Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 91937 |
|---|---|
| ensemblid | ENSG00000145850.9 |
| hgncid | 25132 |
| symbol | TIMD4 |
| name | T cell immunoglobulin and mucin domain containing 4 |
| refseq_nuc | NM_138379.3 |
| refseq_prot | NP_612388.2 |
| ensembl_nuc | ENST00000274532.7 |
| ensembl_prot | ENSP00000274532.2 |
| mane_status | MANE Select |
| chr | chr5 |
| start | 156919292 |
| end | 156963226 |
| strand | - |
| ver | v1.2 |
| region | chr5:156919292-156963226 |
| region5000 | chr5:156914292-156968226 |
| regionname0 | TIMD4_chr5_156919292_156963226 |
| regionname5000 | TIMD4_chr5_156914292_156968226 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 378 | 289 | 73 | 60 | 112 | 16 | 27 | 78 | TIMD4_chr5_156914292_156968226 | TIMD4 | copy fasta | chr5 | 156914292 | 156968226 |
| a0002 | 0/0 | 378 | 7 | 4 | 3 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | copy fasta | chr5 | 156914292 | 156968226 |
| a0003 | 0/0 | 378 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | copy fasta | chr5 | 156914292 | 156968226 |
| a0004 | 1/0 | 378 | 4 | 0 | 3 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | copy fasta | chr5 | 156914292 | 156968226 |
| a0005 | 0/0 | 378 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | copy fasta | chr5 | 156914292 | 156968226 |
| a0006 | 0/0 | 378 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | copy fasta | chr5 | 156914292 | 156968226 |
| a0007 | 0/0 | 378 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | copy fasta | chr5 | 156914292 | 156968226 |
| a0008 | 0/0 | 378 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | copy fasta | chr5 | 156914292 | 156968226 |
| a0009 | 0/0 | 378 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | copy fasta | chr5 | 156914292 | 156968226 |
| chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/1 | 1137 | 274 | 70 | 59 | 103 | 16 | 25 | TIMD4_chr5_156914292_156968226 | TIMD4 | copy fasta | chr5 | 156914292 | 156968226 |
| c0002 | 0/0 | 1137 | 11 | 1 | 1 | 7 | 0 | 2 | TIMD4_chr5_156914292_156968226 | TIMD4 | copy fasta | chr5 | 156914292 | 156968226 |
| c0003 | 0/0 | 1137 | 6 | 3 | 3 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | copy fasta | chr5 | 156914292 | 156968226 |
| c0004 | 0/0 | 1137 | 6 | 6 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | copy fasta | chr5 | 156914292 | 156968226 |
| c0005 | 1/0 | 1137 | 4 | 0 | 3 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | copy fasta | chr5 | 156914292 | 156968226 |
| c0006 | 0/0 | 1137 | 2 | 2 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | copy fasta | chr5 | 156914292 | 156968226 |
| c0007 | 0/0 | 1137 | 2 | 0 | 0 | 2 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | copy fasta | chr5 | 156914292 | 156968226 |
| c0008 | 0/0 | 1137 | 2 | 2 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | copy fasta | chr5 | 156914292 | 156968226 |
| c0009 | 0/0 | 1137 | 1 | 0 | 0 | 0 | 0 | 1 | TIMD4_chr5_156914292_156968226 | TIMD4 | copy fasta | chr5 | 156914292 | 156968226 |
| c0010 | 0/0 | 1137 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | copy fasta | chr5 | 156914292 | 156968226 |
| c0011 | 0/0 | 1137 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | copy fasta | chr5 | 156914292 | 156968226 |
| c0012 | 0/0 | 1137 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | copy fasta | chr5 | 156914292 | 156968226 |
| c0013 | 0/0 | 1137 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | copy fasta | chr5 | 156914292 | 156968226 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 194 | 272 | 65 | 64 | 98 | 16 | 27 | TIMD4_chr5_156914292_156968226 | TIMD4 | copy fasta | chr5 | 156914292 | 156968226 |
| t0002 | 0/0 | 194 | 26 | 9 | 2 | 14 | 0 | 1 | TIMD4_chr5_156914292_156968226 | TIMD4 | copy fasta | chr5 | 156914292 | 156968226 |
| t0003 | 0/0 | 193 | 14 | 14 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | copy fasta | chr5 | 156914292 | 156968226 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0003 | 0/1 | 3 | 0 | 0 | 0 | 2 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0008 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0012 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0013 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0228 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0248 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0249 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0250 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0254 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0256 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 1137 | 274 | 70 | 59 | 103 | 16 | 25 | TIMD4_chr5_156914292_156968226 | TIMD4 | copy fasta | chr5 | 156914292 | 156968226 |
| a0001c0002 | 0/0 | 1137 | 11 | 1 | 1 | 7 | 0 | 2 | TIMD4_chr5_156914292_156968226 | TIMD4 | copy fasta | chr5 | 156914292 | 156968226 |
| a0001c0007 | 0/0 | 1137 | 2 | 0 | 0 | 2 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | copy fasta | chr5 | 156914292 | 156968226 |
| a0001c0008 | 0/0 | 1137 | 2 | 2 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | copy fasta | chr5 | 156914292 | 156968226 |
| a0002c0003 | 0/0 | 1137 | 6 | 3 | 3 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | copy fasta | chr5 | 156914292 | 156968226 |
| a0002c0010 | 0/0 | 1137 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | copy fasta | chr5 | 156914292 | 156968226 |
| a0003c0004 | 0/0 | 1137 | 6 | 6 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | copy fasta | chr5 | 156914292 | 156968226 |
| a0004c0005 | 1/0 | 1137 | 4 | 0 | 3 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | copy fasta | chr5 | 156914292 | 156968226 |
| a0005c0006 | 0/0 | 1137 | 2 | 2 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | copy fasta | chr5 | 156914292 | 156968226 |
| a0006c0013 | 0/0 | 1137 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | copy fasta | chr5 | 156914292 | 156968226 |
| a0007c0011 | 0/0 | 1137 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | copy fasta | chr5 | 156914292 | 156968226 |
| a0008c0012 | 0/0 | 1137 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | copy fasta | chr5 | 156914292 | 156968226 |
| a0009c0009 | 0/0 | 1137 | 1 | 0 | 0 | 0 | 0 | 1 | TIMD4_chr5_156914292_156968226 | TIMD4 | copy fasta | chr5 | 156914292 | 156968226 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 1330 | 234 | 47 | 57 | 89 | 16 | 24 | TIMD4_chr5_156914292_156968226 | TIMD4 | copy fasta | chr5 | 156914292 | 156968226 |
| a0001c0001t0002 | 0/0 | 1330 | 26 | 9 | 2 | 14 | 0 | 1 | TIMD4_chr5_156914292_156968226 | TIMD4 | copy fasta | chr5 | 156914292 | 156968226 |
| a0001c0001t0003 | 0/0 | 1329 | 14 | 14 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | copy fasta | chr5 | 156914292 | 156968226 |
| a0001c0002t0001 | 0/0 | 1330 | 11 | 1 | 1 | 7 | 0 | 2 | TIMD4_chr5_156914292_156968226 | TIMD4 | copy fasta | chr5 | 156914292 | 156968226 |
| a0001c0007t0001 | 0/0 | 1330 | 2 | 0 | 0 | 2 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | copy fasta | chr5 | 156914292 | 156968226 |
| a0001c0008t0001 | 0/0 | 1330 | 2 | 2 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | copy fasta | chr5 | 156914292 | 156968226 |
| a0002c0003t0001 | 0/0 | 1330 | 6 | 3 | 3 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | copy fasta | chr5 | 156914292 | 156968226 |
| a0002c0010t0001 | 0/0 | 1330 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | copy fasta | chr5 | 156914292 | 156968226 |
| a0003c0004t0001 | 0/0 | 1330 | 6 | 6 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | copy fasta | chr5 | 156914292 | 156968226 |
| a0004c0005t0001 | 1/0 | 1330 | 4 | 0 | 3 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | copy fasta | chr5 | 156914292 | 156968226 |
| a0005c0006t0001 | 0/0 | 1330 | 2 | 2 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | copy fasta | chr5 | 156914292 | 156968226 |
| a0006c0013t0001 | 0/0 | 1330 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | copy fasta | chr5 | 156914292 | 156968226 |
| a0007c0011t0001 | 0/0 | 1330 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | copy fasta | chr5 | 156914292 | 156968226 |
| a0008c0012t0001 | 0/0 | 1330 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | copy fasta | chr5 | 156914292 | 156968226 |
| a0009c0009t0001 | 0/0 | 1330 | 1 | 0 | 0 | 0 | 0 | 1 | TIMD4_chr5_156914292_156968226 | TIMD4 | copy fasta | chr5 | 156914292 | 156968226 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0003 | 0/1 | 3 | 0 | 0 | 0 | 2 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0012 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0002g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0002g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0002g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0002g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0002g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0002g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0002g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0002g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0002g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0002g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0002g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0002g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0003g0001 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0003g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0003g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0003g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0003g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0003g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0003g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0003g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0003g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0003g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0003g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0003g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0002t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0002t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0002t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0002t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0002t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0002t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0002t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0007t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0007t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0008t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0008t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0002c0003t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0002c0003t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0002c0003t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0002c0003t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0002c0003t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0002c0003t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0002c0010t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0003c0004t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0003c0004t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0003c0004t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0003c0004t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0003c0004t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0003c0004t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0004c0005t0001g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0004c0005t0001g0254 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0004c0005t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0005c0006t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0005c0006t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0006c0013t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0007c0011t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0008c0012t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0009c0009t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0013 | EUR | GBR | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0117 | EUR | GBR | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0174 | EUR | GBR | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0083 | EUR | GBR | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0013 | EUR | FIN | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0250 | EUR | FIN | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | CHS | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG00408 | hp2 | a0001 | c0002 | t0001 | g0006 | EAS | CHS | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG00423 | hp1 | a0001 | c0002 | t0001 | g0053 | EAS | CHS | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | CHS | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | CHS | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | CHS | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | CHS | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0262 | EAS | CHS | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0090 | AMR | PUR | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0130 | AMR | PUR | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG00673 | hp1 | a0001 | c0002 | t0001 | g0006 | EAS | CHS | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | CHS | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0081 | AMR | PUR | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0207 | AMR | PUR | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0267 | AMR | PUR | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0210 | AMR | PUR | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0214 | AMR | PUR | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0247 | AMR | PUR | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0282 | AMR | PUR | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0108 | AMR | PUR | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG01070 | hp2 | a0002 | c0003 | t0001 | g0235 | AMR | PUR | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0158 | AMR | PUR | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0281 | AMR | PUR | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0137 | AMR | PUR | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0168 | AMR | PUR | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0109 | AMR | PUR | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0219 | AMR | PUR | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0185 | AMR | PUR | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0231 | AMR | PUR | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0097 | AMR | PUR | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG01167 | hp2 | a0002 | c0003 | t0001 | g0236 | AMR | PUR | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0252 | AMR | PUR | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0194 | AMR | PUR | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0251 | AMR | PUR | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG01169 | hp2 | a0002 | c0003 | t0001 | g0237 | AMR | PUR | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0119 | AMR | PUR | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0116 | AMR | PUR | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0205 | AMR | PUR | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0068 | AMR | PUR | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG01255 | hp1 | a0004 | c0005 | t0001 | g0255 | AMR | CLM | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0211 | AMR | CLM | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0181 | AMR | CLM | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | CLM | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG01257 | hp2 | a0004 | c0005 | t0001 | g0014 | AMR | CLM | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG01258 | hp1 | a0004 | c0005 | t0001 | g0014 | AMR | CLM | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0169 | AMR | CLM | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0091 | AMR | CLM | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0233 | AMR | CLM | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0190 | AMR | CLM | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0206 | AMR | CLM | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG01358 | hp2 | a0001 | c0002 | t0001 | g0043 | AMR | CLM | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0088 | AMR | CLM | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0220 | AMR | CLM | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0225 | AMR | CLM | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0224 | AMR | CLM | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0157 | EUR | IBS | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0059 | EUR | IBS | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0256 | EUR | IBS | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | IBS | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | IBS | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0084 | EUR | IBS | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG01884 | hp1 | a0006 | c0013 | t0001 | g0155 | AFR | ACB | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG01884 | hp2 | a0001 | c0001 | t0003 | g0037 | AFR | ACB | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0064 | AFR | ACB | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG01891 | hp2 | a0002 | c0003 | t0001 | g0048 | AFR | ACB | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0213 | AMR | PEL | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0096 | AMR | PEL | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | PEL | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0131 | AMR | PEL | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0172 | AMR | PEL | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0175 | AMR | PEL | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | KHV | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | KHV | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | KHV | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | KHV | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0243 | AFR | ACB | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0283 | AFR | ACB | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | KHV | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | KHV | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | KHV | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | KHV | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | KHV | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | KHV | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | KHV | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | KHV | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | KHV | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | KHV | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | KHV | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0056 | AMR | PEL | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0122 | AMR | PEL | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CDX | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | CDX | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | CDX | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | CDX | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0110 | AFR | ACB | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0290 | AFR | ACB | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0244 | AFR | ACB | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0067 | AFR | ACB | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0098 | AMR | PEL | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0092 | AMR | PEL | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0212 | AMR | PEL | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0123 | AMR | PEL | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0140 | AMR | PEL | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG02451 | hp1 | a0003 | c0004 | t0001 | g0028 | AFR | ACB | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | ACB | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | KHV | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0287 | AFR | GWD | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0066 | AFR | GWD | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG02615 | hp1 | a0001 | c0001 | t0003 | g0041 | AFR | GWD | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0292 | AFR | GWD | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0065 | AFR | GWD | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG02630 | hp1 | a0001 | c0001 | t0003 | g0156 | AFR | GWD | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0114 | AFR | GWD | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0113 | AFR | GWD | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG02647 | hp2 | a0001 | c0002 | t0001 | g0052 | AFR | GWD | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0074 | SAS | PJL | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0150 | SAS | PJL | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0082 | SAS | PJL | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0176 | SAS | PJL | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG02717 | hp1 | a0001 | c0001 | t0002 | g0264 | AFR | GWD | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG02717 | hp2 | a0008 | c0012 | t0001 | g0069 | AFR | GWD | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG02723 | hp1 | a0002 | c0003 | t0001 | g0238 | AFR | GWD | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG02723 | hp2 | a0002 | c0010 | t0001 | g0241 | AFR | GWD | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0094 | SAS | PJL | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0208 | SAS | PJL | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0016 | SAS | PJL | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0095 | SAS | PJL | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0173 | AFR | GWD | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0279 | AFR | GWD | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG02818 | hp1 | a0001 | c0001 | t0003 | g0032 | AFR | GWD | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0289 | AFR | GWD | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0280 | AFR | GWD | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0183 | AFR | GWD | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0167 | AFR | GWD | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG02896 | hp2 | a0001 | c0001 | t0003 | g0036 | AFR | GWD | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG02897 | hp1 | a0001 | c0001 | t0003 | g0042 | AFR | GWD | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0166 | AFR | GWD | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0076 | AFR | ESN | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | ESN | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0291 | AFR | ESN | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | ESN | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0278 | AFR | ESN | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG02970 | hp2 | a0001 | c0001 | t0003 | g0001 | AFR | ESN | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG02976 | hp1 | a0001 | c0001 | t0003 | g0001 | AFR | ESN | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG02976 | hp2 | a0002 | c0003 | t0001 | g0121 | AFR | ESN | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0019 | SAS | PJL | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0189 | SAS | PJL | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | GWD | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG03041 | hp2 | a0001 | c0001 | t0003 | g0035 | AFR | GWD | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | MSL | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG03098 | hp2 | a0001 | c0001 | t0002 | g0034 | AFR | MSL | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG03130 | hp1 | a0001 | c0001 | t0002 | g0031 | AFR | ESN | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG03130 | hp2 | a0001 | c0001 | t0003 | g0040 | AFR | ESN | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0288 | AFR | ESN | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG03139 | hp2 | a0001 | c0001 | t0002 | g0242 | AFR | ESN | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG03195 | hp1 | a0007 | c0011 | t0001 | g0022 | AFR | ESN | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0294 | AFR | ESN | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0293 | AFR | MSL | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0182 | AFR | MSL | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG03225 | hp1 | a0003 | c0004 | t0001 | g0023 | AFR | MSL | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG03225 | hp2 | a0001 | c0001 | t0003 | g0038 | AFR | MSL | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | MSL | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0266 | AFR | MSL | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0240 | AFR | MSL | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0070 | AFR | MSL | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG03491 | hp1 | a0001 | c0002 | t0001 | g0045 | SAS | PJL | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0060 | SAS | PJL | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | GWD | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0263 | AFR | GWD | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG03579 | hp1 | a0003 | c0004 | t0001 | g0025 | AFR | MSL | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0111 | AFR | MSL | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0127 | SAS | PJL | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0232 | SAS | PJL | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0229 | SAS | PJL | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0203 | SAS | PJL | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0209 | SAS | PJL | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0273 | SAS | PJL | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0191 | SAS | BEB | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0163 | SAS | BEB | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0269 | SAS | BEB | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG03942 | hp2 | a0001 | c0002 | t0001 | g0046 | SAS | BEB | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG04204 | hp1 | a0009 | c0009 | t0001 | g0044 | SAS | STU | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | STU | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0080 | SAS | STU | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0227 | SAS | STU | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA18522 | hp1 | a0001 | c0008 | t0001 | g0180 | AFR | YRI | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0284 | AFR | YRI | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | CHB | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | CHB | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA18906 | hp1 | a0001 | c0001 | t0003 | g0039 | AFR | YRI | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0029 | AFR | YRI | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA18941 | hp2 | a0001 | c0001 | t0002 | g0259 | EAS | JPT | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA18945 | hp1 | a0001 | c0007 | t0001 | g0138 | EAS | JPT | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0261 | EAS | JPT | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA18953 | hp2 | a0001 | c0001 | t0002 | g0275 | EAS | JPT | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA18956 | hp1 | a0001 | c0001 | t0002 | g0258 | EAS | JPT | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA18966 | hp1 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA18970 | hp2 | a0001 | c0002 | t0001 | g0055 | EAS | JPT | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA18978 | hp1 | a0001 | c0001 | t0002 | g0274 | EAS | JPT | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0199 | EAS | JPT | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA19001 | hp2 | a0001 | c0001 | t0002 | g0271 | EAS | JPT | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0260 | EAS | JPT | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0257 | EAS | JPT | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA19011 | hp1 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0270 | EAS | JPT | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0115 | AFR | LWK | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0277 | AFR | LWK | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA19062 | hp2 | a0001 | c0007 | t0001 | g0139 | EAS | JPT | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA19066 | hp2 | a0001 | c0002 | t0001 | g0054 | EAS | JPT | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA19090 | hp1 | a0001 | c0001 | t0002 | g0272 | EAS | JPT | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA19240 | hp1 | a0001 | c0001 | t0003 | g0001 | AFR | YRI | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA19240 | hp2 | a0003 | c0004 | t0001 | g0026 | AFR | YRI | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA20129 | hp1 | a0001 | c0008 | t0001 | g0234 | AFR | ASW | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0265 | AFR | ASW | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0228 | EUR | TSI | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0249 | EUR | TSI | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0248 | EUR | TSI | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0159 | EUR | TSI | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0177 | SAS | GIH | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0058 | SAS | GIH | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0230 | AMR | CLM | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG02109 | hp2 | a0005 | c0006 | t0001 | g0239 | AFR | ACB | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG02486 | hp1 | a0001 | c0001 | t0003 | g0285 | AFR | ACB | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0246 | AFR | ACB | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0118 | AFR | ACB | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG02559 | hp2 | a0003 | c0004 | t0001 | g0024 | AFR | ACB | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG03471 | hp1 | a0005 | c0006 | t0001 | g0276 | AFR | MSL | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0245 | AFR | MSL | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | USA | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG06807 | hp2 | a0003 | c0004 | t0001 | g0027 | AFR | USA | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0286 | AFR | USA | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | USA | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0003 | REF | REF | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| homoSapiens_grch38 | hp1 | a0004 | c0005 | t0001 | g0254 | REF | REF | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:156919501
|
C | T | 2 | a0007a0008 | 2 | HG02717.hp2 HG03195.hp1 |
missense_variant | MODERATE | c.1093G>A | p.Val365Met | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 9/9 | 1121/1330 | 1093/1137 | 365/378 | chr5 | 156919501 | ||
| chr5:156949692
|
A | G | 8 | a0001a0002a0003others(5): Show | 308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): Show |
missense_variant | MODERATE | c.719T>C | p.Val240Ala | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 4/9 | 747/1330 | 719/1137 | 240/378 | chr5 | 156949692 | ||
| chr5:156951575
|
G | T | 1 | a0009 | 1 | HG04204.hp1 | missense_variant | MODERATE | c.616C>A | p.Pro206Thr | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 3/9 | 644/1330 | 616/1137 | 206/378 | chr5 | 156951575 | ||
| chr5:156951655
|
G | A | 2 | a0003a0007 | 7 | HG02451.hp1 HG02559.hp2 HG03195.hp1 others(4): Show |
missense_variant | MODERATE | c.536C>T | p.Thr179Ile | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 3/9 | 564/1330 | 536/1137 | 179/378 | chr5 | 156951655 | ||
| chr5:156951677
|
C | T | 1 | a0005 | 2 | HG02109.hp2 HG03471.hp1 |
missense_variant | MODERATE | c.514G>A | p.Val172Met | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 3/9 | 542/1330 | 514/1137 | 172/378 | chr5 | 156951677 | ||
| chr5:156951682
|
G | T | 4 | a0002a0003a0006others(1): Show | 15 | HG01070.hp2 HG01167.hp2 HG01169.hp2 others(12): Show |
missense_variant | MODERATE | c.509C>A | p.Thr170Lys | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 3/9 | 537/1330 | 509/1137 | 170/378 | chr5 | 156951682 | ||
| chr5:156954543
|
G | A | 1 | a0006 | 1 | HG01884.hp1 | missense_variant | MODERATE | c.272C>T | p.Pro91Leu | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 2/9 | 300/1330 | 272/1137 | 91/378 | chr5 | 156954543 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:156919499
|
C | G | 1 | a0001c0007 | 2 | NA18945.hp1 NA19062.hp2 |
synonymous_variant | LOW | c.1095G>C | p.Val365Val | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 9/9 | 1123/1330 | 1095/1137 | 365/378 | chr5 | 156919499 | ||
| chr5:156919517
|
T | C | 2 | a0001c0008a0002c0010 | 3 | HG02723.hp2 NA18522.hp1 NA20129.hp1 |
synonymous_variant | LOW | c.1077A>G | p.Lys359Lys | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 9/9 | 1105/1330 | 1077/1137 | 359/378 | chr5 | 156919517 | ||
| chr5:156954620
|
C | T | 2 | a0001c0002a0009c0009 | 12 | HG00408.hp2 HG00423.hp1 HG00673.hp1 others(9): Show |
synonymous_variant | LOW | c.195G>A | p.Lys65Lys | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 2/9 | 223/1330 | 195/1137 | 65/378 | chr5 | 156954620 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:156919423
|
GC | G | 1 | a0001c0001t0003 | 14 | HG01884.hp2 HG02486.hp1 HG02615.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*33delG | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 9/9 | 33 | chr5 | 156919423 | |||||
| chr5:156919453
|
G | A | 1 | a0001c0001t0002 | 26 | HG00597.hp2 HG01069.hp2 HG01071.hp2 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*4C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 9/9 | 4 | chr5 | 156919453 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:156919830
|
C | T | 24 | a0001c0001t0001g0051a0001c0001t0001g0065a0001c0001t0001g0066others(21): Show | 26 | HG01070.hp2 HG01167.hp2 HG01169.hp2 others(23): Show |
intron_variant | MODIFIER | c.1053-289G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 8/8 | chr5 | 156919830 | ||||||
| chr5:156919895
|
G | A | 12 | a0001c0001t0001g0051a0001c0001t0001g0065a0001c0001t0001g0066others(9): Show | 12 | HG01070.hp2 HG01167.hp2 HG01169.hp2 others(9): Show |
intron_variant | MODIFIER | c.1053-354C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 8/8 | chr5 | 156919895 | ||||||
| chr5:156920171
|
C | G | 12 | a0001c0001t0001g0051a0001c0001t0001g0065a0001c0001t0001g0066others(9): Show | 12 | HG01070.hp2 HG01167.hp2 HG01169.hp2 others(9): Show |
intron_variant | MODIFIER | c.1052+293G>C | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 8/8 | chr5 | 156920171 | ||||||
| chr5:156920203
|
C | T | 29 | a0001c0001t0001g0082a0001c0001t0001g0108a0001c0001t0001g0129others(26): Show | 29 | HG00140.hp1 HG00735.hp2 HG00738.hp2 others(26): Show |
intron_variant | MODIFIER | c.1052+261G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 8/8 | chr5 | 156920203 | ||||||
| chr5:156920261
|
C | T | 3 | a0001c0008t0001g0180a0001c0008t0001g0234a0002c0010t0001g0241 | 3 | HG02723.hp2 NA18522.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1052+203G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 8/8 | chr5 | 156920261 | ||||||
| chr5:156920267
|
T | C | 1 | a0001c0001t0001g0265 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1052+197A>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 8/8 | chr5 | 156920267 | ||||||
| chr5:156920341
|
C | T | 11 | a0001c0001t0003g0001a0001c0001t0003g0032a0001c0001t0003g0035others(8): Show | 13 | HG01884.hp2 HG02486.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.1052+123G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 8/8 | chr5 | 156920341 | ||||||
| chr5:156920541
|
C | T | 1 | a0001c0001t0001g0065 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1013-38G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 7/8 | chr5 | 156920541 | ||||||
| chr5:156920701
|
A | G | 24 | a0001c0001t0002g0004a0001c0001t0002g0015a0001c0001t0002g0029others(21): Show | 26 | HG00597.hp2 HG01069.hp2 HG01071.hp2 others(23): Show |
intron_variant | MODIFIER | c.1013-198T>C | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 7/8 | chr5 | 156920701 | ||||||
| chr5:156920805
|
C | G | 3 | a0001c0008t0001g0180a0001c0008t0001g0234a0002c0010t0001g0241 | 3 | HG02723.hp2 NA18522.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1013-302G>C | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 7/8 | chr5 | 156920805 | ||||||
| chr5:156920846
|
G | A | 1 | a0001c0001t0003g0036 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1013-343C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 7/8 | chr5 | 156920846 | ||||||
| chr5:156920908
|
G | A | 53 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0049others(50): Show | 56 | HG00140.hp1 HG00639.hp2 HG00735.hp2 others(53): Show |
intron_variant | MODIFIER | c.1013-405C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 7/8 | chr5 | 156920908 | ||||||
| chr5:156921054
|
C | T | 1 | a0001c0001t0001g0128 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1013-551G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 7/8 | chr5 | 156921054 | ||||||
| chr5:156921198
|
T | C | 1 | a0001c0001t0001g0190 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1013-695A>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 7/8 | chr5 | 156921198 | ||||||
| chr5:156921282
|
G | A | 1 | a0001c0001t0001g0130 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1013-779C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 7/8 | chr5 | 156921282 | ||||||
| chr5:156921551
|
C | T | 1 | a0001c0001t0001g0085 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1012+548G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 7/8 | chr5 | 156921551 | ||||||
| chr5:156921616
|
C | CA | 19 | a0001c0001t0001g0021a0001c0001t0001g0047a0001c0001t0001g0064others(16): Show | 19 | HG01346.hp2 HG01891.hp1 HG02027.hp2 others(16): Show |
intron_variant | MODIFIER | c.1012+482dupT | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 7/8 | chr5 | 156921616 | ||||||
| chr5:156921616
|
CA | C | 11 | a0001c0001t0001g0063a0001c0001t0001g0106a0001c0001t0001g0126others(8): Show | 11 | HG00558.hp1 HG01069.hp1 HG02080.hp2 others(8): Show |
intron_variant | MODIFIER | c.1012+482delT | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 7/8 | chr5 | 156921616 | ||||||
| chr5:156921616
|
CAAA | C | 15 | a0001c0001t0002g0031a0001c0001t0002g0242a0001c0001t0002g0243others(12): Show | 15 | HG01069.hp2 HG01071.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.1012+480_1012+482d others(5): Show |
TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 7/8 | chr5 | 156921616 | ||||||
| chr5:156921616
|
CAAAA | C | 13 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0001g0067others(10): Show | 14 | HG00597.hp2 HG01243.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.1012+479_1012+482d others(6): Show |
TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 7/8 | chr5 | 156921616 | ||||||
| chr5:156921616
|
CAAAAA | C | 15 | a0001c0001t0001g0012a0001c0001t0001g0131a0001c0001t0001g0175others(12): Show | 18 | HG01978.hp2 HG02004.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.1012+478_1012+482d others(7): Show |
TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 7/8 | chr5 | 156921616 | ||||||
| chr5:156921616
|
CAAAAAA | C | 62 | a0001c0001t0001g0003a0001c0001t0001g0020a0001c0001t0001g0030others(59): Show | 64 | HG00140.hp1 HG00639.hp2 HG00735.hp2 others(61): Show |
intron_variant | MODIFIER | c.1012+477_1012+482d others(8): Show |
TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 7/8 | chr5 | 156921616 | ||||||
| chr5:156921616
|
CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0001g0074 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1012+473_1012+482d others(12): Show |
TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 7/8 | chr5 | 156921616 | ||||||
| chr5:156921617
|
A | C | 2 | a0001c0008t0001g0180a0002c0010t0001g0241 | 2 | HG02723.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1012+482T>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 7/8 | chr5 | 156921617 | ||||||
| chr5:156921618
|
A | C | 1 | a0001c0008t0001g0234 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1012+481T>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 7/8 | chr5 | 156921618 | ||||||
| chr5:156921644
|
A | G | 2 | a0001c0008t0001g0180a0002c0010t0001g0241 | 2 | HG02723.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1012+455T>C | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 7/8 | chr5 | 156921644 | ||||||
| chr5:156921706
|
G | C | 1 | a0001c0001t0001g0201 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1012+393C>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 7/8 | chr5 | 156921706 | ||||||
| chr5:156922066
|
G | A | 1 | a0001c0001t0001g0265 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1012+33C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 7/8 | chr5 | 156922066 | ||||||
| chr5:156922351
|
T | C | 90 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0020others(87): Show | 95 | HG00140.hp1 HG00639.hp2 HG00735.hp2 others(92): Show |
intron_variant | MODIFIER | c.895-135A>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 6/8 | chr5 | 156922351 | ||||||
| chr5:156922390
|
C | T | 4 | a0001c0001t0001g0144a0001c0001t0002g0004a0001c0001t0002g0029others(1): Show | 5 | HG03130.hp1 HG03453.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.895-174G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 6/8 | chr5 | 156922390 | ||||||
| chr5:156922650
|
