| geneid | 23471 |
|---|---|
| ensemblid | ENSG00000067167.8 |
| hgncid | 20568 |
| symbol | TRAM1 |
| name | translocation associated membrane protein 1 |
| refseq_nuc | NM_014294.6 |
| refseq_prot | NP_055109.1 |
| ensembl_nuc | ENST00000262213.7 |
| ensembl_prot | ENSP00000262213.2 |
| mane_status | MANE Select |
| chr | chr8 |
| start | 70573218 |
| end | 70608416 |
| strand | - |
| ver | v1.2 |
| region | chr8:70573218-70608416 |
| region5000 | chr8:70568218-70613416 |
| regionname0 | TRAM1_chr8_70573218_70608416 |
| regionname5000 | TRAM1_chr8_70568218_70613416 |
| 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 | 374 | 321 | 80 | 62 | 131 | 12 | 34 | 109 | TRAM1_chr8_70568218_70613416 | TRAM1 | copy fasta | chr8 | 70568218 | 70613416 |
| a0002 | 0/0 | 374 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | copy fasta | chr8 | 70568218 | 70613416 |
| a0003 | 0/0 | 374 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TRAM1_chr8_70568218_70613416 | TRAM1 | copy fasta | chr8 | 70568218 | 70613416 |
| a0004 | 0/0 | 374 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | copy fasta | chr8 | 70568218 | 70613416 |
| a0005 | 0/0 | 374 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | copy fasta | chr8 | 70568218 | 70613416 |
| 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 | 1125 | 318 | 80 | 62 | 128 | 12 | 34 | TRAM1_chr8_70568218_70613416 | TRAM1 | copy fasta | chr8 | 70568218 | 70613416 |
| c0002 | 0/0 | 1125 | 6 | 6 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | copy fasta | chr8 | 70568218 | 70613416 |
| c0003 | 0/0 | 1125 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | copy fasta | chr8 | 70568218 | 70613416 |
| c0004 | 0/0 | 1125 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | copy fasta | chr8 | 70568218 | 70613416 |
| c0005 | 0/0 | 1125 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | copy fasta | chr8 | 70568218 | 70613416 |
| c0006 | 0/0 | 1125 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | copy fasta | chr8 | 70568218 | 70613416 |
| c0007 | 0/0 | 1125 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | copy fasta | chr8 | 70568218 | 70613416 |
| c0008 | 0/0 | 1125 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | copy fasta | chr8 | 70568218 | 70613416 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/1 | 1933 | 188 | 41 | 29 | 89 | 8 | 20 | TRAM1_chr8_70568218_70613416 | TRAM1 | copy fasta | chr8 | 70568218 | 70613416 |
| t0002 | 1/0 | 1932 | 56 | 5 | 14 | 32 | 1 | 3 | TRAM1_chr8_70568218_70613416 | TRAM1 | copy fasta | chr8 | 70568218 | 70613416 |
| t0003 | 0/0 | 1933 | 49 | 30 | 7 | 6 | 0 | 6 | TRAM1_chr8_70568218_70613416 | TRAM1 | copy fasta | chr8 | 70568218 | 70613416 |
| t0004 | 0/0 | 1934 | 9 | 0 | 2 | 3 | 0 | 4 | TRAM1_chr8_70568218_70613416 | TRAM1 | copy fasta | chr8 | 70568218 | 70613416 |
| t0005 | 0/0 | 1933 | 7 | 1 | 4 | 0 | 2 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | copy fasta | chr8 | 70568218 | 70613416 |
| t0006 | 0/0 | 1933 | 3 | 1 | 1 | 0 | 1 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | copy fasta | chr8 | 70568218 | 70613416 |
| t0007 | 0/0 | 1931 | 3 | 2 | 1 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | copy fasta | chr8 | 70568218 | 70613416 |
| t0008 | 0/0 | 1933 | 3 | 3 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | copy fasta | chr8 | 70568218 | 70613416 |
| t0009 | 0/0 | 1935 | 2 | 1 | 1 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | copy fasta | chr8 | 70568218 | 70613416 |
| t0010 | 0/0 | 1933 | 2 | 2 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | copy fasta | chr8 | 70568218 | 70613416 |
| t0011 | 0/0 | 1934 | 2 | 1 | 1 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | copy fasta | chr8 | 70568218 | 70613416 |
| t0012 | 0/0 | 1933 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | copy fasta | chr8 | 70568218 | 70613416 |
| t0013 | 0/0 | 1933 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | copy fasta | chr8 | 70568218 | 70613416 |
| t0014 | 0/0 | 1933 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | copy fasta | chr8 | 70568218 | 70613416 |
| t0015 | 0/0 | 1935 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM1_chr8_70568218_70613416 | TRAM1 | copy fasta | chr8 | 70568218 | 70613416 |
| t0016 | 0/0 | 1933 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | copy fasta | chr8 | 70568218 | 70613416 |
| t0017 | 0/0 | 1933 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | copy fasta | chr8 | 70568218 | 70613416 |
| 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 | 12 | 0 | 2 | 9 | 0 | 1 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0002 | 0/0 | 12 | 0 | 0 | 11 | 0 | 1 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0003 | 0/0 | 9 | 4 | 2 | 2 | 0 | 1 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0004 | 0/0 | 8 | 0 | 6 | 2 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0005 | 0/0 | 6 | 0 | 4 | 0 | 0 | 2 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0006 | 0/0 | 6 | 0 | 2 | 0 | 2 | 2 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0007 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0008 | 0/0 | 5 | 1 | 3 | 0 | 1 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0009 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0010 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0011 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0012 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0013 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0014 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0015 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0016 | 0/0 | 4 | 0 | 3 | 0 | 0 | 1 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0017 | 1/0 | 3 | 0 | 1 | 0 | 1 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0018 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0020 | 0/0 | 3 | 1 | 1 | 0 | 1 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0021 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0024 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0025 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0026 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0032 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0034 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0038 | 0/1 | 2 | 0 | 0 | 0 | 0 | 1 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0184 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0194 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| 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 | 1125 | 318 | 80 | 62 | 128 | 12 | 34 | TRAM1_chr8_70568218_70613416 | TRAM1 | copy fasta | chr8 | 70568218 | 70613416 |
| a0001c0003 | 0/0 | 1125 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | copy fasta | chr8 | 70568218 | 70613416 |
| a0001c0007 | 0/0 | 1125 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | copy fasta | chr8 | 70568218 | 70613416 |
| a0001c0008 | 0/0 | 1125 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | copy fasta | chr8 | 70568218 | 70613416 |
| a0002c0002 | 0/0 | 1125 | 6 | 6 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | copy fasta | chr8 | 70568218 | 70613416 |
| a0003c0004 | 0/0 | 1125 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | copy fasta | chr8 | 70568218 | 70613416 |
| a0004c0006 | 0/0 | 1125 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | copy fasta | chr8 | 70568218 | 70613416 |
| a0005c0005 | 0/0 | 1125 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | copy fasta | chr8 | 70568218 | 70613416 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 3057 | 183 | 40 | 29 | 85 | 8 | 20 | TRAM1_chr8_70568218_70613416 | TRAM1 | copy fasta | chr8 | 70568218 | 70613416 |
| a0001c0001t0002 | 1/0 | 3056 | 56 | 5 | 14 | 32 | 1 | 3 | TRAM1_chr8_70568218_70613416 | TRAM1 | copy fasta | chr8 | 70568218 | 70613416 |
| a0001c0001t0003 | 0/0 | 3057 | 45 | 26 | 7 | 6 | 0 | 6 | TRAM1_chr8_70568218_70613416 | TRAM1 | copy fasta | chr8 | 70568218 | 70613416 |
| a0001c0001t0004 | 0/0 | 3058 | 9 | 0 | 2 | 3 | 0 | 4 | TRAM1_chr8_70568218_70613416 | TRAM1 | copy fasta | chr8 | 70568218 | 70613416 |
| a0001c0001t0005 | 0/0 | 3057 | 7 | 1 | 4 | 0 | 2 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | copy fasta | chr8 | 70568218 | 70613416 |
| a0001c0001t0006 | 0/0 | 3057 | 3 | 1 | 1 | 0 | 1 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | copy fasta | chr8 | 70568218 | 70613416 |
| a0001c0001t0007 | 0/0 | 3055 | 3 | 2 | 1 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | copy fasta | chr8 | 70568218 | 70613416 |
| a0001c0001t0008 | 0/0 | 3057 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | copy fasta | chr8 | 70568218 | 70613416 |
| a0001c0001t0009 | 0/0 | 3059 | 2 | 1 | 1 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | copy fasta | chr8 | 70568218 | 70613416 |
| a0001c0001t0010 | 0/0 | 3057 | 2 | 2 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | copy fasta | chr8 | 70568218 | 70613416 |
| a0001c0001t0011 | 0/0 | 3058 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | copy fasta | chr8 | 70568218 | 70613416 |
| a0001c0001t0012 | 0/0 | 3057 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | copy fasta | chr8 | 70568218 | 70613416 |
| a0001c0001t0013 | 0/0 | 3057 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | copy fasta | chr8 | 70568218 | 70613416 |
| a0001c0001t0014 | 0/0 | 3057 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | copy fasta | chr8 | 70568218 | 70613416 |
| a0001c0001t0015 | 0/0 | 3059 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM1_chr8_70568218_70613416 | TRAM1 | copy fasta | chr8 | 70568218 | 70613416 |
| a0001c0001t0016 | 0/0 | 3057 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | copy fasta | chr8 | 70568218 | 70613416 |
| a0001c0001t0017 | 0/0 | 3057 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | copy fasta | chr8 | 70568218 | 70613416 |
| a0001c0003t0001 | 0/0 | 3057 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | copy fasta | chr8 | 70568218 | 70613416 |
| a0001c0007t0001 | 0/0 | 3057 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | copy fasta | chr8 | 70568218 | 70613416 |
| a0001c0008t0001 | 0/0 | 3057 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | copy fasta | chr8 | 70568218 | 70613416 |
| a0002c0002t0003 | 0/0 | 3057 | 4 | 4 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | copy fasta | chr8 | 70568218 | 70613416 |
| a0002c0002t0008 | 0/0 | 3057 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | copy fasta | chr8 | 70568218 | 70613416 |
| a0002c0002t0011 | 0/0 | 3058 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | copy fasta | chr8 | 70568218 | 70613416 |
| a0003c0004t0001 | 0/0 | 3057 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | copy fasta | chr8 | 70568218 | 70613416 |
| a0004c0006t0008 | 0/0 | 3057 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | copy fasta | chr8 | 70568218 | 70613416 |
| a0005c0005t0001 | 0/0 | 3057 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | copy fasta | chr8 | 70568218 | 70613416 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 12 | 0 | 0 | 11 | 0 | 1 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0003 | 0/0 | 9 | 4 | 2 | 2 | 0 | 1 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0006 | 0/0 | 6 | 0 | 2 | 0 | 2 | 2 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0007 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0013 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0014 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0016 | 0/0 | 4 | 0 | 3 | 0 | 0 | 1 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0018 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0026 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0038 | 0/1 | 2 | 0 | 0 | 0 | 0 | 1 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0002g0001 | 0/0 | 12 | 0 | 2 | 9 | 0 | 1 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0002g0004 | 0/0 | 8 | 0 | 6 | 2 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0002g0009 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0002g0010 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0002g0011 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0002g0017 | 1/0 | 3 | 0 | 1 | 0 | 1 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0002g0021 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0002g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0002g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0003g0005 | 0/0 | 6 | 0 | 4 | 0 | 0 | 2 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0003g0012 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0003g0015 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0003g0032 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0003g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0003g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0003g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0003g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0003g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0003g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0003g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0003g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0003g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0003g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0003g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0003g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0003g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0003g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0003g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0003g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0003g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0003g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0003g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0003g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0003g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0003g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0003g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0003g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0003g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0003g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0004g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0004g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0004g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0004g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0004g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0004g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0004g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0004g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0004g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0005g0008 | 0/0 | 5 | 1 | 3 | 0 | 1 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0005g0184 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0005g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0006g0020 | 0/0 | 3 | 1 | 1 | 0 | 1 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0007g0034 