Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 51075 |
|---|---|
| ensemblid | ENSG00000213593.10 |
| hgncid | 30739 |
| symbol | TMX2 |
| name | thioredoxin related transmembrane protein 2 |
| refseq_nuc | NM_015959.4 |
| refseq_prot | NP_057043.1 |
| ensembl_nuc | ENST00000278422.9 |
| ensembl_prot | ENSP00000278422.4 |
| mane_status | MANE Select |
| chr | chr11 |
| start | 57712593 |
| end | 57740973 |
| strand | + |
| ver | v1.2 |
| region | chr11:57712593-57740973 |
| region5000 | chr11:57707593-57745973 |
| regionname0 | TMX2_chr11_57712593_57740973 |
| regionname5000 | TMX2_chr11_57707593_57745973 |
| chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/0 | 891 | 342 | 85 | 66 | 137 | 14 | 40 | TMX2_chr11_57707593_57745973 | TMX2 | copy fasta | chr11 | 57707593 | 57745973 |
| c0002 | 0/0 | 891 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | copy fasta | chr11 | 57707593 | 57745973 |
| c0003 | 0/0 | 891 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | copy fasta | chr11 | 57707593 | 57745973 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 755 | 271 | 74 | 48 | 112 | 8 | 29 | TMX2_chr11_57707593_57745973 | TMX2 | copy fasta | chr11 | 57707593 | 57745973 |
| t0002 | 0/0 | 755 | 56 | 7 | 14 | 19 | 6 | 10 | TMX2_chr11_57707593_57745973 | TMX2 | copy fasta | chr11 | 57707593 | 57745973 |
| t0003 | 0/0 | 755 | 4 | 4 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | copy fasta | chr11 | 57707593 | 57745973 |
| t0004 | 0/0 | 757 | 3 | 0 | 0 | 3 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | copy fasta | chr11 | 57707593 | 57745973 |
| t0005 | 0/0 | 755 | 2 | 0 | 0 | 2 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | copy fasta | chr11 | 57707593 | 57745973 |
| t0006 | 0/0 | 755 | 1 | 0 | 0 | 0 | 0 | 1 | TMX2_chr11_57707593_57745973 | TMX2 | copy fasta | chr11 | 57707593 | 57745973 |
| t0007 | 0/0 | 755 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | copy fasta | chr11 | 57707593 | 57745973 |
| t0008 | 0/0 | 755 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | copy fasta | chr11 | 57707593 | 57745973 |
| t0009 | 0/0 | 755 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | copy fasta | chr11 | 57707593 | 57745973 |
| t0010 | 0/0 | 755 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | copy fasta | chr11 | 57707593 | 57745973 |
| t0011 | 0/0 | 755 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | copy fasta | chr11 | 57707593 | 57745973 |
| t0012 | 0/0 | 755 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | copy fasta | chr11 | 57707593 | 57745973 |
| t0013 | 0/0 | 755 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | copy fasta | chr11 | 57707593 | 57745973 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0005 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0037 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0044 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0273 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0283 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0298 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0330 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0334 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 891 | 342 | 85 | 66 | 137 | 14 | 40 | TMX2_chr11_57707593_57745973 | TMX2 | copy fasta | chr11 | 57707593 | 57745973 |
| a0001c0003 | 0/0 | 891 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | copy fasta | chr11 | 57707593 | 57745973 |
| a0002c0002 | 0/0 | 891 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | copy fasta | chr11 | 57707593 | 57745973 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 1645 | 270 | 74 | 48 | 111 | 8 | 29 | TMX2_chr11_57707593_57745973 | TMX2 | copy fasta | chr11 | 57707593 | 57745973 |
| a0001c0001t0002 | 0/0 | 1645 | 56 | 7 | 14 | 19 | 6 | 10 | TMX2_chr11_57707593_57745973 | TMX2 | copy fasta | chr11 | 57707593 | 57745973 |
| a0001c0001t0003 | 0/0 | 1645 | 4 | 4 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | copy fasta | chr11 | 57707593 | 57745973 |
| a0001c0001t0004 | 0/0 | 1647 | 3 | 0 | 0 | 3 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | copy fasta | chr11 | 57707593 | 57745973 |
| a0001c0001t0005 | 0/0 | 1645 | 2 | 0 | 0 | 2 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | copy fasta | chr11 | 57707593 | 57745973 |
| a0001c0001t0006 | 0/0 | 1645 | 1 | 0 | 0 | 0 | 0 | 1 | TMX2_chr11_57707593_57745973 | TMX2 | copy fasta | chr11 | 57707593 | 57745973 |
| a0001c0001t0007 | 0/0 | 1645 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | copy fasta | chr11 | 57707593 | 57745973 |
| a0001c0001t0008 | 0/0 | 1645 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | copy fasta | chr11 | 57707593 | 57745973 |
| a0001c0001t0009 | 0/0 | 1645 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | copy fasta | chr11 | 57707593 | 57745973 |
| a0001c0001t0011 | 0/0 | 1645 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | copy fasta | chr11 | 57707593 | 57745973 |
| a0001c0001t0012 | 0/0 | 1645 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | copy fasta | chr11 | 57707593 | 57745973 |
| a0001c0001t0013 | 0/0 | 1645 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | copy fasta | chr11 | 57707593 | 57745973 |
| a0001c0003t0010 | 0/0 | 1645 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | copy fasta | chr11 | 57707593 | 57745973 |
| a0002c0002t0001 | 0/0 | 1645 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | copy fasta | chr11 | 57707593 | 57745973 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0002g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0002g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0002g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0002g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0002g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0002g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0002g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0002g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0002g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0002g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0002g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0002g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0002g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0002g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0003g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0003g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0003g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0003g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0004g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0004g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0004g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0005g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0005g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0006g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0007g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0008g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0009g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0011g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0012g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0013g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0003t0010g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0002c0002t0001g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0137 | EUR | GBR | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0060 | EUR | GBR | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0037 | EUR | FIN | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0298 | EUR | FIN | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG00408 | hp1 | a0001 | c0001 | t0002 | g0054 | EAS | CHS | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | CHS | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0302 | EAS | CHS | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0081 | EAS | CHS | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | CHS | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | CHS | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0305 | EAS | CHS | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0339 | EAS | CHS | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0317 | EAS | CHS | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | CHS | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | CHS | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | CHS | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | CHS | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | CHS | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG00639 | hp1 | a0001 | c0001 | t0011 | g0139 | AMR | PUR | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0269 | AMR | PUR | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0058 | AMR | PUR | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0167 | AMR | PUR | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | CHS | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | CHS | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0209 | AMR | PUR | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0232 | AMR | PUR | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0245 | AMR | PUR | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0130 | AMR | PUR | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0275 | AMR | PUR | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0112 | AMR | PUR | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | PUR | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0040 | AMR | PUR | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0149 | AMR | PUR | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0036 | AMR | PUR | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0059 | AMR | PUR | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0126 | AMR | PUR | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0038 | AMR | PUR | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0129 | AMR | PUR | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0048 | AMR | PUR | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0247 | AMR | PUR | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0061 | AMR | PUR | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0315 | AMR | PUR | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0125 | AMR | PUR | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0067 | AMR | PUR | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0270 | AMR | PUR | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0169 | AMR | PUR | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0042 | AMR | PUR | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0147 | AMR | PUR | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0260 | AMR | PUR | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0182 | AMR | PUR | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0243 | AMR | PUR | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0133 | AMR | PUR | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG01192 | hp2 | a0001 | c0001 | t0013 | g0316 | AMR | PUR | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0064 | AMR | CLM | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0295 | AMR | CLM | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0310 | AMR | CLM | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0078 | AMR | CLM | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0159 | AMR | CLM | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0309 | AMR | CLM | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0080 | AMR | CLM | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0194 | AMR | CLM | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0162 | AMR | CLM | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0323 | AMR | CLM | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0331 | AMR | CLM | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0294 | AMR | CLM | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG01361 | hp1 | a0001 | c0001 | t0007 | g0213 | AMR | CLM | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0161 | AMR | CLM | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0174 | AMR | CLM | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0088 | AMR | CLM | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0180 | EUR | IBS | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0044 | EUR | IBS | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0071 | EUR | IBS | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0166 | EUR | IBS | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0041 | EUR | IBS | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0073 | EUR | IBS | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0152 | AFR | ACB | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | ACB | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0146 | AFR | ACB | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0039 | AFR | ACB | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0272 | AMR | PEL | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0135 | AMR | PEL | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0156 | AMR | PEL | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0325 | AMR | PEL | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG01981 | hp1 | a0001 | c0001 | t0008 | g0321 | AMR | PEL | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0210 | AMR | PEL | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0256 | AMR | PEL | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0141 | AMR | PEL | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0312 | AMR | PEL | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0187 | AMR | PEL | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0068 | EAS | KHV | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | KHV | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0033 | EAS | KHV | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | KHV | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | ACB | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG02055 | hp2 | a0001 | c0001 | t0002 | g0332 | AFR | ACB | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | KHV | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | KHV | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0065 | EAS | KHV | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | KHV | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | KHV | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0276 | EAS | KHV | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | KHV | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | KHV | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0057 | EAS | KHV | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG02129 | hp2 | a0001 | c0001 | t0005 | g0259 | EAS | KHV | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | KHV | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0070 | EAS | KHV | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0202 | AFR | ACB | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0095 | AFR | ACB | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | CDX | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG02155 | hp2 | a0002 | c0002 | t0001 | g0337 | EAS | CDX | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | CDX | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0286 | EAS | CDX | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | ACB | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0160 | AFR | ACB | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0097 | AFR | ACB | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0177 | AFR | ACB | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0288 | AMR | PEL | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0211 | AMR | PEL | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | ACB | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0249 | AFR | ACB | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0319 | AMR | PEL | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG02293 | hp2 | a0001 | c0001 | t0002 | g0043 | AMR | PEL | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0246 | AMR | PEL | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0140 | AMR | PEL | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG02451 | hp2 | a0001 | c0001 | t0003 | g0106 | AFR | ACB | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0163 | AFR | GWD | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0099 | AFR | GWD | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0136 | SAS | PJL | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0056 | SAS | PJL | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG02615 | hp1 | a0001 | c0001 | t0002 | g0074 | AFR | GWD | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0118 | AFR | GWD | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | GWD | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0184 | AFR | GWD | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0165 | AFR | GWD | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0233 | AFR | GWD | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0264 | AFR | GWD | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG02647 | hp2 | a0001 | c0001 | t0003 | g0104 | AFR | GWD | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0280 | SAS | PJL | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0049 | SAS | PJL | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0183 | AFR | GWD | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0100 | AFR | GWD | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0248 | AFR | GWD | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | GWD | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0047 | SAS | PJL | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0262 | SAS | PJL | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0085 | SAS | PJL | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0188 | SAS | PJL | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0090 | AFR | GWD | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0110 | AFR | GWD | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0094 | AFR | GWD | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0119 | AFR | GWD | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0282 | AFR | GWD | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0292 | AFR | GWD | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0267 | AFR | GWD | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0108 | AFR | GWD | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | GWD | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0087 | AFR | GWD | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | ESN | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0115 | AFR | ESN | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0190 | AFR | ESN | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0204 | AFR | ESN | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0326 | AFR | ESN | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0102 | AFR | ESN | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0201 | AFR | ESN | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG02976 | hp2 | a0001 | c0001 | t0003 | g0123 | AFR | ESN | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0291 | SAS | PJL | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0062 | SAS | PJL | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0281 | AFR | GWD | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0200 | AFR | GWD | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0153 | AFR | MSL | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0101 | AFR | MSL | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG03130 | hp1 | a0001 | c0001 | t0002 | g0077 | AFR | ESN | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0241 | AFR | ESN | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0076 | AFR | ESN | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0191 | AFR | ESN | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | MSL | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0192 | AFR | MSL | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | MSL | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0203 | AFR | MSL | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0063 | SAS | PJL | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0285 | SAS | PJL | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0089 | AFR | MSL | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0196 | AFR | MSL | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0186 | SAS | PJL | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0254 | SAS | PJL | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0154 | SAS | PJL | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG03516 | hp1 | a0001 | c0003 | t0010 | g0193 | AFR | ESN | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0195 | AFR | ESN | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0265 | AFR | GWD | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0263 | AFR | GWD | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0117 | AFR | MSL | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0114 | AFR | MSL | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0164 | SAS | STU | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0242 | SAS | STU | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0333 | SAS | PJL | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0290 | SAS | PJL | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0127 | SAS | PJL | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0142 | SAS | PJL | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG03831 | hp1 | a0001 | c0001 | t0006 | g0084 | SAS | BEB | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0024 | SAS | BEB | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0066 | SAS | BEB | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0255 | SAS | BEB | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0026 | SAS | BEB | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0027 | SAS | BEB | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0303 | SAS | STU | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0228 | SAS | STU | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0330 | SAS | BEB | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0172 | SAS | BEB | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0296 | SAS | STU | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0109 | SAS | STU | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0170 | SAS | STU | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0082 | SAS | STU | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0229 | SAS | STU | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0334 | SAS | STU | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0311 | AFR | YRI | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0266 | AFR | YRI | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0277 | EAS | CHB | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | CHB | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0098 | AFR | YRI | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | YRI | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA18945 | hp1 | a0001 | c0001 | t0004 | g0215 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA18946 | hp1 | a0001 | c0001 | t0002 | g0055 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0307 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA18948 | hp1 | a0001 | c0001 | t0009 | g0010 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0322 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA18959 | hp2 | a0001 | c0001 | t0004 | g0208 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA18961 | hp1 | a0001 | c0001 | t0002 | g0046 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA18964 | hp1 | a0001 | c0001 | t0005 | g0320 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA18976 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA18976 | hp2 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0052 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0318 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0308 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0324 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0069 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0086 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA19010 | hp2 | a0001 | c0001 | t0004 | g0221 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0185 | AFR | LWK | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0313 | AFR | LWK | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0234 | AFR | LWK | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0148 | AFR | LWK | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0314 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA19064 | hp1 | a0001 | c0001 | t0002 | g0050 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA19075 | hp2 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0328 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA19076 | hp2 | a0001 | c0001 | t0012 | g0216 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0336 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0327 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA19078 | hp2 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0338 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA19086 | hp1 | a0001 | c0001 | t0002 | g0051 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA19087 | hp2 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0045 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0329 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0128 | EUR | TSI | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0273 | EUR | TSI | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0283 | EUR | TSI | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0131 | EUR | TSI | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0219 | SAS | GIH | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0072 | SAS | GIH | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0284 | AFR | ACB | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0250 | AFR | ACB | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0116 | AFR | ACB | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG02486 | hp2 | a0001 | c0001 | t0002 | g0075 | AFR | ACB | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0197 | AFR | MSL | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG03471 | hp2 | a0001 | c0001 | t0002 | g0079 | AFR | MSL | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG06807 | hp1 | a0001 | c0001 | t0003 | g0105 | AFR | USA | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0113 | AFR | USA | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0158 | AFR | LWK | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0335 | AFR | LWK | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:57738023
|
A | G | 1 | a0002 | 1 | HG02155.hp2 | missense_variant | MODERATE | c.361A>G | p.Ile121Val | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 3/8 | 387/1645 | 361/891 | 121/296 | chr11 | 57738023 |
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:57737983
|
C | T | 1 | a0001c0003 | 1 | HG03516.hp1 | synonymous_variant | LOW | c.321C>T | p.Arg107Arg | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 3/8 | 347/1645 | 321/891 | 107/296 | chr11 | 57737983 |
| chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:57740254
|
C | CTT | 1 | a0001c0001t0004 | 3 | NA18945.hp1 NA18959.hp2 NA19010.hp2 |
3_prime_UTR_variant | MODIFIER | c.*11_*12dupTT | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 8/8 | 13 | INFO_REALIGN_3_PRIME | chr11 | 57740254 | ||||
| chr11:57740260
|
C | T | 1 | a0001c0001t0013 | 1 | HG01192.hp2 | 3_prime_UTR_variant | MODIFIER | c.*15C>T | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 8/8 | 15 | chr11 | 57740260 | |||||
| chr11:57740264
|
G | A | 1 | a0001c0001t0006 | 1 | HG03831.hp1 | 3_prime_UTR_variant | MODIFIER | c.*19G>A | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 8/8 | 19 | chr11 | 57740264 | |||||
| chr11:57740436
|
G | T | 1 | a0001c0001t0012 | 1 | NA19076.hp2 | 3_prime_UTR_variant | MODIFIER | c.*191G>T | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 8/8 | 191 | chr11 | 57740436 | |||||
| chr11:57740511
|
C | T | 2 | a0001c0001t0002a0001c0001t0006 | 57 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(54): Show |
3_prime_UTR_variant | MODIFIER | c.*266C>T | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 8/8 | 266 | chr11 | 57740511 | |||||
| chr11:57740567
|
T | A | 1 | a0001c0001t0007 | 1 | HG01361.hp1 | 3_prime_UTR_variant | MODIFIER | c.*322T>A | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 8/8 | 322 | chr11 | 57740567 | |||||
| chr11:57740603
|
C | T | 1 | a0001c0001t0005 | 2 | HG02129.hp2 NA18964.hp1 |
3_prime_UTR_variant | MODIFIER | c.*358C>T | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 8/8 | 358 | chr11 | 57740603 | |||||
| chr11:57740645
|
G | C | 1 | a0001c0001t0003 | 4 | HG02451.hp2 HG02647.hp2 HG02976.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*400G>C | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 8/8 | 400 | chr11 | 57740645 | |||||
| chr11:57740798
|
T | G | 1 | a0001c0001t0008 | 1 | HG01981.hp1 | 3_prime_UTR_variant | MODIFIER | c.*553T>G | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 8/8 | 553 | chr11 | 57740798 | |||||
| chr11:57740809
|
C | T | 1 | a0001c0001t0011 | 1 | HG00639.hp1 | 3_prime_UTR_variant | MODIFIER | c.*564C>T | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 8/8 | 564 | chr11 | 57740809 | |||||
| chr11:57740813
|
T | C | 1 | a0001c0001t0008 | 1 | HG01981.hp1 | 3_prime_UTR_variant | MODIFIER | c.*568T>C | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 8/8 | 568 | chr11 | 57740813 | |||||
| chr11:57740824
|
G | A | 1 | a0001c0001t0009 | 1 | NA18948.hp1 | 3_prime_UTR_variant | MODIFIER | c.*579G>A | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 8/8 | 579 | chr11 | 57740824 | |||||
| chr11:57740907
|
C | G | 1 | a0001c0003t0010 | 1 | HG03516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*662C>G | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 8/8 | 662 | chr11 | 57740907 |
| chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:57712814
|
C | T | 4 | a0001c0001t0001g0336a0001c0001t0001g0338a0001c0001t0001g0339others(1): Show | 4 | HG00558.hp2 HG02155.hp2 NA19077.hp2 others(1): Show |
splice_region_variant&intron_variant | LOW | c.189+7C>T | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57712814 | ||||||
| chr11:57712828
|
T | G | 20 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(17): Show | 20 | HG00673.hp1 HG02056.hp1 HG02071.hp2 others(17): Show |
intron_variant | MODIFIER | c.189+21T>G | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57712828 | ||||||
| chr11:57712829
|
A | AC | 7 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(4): Show | 7 | HG02622.hp1 HG03927.hp1 HG03927.hp2 others(4): Show |
intron_variant | MODIFIER | c.189+26dupC | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57712829 | |||||
| chr11:57712859
|
C | T | 1 | a0001c0001t0001g0335 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.189+52C>T | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57712859 | ||||||
| chr11:57712985
|
A | G | 1 | a0001c0001t0001g0334 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.189+178A>G | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57712985 | ||||||
| chr11:57713093
|
C | T | 1 | a0001c0001t0001g0333 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.189+286C>T | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57713093 | ||||||
| chr11:57713151
|
C | A | 73 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(70): Show | 73 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(70): Show |
intron_variant | MODIFIER | c.189+344C>A | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57713151 | ||||||
| chr11:57713151
|
C | G | 2 | a0001c0001t0002g0331a0001c0001t0002g0332 | 2 | HG01358.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.189+344C>G | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57713151 | ||||||
| chr11:57713245
|
C | G | 159 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(156): Show | 161 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(158): Show |
intron_variant | MODIFIER | c.189+438C>G | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57713245 | ||||||
| chr11:57713406
|
G | A | 47 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(44): Show | 47 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(44): Show |
intron_variant | MODIFIER | c.189+599G>A | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57713406 | ||||||
| chr11:57713546
|
