131078 | ||||||
| chr12:71131157
|
T | C | 145 | a0001c0001t0004g0058a0001c0003t0001g0003a0001c0003t0001g0013others(142): Show | 188 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(185): Show |
intron_variant | MODIFIER | c.576+1536A>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 7/8 | chr12 | 71131157 | ||||||
| chr12:71131190
|
T | C | 1 | a0001c0003t0001g0191 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.576+1503A>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 7/8 | chr12 | 71131190 | ||||||
| chr12:71131351
|
G | A | 145 | a0001c0001t0004g0058a0001c0003t0001g0003a0001c0003t0001g0013others(142): Show | 188 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(185): Show |
intron_variant | MODIFIER | c.576+1342C>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 7/8 | chr12 | 71131351 | ||||||
| chr12:71131490
|
T | A | 145 | a0001c0001t0004g0058a0001c0003t0001g0003a0001c0003t0001g0013others(142): Show | 188 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(185): Show |
intron_variant | MODIFIER | c.576+1203A>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 7/8 | chr12 | 71131490 | ||||||
| chr12:71131685
|
G | GAAGAATA others(329): Show |
1 | a0002c0002t0002g0081 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.576+1007_576+1008i others(338): Show |
TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 7/8 | chr12 | 71131685 | ||||||
| chr12:71131685
|
G | GAAGAATA others(314): Show |
1 | a0002c0002t0002g0103 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.576+1007_576+1008i others(323): Show |
TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 7/8 | chr12 | 71131685 | ||||||
| chr12:71131685
|
G | GAAGAATA others(313): Show |
2 | a0002c0002t0002g0029a0002c0002t0002g0078 | 3 | NA18942.hp2 NA18982.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.576+1007_576+1008i others(322): Show |
TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 7/8 | chr12 | 71131685 | ||||||
| chr12:71131685
|
G | GAAGAATA others(314): Show |
49 | a0002c0002t0002g0004a0002c0002t0002g0010a0002c0002t0002g0028others(46): Show | 66 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(63): Show |
intron_variant | MODIFIER | c.576+1007_576+1008i others(323): Show |
TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 7/8 | chr12 | 71131685 | ||||||
| chr12:71131685
|
G | GAAGAATA others(315): Show |
7 | a0002c0002t0001g0239a0002c0002t0002g0045a0002c0002t0002g0095others(4): Show | 8 | HG00738.hp2 HG01175.hp2 NA18977.hp2 others(5): Show |
intron_variant | MODIFIER | c.576+1007_576+1008i others(324): Show |
TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 7/8 | chr12 | 71131685 | ||||||
| chr12:71131685
|
G | GAAGAATA others(325): Show |
2 | a0004c0005t0002g0037a0004c0005t0002g0129 | 3 | HG02280.hp2 HG03209.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.576+1007_576+1008i others(334): Show |
TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 7/8 | chr12 | 71131685 | ||||||
| chr12:71131685
|
G | GAAGAATA others(326): Show |
4 | a0001c0001t0004g0058a0004c0005t0002g0069a0004c0005t0002g0134others(1): Show | 4 | HG02559.hp2 HG02896.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.576+1007_576+1008i others(335): Show |
TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 7/8 | chr12 | 71131685 | ||||||
| chr12:71131685
|
G | GAAGAATA others(327): Show |
1 | a0004c0005t0002g0291 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.576+1007_576+1008i others(336): Show |
TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 7/8 | chr12 | 71131685 | ||||||
| chr12:71131685
|
G | GAAGAATA others(328): Show |
1 | a0002c0002t0002g0084 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.576+1007_576+1008i others(337): Show |
TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 7/8 | chr12 | 71131685 | ||||||
| chr12:71131685
|
G | GAAGAATA others(329): Show |
5 | a0002c0002t0002g0014a0002c0002t0002g0118a0002c0002t0002g0124others(2): Show | 7 | HG01106.hp2 HG02145.hp2 HG02300.hp1 others(4): Show |
intron_variant | MODIFIER | c.576+1007_576+1008i others(338): Show |
TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 7/8 | chr12 | 71131685 | ||||||
| chr12:71131685
|
G | GAAGAATA others(330): Show |
2 | a0002c0002t0002g0085a0002c0002t0002g0125 | 2 | HG01884.hp1 HG01952.hp2 |
intron_variant | MODIFIER | c.576+1007_576+1008i others(339): Show |
TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 7/8 | chr12 | 71131685 | ||||||
| chr12:71131685
|
G | GAAGAATA others(314): Show |
3 | a0002c0002t0002g0030a0002c0002t0002g0105a0002c0002t0002g0128 | 4 | NA18968.hp1 NA18974.hp1 NA19063.hp2 others(1): Show |
intron_variant | MODIFIER | c.576+1007_576+1008i others(323): Show |
TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 7/8 | chr12 | 71131685 | ||||||
| chr12:71131687
|
A | AGAATAAC others(327): Show |
1 | a0001c0003t0001g0226 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.576+1005_576+1006i others(336): Show |
TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 7/8 | chr12 | 71131687 | ||||||
| chr12:71131687
|
A | AGAATAAC others(326): Show |
8 | a0001c0003t0001g0136a0001c0003t0001g0148a0001c0003t0001g0162others(5): Show | 8 | HG00423.hp2 HG00558.hp1 HG02056.hp1 others(5): Show |
intron_variant | MODIFIER | c.576+1005_576+1006i others(335): Show |
TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 7/8 | chr12 | 71131687 | ||||||
| chr12:71131687
|
A | AGAATAAC others(325): Show |
29 | a0001c0003t0001g0013a0001c0003t0001g0018a0001c0003t0001g0046others(26): Show | 37 | HG01175.hp1 HG01192.hp1 HG01255.hp1 others(34): Show |
intron_variant | MODIFIER | c.576+1005_576+1006i others(334): Show |
TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 7/8 | chr12 | 71131687 | ||||||
| chr12:71131687
|
A | AGAATAAC others(324): Show |
26 | a0001c0003t0001g0003a0001c0003t0001g0015a0001c0003t0001g0019others(23): Show | 38 | HG00544.hp1 HG00639.hp2 HG01123.hp1 others(35): Show |
intron_variant | MODIFIER | c.576+1005_576+1006i others(333): Show |
TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 7/8 | chr12 | 71131687 | ||||||
| chr12:71131687
|
A | AGAATAAC others(323): Show |
3 | a0001c0003t0001g0187a0001c0003t0001g0193a0001c0003t0001g0198 | 3 | HG01169.hp2 HG02257.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.576+1005_576+1006i others(332): Show |
TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 7/8 | chr12 | 71131687 | ||||||
| chr12:71131943
|
C | T | 145 | a0001c0001t0004g0058a0001c0003t0001g0003a0001c0003t0001g0013others(142): Show | 188 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(185): Show |
intron_variant | MODIFIER | c.576+750G>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 7/8 | chr12 | 71131943 | ||||||
| chr12:71131978
|
G | A | 1 | a0001c0003t0001g0138 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.576+715C>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 7/8 | chr12 | 71131978 | ||||||
| chr12:71131998
|
G | T | 4 | a0001c0001t0001g0262a0001c0001t0003g0024a0001c0001t0003g0066others(1): Show | 5 | HG01069.hp2 HG03098.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.576+695C>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 7/8 | chr12 | 71131998 | ||||||
| chr12:71132167
|
G | A | 145 | a0001c0001t0004g0058a0001c0003t0001g0003a0001c0003t0001g0013others(142): Show | 188 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(185): Show |
intron_variant | MODIFIER | c.576+526C>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 7/8 | chr12 | 71132167 | ||||||
| chr12:71132284
|
T | C | 145 | a0001c0001t0004g0058a0001c0003t0001g0003a0001c0003t0001g0013others(142): Show | 188 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(185): Show |
intron_variant | MODIFIER | c.576+409A>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 7/8 | chr12 | 71132284 | ||||||
| chr12:71132288
|
G | A | 4 | a0004c0005t0002g0037a0004c0005t0002g0129a0004c0005t0002g0134others(1): Show | 5 | HG02280.hp2 HG02559.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.576+405C>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 7/8 | chr12 | 71132288 | ||||||
| chr12:71132328
|
T | C | 1 | a0001c0001t0001g0290 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.576+365A>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 7/8 | chr12 | 71132328 | ||||||
| chr12:71132507
|
C | A | 145 | a0001c0001t0004g0058a0001c0003t0001g0003a0001c0003t0001g0013others(142): Show | 188 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(185): Show |
intron_variant | MODIFIER | c.576+186G>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 7/8 | chr12 | 71132507 | ||||||
| chr12:71132531
|
C | A | 2 | a0001c0001t0003g0025a0001c0001t0003g0068 | 3 | HG01167.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.576+162G>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 7/8 | chr12 | 71132531 | ||||||
| chr12:71132634
|
T | C | 145 | a0001c0001t0004g0058a0001c0003t0001g0003a0001c0003t0001g0013others(142): Show | 188 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(185): Show |
intron_variant | MODIFIER | c.576+59A>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 7/8 | chr12 | 71132634 | ||||||
| chr12:71132845
|
T | G | 6 | a0001c0001t0003g0025a0001c0001t0003g0068a0001c0006t0001g0007others(3): Show | 12 | HG01167.hp2 HG02896.hp1 HG02897.hp2 others(9): Show |
intron_variant | MODIFIER | c.445-21A>C | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71132845 | ||||||
| chr12:71132897
|
A | G | 76 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0012others(73): Show | 120 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(117): Show |
intron_variant | MODIFIER | c.445-73T>C | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71132897 | ||||||
| chr12:71132929
|
C | T | 145 | a0001c0001t0004g0058a0001c0003t0001g0003a0001c0003t0001g0013others(142): Show | 188 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(185): Show |
intron_variant | MODIFIER | c.445-105G>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71132929 | ||||||
| chr12:71133137
|
G | T | 1 | a0002c0002t0002g0092 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.445-313C>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71133137 | ||||||
| chr12:71133144
|
C | T | 6 | a0001c0001t0003g0025a0001c0001t0003g0068a0001c0006t0001g0007others(3): Show | 12 | HG01167.hp2 HG02896.hp1 HG02897.hp2 others(9): Show |
intron_variant | MODIFIER | c.445-320G>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71133144 | ||||||
| chr12:71133147
|
G | A | 145 | a0001c0001t0004g0058a0001c0003t0001g0003a0001c0003t0001g0013others(142): Show | 188 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(185): Show |
intron_variant | MODIFIER | c.445-323C>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71133147 | ||||||
| chr12:71133152
|
C | T | 1 | a0002c0002t0002g0081 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.445-328G>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71133152 | ||||||
| chr12:71133259
|
G | T | 7 | a0001c0001t0001g0012a0001c0001t0001g0056a0001c0001t0001g0168others(4): Show | 11 | HG01361.hp1 HG01891.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.445-435C>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71133259 | ||||||
| chr12:71133276
|
C | T | 2 | a0001c0001t0003g0025a0001c0001t0003g0068 | 3 | HG01167.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.445-452G>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71133276 | ||||||
| chr12:71133277
|
G | A | 2 | a0001c0003t0001g0193a0001c0003t0003g0065 | 2 | HG03579.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.445-453C>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71133277 | ||||||
| chr12:71133285
|
C | A | 4 | a0001c0006t0001g0007a0001c0006t0001g0038a0001c0006t0001g0137others(1): Show | 9 | NA18964.hp1 NA18966.hp2 NA18970.hp1 others(6): Show |
intron_variant | MODIFIER | c.445-461G>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71133285 | ||||||
| chr12:71133430
|
T | C | 145 | a0001c0001t0004g0058a0001c0003t0001g0003a0001c0003t0001g0013others(142): Show | 188 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(185): Show |
intron_variant | MODIFIER | c.445-606A>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71133430 | ||||||
| chr12:71133458
|
G | T | 1 | a0001c0001t0004g0058 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.445-634C>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71133458 | ||||||
| chr12:71133541
|
C | T | 4 | a0001c0006t0001g0007a0001c0006t0001g0038a0001c0006t0001g0137others(1): Show | 9 | NA18964.hp1 NA18966.hp2 NA18970.hp1 others(6): Show |
intron_variant | MODIFIER | c.445-717G>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71133541 | ||||||
| chr12:71133771
|