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0007g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0008g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0009g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0009g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0010g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0010g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0011g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0012g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0013g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0014g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0015g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0016g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0017g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0003t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0007t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0008t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0002c0002t0003g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0002c0002t0003g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0002c0002t0003g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0002c0002t0003g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0002c0002t0008g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0002c0002t0011g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0003c0004t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0004c0006t0008g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0005c0005t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0017 | EUR | GBR | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0025 | EUR | GBR | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0006 | EUR | GBR | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG00140 | hp2 | a0001 | c0001 | t0006 | g0020 | EUR | GBR | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0128 | EUR | FIN | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG00323 | hp2 | a0001 | c0001 | t0005 | g0184 | EUR | FIN | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | CHS | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | CHS | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | CHS | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG00609 | hp2 | a0001 | c0008 | t0001 | g0211 | EAS | CHS | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | CHS | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | CHS | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0017 | AMR | PUR | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0070 | AMR | PUR | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG00673 | hp1 | a0001 | c0001 | t0003 | g0171 | EAS | CHS | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | CHS | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0198 | AMR | PUR | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0209 | AMR | PUR | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG00738 | hp2 | a0001 | c0001 | t0003 | g0173 | AMR | PUR | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG01071 | hp1 | a0001 | c0001 | t0006 | g0020 | AMR | PUR | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0102 | AMR | PUR | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0075 | AMR | PUR | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0117 | AMR | PUR | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0139 | AMR | PUR | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG01106 | hp2 | a0001 | c0001 | t0009 | g0174 | AMR | PUR | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG01109 | hp1 | a0001 | c0001 | t0007 | g0034 | AMR | PUR | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0188 | AMR | PUR | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG01167 | hp2 | a0001 | c0001 | t0016 | g0159 | AMR | PUR | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG01168 | hp1 | a0001 | c0001 | t0005 | g0008 | AMR | PUR | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0068 | AMR | PUR | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0069 | AMR | PUR | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG01175 | hp1 | a0001 | c0001 | t0005 | g0185 | AMR | PUR | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0104 | AMR | PUR | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG01192 | hp1 | a0001 | c0001 | t0011 | g0220 | AMR | PUR | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0011 | AMR | PUR | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0089 | AMR | PUR | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG01243 | hp2 | a0001 | c0001 | t0003 | g0165 | AMR | PUR | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG01255 | hp1 | a0001 | c0001 | t0003 | g0005 | AMR | CLM | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0197 | AMR | CLM | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | CLM | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG01256 | hp2 | a0001 | c0001 | t0005 | g0008 | AMR | CLM | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | CLM | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG01261 | hp2 | a0001 | c0001 | t0004 | g0216 | AMR | CLM | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG01433 | hp1 | a0001 | c0001 | t0005 | g0008 | AMR | CLM | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | CLM | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | CLM | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | CLM | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0006 | EUR | IBS | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0107 | EUR | IBS | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | ACB | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG01884 | hp2 | a0001 | c0001 | t0003 | g0015 | AFR | ACB | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG01891 | hp1 | a0001 | c0001 | t0003 | g0161 | AFR | ACB | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0115 | AFR | ACB | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0055 | AMR | PEL | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG01934 | hp2 | a0001 | c0001 | t0004 | g0214 | AMR | PEL | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PEL | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0011 | AMR | PEL | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG01978 | hp1 | a0001 | c0001 | t0003 | g0032 | AMR | PEL | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG01978 | hp2 | a0001 | c0001 | t0003 | g0005 | AMR | PEL | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG01993 | hp2 | a0001 | c0001 | t0003 | g0005 | AMR | PEL | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0196 | AMR | PEL | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | PEL | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | KHV | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | KHV | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG02055 | hp1 | a0001 | c0001 | t0003 | g0160 | AFR | ACB | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG02055 | hp2 | a0001 | c0001 | t0003 | g0035 | AFR | ACB | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | KHV | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG02071 | hp2 | a0001 | c0001 | t0002 | g0050 | EAS | KHV | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0052 | EAS | KHV | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | KHV | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0057 | EAS | KHV | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | KHV | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | KHV | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0097 | AFR | ACB | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG02145 | hp2 | a0001 | c0001 | t0003 | g0177 | AFR | ACB | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG02148 | hp1 | a0001 | c0001 | t0003 | g0005 | AMR | PEL | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG02148 | hp2 | a0001 | c0001 | t0002 | g0042 | AMR | PEL | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG02257 | hp1 | a0001 | c0001 | t0006 | g0020 | AFR | ACB | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ACB | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0208 | AFR | ACB | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0190 | AFR | ACB | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG02280 | hp2 | a0001 | c0001 | t0007 | g0034 | AFR | ACB | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0138 | AMR | PEL | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG02293 | hp2 | a0001 | c0001 | t0002 | g0011 | AMR | PEL | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG02451 | hp1 | a0001 | c0001 | t0003 | g0012 | AFR | ACB | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG02451 | hp2 | a0001 | c0001 | t0002 | g0009 | AFR | ACB | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG02572 | hp1 | a0001 | c0001 | t0009 | g0162 | AFR | GWD | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG02572 | hp2 | a0001 | c0001 | t0003 | g0012 | AFR | GWD | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | GWD | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG02615 | hp2 | a0001 | c0001 | t0002 | g0009 | AFR | GWD | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0066 | AFR | GWD | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG02622 | hp2 | a0001 | c0001 | t0003 | g0064 | AFR | GWD | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0112 | AFR | GWD | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG02630 | hp2 | a0001 | c0001 | t0003 | g0098 | AFR | GWD | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG02647 | hp1 | a0001 | c0001 | t0010 | g0166 | AFR | GWD | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG02683 | hp1 | a0001 | c0001 | t0003 | g0172 | SAS | PJL | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG02717 | hp1 | a0001 | c0001 | t0003 | g0168 | AFR | GWD | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG02717 | hp2 | a0001 | c0001 | t0003 | g0084 | AFR | GWD | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0101 | AFR | GWD | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG02723 | hp2 | a0001 | c0001 | t0003 | g0164 | AFR | GWD | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0076 | SAS | PJL | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0021 | SAS | PJL | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0073 | SAS | PJL | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG02738 | hp2 | a0001 | c0001 | t0004 | g0222 | SAS | PJL | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG02809 | hp1 | a0001 | c0001 | t0002 | g0041 | AFR | GWD | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG02809 | hp2 | a0001 | c0001 | t0003 | g0015 | AFR | GWD | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | GWD | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | GWD | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0151 | AFR | GWD | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0124 | AFR | GWD | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG02897 | hp2 | a0001 | c0001 | t0002 | g0009 | AFR | GWD | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0088 | AFR | ESN | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0110 | AFR | ESN | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG02965 | hp1 | a0001 | c0001 | t0003 | g0012 | AFR | ESN | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | ESN | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0009 | AFR | ESN | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG02970 | hp2 | a0001 | c0001 | t0008 | g0153 | AFR | ESN | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG02976 | hp1 | a0001 | c0001 | t0003 | g0035 | AFR | ESN | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG02976 | hp2 | a0001 | c0001 | t0003 | g0079 | AFR | ESN | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0126 | SAS | PJL | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | GWD | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0148 | AFR | GWD | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0100 | AFR | MSL | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | MSL | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG03139 | hp1 | a0004 | c0006 | t0008 | g0154 | AFR | ESN | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG03195 | hp2 | a0001 | c0001 | t0007 | g0077 | AFR | ESN | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG03209 | hp1 | a0002 | c0002 | t0003 | g0180 | AFR | MSL | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG03209 | hp2 | a0001 | c0001 | t0003 | g0178 | AFR | MSL | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG03225 | hp1 | a0001 | c0001 | t0003 | g0170 | AFR | MSL | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG03225 | hp2 | a0001 | c0001 | t0010 | g0167 | AFR | MSL | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0016 | SAS | PJL | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | MSL | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG03453 | hp2 | a0002 | c0002 | t0003 | g0179 | AFR | MSL | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0087 | AFR | MSL | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG03486 | hp2 | a0001 | c0001 | t0003 | g0080 | AFR | MSL | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0024 | SAS | PJL | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0193 | SAS | PJL | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0024 | SAS | PJL | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG03516 | hp1 | a0002 | c0002 | t0011 | g0221 | AFR | ESN | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0067 | AFR | ESN | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0095 | AFR | GWD | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG03579 | hp1 | a0001 | c0001 | t0003 | g0012 | AFR | MSL | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | MSL | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG03669 | hp1 | a0001 | c0001 | t0003 | g0005 | SAS | PJL | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG03669 | hp2 | a0001 | c0001 | t0003 | g0182 | SAS | PJL | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0026 | SAS | PJL | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0021 | SAS | PJL | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0114 | SAS | PJL | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0038 | SAS | PJL | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG03831 | hp1 | a0001 | c0001 | t0004 | g0217 | SAS | BEB | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG03831 | hp2 | a0001 | c0001 | t0004 | g0215 | SAS | BEB | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG03927 | hp1 | a0001 | c0001 | t0003 | g0175 | SAS | BEB | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0133 | SAS | BEB | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG03942 | hp1 | a0001 | c0001 | t0015 | g0103 | SAS | BEB | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0200 | SAS | BEB | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0096 | SAS | BEB | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG04184 | hp2 | a0001 | c0001 | t0004 | g0219 | SAS | BEB | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG04199 | hp1 | a0001 | c0001 | t0003 | g0005 | SAS | STU | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0113 | SAS | STU | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | STU | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG04204 | hp2 | a0001 | c0001 | t0003 | g0176 | SAS | STU | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0141 | SAS | STU | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0150 | SAS | STU | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA18522 | hp1 | a0002 | c0002 | t0003 | g0155 | AFR | YRI | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA18522 | hp2 | a0001 | c0001 | t0014 | g0078 | AFR | YRI | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA18906 | hp1 | a0001 | c0001 | t0003 | g0036 | AFR | YRI | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0090 | AFR | YRI | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA18939 | hp1 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0047 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0045 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA18954 | hp2 | a0001 | c0001 | t0002 | g0044 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA18959 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA18962 | hp1 | a0003 | c0004 | t0001 | g0061 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA18965 