C | G | 14 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0001g0092others(11): Show | 14 | HG01884.hp2 HG02145.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.189+739C>G | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57713546 | ||||||
| chr11:57713555
|
T | C | 5 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0003g0104others(2): Show | 5 | HG02451.hp2 HG02647.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.189+748T>C | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57713555 | ||||||
| chr11:57713562
|
T | A | 1 | a0001c0001t0001g0109 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.189+755T>A | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57713562 | ||||||
| chr11:57713623
|
C | T | 159 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(156): Show | 161 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(158): Show |
intron_variant | MODIFIER | c.189+816C>T | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57713623 | ||||||
| chr11:57713683
|
G | A | 57 | a0001c0001t0002g0026a0001c0001t0002g0033a0001c0001t0002g0034others(54): Show | 57 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(54): Show |
intron_variant | MODIFIER | c.189+876G>A | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57713683 | ||||||
| chr11:57713864
|
C | G | 159 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(156): Show | 161 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(158): Show |
intron_variant | MODIFIER | c.189+1057C>G | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57713864 | ||||||
| chr11:57713866
|
A | G | 5 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0003g0104others(2): Show | 5 | HG02451.hp2 HG02647.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.189+1059A>G | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57713866 | ||||||
| chr11:57713869
|
G | C | 2 | a0001c0001t0001g0110a0001c0001t0001g0111 | 2 | HG02055.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.189+1062G>C | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57713869 | ||||||
| chr11:57714057
|
C | T | 6 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0201others(3): Show | 6 | HG02145.hp1 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.189+1250C>T | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57714057 | ||||||
| chr11:57714122
|
T | C | 3 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089 | 3 | HG01496.hp2 HG02897.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.189+1315T>C | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57714122 | ||||||
| chr11:57714310
|
C | G | 1 | a0001c0001t0001g0330 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.189+1503C>G | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57714310 | ||||||
| chr11:57714332
|
A | T | 1 | a0001c0001t0001g0200 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.189+1525A>T | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57714332 | ||||||
| chr11:57714543
|
C | T | 2 | a0001c0001t0001g0230a0001c0001t0001g0231 | 2 | NA19009.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.189+1736C>T | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57714543 | ||||||
| chr11:57714763
|
T | A | 1 | a0001c0001t0001g0112 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.189+1956T>A | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57714763 | ||||||
| chr11:57714886
|
C | T | 1 | a0001c0001t0001g0229 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.189+2079C>T | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57714886 | ||||||
| chr11:57714894
|
T | TA | 8 | a0001c0001t0001g0001a0001c0001t0001g0113a0001c0001t0001g0114others(5): Show | 9 | HG02451.hp1 HG02486.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.189+2093dupA | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57714894 | |||||
| chr11:57715179
|
T | C | 1 | a0001c0001t0001g0120 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.189+2372T>C | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57715179 | ||||||
| chr11:57715209
|
G | C | 3 | a0001c0001t0001g0002a0001c0001t0001g0121a0001c0001t0001g0122 | 4 | NA18943.hp2 NA18985.hp2 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.189+2402G>C | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57715209 | ||||||
| chr11:57715376
|
G | A | 1 | a0001c0001t0001g0232 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.189+2569G>A | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57715376 | ||||||
| chr11:57715378
|
G | A | 1 | a0001c0001t0001g0232 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.189+2571G>A | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57715378 | ||||||
| chr11:57715379
|
C | G | 1 | a0001c0001t0001g0232 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.189+2572C>G | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57715379 | ||||||
| chr11:57715384
|
A | G | 1 | a0001c0001t0001g0232 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.189+2577A>G | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57715384 | ||||||
| chr11:57715394
|
T | G | 1 | a0001c0001t0001g0232 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.189+2587T>G | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57715394 | ||||||
| chr11:57715395
|
C | CAATACGA others(3): Show |
1 | a0001c0001t0001g0232 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.189+2588_189+2589i others(12): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57715395 | ||||||
| chr11:57715396
|
T | A | 1 | a0001c0001t0001g0232 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.189+2589T>A | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57715396 | ||||||
| chr11:57715422
|
A | T | 1 | a0001c0001t0001g0232 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.189+2615A>T | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57715422 | ||||||
| chr11:57715430
|
A | G | 1 | a0001c0001t0001g0232 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.189+2623A>G | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57715430 | ||||||
| chr11:57715434
|
T | A | 1 | a0001c0001t0001g0232 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.189+2627T>A | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57715434 | ||||||
| chr11:57715438
|
T | C | 1 | a0001c0001t0001g0232 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.189+2631T>C | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57715438 | ||||||
| chr11:57715455
|
G | A | 1 | a0001c0001t0001g0232 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.189+2648G>A | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57715455 | ||||||
| chr11:57715493
|
A | G | 1 | a0001c0001t0001g0025 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.189+2686A>G | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57715493 | ||||||
| chr11:57715567
|
A | T | 75 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(72): Show | 75 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(72): Show |
intron_variant | MODIFIER | c.189+2760A>T | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57715567 | ||||||
| chr11:57715586
|
C | CTTTCTTT others(4): Show |
1 | a0001c0001t0001g0336 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.189+2782_189+2783i others(13): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57715586 | |||||
| chr11:57715586
|
C | CTTTTTTT others(1): Show |
18 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0090others(15): Show | 18 | HG01496.hp2 HG01884.hp2 HG02027.hp1 others(15): Show |
intron_variant | MODIFIER | c.189+2782_189+2789d others(10): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57715586 | |||||
| chr11:57715586
|
C | CTTTTTTT others(2): Show |
56 | a0001c0001t0001g0001a0001c0001t0001g0089a0001c0001t0001g0114others(53): Show | 57 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(54): Show |
intron_variant | MODIFIER | c.189+2781_189+2789d others(11): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57715586 | |||||
| chr11:57715586
|
C | CTTTTTTT others(3): Show |
23 | a0001c0001t0001g0008a0001c0001t0001g0107a0001c0001t0001g0108others(20): Show | 23 | HG02074.hp1 HG02145.hp1 HG02486.hp1 others(20): Show |
intron_variant | MODIFIER | c.189+2780_189+2789d others(12): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57715586 | |||||
| chr11:57715586
|
C | CTTTTTTT others(4): Show |
141 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0009others(138): Show | 143 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(140): Show |
intron_variant | MODIFIER | c.189+2789_189+2790i others(13): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57715586 | |||||
| chr11:57715586
|
C | CTTTTTTT others(5): Show |
17 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0227others(14): Show | 17 | HG01346.hp2 HG01978.hp2 HG01981.hp1 others(14): Show |
intron_variant | MODIFIER | c.189+2789_189+2790i others(14): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57715586 | |||||
| chr11:57715593
|
T | TTTTTTTT others(4): Show |
1 | a0001c0001t0001g0205 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.189+2789_189+2790i others(13): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57715593 | |||||
| chr11:57715789
|
C | T | 1 | a0001c0001t0001g0189 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.189+2982C>T | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57715789 | ||||||
| chr11:57715864
|
A | G | 17 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(14): Show | 17 | HG01496.hp2 HG01884.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.189+3057A>G | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57715864 | ||||||
| chr11:57715894
|
T | C | 1 | a0001c0001t0001g0201 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.189+3087T>C | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57715894 | ||||||
| chr11:57715934
|
G | A | 1 | a0001c0001t0001g0236 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.189+3127G>A | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57715934 | ||||||
| chr11:57716111
|
C | CG | 4 | a0001c0001t0001g0027a0001c0001t0001g0237a0001c0001t0002g0034others(1): Show | 4 | HG03927.hp2 NA18994.hp1 NA19075.hp2 others(1): Show |
intron_variant | MODIFIER | c.189+3308dupG | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57716111 | |||||
| chr11:57716147
|
T | C | 23 | a0001c0001t0001g0001a0001c0001t0001g0107a0001c0001t0001g0108others(20): Show | 24 | HG01261.hp2 HG02145.hp1 HG02451.hp1 others(21): Show |
intron_variant | MODIFIER | c.189+3340T>C | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57716147 | ||||||
| chr11:57716185
|
G | A | 2 | a0001c0001t0001g0191a0001c0001t0001g0192 | 2 | HG03139.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.189+3378G>A | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57716185 | ||||||
| chr11:57716201
|
C | T | 157 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(154): Show | 159 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(156): Show |
intron_variant | MODIFIER | c.189+3394C>T | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57716201 | ||||||
| chr11:57716250
|
C | G | 2 | a0001c0001t0002g0026a0001c0001t0002g0082 | 2 | HG03927.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.189+3443C>G | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57716250 | ||||||
| chr11:57716254
|
C | T | 6 | a0001c0001t0001g0098a0001c0001t0001g0099a0001c0001t0001g0100others(3): Show | 6 | HG02572.hp2 HG02717.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.189+3447C>T | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57716254 | ||||||
| chr11:57716264
|
A | AC | 23 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(20): Show | 23 | HG00438.hp2 HG00597.hp1 HG00673.hp1 others(20): Show |
intron_variant | MODIFIER | c.189+3466dupC | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57716264 | |||||
| chr11:57716338
|
G | C | 1 | a0001c0001t0001g0237 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.189+3531G>C | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57716338 | ||||||
| chr11:57716353
|
A | C | 57 | a0001c0001t0002g0026a0001c0001t0002g0033a0001c0001t0002g0034others(54): Show | 57 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(54): Show |
intron_variant | MODIFIER | c.189+3546A>C | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57716353 | ||||||
| chr11:57716366
|
G | A | 4 | a0001c0001t0003g0104a0001c0001t0003g0105a0001c0001t0003g0106others(1): Show | 4 | HG02451.hp2 HG02647.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.189+3559G>A | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57716366 | ||||||
| chr11:57716366
|
G | T | 57 | a0001c0001t0002g0026a0001c0001t0002g0033a0001c0001t0002g0034others(54): Show | 57 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(54): Show |
intron_variant | MODIFIER | c.189+3559G>T | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57716366 | ||||||
| chr11:57716386
|
C | CT | 57 | a0001c0001t0002g0026a0001c0001t0002g0033a0001c0001t0002g0034others(54): Show | 57 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(54): Show |
intron_variant | MODIFIER | c.189+3579_189+3580i others(3): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57716386 | ||||||
| chr11:57716388
|
AGGGGCTG others(42): Show |
A | 1 | a0001c0001t0003g0123 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.189+3629_189+3677d others(51): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57716388 | |||||
| chr11:57716394
|
T | TCCTCACT others(22): Show |
1 | a0001c0001t0002g0083 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.189+3587_189+3588i others(31): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57716394 | ||||||
| chr11:57716395
|
G | C | 56 | a0001c0001t0002g0026a0001c0001t0002g0033a0001c0001t0002g0034others(53): Show | 56 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(53): Show |
intron_variant | MODIFIER | c.189+3588G>C | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57716395 | ||||||
| chr11:57716396
|
A | C | 56 | a0001c0001t0002g0026a0001c0001t0002g0033a0001c0001t0002g0034others(53): Show | 56 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(53): Show |
intron_variant | MODIFIER | c.189+3589A>C | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57716396 | ||||||
| chr11:57716397
|
C | G | 1 | a0001c0001t0002g0083 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.189+3590C>G | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57716397 | ||||||
| chr11:57716397
|
C | T | 56 | a0001c0001t0002g0026a0001c0001t0002g0033a0001c0001t0002g0034others(53): Show | 56 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(53): Show |
intron_variant | MODIFIER | c.189+3590C>T | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57716397 | ||||||
| chr11:57716398
|
C | G | 1 | a0001c0001t0002g0083 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.189+3591C>G | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57716398 | ||||||
| chr11:57716399
|
C | A | 56 | a0001c0001t0002g0026a0001c0001t0002g0033a0001c0001t0002g0034others(53): Show | 56 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(53): Show |
intron_variant | MODIFIER | c.189+3592C>A | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57716399 | ||||||
| chr11:57716400
|
C | CTT | 56 | a0001c0001t0002g0026a0001c0001t0002g0033a0001c0001t0002g0034others(53): Show | 56 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(53): Show |
intron_variant | MODIFIER | c.189+3593_189+3594i others(4): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57716400 | ||||||
| chr11:57716400
|
C | G | 1 | a0001c0001t0002g0083 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.189+3593C>G | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57716400 | ||||||
| chr11:57716404
|
A | AGTAGGGG others(18): Show |
55 | a0001c0001t0002g0026a0001c0001t0002g0033a0001c0001t0002g0034others(52): Show | 55 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(52): Show |
intron_variant | MODIFIER | c.189+3597_189+3598i others(27): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57716404 | ||||||
| chr11:57716404
|
A | AGTAGGGG others(19): Show |
1 | a0001c0001t0002g0085 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.189+3597_189+3598i others(28): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57716404 | ||||||
| chr11:57716404
|
A | C | 1 | a0001c0001t0002g0083 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.189+3597A>C | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57716404 | ||||||
| chr11:57716405