A | G | 1 | a0001c0001t0001g0288 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.895-434T>C | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 6/8 | chr5 | 156922650 | ||||||
| chr5:156922652
|
C | T | 1 | a0001c0001t0001g0248 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.895-436G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 6/8 | chr5 | 156922652 | ||||||
| chr5:156922780
|
AGAGAT | A | 89 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0020others(86): Show | 94 | HG00140.hp1 HG00639.hp2 HG00735.hp2 others(91): Show |
intron_variant | MODIFIER | c.895-569_895-565del others(5): Show |
TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 6/8 | chr5 | 156922780 | ||||||
| chr5:156922862
|
G | C | 115 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0020others(112): Show | 122 | HG00140.hp1 HG00597.hp2 HG00639.hp2 others(119): Show |
intron_variant | MODIFIER | c.895-646C>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 6/8 | chr5 | 156922862 | ||||||
| chr5:156922984
|
T | A | 1 | a0001c0001t0001g0223 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.895-768A>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 6/8 | chr5 | 156922984 | ||||||
| chr5:156923036
|
A | T | 1 | a0001c0001t0001g0198 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.895-820T>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 6/8 | chr5 | 156923036 | ||||||
| chr5:156923049
|
A | G | 3 | a0001c0008t0001g0180a0001c0008t0001g0234a0002c0010t0001g0241 | 3 | HG02723.hp2 NA18522.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.895-833T>C | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 6/8 | chr5 | 156923049 | ||||||
| chr5:156923090
|
G | A | 5 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0001g0067others(2): Show | 5 | HG01243.hp2 HG02258.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.895-874C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 6/8 | chr5 | 156923090 | ||||||
| chr5:156923096
|
C | T | 49 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0049others(46): Show | 52 | HG00140.hp1 HG00639.hp2 HG00735.hp2 others(49): Show |
intron_variant | MODIFIER | c.895-880G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 6/8 | chr5 | 156923096 | ||||||
| chr5:156923143
|
A | AT | 8 | a0001c0001t0001g0073a0001c0001t0001g0133a0001c0001t0001g0134others(5): Show | 8 | HG02572.hp1 HG03471.hp2 HG03491.hp1 others(5): Show |
intron_variant | MODIFIER | c.895-928dupA | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 6/8 | chr5 | 156923143 | ||||||
| chr5:156923143
|
ATTTTT | A | 33 | a0001c0001t0001g0020a0001c0001t0001g0030a0001c0001t0001g0265others(30): Show | 34 | HG00597.hp2 HG01069.hp2 HG01071.hp2 others(31): Show |
intron_variant | MODIFIER | c.895-932_895-928del others(5): Show |
TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 6/8 | chr5 | 156923143 | ||||||
| chr5:156923143
|
ATTTTTT | A | 79 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0049others(76): Show | 84 | HG00140.hp1 HG00639.hp2 HG00735.hp2 others(81): Show |
intron_variant | MODIFIER | c.895-933_895-928del others(6): Show |
TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 6/8 | chr5 | 156923143 | ||||||
| chr5:156923256
|
C | T | 1 | a0001c0001t0001g0291 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.895-1040G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 6/8 | chr5 | 156923256 | ||||||
| chr5:156923309
|
C | T | 1 | a0001c0001t0001g0065 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.895-1093G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 6/8 | chr5 | 156923309 | ||||||
| chr5:156923438
|
T | A | 4 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0001g0067others(1): Show | 4 | HG01243.hp2 HG02258.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.895-1222A>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 6/8 | chr5 | 156923438 | ||||||
| chr5:156923449
|
TA | T | 63 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0020others(60): Show | 66 | HG00140.hp1 HG00639.hp2 HG00735.hp2 others(63): Show |
intron_variant | MODIFIER | c.895-1234delT | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 6/8 | chr5 | 156923449 | ||||||
| chr5:156923539
|
A | AT | 27 | a0001c0001t0002g0004a0001c0001t0002g0015a0001c0001t0002g0029others(24): Show | 29 | HG00597.hp2 HG01069.hp2 HG01071.hp2 others(26): Show |
intron_variant | MODIFIER | c.895-1324dupA | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 6/8 | chr5 | 156923539 | ||||||
| chr5:156923580
|
C | T | 89 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0020others(86): Show | 94 | HG00140.hp1 HG00639.hp2 HG00735.hp2 others(91): Show |
intron_variant | MODIFIER | c.895-1364G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 6/8 | chr5 | 156923580 | ||||||
| chr5:156923704
|
AT | A | 55 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0049others(52): Show | 58 | HG00140.hp1 HG00639.hp2 HG00735.hp2 others(55): Show |
intron_variant | MODIFIER | c.895-1489delA | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 6/8 | chr5 | 156923704 | ||||||
| chr5:156923739
|
T | G | 9 | a0001c0001t0001g0033a0001c0001t0001g0076a0001c0001t0001g0077others(6): Show | 9 | HG02451.hp2 HG02572.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.895-1523A>C | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 6/8 | chr5 | 156923739 | ||||||
| chr5:156923797
|
C | T | 4 | a0001c0001t0001g0090a0001c0001t0001g0116a0001c0001t0001g0117others(1): Show | 4 | HG00099.hp2 HG00639.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.895-1581G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 6/8 | chr5 | 156923797 | ||||||
| chr5:156924020
|
T | C | 89 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0020others(86): Show | 94 | HG00140.hp1 HG00639.hp2 HG00735.hp2 others(91): Show |
intron_variant | MODIFIER | c.895-1804A>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 6/8 | chr5 | 156924020 | ||||||
| chr5:156924028
|
G | C | 2 | a0007c0011t0001g0022a0008c0012t0001g0069 | 2 | HG02717.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.895-1812C>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 6/8 | chr5 | 156924028 | ||||||
| chr5:156924035
|
C | T | 1 | a0001c0001t0001g0240 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.895-1819G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 6/8 | chr5 | 156924035 | ||||||
| chr5:156924246
|
C | T | 3 | a0001c0008t0001g0180a0001c0008t0001g0234a0002c0010t0001g0241 | 3 | HG02723.hp2 NA18522.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.894+2017G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 6/8 | chr5 | 156924246 | ||||||
| chr5:156924254
|
T | C | 4 | a0001c0001t0002g0242a0001c0001t0002g0243a0001c0001t0002g0263others(1): Show | 4 | HG02055.hp1 HG02717.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.894+2009A>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 6/8 | chr5 | 156924254 | ||||||
| chr5:156924336
|
T | C | 74 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0020others(71): Show | 79 | HG00140.hp1 HG00639.hp2 HG00735.hp2 others(76): Show |
intron_variant | MODIFIER | c.894+1927A>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 6/8 | chr5 | 156924336 | ||||||
| chr5:156924375
|
C | A | 2 | a0001c0001t0001g0192a0001c0001t0001g0226 | 2 | NA18961.hp2 NA18987.hp1 |
intron_variant | MODIFIER | c.894+1888G>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 6/8 | chr5 | 156924375 | ||||||
| chr5:156924492
|
G | C | 89 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0020others(86): Show | 94 | HG00140.hp1 HG00639.hp2 HG00735.hp2 others(91): Show |
intron_variant | MODIFIER | c.894+1771C>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 6/8 | chr5 | 156924492 | ||||||
| chr5:156924635
|
A | C | 4 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0001g0067others(1): Show | 4 | HG01243.hp2 HG02258.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.894+1628T>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 6/8 | chr5 | 156924635 | ||||||
| chr5:156924663
|
G | A | 89 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0020others(86): Show | 94 | HG00140.hp1 HG00639.hp2 HG00735.hp2 others(91): Show |
intron_variant | MODIFIER | c.894+1600C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 6/8 | chr5 | 156924663 | ||||||
| chr5:156924665
|
G | A | 1 | a0001c0001t0002g0243 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.894+1598C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 6/8 | chr5 | 156924665 | ||||||
| chr5:156925225
|
G | A | 89 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0020others(86): Show | 94 | HG00140.hp1 HG00639.hp2 HG00735.hp2 others(91): Show |
intron_variant | MODIFIER | c.894+1038C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 6/8 | chr5 | 156925225 | ||||||
| chr5:156925267
|
A | G | 92 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0020others(89): Show | 97 | HG00140.hp1 HG00639.hp2 HG00735.hp2 others(94): Show |
intron_variant | MODIFIER | c.894+996T>C | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 6/8 | chr5 | 156925267 | ||||||
| chr5:156925369
|
C | T | 2 | a0001c0001t0001g0182a0001c0001t0001g0183 | 2 | HG02886.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.894+894G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 6/8 | chr5 | 156925369 | ||||||
| chr5:156925575
|
C | T | 4 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0001g0067others(1): Show | 4 | HG01243.hp2 HG02258.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.894+688G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 6/8 | chr5 | 156925575 | ||||||
| chr5:156925742
|
G | T | 2 | a0001c0001t0002g0242a0001c0001t0002g0243 | 2 | HG02055.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.894+521C>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 6/8 | chr5 | 156925742 | ||||||
| chr5:156925766
|
G | C | 1 | a0001c0001t0001g0137 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.894+497C>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 6/8 | chr5 | 156925766 | ||||||
| chr5:156925951
|
T | C | 5 | a0001c0001t0001g0082a0001c0001t0001g0159a0001c0001t0001g0166others(2): Show | 5 | HG02698.hp1 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.894+312A>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 6/8 | chr5 | 156925951 | ||||||
| chr5:156926058
|
C | T | 1 | a0001c0001t0001g0217 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.894+205G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 6/8 | chr5 | 156926058 | ||||||
| chr5:156926170
|
C | G | 1 | a0001c0001t0002g0262 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.894+93G>C | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 6/8 | chr5 | 156926170 | ||||||
| chr5:156926397
|
T | A | 4 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0001g0067others(1): Show | 4 | HG01243.hp2 HG02258.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.845-85A>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156926397 | ||||||
| chr5:156926434
|
C | T | 1 | a0001c0001t0001g0148 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.845-122G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156926434 | ||||||
| chr5:156926677
|
T | C | 2 | a0001c0001t0001g0151a0001c0001t0001g0222 | 2 | NA18945.hp2 NA18985.hp2 |
intron_variant | MODIFIER | c.845-365A>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156926677 | ||||||
| chr5:156926686
|
C | T | 1 | a0001c0001t0001g0051 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.845-374G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156926686 | ||||||
| chr5:156926725
|
A | G | 54 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0049others(51): Show | 57 | HG00140.hp1 HG00639.hp2 HG00735.hp2 others(54): Show |
intron_variant | MODIFIER | c.845-413T>C | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156926725 | ||||||
| chr5:156926892
|
T | C | 4 | a0001c0001t0002g0242a0001c0001t0002g0243a0001c0001t0002g0263others(1): Show | 4 | HG02055.hp1 HG02717.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.845-580A>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156926892 | ||||||
| chr5:156927003
|
C | T | 1 | a0001c0001t0001g0224 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.845-691G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156927003 | ||||||
| chr5:156927089
|
T | A | 2 | a0005c0006t0001g0239a0005c0006t0001g0276 | 2 | HG02109.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.845-777A>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156927089 | ||||||
| chr5:156927133
|
C | T | 11 | a0001c0001t0003g0001a0001c0001t0003g0032a0001c0001t0003g0035others(8): Show | 13 | HG01884.hp2 HG02486.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.845-821G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156927133 | ||||||
| chr5:156927163
|
G | T | 3 | a0001c0001t0002g0004a0001c0001t0002g0029a0001c0001t0002g0031 | 4 | HG03130.hp1 HG03453.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.845-851C>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156927163 | ||||||
| chr5:156927184
|
A | G | 1 | a0001c0001t0001g0189 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.845-872T>C | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156927184 | ||||||
| chr5:156927272
|
T | A | 6 | a0001c0001t0001g0240a0001c0001t0001g0265a0002c0003t0001g0235others(3): Show | 6 | HG01070.hp2 HG01167.hp2 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.845-960A>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156927272 | ||||||
| chr5:156927297
|
A | G | 1 | a0001c0001t0001g0021 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.845-985T>C | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156927297 | ||||||
| chr5:156927409
|
C | T | 3 | a0001c0001t0001g0059a0001c0001t0001g0083a0001c0001t0001g0084 | 3 | HG00140.hp2 HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.845-1097G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156927409 | ||||||
| chr5:156927466
|
G | A | 106 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0013others(103): Show | 109 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(106): Show |
intron_variant | MODIFIER | c.845-1154C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156927466 | ||||||
| chr5:156927591
|
G | A | 2 | a0001c0001t0003g0041a0001c0001t0003g0042 | 2 | HG02615.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.845-1279C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156927591 | ||||||
| chr5:156927708
|
T | A | 1 | a0001c0001t0001g0099 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.845-1396A>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156927708 | ||||||
| chr5:156927888
|
A | C | 1 | a0001c0001t0001g0279 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.845-1576T>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156927888 | ||||||
| chr5:156928140
|
C | A | 116 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0020others(113): Show | 123 | HG00140.hp1 HG00597.hp2 HG00639.hp2 others(120): Show |
intron_variant | MODIFIER | c.845-1828G>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156928140 | ||||||
| chr5:156928157
|
G | C | 2 | a0001c0001t0001g0214a0001c0001t0001g0231 | 2 | HG00741.hp1 HG01109.hp2 |
intron_variant | MODIFIER | c.845-1845C>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156928157 | ||||||
| chr5:156928170
|
C | T | 24 | a0001c0001t0002g0004a0001c0001t0002g0015a0001c0001t0002g0029others(21): Show | 26 | HG00597.hp2 HG01069.hp2 HG01071.hp2 others(23): Show |
intron_variant | MODIFIER | c.845-1858G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156928170 | ||||||
| chr5:156928246
|
C | A | 20 | a0001c0001t0002g0015a0001c0001t0002g0034a0001c0001t0002g0242others(17): Show | 21 | HG00597.hp2 HG01069.hp2 HG01071.hp2 others(18): Show |
intron_variant | MODIFIER | c.845-1934G>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156928246 | ||||||
| chr5:156928295
|
T | TA | 15 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0072others(12): Show | 18 | HG00558.hp2 HG02027.hp2 HG02056.hp1 others(15): Show |
intron_variant | MODIFIER | c.845-1984dupT | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156928295 | ||||||
| chr5:156928295
|
T | TAA | 65 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0020others(62): Show | 68 | HG00140.hp1 HG00639.hp2 HG00735.hp2 others(65): Show |
intron_variant | MODIFIER | c.845-1985_845-1984d others(4): Show |
TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156928295 | ||||||
| chr5:156928352
|
A | G | 20 | a0001c0001t0002g0015a0001c0001t0002g0034a0001c0001t0002g0242others(17): Show | 21 | HG00597.hp2 HG01069.hp2 HG01071.hp2 others(18): Show |
intron_variant | MODIFIER | c.845-2040T>C | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156928352 | ||||||
| chr5:156928364
|
A | G | 116 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0020others(113): Show | 123 | HG00140.hp1 HG00597.hp2 HG00639.hp2 others(120): Show |
intron_variant | MODIFIER | c.845-2052T>C | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156928364 | ||||||
| chr5:156928391
|
G | T | 6 | a0001c0001t0001g0240a0002c0003t0001g0121a0002c0003t0001g0235others(3): Show | 6 | HG01070.hp2 HG01167.hp2 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.845-2079C>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156928391 | ||||||
| chr5:156928459
|
C | T | 23 | a0001c0001t0002g0004a0001c0001t0002g0015a0001c0001t0002g0029others(20): Show | 25 | HG00597.hp2 HG01069.hp2 HG01071.hp2 others(22): Show |
intron_variant | MODIFIER | c.845-2147G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156928459 | ||||||
| chr5:156928490
|
G | A | 4 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0001g0067others(1): Show | 4 | HG01243.hp2 HG02258.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.845-2178C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156928490 | ||||||
| chr5:156928663
|
A | G | 1 | a0001c0001t0001g0147 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.845-2351T>C | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156928663 | ||||||
| chr5:156928710
|
T | C | 1 | a0001c0001t0001g0007 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.845-2398A>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156928710 | ||||||
| chr5:156928794
|
T | C | 1 | a0001c0001t0003g0036 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.845-2482A>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156928794 | ||||||
| chr5:156928949
|
G | A | 1 | a0001c0001t0001g0016 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.845-2637C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156928949 | ||||||
| chr5:156929038
|
T | C | 1 | a0001c0001t0001g0233 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.845-2726A>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156929038 | ||||||
| chr5:156929283
|
T | C | 16 | a0001c0001t0002g0015a0001c0001t0002g0034a0001c0001t0002g0257others(13): Show | 17 | HG00597.hp2 HG01069.hp2 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.845-2971A>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156929283 | ||||||
| chr5:156929295
|
C | A | 2 | a0001c0001t0002g0281a0001c0001t0002g0282 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.845-2983G>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156929295 | ||||||
| chr5:156929338
|
G | A | 2 | a0005c0006t0001g0239a0005c0006t0001g0276 | 2 | HG02109.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.845-3026C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156929338 | ||||||
| chr5:156929467
|
A | G | 72 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0020others(69): Show | 75 | HG00140.hp1 HG00639.hp2 HG00735.hp2 others(72): Show |
intron_variant | MODIFIER | c.845-3155T>C | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156929467 | ||||||
| chr5:156929566
|
CGA | C | 11 | a0001c0001t0003g0001a0001c0001t0003g0032a0001c0001t0003g0035others(8): Show | 13 | HG01884.hp2 HG02486.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.845-3256_845-3255d others(4): Show |
TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156929566 | ||||||
| chr5:156929723
|
A | G | 1 | a0001c0002t0001g0055 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.845-3411T>C | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156929723 | ||||||
| chr5:156929806
|
C | T | 1 | a0001c0001t0001g0116 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.845-3494G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156929806 | ||||||
| chr5:156929897
|
C | T | 2 | a0001c0001t0001g0074a0001c0001t0001g0080 | 2 | HG02683.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.845-3585G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156929897 | ||||||
| chr5:156929962
|
T | C | 1 | a0001c0001t0002g0031 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.845-3650A>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156929962 | ||||||
| chr5:156930005
|
C | T | 3 | a0001c0001t0001g0008a0001c0001t0001g0058a0001c0001t0001g0060 | 4 | HG01099.hp1 HG03491.hp2 HG04204.hp2 others(1): Show |