A | G | 1 | a0001c0003t0001g0207 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.445-947T>C | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71133771 | ||||||
| chr12:71133866
|
T | A | 76 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0012others(73): Show | 120 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(117): Show |
intron_variant | MODIFIER | c.445-1042A>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71133866 | ||||||
| chr12:71133927
|
A | C | 76 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0012others(73): Show | 120 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(117): Show |
intron_variant | MODIFIER | c.445-1103T>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71133927 | ||||||
| chr12:71134005
|
A | T | 145 | a0001c0001t0004g0058a0001c0003t0001g0003a0001c0003t0001g0013others(142): Show | 188 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(185): Show |
intron_variant | MODIFIER | c.445-1181T>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71134005 | ||||||
| chr12:71134148
|
C | A | 1 | a0003c0004t0001g0143 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.445-1324G>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71134148 | ||||||
| chr12:71134423
|
T | C | 1 | a0004c0005t0005g0234 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.445-1599A>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71134423 | ||||||
| chr12:71134657
|
A | T | 1 | a0001c0003t0001g0229 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.445-1833T>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71134657 | ||||||
| chr12:71134713
|
TC | T | 5 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0062others(2): Show | 5 | HG01109.hp2 HG02818.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.445-1890delG | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71134713 | ||||||
| chr12:71134720
|
T | C | 1 | a0001c0001t0004g0058 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.445-1896A>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71134720 | ||||||
| chr12:71134721
|
A | G | 18 | a0003c0004t0001g0002a0003c0004t0001g0008a0003c0004t0001g0016others(15): Show | 36 | HG01257.hp1 HG01496.hp1 HG01934.hp1 others(33): Show |
intron_variant | MODIFIER | c.445-1897T>C | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71134721 | ||||||
| chr12:71134747
|
G | A | 227 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0012others(224): Show | 320 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(317): Show |
intron_variant | MODIFIER | c.445-1923C>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71134747 | ||||||
| chr12:71134808
|
T | C | 227 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0012others(224): Show | 320 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(317): Show |
intron_variant | MODIFIER | c.445-1984A>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71134808 | ||||||
| chr12:71134848
|
C | T | 1 | a0001c0003t0001g0186 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.445-2024G>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71134848 | ||||||
| chr12:71134957
|
A | G | 1 | a0002c0002t0002g0092 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.445-2133T>C | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71134957 | ||||||
| chr12:71135036
|
C | T | 1 | a0003c0004t0001g0131 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.445-2212G>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71135036 | ||||||
| chr12:71135067
|
A | T | 5 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0062others(2): Show | 5 | HG01109.hp2 HG02818.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.445-2243T>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71135067 | ||||||
| chr12:71135116
|
C | T | 145 | a0001c0001t0004g0058a0001c0003t0001g0003a0001c0003t0001g0013others(142): Show | 188 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(185): Show |
intron_variant | MODIFIER | c.445-2292G>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71135116 | ||||||
| chr12:71135216
|
GAGGAGGA others(52): Show |
G | 142 | a0001c0003t0001g0003a0001c0003t0001g0013a0001c0003t0001g0015others(139): Show | 185 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(182): Show |
intron_variant | MODIFIER | c.445-2451_445-2393d others(61): Show |
TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71135216 | ||||||
| chr12:71135218
|
GGAGGAAG others(55): Show |
G | 2 | a0001c0001t0004g0058a0001c0003t0001g0086 | 2 | HG03540.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.445-2456_445-2395d others(64): Show |
TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71135218 | ||||||
| chr12:71135219
|
GAGGAAGA others(49): Show |
G | 1 | a0001c0003t0001g0217 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.445-2451_445-2396d others(58): Show |
TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71135219 | ||||||
| chr12:71135224
|
A | G | 5 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0062others(2): Show | 5 | HG01109.hp2 HG02818.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.445-2400T>C | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71135224 | ||||||
| chr12:71135229
|
AAGG | A | 27 | a0001c0001t0001g0043a0001c0001t0001g0060a0001c0001t0001g0061others(24): Show | 47 | HG00423.hp1 HG01109.hp2 HG01167.hp2 others(44): Show |
intron_variant | MODIFIER | c.445-2408_445-2406d others(5): Show |
TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71135229 | ||||||
| chr12:71135232
|
G | A | 57 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0012others(54): Show | 88 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(85): Show |
intron_variant | MODIFIER | c.445-2408C>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71135232 | ||||||
| chr12:71135234
|
G | A | 53 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0012others(50): Show | 79 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(76): Show |
intron_variant | MODIFIER | c.445-2410C>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71135234 | ||||||
| chr12:71135235
|
G | A | 25 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0062others(22): Show | 44 | HG01109.hp2 HG01167.hp2 HG01257.hp1 others(41): Show |
intron_variant | MODIFIER | c.445-2411C>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71135235 | ||||||
| chr12:71135237
|
G | A | 18 | a0003c0004t0001g0002a0003c0004t0001g0008a0003c0004t0001g0016others(15): Show | 36 | HG01257.hp1 HG01496.hp1 HG01934.hp1 others(33): Show |
intron_variant | MODIFIER | c.445-2413C>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71135237 | ||||||
| chr12:71135238
|
G | A | 5 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0062others(2): Show | 5 | HG01109.hp2 HG02818.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.445-2414C>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71135238 | ||||||
| chr12:71135272
|
G | A | 5 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0062others(2): Show | 5 | HG01109.hp2 HG02818.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.445-2448C>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71135272 | ||||||
| chr12:71135275
|
A | G | 5 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0062others(2): Show | 5 | HG01109.hp2 HG02818.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.445-2451T>C | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71135275 | ||||||
| chr12:71135277
|
G | A | 6 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0062others(3): Show | 6 | HG01109.hp2 HG02818.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.445-2453C>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71135277 | ||||||
| chr12:71135291
|
A | G | 23 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0062others(20): Show | 41 | HG01109.hp2 HG01257.hp1 HG01496.hp1 others(38): Show |
intron_variant | MODIFIER | c.445-2467T>C | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71135291 | ||||||
| chr12:71135294
|
G | A | 2 | a0002c0002t0002g0102a0002c0002t0002g0103 | 2 | HG03710.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.445-2470C>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71135294 | ||||||
| chr12:71135295
|
A | AGGG | 5 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0062others(2): Show | 5 | HG01109.hp2 HG02818.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.445-2472_445-2471i others(5): Show |
TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71135295 | ||||||
| chr12:71135297
|
GA | G | 2 | a0001c0001t0003g0025a0001c0001t0003g0068 | 3 | HG01167.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.445-2474delT | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71135297 | ||||||
| chr12:71135340
|
G | A | 1 | a0001c0003t0001g0212 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.445-2516C>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71135340 | ||||||
| chr12:71135356
|
AAAG | A | 2 | a0001c0001t0003g0025a0001c0001t0003g0068 | 3 | HG01167.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.445-2535_445-2533d others(5): Show |
TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71135356 | ||||||
| chr12:71135369
|
A | AAGG | 4 | a0001c0006t0001g0007a0001c0006t0001g0038a0001c0006t0001g0137others(1): Show | 9 | NA18964.hp1 NA18966.hp2 NA18970.hp1 others(6): Show |
intron_variant | MODIFIER | c.445-2548_445-2546d others(5): Show |
TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71135369 | ||||||
| chr12:71135379
|
A | G | 53 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0012others(50): Show | 79 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(76): Show |
intron_variant | MODIFIER | c.445-2555T>C | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71135379 | ||||||
| chr12:71135425
|
AGAG | A | 2 | a0001c0001t0001g0027a0001c0001t0001g0070 | 3 | HG00735.hp1 HG01952.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.444+2525_444+2527d others(5): Show |
TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71135425 | ||||||
| chr12:71135524
|
A | AGAAGGG | 223 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0012others(220): Show | 316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.444+2423_444+2428d others(8): Show |
TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71135524 | ||||||
| chr12:71135529
|
G | GGGAAGA | 5 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0062others(2): Show | 5 | HG01109.hp2 HG02818.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.444+2423_444+2424i others(8): Show |
TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71135529 | ||||||
| chr12:71135566
|
G | A | 145 | a0001c0001t0004g0058a0001c0003t0001g0003a0001c0003t0001g0013others(142): Show | 188 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(185): Show |
intron_variant | MODIFIER | c.444+2387C>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71135566 | ||||||
| chr12:71135607
|
G | T | 227 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0012others(224): Show | 320 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(317): Show |
intron_variant | MODIFIER | c.444+2346C>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71135607 | ||||||
| chr12:71135711
|
G | A | 78 | a0001c0001t0004g0058a0002c0002t0001g0239a0002c0002t0002g0004others(75): Show | 101 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.444+2242C>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71135711 | ||||||
| chr12:71135762
|
A | G | 1 | a0001c0003t0001g0213 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.444+2191T>C | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71135762 | ||||||
| chr12:71135782
|
T | G | 4 | a0001c0001t0001g0023a0001c0001t0001g0266a0001c0001t0001g0267others(1): Show | 6 | HG01361.hp1 HG01361.hp2 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.444+2171A>C | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71135782 | ||||||
| chr12:71135874
|
T | G | 227 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0012others(224): Show | 320 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(317): Show |
intron_variant | MODIFIER | c.444+2079A>C | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71135874 | ||||||
| chr12:71135918
|
C | T | 2 | a0001c0001t0001g0253a0001c0001t0001g0254 | 2 | HG00639.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.444+2035G>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71135918 | ||||||
| chr12:71135948
|
C | T | 79 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0012others(76): Show | 130 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.444+2005G>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71135948 | ||||||
| chr12:71135969
|
A | G | 1 | a0001c0001t0001g0285 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.444+1984T>C | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71135969 | ||||||