|
C | T | 1 | a0001c0001t0002g0083 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.189+3598C>T | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57716405 | ||||||
| chr11:57716407
|
T | A | 1 | a0001c0001t0002g0083 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.189+3600T>A | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57716407 | ||||||
| chr11:57716408
|
C | CA | 56 | a0001c0001t0002g0026a0001c0001t0002g0033a0001c0001t0002g0034others(53): Show | 56 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(53): Show |
intron_variant | MODIFIER | c.189+3601_189+3602i others(3): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57716408 | ||||||
| chr11:57716435
|
C | G | 1 | a0001c0001t0002g0035 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.189+3628C>G | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57716435 | ||||||
| chr11:57716435
|
C | T | 56 | a0001c0001t0002g0026a0001c0001t0002g0033a0001c0001t0002g0034others(53): Show | 56 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(53): Show |
intron_variant | MODIFIER | c.189+3628C>T | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57716435 | ||||||
| chr11:57716451
|
C | A | 1 | a0001c0001t0001g0240 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.189+3644C>A | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57716451 | ||||||
| chr11:57716480
|
C | T | 17 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(14): Show | 17 | HG01496.hp2 HG01884.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.189+3673C>T | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57716480 | ||||||
| chr11:57716481
|
G | C | 57 | a0001c0001t0002g0026a0001c0001t0002g0033a0001c0001t0002g0034others(54): Show | 57 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(54): Show |
intron_variant | MODIFIER | c.189+3674G>C | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57716481 | ||||||
| chr11:57716485
|
T | A | 57 | a0001c0001t0002g0026a0001c0001t0002g0033a0001c0001t0002g0034others(54): Show | 57 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(54): Show |
intron_variant | MODIFIER | c.189+3678T>A | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57716485 | ||||||
| chr11:57716517
|
C | CGGGCAGA others(120): Show |
171 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(168): Show | 173 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(170): Show |
intron_variant | MODIFIER | c.189+3769_189+3770i others(129): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57716517 | |||||
| chr11:57716517
|
C | CGGGCAGA others(120): Show |
1 | a0001c0001t0001g0198 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.189+3769_189+3770i others(129): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57716517 | |||||
| chr11:57716517
|
C | CGGGCAGA others(121): Show |
4 | a0001c0001t0001g0024a0001c0001t0001g0027a0001c0001t0001g0225others(1): Show | 4 | HG03831.hp2 HG03927.hp2 NA19063.hp1 others(1): Show |
intron_variant | MODIFIER | c.189+3769_189+3770i others(130): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57716517 | |||||
| chr11:57716517
|
C | CGGGCAGA others(121): Show |
2 | a0001c0001t0001g0199a0001c0001t0001g0226 | 2 | HG02056.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.189+3761_189+3762i others(130): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57716517 | |||||
| chr11:57716517
|
C | CGGGCAGA others(120): Show |
17 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(14): Show | 17 | HG01496.hp2 HG01884.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.189+3754_189+3755i others(129): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57716517 | |||||
| chr11:57716517
|
C | CGGGCAGA others(119): Show |
1 | a0001c0001t0001g0328 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.189+3733_189+3734i others(128): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57716517 | |||||
| chr11:57716517
|
C | T | 57 | a0001c0001t0002g0026a0001c0001t0002g0033a0001c0001t0002g0034others(54): Show | 57 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(54): Show |
intron_variant | MODIFIER | c.189+3710C>T | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57716517 | ||||||
| chr11:57716527
|
C | CGCCCCTC others(120): Show |
1 | a0001c0001t0001g0204 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.189+3769_189+3770i others(129): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57716527 | |||||
| chr11:57716528
|
G | A | 1 | a0001c0001t0001g0124 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.189+3721G>A | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57716528 | ||||||
| chr11:57716551
|
G | GGCTGGCC others(120): Show |
1 | a0001c0001t0001g0335 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.189+3754_189+3755i others(129): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57716551 | |||||
| chr11:57716562
|
C | CGGGGGGC others(121): Show |
1 | a0001c0001t0001g0025 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.189+3769_189+3770i others(130): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57716562 | |||||
| chr11:57716574
|
CCCACCTC others(137): Show |
C | 1 | a0001c0001t0001g0224 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.189+3770_189+3913d others(2): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57716574 | |||||
| chr11:57716581
|
C | CCCTCCCG others(71): Show |
2 | a0001c0001t0001g0001a0001c0001t0001g0114 | 3 | HG02451.hp1 HG03579.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.189+3797_189+3798i others(80): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57716581 | |||||
| chr11:57716591
|
C | T | 6 | a0001c0001t0001g0113a0001c0001t0001g0115a0001c0001t0001g0116others(3): Show | 6 | HG02486.hp1 HG02615.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.189+3784C>T | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57716591 | ||||||
| chr11:57716608
|
T | C | 2 | a0001c0001t0001g0001a0001c0001t0001g0114 | 3 | HG02451.hp1 HG03579.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.189+3801T>C | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57716608 | ||||||
| chr11:57716610
|
G | A | 7 | a0001c0001t0001g0125a0001c0001t0001g0126a0001c0001t0001g0127others(4): Show | 7 | HG00735.hp2 HG01070.hp2 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.189+3803G>A | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57716610 | ||||||
| chr11:57716619
|
C | T | 1 | a0001c0001t0001g0229 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.189+3812C>T | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57716619 | ||||||
| chr11:57716640
|
C | T | 2 | a0001c0001t0001g0001a0001c0001t0001g0114 | 3 | HG02451.hp1 HG03579.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.189+3833C>T | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57716640 | ||||||
| chr11:57716655
|
A | G | 2 | a0001c0001t0001g0001a0001c0001t0001g0114 | 3 | HG02451.hp1 HG03579.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.189+3848A>G | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57716655 | ||||||
| chr11:57716657
|
C | T | 2 | a0001c0001t0001g0001a0001c0001t0001g0114 | 3 | HG02451.hp1 HG03579.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.189+3850C>T | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57716657 | ||||||
| chr11:57716658
|
G | C | 75 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(72): Show | 75 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(72): Show |
intron_variant | MODIFIER | c.189+3851G>C | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57716658 | ||||||
| chr11:57716698
|
A | T | 1 | a0001c0001t0001g0186 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.189+3891A>T | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57716698 | ||||||
| chr11:57716723
|
C | A | 1 | a0001c0003t0010g0193 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.189+3916C>A | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57716723 | ||||||
| chr11:57716743
|
T | C | 1 | a0001c0001t0001g0224 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.189+3936T>C | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57716743 | ||||||
| chr11:57716752
|
A | C | 1 | a0001c0001t0001g0224 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.189+3945A>C | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57716752 | ||||||
| chr11:57716779
|
A | G | 1 | a0001c0001t0001g0114 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.189+3972A>G | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57716779 | ||||||
| chr11:57716843
|
A | AC | 20 | a0001c0001t0001g0025a0001c0001t0001g0087a0001c0001t0001g0088others(17): Show | 20 | HG01496.hp2 HG01884.hp2 HG02056.hp1 others(17): Show |
intron_variant | MODIFIER | c.189+4044dupC | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57716843 | |||||
| chr11:57716889
|
G | T | 17 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(14): Show | 17 | HG01496.hp2 HG01884.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.189+4082G>T | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57716889 | ||||||
| chr11:57716992
|
G | A | 1 | a0001c0001t0001g0315 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.189+4185G>A | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57716992 | ||||||
| chr11:57717015
|
CTCCCAGA others(109): Show |
C | 6 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0194others(3): Show | 6 | HG01261.hp2 HG03139.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.189+4216_189+4331d others(2): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57717015 | |||||
| chr11:57717032
|
G | A | 1 | a0001c0001t0001g0125 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.189+4225G>A | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57717032 | ||||||
| chr11:57717035
|
C | T | 1 | a0001c0003t0010g0193 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.189+4228C>T | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57717035 | ||||||
| chr11:57717069
|
G | A | 1 | a0001c0001t0001g0241 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.189+4262G>A | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57717069 | ||||||
| chr11:57717108
|
G | A | 57 | a0001c0001t0002g0026a0001c0001t0002g0033a0001c0001t0002g0034others(54): Show | 57 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(54): Show |
intron_variant | MODIFIER | c.189+4301G>A | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57717108 | ||||||
| chr11:57717176
|
A | G | 1 | a0001c0001t0001g0223 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.189+4369A>G | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57717176 | ||||||
| chr11:57717188
|
G | A | 75 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(72): Show | 75 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(72): Show |
intron_variant | MODIFIER | c.189+4381G>A | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57717188 | ||||||
| chr11:57717263
|
C | T | 1 | a0001c0001t0001g0314 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.189+4456C>T | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57717263 | ||||||
| chr11:57717458
|
C | T | 1 | a0001c0001t0001g0231 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.189+4651C>T | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57717458 | ||||||
| chr11:57717459
|
G | C | 1 | a0001c0001t0001g0231 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.189+4652G>C | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57717459 | ||||||
| chr11:57717529
|
C | T | 1 | a0001c0001t0001g0192 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.189+4722C>T | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57717529 | ||||||
| chr11:57717640
|
C | T | 6 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0194others(3): Show | 6 | HG01261.hp2 HG03139.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.189+4833C>T | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57717640 | ||||||
| chr11:57717667
|
C | T | 159 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(156): Show | 161 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(158): Show |
intron_variant | MODIFIER | c.189+4860C>T | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57717667 | ||||||
| chr11:57717689
|
C | T | 3 | a0001c0001t0001g0183a0001c0001t0001g0184a0001c0001t0001g0185 | 3 | HG02622.hp2 HG02717.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.189+4882C>T | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57717689 | ||||||
| chr11:57717714
|
C | CGAGAGGG others(13): Show |
1 | a0001c0001t0001g0328 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.189+4917_189+4918i others(22): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57717714 | |||||
| chr11:57717717
|
G | GAGGGAGA | 57 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0110others(54): Show | 59 | HG00140.hp1 HG00609.hp1 HG00621.hp1 others(56): Show |
intron_variant | MODIFIER | c.189+4911_189+4917d others(9): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57717717 | |||||
| chr11:57717718
|
A | AGGGAGAA others(7): Show |
19 | a0001c0001t0001g0131a0001c0001t0001g0224a0001c0001t0001g0251others(16): Show | 19 | HG00323.hp1 HG00597.hp2 HG00741.hp2 others(16): Show |
intron_variant | MODIFIER | c.189+4917_189+4918i others(16): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57717718 | |||||
| chr11:57717718
|
A | AGGGAGAA others(20): Show |
1 | a0001c0001t0001g0242 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.189+4917_189+4918i others(29): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57717718 | |||||
| chr11:57717718
|
A | AGGGAGAA others(14): Show |
11 | a0001c0001t0001g0098a0001c0001t0001g0309a0001c0001t0001g0310others(8): Show | 11 | HG01074.hp1 HG01257.hp1 HG01258.hp2 others(8): Show |
intron_variant | MODIFIER | c.189+4917_189+4918i others(23): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57717718 | |||||
| chr11:57717718
|
A | AGGGAGAA others(21): Show |
23 | a0001c0001t0002g0026a0001c0001t0002g0034a0001c0001t0002g0052others(20): Show | 23 | HG00140.hp2 HG00408.hp1 HG00438.hp2 others(20): Show |
intron_variant | MODIFIER | c.189+4917_189+4918i others(30): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57717718 | |||||
| chr11:57717718
|
A | AGGGAGAA others(28): Show |
5 | a0001c0001t0002g0069a0001c0001t0002g0070a0001c0001t0002g0071others(2): Show | 5 | HG01516.hp1 HG01517.hp2 HG02135.hp2 others(2): Show |
intron_variant | MODIFIER | c.189+4917_189+4918i others(37): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57717718 | |||||
| chr11:57717718
|
A | AGGGAGAA others(35): Show |
2 | a0001c0001t0002g0033a0001c0001t0002g0074 | 2 | HG02027.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.189+4917_189+4918i others(44): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57717718 | |||||
| chr11:57717718
|
A | AGGGAGAA others(42): Show |
2 | a0001c0001t0002g0078a0001c0001t0002g0079 | 2 | HG01257.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.189+4917_189+4918i others(51): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57717718 | |||||
| chr11:57717718
|
A | AGGGAGAA others(22): Show |
1 | a0001c0001t0002g0085 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.189+4917_189+4918i others(31): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57717718 | |||||
| chr11:57717725
|
G | A | 199 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(196): Show | 202 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(199): Show |
intron_variant | MODIFIER | c.189+4918G>A | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57717725 | ||||||
| chr11:57717731
|
A | AGGGGAGA others(8): Show |
1 | a0001c0001t0001g0327 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.189+4928_189+4942d others(17): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57717731 | |||||
| chr11:57717746
|
G | GGGGAGAG others(14): Show |
1 | a0001c0001t0001g0231 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.189+4952_189+4953i others(23): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57717746 | |||||
| chr11:57717746
|
G | GGGGAGAG others(6): Show |
22 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0198others(19): Show | 22 | HG00544.hp2 HG00735.hp1 HG01074.hp2 others(19): Show |
intron_variant | MODIFIER | c.189+4948_189+4949i others(15): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57717746 | |||||
| chr11:57717746
|
G | GGGGAGAG others(13): Show |
150 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(147): Show | 153 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(150): Show |