intron_variant | MODIFIER | c.845-3693G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156930005 | ||||||
| chr5:156930018
|
T | C | 4 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0001g0067others(1): Show | 4 | HG01243.hp2 HG02258.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.845-3706A>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156930018 | ||||||
| chr5:156930059
|
C | G | 2 | a0001c0001t0001g0278a0001c0001t0001g0279 | 2 | HG02809.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.845-3747G>C | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156930059 | ||||||
| chr5:156930074
|
G | A | 1 | a0001c0001t0001g0105 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.845-3762C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156930074 | ||||||
| chr5:156930127
|
A | G | 66 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0020others(63): Show | 69 | HG00140.hp1 HG00639.hp2 HG00735.hp2 others(66): Show |
intron_variant | MODIFIER | c.845-3815T>C | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156930127 | ||||||
| chr5:156930133
|
T | C | 11 | a0001c0001t0003g0001a0001c0001t0003g0032a0001c0001t0003g0035others(8): Show | 13 | HG01884.hp2 HG02486.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.845-3821A>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156930133 | ||||||
| chr5:156930146
|
G | T | 12 | a0001c0001t0001g0020a0001c0001t0001g0030a0001c0001t0001g0051others(9): Show | 12 | HG02055.hp2 HG02109.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.845-3834C>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156930146 | ||||||
| chr5:156930150
|
C | T | 1 | a0001c0001t0001g0174 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.845-3838G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156930150 | ||||||
| chr5:156930159
|
G | T | 3 | a0001c0008t0001g0180a0001c0008t0001g0234a0002c0010t0001g0241 | 3 | HG02723.hp2 NA18522.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.845-3847C>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156930159 | ||||||
| chr5:156930425
|
T | C | 11 | a0001c0001t0003g0001a0001c0001t0003g0032a0001c0001t0003g0035others(8): Show | 13 | HG01884.hp2 HG02486.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.845-4113A>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156930425 | ||||||
| chr5:156930451
|
A | T | 2 | a0007c0011t0001g0022a0008c0012t0001g0069 | 2 | HG02717.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.845-4139T>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156930451 | ||||||
| chr5:156930587
|
A | G | 1 | a0001c0001t0001g0212 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.845-4275T>C | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156930587 | ||||||
| chr5:156930863
|
T | C | 6 | a0001c0001t0001g0240a0002c0003t0001g0121a0002c0003t0001g0235others(3): Show | 6 | HG01070.hp2 HG01167.hp2 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.845-4551A>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156930863 | ||||||
| chr5:156931008
|
G | T | 6 | a0003c0004t0001g0023a0003c0004t0001g0024a0003c0004t0001g0025others(3): Show | 6 | HG02451.hp1 HG02559.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.845-4696C>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156931008 | ||||||
| chr5:156931452
|
T | C | 1 | a0001c0001t0003g0038 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.845-5140A>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156931452 | ||||||
| chr5:156931659
|
A | G | 2 | a0007c0011t0001g0022a0008c0012t0001g0069 | 2 | HG02717.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.845-5347T>C | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156931659 | ||||||
| chr5:156931842
|
G | C | 16 | a0001c0001t0002g0015a0001c0001t0002g0034a0001c0001t0002g0257others(13): Show | 17 | HG00597.hp2 HG01069.hp2 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.845-5530C>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156931842 | ||||||
| chr5:156931843
|
C | A | 16 | a0001c0001t0002g0015a0001c0001t0002g0034a0001c0001t0002g0257others(13): Show | 17 | HG00597.hp2 HG01069.hp2 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.845-5531G>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156931843 | ||||||
| chr5:156931845
|
AAGATACT others(164): Show |
A | 16 | a0001c0001t0002g0015a0001c0001t0002g0034a0001c0001t0002g0257others(13): Show | 17 | HG00597.hp2 HG01069.hp2 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.845-5704_845-5534d others(2): Show |
TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156931845 | ||||||
| chr5:156932018
|
CT | C | 16 | a0001c0001t0002g0015a0001c0001t0002g0034a0001c0001t0002g0257others(13): Show | 17 | HG00597.hp2 HG01069.hp2 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.845-5707delA | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156932018 | ||||||
| chr5:156932020
|
T | C | 16 | a0001c0001t0002g0015a0001c0001t0002g0034a0001c0001t0002g0257others(13): Show | 17 | HG00597.hp2 HG01069.hp2 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.845-5708A>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156932020 | ||||||
| chr5:156932026
|
A | T | 16 | a0001c0001t0002g0015a0001c0001t0002g0034a0001c0001t0002g0257others(13): Show | 17 | HG00597.hp2 HG01069.hp2 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.845-5714T>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156932026 | ||||||
| chr5:156932028
|
G | C | 16 | a0001c0001t0002g0015a0001c0001t0002g0034a0001c0001t0002g0257others(13): Show | 17 | HG00597.hp2 HG01069.hp2 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.845-5716C>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156932028 | ||||||
| chr5:156932029
|
G | A | 16 | a0001c0001t0002g0015a0001c0001t0002g0034a0001c0001t0002g0257others(13): Show | 17 | HG00597.hp2 HG01069.hp2 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.845-5717C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156932029 | ||||||
| chr5:156932030
|
A | T | 16 | a0001c0001t0002g0015a0001c0001t0002g0034a0001c0001t0002g0257others(13): Show | 17 | HG00597.hp2 HG01069.hp2 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.845-5718T>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156932030 | ||||||
| chr5:156932038
|
T | C | 3 | a0001c0008t0001g0180a0001c0008t0001g0234a0002c0010t0001g0241 | 3 | HG02723.hp2 NA18522.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.845-5726A>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156932038 | ||||||
| chr5:156932072
|
T | C | 4 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0001g0067others(1): Show | 4 | HG01243.hp2 HG02258.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.845-5760A>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156932072 | ||||||
| chr5:156932081
|
T | C | 12 | a0001c0001t0001g0020a0001c0001t0001g0030a0001c0001t0001g0051others(9): Show | 12 | HG02055.hp2 HG02109.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.845-5769A>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156932081 | ||||||
| chr5:156932264
|
T | C | 1 | a0001c0001t0001g0163 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.845-5952A>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156932264 | ||||||
| chr5:156932283
|
T | G | 3 | a0001c0001t0002g0004a0001c0001t0002g0029a0001c0001t0002g0031 | 4 | HG03130.hp1 HG03453.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.845-5971A>C | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156932283 | ||||||
| chr5:156932391
|
A | G | 20 | a0001c0001t0002g0015a0001c0001t0002g0034a0001c0001t0002g0242others(17): Show | 21 | HG00597.hp2 HG01069.hp2 HG01071.hp2 others(18): Show |
intron_variant | MODIFIER | c.845-6079T>C | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156932391 | ||||||
| chr5:156932424
|
A | G | 1 | a0001c0001t0001g0223 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.845-6112T>C | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156932424 | ||||||
| chr5:156932469
|
C | G | 2 | a0007c0011t0001g0022a0008c0012t0001g0069 | 2 | HG02717.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.845-6157G>C | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156932469 | ||||||
| chr5:156932488
|
G | T | 1 | a0001c0001t0001g0113 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.845-6176C>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156932488 | ||||||
| chr5:156932531
|
C | T | 3 | a0001c0008t0001g0180a0001c0008t0001g0234a0002c0010t0001g0241 | 3 | HG02723.hp2 NA18522.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.845-6219G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156932531 | ||||||
| chr5:156932717
|
G | A | 23 | a0001c0001t0002g0004a0001c0001t0002g0015a0001c0001t0002g0029others(20): Show | 25 | HG00597.hp2 HG01069.hp2 HG01071.hp2 others(22): Show |
intron_variant | MODIFIER | c.845-6405C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156932717 | ||||||
| chr5:156932754
|
C | A | 13 | a0001c0001t0002g0015a0001c0001t0002g0257a0001c0001t0002g0258others(10): Show | 14 | HG00597.hp2 HG03704.hp2 NA18941.hp2 others(11): Show |
intron_variant | MODIFIER | c.845-6442G>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156932754 | ||||||
| chr5:156932784
|
A | G | 3 | a0001c0008t0001g0180a0001c0008t0001g0234a0002c0010t0001g0241 | 3 | HG02723.hp2 NA18522.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.845-6472T>C | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156932784 | ||||||
| chr5:156932866
|
T | G | 1 | a0001c0001t0001g0265 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.845-6554A>C | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156932866 | ||||||
| chr5:156932897
|
C | A | 4 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0001g0067others(1): Show | 4 | HG01243.hp2 HG02258.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.845-6585G>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156932897 | ||||||
| chr5:156933003
|
C | CAA | 23 | a0001c0001t0002g0004a0001c0001t0002g0015a0001c0001t0002g0029others(20): Show | 25 | HG00597.hp2 HG01069.hp2 HG01071.hp2 others(22): Show |
intron_variant | MODIFIER | c.845-6693_845-6692d others(4): Show |
TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156933003 | ||||||
| chr5:156933006
|
A | AAAAAG | 51 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0049others(48): Show | 54 | HG00140.hp1 HG00639.hp2 HG00735.hp2 others(51): Show |
intron_variant | MODIFIER | c.845-6699_845-6695d others(7): Show |
TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156933006 | ||||||
| chr5:156933006
|
A | AAAAAGAA others(3): Show |
2 | a0001c0001t0001g0214a0001c0001t0001g0291 | 2 | HG00741.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.845-6704_845-6695d others(12): Show |
TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156933006 | ||||||
| chr5:156933006
|
A | AAAAAGAA others(8): Show |
6 | a0001c0001t0001g0020a0001c0001t0001g0208a0001c0001t0001g0279others(3): Show | 6 | HG02055.hp2 HG02735.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.845-6709_845-6695d others(17): Show |
TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156933006 | ||||||
| chr5:156933006
|
A | AAAAAGAA others(13): Show |
2 | a0001c0001t0001g0110a0001c0001t0001g0278 | 2 | HG02257.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.845-6714_845-6695d others(22): Show |
TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156933006 | ||||||
| chr5:156933006
|
A | AAAAAGAA others(18): Show |
3 | a0001c0001t0001g0030a0001c0001t0001g0051a0001c0001t0001g0293 | 3 | HG02922.hp2 HG02965.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.845-6719_845-6695d others(27): Show |
TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156933006 | ||||||
| chr5:156933006
|
A | AAAAAGAA others(38): Show |
1 | a0005c0006t0001g0276 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.845-6695_845-6694i others(47): Show |
TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156933006 | ||||||
| chr5:156933006
|
A | AAAAAGAA others(43): Show |
1 | a0005c0006t0001g0239 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.845-6695_845-6694i others(52): Show |
TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156933006 | ||||||
| chr5:156933144
|
T | G | 5 | a0001c0001t0001g0009a0001c0001t0001g0075a0001c0001t0001g0079others(2): Show | 6 | HG00558.hp2 HG02056.hp1 HG02074.hp1 others(3): Show |
intron_variant | MODIFIER | c.845-6832A>C | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156933144 | ||||||
| chr5:156933172
|
G | C | 113 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0013others(110): Show | 118 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.845-6860C>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156933172 | ||||||
| chr5:156933182
|
A | C | 89 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0020others(86): Show | 94 | HG00140.hp1 HG00597.hp2 HG00639.hp2 others(91): Show |
intron_variant | MODIFIER | c.845-6870T>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156933182 | ||||||
| chr5:156933211
|
G | A | 1 | a0001c0001t0001g0088 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.845-6899C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156933211 | ||||||
| chr5:156933263
|
T | C | 2 | a0001c0001t0001g0141a0001c0001t0001g0143 | 2 | NA18942.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.845-6951A>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156933263 | ||||||
| chr5:156933297
|
G | A | 1 | a0001c0001t0001g0185 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.845-6985C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156933297 | ||||||
| chr5:156933338
|
A | G | 54 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0049others(51): Show | 57 | HG00140.hp1 HG00639.hp2 HG00735.hp2 others(54): Show |
intron_variant | MODIFIER | c.845-7026T>C | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156933338 | ||||||
| chr5:156933371
|
A | G | 11 | a0001c0001t0003g0001a0001c0001t0003g0032a0001c0001t0003g0035others(8): Show | 13 | HG01884.hp2 HG02486.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.845-7059T>C | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156933371 | ||||||
| chr5:156933440
|
T | C | 109 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0020others(106): Show | 116 | HG00140.hp1 HG00597.hp2 HG00639.hp2 others(113): Show |
intron_variant | MODIFIER | c.845-7128A>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156933440 | ||||||
| chr5:156933457
|
A | AC | 16 | a0001c0001t0001g0020a0001c0001t0001g0030a0001c0001t0001g0049others(13): Show | 16 | HG02027.hp1 HG02027.hp2 HG02074.hp1 others(13): Show |
intron_variant | MODIFIER | c.845-7146dupG | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156933457 | ||||||
| chr5:156933544
|
G | GTTGTT | 58 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0020others(55): Show | 61 | HG00140.hp1 HG00639.hp2 HG00735.hp2 others(58): Show |
intron_variant | MODIFIER | c.845-7237_845-7233d others(7): Show |
TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156933544 | ||||||
| chr5:156933544
|
G | GTTGTTTT others(3): Show |
16 | a0001c0001t0001g0030a0001c0001t0001g0082a0001c0001t0001g0173others(13): Show | 16 | HG01928.hp1 HG02055.hp2 HG02698.hp1 others(13): Show |
intron_variant | MODIFIER | c.845-7242_845-7233d others(12): Show |
TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156933544 | ||||||
| chr5:156933544
|
G | GTTGTTTT others(8): Show |
13 | a0001c0001t0002g0015a0001c0001t0002g0258a0001c0001t0002g0259others(10): Show | 14 | HG00597.hp2 HG01069.hp2 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.845-7247_845-7233d others(17): Show |
TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156933544 | ||||||
| chr5:156933544
|
G | GTTGTTTT others(13): Show |
4 | a0001c0001t0002g0004a0001c0001t0002g0029a0001c0001t0002g0031others(1): Show | 5 | HG03130.hp1 HG03453.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.845-7252_845-7233d others(22): Show |
TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156933544 | ||||||
| chr5:156933544
|
GTTGTT | G | 178 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(175): Show | 188 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(185): Show |
intron_variant | MODIFIER | c.845-7237_845-7233d others(7): Show |
TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156933544 | ||||||
| chr5:156933544
|
GTTGTTTT others(3): Show |
G | 2 | a0001c0001t0001g0151a0001c0001t0001g0222 | 2 | NA18945.hp2 NA18985.hp2 |
intron_variant | MODIFIER | c.845-7242_845-7233d others(12): Show |
TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156933544 | ||||||
| chr5:156933606
|
C | A | 2 | a0001c0001t0002g0259a0001c0001t0002g0261 | 2 | NA18941.hp2 NA18950.hp1 |
intron_variant | MODIFIER | c.845-7294G>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156933606 | ||||||
| chr5:156933716
|
G | A | 1 | a0008c0012t0001g0069 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.845-7404C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156933716 | ||||||
| chr5:156933805
|
C | A | 7 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0001g0067others(4): Show | 7 | HG01243.hp2 HG02258.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.845-7493G>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156933805 | ||||||
| chr5:156933893
|
C | T | 4 | a0001c0001t0001g0157a0001c0001t0001g0181a0001c0001t0001g0206others(1): Show | 4 | HG00735.hp2 HG01256.hp2 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.845-7581G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156933893 | ||||||
| chr5:156933942
|
A | G | 1 | a0001c0001t0001g0067 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.845-7630T>C | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156933942 | ||||||
| chr5:156934129
|
C | T | 3 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0114 | 3 | HG02630.hp2 HG02922.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.845-7817G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156934129 | ||||||
| chr5:156934152
|
CT | C | 8 | a0001c0001t0001g0020a0001c0001t0001g0030a0001c0001t0001g0278others(5): Show | 8 | HG02055.hp2 HG02809.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.845-7841delA | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156934152 | ||||||
| chr5:156934246
|
T | G | 1 | a0001c0001t0001g0244 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.845-7934A>C | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156934246 | ||||||
| chr5:156934288
|
T | TA | 3 | a0001c0001t0002g0004a0001c0001t0002g0029a0001c0001t0002g0031 | 4 | HG03130.hp1 HG03453.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.845-7977dupT | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156934288 | ||||||
| chr5:156934315
|
G | T | 1 | a0001c0007t0001g0138 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.845-8003C>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156934315 | ||||||
| chr5:156934431
|
G | A | 11 | a0001c0001t0003g0001a0001c0001t0003g0032a0001c0001t0003g0035others(8): Show | 13 | HG01884.hp2 HG02486.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.845-8119C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156934431 | ||||||
| chr5:156934431
|
G | T | 9 | a0001c0001t0001g0003a0001c0001t0001g0049a0001c0001t0001g0050others(6): Show | 11 | HG01261.hp1 HG01516.hp2 HG01517.hp1 others(8): Show |
intron_variant | MODIFIER | c.845-8119C>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156934431 | ||||||
| chr5:156934440
|
G | T | 2 | a0001c0001t0001g0051a0001c0001t0001g0110 | 2 | HG02257.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.845-8128C>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156934440 | ||||||
| chr5:156934529
|
T | C | 2 | a0007c0011t0001g0022a0008c0012t0001g0069 | 2 | HG02717.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.845-8217A>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156934529 | ||||||
| chr5:156934541
|
G | C | 116 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0020others(113): Show | 123 | HG00140.hp1 HG00597.hp2 HG00639.hp2 others(120): Show |
intron_variant | MODIFIER | c.845-8229C>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156934541 | ||||||
| chr5:156934564
|
T | A | 1 | a0001c0001t0001g0104 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.845-8252A>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156934564 | ||||||
| chr5:156934665
|
G | T | 1 | a0001c0001t0001g0253 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.845-8353C>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156934665 | ||||||
| chr5:156934705
|
T | C | 1 | a0001c0001t0001g0196 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.845-8393A>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156934705 | ||||||
| chr5:156934773
|
C | T | 1 | a0001c0001t0001g0277 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.845-8461G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156934773 | ||||||
| chr5:156935006
|