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA18968 | hp2 | a0001 | c0001 | t0003 | g0158 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA18972 | hp1 | a0001 | c0001 | t0003 | g0033 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA18974 | hp2 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA18975 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA18981 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA18992 | hp1 | a0001 | c0001 | t0002 | g0043 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA18993 | hp2 | a0001 | c0001 | t0002 | g0046 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA18997 | hp1 | a0001 | c0001 | t0002 | g0054 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA18999 | hp2 | a0001 | c0001 | t0012 | g0060 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA19005 | hp2 | a0001 | c0001 | t0003 | g0033 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA19010 | hp1 | a0001 | c0001 | t0004 | g0218 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA19010 | hp2 | a0001 | c0001 | t0004 | g0223 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA19012 | hp1 | a0001 | c0001 | t0004 | g0213 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA19030 | hp1 | a0001 | c0001 | t0003 | g0169 | AFR | LWK | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0072 | AFR | LWK | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | LWK | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA19043 | hp2 | a0001 | c0001 | t0003 | g0163 | AFR | LWK | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA19054 | hp1 | a0001 | c0003 | t0001 | g0187 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA19055 | hp2 | a0001 | c0001 | t0002 | g0059 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA19058 | hp2 | a0001 | c0001 | t0002 | g0051 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0049 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA19066 | hp2 | a0001 | c0001 | t0013 | g0111 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA19068 | hp1 | a0001 | c0007 | t0001 | g0149 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA19068 | hp2 | a0001 | c0001 | t0003 | g0032 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA19072 | hp1 | a0001 | c0001 | t0002 | g0056 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA19074 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA19077 | hp2 | a0001 | c0001 | t0003 | g0157 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA19081 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0058 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA19240 | hp1 | a0001 | c0001 | t0003 | g0036 | AFR | YRI | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | YRI | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA20129 | hp1 | a0001 | c0001 | t0005 | g0008 | AFR | ASW | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA20129 | hp2 | a0001 | c0001 | t0003 | g0015 | AFR | ASW | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA20752 | hp1 | a0001 | c0001 | t0005 | g0008 | EUR | TSI | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0082 | EUR | TSI | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0118 | EUR | TSI | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0194 | EUR | TSI | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0106 | AMR | CLM | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG01123 | hp2 | a0001 | c0001 | t0017 | g0212 | AMR | CLM | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0065 | AFR | MSL | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | MSL | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG06807 | hp1 | a0001 | c0001 | t0003 | g0015 | AFR | USA | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG06807 | hp2 | a0002 | c0002 | t0008 | g0156 | AFR | USA | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | USA | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA20300 | hp2 | a0002 | c0002 | t0003 | g0181 | AFR | USA | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA21309 | hp1 | a0005 | c0005 | t0001 | g0152 | AFR | LWK | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | LWK | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0038 | REF | REF | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0017 | REF | REF | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:70574975
|
T | C | 1 | a0004 | 1 | HG03139.hp1 | missense_variant | MODERATE | c.1082A>G | p.Asn361Ser | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 11/11 | 1299/3056 | 1082/1125 | 361/374 | chr8 | 70574975 | ||
| chr8:70583738
|
A | T | 1 | a0005 | 1 | NA21309.hp1 | missense_variant | MODERATE | c.802T>A | p.Ser268Thr | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 9/11 | 1019/3056 | 802/1125 | 268/374 | chr8 | 70583738 | ||
| chr8:70596265
|
C | T | 1 | a0003 | 1 | NA18962.hp1 | missense_variant&splice_region_variant | MODERATE | c.483G>A | p.Met161Ile | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 5/11 | 700/3056 | 483/1125 | 161/374 | chr8 | 70596265 | ||
| chr8:70596318
|
T | C | 1 | a0002 | 6 | HG03209.hp1 HG03453.hp2 HG03516.hp1 others(3): Show |
missense_variant | MODERATE | c.430A>G | p.Asn144Asp | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 5/11 | 647/3056 | 430/1125 | 144/374 | chr8 | 70596318 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:70583314
|
G | A | 1 | a0001c0007 | 1 | NA19068.hp1 | synonymous_variant | LOW | c.901C>T | p.Leu301Leu | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 10/11 | 1118/3056 | 901/1125 | 301/374 | chr8 | 70583314 | ||
| chr8:70597940
|
C | T | 1 | a0001c0003 | 1 | NA19054.hp1 | synonymous_variant | LOW | c.381G>A | p.Ala127Ala | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 4/11 | 598/3056 | 381/1125 | 127/374 | chr8 | 70597940 | ||
| chr8:70608101
|
G | A | 1 | a0001c0008 | 1 | HG00609.hp2 | synonymous_variant | LOW | c.99C>T | p.Val33Val | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/11 | 316/3056 | 99/1125 | 33/374 | chr8 | 70608101 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:70573247
|
T | C | 3 | a0001c0001t0008a0002c0002t0008a0004c0006t0008 | 3 | HG02970.hp2 HG03139.hp1 HG06807.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1685A>G | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 11/11 | 1685 | chr8 | 70573247 | |||||
| chr8:70573283
|
C | A | 1 | a0001c0001t0010 | 2 | HG02647.hp1 HG03225.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1649G>T | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 11/11 | 1649 | chr8 | 70573283 | |||||
| chr8:70573408
|
A | T | 14 | a0001c0001t0001a0001c0001t0004a0001c0001t0005others(11): Show | 210 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(207): Show |
3_prime_UTR_variant | MODIFIER | c.*1524T>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 11/11 | 1524 | chr8 | 70573408 | |||||
| chr8:70573793
|
A | G | 2 | a0001c0001t0014a0001c0001t0016 | 2 | HG01167.hp2 NA18522.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1139T>C | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 11/11 | 1139 | chr8 | 70573793 | |||||
| chr8:70573850
|
A | C | 14 | a0001c0001t0001a0001c0001t0004a0001c0001t0005others(11): Show | 210 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(207): Show |
3_prime_UTR_variant | MODIFIER | c.*1082T>G | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 11/11 | 1082 | chr8 | 70573850 | |||||
| chr8:70573851
|
G | A | 1 | a0001c0001t0005 | 7 | HG00323.hp2 HG01168.hp1 HG01175.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1081C>T | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 11/11 | 1081 | chr8 | 70573851 | |||||
| chr8:70573857
|
A | AAT | 2 | a0001c0001t0009a0001c0001t0015 | 3 | HG01106.hp2 HG02572.hp1 HG03942.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1073_*1074dupAT | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 11/11 | 1074 | chr8 | 70573857 | |||||
| chr8:70573857
|
AAT | A | 1 | a0001c0001t0007 | 3 | HG01109.hp1 HG02280.hp2 HG03195.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1073_*1074delAT | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 11/11 | 1073 | chr8 | 70573857 | |||||
| chr8:70573964
|
G | T | 1 | a0001c0001t0006 | 3 | HG00140.hp2 HG01071.hp1 HG02257.hp1 |
3_prime_UTR_variant | MODIFIER | c.*968C>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 11/11 | 968 | chr8 | 70573964 | |||||
| chr8:70574333
|
G | C | 17 | a0001c0001t0001a0001c0001t0004a0001c0001t0005others(14): Show | 213 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(210): Show |
3_prime_UTR_variant | MODIFIER | c.*599C>G | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 11/11 | 599 | chr8 | 70574333 | |||||
| chr8:70574556
|
T | G | 3 | a0001c0001t0008a0002c0002t0008a0004c0006t0008 | 3 | HG02970.hp2 HG03139.hp1 HG06807.hp2 |
3_prime_UTR_variant | MODIFIER | c.*376A>C | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 11/11 | 376 | chr8 | 70574556 | |||||
| chr8:70574557
|
T | C | 3 | a0001c0001t0008a0002c0002t0008a0004c0006t0008 | 3 | HG02970.hp2 HG03139.hp1 HG06807.hp2 |
3_prime_UTR_variant | MODIFIER | c.*375A>G | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 11/11 | 375 | chr8 | 70574557 | |||||
| chr8:70574809
|
C | T | 2 | a0001c0001t0013a0001c0001t0014 | 2 | NA18522.hp2 NA19066.hp2 |
3_prime_UTR_variant | MODIFIER | c.*123G>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 11/11 | 123 | chr8 | 70574809 | |||||
| chr8:70608218
|
G | T | 1 | a0001c0001t0012 | 1 | NA18999.hp2 | 5_prime_UTR_variant | MODIFIER | c.-19C>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/11 | 19 | chr8 | 70608218 | |||||
| chr8:70608298
|
G | A | 1 | a0001c0001t0017 | 1 | HG01123.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-99C>T | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/11 | chr8 | 70608298 | ||||||
| chr8:70608373
|
G | GA | 22 | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(19): Show | 263 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(260): Show |
5_prime_UTR_variant | MODIFIER | c.-175dupT | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/11 | 175 | chr8 | 70608373 | |||||
| chr8:70608373
|
G | GAA | 3 | a0001c0001t0004a0001c0001t0011a0002c0002t0011 | 11 | HG01192.hp1 HG01261.hp2 HG01934.hp2 others(8): Show |
5_prime_UTR_variant | MODIFIER | c.-176_-175dupTT | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/11 | 175 | chr8 | 70608373 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:70575159
|
T | G | 4 | a0001c0001t0003g0035a0001c0001t0003g0168a0001c0001t0003g0169others(1): Show | 5 | HG02055.hp2 HG02717.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1052-154A>C | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 10/10 | chr8 | 70575159 | ||||||
| chr8:70575403
|
G | A | 1 | a0001c0001t0001g0204 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1052-398C>T | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 10/10 | chr8 | 70575403 | ||||||
| chr8:70575871
|
G | A | 1 | a0001c0001t0001g0144 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1052-866C>T | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 10/10 | chr8 | 70575871 | ||||||
| chr8:70576009
|
T | C | 2 | a0001c0001t0001g0031a0001c0001t0001g0130 | 3 | HG02015.hp2 HG02132.hp2 NA18952.hp1 |
intron_variant | MODIFIER | c.1052-1004A>G | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 10/10 | chr8 | 70576009 | ||||||
| chr8:70576025
|
C | G | 8 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(5): Show | 8 | HG01243.hp1 HG01884.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.1052-1020G>C | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 10/10 | chr8 | 70576025 | ||||||
| chr8:70576069
|
T | TA | 14 | a0001c0001t0001g0076a0001c0001t0001g0104a0001c0001t0001g0112others(11): Show | 14 | HG01167.hp2 HG01175.hp2 HG02071.hp1 others(11): Show |
intron_variant | MODIFIER | c.1052-1065dupT | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 10/10 | chr8 | 70576069 | ||||||
| chr8:70576069
|
TAAAAAAA others(6): Show |
T | 1 | a0001c0001t0004g0219 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1052-1077_1052-106 others(17): Show |
TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 10/10 | chr8 | 70576069 | ||||||
| chr8:70576070
|
AAAAAAAA others(3): Show |
A | 50 | a0001c0001t0001g0006a0001c0001t0001g0016a0001c0001t0001g0022others(47): Show | 67 | HG00140.hp1 HG00323.hp2 HG00733.hp2 others(64): Show |
intron_variant | MODIFIER | c.1052-1075_1052-106 others(14): Show |
TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 10/10 | chr8 | 70576070 | ||||||
| chr8:70576079
|
AG | A | 15 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0065others(12): Show | 17 | HG00642.hp1 HG01074.hp2 HG01168.hp2 others(14): Show |
intron_variant | MODIFIER | c.1052-1075delC | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 10/10 | chr8 | 70576079 | ||||||
| chr8:70576080
|
G | A | 87 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(84): Show | 128 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(125): Show |
intron_variant | MODIFIER | c.1052-1075C>T | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 10/10 | chr8 | 70576080 | ||||||
| chr8:70576102
|
A | C | 1 | a0001c0001t0014g0078 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1052-1097T>G | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 10/10 | chr8 | 70576102 | ||||||
| chr8:70576103
|
A | C | 29 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0010others(26): Show | 55 | HG00408.hp2 HG00544.hp2 HG00621.hp1 others(52): Show |
intron_variant | MODIFIER | c.1052-1098T>G | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 10/10 | chr8 | 70576103 | ||||||
| chr8:70576107
|
A | C | 52 | a0001c0001t0001g0006a0001c0001t0001g0016a0001c0001t0001g0022others(49): Show | 69 | HG00140.hp1 HG00323.hp2 HG00733.hp2 others(66): Show |
intron_variant | MODIFIER | c.1052-1102T>G | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 10/10 | chr8 | 70576107 | ||||||
| chr8:70576445
|
C | T | 1 | a0001c0001t0001g0206 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.1052-1440G>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 10/10 | chr8 | 70576445 | ||||||
| chr8:70576472
|
G | A | 4 | a0001c0001t0001g0027a0001c0001t0001g0106a0001c0001t0001g0139others(1): Show | 5 | HG01081.hp1 HG01106.hp1 HG01123.hp1 others(2): Show |
intron_variant | MODIFIER | c.1052-1467C>T | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 10/10 | chr8 | 70576472 | ||||||
| chr8:70576842
|
C | G | 191 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(188): Show | 266 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(263): Show |
intron_variant | MODIFIER | c.1052-1837G>C | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 10/10 | chr8 | 70576842 | ||||||
| chr8:70576845
|
T | G | 191 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(188): Show | 266 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(263): Show |
intron_variant | MODIFIER | c.1052-1840A>C | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 10/10 | chr8 | 70576845 | ||||||
| chr8:70576850
|
A | G | 153 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(150): Show | 212 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(209): Show |
intron_variant | MODIFIER | c.1052-1845T>C | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 10/10 | chr8 | 70576850 | ||||||
| chr8:70576921
|
G | A | 2 | a0001c0001t0007g0034a0001c0001t0007g0077 | 3 | HG01109.hp1 HG02280.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1052-1916C>T | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 10/10 | chr8 | 70576921 | ||||||
| chr8:70576954
|
C | G | 14 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0065others(11): Show | 16 | HG00642.hp1 HG01074.hp2 HG01168.hp2 others(13): Show |