intron_variant | MODIFIER | c.189+4948_189+4949i others(22): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57717746 | |||||
| chr11:57717746
|
G | GGGGAGAG others(20): Show |
10 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0099others(7): Show | 10 | HG01496.hp2 HG02004.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.189+4948_189+4949i others(29): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57717746 | |||||
| chr11:57717746
|
G | GGGGAGAG others(27): Show |
7 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(4): Show | 7 | HG03516.hp1 HG03831.hp2 NA18961.hp2 others(4): Show |
intron_variant | MODIFIER | c.189+4948_189+4949i others(36): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57717746 | |||||
| chr11:57717746
|
G | GGGGAGAG others(14): Show |
1 | a0001c0001t0001g0032 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.189+4948_189+4949i others(23): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57717746 | |||||
| chr11:57717751
|
G | A | 1 | a0001c0001t0001g0132 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.189+4944G>A | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57717751 | ||||||
| chr11:57717752
|
A | AGGGGAGA others(36): Show |
3 | a0001c0001t0002g0075a0001c0001t0002g0076a0001c0001t0002g0077 | 3 | HG02486.hp2 HG03130.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.189+4948_189+4949i others(45): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57717752 | |||||
| chr11:57717752
|
A | AGGGGAGA others(43): Show |
1 | a0001c0001t0001g0335 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.189+4948_189+4949i others(52): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57717752 | |||||
| chr11:57717755
|
G | C | 6 | a0001c0001t0002g0034a0001c0001t0002g0052a0001c0001t0002g0053others(3): Show | 6 | HG00408.hp1 HG00438.hp2 NA18946.hp1 others(3): Show |
intron_variant | MODIFIER | c.189+4948G>C | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57717755 | ||||||
| chr11:57717755
|
G | GGAGAGGG others(25): Show |
1 | a0002c0002t0001g0337 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.189+4948_189+4949i others(34): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57717755 | ||||||
| chr11:57717755
|
G | GGAGAGGG others(25): Show |
1 | a0001c0001t0001g0229 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.189+4948_189+4949i others(34): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57717755 | ||||||
| chr11:57717755
|
G | GGAGAGGG others(24): Show |
1 | a0001c0001t0002g0035 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.189+4948_189+4949i others(33): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57717755 | ||||||
| chr11:57717761
|
C | G | 2 | a0001c0001t0001g0335a0001c0001t0003g0106 | 2 | HG02451.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.189+4954C>G | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57717761 | ||||||
| chr11:57717767
|
C | G | 1 | a0001c0001t0001g0335 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.189+4960C>G | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57717767 | ||||||
| chr11:57718016
|
T | G | 1 | a0001c0001t0001g0253 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.189+5209T>G | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57718016 | ||||||
| chr11:57718297
|
C | A | 1 | a0001c0001t0001g0015 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.189+5490C>A | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57718297 | ||||||
| chr11:57718298
|
A | AT | 158 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(155): Show | 160 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(157): Show |
intron_variant | MODIFIER | c.189+5492dupT | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57718298 | |||||
| chr11:57718298
|
A | T | 1 | a0001c0001t0001g0015 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.189+5491A>T | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57718298 | ||||||
| chr11:57718300
|
A | G | 159 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(156): Show | 161 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(158): Show |
intron_variant | MODIFIER | c.189+5493A>G | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57718300 | ||||||
| chr11:57718330
|
G | C | 1 | a0001c0001t0001g0117 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.189+5523G>C | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57718330 | ||||||
| chr11:57718424
|
C | T | 3 | a0001c0001t0002g0071a0001c0001t0002g0072a0001c0001t0002g0073 | 3 | HG01516.hp1 HG01517.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.189+5617C>T | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57718424 | ||||||
| chr11:57718587
|
A | G | 1 | a0001c0001t0002g0068 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.189+5780A>G | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57718587 | ||||||
| chr11:57718653
|
C | CT | 11 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0022others(8): Show | 11 | HG02055.hp1 HG02293.hp1 HG02818.hp2 others(8): Show |
intron_variant | MODIFIER | c.189+5866dupT | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57718653 | |||||
| chr11:57718653
|
CT | C | 82 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(79): Show | 82 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(79): Show |
intron_variant | MODIFIER | c.189+5866delT | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57718653 | |||||
| chr11:57718781
|
G | A | 1 | a0001c0001t0001g0109 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.189+5974G>A | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57718781 | ||||||
| chr11:57718901
|
C | T | 9 | a0001c0001t0001g0031a0001c0001t0001g0257a0001c0001t0001g0304others(6): Show | 9 | HG00558.hp1 NA18946.hp1 NA18946.hp2 others(6): Show |
intron_variant | MODIFIER | c.189+6094C>T | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57718901 | ||||||
| chr11:57719020
|
CAT | C | 13 | a0001c0001t0001g0203a0001c0001t0001g0302a0001c0001t0001g0303others(10): Show | 13 | HG00438.hp1 HG00438.hp2 HG01106.hp1 others(10): Show |
intron_variant | MODIFIER | c.189+6226_189+6227d others(4): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57719020 | |||||
| chr11:57719020
|
CATAT | C | 17 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(14): Show | 17 | HG01496.hp2 HG02145.hp2 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.189+6224_189+6227d others(6): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57719020 | |||||
| chr11:57719025
|
A | G | 1 | a0001c0001t0003g0105 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.189+6218A>G | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57719025 | ||||||
| chr11:57719030
|
TATA | T | 46 | a0001c0001t0002g0026a0001c0001t0002g0033a0001c0001t0002g0035others(43): Show | 46 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(43): Show |
intron_variant | MODIFIER | c.189+6224_189+6226d others(5): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57719030 | ||||||
| chr11:57719031
|
A | T | 12 | a0001c0001t0001g0001a0001c0001t0001g0107a0001c0001t0001g0108others(9): Show | 13 | HG02451.hp1 HG02486.hp1 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.189+6224A>T | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57719031 | ||||||
| chr11:57719033
|
A | AT | 12 | a0001c0001t0001g0161a0001c0001t0001g0162a0001c0001t0001g0163others(9): Show | 12 | HG01175.hp1 HG01346.hp1 HG01361.hp2 others(9): Show |
intron_variant | MODIFIER | c.189+6248dupT | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57719033 | |||||
| chr11:57719033
|
A | T | 29 | a0001c0001t0001g0001a0001c0001t0001g0107a0001c0001t0001g0108others(26): Show | 30 | HG00438.hp2 HG00642.hp2 HG01106.hp1 others(27): Show |
intron_variant | MODIFIER | c.189+6226A>T | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57719033 | ||||||
| chr11:57719033
|
AT | A | 16 | a0001c0001t0001g0022a0001c0001t0001g0030a0001c0001t0001g0126others(13): Show | 16 | HG00323.hp2 HG00597.hp2 HG01070.hp2 others(13): Show |
intron_variant | MODIFIER | c.189+6248delT | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57719033 | |||||
| chr11:57719033
|
ATT | A | 142 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(139): Show | 144 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(141): Show |
intron_variant | MODIFIER | c.189+6247_189+6248d others(4): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57719033 | |||||
| chr11:57719035
|
T | A | 5 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0135others(2): Show | 5 | HG01167.hp1 HG01928.hp2 HG02004.hp2 others(2): Show |
intron_variant | MODIFIER | c.189+6228T>A | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57719035 | ||||||
| chr11:57719036
|
T | A | 5 | a0001c0001t0001g0205a0001c0001t0001g0224a0001c0001t0001g0261others(2): Show | 5 | HG00597.hp2 HG02080.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.189+6229T>A | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57719036 | ||||||
| chr11:57719037
|
T | A | 30 | a0001c0001t0001g0007a0001c0001t0001g0027a0001c0001t0001g0198others(27): Show | 30 | HG00544.hp1 HG00544.hp2 HG00733.hp1 others(27): Show |
intron_variant | MODIFIER | c.189+6230T>A | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57719037 | ||||||
| chr11:57719038
|
T | A | 3 | a0001c0001t0001g0205a0001c0001t0001g0224a0001c0001t0001g0310 | 3 | HG00597.hp2 HG01257.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.189+6231T>A | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57719038 | ||||||
| chr11:57719039
|
T | A | 5 | a0001c0001t0001g0243a0001c0001t0001g0244a0001c0001t0001g0245others(2): Show | 5 | HG00735.hp1 HG01099.hp1 HG01175.hp2 others(2): Show |
intron_variant | MODIFIER | c.189+6232T>A | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57719039 | ||||||
| chr11:57719040
|
T | A | 1 | a0001c0001t0001g0205 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.189+6233T>A | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57719040 | ||||||
| chr11:57719179
|
G | A | 57 | a0001c0001t0002g0026a0001c0001t0002g0033a0001c0001t0002g0034others(54): Show | 57 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(54): Show |
intron_variant | MODIFIER | c.189+6372G>A | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57719179 | ||||||
| chr11:57719240
|
T | C | 6 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0194others(3): Show | 6 | HG01261.hp2 HG03139.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.189+6433T>C | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57719240 | ||||||
| chr11:57719324
|
C | T | 1 | a0001c0001t0001g0160 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.189+6517C>T | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57719324 | ||||||
| chr11:57719514
|
C | CT | 81 | a0001c0001t0001g0088a0001c0001t0001g0089a0001c0001t0001g0095others(78): Show | 81 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(78): Show |
intron_variant | MODIFIER | c.189+6731dupT | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57719514 | |||||
| chr11:57719514
|
C | CTT | 129 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(126): Show | 131 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(128): Show |
intron_variant | MODIFIER | c.189+6730_189+6731d others(4): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57719514 | |||||
| chr11:57719514
|
C | CTTT | 45 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(42): Show | 45 | HG00544.hp1 HG00544.hp2 HG00597.hp1 others(42): Show |
intron_variant | MODIFIER | c.189+6729_189+6731d others(5): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57719514 | |||||
| chr11:57719682
|
A | G | 3 | a0001c0001t0001g0134a0001c0001t0001g0150a0001c0001t0001g0151 | 3 | HG02015.hp2 NA18964.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.189+6875A>G | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57719682 | ||||||
| chr11:57719780
|
A | G | 1 | a0001c0001t0001g0095 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.189+6973A>G | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57719780 | ||||||
| chr11:57720133
|
A | G | 3 | a0001c0001t0003g0104a0001c0001t0003g0105a0001c0001t0003g0106 | 3 | HG02451.hp2 HG02647.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.189+7326A>G | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57720133 | ||||||
| chr11:57720134
|
C | CA | 49 | a0001c0001t0001g0096a0001c0001t0001g0118a0001c0001t0001g0202others(46): Show | 49 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(46): Show |
intron_variant | MODIFIER | c.189+7346dupA | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57720134 | |||||
| chr11:57720134
|
C | CAA | 10 | a0001c0001t0002g0026a0001c0001t0002g0033a0001c0001t0002g0035others(7): Show | 10 | HG00408.hp1 HG00642.hp1 HG01069.hp2 others(7): Show |
intron_variant | MODIFIER | c.189+7345_189+7346d others(4): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57720134 | |||||
| chr11:57720134
|
CA | C | 81 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0110others(78): Show | 83 | HG00140.hp1 HG00544.hp2 HG00609.hp1 others(80): Show |
intron_variant | MODIFIER | c.189+7346delA | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57720134 | |||||
| chr11:57720134
|
CAAAA | C | 7 | a0001c0001t0001g0027a0001c0001t0001g0031a0001c0001t0001g0243others(4): Show | 7 | HG01175.hp2 HG02300.hp1 HG03927.hp2 others(4): Show |
intron_variant | MODIFIER | c.189+7343_189+7346d others(6): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57720134 | |||||
| chr11:57720134
|
CAAAAA | C | 152 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(149): Show | 154 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(151): Show |
intron_variant | MODIFIER | c.189+7342_189+7346d others(7): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57720134 | |||||
| chr11:57720202
|
C | T | 1 | a0001c0001t0001g0291 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.189+7395C>T | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57720202 | ||||||
| chr11:57720349
|
A | G | 2 | a0001c0001t0001g0133a0001c0001t0001g0149 | 2 | HG01069.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.189+7542A>G | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57720349 | ||||||
| chr11:57720503
|
C | T | 2 | a0001c0001t0001g0202a0001c0001t0001g0203 | 2 | HG02145.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.189+7696C>T | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57720503 | ||||||
| chr11:57720688
|
G | A | 159 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(156): Show | 161 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(158): Show |
intron_variant | MODIFIER | c.189+7881G>A | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57720688 | ||||||
| chr11:57720776
|
A | G | 1 | a0001c0001t0001g0148 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.189+7969A>G | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57720776 | ||||||
| chr11:57720872
|
A | G | 1 | a0001c0001t0001g0227 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.189+8065A>G | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57720872 | ||||||
| chr11:57721007
|
G | GT | 230 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(227): Show | 232 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(229): Show |
intron_variant | MODIFIER | c.189+8214dupT | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57721007 | |||||
| chr11:57721007
|
G | GTT | 6 | a0001c0001t0001g0212a0001c0001t0001g0224a0001c0001t0001g0249others(3): Show | 6 | HG00597.hp2 HG02027.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.189+8213_189+8214d others(4): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57721007 | |||||
| chr11:57721099
|
C | T | 1 | a0001c0001t0001g0151 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.189+8292C>T | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57721099 | ||||||
| chr11:57721119
|
C | T | 1 | a0001c0001t0001g0202 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.189+8312C>T | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57721119 | ||||||
| chr11:57721131
|
G | A | 1 | a0001c0001t0001g0154 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.189+8324G>A | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57721131 | ||||||
| chr11:57721285
|
A | C | 1 | a0001c0001t0001g0262 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.189+8478A>C | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57721285 | ||||||
| chr11:57721345
|