| chr12:71136005
|
A | G | 1 | a0001c0003t0001g0195 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.444+1948T>C | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71136005 | ||||||
| chr12:71136093
|
G | GAA | 144 | a0001c0001t0004g0058a0001c0003t0001g0003a0001c0003t0001g0013others(141): Show | 187 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(184): Show |
intron_variant | MODIFIER | c.444+1858_444+1859d others(4): Show |
TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71136093 | ||||||
| chr12:71136099
|
A | AAG | 5 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0062others(2): Show | 5 | HG01109.hp2 HG02818.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.444+1853_444+1854i others(4): Show |
TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71136099 | ||||||
| chr12:71136170
|
GAAC | G | 5 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0062others(2): Show | 5 | HG01109.hp2 HG02818.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.444+1780_444+1782d others(5): Show |
TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71136170 | ||||||
| chr12:71136310
|
T | C | 1 | a0001c0001t0001g0072 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.444+1643A>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71136310 | ||||||
| chr12:71136379
|
C | T | 67 | a0001c0003t0001g0003a0001c0003t0001g0013a0001c0003t0001g0015others(64): Show | 87 | HG00423.hp2 HG00544.hp1 HG00558.hp1 others(84): Show |
intron_variant | MODIFIER | c.444+1574G>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71136379 | ||||||
| chr12:71136441
|
A | T | 6 | a0001c0001t0003g0025a0001c0001t0003g0068a0001c0006t0001g0007others(3): Show | 12 | HG01167.hp2 HG02896.hp1 HG02897.hp2 others(9): Show |
intron_variant | MODIFIER | c.444+1512T>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71136441 | ||||||
| chr12:71136851
|
T | C | 18 | a0003c0004t0001g0002a0003c0004t0001g0008a0003c0004t0001g0016others(15): Show | 36 | HG01257.hp1 HG01496.hp1 HG01934.hp1 others(33): Show |
intron_variant | MODIFIER | c.444+1102A>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71136851 | ||||||
| chr12:71136856
|
C | T | 68 | a0001c0001t0004g0058a0001c0003t0001g0003a0001c0003t0001g0013others(65): Show | 88 | HG00423.hp2 HG00544.hp1 HG00558.hp1 others(85): Show |
intron_variant | MODIFIER | c.444+1097G>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71136856 | ||||||
| chr12:71136978
|
G | C | 5 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0062others(2): Show | 5 | HG01109.hp2 HG02818.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.444+975C>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71136978 | ||||||
| chr12:71136996
|
T | C | 5 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0062others(2): Show | 5 | HG01109.hp2 HG02818.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.444+957A>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71136996 | ||||||
| chr12:71137008
|
C | T | 1 | a0004c0005t0005g0234 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.444+945G>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71137008 | ||||||
| chr12:71137009
|
G | A | 1 | a0001c0003t0001g0226 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.444+944C>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71137009 | ||||||
| chr12:71137025
|
A | C | 5 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0062others(2): Show | 5 | HG01109.hp2 HG02818.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.444+928T>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71137025 | ||||||
| chr12:71137166
|
A | G | 5 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0062others(2): Show | 5 | HG01109.hp2 HG02818.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.444+787T>C | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71137166 | ||||||
| chr12:71137194
|
C | G | 9 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0062others(6): Show | 14 | HG01109.hp2 HG02818.hp1 HG02976.hp1 others(11): Show |
intron_variant | MODIFIER | c.444+759G>C | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71137194 | ||||||
| chr12:71137213
|
A | G | 5 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0062others(2): Show | 5 | HG01109.hp2 HG02818.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.444+740T>C | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71137213 | ||||||
| chr12:71137235
|
A | G | 5 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0062others(2): Show | 5 | HG01109.hp2 HG02818.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.444+718T>C | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71137235 | ||||||
| chr12:71137309
|
G | A | 54 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0012others(51): Show | 81 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(78): Show |
intron_variant | MODIFIER | c.444+644C>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71137309 | ||||||
| chr12:71137358
|
G | T | 5 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0062others(2): Show | 5 | HG01109.hp2 HG02818.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.444+595C>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71137358 | ||||||
| chr12:71137387
|
T | C | 1 | a0001c0001t0001g0170 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.444+566A>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71137387 | ||||||
| chr12:71137400
|
A | G | 1 | a0002c0002t0002g0199 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.444+553T>C | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71137400 | ||||||
| chr12:71137436
|
T | C | 7 | a0001c0001t0001g0023a0001c0001t0001g0265a0001c0001t0001g0266others(4): Show | 9 | HG01361.hp2 HG01433.hp1 HG03017.hp2 others(6): Show |
intron_variant | MODIFIER | c.444+517A>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71137436 | ||||||
| chr12:71137443
|
AC | A | 5 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0062others(2): Show | 5 | HG01109.hp2 HG02818.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.444+509delG | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71137443 | ||||||
| chr12:71137457
|
G | A | 1 | a0001c0001t0004g0058 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.444+496C>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71137457 | ||||||
| chr12:71137477
|
G | A | 5 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0062others(2): Show | 5 | HG01109.hp2 HG02818.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.444+476C>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71137477 | ||||||
| chr12:71137494
|
G | T | 5 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0062others(2): Show | 5 | HG01109.hp2 HG02818.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.444+459C>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71137494 | ||||||
| chr12:71137536
|
G | A | 1 | a0001c0003t0001g0152 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.444+417C>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71137536 | ||||||
| chr12:71137603
|
C | A | 1 | a0001c0001t0001g0177 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.444+350G>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71137603 | ||||||
| chr12:71137604
|
C | A | 1 | a0001c0001t0004g0058 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.444+349G>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71137604 | ||||||
| chr12:71137604
|
CA | C | 154 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0012others(151): Show | 228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.444+348delT | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71137604 | ||||||
| chr12:71137605
|
A | C | 1 | a0004c0005t0002g0069 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.444+348T>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71137605 | ||||||
| chr12:71137611
|
A | G | 1 | a0002c0002t0002g0106 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.444+342T>C | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71137611 | ||||||
| chr12:71137747
|
C | G | 1 | a0001c0006t0001g0156 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.444+206G>C | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71137747 | ||||||
| chr12:71137859
|
G | A | 77 | a0002c0002t0001g0239a0002c0002t0002g0004a0002c0002t0002g0010others(74): Show | 100 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.444+94C>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71137859 | ||||||
| chr12:71137883
|
A | T | 77 | a0002c0002t0001g0239a0002c0002t0002g0004a0002c0002t0002g0010others(74): Show | 100 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.444+70T>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71137883 | ||||||
| chr12:71137910
|
A | C | 1 | a0002c0002t0002g0091 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.444+43T>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71137910 | ||||||
| chr12:71137939
|
T | C | 4 | a0004c0005t0002g0037a0004c0005t0002g0129a0004c0005t0002g0134others(1): Show | 5 | HG02280.hp2 HG02559.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.444+14A>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71137939 | ||||||
| chr12:71138102
|
T | G | 5 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0062others(2): Show | 5 | HG01109.hp2 HG02818.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.337-42A>C | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 5/8 | chr12 | 71138102 | ||||||
| chr12:71138109
|
T | C | 73 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0012others(70): Show | 118 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(115): Show |
intron_variant | MODIFIER | c.336+47A>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 5/8 | chr12 | 71138109 | ||||||
| chr12:71138319
|
G | A | 77 | a0002c0002t0001g0239a0002c0002t0002g0004a0002c0002t0002g0010others(74): Show | 100 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.262-89C>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 4/8 | chr12 | 71138319 | ||||||
| chr12:71138392
|
G | A | 1 | a0001c0003t0001g0184 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.262-162C>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 4/8 | chr12 | 71138392 | ||||||
| chr12:71138407
|
C | T | 1 | a0003c0004t0001g0143 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.262-177G>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 4/8 | chr12 | 71138407 | ||||||
| chr12:71138414
|
T | C | 5 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0062others(2): Show | 5 | HG01109.hp2 HG02818.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.262-184A>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 4/8 | chr12 | 71138414 | ||||||
| chr12:71138458
|
T | G | 68 | a0001c0001t0004g0058a0001c0003t0001g0003a0001c0003t0001g0013others(65): Show | 88 | HG00423.hp2 HG00544.hp1 HG00558.hp1 others(85): Show |
intron_variant | MODIFIER | c.262-228A>C | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 4/8 | chr12 | 71138458 | ||||||
| chr12:71138521
|
G | C | 5 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0062others(2): Show | 5 | HG01109.hp2 HG02818.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.262-291C>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 4/8 | chr12 | 71138521 | ||||||
| chr12:71138548
|
C | T | 5 | a0001c0001t0001g0005a0001c0001t0001g0034a0001c0001t0001g0088others(2): Show | 10 | HG00558.hp2 HG02132.hp2 HG02523.hp1 others(7): Show |
intron_variant | MODIFIER | c.262-318G>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 4/8 | chr12 | 71138548 | ||||||
| chr12:71138587
|
T | C | 4 | a0001c0001t0001g0262a0001c0001t0003g0024a0001c0001t0003g0066others(1): Show | 5 | HG01069.hp2 HG03098.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.262-357A>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 4/8 | chr12 | 71138587 | ||||||
| chr12:71138646
|
T | G | 4 | a0001c0006t0001g0007a0001c0006t0001g0038a0001c0006t0001g0137others(1): Show | 9 | NA18964.hp1 NA18966.hp2 NA18970.hp1 others(6): Show |
intron_variant | MODIFIER | c.262-416A>C | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 4/8 | chr12 | 71138646 | ||||||
| chr12:71138660
|
C | T | 1 | a0001c0001t0001g0245 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.262-430G>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 4/8 | chr12 | 71138660 | ||||||
| chr12:71138807
|
G | A | 5 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0062others(2): Show | 5 | HG01109.hp2 HG02818.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.262-577C>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 4/8 | chr12 | 71138807 | ||||||
| chr12:71138853
|