intron_variant | MODIFIER | c.1052-1949G>C | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 10/10 | chr8 | 70576954 | ||||||
| chr8:70576965
|
A | G | 153 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(150): Show | 212 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(209): Show |
intron_variant | MODIFIER | c.1052-1960T>C | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 10/10 | chr8 | 70576965 | ||||||
| chr8:70576980
|
C | T | 1 | a0001c0001t0001g0076 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1052-1975G>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 10/10 | chr8 | 70576980 | ||||||
| chr8:70577042
|
G | A | 1 | a0001c0001t0003g0084 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1052-2037C>T | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 10/10 | chr8 | 70577042 | ||||||
| chr8:70577092
|
C | T | 5 | a0001c0001t0001g0088a0001c0001t0001g0095a0001c0001t0008g0153others(2): Show | 5 | HG02922.hp1 HG02970.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1052-2087G>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 10/10 | chr8 | 70577092 | ||||||
| chr8:70577171
|
C | T | 1 | a0001c0001t0003g0172 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1052-2166G>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 10/10 | chr8 | 70577171 | ||||||
| chr8:70577197
|
G | A | 2 | a0001c0001t0001g0113a0001c0001t0001g0114 | 2 | HG03710.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.1052-2192C>T | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 10/10 | chr8 | 70577197 | ||||||
| chr8:70577325
|
C | T | 5 | a0001c0001t0009g0162a0002c0002t0003g0179a0002c0002t0003g0180others(2): Show | 5 | HG02572.hp1 HG03209.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.1052-2320G>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 10/10 | chr8 | 70577325 | ||||||
| chr8:70577447
|
C | A | 153 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(150): Show | 212 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(209): Show |
intron_variant | MODIFIER | c.1052-2442G>T | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 10/10 | chr8 | 70577447 | ||||||
| chr8:70577463
|
T | C | 1 | a0001c0001t0001g0208 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1052-2458A>G | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 10/10 | chr8 | 70577463 | ||||||
| chr8:70577672
|
G | A | 9 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0093others(6): Show | 11 | NA18943.hp2 NA18969.hp2 NA18977.hp2 others(8): Show |
intron_variant | MODIFIER | c.1052-2667C>T | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 10/10 | chr8 | 70577672 | ||||||
| chr8:70577674
|
C | T | 4 | a0001c0001t0001g0023a0001c0001t0001g0065a0001c0001t0001g0067others(1): Show | 5 | HG02965.hp2 HG03098.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.1052-2669G>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 10/10 | chr8 | 70577674 | ||||||
| chr8:70577815
|
C | T | 1 | a0001c0001t0006g0020 | 3 | HG00140.hp2 HG01071.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.1052-2810G>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 10/10 | chr8 | 70577815 | ||||||
| chr8:70577887
|
C | T | 1 | a0001c0001t0001g0136 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.1052-2882G>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 10/10 | chr8 | 70577887 | ||||||
| chr8:70577929
|
G | A | 1 | a0001c0001t0014g0078 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1052-2924C>T | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 10/10 | chr8 | 70577929 | ||||||
| chr8:70578211
|
G | A | 14 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0065others(11): Show | 16 | HG00642.hp1 HG01074.hp2 HG01168.hp2 others(13): Show |
intron_variant | MODIFIER | c.1052-3206C>T | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 10/10 | chr8 | 70578211 | ||||||
| chr8:70578258
|
A | C | 3 | a0001c0001t0001g0129a0001c0001t0001g0132a0001c0001t0001g0135 | 3 | NA18975.hp1 NA19055.hp1 NA19072.hp2 |
intron_variant | MODIFIER | c.1052-3253T>G | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 10/10 | chr8 | 70578258 | ||||||
| chr8:70578304
|
T | C | 26 | a0001c0001t0003g0005a0001c0001t0003g0015a0001c0001t0003g0035others(23): Show | 38 | HG00140.hp2 HG00673.hp1 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.1052-3299A>G | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 10/10 | chr8 | 70578304 | ||||||
| chr8:70578588
|
G | A | 1 | a0001c0001t0001g0114 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1052-3583C>T | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 10/10 | chr8 | 70578588 | ||||||
| chr8:70578867
|
C | T | 3 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0004g0214 | 3 | HG01168.hp2 HG01169.hp1 HG01934.hp2 |
intron_variant | MODIFIER | c.1052-3862G>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 10/10 | chr8 | 70578867 | ||||||
| chr8:70578885
|
A | G | 4 | a0001c0001t0003g0035a0001c0001t0003g0168a0001c0001t0003g0169others(1): Show | 5 | HG02055.hp2 HG02717.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1052-3880T>C | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 10/10 | chr8 | 70578885 | ||||||
| chr8:70579081
|
T | C | 27 | a0001c0001t0003g0005a0001c0001t0003g0015a0001c0001t0003g0035others(24): Show | 39 | HG00140.hp2 HG00673.hp1 HG00738.hp2 others(36): Show |
intron_variant | MODIFIER | c.1052-4076A>G | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 10/10 | chr8 | 70579081 | ||||||
| chr8:70579111
|
G | T | 1 | a0001c0001t0012g0060 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1051+4053C>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 10/10 | chr8 | 70579111 | ||||||
| chr8:70579115
|
T | C | 2 | a0001c0001t0001g0151a0005c0005t0001g0152 | 2 | HG02895.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1051+4049A>G | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 10/10 | chr8 | 70579115 | ||||||
| chr8:70579161
|
C | T | 151 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(148): Show | 210 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(207): Show |
intron_variant | MODIFIER | c.1051+4003G>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 10/10 | chr8 | 70579161 | ||||||
| chr8:70579258
|
G | T | 1 | a0002c0002t0003g0155 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1051+3906C>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 10/10 | chr8 | 70579258 | ||||||
| chr8:70579309
|
GTATCTAA others(3): Show |
G | 1 | a0001c0001t0001g0107 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1051+3845_1051+385 others(14): Show |
TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 10/10 | chr8 | 70579309 | ||||||
| chr8:70579365
|
T | C | 1 | a0001c0001t0003g0165 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1051+3799A>G | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 10/10 | chr8 | 70579365 | ||||||
| chr8:70579453
|
T | C | 1 | a0001c0001t0001g0150 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1051+3711A>G | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 10/10 | chr8 | 70579453 | ||||||
| chr8:70579760
|
C | T | 1 | a0001c0001t0001g0071 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1051+3404G>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 10/10 | chr8 | 70579760 | ||||||
| chr8:70579783
|
G | A | 1 | a0001c0001t0001g0195 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1051+3381C>T | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 10/10 | chr8 | 70579783 | ||||||
| chr8:70579877
|
C | T | 4 | a0001c0001t0003g0012a0001c0001t0003g0079a0001c0001t0003g0160others(1): Show | 7 | HG01891.hp1 HG02055.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.1051+3287G>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 10/10 | chr8 | 70579877 | ||||||
| chr8:70579923
|
G | C | 2 | a0001c0001t0007g0034a0001c0001t0007g0077 | 3 | HG01109.hp1 HG02280.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1051+3241C>G | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 10/10 | chr8 | 70579923 | ||||||
| chr8:70579956
|
A | G | 1 | a0001c0001t0014g0078 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1051+3208T>C | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 10/10 | chr8 | 70579956 | ||||||
| chr8:70580118
|
C | T | 2 | a0001c0001t0001g0006a0001c0001t0001g0209 | 7 | HG00140.hp1 HG00735.hp2 HG01258.hp2 others(4): Show |
intron_variant | MODIFIER | c.1051+3046G>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 10/10 | chr8 | 70580118 | ||||||
| chr8:70580219
|
T | A | 1 | a0001c0001t0003g0164 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1051+2945A>T | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 10/10 | chr8 | 70580219 | ||||||
| chr8:70580243
|
A | G | 4 | a0002c0002t0003g0179a0002c0002t0003g0180a0002c0002t0003g0181others(1): Show | 4 | HG03209.hp1 HG03453.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1051+2921T>C | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 10/10 | chr8 | 70580243 | ||||||
| chr8:70580383
|
G | A | 1 | a0001c0001t0014g0078 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1051+2781C>T | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 10/10 | chr8 | 70580383 | ||||||
| chr8:70580388
|
G | A | 2 | a0001c0001t0007g0034a0001c0001t0007g0077 | 3 | HG01109.hp1 HG02280.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1051+2776C>T | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 10/10 | chr8 | 70580388 | ||||||
| chr8:70580487
|
A | G | 1 | a0001c0001t0003g0160 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1051+2677T>C | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 10/10 | chr8 | 70580487 | ||||||
| chr8:70580488
|
T | C | 1 | a0001c0001t0001g0140 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1051+2676A>G | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 10/10 | chr8 | 70580488 | ||||||
| chr8:70580862
|
T | C | 2 | a0001c0001t0003g0160a0001c0001t0003g0161 | 2 | HG01891.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.1051+2302A>G | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 10/10 | chr8 | 70580862 | ||||||
| chr8:70581053
|
A | T | 1 | a0001c0001t0003g0161 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1051+2111T>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 10/10 | chr8 | 70581053 | ||||||
| chr8:70581107
|
G | A | 3 | a0001c0001t0001g0031a0001c0001t0001g0130a0001c0001t0001g0131 | 4 | HG02015.hp2 HG02132.hp2 HG02135.hp2 others(1): Show |
intron_variant | MODIFIER | c.1051+2057C>T | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 10/10 | chr8 | 70581107 | ||||||
| chr8:70581312
|
C | T | 8 | a0001c0001t0001g0029a0001c0001t0001g0081a0001c0001t0001g0085others(5): Show | 9 | HG00438.hp1 HG00609.hp1 HG02071.hp1 others(6): Show |
intron_variant | MODIFIER | c.1051+1852G>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 10/10 | chr8 | 70581312 | ||||||
| chr8:70581375
|
G | A | 2 | a0001c0001t0001g0094a0001c0001t0001g0201 | 2 | NA18971.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.1051+1789C>T | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 10/10 | chr8 | 70581375 | ||||||
| chr8:70581549
|
T | C | 1 | a0001c0001t0001g0141 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1051+1615A>G | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 10/10 | chr8 | 70581549 | ||||||
| chr8:70581613
|
T | C | 1 | a0001c0001t0002g0052 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1051+1551A>G | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 10/10 | chr8 | 70581613 | ||||||
| chr8:70581687
|
T | C | 81 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(78): Show | 121 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.1051+1477A>G | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 10/10 | chr8 | 70581687 | ||||||
| chr8:70581801
|
T | C | 1 | a0001c0001t0014g0078 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1051+1363A>G | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 10/10 | chr8 | 70581801 | ||||||
| chr8:70581879
|
T | G | 26 | a0001c0001t0003g0005a0001c0001t0003g0015a0001c0001t0003g0035others(23): Show | 38 | HG00140.hp2 HG00673.hp1 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.1051+1285A>C | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 10/10 | chr8 | 70581879 | ||||||
| chr8:70582179
|
A | G | 1 | a0001c0001t0001g0197 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1051+985T>C | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 10/10 | chr8 | 70582179 | ||||||
| chr8:70582199
|
T | C | 1 | a0001c0001t0003g0080 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1051+965A>G | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 10/10 | chr8 | 70582199 | ||||||
| chr8:70582273
|
T | C | 3 | a0001c0001t0008g0153a0002c0002t0008g0156a0004c0006t0008g0154 | 3 | HG02970.hp2 HG03139.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1051+891A>G | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 10/10 | chr8 | 70582273 | ||||||
| chr8:70582277
|
C | G | 1 | a0001c0007t0001g0149 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1051+887G>C | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 10/10 | chr8 | 70582277 | ||||||
| chr8:70582289
|
A | AT | 18 | a0001c0001t0001g0014a0001c0001t0001g0023a0001c0001t0001g0024others(15): Show | 23 | HG00642.hp1 HG01074.hp2 HG01168.hp2 others(20): Show |
intron_variant | MODIFIER | c.1051+874dupA | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 10/10 | chr8 | 70582289 | ||||||
| chr8:70582289
|
AT | A | 10 | a0001c0001t0001g0115a0001c0001t0001g0122a0001c0001t0001g0135others(7): Show | 10 | HG01891.hp2 HG03209.hp1 HG03453.hp2 others(7): Show |
intron_variant | MODIFIER | c.1051+874delA | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 10/10 | chr8 | 70582289 | ||||||
| chr8:70582519
|
GA | G | 7 | a0001c0001t0002g0047a0001c0001t0002g0050a0001c0001t0003g0158others(4): Show | 9 | HG00140.hp2 HG01071.hp1 HG02071.hp2 others(6): Show |
intron_variant | MODIFIER | c.1051+644delT | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 10/10 | chr8 | 70582519 | ||||||
| chr8:70582545
|
G | T | 137 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(134): Show | 194 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(191): Show |
intron_variant | MODIFIER | c.1051+619C>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 10/10 | chr8 | 70582545 | ||||||
| chr8:70582762
|
T | TA | 2 | a0001c0001t0003g0012a0001c0001t0003g0079 | 5 | HG02451.hp1 HG02572.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.1051+401dupT | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 10/10 | chr8 | 70582762 | ||||||
| chr8:70582782
|
T | C | 1 | a0001c0001t0003g0175 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1051+382A>G | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 10/10 | chr8 | 70582782 | ||||||
| chr8:70583073
|
GAC | G | 15 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0065others(12): Show | 17 | HG00642.hp1 HG01074.hp2 HG01168.hp2 others(14): Show |
intron_variant | MODIFIER | c.1051+89_1051+90del others(2): Show |
TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 10/10 | chr8 | 70583073 | ||||||
| chr8:70583098
|
T | C | 1 | a0001c0001t0001g0116 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1051+66A>G | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 10/10 | chr8 | 70583098 | ||||||
| chr8:70583131
|
C | T | 1 | a0001c0001t0001g0110 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1051+33G>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 10/10 | chr8 | 70583131 | ||||||
| chr8:70583549
|
C | T | 1 | a0001c0001t0003g0080 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.890+101G>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 9/10 | chr8 | 70583549 | ||||||
| chr8:70583612
|
A | G | 14 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0065others(11): Show | 16 | HG00642.hp1 HG01074.hp2 HG01168.hp2 others(13): Show |