G | GT | 7 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0335others(4): Show | 7 | HG02135.hp2 HG02145.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.189+8558dupT | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57721345 | |||||
| chr11:57721345
|
GT | G | 215 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(212): Show | 219 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(216): Show |
intron_variant | MODIFIER | c.189+8558delT | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57721345 | |||||
| chr11:57721345
|
GTT | G | 41 | a0001c0001t0001g0001a0001c0001t0001g0107a0001c0001t0001g0108others(38): Show | 42 | HG00544.hp2 HG00673.hp2 HG01074.hp2 others(39): Show |
intron_variant | MODIFIER | c.189+8557_189+8558d others(4): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57721345 | |||||
| chr11:57721418
|
G | A | 57 | a0001c0001t0002g0026a0001c0001t0002g0033a0001c0001t0002g0034others(54): Show | 57 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(54): Show |
intron_variant | MODIFIER | c.189+8611G>A | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57721418 | ||||||
| chr11:57721952
|
T | G | 1 | a0001c0001t0001g0292 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.189+9145T>G | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57721952 | ||||||
| chr11:57722040
|
C | T | 1 | a0001c0001t0001g0335 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.189+9233C>T | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57722040 | ||||||
| chr11:57722232
|
G | A | 3 | a0001c0001t0001g0202a0001c0001t0001g0203a0001c0001t0001g0204 | 3 | HG02145.hp1 HG02965.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.189+9425G>A | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57722232 | ||||||
| chr11:57722497
|
A | C | 1 | a0001c0001t0001g0206 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.189+9690A>C | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57722497 | ||||||
| chr11:57723041
|
G | A | 1 | a0001c0001t0001g0137 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.189+10234G>A | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57723041 | ||||||
| chr11:57723072
|
A | G | 1 | a0001c0001t0001g0233 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.189+10265A>G | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57723072 | ||||||
| chr11:57723092
|
T | C | 1 | a0001c0001t0001g0090 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.189+10285T>C | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57723092 | ||||||
| chr11:57723106
|
G | A | 6 | a0001c0001t0001g0233a0001c0001t0001g0234a0001c0001t0001g0248others(3): Show | 6 | HG02109.hp2 HG02280.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.189+10299G>A | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57723106 | ||||||
| chr11:57723115
|
AAAAT | A | 16 | a0001c0001t0001g0001a0001c0001t0001g0107a0001c0001t0001g0108others(13): Show | 17 | HG02145.hp1 HG02451.hp1 HG02486.hp1 others(14): Show |
intron_variant | MODIFIER | c.189+10324_189+1032 others(8): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57723115 | |||||
| chr11:57723164
|
A | G | 1 | a0001c0001t0001g0212 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.189+10357A>G | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57723164 | ||||||
| chr11:57723278
|
G | A | 103 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(100): Show | 106 | HG00140.hp1 HG00609.hp1 HG00621.hp1 others(103): Show |
intron_variant | MODIFIER | c.189+10471G>A | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57723278 | ||||||
| chr11:57723335
|
T | G | 1 | a0001c0003t0010g0193 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.189+10528T>G | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57723335 | ||||||
| chr11:57723502
|
C | CA | 7 | a0001c0001t0001g0015a0001c0001t0001g0030a0001c0001t0001g0032others(4): Show | 7 | HG00544.hp2 HG02056.hp2 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.189+10708dupA | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57723502 | |||||
| chr11:57723540
|
C | A | 1 | a0001c0001t0002g0078 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.189+10733C>A | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57723540 | ||||||
| chr11:57723805
|
A | AAAT | 77 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0087others(74): Show | 79 | HG00140.hp1 HG00544.hp2 HG00609.hp1 others(76): Show |
intron_variant | MODIFIER | c.189+11028_189+1103 others(7): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57723805 | |||||
| chr11:57723805
|
A | AAATAAT | 15 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0125others(12): Show | 15 | HG00735.hp1 HG01099.hp2 HG01261.hp2 others(12): Show |
intron_variant | MODIFIER | c.189+11025_189+1103 others(10): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57723805 | |||||
| chr11:57723805
|
A | AAATAATA others(2): Show |
21 | a0001c0001t0001g0001a0001c0001t0001g0113a0001c0001t0001g0114others(18): Show | 22 | HG01168.hp1 HG01884.hp1 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.189+11022_189+1103 others(13): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57723805 | |||||
| chr11:57723805
|
A | AAATAATA others(5): Show |
12 | a0001c0001t0002g0026a0001c0001t0002g0036a0001c0001t0002g0038others(9): Show | 12 | HG01069.hp2 HG01071.hp1 HG01358.hp1 others(9): Show |
intron_variant | MODIFIER | c.189+11019_189+1103 others(16): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57723805 | |||||
| chr11:57723805
|
A | AAATAATA others(8): Show |
37 | a0001c0001t0002g0033a0001c0001t0002g0035a0001c0001t0002g0037others(34): Show | 37 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(34): Show |
intron_variant | MODIFIER | c.189+11016_189+1103 others(19): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57723805 | |||||
| chr11:57723805
|
A | AAATAATA others(11): Show |
5 | a0001c0001t0002g0049a0001c0001t0002g0050a0001c0001t0002g0066others(2): Show | 5 | HG02683.hp2 HG03834.hp1 NA19064.hp1 others(2): Show |
intron_variant | MODIFIER | c.189+11013_189+1103 others(22): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57723805 | |||||
| chr11:57723805
|
A | AAATAATA others(14): Show |
1 | a0001c0001t0002g0067 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.189+11010_189+1103 others(25): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57723805 | |||||
| chr11:57723805
|
AAATAATA others(8): Show |
A | 1 | a0001c0001t0001g0167 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.189+11016_189+1103 others(19): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57723805 | |||||
| chr11:57723899
|
T | A | 103 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(100): Show | 106 | HG00140.hp1 HG00609.hp1 HG00621.hp1 others(103): Show |
intron_variant | MODIFIER | c.189+11092T>A | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57723899 | ||||||
| chr11:57723900
|
T | A | 103 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(100): Show | 106 | HG00140.hp1 HG00609.hp1 HG00621.hp1 others(103): Show |
intron_variant | MODIFIER | c.189+11093T>A | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57723900 | ||||||
| chr11:57723968
|
A | G | 1 | a0001c0001t0001g0159 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.189+11161A>G | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57723968 | ||||||
| chr11:57724019
|
G | A | 4 | a0001c0001t0001g0264a0001c0001t0001g0265a0001c0001t0001g0266others(1): Show | 4 | HG02647.hp1 HG02895.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.189+11212G>A | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57724019 | ||||||
| chr11:57724021
|
A | G | 2 | a0001c0001t0001g0290a0001c0001t0001g0296 | 2 | HG03704.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.189+11214A>G | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57724021 | ||||||
| chr11:57724647
|
T | TA | 8 | a0001c0001t0001g0001a0001c0001t0001g0113a0001c0001t0001g0114others(5): Show | 9 | HG02451.hp1 HG02486.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.189+11845dupA | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57724647 | |||||
| chr11:57724697
|
C | A | 1 | a0001c0001t0002g0046 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.189+11890C>A | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57724697 | ||||||
| chr11:57724754
|
A | G | 76 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0109others(73): Show | 78 | HG00140.hp1 HG00609.hp1 HG00621.hp1 others(75): Show |
intron_variant | MODIFIER | c.189+11947A>G | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57724754 | ||||||
| chr11:57725012
|
C | T | 1 | a0001c0001t0001g0206 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.189+12205C>T | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57725012 | ||||||
| chr11:57725038
|
C | CA | 24 | a0001c0001t0001g0028a0001c0001t0001g0111a0001c0001t0001g0138others(21): Show | 24 | HG00733.hp1 HG01192.hp2 HG01358.hp2 others(21): Show |
intron_variant | MODIFIER | c.189+12248dupA | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57725038 | |||||
| chr11:57725052
|
A | G | 16 | a0001c0001t0001g0001a0001c0001t0001g0107a0001c0001t0001g0108others(13): Show | 17 | HG02145.hp1 HG02451.hp1 HG02486.hp1 others(14): Show |
intron_variant | MODIFIER | c.189+12245A>G | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57725052 | ||||||
| chr11:57725056
|
G | A | 2 | a0001c0001t0001g0258a0001c0001t0001g0268 | 2 | NA18985.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.189+12249G>A | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57725056 | ||||||
| chr11:57725057
|
A | G | 1 | a0001c0001t0001g0258 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.189+12250A>G | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57725057 | ||||||
| chr11:57725666
|
G | C | 1 | a0001c0001t0001g0102 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.190-11942G>C | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57725666 | ||||||
| chr11:57725765
|
C | G | 2 | a0001c0001t0001g0230a0001c0001t0001g0231 | 2 | NA19009.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.190-11843C>G | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57725765 | ||||||
| chr11:57725785
|
GTAC | G | 4 | a0001c0001t0001g0209a0001c0001t0001g0210a0001c0001t0001g0211others(1): Show | 4 | HG00733.hp1 HG01361.hp1 HG01981.hp2 others(1): Show |
intron_variant | MODIFIER | c.190-11820_190-1181 others(7): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57725785 | |||||
| chr11:57725923
|
A | C | 1 | a0001c0001t0001g0256 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.190-11685A>C | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57725923 | ||||||
| chr11:57726024
|
A | G | 1 | a0001c0001t0001g0237 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.190-11584A>G | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57726024 | ||||||
| chr11:57726150
|
C | A | 51 | a0001c0001t0002g0026a0001c0001t0002g0034a0001c0001t0002g0035others(48): Show | 51 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(48): Show |
intron_variant | MODIFIER | c.190-11458C>A | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57726150 | ||||||
| chr11:57726285
|
C | T | 1 | a0001c0001t0003g0123 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.190-11323C>T | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57726285 | ||||||
| chr11:57726338
|
G | A | 16 | a0001c0001t0001g0001a0001c0001t0001g0107a0001c0001t0001g0108others(13): Show | 17 | HG02145.hp1 HG02451.hp1 HG02486.hp1 others(14): Show |
intron_variant | MODIFIER | c.190-11270G>A | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57726338 | ||||||
| chr11:57726726
|
T | C | 76 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0109others(73): Show | 78 | HG00140.hp1 HG00609.hp1 HG00621.hp1 others(75): Show |
intron_variant | MODIFIER | c.190-10882T>C | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57726726 | ||||||
| chr11:57727015
|
A | C | 159 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(156): Show | 161 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(158): Show |
intron_variant | MODIFIER | c.190-10593A>C | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57727015 | ||||||
| chr11:57727038
|
T | C | 1 | a0001c0001t0001g0227 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.190-10570T>C | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57727038 | ||||||
| chr11:57727562
|
T | G | 2 | a0001c0001t0001g0009a0001c0001t0001g0022 | 2 | NA18960.hp1 NA18978.hp2 |
intron_variant | MODIFIER | c.190-10046T>G | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57727562 | ||||||
| chr11:57727765
|
G | C | 1 | a0001c0001t0001g0173 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.190-9843G>C | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57727765 | ||||||
| chr11:57728014
|
TTTGA | T | 23 | a0001c0001t0001g0001a0001c0001t0001g0107a0001c0001t0001g0108others(20): Show | 24 | HG01261.hp2 HG02145.hp1 HG02451.hp1 others(21): Show |
intron_variant | MODIFIER | c.190-9588_190-9585d others(6): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57728014 | |||||
| chr11:57728169
|
C | CT | 77 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0024others(74): Show | 79 | HG00140.hp1 HG00609.hp1 HG00621.hp1 others(76): Show |
intron_variant | MODIFIER | c.190-9428dupT | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57728169 | |||||
| chr11:57728174
|
T | G | 1 | a0001c0001t0001g0335 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.190-9434T>G | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57728174 | ||||||
| chr11:57728202
|
G | A | 159 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(156): Show | 161 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(158): Show |
intron_variant | MODIFIER | c.190-9406G>A | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57728202 | ||||||
| chr11:57728414
|
C | T | 8 | a0001c0001t0001g0003a0001c0001t0001g0134a0001c0001t0001g0144others(5): Show | 9 | HG00621.hp1 HG02015.hp2 NA18964.hp2 others(6): Show |
intron_variant | MODIFIER | c.190-9194C>T | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57728414 | ||||||
| chr11:57728681
|
C | G | 6 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(3): Show | 6 | HG03831.hp2 NA18961.hp2 NA18999.hp1 others(3): Show |
intron_variant | MODIFIER | c.190-8927C>G | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57728681 | ||||||
| chr11:57728713
|
A | C | 1 | a0001c0001t0003g0123 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.190-8895A>C | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57728713 | ||||||
| chr11:57728733
|
CAT | C | 3 | a0001c0001t0001g0183a0001c0001t0001g0184a0001c0001t0001g0185 | 3 | HG02622.hp2 HG02717.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.190-8873_190-8872d others(4): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57728733 | |||||
| chr11:57729018
|
C | T | 7 | a0001c0001t0001g0232a0001c0001t0001g0256a0001c0001t0001g0268others(4): Show | 7 | HG00733.hp2 HG01192.hp2 HG01993.hp1 others(4): Show |
intron_variant | MODIFIER | c.190-8590C>T | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57729018 | ||||||
| chr11:57729168
|
A | T | 1 | a0001c0001t0001g0191 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.190-8440A>T | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57729168 | ||||||
| chr11:57729348
|
C | T | 57 | a0001c0001t0002g0026a0001c0001t0002g0033a0001c0001t0002g0034others(54): Show | 57 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(54): Show |
intron_variant | MODIFIER | c.190-8260C>T | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57729348 | ||||||
| chr11:57729363
|
G | C | 1 | a0001c0001t0001g0004 | 2 | NA18970.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.190-8245G>C | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57729363 | ||||||
| chr11:57729539
|
C | A | 57 | a0001c0001t0002g0026a0001c0001t0002g0033a0001c0001t0002g0034others(54): Show | 57 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(54): Show |
intron_variant | MODIFIER | c.190-8069C>A | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57729539 | ||||||
| chr11:57729541
|
C | T | 2 | a0001c0001t0001g0166a0001c0001t0001g0167 | 2 | HG00642.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.190-8067C>T | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57729541 | ||||||
| chr11:57729838
|
T | C | 1 | a0001c0001t0009g0010 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.190-7770T>C | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57729838 | ||||||