C | G | 1 | a0001c0001t0001g0130 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.262-623G>C | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 4/8 | chr12 | 71138853 | ||||||
| chr12:71138856
|
T | C | 1 | a0001c0003t0001g0182 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.262-626A>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 4/8 | chr12 | 71138856 | ||||||
| chr12:71139099
|
A | G | 18 | a0003c0004t0001g0002a0003c0004t0001g0008a0003c0004t0001g0016others(15): Show | 36 | HG01257.hp1 HG01496.hp1 HG01934.hp1 others(33): Show |
intron_variant | MODIFIER | c.261+612T>C | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 4/8 | chr12 | 71139099 | ||||||
| chr12:71139142
|
A | C | 3 | a0001c0001t0001g0130a0001c0001t0001g0132a0001c0001t0001g0249 | 3 | HG02886.hp2 HG02895.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.261+569T>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 4/8 | chr12 | 71139142 | ||||||
| chr12:71139176
|
C | A | 5 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0062others(2): Show | 5 | HG01109.hp2 HG02818.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.261+535G>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 4/8 | chr12 | 71139176 | ||||||
| chr12:71139192
|
C | T | 6 | a0001c0003t0001g0013a0001c0003t0001g0182a0001c0003t0001g0203others(3): Show | 9 | HG00558.hp1 HG01255.hp1 HG01358.hp1 others(6): Show |
intron_variant | MODIFIER | c.261+519G>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 4/8 | chr12 | 71139192 | ||||||
| chr12:71139208
|
C | A | 1 | a0002c0002t0002g0040 | 2 | HG00544.hp2 HG02155.hp2 |
intron_variant | MODIFIER | c.261+503G>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 4/8 | chr12 | 71139208 | ||||||
| chr12:71139430
|
C | T | 69 | a0002c0002t0001g0239a0002c0002t0002g0004a0002c0002t0002g0010others(66): Show | 91 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.261+281G>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 4/8 | chr12 | 71139430 | ||||||
| chr12:71139458
|
G | T | 77 | a0002c0002t0001g0239a0002c0002t0002g0004a0002c0002t0002g0010others(74): Show | 100 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.261+253C>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 4/8 | chr12 | 71139458 | ||||||
| chr12:71139568
|
A | G | 3 | a0001c0001t0001g0252a0001c0001t0002g0021a0001c0001t0002g0260 | 5 | HG01516.hp1 HG01517.hp1 HG01891.hp1 others(2): Show |
intron_variant | MODIFIER | c.261+143T>C | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 4/8 | chr12 | 71139568 | ||||||
| chr12:71139628
|
C | T | 5 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0062others(2): Show | 5 | HG01109.hp2 HG02818.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.261+83G>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 4/8 | chr12 | 71139628 | ||||||
| chr12:71139972
|
C | CCTTCATT others(491): Show |
18 | a0003c0004t0001g0002a0003c0004t0001g0008a0003c0004t0001g0016others(15): Show | 36 | HG01257.hp1 HG01496.hp1 HG01934.hp1 others(33): Show |
intron_variant | MODIFIER | c.124-125_124-124ins others(498): Show |
TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 3/8 | chr12 | 71139972 | ||||||
| chr12:71139972
|
C | CCTTCATT others(491): Show |
54 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0012others(51): Show | 81 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(78): Show |
intron_variant | MODIFIER | c.124-125_124-124ins others(498): Show |
TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 3/8 | chr12 | 71139972 | ||||||
| chr12:71139972
|
C | CCTTCATT others(495): Show |
1 | a0001c0001t0001g0132 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.124-125_124-124ins others(502): Show |
TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 3/8 | chr12 | 71139972 | ||||||
| chr12:71139972
|
C | CCTTCATT others(495): Show |
6 | a0001c0001t0003g0025a0001c0001t0003g0068a0001c0006t0001g0007others(3): Show | 12 | HG01167.hp2 HG02896.hp1 HG02897.hp2 others(9): Show |
intron_variant | MODIFIER | c.124-125_124-124ins others(502): Show |
TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 3/8 | chr12 | 71139972 | ||||||
| chr12:71139974
|
G | A | 1 | a0001c0001t0001g0088 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.124-126C>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 3/8 | chr12 | 71139974 | ||||||
| chr12:71139974
|
G | T | 79 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0012others(76): Show | 130 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.124-126C>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 3/8 | chr12 | 71139974 | ||||||
| chr12:71140015
|
C | CA | 6 | a0001c0001t0003g0025a0001c0001t0003g0068a0001c0006t0001g0007others(3): Show | 12 | HG01167.hp2 HG02896.hp1 HG02897.hp2 others(9): Show |
intron_variant | MODIFIER | c.124-168dupT | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 3/8 | chr12 | 71140015 | ||||||
| chr12:71140072
|
A | C | 1 | a0001c0001t0001g0270 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.124-224T>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 3/8 | chr12 | 71140072 | ||||||
| chr12:71140083
|
G | GT | 8 | a0001c0001t0001g0050a0001c0001t0001g0240a0001c0001t0001g0242others(5): Show | 9 | HG00621.hp1 HG02132.hp1 HG03927.hp1 others(6): Show |
intron_variant | MODIFIER | c.124-236dupA | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 3/8 | chr12 | 71140083 | ||||||
| chr12:71140094
|
C | T | 79 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0012others(76): Show | 130 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.124-246G>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 3/8 | chr12 | 71140094 | ||||||
| chr12:71140196
|
T | A | 6 | a0001c0001t0003g0025a0001c0001t0003g0068a0001c0006t0001g0007others(3): Show | 12 | HG01167.hp2 HG02896.hp1 HG02897.hp2 others(9): Show |
intron_variant | MODIFIER | c.124-348A>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 3/8 | chr12 | 71140196 | ||||||
| chr12:71140216
|
C | A | 1 | a0001c0001t0001g0232 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.124-368G>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 3/8 | chr12 | 71140216 | ||||||
| chr12:71140314
|
A | G | 1 | a0001c0001t0004g0058 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.124-466T>C | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 3/8 | chr12 | 71140314 | ||||||
| chr12:71140446
|
C | A | 1 | a0001c0003t0003g0065 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.124-598G>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 3/8 | chr12 | 71140446 | ||||||
| chr12:71140476
|
C | T | 1 | a0002c0002t0002g0032 | 2 | HG01192.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.124-628G>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 3/8 | chr12 | 71140476 | ||||||
| chr12:71140644
|
C | T | 1 | a0001c0001t0001g0052 | 2 | HG01346.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.124-796G>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 3/8 | chr12 | 71140644 | ||||||
| chr12:71140806
|
T | C | 1 | a0004c0005t0002g0069 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.124-958A>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 3/8 | chr12 | 71140806 | ||||||
| chr12:71140819
|
C | T | 5 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0062others(2): Show | 5 | HG01109.hp2 HG02818.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.124-971G>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 3/8 | chr12 | 71140819 | ||||||
| chr12:71141083
|
T | C | 1 | a0002c0002t0002g0096 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.124-1235A>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 3/8 | chr12 | 71141083 | ||||||
| chr12:71141105
|
A | G | 17 | a0003c0004t0001g0002a0003c0004t0001g0008a0003c0004t0001g0016others(14): Show | 35 | HG01257.hp1 HG01496.hp1 HG01934.hp1 others(32): Show |
intron_variant | MODIFIER | c.124-1257T>C | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 3/8 | chr12 | 71141105 | ||||||
| chr12:71141108
|
A | C | 1 | a0001c0001t0001g0275 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.124-1260T>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 3/8 | chr12 | 71141108 | ||||||
| chr12:71141122
|
G | A | 5 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0062others(2): Show | 5 | HG01109.hp2 HG02818.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.124-1274C>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 3/8 | chr12 | 71141122 | ||||||
| chr12:71141153
|
T | C | 1 | a0002c0002t0002g0294 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.124-1305A>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 3/8 | chr12 | 71141153 | ||||||
| chr12:71141234
|
A | T | 1 | a0002c0002t0002g0100 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.124-1386T>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 3/8 | chr12 | 71141234 | ||||||
| chr12:71141249
|
G | A | 155 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0012others(152): Show | 223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.124-1401C>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 3/8 | chr12 | 71141249 | ||||||
| chr12:71141315
|
T | C | 73 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0012others(70): Show | 118 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(115): Show |
intron_variant | MODIFIER | c.124-1467A>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 3/8 | chr12 | 71141315 | ||||||
| chr12:71141393
|
G | A | 4 | a0001c0001t0001g0262a0001c0001t0003g0024a0001c0001t0003g0066others(1): Show | 5 | HG01069.hp2 HG03098.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.124-1545C>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 3/8 | chr12 | 71141393 | ||||||
| chr12:71141531
|
CA | C | 73 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0012others(70): Show | 118 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(115): Show |
intron_variant | MODIFIER | c.124-1684delT | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 3/8 | chr12 | 71141531 | ||||||
| chr12:71141902
|
C | T | 1 | a0003c0004t0001g0149 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.124-2054G>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 3/8 | chr12 | 71141902 | ||||||
| chr12:71142087
|
T | C | 2 | a0001c0001t0003g0025a0001c0001t0003g0068 | 3 | HG01167.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.123+2064A>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 3/8 | chr12 | 71142087 | ||||||
| chr12:71142091
|
A | G | 1 | a0001c0001t0001g0113 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.123+2060T>C | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 3/8 | chr12 | 71142091 | ||||||
| chr12:71142377
|
C | T | 77 | a0002c0002t0001g0239a0002c0002t0002g0004a0002c0002t0002g0010others(74): Show | 100 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.123+1774G>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 3/8 | chr12 | 71142377 | ||||||
| chr12:71142411
|
A | C | 1 | a0003c0004t0001g0150 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.123+1740T>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 3/8 | chr12 | 71142411 | ||||||
| chr12:71142517
|
T | C | 5 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0062others(2): Show | 5 | HG01109.hp2 HG02818.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.123+1634A>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 3/8 | chr12 | 71142517 | ||||||
| chr12:71142561
|
T | A | 1 | a0001c0001t0001g0072 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.123+1590A>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 3/8 | chr12 | 71142561 | ||||||
| chr12:71142622
|
C | T | 5 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0062others(2): Show | 5 | HG01109.hp2 HG02818.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.123+1529G>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 3/8 | chr12 | 71142622 | ||||||
| chr12:71142701
|
A | C | 4 | a0001c0006t0001g0007a0001c0006t0001g0038a0001c0006t0001g0137others(1): Show | 9 | NA18964.hp1 NA18966.hp2 NA18970.hp1 others(6): Show |
intron_variant | MODIFIER | c.123+1450T>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 3/8 | chr12 | 71142701 | ||||||
| chr12:71142756
|
G | A | 2 | a0001c0001t0003g0025a0001c0001t0003g0068 | 3 | HG01167.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.123+1395C>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 3/8 | chr12 | 71142756 | ||||||
| chr12:71142847
|
C | CA | 108 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0052others(105): Show | 164 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(161): Show |
intron_variant | MODIFIER | c.123+1303dupT | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 3/8 | chr12 | 71142847 | ||||||
| chr12:71142847
|
C | CAA | 54 | a0001c0001t0001g0055a0001c0001t0001g0279a0001c0001t0001g0286others(51): Show | 70 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(67): Show |