intron_variant | MODIFIER | c.890+38T>C | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 9/10 | chr8 | 70583612 | ||||||
| chr8:70583810
|
G | A | 1 | a0001c0001t0014g0078 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.747-17C>T | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 8/10 | chr8 | 70583810 | ||||||
| chr8:70583904
|
T | C | 3 | a0001c0001t0003g0012a0001c0001t0003g0079a0001c0001t0003g0080 | 6 | HG02451.hp1 HG02572.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.747-111A>G | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 8/10 | chr8 | 70583904 | ||||||
| chr8:70584120
|
G | A | 4 | a0001c0001t0001g0018a0001c0001t0001g0082a0001c0001t0001g0102others(1): Show | 6 | HG00639.hp2 HG00738.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.747-327C>T | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 8/10 | chr8 | 70584120 | ||||||
| chr8:70584160
|
A | G | 2 | a0001c0001t0002g0041a0001c0001t0003g0064 | 2 | HG02622.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.747-367T>C | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 8/10 | chr8 | 70584160 | ||||||
| chr8:70584505
|
C | A | 1 | a0001c0001t0002g0021 | 2 | HG02735.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.747-712G>T | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 8/10 | chr8 | 70584505 | ||||||
| chr8:70584583
|
A | T | 1 | a0001c0001t0001g0209 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.747-790T>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 8/10 | chr8 | 70584583 | ||||||
| chr8:70584726
|
T | C | 14 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0065others(11): Show | 16 | HG00642.hp1 HG01074.hp2 HG01168.hp2 others(13): Show |
intron_variant | MODIFIER | c.747-933A>G | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 8/10 | chr8 | 70584726 | ||||||
| chr8:70584756
|
A | T | 1 | a0001c0001t0001g0194 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.747-963T>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 8/10 | chr8 | 70584756 | ||||||
| chr8:70584816
|
A | G | 153 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(150): Show | 212 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(209): Show |
intron_variant | MODIFIER | c.747-1023T>C | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 8/10 | chr8 | 70584816 | ||||||
| chr8:70584844
|
G | C | 1 | a0001c0001t0003g0098 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.747-1051C>G | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 8/10 | chr8 | 70584844 | ||||||
| chr8:70584961
|
C | T | 1 | a0001c0001t0014g0078 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.747-1168G>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 8/10 | chr8 | 70584961 | ||||||
| chr8:70584979
|
C | T | 1 | a0001c0001t0014g0078 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.747-1186G>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 8/10 | chr8 | 70584979 | ||||||
| chr8:70584984
|
C | T | 1 | a0001c0001t0003g0161 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.747-1191G>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 8/10 | chr8 | 70584984 | ||||||
| chr8:70585041
|
C | T | 2 | a0001c0001t0002g0049a0001c0001t0002g0056 | 2 | NA19065.hp1 NA19072.hp1 |
intron_variant | MODIFIER | c.747-1248G>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 8/10 | chr8 | 70585041 | ||||||
| chr8:70585046
|
T | A | 1 | a0001c0001t0014g0078 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.747-1253A>T | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 8/10 | chr8 | 70585046 | ||||||
| chr8:70585141
|
C | T | 1 | a0001c0001t0001g0074 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.747-1348G>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 8/10 | chr8 | 70585141 | ||||||
| chr8:70585529
|
G | C | 10 | a0001c0001t0001g0024a0001c0001t0001g0066a0001c0001t0001g0068others(7): Show | 11 | HG00642.hp1 HG01074.hp2 HG01168.hp2 others(8): Show |
intron_variant | MODIFIER | c.746+1366C>G | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 8/10 | chr8 | 70585529 | ||||||
| chr8:70585583
|
A | AAAAC | 152 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(149): Show | 211 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(208): Show |
intron_variant | MODIFIER | c.746+1308_746+1311d others(6): Show |
TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 8/10 | chr8 | 70585583 | ||||||
| chr8:70585741
|
AG | A | 152 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(149): Show | 211 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(208): Show |
intron_variant | MODIFIER | c.746+1153delC | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 8/10 | chr8 | 70585741 | ||||||
| chr8:70585749
|
T | C | 2 | a0001c0001t0001g0090a0001c0001t0014g0078 | 2 | NA18522.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.746+1146A>G | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 8/10 | chr8 | 70585749 | ||||||
| chr8:70585782
|
G | A | 2 | a0001c0001t0003g0163a0001c0001t0003g0164 | 2 | HG02723.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.746+1113C>T | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 8/10 | chr8 | 70585782 | ||||||
| chr8:70585822
|
C | G | 190 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(187): Show | 265 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(262): Show |
intron_variant | MODIFIER | c.746+1073G>C | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 8/10 | chr8 | 70585822 | ||||||
| chr8:70585909
|
C | A | 190 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(187): Show | 265 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(262): Show |
intron_variant | MODIFIER | c.746+986G>T | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 8/10 | chr8 | 70585909 | ||||||
| chr8:70585928
|
T | C | 14 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0065others(11): Show | 16 | HG00642.hp1 HG01074.hp2 HG01168.hp2 others(13): Show |
intron_variant | MODIFIER | c.746+967A>G | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 8/10 | chr8 | 70585928 | ||||||
| chr8:70585987
|
G | A | 2 | a0001c0001t0007g0034a0001c0001t0007g0077 | 3 | HG01109.hp1 HG02280.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.746+908C>T | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 8/10 | chr8 | 70585987 | ||||||
| chr8:70586059
|
G | A | 1 | a0001c0001t0003g0160 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.746+836C>T | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 8/10 | chr8 | 70586059 | ||||||
| chr8:70586278
|
T | TG | 190 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(187): Show | 265 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(262): Show |
intron_variant | MODIFIER | c.746+616dupC | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 8/10 | chr8 | 70586278 | ||||||
| chr8:70586284
|
A | G | 1 | a0001c0001t0003g0175 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.746+611T>C | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 8/10 | chr8 | 70586284 | ||||||
| chr8:70586382
|
C | A | 14 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0065others(11): Show | 16 | HG00642.hp1 HG01074.hp2 HG01168.hp2 others(13): Show |
intron_variant | MODIFIER | c.746+513G>T | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 8/10 | chr8 | 70586382 | ||||||
| chr8:70586507
|
C | T | 1 | a0001c0001t0001g0206 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.746+388G>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 8/10 | chr8 | 70586507 | ||||||
| chr8:70586776
|
A | T | 26 | a0001c0001t0003g0005a0001c0001t0003g0015a0001c0001t0003g0035others(23): Show | 38 | HG00140.hp2 HG00673.hp1 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.746+119T>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 8/10 | chr8 | 70586776 | ||||||
| chr8:70586874
|
T | C | 14 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0065others(11): Show | 16 | HG00642.hp1 HG01074.hp2 HG01168.hp2 others(13): Show |
intron_variant | MODIFIER | c.746+21A>G | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 8/10 | chr8 | 70586874 | ||||||
| chr8:70587344
|
T | C | 1 | a0001c0001t0001g0134 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.571-168A>G | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 6/10 | chr8 | 70587344 | ||||||
| chr8:70587377
|
GA | G | 2 | a0001c0001t0001g0014a0001c0001t0001g0124 | 5 | HG02257.hp2 HG02647.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.571-202delT | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 6/10 | chr8 | 70587377 | ||||||
| chr8:70587426
|
C | T | 1 | a0001c0001t0001g0193 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.571-250G>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 6/10 | chr8 | 70587426 | ||||||
| chr8:70587504
|
A | T | 5 | a0002c0002t0003g0155a0002c0002t0003g0179a0002c0002t0003g0180others(2): Show | 5 | HG03209.hp1 HG03453.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.571-328T>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 6/10 | chr8 | 70587504 | ||||||
| chr8:70587610
|
A | C | 1 | a0001c0001t0014g0078 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.571-434T>G | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 6/10 | chr8 | 70587610 | ||||||
| chr8:70588014
|
C | T | 192 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(189): Show | 270 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(267): Show |
intron_variant | MODIFIER | c.571-838G>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 6/10 | chr8 | 70588014 | ||||||
| chr8:70588034
|
C | G | 1 | a0001c0001t0002g0046 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.571-858G>C | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 6/10 | chr8 | 70588034 | ||||||
| chr8:70588038
|
A | G | 1 | a0001c0001t0014g0078 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.571-862T>C | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 6/10 | chr8 | 70588038 | ||||||
| chr8:70588066
|
T | G | 2 | a0001c0001t0007g0034a0001c0001t0007g0077 | 3 | HG01109.hp1 HG02280.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.571-890A>C | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 6/10 | chr8 | 70588066 | ||||||
| chr8:70588315
|
A | C | 4 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(1): Show | 4 | NA18969.hp2 NA18979.hp2 NA19010.hp2 others(1): Show |
intron_variant | MODIFIER | c.571-1139T>G | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 6/10 | chr8 | 70588315 | ||||||
| chr8:70588353
|
A | G | 1 | a0001c0001t0001g0189 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.571-1177T>C | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 6/10 | chr8 | 70588353 | ||||||
| chr8:70588830
|
C | T | 2 | a0001c0001t0001g0014a0001c0001t0001g0124 | 5 | HG02257.hp2 HG02647.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.571-1654G>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 6/10 | chr8 | 70588830 | ||||||
| chr8:70588831
|
G | A | 4 | a0002c0002t0003g0179a0002c0002t0003g0180a0002c0002t0003g0181others(1): Show | 4 | HG03209.hp1 HG03453.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.571-1655C>T | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 6/10 | chr8 | 70588831 | ||||||
| chr8:70588870
|
C | T | 1 | a0001c0001t0003g0080 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.571-1694G>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 6/10 | chr8 | 70588870 | ||||||
| chr8:70589023
|
C | T | 7 | a0001c0001t0001g0037a0001c0001t0001g0086a0001c0001t0001g0186others(4): Show | 8 | NA18954.hp1 NA18957.hp1 NA18982.hp2 others(5): Show |
intron_variant | MODIFIER | c.571-1847G>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 6/10 | chr8 | 70589023 | ||||||
| chr8:70589057
|
G | A | 2 | a0001c0001t0001g0118a0001c0001t0004g0219 | 2 | HG04184.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.571-1881C>T | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 6/10 | chr8 | 70589057 | ||||||
| chr8:70589239
|
A | C | 27 | a0001c0001t0001g0196a0001c0001t0003g0005a0001c0001t0003g0015others(24): Show | 39 | HG00140.hp2 HG00673.hp1 HG00738.hp2 others(36): Show |
intron_variant | MODIFIER | c.571-2063T>G | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 6/10 | chr8 | 70589239 | ||||||
| chr8:70589665
|
C | T | 2 | a0001c0001t0001g0145a0001c0001t0001g0146 | 2 | NA18990.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.571-2489G>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 6/10 | chr8 | 70589665 | ||||||
| chr8:70589710
|
T | C | 16 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0065others(13): Show | 21 | HG00642.hp1 HG01074.hp2 HG01168.hp2 others(18): Show |
intron_variant | MODIFIER | c.571-2534A>G | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 6/10 | chr8 | 70589710 | ||||||
| chr8:70589786
|
C | G | 154 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(151): Show | 212 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(209): Show |
intron_variant | MODIFIER | c.571-2610G>C | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 6/10 | chr8 | 70589786 | ||||||
| chr8:70590097
|
T | C | 14 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0065others(11): Show | 16 | HG00642.hp1 HG01074.hp2 HG01168.hp2 others(13): Show |
intron_variant | MODIFIER | c.571-2921A>G | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 6/10 | chr8 | 70590097 | ||||||
| chr8:70590141
|
T | TA | 8 | a0001c0001t0001g0129a0001c0001t0001g0138a0001c0001t0002g0011others(5): Show | 11 | HG00621.hp1 HG01192.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.571-2966dupT | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 6/10 | chr8 | 70590141 | ||||||
| chr8:70590141
|
TA | T | 102 | a0001c0001t0001g0006a0001c0001t0001g0016a0001c0001t0001g0022others(99): Show | 135 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(132): Show |
intron_variant | MODIFIER | c.571-2966delT | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 6/10 | chr8 | 70590141 | ||||||
| chr8:70590141
|
TAA | T | 7 | a0001c0001t0001g0192a0001c0001t0014g0078a0002c0002t0003g0155others(4): Show | 7 | HG03209.hp1 HG03453.hp2 HG03516.hp1 others(4): Show |
intron_variant | MODIFIER | c.571-2967_571-2966d others(4): Show |
TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 6/10 | chr8 | 70590141 | ||||||
| chr8:70590202
|
AT | A | 18 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0065others(15): Show | 20 | HG00642.hp1 HG01074.hp2 HG01168.hp2 others(17): Show |
intron_variant | MODIFIER | c.571-3027delA | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 6/10 | chr8 | 70590202 | ||||||
| chr8:70590308
|
T | C | 1 | a0001c0001t0001g0141 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.571-3132A>G | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 6/10 | chr8 | 70590308 | ||||||
| chr8:70590333
|
C | G | 1 | a0001c0001t0001g0191 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.571-3157G>C | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 6/10 | chr8 | 70590333 | ||||||
| chr8:70590340
|
T | C | 15 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0065others(12): Show | 17 | HG00642.hp1 HG01074.hp2 HG01168.hp2 others(14): Show |
intron_variant | MODIFIER | c.571-3164A>G | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 6/10 | chr8 | 70590340 | ||||||
| chr8:70590363
|
C | T | 1 | a0001c0001t0001g0205 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.571-3187G>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 6/10 | chr8 | 70590363 | ||||||
| chr8:70590404
|
G | A | 1 | a0001c0001t0002g0052 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.571-3228C>T | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 6/10 | chr8 | 70590404 | ||||||
| chr8:70590577
|