A | G | 3 | a0001c0001t0001g0008a0001c0001t0001g0058a0001c0001t0001g0060 | 4 | HG01099.hp1 HG03491.hp2 HG04204.hp2 others(1): Show |
intron_variant | MODIFIER | c.845-8694T>C | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156935006 | ||||||
| chr5:156935031
|
C | A | 1 | a0001c0001t0002g0271 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.845-8719G>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156935031 | ||||||
| chr5:156935062
|
C | T | 1 | a0001c0001t0002g0270 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.845-8750G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156935062 | ||||||
| chr5:156935070
|
T | C | 1 | a0001c0001t0001g0193 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.845-8758A>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156935070 | ||||||
| chr5:156935135
|
T | C | 4 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0001g0067others(1): Show | 4 | HG01243.hp2 HG02258.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.845-8823A>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156935135 | ||||||
| chr5:156935182
|
C | CT | 20 | a0001c0001t0002g0015a0001c0001t0002g0034a0001c0001t0002g0242others(17): Show | 21 | HG00597.hp2 HG01069.hp2 HG01071.hp2 others(18): Show |
intron_variant | MODIFIER | c.845-8871dupA | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156935182 | ||||||
| chr5:156935473
|
C | A | 1 | a0001c0001t0001g0099 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.845-9161G>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156935473 | ||||||
| chr5:156935713
|
C | A | 1 | a0001c0001t0001g0075 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.845-9401G>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156935713 | ||||||
| chr5:156936040
|
A | C | 1 | a0001c0001t0001g0092 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.845-9728T>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156936040 | ||||||
| chr5:156936067
|
C | T | 11 | a0001c0001t0003g0001a0001c0001t0003g0032a0001c0001t0003g0035others(8): Show | 13 | HG01884.hp2 HG02486.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.845-9755G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156936067 | ||||||
| chr5:156936119
|
G | A | 3 | a0001c0008t0001g0180a0001c0008t0001g0234a0002c0010t0001g0241 | 3 | HG02723.hp2 NA18522.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.845-9807C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156936119 | ||||||
| chr5:156936141
|
C | A | 2 | a0007c0011t0001g0022a0008c0012t0001g0069 | 2 | HG02717.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.845-9829G>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156936141 | ||||||
| chr5:156936142
|
G | A | 1 | a0001c0001t0001g0021 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.845-9830C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156936142 | ||||||
| chr5:156936153
|
C | T | 91 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0020others(88): Show | 96 | HG00140.hp1 HG00597.hp2 HG00639.hp2 others(93): Show |
intron_variant | MODIFIER | c.845-9841G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156936153 | ||||||
| chr5:156936173
|
A | G | 2 | a0001c0001t0002g0260a0001c0001t0002g0272 | 2 | NA19005.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.845-9861T>C | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156936173 | ||||||
| chr5:156936216
|
G | A | 8 | a0001c0001t0001g0020a0001c0001t0001g0030a0001c0001t0001g0278others(5): Show | 8 | HG02055.hp2 HG02809.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.845-9904C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156936216 | ||||||
| chr5:156936622
|
T | C | 4 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0001g0067others(1): Show | 4 | HG01243.hp2 HG02258.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.845-10310A>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156936622 | ||||||
| chr5:156936800
|
C | T | 1 | a0005c0006t0001g0239 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.845-10488G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156936800 | ||||||
| chr5:156936919
|
G | A | 1 | a0001c0001t0001g0088 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.845-10607C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156936919 | ||||||
| chr5:156936932
|
G | GA | 50 | a0001c0001t0001g0020a0001c0001t0001g0030a0001c0001t0001g0051others(47): Show | 54 | HG00597.hp2 HG01069.hp2 HG01071.hp2 others(51): Show |
intron_variant | MODIFIER | c.845-10621dupT | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156936932 | ||||||
| chr5:156937027
|
C | T | 2 | a0005c0006t0001g0239a0005c0006t0001g0276 | 2 | HG02109.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.845-10715G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156937027 | ||||||
| chr5:156937028
|
G | A | 1 | a0001c0001t0001g0126 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.845-10716C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156937028 | ||||||
| chr5:156937192
|
C | T | 1 | a0001c0001t0001g0007 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.845-10880G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156937192 | ||||||
| chr5:156937196
|
G | A | 1 | a0001c0001t0001g0132 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.845-10884C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156937196 | ||||||
| chr5:156937382
|
C | CAG | 58 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0049others(55): Show | 61 | HG00140.hp1 HG00639.hp2 HG00735.hp2 others(58): Show |
intron_variant | MODIFIER | c.844+11032_844+1103 others(6): Show |
TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156937382 | ||||||
| chr5:156937437
|
G | T | 8 | a0001c0001t0001g0020a0001c0001t0001g0030a0001c0001t0001g0278others(5): Show | 8 | HG02055.hp2 HG02809.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.844+10979C>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156937437 | ||||||
| chr5:156937465
|
C | G | 2 | a0001c0008t0001g0180a0002c0010t0001g0241 | 2 | HG02723.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.844+10951G>C | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156937465 | ||||||
| chr5:156937477
|
C | T | 1 | a0009c0009t0001g0044 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.844+10939G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156937477 | ||||||
| chr5:156937586
|
A | AC | 6 | a0001c0001t0001g0240a0002c0003t0001g0121a0002c0003t0001g0235others(3): Show | 6 | HG01070.hp2 HG01167.hp2 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.844+10829dupG | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156937586 | ||||||
| chr5:156937998
|
C | T | 1 | a0001c0001t0001g0146 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.844+10418G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156937998 | ||||||
| chr5:156938044
|
T | C | 4 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0001g0067others(1): Show | 4 | HG01243.hp2 HG02258.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.844+10372A>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156938044 | ||||||
| chr5:156938239
|
C | G | 1 | a0001c0001t0001g0117 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.844+10177G>C | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156938239 | ||||||
| chr5:156938355
|
T | A | 89 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0020others(86): Show | 94 | HG00140.hp1 HG00597.hp2 HG00639.hp2 others(91): Show |
intron_variant | MODIFIER | c.844+10061A>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156938355 | ||||||
| chr5:156938461
|
A | C | 91 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0020others(88): Show | 96 | HG00140.hp1 HG00597.hp2 HG00639.hp2 others(93): Show |
intron_variant | MODIFIER | c.844+9955T>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156938461 | ||||||
| chr5:156938565
|
G | A | 91 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0020others(88): Show | 96 | HG00140.hp1 HG00597.hp2 HG00639.hp2 others(93): Show |
intron_variant | MODIFIER | c.844+9851C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156938565 | ||||||
| chr5:156938669
|
G | A | 5 | a0001c0001t0001g0030a0001c0001t0001g0293a0001c0001t0002g0004others(2): Show | 6 | HG02965.hp2 HG03130.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.844+9747C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156938669 | ||||||
| chr5:156938725
|
G | A | 2 | a0001c0001t0001g0151a0001c0001t0001g0222 | 2 | NA18945.hp2 NA18985.hp2 |
intron_variant | MODIFIER | c.844+9691C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156938725 | ||||||
| chr5:156938836
|
C | T | 10 | a0001c0001t0003g0001a0001c0001t0003g0032a0001c0001t0003g0035others(7): Show | 12 | HG01884.hp2 HG02615.hp1 HG02818.hp1 others(9): Show |
intron_variant | MODIFIER | c.844+9580G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156938836 | ||||||
| chr5:156938912
|
G | A | 11 | a0001c0001t0003g0001a0001c0001t0003g0032a0001c0001t0003g0035others(8): Show | 13 | HG01884.hp2 HG02486.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.844+9504C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156938912 | ||||||
| chr5:156939094
|
C | A | 1 | a0001c0001t0001g0127 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.844+9322G>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156939094 | ||||||
| chr5:156939170
|
G | A | 91 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0020others(88): Show | 96 | HG00140.hp1 HG00597.hp2 HG00639.hp2 others(93): Show |
intron_variant | MODIFIER | c.844+9246C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156939170 | ||||||
| chr5:156939285
|
T | C | 91 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0020others(88): Show | 96 | HG00140.hp1 HG00597.hp2 HG00639.hp2 others(93): Show |
intron_variant | MODIFIER | c.844+9131A>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156939285 | ||||||
| chr5:156939355
|
G | A | 8 | a0001c0001t0001g0020a0001c0001t0001g0030a0001c0001t0001g0278others(5): Show | 8 | HG02055.hp2 HG02809.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.844+9061C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156939355 | ||||||
| chr5:156939448
|
G | T | 1 | a0001c0002t0001g0046 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.844+8968C>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156939448 | ||||||
| chr5:156939677
|
T | C | 11 | a0001c0001t0003g0001a0001c0001t0003g0032a0001c0001t0003g0035others(8): Show | 13 | HG01884.hp2 HG02486.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.844+8739A>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156939677 | ||||||
| chr5:156939775
|
G | A | 14 | a0001c0001t0002g0260a0001c0001t0003g0001a0001c0001t0003g0032others(11): Show | 16 | HG01884.hp2 HG02486.hp1 HG02615.hp1 others(13): Show |
intron_variant | MODIFIER | c.844+8641C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156939775 | ||||||
| chr5:156939977
|
G | A | 2 | a0001c0008t0001g0180a0002c0010t0001g0241 | 2 | HG02723.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.844+8439C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156939977 | ||||||
| chr5:156940081
|
T | C | 233 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0010others(230): Show | 246 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(243): Show |
intron_variant | MODIFIER | c.844+8335A>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156940081 | ||||||
| chr5:156940189
|
C | T | 2 | a0001c0001t0001g0128a0001c0001t0001g0193 | 2 | NA18960.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.844+8227G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156940189 | ||||||
| chr5:156940204
|
C | T | 4 | a0001c0001t0001g0265a0001c0008t0001g0180a0001c0008t0001g0234others(1): Show | 4 | HG02723.hp2 NA18522.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.844+8212G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156940204 | ||||||
| chr5:156940246
|
A | G | 91 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0020others(88): Show | 96 | HG00140.hp1 HG00597.hp2 HG00639.hp2 others(93): Show |
intron_variant | MODIFIER | c.844+8170T>C | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156940246 | ||||||
| chr5:156940289
|
G | A | 53 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0049others(50): Show | 56 | HG00140.hp1 HG00639.hp2 HG00735.hp2 others(53): Show |
intron_variant | MODIFIER | c.844+8127C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156940289 | ||||||
| chr5:156940317
|
T | A | 1 | a0001c0002t0001g0054 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.844+8099A>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156940317 | ||||||
| chr5:156940324
|
C | T | 15 | a0001c0001t0001g0051a0001c0001t0001g0110a0001c0001t0003g0001others(12): Show | 17 | HG01884.hp2 HG02109.hp2 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.844+8092G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156940324 | ||||||
| chr5:156940369
|
G | T | 1 | a0001c0001t0001g0193 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.844+8047C>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156940369 | ||||||
| chr5:156940399
|
G | A | 1 | a0001c0001t0001g0202 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.844+8017C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156940399 | ||||||
| chr5:156940419
|
C | G | 4 | a0001c0001t0001g0051a0001c0001t0001g0110a0005c0006t0001g0239others(1): Show | 4 | HG02109.hp2 HG02257.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.844+7997G>C | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156940419 | ||||||
| chr5:156940447
|
C | T | 1 | a0001c0001t0001g0163 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.844+7969G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156940447 | ||||||
| chr5:156940475
|
G | A | 3 | a0001c0001t0002g0004a0001c0001t0002g0029a0001c0001t0002g0031 | 4 | HG03130.hp1 HG03453.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.844+7941C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156940475 | ||||||
| chr5:156940515
|
A | G | 97 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0020others(94): Show | 102 | HG00140.hp1 HG00597.hp2 HG00639.hp2 others(99): Show |
intron_variant | MODIFIER | c.844+7901T>C | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156940515 | ||||||
| chr5:156940528
|
C | T | 29 | a0001c0001t0001g0082a0001c0001t0001g0108a0001c0001t0001g0129others(26): Show | 29 | HG00140.hp1 HG00639.hp2 HG00735.hp2 others(26): Show |
intron_variant | MODIFIER | c.844+7888G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156940528 | ||||||
| chr5:156940573
|
G | A | 1 | a0005c0006t0001g0276 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.844+7843C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156940573 | ||||||
| chr5:156940592
|
CCTCTGCC others(30): Show |
C | 12 | a0001c0001t0001g0020a0001c0001t0001g0030a0001c0001t0001g0051others(9): Show | 12 | HG02055.hp2 HG02109.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.844+7787_844+7823d others(39): Show |
TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156940592 | ||||||
| chr5:156940650
|
A | G | 91 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0020others(88): Show | 96 | HG00140.hp1 HG00597.hp2 HG00639.hp2 others(93): Show |
intron_variant | MODIFIER | c.844+7766T>C | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156940650 | ||||||
| chr5:156940727
|
G | A | 2 | a0001c0001t0001g0141a0001c0001t0001g0143 | 2 | NA18942.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.844+7689C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156940727 | ||||||
| chr5:156940744
|
A | C | 90 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0020others(87): Show | 95 | HG00140.hp1 HG00597.hp2 HG00639.hp2 others(92): Show |
intron_variant | MODIFIER | c.844+7672T>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156940744 | ||||||
| chr5:156940792
|
G | A | 2 | a0001c0001t0001g0160a0001c0001t0001g0162 | 2 | HG02129.hp1 HG02155.hp2 |
intron_variant | MODIFIER | c.844+7624C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156940792 | ||||||
| chr5:156940799
|
G | A | 1 | a0001c0001t0001g0100 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.844+7617C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156940799 | ||||||
| chr5:156940818
|
C | T | 88 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0020others(85): Show | 93 | HG00140.hp1 HG00597.hp2 HG00639.hp2 others(90): Show |
intron_variant | MODIFIER | c.844+7598G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156940818 | ||||||
| chr5:156941021
|
G | C | 108 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0020others(105): Show | 115 | HG00140.hp1 HG00597.hp2 HG00639.hp2 others(112): Show |
intron_variant | MODIFIER | c.844+7395C>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156941021 | ||||||
| chr5:156941040
|
T | A | 6 | a0001c0001t0001g0109a0001c0001t0001g0160a0001c0001t0001g0162others(3): Show | 6 | HG01081.hp2 HG01361.hp2 HG02129.hp1 others(3): Show |
intron_variant | MODIFIER | c.844+7376A>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156941040 | ||||||
| chr5:156941051
|
A | C | 19 | a0001c0001t0001g0020a0001c0001t0001g0030a0001c0001t0001g0051others(16): Show | 20 | HG02055.hp1 HG02055.hp2 HG02109.hp2 others(17): Show |
intron_variant | MODIFIER | c.844+7365T>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156941051 | ||||||
| chr5:156941093
|
T | C | 3 | a0001c0001t0001g0100a0001c0001t0001g0105a0001c0001t0001g0106 | 3 | HG00558.hp1 HG02135.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.844+7323A>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156941093 | ||||||
| chr5:156941185
|
C | T | 2 | a0007c0011t0001g0022a0008c0012t0001g0069 | 2 | HG02717.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.844+7231G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156941185 | ||||||
| chr5:156941186
|
G | A | 17 | a0001c0001t0001g0020a0001c0001t0001g0030a0001c0001t0001g0051others(14): Show | 18 | HG01243.hp2 HG02055.hp2 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.844+7230C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156941186 | ||||||
| chr5:156942052
|
G | A | 14 | a0001c0001t0002g0004a0001c0001t0002g0029a0001c0001t0002g0031others(11): Show | 17 | HG01884.hp2 HG02615.hp1 HG02818.hp1 others(14): Show |
intron_variant | MODIFIER | c.844+6364C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156942052 | ||||||
| chr5:156942138
|
G | A | 2 | a0002c0003t0001g0048a0006c0013t0001g0155 | 2 | HG01884.hp1 HG01891.hp2 |
intron_variant | MODIFIER | c.844+6278C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156942138 | ||||||
| chr5:156942160
|
C | T | 237 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0010others(234): Show | 250 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(247): Show |
intron_variant | MODIFIER | c.844+6256G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156942160 | ||||||
| chr5:156942175
|
C | T | 12 | a0001c0001t0001g0240a0001c0001t0001g0265a0001c0002t0001g0005others(9): Show | 14 | HG00408.hp2 HG00423.hp1 HG00673.hp1 others(11): Show |
intron_variant | MODIFIER | c.844+6241G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156942175 | ||||||
| chr5:156942205
|
T | C | 1 | a0001c0001t0001g0277 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.844+6211A>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156942205 | ||||||
| chr5:156942287
|
C | T | 2 | a0007c0011t0001g0022a0008c0012t0001g0069 | 2 | HG02717.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.844+6129G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156942287 | ||||||
| chr5:156942359
|
T | C | 10 | a0001c0001t0001g0051a0001c0008t0001g0234a0002c0003t0001g0048others(7): Show | 10 | HG01070.hp2 HG01167.hp2 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.844+6057A>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156942359 | ||||||
| chr5:156942463
|
C | T | 10 | a0001c0001t0001g0051a0001c0008t0001g0234a0002c0003t0001g0048others(7): Show | 10 | HG01070.hp2 HG01167.hp2 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.844+5953G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156942463 | ||||||
| chr5:156942657
|
C | A | 3 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0008t0001g0180 | 3 | HG02886.hp2 HG03209.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.844+5759G>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156942657 | ||||||
| chr5:156942658
|
C | T | 2 | a0001c0001t0001g0007a0001c0008t0001g0234 | 3 | HG01256.hp1 HG01258.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.844+5758G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156942658 | ||||||
| chr5:156942748
|
T | C | 1 | a0001c0001t0001g0225 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.844+5668A>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156942748 | ||||||
| chr5:156942761
|
T | C | 2 | a0007c0011t0001g0022a0008c0012t0001g0069 | 2 | HG02717.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.844+5655A>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156942761 | ||||||