intron_variant | MODIFIER | c.123+1302_123+1303d others(4): Show |
TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 3/8 | chr12 | 71142847 | ||||||
| chr12:71142848
|
A | AAC | 5 | a0002c0002t0002g0032a0002c0002t0002g0089a0004c0005t0002g0237others(2): Show | 6 | HG00099.hp1 HG01192.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.123+1302_123+1303i others(4): Show |
TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 3/8 | chr12 | 71142848 | ||||||
| chr12:71142849
|
A | AAAC | 5 | a0001c0006t0001g0007a0001c0006t0001g0038a0001c0006t0001g0137others(2): Show | 10 | HG03831.hp2 NA18964.hp1 NA18966.hp2 others(7): Show |
intron_variant | MODIFIER | c.123+1301_123+1302i others(5): Show |
TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 3/8 | chr12 | 71142849 | ||||||
| chr12:71142849
|
A | AAC | 12 | a0001c0001t0001g0012a0001c0001t0001g0056a0001c0001t0001g0168others(9): Show | 17 | HG01361.hp1 HG01891.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.123+1301_123+1302i others(4): Show |
TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 3/8 | chr12 | 71142849 | ||||||
| chr12:71142850
|
A | AAC | 14 | a0002c0002t0002g0010a0002c0002t0002g0030a0002c0002t0002g0031others(11): Show | 19 | HG00438.hp2 HG02027.hp2 HG02135.hp1 others(16): Show |
intron_variant | MODIFIER | c.123+1300_123+1301i others(4): Show |
TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 3/8 | chr12 | 71142850 | ||||||
| chr12:71142850
|
A | AC | 23 | a0001c0001t0001g0009a0001c0001t0001g0060a0001c0001t0001g0061others(20): Show | 28 | HG00140.hp1 HG00738.hp1 HG01106.hp1 others(25): Show |
intron_variant | MODIFIER | c.123+1300_123+1301i others(3): Show |
TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 3/8 | chr12 | 71142850 | ||||||
| chr12:71142851
|
A | C | 3 | a0001c0001t0003g0025a0001c0001t0003g0068a0002c0002t0002g0089 | 4 | HG00099.hp1 HG01167.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.123+1300T>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 3/8 | chr12 | 71142851 | ||||||
| chr12:71143281
|
T | C | 1 | a0002c0002t0002g0117 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.123+870A>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 3/8 | chr12 | 71143281 | ||||||
| chr12:71143454
|
C | T | 1 | a0001c0003t0001g0224 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.123+697G>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 3/8 | chr12 | 71143454 | ||||||
| chr12:71143476
|
G | A | 2 | a0001c0001t0003g0025a0001c0001t0003g0068 | 3 | HG01167.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.123+675C>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 3/8 | chr12 | 71143476 | ||||||
| chr12:71143507
|
G | C | 1 | a0001c0001t0001g0231 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.123+644C>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 3/8 | chr12 | 71143507 | ||||||
| chr12:71143531
|
A | G | 5 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0062others(2): Show | 5 | HG01109.hp2 HG02818.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.123+620T>C | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 3/8 | chr12 | 71143531 | ||||||
| chr12:71143549
|
T | C | 77 | a0002c0002t0001g0239a0002c0002t0002g0004a0002c0002t0002g0010others(74): Show | 100 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.123+602A>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 3/8 | chr12 | 71143549 | ||||||
| chr12:71144052
|
T | C | 2 | a0001c0001t0003g0025a0001c0001t0003g0068 | 3 | HG01167.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.123+99A>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 3/8 | chr12 | 71144052 | ||||||
| chr12:71144089
|
T | G | 1 | a0001c0001t0001g0259 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.123+62A>C | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 3/8 | chr12 | 71144089 | ||||||
| chr12:71144274
|
C | T | 1 | a0006c0008t0001g0051 | 2 | HG02486.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.61-61G>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71144274 | ||||||
| chr12:71144292
|
C | T | 5 | a0001c0001t0001g0247a0001c0006t0001g0007a0001c0006t0001g0038others(2): Show | 10 | HG01255.hp2 NA18964.hp1 NA18966.hp2 others(7): Show |
intron_variant | MODIFIER | c.61-79G>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71144292 | ||||||
| chr12:71144416
|
A | G | 18 | a0001c0001t0001g0023a0001c0001t0001g0050a0001c0001t0001g0240others(15): Show | 22 | HG00621.hp1 HG01361.hp2 HG01433.hp1 others(19): Show |
intron_variant | MODIFIER | c.61-203T>C | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71144416 | ||||||
| chr12:71144530
|
T | C | 53 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0012others(50): Show | 80 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(77): Show |
intron_variant | MODIFIER | c.61-317A>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71144530 | ||||||
| chr12:71144976
|
T | C | 2 | a0001c0001t0001g0230a0001c0001t0001g0231 | 2 | HG02630.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.61-763A>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71144976 | ||||||
| chr12:71144982
|
C | T | 68 | a0001c0001t0001g0181a0001c0001t0001g0236a0001c0003t0001g0003others(65): Show | 88 | HG00423.hp2 HG00544.hp1 HG00558.hp1 others(85): Show |
intron_variant | MODIFIER | c.61-769G>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71144982 | ||||||
| chr12:71145044
|
C | T | 1 | a0001c0001t0001g0053 | 2 | HG02145.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.61-831G>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71145044 | ||||||
| chr12:71145064
|
T | C | 66 | a0001c0001t0001g0181a0001c0001t0001g0236a0001c0003t0001g0003others(63): Show | 86 | HG00423.hp2 HG00544.hp1 HG00558.hp1 others(83): Show |
intron_variant | MODIFIER | c.61-851A>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71145064 | ||||||
| chr12:71145351
|
G | A | 1 | a0002c0002t0002g0083 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.61-1138C>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71145351 | ||||||
| chr12:71145497
|
C | T | 3 | a0002c0002t0002g0100a0002c0002t0002g0101a0002c0002t0002g0119 | 3 | HG03942.hp1 HG04184.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.61-1284G>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71145497 | ||||||
| chr12:71145527
|
T | C | 1 | a0001c0001t0001g0256 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.61-1314A>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71145527 | ||||||
| chr12:71145866
|
C | A | 93 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(90): Show | 148 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(145): Show |
intron_variant | MODIFIER | c.61-1653G>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71145866 | ||||||
| chr12:71145910
|
C | A | 1 | a0002c0002t0002g0097 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.61-1697G>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71145910 | ||||||
| chr12:71145984
|
C | T | 1 | a0001c0001t0001g0164 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.61-1771G>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71145984 | ||||||
| chr12:71145991
|
C | T | 204 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(201): Show | 291 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(288): Show |
intron_variant | MODIFIER | c.61-1778G>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71145991 | ||||||
| chr12:71146060
|
C | T | 66 | a0001c0001t0001g0181a0001c0001t0001g0236a0001c0003t0001g0003others(63): Show | 86 | HG00423.hp2 HG00544.hp1 HG00558.hp1 others(83): Show |
intron_variant | MODIFIER | c.61-1847G>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71146060 | ||||||
| chr12:71146135
|
A | C | 279 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(276): Show | 392 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(389): Show |
intron_variant | MODIFIER | c.61-1922T>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71146135 | ||||||
| chr12:71146135
|
A | T | 11 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0001g0281others(8): Show | 13 | HG02258.hp1 HG02280.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.61-1922T>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71146135 | ||||||
| chr12:71146237
|
C | T | 66 | a0001c0001t0001g0181a0001c0001t0001g0236a0001c0003t0001g0003others(63): Show | 86 | HG00423.hp2 HG00544.hp1 HG00558.hp1 others(83): Show |
intron_variant | MODIFIER | c.61-2024G>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71146237 | ||||||
| chr12:71146306
|
T | C | 207 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(204): Show | 294 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(291): Show |
intron_variant | MODIFIER | c.61-2093A>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71146306 | ||||||
| chr12:71146359
|
T | C | 1 | a0001c0001t0001g0164 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.61-2146A>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71146359 | ||||||
| chr12:71146385
|
C | A | 63 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0020others(60): Show | 91 | HG00099.hp2 HG00140.hp2 HG00621.hp1 others(88): Show |
intron_variant | MODIFIER | c.61-2172G>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71146385 | ||||||
| chr12:71146492
|
A | G | 66 | a0001c0001t0001g0181a0001c0001t0001g0236a0001c0003t0001g0003others(63): Show | 86 | HG00423.hp2 HG00544.hp1 HG00558.hp1 others(83): Show |
intron_variant | MODIFIER | c.61-2279T>C | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71146492 | ||||||
| chr12:71146806
|
A | C | 4 | a0001c0001t0001g0263a0001c0001t0001g0276a0001c0001t0001g0277others(1): Show | 4 | HG01884.hp2 HG02257.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.61-2593T>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71146806 | ||||||
| chr12:71146858
|
A | G | 5 | a0001c0001t0001g0173a0001c0001t0001g0174a0001c0001t0001g0267others(2): Show | 5 | HG01361.hp1 HG02055.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.61-2645T>C | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71146858 | ||||||
| chr12:71146881
|
C | T | 2 | a0001c0001t0001g0130a0001c0001t0001g0133 | 2 | HG02109.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.61-2668G>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71146881 | ||||||
| chr12:71147041
|
C | T | 2 | a0002c0002t0002g0084a0002c0002t0002g0085 | 2 | HG01884.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.61-2828G>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71147041 | ||||||
| chr12:71147042
|
G | A | 1 | a0002c0002t0002g0110 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.61-2829C>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71147042 | ||||||
| chr12:71147210
|
A | G | 1 | a0001c0001t0001g0249 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.61-2997T>C | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71147210 | ||||||
| chr12:71147336
|
G | A | 1 | a0001c0003t0001g0195 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.61-3123C>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71147336 | ||||||
| chr12:71147415
|
G | A | 1 | a0001c0001t0001g0264 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.61-3202C>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71147415 | ||||||
| chr12:71147445
|
T | G | 10 | a0001c0001t0001g0055a0001c0001t0001g0263a0001c0001t0001g0276others(7): Show | 12 | HG01884.hp2 HG02257.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.61-3232A>C | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71147445 | ||||||
| chr12:71147599
|
C | A | 3 | a0002c0002t0002g0100a0002c0002t0002g0101a0002c0002t0002g0119 | 3 | HG03942.hp1 HG04184.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.61-3386G>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71147599 | ||||||
| chr12:71147652
|
C | G | 7 | a0001c0001t0001g0130a0001c0001t0001g0132a0001c0001t0001g0133others(4): Show | 8 | HG02109.hp1 HG02280.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.61-3439G>C | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71147652 | ||||||
| chr12:71147726
|
G | C | 1 | a0001c0001t0004g0059 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.61-3513C>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71147726 | ||||||
| chr12:71147751
|
A | G | 1 | a0004c0005t0002g0291 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.61-3538T>C | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71147751 | ||||||
| chr12:71147925
|
A | G | 1 | a0001c0001t0004g0058 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.61-3712T>C | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71147925 | ||||||
| chr12:71147934
|