T | C | 5 | a0002c0002t0003g0155a0002c0002t0003g0179a0002c0002t0003g0180others(2): Show | 5 | HG03209.hp1 HG03453.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.571-3401A>G | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 6/10 | chr8 | 70590577 | ||||||
| chr8:70590632
|
G | A | 1 | a0001c0001t0001g0123 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.571-3456C>T | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 6/10 | chr8 | 70590632 | ||||||
| chr8:70590689
|
A | T | 4 | a0002c0002t0003g0179a0002c0002t0003g0180a0002c0002t0003g0181others(1): Show | 4 | HG03209.hp1 HG03453.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.571-3513T>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 6/10 | chr8 | 70590689 | ||||||
| chr8:70590927
|
T | C | 3 | a0001c0001t0007g0034a0001c0001t0007g0077a0001c0001t0016g0159 | 4 | HG01109.hp1 HG01167.hp2 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.570+3579A>G | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 6/10 | chr8 | 70590927 | ||||||
| chr8:70591004
|
T | TAC | 9 | a0001c0001t0001g0024a0001c0001t0001g0068a0001c0001t0001g0069others(6): Show | 10 | HG00642.hp1 HG01074.hp2 HG01168.hp2 others(7): Show |
intron_variant | MODIFIER | c.570+3501_570+3502i others(4): Show |
TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 6/10 | chr8 | 70591004 | ||||||
| chr8:70591005
|
A | AC | 5 | a0001c0001t0001g0023a0001c0001t0001g0065a0001c0001t0001g0066others(2): Show | 6 | HG02622.hp1 HG02965.hp2 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.570+3500_570+3501i others(3): Show |
TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 6/10 | chr8 | 70591005 | ||||||
| chr8:70591007
|
T | A | 16 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0065others(13): Show | 18 | HG00642.hp1 HG01074.hp2 HG01168.hp2 others(15): Show |
intron_variant | MODIFIER | c.570+3499A>T | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 6/10 | chr8 | 70591007 | ||||||
| chr8:70591070
|
A | C | 1 | a0001c0001t0003g0161 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.570+3436T>G | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 6/10 | chr8 | 70591070 | ||||||
| chr8:70591076
|
C | A | 1 | a0001c0001t0003g0169 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.570+3430G>T | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 6/10 | chr8 | 70591076 | ||||||
| chr8:70591350
|
C | T | 1 | a0001c0001t0001g0018 | 3 | HG00639.hp2 HG00738.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.570+3156G>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 6/10 | chr8 | 70591350 | ||||||
| chr8:70591517
|
A | C | 155 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(152): Show | 214 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(211): Show |
intron_variant | MODIFIER | c.570+2989T>G | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 6/10 | chr8 | 70591517 | ||||||
| chr8:70591726
|
C | T | 4 | a0002c0002t0003g0179a0002c0002t0003g0180a0002c0002t0003g0181others(1): Show | 4 | HG03209.hp1 HG03453.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.570+2780G>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 6/10 | chr8 | 70591726 | ||||||
| chr8:70591727
|
A | C | 1 | a0001c0001t0002g0048 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.570+2779T>G | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 6/10 | chr8 | 70591727 | ||||||
| chr8:70591916
|
A | G | 2 | a0001c0001t0003g0160a0001c0001t0003g0161 | 2 | HG01891.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.570+2590T>C | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 6/10 | chr8 | 70591916 | ||||||
| chr8:70592041
|
T | A | 1 | a0001c0001t0014g0078 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.570+2465A>T | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 6/10 | chr8 | 70592041 | ||||||
| chr8:70592181
|
T | C | 3 | a0001c0001t0003g0012a0001c0001t0003g0079a0001c0001t0003g0080 | 6 | HG02451.hp1 HG02572.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.570+2325A>G | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 6/10 | chr8 | 70592181 | ||||||
| chr8:70592237
|
A | C | 192 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(189): Show | 267 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(264): Show |
intron_variant | MODIFIER | c.570+2269T>G | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 6/10 | chr8 | 70592237 | ||||||
| chr8:70592699
|
C | T | 2 | a0001c0001t0003g0012a0001c0001t0003g0079 | 5 | HG02451.hp1 HG02572.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.570+1807G>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 6/10 | chr8 | 70592699 | ||||||
| chr8:70592827
|
C | T | 6 | a0001c0001t0003g0012a0001c0001t0003g0079a0001c0001t0003g0080others(3): Show | 9 | HG01891.hp1 HG02055.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.570+1679G>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 6/10 | chr8 | 70592827 | ||||||
| chr8:70592888
|
A | G | 3 | a0001c0001t0003g0012a0001c0001t0003g0079a0001c0001t0003g0080 | 6 | HG02451.hp1 HG02572.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.570+1618T>C | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 6/10 | chr8 | 70592888 | ||||||
| chr8:70592911
|
C | T | 24 | a0001c0001t0003g0005a0001c0001t0003g0015a0001c0001t0003g0035others(21): Show | 36 | HG00140.hp2 HG00673.hp1 HG00738.hp2 others(33): Show |
intron_variant | MODIFIER | c.570+1595G>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 6/10 | chr8 | 70592911 | ||||||
| chr8:70592985
|
T | C | 14 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0065others(11): Show | 16 | HG00642.hp1 HG01074.hp2 HG01168.hp2 others(13): Show |
intron_variant | MODIFIER | c.570+1521A>G | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 6/10 | chr8 | 70592985 | ||||||
| chr8:70593407
|
A | G | 4 | a0002c0002t0003g0179a0002c0002t0003g0180a0002c0002t0003g0181others(1): Show | 4 | HG03209.hp1 HG03453.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.570+1099T>C | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 6/10 | chr8 | 70593407 | ||||||
| chr8:70593428
|
C | T | 14 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0065others(11): Show | 16 | HG00642.hp1 HG01074.hp2 HG01168.hp2 others(13): Show |
intron_variant | MODIFIER | c.570+1078G>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 6/10 | chr8 | 70593428 | ||||||
| chr8:70593458
|
A | G | 1 | a0001c0001t0003g0182 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.570+1048T>C | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 6/10 | chr8 | 70593458 | ||||||
| chr8:70593527
|
C | A | 1 | a0001c0001t0016g0159 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.570+979G>T | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 6/10 | chr8 | 70593527 | ||||||
| chr8:70593528
|
C | T | 1 | a0001c0001t0001g0130 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.570+978G>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 6/10 | chr8 | 70593528 | ||||||
| chr8:70593596
|
T | TA | 3 | a0001c0001t0003g0012a0001c0001t0003g0079a0001c0001t0014g0078 | 6 | HG02451.hp1 HG02572.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.570+909dupT | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 6/10 | chr8 | 70593596 | ||||||
| chr8:70593596
|
TA | T | 67 | a0001c0001t0001g0006a0001c0001t0001g0016a0001c0001t0001g0022others(64): Show | 84 | HG00140.hp1 HG00323.hp2 HG00733.hp2 others(81): Show |
intron_variant | MODIFIER | c.570+909delT | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 6/10 | chr8 | 70593596 | ||||||
| chr8:70594066
|
A | C | 1 | a0001c0001t0003g0173 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.570+440T>G | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 6/10 | chr8 | 70594066 | ||||||
| chr8:70594165
|
C | T | 1 | a0002c0002t0003g0155 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.570+341G>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 6/10 | chr8 | 70594165 | ||||||
| chr8:70594305
|
G | GT | 149 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(146): Show | 213 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(210): Show |
intron_variant | MODIFIER | c.570+200dupA | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 6/10 | chr8 | 70594305 | ||||||
| chr8:70594305
|
G | GTT | 8 | a0001c0001t0001g0039a0001c0001t0001g0100a0001c0001t0001g0190others(5): Show | 13 | HG01109.hp1 HG02280.hp1 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.570+199_570+200dup others(2): Show |
TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 6/10 | chr8 | 70594305 | ||||||
| chr8:70594305
|
GT | G | 6 | a0001c0001t0003g0173a0002c0002t0003g0155a0002c0002t0003g0179others(3): Show | 6 | HG00738.hp2 HG03209.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.570+200delA | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 6/10 | chr8 | 70594305 | ||||||
| chr8:70594311
|
T | TG | 9 | a0001c0001t0001g0029a0001c0001t0001g0081a0001c0001t0001g0085others(6): Show | 10 | HG00438.hp1 HG00609.hp1 HG02071.hp1 others(7): Show |
intron_variant | MODIFIER | c.570+194_570+195ins others(1): Show |
TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 6/10 | chr8 | 70594311 | ||||||
| chr8:70594361
|
G | A | 1 | a0002c0002t0003g0155 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.570+145C>T | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 6/10 | chr8 | 70594361 | ||||||
| chr8:70594399
|
G | C | 44 | a0001c0001t0001g0006a0001c0001t0001g0016a0001c0001t0001g0022others(41): Show | 61 | HG00140.hp1 HG00323.hp2 HG00733.hp2 others(58): Show |
intron_variant | MODIFIER | c.570+107C>G | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 6/10 | chr8 | 70594399 | ||||||
| chr8:70594639
|
T | A | 2 | a0001c0001t0003g0012a0001c0001t0003g0079 | 5 | HG02451.hp1 HG02572.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.486-49A>T | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 5/10 | chr8 | 70594639 | ||||||
| chr8:70594640
|
A | T | 9 | a0001c0001t0001g0027a0001c0001t0001g0106a0001c0001t0001g0128others(6): Show | 10 | HG00323.hp1 HG01081.hp1 HG01106.hp1 others(7): Show |
intron_variant | MODIFIER | c.486-50T>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 5/10 | chr8 | 70594640 | ||||||
| chr8:70594777
|
T | C | 14 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0065others(11): Show | 16 | HG00642.hp1 HG01074.hp2 HG01168.hp2 others(13): Show |
intron_variant | MODIFIER | c.486-187A>G | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 5/10 | chr8 | 70594777 | ||||||
| chr8:70595038
|
G | GT | 166 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(163): Show | 233 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.486-449dupA | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 5/10 | chr8 | 70595038 | ||||||
| chr8:70595038
|
GT | G | 13 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0065others(10): Show | 15 | HG00642.hp1 HG01074.hp2 HG01168.hp2 others(12): Show |
intron_variant | MODIFIER | c.486-449delA | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 5/10 | chr8 | 70595038 | ||||||
| chr8:70595212
|
A | T | 1 | a0001c0001t0014g0078 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.486-622T>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 5/10 | chr8 | 70595212 | ||||||
| chr8:70595380
|
A | G | 1 | a0002c0002t0003g0179 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.486-790T>C | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 5/10 | chr8 | 70595380 | ||||||
| chr8:70595462
|
C | T | 24 | a0001c0001t0003g0005a0001c0001t0003g0015a0001c0001t0003g0035others(21): Show | 36 | HG00140.hp2 HG00673.hp1 HG00738.hp2 others(33): Show |
intron_variant | MODIFIER | c.485+801G>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 5/10 | chr8 | 70595462 | ||||||
| chr8:70595955
|
T | G | 1 | a0001c0001t0001g0125 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.485+308A>C | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 5/10 | chr8 | 70595955 | ||||||
| chr8:70596496
|
T | C | 2 | a0001c0001t0001g0126a0001c0001t0004g0215 | 2 | HG03017.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.427-175A>G | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 4/10 | chr8 | 70596496 | ||||||
| chr8:70596670
|
A | C | 81 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(78): Show | 121 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.427-349T>G | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 4/10 | chr8 | 70596670 | ||||||
| chr8:70596677
|
A | G | 1 | a0001c0001t0003g0079 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.427-356T>C | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 4/10 | chr8 | 70596677 | ||||||
| chr8:70596700
|
A | G | 1 | a0001c0001t0001g0038 | 2 | HG03710.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.427-379T>C | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 4/10 | chr8 | 70596700 | ||||||
| chr8:70596749
|
C | T | 1 | a0001c0001t0001g0189 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.427-428G>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 4/10 | chr8 | 70596749 | ||||||
| chr8:70596819
|
T | TA | 19 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0030others(16): Show | 22 | HG00642.hp1 HG01074.hp2 HG01168.hp2 others(19): Show |
intron_variant | MODIFIER | c.427-499dupT | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 4/10 | chr8 | 70596819 | ||||||
| chr8:70596819
|
TA | T | 30 | a0001c0001t0001g0086a0001c0001t0001g0127a0001c0001t0001g0151others(27): Show | 42 | HG00140.hp2 HG00673.hp1 HG00738.hp2 others(39): Show |
intron_variant | MODIFIER | c.427-499delT | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 4/10 | chr8 | 70596819 | ||||||
| chr8:70596820
|
A | T | 4 | a0002c0002t0003g0179a0002c0002t0003g0180a0002c0002t0003g0181others(1): Show | 4 | HG03209.hp1 HG03453.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.427-499T>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 4/10 | chr8 | 70596820 | ||||||
| chr8:70596967
|
T | G | 1 | a0001c0001t0003g0175 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.427-646A>C | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 4/10 | chr8 | 70596967 | ||||||
| chr8:70597296
|
A | G | 155 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(152): Show | 214 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(211): Show |
intron_variant | MODIFIER | c.426+599T>C | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 4/10 | chr8 | 70597296 | ||||||
| chr8:70597656
|
G | A | 1 | a0001c0001t0017g0212 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.426+239C>T | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 4/10 | chr8 | 70597656 | ||||||
| chr8:70597668
|
C | CA | 84 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0013others(81): Show | 120 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(117): Show |
intron_variant | MODIFIER | c.426+226dupT | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 4/10 | chr8 | 70597668 | ||||||
| chr8:70597668
|
C | CAA | 53 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0031others(50): Show | 79 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(76): Show |
intron_variant | MODIFIER | c.426+225_426+226dup others(2): Show |
TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 4/10 | chr8 | 70597668 | ||||||
| chr8:70597668
|
C | CAAA | 8 | a0001c0001t0001g0097a0001c0001t0001g0104a0001c0001t0001g0137others(5): Show | 9 | HG01175.hp2 HG02055.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.426+224_426+226dup others(3): Show |
TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 4/10 | chr8 | 70597668 | ||||||
| chr8:70597853
|
T | C | 4 | a0001c0001t0003g0035a0001c0001t0003g0168a0001c0001t0003g0169others(1): Show | 5 | HG02055.hp2 HG02717.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.426+42A>G | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 4/10 | chr8 | 70597853 | ||||||
| chr8:70597858
|