| chr5:156942985
|
T | C | 1 | a0001c0001t0001g0110 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.844+5431A>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156942985 | ||||||
| chr5:156943018
|
T | C | 1 | a0001c0001t0001g0110 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.844+5398A>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156943018 | ||||||
| chr5:156943057
|
C | T | 2 | a0001c0001t0001g0219a0001c0001t0001g0232 | 2 | HG01099.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.844+5359G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156943057 | ||||||
| chr5:156943162
|
C | A | 2 | a0001c0001t0001g0078a0001c0001t0001g0134 | 2 | NA18985.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.844+5254G>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156943162 | ||||||
| chr5:156943240
|
T | C | 4 | a0002c0003t0001g0235a0002c0003t0001g0236a0002c0003t0001g0237others(1): Show | 4 | HG01070.hp2 HG01167.hp2 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.844+5176A>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156943240 | ||||||
| chr5:156943298
|
G | T | 1 | a0001c0008t0001g0234 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.844+5118C>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156943298 | ||||||
| chr5:156943362
|
G | A | 3 | a0002c0003t0001g0048a0002c0003t0001g0121a0006c0013t0001g0155 | 3 | HG01884.hp1 HG01891.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.844+5054C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156943362 | ||||||
| chr5:156943393
|
T | C | 10 | a0001c0001t0001g0051a0001c0008t0001g0234a0002c0003t0001g0048others(7): Show | 10 | HG01070.hp2 HG01167.hp2 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.844+5023A>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156943393 | ||||||
| chr5:156943555
|
T | A | 1 | a0001c0001t0001g0150 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.844+4861A>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156943555 | ||||||
| chr5:156943558
|
G | C | 10 | a0001c0001t0001g0051a0001c0008t0001g0234a0002c0003t0001g0048others(7): Show | 10 | HG01070.hp2 HG01167.hp2 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.844+4858C>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156943558 | ||||||
| chr5:156943602
|
A | G | 1 | a0001c0001t0001g0229 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.844+4814T>C | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156943602 | ||||||
| chr5:156943653
|
T | G | 1 | a0001c0001t0001g0047 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.844+4763A>C | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156943653 | ||||||
| chr5:156943663
|
T | A | 1 | a0001c0001t0001g0184 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.844+4753A>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156943663 | ||||||
| chr5:156943818
|
A | G | 276 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(273): Show | 293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.844+4598T>C | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156943818 | ||||||
| chr5:156943878
|
C | T | 1 | a0001c0008t0001g0234 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.844+4538G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156943878 | ||||||
| chr5:156943879
|
G | A | 1 | a0001c0001t0001g0165 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.844+4537C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156943879 | ||||||
| chr5:156943895
|
C | CA | 19 | a0001c0001t0001g0013a0001c0001t0001g0051a0001c0001t0001g0086others(16): Show | 20 | HG00099.hp1 HG00323.hp1 HG00738.hp1 others(17): Show |
intron_variant | MODIFIER | c.844+4520dupT | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156943895 | ||||||
| chr5:156943895
|
CA | C | 13 | a0001c0001t0001g0056a0001c0001t0002g0015a0001c0001t0002g0257others(10): Show | 14 | HG00597.hp2 HG01884.hp1 HG02148.hp1 others(11): Show |
intron_variant | MODIFIER | c.844+4520delT | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156943895 | ||||||
| chr5:156943987
|
G | A | 10 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0043others(7): Show | 12 | HG00408.hp2 HG00423.hp1 HG00673.hp1 others(9): Show |
intron_variant | MODIFIER | c.844+4429C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156943987 | ||||||
| chr5:156944073
|
AG | A | 7 | a0001c0001t0001g0051a0001c0008t0001g0234a0002c0003t0001g0235others(4): Show | 7 | HG01070.hp2 HG01167.hp2 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.844+4342delC | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156944073 | ||||||
| chr5:156944483
|
C | T | 3 | a0001c0001t0001g0059a0001c0001t0001g0083a0001c0001t0001g0084 | 3 | HG00140.hp2 HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.844+3933G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156944483 | ||||||
| chr5:156944495
|
C | CT | 42 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0060others(39): Show | 43 | HG00140.hp2 HG00558.hp2 HG00597.hp1 others(40): Show |
intron_variant | MODIFIER | c.844+3920dupA | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156944495 | ||||||
| chr5:156944495
|
C | CTT | 8 | a0001c0001t0001g0009a0001c0001t0001g0086a0001c0001t0001g0277others(5): Show | 9 | HG01071.hp2 HG02055.hp2 HG02056.hp1 others(6): Show |
intron_variant | MODIFIER | c.844+3919_844+3920d others(4): Show |
TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156944495 | ||||||
| chr5:156944495
|
CT | C | 144 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0010others(141): Show | 154 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.844+3920delA | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156944495 | ||||||
| chr5:156944495
|
CTT | C | 6 | a0001c0001t0001g0166a0001c0001t0001g0167a0001c0001t0002g0275others(3): Show | 6 | HG01884.hp1 HG01891.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.844+3919_844+3920d others(4): Show |
TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156944495 | ||||||
| chr5:156944495
|
CTTTTTTT others(5): Show |
C | 2 | a0001c0001t0001g0064a0001c0001t0001g0228 | 2 | HG01891.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.844+3909_844+3920d others(14): Show |
TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156944495 | ||||||
| chr5:156944502
|
T | C | 3 | a0002c0003t0001g0048a0002c0003t0001g0121a0006c0013t0001g0155 | 3 | HG01884.hp1 HG01891.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.844+3914A>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156944502 | ||||||
| chr5:156944727
|
G | A | 1 | a0001c0001t0001g0119 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.844+3689C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156944727 | ||||||
| chr5:156944740
|
C | T | 1 | a0001c0001t0001g0245 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.844+3676G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156944740 | ||||||
| chr5:156944747
|
C | T | 8 | a0002c0003t0001g0048a0002c0003t0001g0121a0002c0003t0001g0235others(5): Show | 8 | HG01070.hp2 HG01167.hp2 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.844+3669G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156944747 | ||||||
| chr5:156944817
|
G | A | 1 | a0001c0001t0001g0110 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.844+3599C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156944817 | ||||||
| chr5:156944820
|
A | C | 1 | a0001c0001t0001g0051 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.844+3596T>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156944820 | ||||||
| chr5:156944874
|
C | T | 1 | a0001c0001t0001g0291 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.844+3542G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156944874 | ||||||
| chr5:156944881
|
T | C | 1 | a0001c0001t0001g0110 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.844+3535A>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156944881 | ||||||
| chr5:156945126
|
T | A | 2 | a0005c0006t0001g0239a0005c0006t0001g0276 | 2 | HG02109.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.844+3290A>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156945126 | ||||||
| chr5:156945233
|
A | G | 1 | a0001c0001t0001g0007 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.844+3183T>C | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156945233 | ||||||
| chr5:156945448
|
G | T | 1 | a0001c0001t0001g0065 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.844+2968C>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156945448 | ||||||
| chr5:156945573
|
A | G | 11 | a0001c0001t0001g0051a0001c0001t0001g0110a0001c0008t0001g0234others(8): Show | 11 | HG01070.hp2 HG01167.hp2 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.844+2843T>C | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156945573 | ||||||
| chr5:156945648
|
T | C | 1 | a0002c0010t0001g0241 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.844+2768A>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156945648 | ||||||
| chr5:156945671
|
A | G | 3 | a0001c0001t0001g0286a0005c0006t0001g0239a0005c0006t0001g0276 | 3 | HG02109.hp2 HG03471.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.844+2745T>C | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156945671 | ||||||
| chr5:156945767
|
T | G | 1 | a0001c0001t0001g0176 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.844+2649A>C | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156945767 | ||||||
| chr5:156945932
|
C | T | 1 | a0001c0002t0001g0043 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.844+2484G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156945932 | ||||||
| chr5:156946256
|
T | C | 1 | a0005c0006t0001g0239 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.844+2160A>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156946256 | ||||||
| chr5:156946373
|
G | A | 3 | a0001c0001t0001g0244a0001c0001t0001g0245a0001c0001t0001g0266 | 3 | HG02258.hp1 HG03453.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.844+2043C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156946373 | ||||||
| chr5:156946406
|
T | G | 1 | a0001c0001t0001g0071 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.844+2010A>C | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156946406 | ||||||
| chr5:156946422
|
T | G | 1 | a0002c0010t0001g0241 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.844+1994A>C | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156946422 | ||||||
| chr5:156946479
|
T | G | 1 | a0001c0001t0001g0291 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.844+1937A>C | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156946479 | ||||||
| chr5:156946513
|
G | T | 10 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0043others(7): Show | 12 | HG00408.hp2 HG00423.hp1 HG00673.hp1 others(9): Show |
intron_variant | MODIFIER | c.844+1903C>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156946513 | ||||||
| chr5:156946578
|
G | A | 17 | a0001c0001t0001g0020a0001c0001t0001g0277a0001c0001t0001g0278others(14): Show | 17 | HG01069.hp2 HG01071.hp2 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.844+1838C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156946578 | ||||||
| chr5:156946602
|
G | A | 1 | a0001c0001t0001g0144 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.844+1814C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156946602 | ||||||
| chr5:156946625
|
C | T | 4 | a0002c0003t0001g0235a0002c0003t0001g0236a0002c0003t0001g0237others(1): Show | 4 | HG01070.hp2 HG01167.hp2 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.844+1791G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156946625 | ||||||
| chr5:156946626
|
G | C | 192 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(189): Show | 200 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(197): Show |
intron_variant | MODIFIER | c.844+1790C>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156946626 | ||||||
| chr5:156946649
|
T | C | 1 | a0001c0001t0001g0110 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.844+1767A>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156946649 | ||||||
| chr5:156946653
|
A | AT | 8 | a0001c0001t0001g0152a0003c0004t0001g0023a0003c0004t0001g0024others(5): Show | 8 | HG02451.hp1 HG02559.hp2 HG03195.hp1 others(5): Show |
intron_variant | MODIFIER | c.844+1762dupA | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156946653 | ||||||
| chr5:156946775
|
G | A | 1 | a0001c0001t0001g0284 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.844+1641C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156946775 | ||||||
| chr5:156946964
|
G | A | 1 | a0001c0001t0001g0233 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.844+1452C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156946964 | ||||||
| chr5:156947003
|
A | C | 18 | a0001c0001t0001g0051a0001c0001t0001g0110a0001c0008t0001g0234others(15): Show | 18 | HG01070.hp2 HG01167.hp2 HG01169.hp2 others(15): Show |
intron_variant | MODIFIER | c.844+1413T>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156947003 | ||||||
| chr5:156947156
|
C | A | 8 | a0002c0003t0001g0048a0002c0003t0001g0121a0002c0003t0001g0235others(5): Show | 8 | HG01070.hp2 HG01167.hp2 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.844+1260G>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156947156 | ||||||
| chr5:156947197
|
C | CA | 13 | a0001c0001t0001g0108a0001c0001t0001g0132a0001c0001t0001g0158others(10): Show | 13 | HG00738.hp2 HG00741.hp1 HG01070.hp1 others(10): Show |
intron_variant | MODIFIER | c.844+1218dupT | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156947197 | ||||||
| chr5:156947213
|
T | C | 3 | a0002c0003t0001g0048a0002c0003t0001g0121a0006c0013t0001g0155 | 3 | HG01884.hp1 HG01891.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.844+1203A>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156947213 | ||||||
| chr5:156947213
|
TAGAA | T | 7 | a0003c0004t0001g0023a0003c0004t0001g0024a0003c0004t0001g0025others(4): Show | 7 | HG02451.hp1 HG02559.hp2 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.844+1199_844+1202d others(6): Show |
TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156947213 | ||||||
| chr5:156947478
|
A | G | 1 | a0001c0001t0001g0070 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.844+938T>C | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156947478 | ||||||
| chr5:156947513
|
A | G | 1 | a0001c0001t0001g0265 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.844+903T>C | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156947513 | ||||||
| chr5:156947639
|
C | T | 2 | a0001c0001t0001g0253a0001c0001t0001g0268 | 2 | HG02015.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.844+777G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156947639 | ||||||
| chr5:156947670
|
A | G | 1 | a0001c0001t0002g0034 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.844+746T>C | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156947670 | ||||||
| chr5:156947683
|
C | T | 3 | a0001c0001t0001g0051a0001c0001t0001g0110a0001c0008t0001g0234 | 3 | HG02257.hp1 HG02922.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.844+733G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156947683 | ||||||
| chr5:156948324
|
C | CAA | 11 | a0001c0001t0001g0051a0001c0001t0001g0110a0001c0008t0001g0234others(8): Show | 11 | HG01070.hp2 HG01167.hp2 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.844+90_844+91dupTT | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156948324 | ||||||
| chr5:156948324
|
CA | C | 7 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0094others(4): Show | 7 | HG01346.hp2 HG02056.hp2 HG02735.hp1 others(4): Show |
intron_variant | MODIFIER | c.844+91delT | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156948324 | ||||||
| chr5:156948361
|
T | A | 31 | a0001c0001t0001g0108a0001c0001t0001g0129a0001c0001t0001g0130others(28): Show | 31 | HG00140.hp1 HG00639.hp2 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.844+55A>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156948361 | ||||||
| chr5:156949209
|
G | T | 1 | a0001c0001t0001g0144 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.760+442C>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 4/8 | chr5 | 156949209 | ||||||
| chr5:156949265
|
C | T | 11 | a0001c0001t0001g0051a0001c0001t0001g0110a0001c0008t0001g0234others(8): Show | 11 | HG01070.hp2 HG01167.hp2 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.760+386G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 4/8 | chr5 | 156949265 | ||||||
| chr5:156949367
|
G | C | 1 | a0001c0001t0002g0034 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.760+284C>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 4/8 | chr5 | 156949367 | ||||||
| chr5:156949418
|
C | CCCT | 8 | a0001c0001t0001g0002a0001c0001t0001g0071a0001c0001t0001g0072others(5): Show | 10 | HG01516.hp1 HG02015.hp2 HG02027.hp2 others(7): Show |
intron_variant | MODIFIER | c.760+230_760+232dup others(3): Show |
TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 4/8 | chr5 | 156949418 | ||||||
| chr5:156949418
|
CCCT | C | 167 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(164): Show | 175 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(172): Show |
intron_variant | MODIFIER | c.760+230_760+232del others(3): Show |
TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 4/8 | chr5 | 156949418 | ||||||
| chr5:156949418
|
CCCTCCT | C | 34 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0049others(31): Show | 39 | HG00423.hp2 HG01261.hp1 HG01346.hp2 others(36): Show |
intron_variant | MODIFIER | c.760+227_760+232del others(6): Show |
TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 4/8 | chr5 | 156949418 | ||||||
| chr5:156949418
|
CCCTCCTC others(2): Show |
C | 13 | a0001c0001t0001g0286a0001c0001t0001g0287a0001c0001t0001g0288others(10): Show | 13 | HG01070.hp2 HG01167.hp2 HG01169.hp2 others(10): Show |
intron_variant | MODIFIER | c.760+224_760+232del others(9): Show |
TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 4/8 | chr5 | 156949418 | ||||||
| chr5:156949429
|
C | T | 1 | a0002c0010t0001g0241 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.760+222G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 4/8 | chr5 | 156949429 | ||||||
| chr5:156949638
|
A | G | 1 | a0001c0001t0002g0257 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.760+13T>C | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 4/8 | chr5 | 156949638 | ||||||
| chr5:156949811
|
T | A | 7 | a0003c0004t0001g0023a0003c0004t0001g0024a0003c0004t0001g0025others(4): Show | 7 | HG02451.hp1 HG02559.hp2 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.680-80A>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 3/8 | chr5 | 156949811 | ||||||
| chr5:156949863
|
G | T | 16 | a0001c0001t0001g0277a0001c0001t0001g0278a0001c0001t0001g0279others(13): Show | 16 | HG01069.hp2 HG01071.hp2 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.680-132C>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 3/8 | chr5 | 156949863 | ||||||
| chr5:156949883
|
T | C | 1 | a0001c0001t0001g0170 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.680-152A>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 3/8 | chr5 | 156949883 | ||||||
| chr5:156950060
|
C | T | 1 | a0001c0001t0001g0211 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.680-329G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 3/8 | chr5 | 156950060 | ||||||
| chr5:156950119
|
CT | C | 213 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(210): Show | 221 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(218): Show |
intron_variant | MODIFIER | c.680-389delA | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 3/8 | chr5 | 156950119 | ||||||
| chr5:156950215
|
G | C | 18 | a0001c0001t0001g0051a0001c0001t0001g0110a0001c0008t0001g0234others(15): Show | 18 | HG01070.hp2 HG01167.hp2 HG01169.hp2 others(15): Show |
intron_variant | MODIFIER | c.680-484C>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 3/8 | chr5 | 156950215 | ||||||
| chr5:156950275
|
T | C | 3 | a0001c0001t0001g0059a0001c0001t0001g0083a0001c0001t0001g0084 | 3 | HG00140.hp2 HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.680-544A>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 3/8 | chr5 | 156950275 | ||||||
| chr5:156950341
|
C | T | 16 | a0001c0001t0001g0277a0001c0001t0001g0278a0001c0001t0001g0279others(13): Show | 16 | HG01069.hp2 HG01071.hp2 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.680-610G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 3/8 | chr5 | 156950341 | ||||||
| chr5:156950471
|
T | C | 1 | a0001c0001t0001g0141 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.680-740A>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 3/8 | chr5 | 156950471 | ||||||
| chr5:156950762
|
G | A | 16 | a0001c0001t0001g0277a0001c0001t0001g0278a0001c0001t0001g0279others(13): Show | 16 | HG01069.hp2 HG01071.hp2 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.679+750C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 3/8 | chr5 | 156950762 | ||||||