T | C | 5 | a0001c0003t0001g0146a0001c0003t0001g0152a0001c0003t0001g0153others(2): Show | 6 | HG00544.hp2 HG01123.hp1 HG01261.hp1 others(3): Show |
intron_variant | MODIFIER | c.61-3721A>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71147934 | ||||||
| chr12:71148029
|
C | T | 4 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0074others(1): Show | 4 | HG00280.hp2 HG02723.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.61-3816G>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71148029 | ||||||
| chr12:71148256
|
A | G | 2 | a0001c0001t0001g0130a0001c0001t0001g0133 | 2 | HG02109.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.61-4043T>C | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71148256 | ||||||
| chr12:71148301
|
T | C | 1 | a0001c0003t0001g0153 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.61-4088A>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71148301 | ||||||
| chr12:71148366
|
C | T | 1 | a0001c0001t0001g0164 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.61-4153G>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71148366 | ||||||
| chr12:71148368
|
C | T | 3 | a0004c0005t0002g0037a0004c0005t0002g0129a0004c0005t0002g0134 | 4 | HG02280.hp2 HG02559.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.61-4155G>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71148368 | ||||||
| chr12:71148561
|
C | T | 7 | a0001c0001t0001g0130a0001c0001t0001g0132a0001c0001t0001g0133others(4): Show | 8 | HG02109.hp1 HG02280.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.61-4348G>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71148561 | ||||||
| chr12:71148573
|
A | G | 3 | a0001c0001t0001g0276a0001c0001t0001g0277a0001c0001t0001g0278 | 3 | HG01884.hp2 HG02257.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.61-4360T>C | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71148573 | ||||||
| chr12:71148789
|
C | T | 7 | a0001c0003t0001g0136a0001c0003t0001g0138a0001c0003t0001g0139others(4): Show | 12 | HG02080.hp2 HG04115.hp2 NA18964.hp1 others(9): Show |
intron_variant | MODIFIER | c.61-4576G>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71148789 | ||||||
| chr12:71149018
|
G | T | 7 | a0001c0003t0001g0136a0001c0003t0001g0138a0001c0003t0001g0139others(4): Show | 12 | HG02080.hp2 HG04115.hp2 NA18964.hp1 others(9): Show |
intron_variant | MODIFIER | c.61-4805C>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71149018 | ||||||
| chr12:71149072
|
T | C | 1 | a0001c0001t0001g0223 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.61-4859A>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71149072 | ||||||
| chr12:71149213
|
A | G | 1 | a0001c0001t0001g0072 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.61-5000T>C | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71149213 | ||||||
| chr12:71149238
|
C | T | 4 | a0002c0002t0002g0029a0002c0002t0002g0082a0002c0002t0002g0083others(1): Show | 5 | NA18942.hp2 NA18960.hp1 NA18962.hp2 others(2): Show |
intron_variant | MODIFIER | c.61-5025G>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71149238 | ||||||
| chr12:71149291
|
C | T | 14 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0168others(11): Show | 21 | HG00140.hp1 HG00738.hp1 HG01106.hp1 others(18): Show |
intron_variant | MODIFIER | c.61-5078G>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71149291 | ||||||
| chr12:71149369
|
C | CA | 48 | a0001c0001t0001g0011a0001c0001t0001g0036a0001c0001t0001g0039others(45): Show | 76 | HG00423.hp1 HG00544.hp2 HG00609.hp2 others(73): Show |
intron_variant | MODIFIER | c.61-5157dupT | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71149369 | ||||||
| chr12:71149369
|
CA | C | 12 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0063others(9): Show | 12 | HG01934.hp2 HG02055.hp1 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.61-5157delT | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71149369 | ||||||
| chr12:71149385
|
A | G | 13 | a0001c0003t0001g0013a0001c0003t0001g0046a0001c0003t0001g0182others(10): Show | 17 | HG00423.hp2 HG00558.hp1 HG01255.hp1 others(14): Show |
intron_variant | MODIFIER | c.61-5172T>C | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71149385 | ||||||
| chr12:71149451
|
C | T | 8 | a0001c0003t0001g0136a0001c0003t0001g0138a0001c0003t0001g0139others(5): Show | 13 | HG02080.hp2 HG02155.hp1 HG04115.hp2 others(10): Show |
intron_variant | MODIFIER | c.61-5238G>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71149451 | ||||||
| chr12:71149590
|
T | C | 218 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(215): Show | 308 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(305): Show |
intron_variant | MODIFIER | c.61-5377A>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71149590 | ||||||
| chr12:71149727
|
G | A | 2 | a0001c0001t0001g0055a0001c0001t0001g0279 | 3 | HG02572.hp1 HG03195.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.61-5514C>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71149727 | ||||||
| chr12:71149730
|
C | T | 1 | a0001c0001t0001g0164 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.61-5517G>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71149730 | ||||||
| chr12:71149731
|
G | A | 2 | a0001c0001t0001g0173a0001c0001t0001g0174 | 2 | HG02055.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.61-5518C>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71149731 | ||||||
| chr12:71149777
|
T | C | 6 | a0001c0003t0001g0136a0001c0003t0001g0138a0001c0006t0001g0007others(3): Show | 11 | HG02080.hp2 NA18964.hp1 NA18965.hp2 others(8): Show |
intron_variant | MODIFIER | c.61-5564A>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71149777 | ||||||
| chr12:71149795
|
G | T | 6 | a0001c0003t0001g0136a0001c0003t0001g0138a0001c0006t0001g0007others(3): Show | 11 | HG02080.hp2 NA18964.hp1 NA18965.hp2 others(8): Show |
intron_variant | MODIFIER | c.61-5582C>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71149795 | ||||||
| chr12:71149856
|
G | A | 1 | a0003c0004t0001g0041 | 2 | NA18951.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.61-5643C>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71149856 | ||||||
| chr12:71149880
|
T | A | 1 | a0002c0002t0001g0239 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.61-5667A>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71149880 | ||||||
| chr12:71149916
|
T | C | 2 | a0002c0002t0002g0102a0002c0002t0002g0103 | 2 | HG03710.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.61-5703A>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71149916 | ||||||
| chr12:71150051
|
C | T | 6 | a0001c0001t0003g0024a0001c0001t0003g0025a0001c0001t0003g0066others(3): Show | 8 | HG01167.hp2 HG02896.hp1 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.61-5838G>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71150051 | ||||||
| chr12:71150094
|
G | A | 1 | a0004c0005t0005g0234 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.61-5881C>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71150094 | ||||||
| chr12:71150141
|
C | T | 57 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0022others(54): Show | 82 | HG00099.hp2 HG00140.hp2 HG00621.hp1 others(79): Show |
intron_variant | MODIFIER | c.61-5928G>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71150141 | ||||||
| chr12:71150186
|
C | T | 57 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0022others(54): Show | 82 | HG00099.hp2 HG00140.hp2 HG00621.hp1 others(79): Show |
intron_variant | MODIFIER | c.61-5973G>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71150186 | ||||||
| chr12:71150344
|
C | T | 1 | a0002c0002t0002g0028 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.61-6131G>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71150344 | ||||||
| chr12:71150353
|
C | G | 4 | a0002c0002t0002g0014a0002c0002t0002g0081a0002c0002t0002g0124others(1): Show | 6 | HG01952.hp2 HG02300.hp1 HG02735.hp1 others(3): Show |
intron_variant | MODIFIER | c.61-6140G>C | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71150353 | ||||||
| chr12:71150374
|
G | A | 3 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0074 | 3 | HG02723.hp1 HG02922.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.61-6161C>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71150374 | ||||||
| chr12:71150501
|
GTCCTACT others(3): Show |
G | 1 | a0005c0007t0002g0141 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.61-6298_61-6289del others(10): Show |
TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71150501 | ||||||
| chr12:71150509
|
GAT | G | 85 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0012others(82): Show | 124 | HG00140.hp1 HG00423.hp1 HG00544.hp2 others(121): Show |
intron_variant | MODIFIER | c.61-6298_61-6297del others(2): Show |
TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71150509 | ||||||
| chr12:71150527
|
C | T | 18 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0165others(15): Show | 25 | HG00140.hp1 HG00738.hp1 HG01106.hp1 others(22): Show |
intron_variant | MODIFIER | c.61-6314G>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71150527 | ||||||
| chr12:71150528
|
G | A | 3 | a0001c0003t0001g0197a0001c0003t0001g0198a0001c0003t0001g0218 | 3 | HG01167.hp1 HG01169.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.61-6315C>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71150528 | ||||||
| chr12:71150612
|
G | A | 1 | a0001c0001t0001g0072 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.61-6399C>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71150612 | ||||||
| chr12:71150627
|
G | A | 3 | a0001c0001t0001g0267a0001c0001t0001g0268a0001c0001t0001g0269 | 3 | HG01361.hp1 HG02622.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.61-6414C>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71150627 | ||||||
| chr12:71150692
|
T | C | 1 | a0001c0001t0001g0278 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.61-6479A>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71150692 | ||||||
| chr12:71150748
|
C | T | 14 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0062others(11): Show | 19 | HG01109.hp2 HG01496.hp2 HG02080.hp2 others(16): Show |
intron_variant | MODIFIER | c.61-6535G>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71150748 | ||||||
| chr12:71150758
|
C | T | 1 | a0003c0004t0001g0143 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.61-6545G>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71150758 | ||||||
| chr12:71150894
|
C | G | 40 | a0001c0001t0001g0181a0001c0001t0001g0194a0001c0003t0001g0003others(37): Show | 55 | HG00544.hp1 HG00639.hp2 HG01167.hp1 others(52): Show |
intron_variant | MODIFIER | c.61-6681G>C | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71150894 | ||||||
| chr12:71150928
|
A | C | 3 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0074 | 3 | HG02723.hp1 HG02922.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.60+6691T>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71150928 | ||||||
| chr12:71151056
|
C | T | 4 | a0001c0003t0001g0015a0001c0003t0001g0075a0001c0003t0001g0135others(1): Show | 6 | NA18974.hp2 NA18975.hp1 NA18980.hp1 others(3): Show |
intron_variant | MODIFIER | c.60+6563G>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71151056 | ||||||
| chr12:71151066
|
A | AT | 78 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0062others(75): Show | 103 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(100): Show |
intron_variant | MODIFIER | c.60+6552dupA | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71151066 | ||||||
| chr12:71151066
|
AT | A | 9 | a0001c0001t0001g0130a0001c0001t0001g0132a0001c0001t0001g0133others(6): Show | 10 | HG02109.hp1 HG02280.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.60+6552delA | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71151066 | ||||||
| chr12:71151069
|
T | A | 6 | a0001c0001t0001g0057a0001c0001t0001g0282a0001c0001t0001g0284others(3): Show | 7 | HG02258.hp1 HG02280.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.60+6550A>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71151069 | ||||||
| chr12:71151221
|
G | A | 4 | a0002c0002t0002g0033a0002c0002t0002g0120a0002c0002t0002g0121others(1): Show | 5 | NA18949.hp1 NA18957.hp2 NA18965.hp1 others(2): Show |
intron_variant | MODIFIER | c.60+6398C>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71151221 | ||||||
| chr12:71151257
|
G | A | 58 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0022others(55): Show | 83 | HG00099.hp2 HG00140.hp2 HG00621.hp1 others(80): Show |
intron_variant | MODIFIER | c.60+6362C>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71151257 | ||||||
| chr12:71151274
|
G | A | 1 | a0001c0001t0001g0132 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.60+6345C>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71151274 | ||||||