A | G | 192 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(189): Show | 267 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(264): Show |
intron_variant | MODIFIER | c.426+37T>C | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 4/10 | chr8 | 70597858 | ||||||
| chr8:70598484
|
G | A | 1 | a0002c0002t0003g0155 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.188-229C>T | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 2/10 | chr8 | 70598484 | ||||||
| chr8:70598511
|
A | G | 1 | a0001c0001t0001g0106 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.188-256T>C | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 2/10 | chr8 | 70598511 | ||||||
| chr8:70598652
|
C | A | 1 | a0001c0001t0014g0078 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.188-397G>T | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 2/10 | chr8 | 70598652 | ||||||
| chr8:70598814
|
A | G | 1 | a0001c0001t0007g0034 | 2 | HG01109.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.188-559T>C | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 2/10 | chr8 | 70598814 | ||||||
| chr8:70598916
|
C | T | 1 | a0001c0001t0003g0160 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.188-661G>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 2/10 | chr8 | 70598916 | ||||||
| chr8:70599040
|
C | T | 1 | a0001c0001t0001g0105 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.188-785G>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 2/10 | chr8 | 70599040 | ||||||
| chr8:70599081
|
G | A | 1 | a0001c0001t0001g0204 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.188-826C>T | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 2/10 | chr8 | 70599081 | ||||||
| chr8:70599261
|
T | C | 1 | a0001c0001t0003g0098 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.187+758A>G | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 2/10 | chr8 | 70599261 | ||||||
| chr8:70599321
|
G | T | 1 | a0001c0001t0005g0184 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.187+698C>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 2/10 | chr8 | 70599321 | ||||||
| chr8:70599502
|
A | G | 3 | a0001c0001t0007g0034a0001c0001t0007g0077a0001c0001t0016g0159 | 4 | HG01109.hp1 HG01167.hp2 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.187+517T>C | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 2/10 | chr8 | 70599502 | ||||||
| chr8:70599933
|
C | T | 1 | a0001c0001t0002g0057 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.187+86G>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 2/10 | chr8 | 70599933 | ||||||
| chr8:70600114
|
A | T | 134 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(131): Show | 191 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(188): Show |
intron_variant | MODIFIER | c.124-32T>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70600114 | ||||||
| chr8:70600142
|
C | T | 80 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(77): Show | 120 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(117): Show |
intron_variant | MODIFIER | c.124-60G>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70600142 | ||||||
| chr8:70600143
|
G | A | 1 | a0001c0001t0014g0078 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.124-61C>T | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70600143 | ||||||
| chr8:70600154
|
A | G | 4 | a0002c0002t0003g0179a0002c0002t0003g0180a0002c0002t0003g0181others(1): Show | 4 | HG03209.hp1 HG03453.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.124-72T>C | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70600154 | ||||||
| chr8:70600176
|
C | T | 3 | a0001c0001t0007g0034a0001c0001t0007g0077a0001c0001t0016g0159 | 4 | HG01109.hp1 HG01167.hp2 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.124-94G>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70600176 | ||||||
| chr8:70600429
|
G | A | 1 | a0001c0001t0003g0170 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.124-347C>T | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70600429 | ||||||
| chr8:70600449
|
G | C | 1 | a0001c0001t0003g0178 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.124-367C>G | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70600449 | ||||||
| chr8:70600561
|
G | A | 1 | a0002c0002t0003g0155 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.124-479C>T | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70600561 | ||||||
| chr8:70600651
|
G | T | 1 | a0001c0001t0014g0078 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.124-569C>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70600651 | ||||||
| chr8:70600666
|
G | T | 1 | a0001c0001t0001g0186 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.124-584C>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70600666 | ||||||
| chr8:70600772
|
T | C | 1 | a0001c0001t0001g0071 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.124-690A>G | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70600772 | ||||||
| chr8:70600797
|
GT | G | 8 | a0001c0001t0003g0015a0001c0001t0003g0036a0001c0001t0003g0163others(5): Show | 12 | HG01243.hp2 HG01884.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.124-716delA | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70600797 | ||||||
| chr8:70600856
|
C | A | 1 | a0001c0001t0001g0139 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.124-774G>T | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70600856 | ||||||
| chr8:70600895
|
T | C | 134 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(131): Show | 191 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(188): Show |
intron_variant | MODIFIER | c.124-813A>G | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70600895 | ||||||
| chr8:70601155
|
T | C | 1 | a0001c0001t0003g0161 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.124-1073A>G | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70601155 | ||||||
| chr8:70601413
|
A | G | 1 | a0001c0001t0001g0072 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.124-1331T>C | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70601413 | ||||||
| chr8:70601546
|
C | G | 1 | a0001c0001t0001g0099 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.124-1464G>C | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70601546 | ||||||
| chr8:70601602
|
G | A | 1 | a0001c0001t0001g0066 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.124-1520C>T | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70601602 | ||||||
| chr8:70601619
|
G | A | 1 | a0001c0001t0001g0140 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.124-1537C>T | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70601619 | ||||||
| chr8:70601684
|
A | C | 1 | a0001c0001t0001g0025 | 2 | HG00099.hp2 HG00733.hp1 |
intron_variant | MODIFIER | c.124-1602T>G | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70601684 | ||||||
| chr8:70601806
|
T | C | 24 | a0001c0001t0003g0005a0001c0001t0003g0015a0001c0001t0003g0035others(21): Show | 36 | HG00140.hp2 HG00673.hp1 HG00738.hp2 others(33): Show |
intron_variant | MODIFIER | c.124-1724A>G | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70601806 | ||||||
| chr8:70601834
|
A | T | 191 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(188): Show | 266 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(263): Show |
intron_variant | MODIFIER | c.124-1752T>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70601834 | ||||||
| chr8:70601853
|
C | A | 1 | a0001c0001t0003g0165 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.124-1771G>T | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70601853 | ||||||
| chr8:70601957
|
G | A | 2 | a0001c0001t0010g0166a0001c0001t0010g0167 | 2 | HG02647.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.124-1875C>T | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70601957 | ||||||
| chr8:70602024
|
A | C | 1 | a0001c0001t0002g0043 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.124-1942T>G | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70602024 | ||||||
| chr8:70602068
|
A | G | 135 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(132): Show | 192 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(189): Show |
intron_variant | MODIFIER | c.124-1986T>C | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70602068 | ||||||
| chr8:70602115
|
A | C | 24 | a0001c0001t0003g0005a0001c0001t0003g0015a0001c0001t0003g0035others(21): Show | 36 | HG00140.hp2 HG00673.hp1 HG00738.hp2 others(33): Show |
intron_variant | MODIFIER | c.124-2033T>G | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70602115 | ||||||
| chr8:70602259
|
T | C | 1 | a0002c0002t0008g0156 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.124-2177A>G | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70602259 | ||||||
| chr8:70602332
|
C | T | 191 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(188): Show | 266 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(263): Show |
intron_variant | MODIFIER | c.124-2250G>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70602332 | ||||||
| chr8:70602379
|
A | G | 1 | a0001c0001t0001g0141 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.124-2297T>C | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70602379 | ||||||
| chr8:70602388
|
G | C | 1 | a0001c0001t0002g0057 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.124-2306C>G | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70602388 | ||||||
| chr8:70602437
|
T | C | 3 | a0001c0001t0007g0034a0001c0001t0007g0077a0001c0001t0016g0159 | 4 | HG01109.hp1 HG01167.hp2 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.124-2355A>G | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70602437 | ||||||
| chr8:70602558
|
C | T | 1 | a0001c0001t0001g0104 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.124-2476G>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70602558 | ||||||
| chr8:70602636
|
G | A | 190 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(187): Show | 265 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(262): Show |
intron_variant | MODIFIER | c.124-2554C>T | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70602636 | ||||||
| chr8:70602721
|
C | A | 1 | a0001c0001t0001g0141 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.124-2639G>T | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70602721 | ||||||
| chr8:70602773
|
T | C | 1 | a0001c0001t0002g0055 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.124-2691A>G | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70602773 | ||||||
| chr8:70602785
|
A | G | 1 | a0001c0001t0015g0103 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.124-2703T>C | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70602785 | ||||||
| chr8:70603020
|
C | T | 9 | a0001c0001t0001g0024a0001c0001t0001g0068a0001c0001t0001g0069others(6): Show | 10 | HG00642.hp1 HG01074.hp2 HG01168.hp2 others(7): Show |
intron_variant | MODIFIER | c.124-2938G>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70603020 | ||||||
| chr8:70603040
|
C | T | 4 | a0002c0002t0003g0179a0002c0002t0003g0180a0002c0002t0003g0181others(1): Show | 4 | HG03209.hp1 HG03453.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.124-2958G>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70603040 | ||||||
| chr8:70603242
|
TTATA | T | 5 | a0001c0001t0003g0012a0001c0001t0003g0079a0001c0001t0003g0080others(2): Show | 8 | HG01891.hp1 HG02055.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.124-3164_124-3161d others(6): Show |
TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70603242 | ||||||
| chr8:70603287
|
C | T | 1 | a0001c0001t0003g0160 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.124-3205G>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70603287 | ||||||
| chr8:70603300
|
T | TTA | 10 | a0001c0001t0003g0005a0001c0001t0003g0036a0001c0001t0003g0175others(7): Show | 16 | HG01106.hp2 HG01192.hp1 HG01255.hp1 others(13): Show |
intron_variant | MODIFIER | c.124-3220_124-3219d others(4): Show |
TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70603300 | ||||||
| chr8:70603303
|
T | TAC | 3 | a0001c0001t0002g0009a0001c0001t0002g0056a0001c0001t0003g0178 | 6 | HG02451.hp2 HG02615.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.124-3223_124-3222d others(4): Show |
TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70603303 | ||||||
| chr8:70603303
|
T | TACACACA others(3): Show |
2 | a0001c0001t0001g0023a0001c0001t0001g0065 | 3 | HG02965.hp2 HG03453.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.124-3231_124-3222d others(12): Show |
TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70603303 | ||||||
| chr8:70603303
|
T | TATACAC | 3 | a0002c0002t0003g0179a0002c0002t0003g0180a0002c0002t0011g0221 | 3 | HG03209.hp1 HG03453.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.124-3222_124-3221i others(8): Show |
TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70603303 | ||||||
| chr8:70603303
|
T | TATACACA others(1): Show |
6 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0070others(3): Show | 6 | HG00642.hp1 HG01168.hp2 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.124-3222_124-3221i others(10): Show |
TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70603303 | ||||||
| chr8:70603303
|
T | TATACACA others(3): Show |
2 | a0001c0001t0001g0066a0001c0001t0001g0072 | 2 | HG02622.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.124-3222_124-3221i others(12): Show |
TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70603303 | ||||||
| chr8:70603303
|
T | TATACACA others(5): Show |
3 | a0001c0001t0001g0024a0001c0001t0001g0073a0001c0001t0001g0074 | 4 | HG02738.hp1 HG03098.hp2 HG03491.hp1 others(1): Show |
intron_variant | MODIFIER | c.124-3222_124-3221i others(14): Show |
TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70603303 | ||||||
| chr8:70603303
|
T | TATACACA others(9): Show |
1 | a0001c0001t0001g0075 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.124-3222_124-3221i others(18): Show |
TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70603303 | ||||||
| chr8:70603303
|
TAC | T | 17 | a0001c0001t0001g0019a0001c0001t0001g0099a0001c0001t0001g0142others(14): Show | 23 | HG02055.hp1 HG02055.hp2 HG02071.hp1 others(20): Show |
intron_variant | MODIFIER | c.124-3223_124-3222d others(4): Show |
TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70603303 | ||||||
| chr8:70603303
|
TACAC | T | 78 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(75): Show | 119 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.124-3225_124-3222d others(6): Show |
TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70603303 | ||||||
| chr8:70603303
|
TACACAC | T | 2 | a0001c0001t0007g0034a0001c0001t0007g0077 | 3 | HG01109.hp1 HG02280.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.124-3227_124-3222d others(8): Show |
TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70603303 | ||||||
| chr8:70603303
|
TACACACA others(1): Show |
T | 3 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102 | 3 | HG01071.hp2 HG02723.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.124-3229_124-3222d others(10): Show |
TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70603303 | ||||||
| chr8:70603303
|
TACACACA others(3): Show |
T | 2 | a0001c0001t0001g0203a0001c0001t0001g0204 | 2 | NA19066.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.124-3231_124-3222d others(12): Show |
TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70603303 | ||||||
| chr8:70603303
|
TACACACA others(5): Show |
T | 53 | a0001c0001t0001g0006a0001c0001t0001g0016a0001c0001t0001g0022others(50): Show | 70 | HG00140.hp1 HG00323.hp2 HG00733.hp2 others(67): Show |
intron_variant | MODIFIER | c.124-3233_124-3222d others(14): Show |
TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70603303 | ||||||
| chr8:70603305
|