| chr11:57729934
|
C | A | 1 | a0001c0001t0002g0066 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.190-7674C>A | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57729934 | ||||||
| chr11:57729937
|
G | A | 1 | a0001c0001t0001g0335 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.190-7671G>A | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57729937 | ||||||
| chr11:57729972
|
G | T | 2 | a0001c0001t0001g0032a0001c0001t0001g0287 | 2 | NA18991.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.190-7636G>T | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57729972 | ||||||
| chr11:57730041
|
T | C | 7 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0194others(4): Show | 7 | HG01261.hp2 HG03139.hp2 HG03209.hp2 others(4): Show |
intron_variant | MODIFIER | c.190-7567T>C | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57730041 | ||||||
| chr11:57730108
|
C | T | 4 | a0001c0001t0001g0209a0001c0001t0001g0210a0001c0001t0001g0211others(1): Show | 4 | HG00733.hp1 HG01361.hp1 HG01981.hp2 others(1): Show |
intron_variant | MODIFIER | c.190-7500C>T | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57730108 | ||||||
| chr11:57730123
|
T | TTA | 44 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0112others(41): Show | 46 | HG00140.hp1 HG00609.hp1 HG00621.hp1 others(43): Show |
intron_variant | MODIFIER | c.190-7471_190-7470d others(4): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57730123 | |||||
| chr11:57730131
|
A | G | 4 | a0001c0001t0001g0209a0001c0001t0001g0210a0001c0001t0001g0211others(1): Show | 4 | HG00733.hp1 HG01361.hp1 HG01981.hp2 others(1): Show |
intron_variant | MODIFIER | c.190-7477A>G | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57730131 | ||||||
| chr11:57730298
|
G | T | 3 | a0001c0001t0001g0177a0001c0001t0001g0180a0001c0001t0001g0182 | 3 | HG01175.hp1 HG01515.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.190-7310G>T | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57730298 | ||||||
| chr11:57730324
|
G | T | 4 | a0001c0001t0001g0194a0001c0001t0001g0195a0001c0001t0001g0196others(1): Show | 4 | HG01261.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.190-7284G>T | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57730324 | ||||||
| chr11:57730375
|
C | T | 57 | a0001c0001t0002g0026a0001c0001t0002g0033a0001c0001t0002g0034others(54): Show | 57 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(54): Show |
intron_variant | MODIFIER | c.190-7233C>T | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57730375 | ||||||
| chr11:57730426
|
T | TA | 9 | a0001c0001t0001g0088a0001c0001t0001g0089a0001c0001t0001g0096others(6): Show | 9 | HG00639.hp2 HG01106.hp2 HG01496.hp2 others(6): Show |
intron_variant | MODIFIER | c.190-7154dupA | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57730426 | |||||
| chr11:57730426
|
TA | T | 161 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(158): Show | 163 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(160): Show |
intron_variant | MODIFIER | c.190-7154delA | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57730426 | |||||
| chr11:57730426
|
TAA | T | 70 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(67): Show | 73 | HG00140.hp1 HG00544.hp2 HG00673.hp2 others(70): Show |
intron_variant | MODIFIER | c.190-7155_190-7154d others(4): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57730426 | |||||
| chr11:57730468
|
G | A | 38 | a0001c0001t0001g0029a0001c0001t0001g0031a0001c0001t0001g0032others(35): Show | 38 | HG00438.hp1 HG00558.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.190-7140G>A | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57730468 | ||||||
| chr11:57730508
|
G | A | 76 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0109others(73): Show | 78 | HG00140.hp1 HG00609.hp1 HG00621.hp1 others(75): Show |
intron_variant | MODIFIER | c.190-7100G>A | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57730508 | ||||||
| chr11:57730652
|
C | G | 1 | a0001c0001t0001g0276 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.190-6956C>G | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57730652 | ||||||
| chr11:57730760
|
C | T | 264 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(261): Show | 269 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(266): Show |
intron_variant | MODIFIER | c.190-6848C>T | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57730760 | ||||||
| chr11:57730834
|
A | G | 8 | a0001c0001t0002g0037a0001c0001t0002g0039a0001c0001t0002g0040others(5): Show | 8 | HG00323.hp1 HG00741.hp2 HG01167.hp2 others(5): Show |
intron_variant | MODIFIER | c.190-6774A>G | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57730834 | ||||||
| chr11:57730857
|
A | G | 3 | a0001c0001t0003g0104a0001c0001t0003g0105a0001c0001t0003g0106 | 3 | HG02451.hp2 HG02647.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.190-6751A>G | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57730857 | ||||||
| chr11:57730988
|
C | CTTAAA | 265 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(262): Show | 270 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(267): Show |
intron_variant | MODIFIER | c.190-6617_190-6616i others(7): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57730988 | |||||
| chr11:57731109
|
C | T | 1 | a0001c0001t0001g0142 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.190-6499C>T | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57731109 | ||||||
| chr11:57731111
|
G | A | 2 | a0001c0001t0001g0311a0001c0001t0001g0313 | 2 | NA18522.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.190-6497G>A | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57731111 | ||||||
| chr11:57731125
|
G | T | 3 | a0001c0001t0002g0039a0001c0001t0002g0040a0001c0001t0002g0042 | 3 | HG00741.hp2 HG01167.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.190-6483G>T | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57731125 | ||||||
| chr11:57731125
|
GTTTT | G | 39 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0013others(36): Show | 39 | HG00438.hp1 HG00673.hp1 HG00733.hp2 others(36): Show |
intron_variant | MODIFIER | c.190-6458_190-6455d others(6): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57731125 | |||||
| chr11:57731125
|
GTTTTT | G | 113 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(110): Show | 115 | HG00323.hp2 HG00408.hp2 HG00544.hp1 others(112): Show |
intron_variant | MODIFIER | c.190-6459_190-6455d others(7): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57731125 | |||||
| chr11:57731125
|
GTTTTTT | G | 11 | a0001c0001t0001g0161a0001c0001t0001g0175a0001c0001t0001g0176others(8): Show | 11 | HG01361.hp2 HG02109.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.190-6460_190-6455d others(8): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57731125 | |||||
| chr11:57731125
|
GTTTTTTT | G | 18 | a0001c0001t0001g0124a0001c0001t0001g0126a0001c0001t0001g0129others(15): Show | 18 | HG00621.hp1 HG00642.hp2 HG00741.hp1 others(15): Show |
intron_variant | MODIFIER | c.190-6461_190-6455d others(9): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57731125 | |||||
| chr11:57731125
|
GTTTTTTT others(1): Show |
G | 65 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0109others(62): Show | 67 | HG00140.hp1 HG00544.hp2 HG00609.hp1 others(64): Show |
intron_variant | MODIFIER | c.190-6462_190-6455d others(10): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57731125 | |||||
| chr11:57731125
|
GTTTTTTT others(2): Show |
G | 18 | a0001c0001t0001g0001a0001c0001t0001g0107a0001c0001t0001g0108others(15): Show | 19 | HG01261.hp2 HG02451.hp1 HG02486.hp1 others(16): Show |
intron_variant | MODIFIER | c.190-6463_190-6455d others(11): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57731125 | |||||
| chr11:57731133
|
T | TTG | 9 | a0001c0001t0002g0034a0001c0001t0002g0036a0001c0001t0002g0040others(6): Show | 9 | HG00741.hp2 HG01069.hp2 HG01261.hp1 others(6): Show |
intron_variant | MODIFIER | c.190-6474_190-6473i others(4): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57731133 | |||||
| chr11:57731134
|
T | TG | 45 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0002g0026others(42): Show | 45 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(42): Show |
intron_variant | MODIFIER | c.190-6474_190-6473i others(3): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57731134 | ||||||
| chr11:57731135
|
T | G | 13 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(10): Show | 13 | HG01496.hp2 HG02258.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.190-6473T>G | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57731135 | ||||||
| chr11:57731136
|
T | G | 2 | a0001c0001t0001g0279a0001c0001t0001g0300 | 2 | NA18976.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.190-6472T>G | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57731136 | ||||||
| chr11:57731137
|
T | G | 4 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0022others(1): Show | 4 | NA18947.hp1 NA18960.hp1 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.190-6471T>G | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57731137 | ||||||
| chr11:57731139
|
T | G | 5 | a0001c0001t0001g0209a0001c0001t0001g0210a0001c0001t0001g0211others(2): Show | 5 | HG00733.hp1 HG01361.hp1 HG01981.hp2 others(2): Show |
intron_variant | MODIFIER | c.190-6469T>G | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57731139 | ||||||
| chr11:57731140
|
T | G | 3 | a0001c0001t0001g0144a0001c0001t0001g0198a0001c0001t0001g0199 | 3 | HG00544.hp2 HG02056.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.190-6468T>G | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57731140 | ||||||
| chr11:57731141
|
T | G | 1 | a0001c0001t0001g0335 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.190-6467T>G | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57731141 | ||||||
| chr11:57731142
|
T | G | 2 | a0001c0001t0001g0255a0001c0001t0001g0280 | 2 | HG02683.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.190-6466T>G | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57731142 | ||||||
| chr11:57731144
|
T | G | 1 | a0001c0001t0001g0004 | 2 | NA18970.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.190-6464T>G | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57731144 | ||||||
| chr11:57731237
|
G | A | 1 | a0001c0001t0001g0140 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.190-6371G>A | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57731237 | ||||||
| chr11:57731433
|
C | CT | 131 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0013others(128): Show | 132 | HG00140.hp1 HG00323.hp1 HG00544.hp2 others(129): Show |
intron_variant | MODIFIER | c.190-6151dupT | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57731433 | |||||
| chr11:57731433
|
C | CTT | 96 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(93): Show | 97 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.190-6152_190-6151d others(4): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57731433 | |||||
| chr11:57731433
|
CT | C | 14 | a0001c0001t0001g0001a0001c0001t0001g0115a0001c0001t0001g0116others(11): Show | 15 | HG01261.hp2 HG02273.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.190-6151delT | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57731433 | |||||
| chr11:57731442
|
T | TC | 6 | a0001c0001t0001g0233a0001c0001t0001g0234a0001c0001t0001g0248others(3): Show | 6 | HG02109.hp2 HG02280.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.190-6166_190-6165i others(3): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57731442 | ||||||
| chr11:57731593
|
C | T | 264 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(261): Show | 269 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(266): Show |
intron_variant | MODIFIER | c.190-6015C>T | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57731593 | ||||||
| chr11:57731726
|
G | A | 322 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(319): Show | 327 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(324): Show |
intron_variant | MODIFIER | c.190-5882G>A | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57731726 | ||||||
| chr11:57731786
|
C | A | 1 | a0001c0001t0001g0272 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.190-5822C>A | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57731786 | ||||||
| chr11:57732000
|
CAT | C | 3 | a0001c0001t0003g0104a0001c0001t0003g0105a0001c0001t0003g0106 | 3 | HG02451.hp2 HG02647.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.190-5605_190-5604d others(4): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57732000 | |||||
| chr11:57732167
|
A | C | 2 | a0001c0001t0001g0289a0001c0001t0001g0322 | 2 | NA18950.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.190-5441A>C | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57732167 | ||||||
| chr11:57732183
|
T | G | 105 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(102): Show | 108 | HG00140.hp1 HG00544.hp2 HG00609.hp1 others(105): Show |
intron_variant | MODIFIER | c.190-5425T>G | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57732183 | ||||||
| chr11:57732251
|
CTG | C | 3 | a0001c0001t0003g0104a0001c0001t0003g0105a0001c0001t0003g0106 | 3 | HG02451.hp2 HG02647.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.190-5354_190-5353d others(4): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57732251 | |||||
| chr11:57732494
|
A | G | 1 | a0001c0001t0001g0335 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.190-5114A>G | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57732494 | ||||||
| chr11:57732607
|
A | T | 1 | a0001c0001t0001g0242 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.190-5001A>T | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57732607 | ||||||
| chr11:57732661
|
C | T | 2 | a0001c0001t0001g0279a0001c0001t0001g0300 | 2 | NA18976.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.190-4947C>T | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57732661 | ||||||
| chr11:57732662
|
A | G | 159 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(156): Show | 161 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(158): Show |
intron_variant | MODIFIER | c.190-4946A>G | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57732662 | ||||||
| chr11:57732702
|
T | G | 1 | a0001c0003t0010g0193 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.190-4906T>G | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57732702 | ||||||
| chr11:57732813
|
A | G | 1 | a0001c0001t0001g0220 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.190-4795A>G | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57732813 | ||||||
| chr11:57732820
|
G | T | 1 | a0001c0001t0001g0250 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.190-4788G>T | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57732820 | ||||||
| chr11:57732870
|
G | A | 1 | a0001c0001t0001g0200 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.190-4738G>A | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57732870 | ||||||
| chr11:57732890
|
T | G | 3 | a0001c0001t0002g0047a0001c0001t0002g0059a0001c0001t0002g0061 | 3 | HG01070.hp1 HG01081.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.190-4718T>G | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57732890 | ||||||
| chr11:57732927
|
T | C | 6 | a0001c0001t0002g0026a0001c0001t0002g0056a0001c0001t0002g0057others(3): Show | 6 | HG02129.hp1 HG02602.hp2 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.190-4681T>C | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57732927 | ||||||
| chr11:57732978
|
G | C | 1 | a0001c0001t0002g0081 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.190-4630G>C | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57732978 | ||||||
| chr11:57733056
|
C | A | 1 | a0001c0001t0001g0256 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.190-4552C>A | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57733056 | ||||||
| chr11:57733115
|
T | C | 1 | a0001c0001t0002g0057 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.190-4493T>C | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57733115 | ||||||
| chr11:57733238
|
C | A | 1 | a0001c0001t0001g0142 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.190-4370C>A | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57733238 | ||||||
| chr11:57733247
|
A | AT | 39 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0013others(36): Show | 39 | HG00597.hp1 HG00597.hp2 HG00609.hp2 others(36): Show |