| chr12:71151354
|
C | T | 1 | a0001c0003t0001g0218 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.60+6265G>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71151354 | ||||||
| chr12:71151391
|
T | C | 7 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0062others(4): Show | 7 | HG01109.hp2 HG01496.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.60+6228A>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71151391 | ||||||
| chr12:71151450
|
C | A | 1 | a0003c0004t0001g0131 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.60+6169G>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71151450 | ||||||
| chr12:71151493
|
A | C | 20 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0165others(17): Show | 27 | HG00140.hp1 HG00738.hp1 HG01106.hp1 others(24): Show |
intron_variant | MODIFIER | c.60+6126T>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71151493 | ||||||
| chr12:71151778
|
T | A | 20 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0165others(17): Show | 27 | HG00140.hp1 HG00738.hp1 HG01106.hp1 others(24): Show |
intron_variant | MODIFIER | c.60+5841A>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71151778 | ||||||
| chr12:71151810
|
A | G | 48 | a0001c0001t0001g0011a0001c0001t0001g0039a0001c0001t0001g0042others(45): Show | 78 | HG00423.hp1 HG00544.hp2 HG00609.hp2 others(75): Show |
intron_variant | MODIFIER | c.60+5809T>C | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71151810 | ||||||
| chr12:71151879
|
G | T | 7 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0062others(4): Show | 7 | HG01109.hp2 HG01496.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.60+5740C>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71151879 | ||||||
| chr12:71152006
|
T | C | 5 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0062others(2): Show | 5 | HG01109.hp2 HG02818.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.60+5613A>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71152006 | ||||||
| chr12:71152042
|
G | C | 1 | a0001c0001t0001g0155 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.60+5577C>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71152042 | ||||||
| chr12:71152158
|
T | C | 12 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0001g0281others(9): Show | 14 | HG02258.hp1 HG02280.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.60+5461A>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71152158 | ||||||
| chr12:71152223
|
G | A | 1 | a0002c0002t0002g0104 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.60+5396C>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71152223 | ||||||
| chr12:71152227
|
G | C | 1 | a0001c0003t0001g0226 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.60+5392C>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71152227 | ||||||
| chr12:71152304
|
T | C | 8 | a0001c0001t0001g0023a0001c0001t0001g0054a0001c0001t0001g0265others(5): Show | 11 | HG01361.hp2 HG01433.hp1 HG03017.hp2 others(8): Show |
intron_variant | MODIFIER | c.60+5315A>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71152304 | ||||||
| chr12:71152482
|
A | G | 56 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0022others(53): Show | 81 | HG00099.hp2 HG00140.hp2 HG00621.hp1 others(78): Show |
intron_variant | MODIFIER | c.60+5137T>C | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71152482 | ||||||
| chr12:71152778
|
A | T | 3 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0070 | 5 | HG00735.hp1 HG01952.hp1 HG01993.hp2 others(2): Show |
intron_variant | MODIFIER | c.60+4841T>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71152778 | ||||||
| chr12:71152928
|
T | C | 12 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0001g0281others(9): Show | 14 | HG02258.hp1 HG02280.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.60+4691A>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71152928 | ||||||
| chr12:71152979
|
C | T | 1 | a0002c0002t0002g0144 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.60+4640G>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71152979 | ||||||
| chr12:71152999
|
A | C | 1 | a0001c0001t0001g0168 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.60+4620T>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71152999 | ||||||
| chr12:71153060
|
C | G | 2 | a0001c0001t0002g0021a0001c0001t0002g0260 | 4 | HG01516.hp1 HG01517.hp1 HG01891.hp1 others(1): Show |
intron_variant | MODIFIER | c.60+4559G>C | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71153060 | ||||||
| chr12:71153152
|
T | C | 2 | a0002c0002t0002g0105a0002c0002t0002g0128 | 2 | NA18974.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.60+4467A>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71153152 | ||||||
| chr12:71153230
|
A | T | 7 | a0001c0003t0001g0136a0001c0003t0001g0138a0001c0003t0001g0139others(4): Show | 12 | HG02080.hp2 HG04115.hp2 NA18964.hp1 others(9): Show |
intron_variant | MODIFIER | c.60+4389T>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71153230 | ||||||
| chr12:71153491
|
C | G | 1 | a0001c0001t0001g0244 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.60+4128G>C | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71153491 | ||||||
| chr12:71153510
|
C | T | 1 | a0002c0002t0002g0080 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.60+4109G>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71153510 | ||||||
| chr12:71153560
|
C | T | 2 | a0001c0001t0001g0235a0001c0001t0001g0236 | 2 | HG02970.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.60+4059G>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71153560 | ||||||
| chr12:71153640
|
T | C | 1 | a0001c0001t0001g0132 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.60+3979A>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71153640 | ||||||
| chr12:71153678
|
G | A | 5 | a0001c0003t0001g0109a0002c0002t0002g0078a0002c0002t0002g0106others(2): Show | 5 | NA18969.hp1 NA18982.hp1 NA18995.hp1 others(2): Show |
intron_variant | MODIFIER | c.60+3941C>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71153678 | ||||||
| chr12:71153715
|
C | T | 1 | a0001c0001t0001g0039 | 2 | NA18946.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.60+3904G>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71153715 | ||||||
| chr12:71153739
|
T | C | 216 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(213): Show | 306 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(303): Show |
intron_variant | MODIFIER | c.60+3880A>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71153739 | ||||||
| chr12:71153837
|
C | T | 6 | a0001c0001t0001g0057a0001c0001t0001g0282a0001c0001t0001g0284others(3): Show | 7 | HG02258.hp1 HG02280.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.60+3782G>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71153837 | ||||||
| chr12:71153878
|
A | T | 1 | a0002c0002t0002g0079 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.60+3741T>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71153878 | ||||||
| chr12:71153936
|
A | C | 1 | a0001c0001t0001g0073 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.60+3683T>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71153936 | ||||||
| chr12:71153950
|
A | T | 216 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(213): Show | 306 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(303): Show |
intron_variant | MODIFIER | c.60+3669T>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71153950 | ||||||
| chr12:71154035
|
G | A | 2 | a0003c0004t0001g0008a0003c0004t0001g0163 | 6 | HG01257.hp1 HG01496.hp1 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.60+3584C>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71154035 | ||||||
| chr12:71154058
|
C | T | 2 | a0001c0003t0001g0183a0001c0003t0001g0184 | 2 | HG03688.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.60+3561G>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71154058 | ||||||
| chr12:71154067
|
A | G | 184 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0020others(181): Show | 265 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(262): Show |
intron_variant | MODIFIER | c.60+3552T>C | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71154067 | ||||||
| chr12:71154145
|
C | A | 1 | a0001c0001t0001g0164 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.60+3474G>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71154145 | ||||||
| chr12:71154177
|
G | A | 1 | a0002c0002t0002g0110 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.60+3442C>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71154177 | ||||||
| chr12:71154210
|
T | C | 39 | a0001c0001t0001g0011a0001c0001t0001g0039a0001c0001t0001g0042others(36): Show | 67 | HG00423.hp1 HG00544.hp2 HG00609.hp2 others(64): Show |
intron_variant | MODIFIER | c.60+3409A>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71154210 | ||||||
| chr12:71154311
|
A | AAAT | 131 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0022others(128): Show | 184 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(181): Show |
intron_variant | MODIFIER | c.60+3305_60+3307dup others(3): Show |
TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71154311 | ||||||
| chr12:71154311
|
A | AAATAAT | 7 | a0001c0001t0001g0060a0001c0001t0001g0063a0001c0003t0001g0182others(4): Show | 7 | HG00558.hp1 HG02074.hp1 HG03516.hp1 others(4): Show |
intron_variant | MODIFIER | c.60+3302_60+3307dup others(6): Show |
TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71154311 | ||||||
| chr12:71154311
|
AAAT | A | 29 | a0001c0001t0001g0009a0001c0001t0001g0020a0001c0001t0001g0026others(26): Show | 40 | HG00140.hp1 HG00735.hp1 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.60+3305_60+3307del others(3): Show |
TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71154311 | ||||||
| chr12:71154311
|
AAATAAT | A | 19 | a0001c0001t0001g0001a0001c0001t0001g0052a0001c0001t0001g0235others(16): Show | 32 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(29): Show |
intron_variant | MODIFIER | c.60+3302_60+3307del others(6): Show |
TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71154311 | ||||||
| chr12:71154311
|
AAATAATA others(2): Show |
A | 48 | a0001c0001t0001g0011a0001c0001t0001g0039a0001c0001t0001g0042others(45): Show | 78 | HG00423.hp1 HG00544.hp2 HG00609.hp2 others(75): Show |
intron_variant | MODIFIER | c.60+3299_60+3307del others(9): Show |
TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71154311 | ||||||
| chr12:71154354
|
A | AATAATC | 4 | a0001c0001t0001g0056a0001c0001t0001g0283a0001c0001t0001g0287others(1): Show | 5 | HG02451.hp1 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.60+3264_60+3265ins others(6): Show |
TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71154354 | ||||||
| chr12:71154354
|
A | C | 5 | a0001c0001t0001g0057a0001c0001t0001g0284a0001c0001t0001g0285others(2): Show | 6 | HG02258.hp1 HG02280.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.60+3265T>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71154354 | ||||||
| chr12:71154442
|
G | A | 1 | a0001c0001t0001g0178 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.60+3177C>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71154442 | ||||||
| chr12:71155110
|
C | T | 55 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0022others(52): Show | 80 | HG00099.hp2 HG00140.hp2 HG00621.hp1 others(77): Show |
intron_variant | MODIFIER | c.60+2509G>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71155110 | ||||||
| chr12:71155192
|
T | C | 2 | a0002c0002t0002g0124a0002c0002t0002g0125 | 2 | HG01952.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.60+2427A>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71155192 | ||||||
| chr12:71155316
|
C | A | 224 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(221): Show | 315 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(312): Show |
intron_variant | MODIFIER | c.60+2303G>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71155316 | ||||||
| chr12:71155332
|
T | A | 2 | a0001c0003t0001g0019a0001c0003t0001g0048 | 5 | NA18947.hp1 NA18978.hp1 NA19000.hp2 others(2): Show |
intron_variant | MODIFIER | c.60+2287A>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71155332 | ||||||
| chr12:71155545
|
A | G | 1 | a0003c0004t0001g0142 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.60+2074T>C | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71155545 | ||||||
| chr12:71155613
|
G | A | 1 | a0001c0001t0001g0232 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.60+2006C>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71155613 | ||||||
| chr12:71155627
|