C | T | 2 | a0001c0001t0003g0161a0001c0001t0003g0171 | 2 | HG00673.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.124-3223G>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70603305 | ||||||
| chr8:70603307
|
C | T | 12 | a0001c0001t0001g0151a0001c0001t0003g0012a0001c0001t0003g0035others(9): Show | 16 | HG02055.hp1 HG02055.hp2 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.124-3225G>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70603307 | ||||||
| chr8:70603309
|
C | T | 6 | a0001c0001t0003g0015a0001c0001t0003g0163a0001c0001t0003g0164others(3): Show | 9 | HG01243.hp2 HG01884.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.124-3227G>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70603309 | ||||||
| chr8:70603312
|
A | T | 1 | a0001c0001t0001g0099 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.124-3230T>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70603312 | ||||||
| chr8:70603450
|
C | T | 1 | a0001c0001t0009g0162 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.124-3368G>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70603450 | ||||||
| chr8:70603494
|
C | T | 1 | a0001c0001t0001g0066 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.124-3412G>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70603494 | ||||||
| chr8:70603506
|
C | A | 2 | a0001c0001t0001g0145a0001c0001t0001g0146 | 2 | NA18990.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.124-3424G>T | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70603506 | ||||||
| chr8:70603585
|
C | T | 1 | a0001c0001t0007g0077 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.124-3503G>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70603585 | ||||||
| chr8:70603586
|
G | A | 1 | a0001c0001t0003g0161 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.124-3504C>T | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70603586 | ||||||
| chr8:70603630
|
T | A | 2 | a0001c0001t0001g0145a0001c0001t0001g0146 | 2 | NA18990.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.124-3548A>T | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70603630 | ||||||
| chr8:70603693
|
G | T | 4 | a0002c0002t0003g0179a0002c0002t0003g0180a0002c0002t0003g0181others(1): Show | 4 | HG03209.hp1 HG03453.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.124-3611C>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70603693 | ||||||
| chr8:70603869
|
TAGA | T | 29 | a0001c0001t0003g0005a0001c0001t0003g0012a0001c0001t0003g0015others(26): Show | 44 | HG00140.hp2 HG00673.hp1 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.124-3790_124-3788d others(5): Show |
TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70603869 | ||||||
| chr8:70604000
|
C | T | 2 | a0001c0001t0001g0151a0005c0005t0001g0152 | 2 | HG02895.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.124-3918G>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70604000 | ||||||
| chr8:70604002
|
C | A | 3 | a0001c0001t0001g0007a0001c0001t0001g0147a0001c0001t0001g0148 | 7 | HG02258.hp1 HG02886.hp2 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.124-3920G>T | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70604002 | ||||||
| chr8:70604058
|
T | C | 1 | a0001c0007t0001g0149 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.124-3976A>G | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70604058 | ||||||
| chr8:70604239
|
C | CAAT | 193 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(190): Show | 271 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(268): Show |
intron_variant | MODIFIER | c.123+3837_123+3838i others(5): Show |
TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70604239 | ||||||
| chr8:70604285
|
C | G | 1 | a0001c0001t0003g0084 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.123+3792G>C | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70604285 | ||||||
| chr8:70604525
|
A | C | 6 | a0002c0002t0003g0155a0002c0002t0003g0179a0002c0002t0003g0180others(3): Show | 6 | HG03209.hp1 HG03453.hp2 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.123+3552T>G | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70604525 | ||||||
| chr8:70604576
|
A | G | 2 | a0001c0001t0003g0012a0001c0001t0003g0079 | 5 | HG02451.hp1 HG02572.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.123+3501T>C | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70604576 | ||||||
| chr8:70604654
|
A | G | 2 | a0001c0001t0001g0013a0001c0001t0001g0083 | 5 | HG00673.hp2 NA18971.hp1 NA19054.hp2 others(2): Show |
intron_variant | MODIFIER | c.123+3423T>C | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70604654 | ||||||
| chr8:70604662
|
A | G | 1 | a0001c0001t0016g0159 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.123+3415T>C | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70604662 | ||||||
| chr8:70604711
|
G | A | 4 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(1): Show | 4 | NA18969.hp2 NA18979.hp2 NA19010.hp2 others(1): Show |
intron_variant | MODIFIER | c.123+3366C>T | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70604711 | ||||||
| chr8:70604784
|
AAT | A | 3 | a0001c0001t0007g0034a0001c0001t0007g0077a0001c0001t0016g0159 | 4 | HG01109.hp1 HG01167.hp2 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.123+3291_123+3292d others(4): Show |
TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70604784 | ||||||
| chr8:70604819
|
C | T | 4 | a0001c0001t0001g0151a0001c0001t0008g0153a0004c0006t0008g0154others(1): Show | 4 | HG02895.hp1 HG02970.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.123+3258G>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70604819 | ||||||
| chr8:70604930
|
T | C | 3 | a0001c0001t0007g0034a0001c0001t0007g0077a0001c0001t0016g0159 | 4 | HG01109.hp1 HG01167.hp2 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.123+3147A>G | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70604930 | ||||||
| chr8:70604954
|
A | G | 1 | a0001c0001t0001g0082 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.123+3123T>C | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70604954 | ||||||
| chr8:70605066
|
A | G | 1 | a0001c0001t0002g0042 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.123+3011T>C | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70605066 | ||||||
| chr8:70605083
|
A | T | 14 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0065others(11): Show | 16 | HG00642.hp1 HG01074.hp2 HG01168.hp2 others(13): Show |
intron_variant | MODIFIER | c.123+2994T>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70605083 | ||||||
| chr8:70605166
|
C | A | 138 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(135): Show | 196 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(193): Show |
intron_variant | MODIFIER | c.123+2911G>T | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70605166 | ||||||
| chr8:70605189
|
G | T | 14 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0065others(11): Show | 16 | HG00642.hp1 HG01074.hp2 HG01168.hp2 others(13): Show |
intron_variant | MODIFIER | c.123+2888C>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70605189 | ||||||
| chr8:70605255
|
A | T | 14 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0065others(11): Show | 16 | HG00642.hp1 HG01074.hp2 HG01168.hp2 others(13): Show |
intron_variant | MODIFIER | c.123+2822T>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70605255 | ||||||
| chr8:70605325
|
C | T | 1 | a0001c0001t0001g0081 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.123+2752G>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70605325 | ||||||
| chr8:70605370
|
T | A | 1 | a0001c0001t0001g0208 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.123+2707A>T | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70605370 | ||||||
| chr8:70605380
|
C | T | 3 | a0001c0001t0005g0008a0001c0001t0005g0184a0001c0001t0005g0185 | 7 | HG00323.hp2 HG01168.hp1 HG01175.hp1 others(4): Show |
intron_variant | MODIFIER | c.123+2697G>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70605380 | ||||||
| chr8:70605598
|
C | T | 1 | a0001c0001t0009g0162 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.123+2479G>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70605598 | ||||||
| chr8:70605628
|
G | C | 1 | a0001c0001t0001g0208 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.123+2449C>G | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70605628 | ||||||
| chr8:70605807
|
A | T | 1 | a0001c0001t0014g0078 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.123+2270T>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70605807 | ||||||
| chr8:70605863
|
A | G | 24 | a0001c0001t0003g0005a0001c0001t0003g0015a0001c0001t0003g0035others(21): Show | 36 | HG00140.hp2 HG00673.hp1 HG00738.hp2 others(33): Show |
intron_variant | MODIFIER | c.123+2214T>C | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70605863 | ||||||
| chr8:70605878
|
G | A | 1 | a0001c0001t0001g0150 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.123+2199C>T | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70605878 | ||||||
| chr8:70605922
|
G | T | 1 | a0001c0001t0001g0065 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.123+2155C>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70605922 | ||||||
| chr8:70606126
|
C | A | 5 | a0001c0001t0003g0012a0001c0001t0003g0079a0001c0001t0003g0080others(2): Show | 8 | HG01891.hp1 HG02055.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.123+1951G>T | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70606126 | ||||||
| chr8:70606136
|
G | A | 221 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(218): Show | 325 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(322): Show |
intron_variant | MODIFIER | c.123+1941C>T | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70606136 | ||||||
| chr8:70606313
|
C | T | 135 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(132): Show | 192 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(189): Show |
intron_variant | MODIFIER | c.123+1764G>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70606313 | ||||||
| chr8:70606314
|
G | T | 14 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0065others(11): Show | 16 | HG00642.hp1 HG01074.hp2 HG01168.hp2 others(13): Show |
intron_variant | MODIFIER | c.123+1763C>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70606314 | ||||||
| chr8:70606334
|
G | A | 5 | a0001c0001t0003g0012a0001c0001t0003g0079a0001c0001t0003g0080others(2): Show | 8 | HG01891.hp1 HG02055.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.123+1743C>T | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70606334 | ||||||
| chr8:70606371
|
T | G | 1 | a0001c0001t0002g0057 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.123+1706A>C | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70606371 | ||||||
| chr8:70606686
|
C | A | 24 | a0001c0001t0003g0005a0001c0001t0003g0015a0001c0001t0003g0035others(21): Show | 36 | HG00140.hp2 HG00673.hp1 HG00738.hp2 others(33): Show |
intron_variant | MODIFIER | c.123+1391G>T | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70606686 | ||||||
| chr8:70606762
|
A | G | 3 | a0001c0001t0003g0012a0001c0001t0003g0079a0001c0001t0003g0080 | 6 | HG02451.hp1 HG02572.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.123+1315T>C | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70606762 | ||||||
| chr8:70606935
|
CATCTT | C | 2 | a0001c0001t0001g0006a0001c0001t0001g0209 | 7 | HG00140.hp1 HG00735.hp2 HG01258.hp2 others(4): Show |
intron_variant | MODIFIER | c.123+1137_123+1141d others(7): Show |
TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70606935 | ||||||
| chr8:70607013
|
T | C | 1 | a0001c0001t0002g0058 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.123+1064A>G | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70607013 | ||||||
| chr8:70607103
|
C | T | 1 | a0001c0001t0014g0078 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.123+974G>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70607103 | ||||||
| chr8:70607165
|
A | G | 1 | a0001c0001t0007g0077 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.123+912T>C | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70607165 | ||||||
| chr8:70607180
|
T | A | 14 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0065others(11): Show | 16 | HG00642.hp1 HG01074.hp2 HG01168.hp2 others(13): Show |
intron_variant | MODIFIER | c.123+897A>T | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70607180 | ||||||
| chr8:70607242
|
T | C | 14 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0065others(11): Show | 16 | HG00642.hp1 HG01074.hp2 HG01168.hp2 others(13): Show |
intron_variant | MODIFIER | c.123+835A>G | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70607242 | ||||||
| chr8:70607365
|
T | C | 4 | a0002c0002t0003g0179a0002c0002t0003g0180a0002c0002t0003g0181others(1): Show | 4 | HG03209.hp1 HG03453.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.123+712A>G | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70607365 | ||||||
| chr8:70607379
|
G | A | 14 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0065others(11): Show | 16 | HG00642.hp1 HG01074.hp2 HG01168.hp2 others(13): Show |
intron_variant | MODIFIER | c.123+698C>T | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70607379 | ||||||
| chr8:70607544
|
G | C | 1 | a0001c0001t0003g0182 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.123+533C>G | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70607544 | ||||||
| chr8:70607582
|
C | A | 1 | a0001c0001t0001g0183 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.123+495G>T | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70607582 | ||||||
| chr8:70607596
|
A | G | 1 | a0001c0001t0001g0076 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.123+481T>C | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70607596 | ||||||
| chr8:70607671
|
C | T | 14 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0065others(11): Show | 16 | HG00642.hp1 HG01074.hp2 HG01168.hp2 others(13): Show |
intron_variant | MODIFIER | c.123+406G>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70607671 | ||||||
| chr8:70607689
|
CCCGAG | C | 40 | a0001c0001t0001g0006a0001c0001t0001g0016a0001c0001t0001g0022others(37): Show | 57 | HG00140.hp1 HG00323.hp2 HG00733.hp2 others(54): Show |
intron_variant | MODIFIER | c.123+383_123+387del others(5): Show |
TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70607689 | ||||||
| chr8:70607712
|
G | A | 1 | a0001c0001t0002g0059 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.123+365C>T | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70607712 | ||||||
| chr8:70607729
|
A | C | 14 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0065others(11): Show | 16 | HG00642.hp1 HG01074.hp2 HG01168.hp2 others(13): Show |
intron_variant | MODIFIER | c.123+348T>G | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70607729 | ||||||
| chr8:70607789
|
T | G | 218 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(215): Show | 319 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(316): Show |
intron_variant | MODIFIER | c.123+288A>C | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70607789 | ||||||
| chr8:70607882
|
C | T | 5 | a0001c0001t0001g0022a0001c0001t0001g0062a0001c0001t0001g0063others(2): Show | 6 | NA18959.hp1 NA18962.hp1 NA18964.hp2 others(3): Show |
intron_variant | MODIFIER | c.123+195G>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70607882 | ||||||
| chr8:70607913
|
G | A | 1 | a0001c0001t0001g0210 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.123+164C>T | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70607913 | ||||||
| chr8:70608023
|
C | T | 1 | a0001c0001t0004g0213 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.123+54G>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70608023 |