| chr5:156950832
|
G | C | 1 | a0001c0001t0001g0113 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.679+680C>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 3/8 | chr5 | 156950832 | ||||||
| chr5:156950848
|
G | A | 1 | a0001c0001t0001g0110 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.679+664C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 3/8 | chr5 | 156950848 | ||||||
| chr5:156950855
|
C | T | 1 | a0001c0008t0001g0180 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.679+657G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 3/8 | chr5 | 156950855 | ||||||
| chr5:156951004
|
T | TCTA | 6 | a0003c0004t0001g0023a0003c0004t0001g0024a0003c0004t0001g0025others(3): Show | 6 | HG02451.hp1 HG02559.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.679+507_679+508ins others(3): Show |
TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 3/8 | chr5 | 156951004 | ||||||
| chr5:156951006
|
G | A | 6 | a0003c0004t0001g0023a0003c0004t0001g0024a0003c0004t0001g0025others(3): Show | 6 | HG02451.hp1 HG02559.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.679+506C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 3/8 | chr5 | 156951006 | ||||||
| chr5:156951007
|
T | C | 6 | a0003c0004t0001g0023a0003c0004t0001g0024a0003c0004t0001g0025others(3): Show | 6 | HG02451.hp1 HG02559.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.679+505A>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 3/8 | chr5 | 156951007 | ||||||
| chr5:156951007
|
T | TAC | 156 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(153): Show | 162 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(159): Show |
intron_variant | MODIFIER | c.679+503_679+504dup others(2): Show |
TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 3/8 | chr5 | 156951007 | ||||||
| chr5:156951007
|
T | TACAC | 11 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0001g0067others(8): Show | 11 | HG01243.hp2 HG01891.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.679+501_679+504dup others(4): Show |
TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 3/8 | chr5 | 156951007 | ||||||
| chr5:156951007
|
T | TACACACA others(1): Show |
3 | a0001c0001t0001g0110a0001c0008t0001g0234a0002c0010t0001g0241 | 3 | HG02257.hp1 HG02723.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.679+497_679+504dup others(8): Show |
TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 3/8 | chr5 | 156951007 | ||||||
| chr5:156951007
|
T | TACACACA others(3): Show |
3 | a0002c0003t0001g0235a0002c0003t0001g0236a0002c0003t0001g0238 | 3 | HG01070.hp2 HG01167.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.679+495_679+504dup others(10): Show |
TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 3/8 | chr5 | 156951007 | ||||||
| chr5:156951007
|
T | TACACACA others(5): Show |
1 | a0002c0003t0001g0237 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.679+493_679+504dup others(12): Show |
TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 3/8 | chr5 | 156951007 | ||||||
| chr5:156951031
|
C | A | 1 | a0001c0001t0001g0280 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.679+481G>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 3/8 | chr5 | 156951031 | ||||||
| chr5:156951038
|
C | T | 1 | a0001c0001t0001g0098 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.679+474G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 3/8 | chr5 | 156951038 | ||||||
| chr5:156951067
|
C | G | 1 | a0001c0001t0001g0051 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.679+445G>C | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 3/8 | chr5 | 156951067 | ||||||
| chr5:156951119
|
A | G | 18 | a0001c0001t0001g0051a0001c0001t0001g0110a0001c0008t0001g0234others(15): Show | 18 | HG01070.hp2 HG01167.hp2 HG01169.hp2 others(15): Show |
intron_variant | MODIFIER | c.679+393T>C | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 3/8 | chr5 | 156951119 | ||||||
| chr5:156951131
|
C | A | 10 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0043others(7): Show | 12 | HG00408.hp2 HG00423.hp1 HG00673.hp1 others(9): Show |
intron_variant | MODIFIER | c.679+381G>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 3/8 | chr5 | 156951131 | ||||||
| chr5:156951272
|
A | G | 1 | a0002c0010t0001g0241 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.679+240T>C | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 3/8 | chr5 | 156951272 | ||||||
| chr5:156951939
|
T | C | 1 | a0001c0001t0001g0051 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.401-149A>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 2/8 | chr5 | 156951939 | ||||||
| chr5:156952019
|
G | C | 3 | a0002c0003t0001g0048a0002c0003t0001g0121a0006c0013t0001g0155 | 3 | HG01884.hp1 HG01891.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.401-229C>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 2/8 | chr5 | 156952019 | ||||||
| chr5:156952042
|
C | T | 8 | a0002c0003t0001g0048a0002c0003t0001g0121a0002c0003t0001g0235others(5): Show | 8 | HG01070.hp2 HG01167.hp2 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.401-252G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 2/8 | chr5 | 156952042 | ||||||
| chr5:156952214
|
T | C | 3 | a0001c0001t0001g0142a0001c0001t0001g0154a0001c0001t0001g0178 | 3 | NA18957.hp1 NA18974.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.401-424A>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 2/8 | chr5 | 156952214 | ||||||
| chr5:156952289
|
C | CA | 19 | a0001c0001t0001g0205a0001c0001t0001g0277a0001c0001t0001g0278others(16): Show | 19 | HG01069.hp2 HG01071.hp2 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.401-500dupT | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 2/8 | chr5 | 156952289 | ||||||
| chr5:156952487
|
C | T | 1 | a0001c0001t0001g0097 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.401-697G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 2/8 | chr5 | 156952487 | ||||||
| chr5:156952511
|
T | G | 1 | a0001c0001t0001g0092 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.401-721A>C | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 2/8 | chr5 | 156952511 | ||||||
| chr5:156952520
|
A | T | 1 | a0001c0001t0001g0097 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.401-730T>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 2/8 | chr5 | 156952520 | ||||||
| chr5:156952529
|
G | A | 1 | a0002c0003t0001g0048 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.401-739C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 2/8 | chr5 | 156952529 | ||||||
| chr5:156952537
|
A | G | 8 | a0001c0001t0001g0277a0001c0001t0001g0278a0001c0001t0001g0279others(5): Show | 8 | HG01069.hp2 HG01071.hp2 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.401-747T>C | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 2/8 | chr5 | 156952537 | ||||||
| chr5:156952669
|
A | G | 1 | a0001c0001t0001g0196 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.401-879T>C | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 2/8 | chr5 | 156952669 | ||||||
| chr5:156952973
|
ACCT | A | 10 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0043others(7): Show | 12 | HG00408.hp2 HG00423.hp1 HG00673.hp1 others(9): Show |
intron_variant | MODIFIER | c.401-1186_401-1184d others(5): Show |
TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 2/8 | chr5 | 156952973 | ||||||
| chr5:156953030
|
C | T | 2 | a0003c0004t0001g0024a0003c0004t0001g0025 | 2 | HG02559.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.401-1240G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 2/8 | chr5 | 156953030 | ||||||
| chr5:156953056
|
T | G | 196 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(193): Show | 204 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(201): Show |
intron_variant | MODIFIER | c.401-1266A>C | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 2/8 | chr5 | 156953056 | ||||||
| chr5:156953467
|
C | T | 2 | a0001c0001t0001g0008a0001c0001t0001g0058 | 3 | HG01099.hp1 HG04204.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.400+948G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 2/8 | chr5 | 156953467 | ||||||
| chr5:156953477
|
G | A | 1 | a0001c0001t0002g0034 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.400+938C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 2/8 | chr5 | 156953477 | ||||||
| chr5:156953579
|
G | A | 1 | a0001c0001t0001g0265 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.400+836C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 2/8 | chr5 | 156953579 | ||||||
| chr5:156953653
|
C | CA | 71 | a0001c0001t0001g0007a0001c0001t0001g0021a0001c0001t0001g0033others(68): Show | 77 | HG00408.hp2 HG00597.hp2 HG00673.hp1 others(74): Show |
intron_variant | MODIFIER | c.400+761dupT | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 2/8 | chr5 | 156953653 | ||||||
| chr5:156953653
|
C | CAA | 145 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(142): Show | 151 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(148): Show |
intron_variant | MODIFIER | c.400+760_400+761dup others(2): Show |
TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 2/8 | chr5 | 156953653 | ||||||
| chr5:156953653
|
CAAAAAAA others(3): Show |
C | 7 | a0003c0004t0001g0023a0003c0004t0001g0024a0003c0004t0001g0025others(4): Show | 7 | HG02451.hp1 HG02559.hp2 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.400+752_400+761del others(10): Show |
TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 2/8 | chr5 | 156953653 | ||||||
| chr5:156953676
|
G | A | 15 | a0001c0001t0001g0030a0001c0001t0002g0004a0001c0001t0002g0029others(12): Show | 18 | HG01884.hp2 HG02615.hp1 HG02818.hp1 others(15): Show |
intron_variant | MODIFIER | c.400+739C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 2/8 | chr5 | 156953676 | ||||||
| chr5:156953678
|
G | A | 15 | a0001c0001t0001g0030a0001c0001t0002g0004a0001c0001t0002g0029others(12): Show | 18 | HG01884.hp2 HG02615.hp1 HG02818.hp1 others(15): Show |
intron_variant | MODIFIER | c.400+737C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 2/8 | chr5 | 156953678 | ||||||
| chr5:156953711
|
T | A | 6 | a0001c0001t0001g0020a0001c0001t0001g0065a0001c0001t0001g0066others(3): Show | 6 | HG01243.hp2 HG02258.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.400+704A>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 2/8 | chr5 | 156953711 | ||||||
| chr5:156953766
|
C | G | 7 | a0003c0004t0001g0023a0003c0004t0001g0024a0003c0004t0001g0025others(4): Show | 7 | HG02451.hp1 HG02559.hp2 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.400+649G>C | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 2/8 | chr5 | 156953766 | ||||||
| chr5:156953856
|
G | A | 1 | a0006c0013t0001g0155 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.400+559C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 2/8 | chr5 | 156953856 | ||||||
| chr5:156953897
|
G | A | 18 | a0001c0001t0001g0051a0001c0001t0001g0110a0001c0008t0001g0234others(15): Show | 18 | HG01070.hp2 HG01167.hp2 HG01169.hp2 others(15): Show |
intron_variant | MODIFIER | c.400+518C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 2/8 | chr5 | 156953897 | ||||||
| chr5:156954026
|
C | A | 1 | a0001c0001t0001g0110 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.400+389G>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 2/8 | chr5 | 156954026 | ||||||
| chr5:156954030
|
T | C | 18 | a0001c0001t0001g0051a0001c0001t0001g0110a0001c0008t0001g0234others(15): Show | 18 | HG01070.hp2 HG01167.hp2 HG01169.hp2 others(15): Show |
intron_variant | MODIFIER | c.400+385A>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 2/8 | chr5 | 156954030 | ||||||
| chr5:156954057
|
T | G | 7 | a0003c0004t0001g0023a0003c0004t0001g0024a0003c0004t0001g0025others(4): Show | 7 | HG02451.hp1 HG02559.hp2 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.400+358A>C | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 2/8 | chr5 | 156954057 | ||||||
| chr5:156954163
|
C | A | 1 | a0001c0001t0001g0078 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.400+252G>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 2/8 | chr5 | 156954163 | ||||||
| chr5:156954172
|
AC | A | 3 | a0001c0001t0001g0051a0001c0001t0001g0110a0001c0008t0001g0234 | 3 | HG02257.hp1 HG02922.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.400+242delG | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 2/8 | chr5 | 156954172 | ||||||
| chr5:156954174
|
G | A | 1 | a0001c0001t0001g0248 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.400+241C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 2/8 | chr5 | 156954174 | ||||||
| chr5:156954359
|
G | A | 214 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(211): Show | 222 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(219): Show |
intron_variant | MODIFIER | c.400+56C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 2/8 | chr5 | 156954359 | ||||||
| chr5:156954884
|
C | CTT | 16 | a0001c0001t0001g0051a0001c0001t0001g0110a0001c0008t0001g0234others(13): Show | 16 | HG01070.hp2 HG01167.hp2 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.59-130_59-129dupAA | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156954884 | ||||||
| chr5:156954884
|
CT | C | 10 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0043others(7): Show | 12 | HG00408.hp2 HG00423.hp1 HG00673.hp1 others(9): Show |
intron_variant | MODIFIER | c.59-129delA | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156954884 | ||||||
| chr5:156954921
|
A | G | 1 | a0005c0006t0001g0276 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.59-165T>C | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156954921 | ||||||
| chr5:156954986
|
T | C | 16 | a0001c0001t0001g0051a0001c0001t0001g0110a0001c0008t0001g0234others(13): Show | 16 | HG01070.hp2 HG01167.hp2 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.59-230A>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156954986 | ||||||
| chr5:156955024
|
C | T | 2 | a0001c0001t0001g0140a0001c0001t0001g0207 | 2 | HG00735.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.59-268G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156955024 | ||||||
| chr5:156955064
|
C | G | 1 | a0001c0001t0001g0265 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.59-308G>C | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156955064 | ||||||
| chr5:156955202
|
G | A | 2 | a0001c0001t0001g0175a0002c0003t0001g0048 | 2 | HG01891.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.59-446C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156955202 | ||||||
| chr5:156955297
|
A | G | 167 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(164): Show | 173 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(170): Show |
intron_variant | MODIFIER | c.59-541T>C | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156955297 | ||||||
| chr5:156955327
|
G | A | 16 | a0001c0001t0001g0051a0001c0001t0001g0110a0001c0008t0001g0234others(13): Show | 16 | HG01070.hp2 HG01167.hp2 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.59-571C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156955327 | ||||||
| chr5:156955431
|
C | T | 1 | a0002c0003t0001g0048 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.59-675G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156955431 | ||||||
| chr5:156955433
|
G | A | 1 | a0002c0010t0001g0241 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.59-677C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156955433 | ||||||
| chr5:156955528
|
C | T | 1 | a0001c0001t0001g0110 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.59-772G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156955528 | ||||||
| chr5:156955535
|
G | A | 16 | a0001c0001t0001g0051a0001c0001t0001g0110a0001c0008t0001g0234others(13): Show | 16 | HG01070.hp2 HG01167.hp2 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.59-779C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156955535 | ||||||
| chr5:156955564
|
G | A | 1 | a0001c0001t0001g0133 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.59-808C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156955564 | ||||||
| chr5:156955738
|
C | T | 1 | a0001c0001t0001g0265 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.59-982G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156955738 | ||||||
| chr5:156955879
|
G | A | 10 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0043others(7): Show | 12 | HG00408.hp2 HG00423.hp1 HG00673.hp1 others(9): Show |
intron_variant | MODIFIER | c.59-1123C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156955879 | ||||||
| chr5:156956001
|
G | A | 16 | a0001c0001t0001g0051a0001c0001t0001g0110a0001c0008t0001g0234others(13): Show | 16 | HG01070.hp2 HG01167.hp2 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.59-1245C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156956001 | ||||||
| chr5:156956147
|
C | T | 1 | a0001c0001t0001g0277 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.59-1391G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156956147 | ||||||
| chr5:156956206
|
T | C | 2 | a0001c0001t0001g0184a0001c0001t0001g0221 | 2 | NA19062.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.59-1450A>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156956206 | ||||||
| chr5:156956254
|
C | G | 10 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0043others(7): Show | 12 | HG00408.hp2 HG00423.hp1 HG00673.hp1 others(9): Show |
intron_variant | MODIFIER | c.59-1498G>C | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156956254 | ||||||
| chr5:156956281
|
C | T | 1 | a0001c0001t0001g0111 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.59-1525G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156956281 | ||||||
| chr5:156956411
|
A | G | 197 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(194): Show | 205 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(202): Show |
intron_variant | MODIFIER | c.59-1655T>C | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156956411 | ||||||
| chr5:156956442
|
G | A | 1 | a0001c0001t0001g0176 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.59-1686C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156956442 | ||||||
| chr5:156956526
|
G | A | 1 | a0002c0010t0001g0241 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.59-1770C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156956526 | ||||||
| chr5:156956724
|
T | C | 2 | a0005c0006t0001g0239a0005c0006t0001g0276 | 2 | HG02109.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.59-1968A>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156956724 | ||||||
| chr5:156956882
|
A | G | 1 | a0002c0003t0001g0048 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.59-2126T>C | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156956882 | ||||||
| chr5:156956918
|
C | T | 1 | a0001c0001t0001g0095 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.59-2162G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156956918 | ||||||
| chr5:156957090
|
C | T | 1 | a0001c0001t0001g0110 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.59-2334G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156957090 | ||||||
| chr5:156957091
|
G | A | 1 | a0001c0001t0001g0051 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.59-2335C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156957091 | ||||||
| chr5:156957242
|
A | G | 2 | a0001c0001t0001g0051a0001c0008t0001g0234 | 2 | HG02922.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.59-2486T>C | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156957242 | ||||||
| chr5:156957504
|
G | C | 229 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(226): Show | 240 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(237): Show |
intron_variant | MODIFIER | c.59-2748C>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156957504 | ||||||
| chr5:156957512
|
C | CAAAAA | 13 | a0001c0001t0001g0051a0002c0003t0001g0048a0002c0003t0001g0236others(10): Show | 13 | HG01167.hp2 HG01169.hp2 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.59-2761_59-2757dup others(5): Show |
TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156957512 | ||||||
| chr5:156957512
|
C | CAAAAAAA | 29 | a0001c0001t0001g0020a0001c0001t0001g0240a0001c0001t0001g0277others(26): Show | 31 | HG00408.hp2 HG00423.hp1 HG00673.hp1 others(28): Show |
intron_variant | MODIFIER | c.59-2763_59-2757dup others(7): Show |
TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156957512 | ||||||
| chr5:156957512
|
C | CAAAAAAA others(1): Show |
29 | a0001c0001t0001g0021a0001c0001t0001g0065a0001c0001t0001g0066others(26): Show | 30 | HG00597.hp2 HG01099.hp2 HG01243.hp2 others(27): Show |
intron_variant | MODIFIER | c.59-2764_59-2757dup others(8): Show |
TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156957512 | ||||||
| chr5:156957512
|
C | CAAAAAAA others(2): Show |
145 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(142): Show | 152 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(149): Show |