T | C | 7 | a0001c0003t0001g0136a0001c0003t0001g0138a0001c0003t0001g0139others(4): Show | 12 | HG02080.hp2 HG04115.hp2 NA18964.hp1 others(9): Show |
intron_variant | MODIFIER | c.60+1992A>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71155627 | ||||||
| chr12:71155736
|
A | AT | 7 | a0001c0001t0001g0055a0001c0001t0001g0166a0001c0001t0001g0167others(4): Show | 8 | HG01884.hp2 HG02257.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.60+1882dupA | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71155736 | ||||||
| chr12:71155736
|
A | ATT | 39 | a0001c0001t0001g0011a0001c0001t0001g0039a0001c0001t0001g0042others(36): Show | 67 | HG00423.hp1 HG00544.hp2 HG00609.hp2 others(64): Show |
intron_variant | MODIFIER | c.60+1881_60+1882dup others(2): Show |
TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71155736 | ||||||
| chr12:71155878
|
C | T | 2 | a0001c0001t0001g0071a0001c0001t0001g0076 | 2 | HG03139.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.60+1741G>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71155878 | ||||||
| chr12:71155891
|
C | G | 2 | a0001c0001t0003g0024a0001c0001t0003g0067 | 3 | HG03471.hp2 HG03516.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.60+1728G>C | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71155891 | ||||||
| chr12:71155892
|
C | T | 2 | a0005c0007t0002g0140a0005c0007t0002g0141 | 2 | HG02683.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.60+1727G>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71155892 | ||||||
| chr12:71156022
|
C | T | 4 | a0001c0001t0001g0181a0001c0003t0001g0215a0001c0003t0001g0216others(1): Show | 4 | HG00544.hp1 HG02165.hp2 NA18981.hp1 others(1): Show |
intron_variant | MODIFIER | c.60+1597G>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71156022 | ||||||
| chr12:71156083
|
C | T | 1 | a0001c0001t0001g0268 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.60+1536G>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71156083 | ||||||
| chr12:71156223
|
C | G | 1 | a0001c0001t0001g0267 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.60+1396G>C | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71156223 | ||||||
| chr12:71156250
|
C | CA | 6 | a0001c0001t0001g0133a0002c0002t0002g0126a0002c0002t0002g0127others(3): Show | 6 | HG02109.hp1 HG02559.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.60+1368dupT | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71156250 | ||||||
| chr12:71156250
|
C | CAAAAAAA | 6 | a0001c0001t0001g0055a0001c0001t0001g0267a0001c0001t0001g0268others(3): Show | 7 | HG02257.hp2 HG02622.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.60+1362_60+1368dup others(7): Show |
TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71156250 | ||||||
| chr12:71156250
|
C | CAAAAAAA others(2): Show |
6 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0269others(3): Show | 7 | HG01167.hp2 HG01361.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.60+1360_60+1368dup others(9): Show |
TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71156250 | ||||||
| chr12:71156250
|
C | CAAAAAAA others(3): Show |
2 | a0001c0001t0001g0270a0001c0001t0001g0271 | 2 | HG03017.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.60+1359_60+1368dup others(10): Show |
TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71156250 | ||||||
| chr12:71156250
|
C | CAAAAAAA others(4): Show |
2 | a0001c0001t0001g0272a0008c0009t0001g0273 | 2 | HG03704.hp2 NA18967.hp1 |
intron_variant | MODIFIER | c.60+1358_60+1368dup others(11): Show |
TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71156250 | ||||||
| chr12:71156250
|
C | CAAAAAAA others(5): Show |
2 | a0001c0001t0004g0058a0004c0005t0002g0069 | 2 | HG03540.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.60+1357_60+1368dup others(12): Show |
TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71156250 | ||||||
| chr12:71156250
|
C | CAAAAAAA others(6): Show |
2 | a0001c0001t0001g0026a0001c0001t0001g0070 | 3 | HG01993.hp2 NA20300.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.60+1356_60+1368dup others(13): Show |
TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71156250 | ||||||
| chr12:71156250
|
C | CAAAAAAA others(7): Show |
4 | a0001c0001t0001g0027a0001c0001t0001g0060a0001c0001t0001g0061others(1): Show | 5 | HG00735.hp1 HG01952.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.60+1355_60+1368dup others(14): Show |
TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71156250 | ||||||
| chr12:71156250
|
C | CAAAAAAA others(8): Show |
6 | a0001c0001t0001g0054a0001c0001t0001g0062a0001c0001t0001g0230others(3): Show | 7 | HG01109.hp2 HG01496.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.60+1354_60+1368dup others(15): Show |
TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71156250 | ||||||
| chr12:71156250
|
C | CAAAAAAA others(9): Show |
2 | a0001c0001t0001g0063a0001c0001t0001g0064 | 2 | HG02818.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.60+1353_60+1368dup others(16): Show |
TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71156250 | ||||||
| chr12:71156250
|
C | CAAAAAAA others(11): Show |
1 | a0001c0001t0001g0274 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.60+1351_60+1368dup others(18): Show |
TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71156250 | ||||||
| chr12:71156250
|
C | CAAAAAAA others(16): Show |
1 | a0001c0001t0001g0164 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.60+1368_60+1369ins others(23): Show |
TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71156250 | ||||||
| chr12:71156255
|
AAAAAAAA others(11): Show |
A | 1 | a0001c0001t0001g0236 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.60+1346_60+1363del others(18): Show |
TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71156255 | ||||||
| chr12:71156257
|
AAAAAAAA others(9): Show |
A | 1 | a0004c0005t0002g0237 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.60+1346_60+1361del others(16): Show |
TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71156257 | ||||||
| chr12:71156258
|
AAAAAAAA others(8): Show |
A | 1 | a0004c0005t0002g0238 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.60+1346_60+1360del others(15): Show |
TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71156258 | ||||||
| chr12:71156260
|
AAAAAAAA others(6): Show |
A | 16 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0166others(13): Show | 23 | HG00140.hp1 HG00738.hp1 HG01106.hp1 others(20): Show |
intron_variant | MODIFIER | c.60+1346_60+1358del others(13): Show |
TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71156260 | ||||||
| chr12:71156261
|
AAAAAAAA others(5): Show |
A | 26 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0050others(23): Show | 43 | HG00099.hp2 HG00140.hp2 HG00621.hp1 others(40): Show |
intron_variant | MODIFIER | c.60+1346_60+1357del others(12): Show |
TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71156261 | ||||||
| chr12:71156262
|
AAAAAAAC others(4): Show |
A | 4 | a0001c0001t0001g0259a0001c0001t0001g0261a0001c0001t0002g0260others(1): Show | 4 | HG01123.hp2 HG01891.hp1 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.60+1346_60+1356del others(11): Show |
TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71156262 | ||||||
| chr12:71156265
|
AAAAC | A | 22 | a0001c0001t0001g0044a0001c0001t0001g0223a0001c0001t0001g0266others(19): Show | 24 | HG00438.hp1 HG00544.hp1 HG00673.hp1 others(21): Show |
intron_variant | MODIFIER | c.60+1350_60+1353del others(4): Show |
TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71156265 | ||||||
| chr12:71156266
|
AAACAAAC | A | 7 | a0001c0003t0001g0135a0001c0003t0001g0136a0001c0003t0001g0138others(4): Show | 12 | HG02080.hp2 HG04115.hp2 NA18964.hp1 others(9): Show |
intron_variant | MODIFIER | c.60+1346_60+1352del others(7): Show |
TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71156266 | ||||||
| chr12:71156267
|
AACAAAC | A | 35 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0039others(32): Show | 61 | HG00544.hp2 HG00609.hp2 HG00639.hp2 others(58): Show |
intron_variant | MODIFIER | c.60+1346_60+1351del others(6): Show |
TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71156267 | ||||||
| chr12:71156268
|
ACAAAC | A | 61 | a0001c0001t0001g0023a0001c0001t0001g0042a0001c0001t0001g0043others(58): Show | 87 | HG00423.hp1 HG00423.hp2 HG00558.hp1 others(84): Show |
intron_variant | MODIFIER | c.60+1346_60+1350del others(5): Show |
TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71156268 | ||||||
| chr12:71156269
|
C | A | 38 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0054others(35): Show | 44 | HG00735.hp1 HG01109.hp2 HG01167.hp2 others(41): Show |
intron_variant | MODIFIER | c.60+1350G>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71156269 | ||||||
| chr12:71156270
|
A | C | 1 | a0004c0005t0002g0129 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.60+1349T>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71156270 | ||||||
| chr12:71156273
|
C | A | 72 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0044others(69): Show | 82 | HG00438.hp1 HG00544.hp1 HG00673.hp1 others(79): Show |
intron_variant | MODIFIER | c.60+1346G>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71156273 | ||||||
| chr12:71156435
|
T | G | 1 | a0001c0001t0001g0233 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.60+1184A>C | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71156435 | ||||||
| chr12:71156441
|
AAGCAGCC others(20): Show |
A | 92 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0056others(89): Show | 121 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.60+1151_60+1177del others(27): Show |
TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71156441 | ||||||
| chr12:71156643
|
T | G | 1 | a0001c0001t0001g0275 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.60+976A>C | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71156643 | ||||||
| chr12:71156649
|
T | C | 60 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0022others(57): Show | 85 | HG00099.hp2 HG00140.hp2 HG00621.hp1 others(82): Show |
intron_variant | MODIFIER | c.60+970A>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71156649 | ||||||
| chr12:71156901
|
T | C | 5 | a0001c0001t0001g0055a0001c0001t0001g0276a0001c0001t0001g0277others(2): Show | 6 | HG01884.hp2 HG02257.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.60+718A>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71156901 | ||||||
| chr12:71156917
|
T | C | 225 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(222): Show | 316 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(313): Show |
intron_variant | MODIFIER | c.60+702A>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71156917 | ||||||
| chr12:71157021
|
T | G | 1 | a0003c0004t0001g0280 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.60+598A>C | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71157021 | ||||||
| chr12:71157060
|
A | C | 1 | a0001c0003t0001g0075 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.60+559T>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71157060 | ||||||
| chr12:71157210
|
C | CA | 12 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0001g0281others(9): Show | 14 | HG02258.hp1 HG02280.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.60+408dupT | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71157210 | ||||||
| chr12:71157217
|
A | G | 3 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0074 | 3 | HG02723.hp1 HG02922.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.60+402T>C | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71157217 | ||||||
| chr12:71157342
|
G | A | 1 | a0004c0005t0002g0291 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.60+277C>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71157342 | ||||||
| chr12:71157412
|
A | G | 5 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0070others(2): Show | 7 | HG00735.hp1 HG01952.hp1 HG01993.hp2 others(4): Show |
intron_variant | MODIFIER | c.60+207T>C | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71157412 | ||||||
| chr12:71157866
|
A | G | 5 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0062others(2): Show | 5 | HG01109.hp2 HG02818.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.-110+64T>C | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 1/8 | chr12 | 71157866 | ||||||
| chr12:71157879
|
GCAAAGGC others(25): Show |
G | 1 | a0002c0002t0002g0294 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-110+19_-110+50del others(32): Show |
TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 1/8 | chr12 | 71157879 | ||||||
| chr12:71157897
|
C | A | 1 | a0003c0004t0001g0293 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.-110+33G>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 1/8 | chr12 | 71157897 |