intron_variant | MODIFIER | c.190-4336dupT | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57733247 | |||||
| chr11:57733247
|
AT | A | 97 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(94): Show | 101 | HG00140.hp1 HG00609.hp1 HG00621.hp1 others(98): Show |
intron_variant | MODIFIER | c.190-4336delT | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57733247 | |||||
| chr11:57733247
|
ATTTTTTT others(3): Show |
A | 1 | a0001c0001t0001g0296 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.190-4345_190-4336d others(12): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57733247 | |||||
| chr11:57733247
|
ATTTTTTT others(4): Show |
A | 1 | a0001c0001t0001g0290 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.190-4346_190-4336d others(13): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57733247 | |||||
| chr11:57733348
|
C | T | 159 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(156): Show | 161 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(158): Show |
intron_variant | MODIFIER | c.190-4260C>T | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57733348 | ||||||
| chr11:57733447
|
G | A | 5 | a0001c0001t0001g0138a0001c0001t0001g0146a0001c0001t0001g0152others(2): Show | 5 | HG01884.hp1 HG01891.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.190-4161G>A | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57733447 | ||||||
| chr11:57733548
|
C | T | 6 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0194others(3): Show | 6 | HG01261.hp2 HG03139.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.190-4060C>T | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57733548 | ||||||
| chr11:57733694
|
G | A | 1 | a0001c0001t0001g0092 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.190-3914G>A | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57733694 | ||||||
| chr11:57733710
|
C | T | 104 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(101): Show | 107 | HG00140.hp1 HG00544.hp2 HG00609.hp1 others(104): Show |
intron_variant | MODIFIER | c.190-3898C>T | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57733710 | ||||||
| chr11:57733748
|
T | G | 2 | a0001c0001t0001g0238a0001c0001t0001g0239 | 2 | HG00609.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.190-3860T>G | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57733748 | ||||||
| chr11:57734067
|
G | A | 3 | a0001c0001t0001g0252a0001c0001t0001g0314a0001c0001t0001g0327 | 3 | NA18973.hp2 NA19056.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.190-3541G>A | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57734067 | ||||||
| chr11:57734157
|
C | CA | 12 | a0001c0001t0001g0101a0001c0001t0001g0168a0001c0001t0001g0172others(9): Show | 12 | HG00323.hp1 HG00733.hp2 HG01069.hp2 others(9): Show |
intron_variant | MODIFIER | c.190-3421dupA | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57734157 | |||||
| chr11:57734157
|
C | CAA | 7 | a0001c0001t0001g0109a0001c0001t0001g0165a0001c0001t0002g0040others(4): Show | 7 | HG00741.hp2 HG01192.hp2 HG01261.hp1 others(4): Show |
intron_variant | MODIFIER | c.190-3422_190-3421d others(4): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57734157 | |||||
| chr11:57734157
|
CA | C | 120 | a0001c0001t0001g0008a0001c0001t0001g0019a0001c0001t0001g0020others(117): Show | 120 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(117): Show |
intron_variant | MODIFIER | c.190-3421delA | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57734157 | |||||
| chr11:57734157
|
CAA | C | 131 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(128): Show | 135 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(132): Show |
intron_variant | MODIFIER | c.190-3422_190-3421d others(4): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57734157 | |||||
| chr11:57734157
|
CAAA | C | 6 | a0001c0001t0001g0234a0001c0001t0001g0260a0001c0001t0001g0275others(3): Show | 6 | HG00738.hp1 HG01168.hp2 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.190-3423_190-3421d others(5): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57734157 | |||||
| chr11:57734157
|
CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0001g0299 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.190-3430_190-3421d others(12): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57734157 | |||||
| chr11:57734157
|
CAAAAAAA others(6): Show |
C | 6 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0194others(3): Show | 6 | HG01261.hp2 HG03139.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.190-3433_190-3421d others(15): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57734157 | |||||
| chr11:57734157
|
CAAAAAAA others(7): Show |
C | 16 | a0001c0001t0001g0001a0001c0001t0001g0108a0001c0001t0001g0113others(13): Show | 17 | HG02145.hp1 HG02451.hp1 HG02486.hp1 others(14): Show |
intron_variant | MODIFIER | c.190-3434_190-3421d others(16): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57734157 | |||||
| chr11:57734157
|
CAAAAAAA others(8): Show |
C | 2 | a0001c0001t0001g0107a0001c0001t0001g0146 | 2 | HG01891.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.190-3435_190-3421d others(17): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57734157 | |||||
| chr11:57734282
|
T | A | 1 | a0001c0001t0001g0229 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.190-3326T>A | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57734282 | ||||||
| chr11:57734442
|
A | G | 2 | a0001c0001t0001g0279a0001c0001t0001g0300 | 2 | NA18976.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.190-3166A>G | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57734442 | ||||||
| chr11:57734466
|
A | C | 1 | a0001c0001t0001g0274 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.190-3142A>C | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57734466 | ||||||
| chr11:57734815
|
A | G | 2 | a0001c0001t0001g0198a0001c0001t0001g0199 | 2 | HG00544.hp2 HG02056.hp2 |
intron_variant | MODIFIER | c.190-2793A>G | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57734815 | ||||||
| chr11:57734825
|
AC | A | 5 | a0001c0001t0002g0035a0001c0001t0002g0052a0001c0001t0002g0053others(2): Show | 5 | HG00408.hp1 HG00438.hp2 NA18975.hp1 others(2): Show |
intron_variant | MODIFIER | c.190-2781delC | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57734825 | |||||
| chr11:57734920
|
G | A | 159 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(156): Show | 161 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(158): Show |
intron_variant | MODIFIER | c.190-2688G>A | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57734920 | ||||||
| chr11:57734953
|
G | A | 1 | a0001c0001t0001g0130 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.190-2655G>A | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57734953 | ||||||
| chr11:57735160
|
G | A | 8 | a0001c0001t0001g0001a0001c0001t0001g0113a0001c0001t0001g0114others(5): Show | 9 | HG02451.hp1 HG02486.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.190-2448G>A | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57735160 | ||||||
| chr11:57735209
|
T | G | 1 | a0001c0001t0001g0334 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.190-2399T>G | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57735209 | ||||||
| chr11:57735277
|
C | T | 2 | a0001c0001t0001g0309a0001c0001t0001g0310 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.190-2331C>T | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57735277 | ||||||
| chr11:57735385
|
A | G | 1 | a0001c0001t0001g0318 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.190-2223A>G | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57735385 | ||||||
| chr11:57735483
|
T | C | 1 | a0001c0001t0002g0078 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.190-2125T>C | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57735483 | ||||||
| chr11:57735506
|
C | T | 2 | a0001c0001t0001g0198a0001c0001t0001g0199 | 2 | HG00544.hp2 HG02056.hp2 |
intron_variant | MODIFIER | c.190-2102C>T | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57735506 | ||||||
| chr11:57735735
|
A | G | 1 | a0001c0003t0010g0193 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.190-1873A>G | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57735735 | ||||||
| chr11:57735745
|
A | G | 1 | a0001c0001t0001g0204 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.190-1863A>G | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57735745 | ||||||
| chr11:57735767
|
G | A | 1 | a0001c0001t0001g0294 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.190-1841G>A | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57735767 | ||||||
| chr11:57735789
|
G | A | 6 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0194others(3): Show | 6 | HG01261.hp2 HG03139.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.190-1819G>A | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57735789 | ||||||
| chr11:57735794
|
G | C | 76 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0109others(73): Show | 78 | HG00140.hp1 HG00609.hp1 HG00621.hp1 others(75): Show |
intron_variant | MODIFIER | c.190-1814G>C | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57735794 | ||||||
| chr11:57736053
|
T | A | 1 | a0001c0001t0001g0253 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.190-1555T>A | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57736053 | ||||||
| chr11:57736108
|
A | G | 1 | a0001c0001t0012g0216 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.190-1500A>G | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57736108 | ||||||
| chr11:57736142
|
T | G | 3 | a0001c0001t0002g0057a0001c0001t0002g0085a0001c0001t0006g0084 | 3 | HG02129.hp1 HG02738.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.190-1466T>G | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57736142 | ||||||
| chr11:57736212
|
C | G | 1 | a0001c0001t0001g0197 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.190-1396C>G | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57736212 | ||||||
| chr11:57736340
|
TA | T | 315 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(312): Show | 320 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(317): Show |
intron_variant | MODIFIER | c.190-1253delA | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57736340 | |||||
| chr11:57736342
|
A | T | 2 | a0001c0001t0001g0191a0001c0001t0001g0192 | 2 | HG03139.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.190-1266A>T | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57736342 | ||||||
| chr11:57736481
|
G | GT | 5 | a0001c0001t0001g0003a0001c0001t0001g0144a0001c0001t0001g0145others(2): Show | 6 | HG00621.hp1 NA18976.hp1 NA18983.hp2 others(3): Show |
intron_variant | MODIFIER | c.190-1126dupT | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57736481 | |||||
| chr11:57736539
|
A | G | 2 | a0001c0001t0001g0238a0001c0001t0001g0239 | 2 | HG00609.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.190-1069A>G | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57736539 | ||||||
| chr11:57736602
|
T | C | 5 | a0001c0001t0001g0168a0001c0001t0001g0175a0001c0001t0001g0176others(2): Show | 5 | NA18945.hp2 NA18950.hp1 NA18957.hp2 others(2): Show |
intron_variant | MODIFIER | c.190-1006T>C | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57736602 | ||||||
| chr11:57736658
|
C | T | 2 | a0001c0001t0001g0126a0001c0001t0001g0129 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.190-950C>T | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57736658 | ||||||
| chr11:57736752
|
G | C | 7 | a0001c0001t0001g0232a0001c0001t0001g0256a0001c0001t0001g0268others(4): Show | 7 | HG00733.hp2 HG01192.hp2 HG01993.hp1 others(4): Show |
intron_variant | MODIFIER | c.190-856G>C | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57736752 | ||||||
| chr11:57736776
|
T | C | 1 | a0001c0001t0001g0006 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.190-832T>C | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57736776 | ||||||
| chr11:57736807
|
G | T | 1 | a0001c0001t0001g0299 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.190-801G>T | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57736807 | ||||||
| chr11:57736883
|
C | CA | 12 | a0001c0001t0001g0031a0001c0001t0001g0235a0001c0001t0001g0257others(9): Show | 12 | HG00558.hp1 HG01257.hp2 HG02683.hp2 others(9): Show |
intron_variant | MODIFIER | c.190-709dupA | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57736883 | |||||
| chr11:57736905
|
CAT | C | 5 | a0001c0001t0001g0233a0001c0001t0001g0234a0001c0001t0001g0248others(2): Show | 5 | HG02109.hp2 HG02280.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.190-702_190-701del others(2): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57736905 | ||||||
| chr11:57737006
|
C | T | 2 | a0001c0001t0001g0230a0001c0001t0001g0231 | 2 | NA19009.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.190-602C>T | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57737006 | ||||||
| chr11:57737061
|
A | C | 1 | a0001c0001t0001g0022 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.190-547A>C | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57737061 | ||||||
| chr11:57737489
|
T | C | 5 | a0001c0001t0001g0168a0001c0001t0001g0175a0001c0001t0001g0176others(2): Show | 5 | NA18945.hp2 NA18950.hp1 NA18957.hp2 others(2): Show |
intron_variant | MODIFIER | c.190-119T>C | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57737489 | ||||||
| chr11:57737750
|
A | G | 1 | a0001c0001t0001g0335 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.250+82A>G | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 2/7 | chr11 | 57737750 | ||||||
| chr11:57738048
|
C | CT | 6 | a0001c0001t0002g0033a0001c0001t0002g0045a0001c0001t0002g0050others(3): Show | 6 | HG02027.hp1 NA19002.hp2 NA19064.hp1 others(3): Show |
intron_variant | MODIFIER | c.364+35dupT | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr11 | 57738048 | |||||
| chr11:57738048
|
CT | C | 11 | a0001c0001t0001g0015a0001c0001t0001g0181a0001c0001t0001g0191others(8): Show | 11 | HG01261.hp2 HG03139.hp2 HG03209.hp2 others(8): Show |
intron_variant | MODIFIER | c.364+35delT | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr11 | 57738048 | |||||
| chr11:57738116
|
T | A | 1 | a0001c0001t0002g0078 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.364+90T>A | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 3/7 | chr11 | 57738116 | ||||||
| chr11:57738475
|
G | A | 1 | a0001c0001t0001g0289 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.441+45G>A | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 4/7 | chr11 | 57738475 | ||||||
| chr11:57739431
|
A | C | 18 | a0001c0001t0001g0029a0001c0001t0001g0032a0001c0001t0001g0232others(15): Show | 18 | HG00597.hp1 HG00733.hp2 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.744+171A>C | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 7/7 | chr11 | 57739431 | ||||||
| chr11:57739500
|
G | A | 1 | a0001c0001t0002g0037 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.744+240G>A | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 7/7 | chr11 | 57739500 | ||||||
| chr11:57739613
|
C | T | 1 | a0001c0001t0001g0177 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.744+353C>T | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 7/7 | chr11 | 57739613 | ||||||
| chr11:57739672
|
G | A | 159 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(156): Show | 161 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(158): Show |
intron_variant | MODIFIER | c.744+412G>A | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 7/7 | chr11 | 57739672 | ||||||
| chr11:57739754
|
GA | G | 10 | a0001c0001t0001g0001a0001c0001t0001g0113a0001c0001t0001g0114others(7): Show | 11 | HG02451.hp1 HG02486.hp1 HG02818.hp2 others(8): Show |
intron_variant | MODIFIER | c.745-332delA | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr11 | 57739754 | |||||
| chr11:57739841
|
A | G | 2 | a0001c0001t0001g0198a0001c0001t0001g0199 | 2 | HG00544.hp2 HG02056.hp2 |
intron_variant | MODIFIER | c.745-258A>G | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 7/7 | chr11 | 57739841 | ||||||
| chr11:57739979
|
G | A | 7 | a0001c0001t0001g0236a0001c0001t0001g0243a0001c0001t0001g0244others(4): Show | 7 | HG00735.hp1 HG01074.hp2 HG01099.hp1 others(4): Show |
intron_variant | MODIFIER | c.745-120G>A | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 7/7 | chr11 | 57739979 |