intron_variant | MODIFIER | c.59-2765_59-2757dup others(9): Show |
TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156957512 | ||||||
| chr5:156957512
|
C | CAAAAAAA others(3): Show |
4 | a0001c0001t0001g0095a0001c0001t0001g0171a0001c0001t0001g0196others(1): Show | 4 | HG02074.hp2 HG02738.hp2 NA18940.hp1 others(1): Show |
intron_variant | MODIFIER | c.59-2766_59-2757dup others(10): Show |
TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156957512 | ||||||
| chr5:156957613
|
C | T | 4 | a0001c0001t0001g0286a0001c0001t0001g0287a0001c0001t0001g0288others(1): Show | 4 | HG02572.hp1 HG03139.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.59-2857G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156957613 | ||||||
| chr5:156957706
|
C | G | 1 | a0001c0001t0001g0172 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.59-2950G>C | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156957706 | ||||||
| chr5:156957767
|
G | T | 1 | a0001c0001t0001g0268 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.59-3011C>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156957767 | ||||||
| chr5:156957942
|
G | T | 4 | a0001c0001t0001g0136a0001c0001t0001g0198a0001c0007t0001g0138others(1): Show | 4 | HG02080.hp2 NA18945.hp1 NA19062.hp2 others(1): Show |
intron_variant | MODIFIER | c.59-3186C>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156957942 | ||||||
| chr5:156957995
|
C | T | 1 | a0001c0001t0001g0207 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.59-3239G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156957995 | ||||||
| chr5:156958042
|
G | A | 1 | a0001c0001t0001g0124 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.59-3286C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156958042 | ||||||
| chr5:156958145
|
G | A | 2 | a0001c0001t0001g0009a0001c0001t0001g0086 | 3 | HG02056.hp1 HG02135.hp2 HG02165.hp1 |
intron_variant | MODIFIER | c.59-3389C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156958145 | ||||||
| chr5:156958145
|
G | T | 1 | a0001c0008t0001g0234 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.59-3389C>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156958145 | ||||||
| chr5:156958170
|
G | A | 15 | a0001c0001t0001g0277a0001c0001t0001g0278a0001c0001t0001g0279others(12): Show | 15 | HG01069.hp2 HG01071.hp2 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.59-3414C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156958170 | ||||||
| chr5:156958171
|
C | T | 15 | a0001c0001t0001g0030a0001c0001t0002g0004a0001c0001t0002g0029others(12): Show | 18 | HG01884.hp2 HG02615.hp1 HG02818.hp1 others(15): Show |
intron_variant | MODIFIER | c.59-3415G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156958171 | ||||||
| chr5:156958196
|
C | T | 13 | a0002c0003t0001g0048a0002c0003t0001g0235a0002c0003t0001g0236others(10): Show | 13 | HG01070.hp2 HG01167.hp2 HG01169.hp2 others(10): Show |
intron_variant | MODIFIER | c.59-3440G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156958196 | ||||||
| chr5:156958216
|
T | G | 13 | a0001c0001t0002g0015a0001c0001t0002g0257a0001c0001t0002g0258others(10): Show | 14 | HG00597.hp2 HG03704.hp2 NA18941.hp2 others(11): Show |
intron_variant | MODIFIER | c.59-3460A>C | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156958216 | ||||||
| chr5:156958305
|
G | GAAGGA | 7 | a0001c0001t0001g0060a0001c0001t0001g0268a0001c0002t0001g0005others(4): Show | 8 | HG01255.hp1 HG01891.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.59-3554_59-3550dup others(5): Show |
TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156958305 | ||||||
| chr5:156958305
|
G | GAAGGAAA others(3): Show |
7 | a0001c0001t0001g0185a0001c0001t0001g0253a0001c0001t0001g0269others(4): Show | 9 | HG00408.hp2 HG00673.hp1 HG01109.hp1 others(6): Show |
intron_variant | MODIFIER | c.59-3559_59-3550dup others(10): Show |
TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156958305 | ||||||
| chr5:156958305
|
G | GAAGGAAA others(8): Show |
1 | a0001c0001t0001g0089 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.59-3564_59-3550dup others(15): Show |
TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156958305 | ||||||
| chr5:156958305
|
GAAGGA | G | 27 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0059others(24): Show | 29 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(26): Show |
intron_variant | MODIFIER | c.59-3554_59-3550del others(5): Show |
TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156958305 | ||||||
| chr5:156958305
|
GAAGGAAA others(3): Show |
G | 28 | a0001c0001t0001g0002a0001c0001t0001g0033a0001c0001t0001g0058others(25): Show | 30 | HG00738.hp1 HG01069.hp1 HG02027.hp2 others(27): Show |
intron_variant | MODIFIER | c.59-3559_59-3550del others(10): Show |
TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156958305 | ||||||
| chr5:156958305
|
GAAGGAAA others(8): Show |
G | 28 | a0001c0001t0001g0012a0001c0001t0001g0049a0001c0001t0001g0050others(25): Show | 29 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.59-3564_59-3550del others(15): Show |
TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156958305 | ||||||
| chr5:156958305
|
GAAGGAAA others(13): Show |
G | 40 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0056others(37): Show | 43 | HG00735.hp2 HG00738.hp2 HG01074.hp2 others(40): Show |
intron_variant | MODIFIER | c.59-3569_59-3550del others(20): Show |
TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156958305 | ||||||
| chr5:156958305
|
GAAGGAAA others(18): Show |
G | 39 | a0001c0001t0001g0013a0001c0001t0001g0016a0001c0001t0001g0094others(36): Show | 42 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(39): Show |
intron_variant | MODIFIER | c.59-3574_59-3550del others(25): Show |
TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156958305 | ||||||
| chr5:156958305
|
GAAGGAAA others(23): Show |
G | 59 | a0001c0001t0001g0011a0001c0001t0001g0018a0001c0001t0001g0019others(56): Show | 60 | HG00423.hp2 HG00558.hp1 HG00673.hp2 others(57): Show |
intron_variant | MODIFIER | c.59-3579_59-3550del others(30): Show |
TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156958305 | ||||||
| chr5:156958305
|
GAAGGAAA others(28): Show |
G | 10 | a0001c0001t0001g0017a0001c0001t0001g0021a0001c0001t0001g0030others(7): Show | 11 | HG01074.hp1 HG01257.hp1 HG02080.hp2 others(8): Show |
intron_variant | MODIFIER | c.59-3584_59-3550del others(35): Show |
TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156958305 | ||||||
| chr5:156958305
|
GAAGGAAA others(33): Show |
G | 13 | a0001c0001t0001g0020a0001c0001t0001g0065a0001c0001t0001g0066others(10): Show | 13 | HG00597.hp2 HG01243.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.59-3589_59-3550del others(40): Show |
TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156958305 | ||||||
| chr5:156958305
|
GAAGGAAA others(38): Show |
G | 17 | a0001c0001t0002g0015a0001c0001t0002g0257a0001c0001t0002g0258others(14): Show | 18 | HG02451.hp1 HG02559.hp2 HG03225.hp1 others(15): Show |
intron_variant | MODIFIER | c.59-3594_59-3550del others(45): Show |
TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156958305 | ||||||
| chr5:156958305
|
GAAGGAAA others(43): Show |
G | 3 | a0001c0001t0001g0134a0001c0001t0002g0259a0007c0011t0001g0022 | 3 | HG03195.hp1 NA18941.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.59-3599_59-3550del others(50): Show |
TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156958305 | ||||||
| chr5:156958313
|
GGAAAGGA others(15): Show |
G | 1 | a0001c0001t0001g0193 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.59-3579_59-3558del others(22): Show |
TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156958313 | ||||||
| chr5:156958374
|
G | T | 1 | a0001c0002t0001g0043 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.59-3618C>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156958374 | ||||||
| chr5:156958697
|
C | T | 7 | a0003c0004t0001g0023a0003c0004t0001g0024a0003c0004t0001g0025others(4): Show | 7 | HG02451.hp1 HG02559.hp2 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.59-3941G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156958697 | ||||||
| chr5:156958796
|
A | G | 2 | a0001c0001t0001g0051a0001c0008t0001g0234 | 2 | HG02922.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.59-4040T>C | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156958796 | ||||||
| chr5:156958821
|
G | A | 4 | a0001c0001t0001g0215a0001c0001t0001g0216a0001c0001t0001g0217others(1): Show | 4 | NA18957.hp2 NA19058.hp1 NA19068.hp2 others(1): Show |
intron_variant | MODIFIER | c.59-4065C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156958821 | ||||||
| chr5:156958894
|
T | C | 7 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0001g0092others(4): Show | 7 | HG00099.hp2 HG00639.hp1 HG01192.hp1 others(4): Show |
intron_variant | MODIFIER | c.59-4138A>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156958894 | ||||||
| chr5:156958934
|
A | G | 1 | a0001c0001t0001g0265 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.59-4178T>C | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156958934 | ||||||
| chr5:156958945
|
A | G | 1 | a0001c0001t0001g0135 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.59-4189T>C | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156958945 | ||||||
| chr5:156958973
|
TA | T | 15 | a0001c0001t0001g0051a0001c0008t0001g0234a0002c0003t0001g0048others(12): Show | 15 | HG01070.hp2 HG01167.hp2 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.58+4167delT | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156958973 | ||||||
| chr5:156959159
|
G | T | 1 | a0001c0001t0001g0134 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.58+3982C>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156959159 | ||||||
| chr5:156959440
|
A | C | 2 | a0001c0001t0001g0051a0001c0008t0001g0234 | 2 | HG02922.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.58+3701T>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156959440 | ||||||
| chr5:156959563
|
C | G | 15 | a0001c0001t0001g0051a0001c0008t0001g0234a0002c0003t0001g0048others(12): Show | 15 | HG01070.hp2 HG01167.hp2 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.58+3578G>C | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156959563 | ||||||
| chr5:156959630
|
A | C | 1 | a0001c0001t0003g0285 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.58+3511T>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156959630 | ||||||
| chr5:156959653
|
C | T | 3 | a0001c0001t0001g0192a0001c0001t0001g0195a0001c0001t0001g0226 | 3 | NA18961.hp2 NA18987.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.58+3488G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156959653 | ||||||
| chr5:156959729
|
A | T | 15 | a0001c0001t0001g0051a0001c0008t0001g0234a0002c0003t0001g0048others(12): Show | 15 | HG01070.hp2 HG01167.hp2 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.58+3412T>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156959729 | ||||||
| chr5:156959877
|
C | G | 16 | a0001c0001t0001g0030a0001c0001t0001g0033a0001c0001t0002g0004others(13): Show | 19 | HG01884.hp2 HG02451.hp2 HG02615.hp1 others(16): Show |
intron_variant | MODIFIER | c.58+3264G>C | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156959877 | ||||||
| chr5:156959906
|
G | T | 2 | a0001c0001t0001g0291a0001c0001t0001g0292 | 2 | HG02622.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.58+3235C>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156959906 | ||||||
| chr5:156959911
|
C | T | 2 | a0001c0001t0001g0132a0001c0001t0001g0133 | 2 | HG02523.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.58+3230G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156959911 | ||||||
| chr5:156959916
|
G | A | 2 | a0001c0001t0001g0219a0001c0001t0001g0232 | 2 | HG01099.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.58+3225C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156959916 | ||||||
| chr5:156959936
|
G | A | 1 | a0001c0001t0001g0265 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.58+3205C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156959936 | ||||||
| chr5:156960096
|
GA | G | 280 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(277): Show | 295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.58+3044delT | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156960096 | ||||||
| chr5:156960096
|
GAA | G | 10 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0043others(7): Show | 12 | HG00408.hp2 HG00423.hp1 HG00673.hp1 others(9): Show |
intron_variant | MODIFIER | c.58+3043_58+3044del others(2): Show |
TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156960096 | ||||||
| chr5:156960126
|
G | C | 167 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(164): Show | 173 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(170): Show |
intron_variant | MODIFIER | c.58+3015C>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156960126 | ||||||
| chr5:156960405
|
C | CT | 20 | a0001c0001t0001g0013a0001c0001t0001g0030a0001c0001t0001g0033others(17): Show | 22 | HG00099.hp1 HG00323.hp1 HG00639.hp2 others(19): Show |
intron_variant | MODIFIER | c.58+2735dupA | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156960405 | ||||||
| chr5:156960405
|
CT | C | 45 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0051others(42): Show | 47 | HG00408.hp2 HG00423.hp1 HG00673.hp1 others(44): Show |
intron_variant | MODIFIER | c.58+2735delA | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156960405 | ||||||
| chr5:156960406
|
T | C | 2 | a0001c0001t0001g0184a0001c0001t0001g0221 | 2 | NA19062.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.58+2735A>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156960406 | ||||||
| chr5:156960409
|
T | G | 1 | a0001c0001t0001g0186 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.58+2732A>C | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156960409 | ||||||
| chr5:156960411
|
T | A | 1 | a0001c0001t0001g0186 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.58+2730A>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156960411 | ||||||
| chr5:156960412
|
T | A | 1 | a0001c0001t0001g0186 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.58+2729A>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156960412 | ||||||
| chr5:156960425
|
C | G | 229 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(226): Show | 240 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(237): Show |
intron_variant | MODIFIER | c.58+2716G>C | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156960425 | ||||||
| chr5:156960429
|
A | C | 1 | a0001c0001t0001g0186 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.58+2712T>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156960429 | ||||||
| chr5:156960443
|
G | C | 1 | a0001c0001t0001g0186 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.58+2698C>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156960443 | ||||||
| chr5:156960444
|
T | C | 1 | a0001c0001t0001g0186 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.58+2697A>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156960444 | ||||||
| chr5:156960463
|
G | A | 1 | a0001c0001t0001g0186 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.58+2678C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156960463 | ||||||
| chr5:156960617
|
G | A | 2 | a0001c0001t0001g0105a0001c0001t0001g0106 | 2 | HG00558.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.58+2524C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156960617 | ||||||
| chr5:156960640
|
C | T | 18 | a0001c0001t0001g0011a0001c0001t0001g0096a0001c0001t0001g0097others(15): Show | 19 | HG00408.hp1 HG00558.hp1 HG00673.hp2 others(16): Show |
intron_variant | MODIFIER | c.58+2501G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156960640 | ||||||
| chr5:156960677
|
G | A | 1 | a0001c0001t0001g0222 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.58+2464C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156960677 | ||||||
| chr5:156960777
|
A | G | 1 | a0002c0003t0001g0121 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.58+2364T>C | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156960777 | ||||||
| chr5:156960795
|
C | T | 6 | a0001c0001t0001g0016a0001c0001t0001g0094a0001c0001t0001g0095others(3): Show | 6 | HG01346.hp2 HG02056.hp2 HG02735.hp1 others(3): Show |
intron_variant | MODIFIER | c.58+2346G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156960795 | ||||||
| chr5:156960817
|
T | C | 1 | a0001c0001t0001g0223 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.58+2324A>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156960817 | ||||||
| chr5:156960834
|
G | C | 1 | a0001c0001t0001g0051 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.58+2307C>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156960834 | ||||||
| chr5:156960869
|
A | G | 1 | a0001c0001t0001g0051 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.58+2272T>C | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156960869 | ||||||
| chr5:156960892
|
C | G | 13 | a0001c0001t0001g0240a0001c0001t0001g0265a0001c0001t0003g0285others(10): Show | 15 | HG00408.hp2 HG00423.hp1 HG00673.hp1 others(12): Show |
intron_variant | MODIFIER | c.58+2249G>C | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156960892 | ||||||
| chr5:156960988
|
G | A | 13 | a0001c0001t0002g0015a0001c0001t0002g0257a0001c0001t0002g0258others(10): Show | 14 | HG00597.hp2 HG03704.hp2 NA18941.hp2 others(11): Show |
intron_variant | MODIFIER | c.58+2153C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156960988 | ||||||
| chr5:156961248
|
G | A | 14 | a0001c0001t0001g0240a0001c0001t0002g0263a0001c0001t0002g0264others(11): Show | 16 | HG00408.hp2 HG00423.hp1 HG00673.hp1 others(13): Show |
intron_variant | MODIFIER | c.58+1893C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156961248 | ||||||
| chr5:156961327
|
C | T | 1 | a0001c0001t0001g0188 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.58+1814G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156961327 | ||||||
| chr5:156961354
|
A | G | 2 | a0005c0006t0001g0239a0005c0006t0001g0276 | 2 | HG02109.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.58+1787T>C | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156961354 | ||||||
| chr5:156961360
|
T | G | 1 | a0005c0006t0001g0239 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.58+1781A>C | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156961360 | ||||||
| chr5:156961451
|
C | T | 5 | a0001c0001t0001g0057a0001c0001t0001g0061a0001c0001t0001g0062others(2): Show | 5 | HG00597.hp1 HG02071.hp1 NA18951.hp2 others(2): Show |
intron_variant | MODIFIER | c.58+1690G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156961451 | ||||||
| chr5:156961512
|
G | A | 2 | a0001c0001t0001g0240a0001c0001t0003g0285 | 2 | HG02486.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.58+1629C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156961512 | ||||||
| chr5:156961657
|
G | GCCAGGCA others(21): Show |
16 | a0001c0001t0001g0030a0001c0001t0001g0033a0001c0001t0002g0004others(13): Show | 19 | HG01884.hp2 HG02451.hp2 HG02615.hp1 others(16): Show |
intron_variant | MODIFIER | c.58+1456_58+1483dup others(28): Show |
TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156961657 | ||||||
| chr5:156961702
|
C | T | 1 | a0001c0001t0001g0188 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.58+1439G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156961702 | ||||||
| chr5:156961720
|
G | A | 7 | a0001c0001t0001g0187a0003c0004t0001g0023a0003c0004t0001g0024others(4): Show | 7 | HG02451.hp1 HG02559.hp2 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.58+1421C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156961720 | ||||||
| chr5:156961751
|
C | T | 1 | a0002c0010t0001g0241 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.58+1390G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156961751 | ||||||
| chr5:156961765
|
T | C | 40 | a0001c0001t0001g0030a0001c0001t0001g0033a0001c0001t0001g0051others(37): Show | 45 | HG00408.hp2 HG00423.hp1 HG00673.hp1 others(42): Show |
intron_variant | MODIFIER | c.58+1376A>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156961765 | ||||||
| chr5:156961803
|
C | T | 11 | a0001c0001t0001g0051a0001c0002t0001g0005a0001c0002t0001g0006others(8): Show | 13 | HG00408.hp2 HG00423.hp1 HG00673.hp1 others(10): Show |
intron_variant | MODIFIER | c.58+1338G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156961803 | ||||||
| chr5:156961808
|
C | CA | 39 | a0001c0001t0001g0011a0001c0001t0001g0093a0001c0001t0001g0094others(36): Show | 40 | HG00099.hp2 HG00558.hp1 HG00673.hp2 others(37): Show |
intron_variant | MODIFIER | c.58+1332dupT | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156961808 | ||||||
| chr5:156961808
|
C | CAA | 72 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0047others(69): Show | 75 | HG00140.hp1 HG00408.hp1 HG00639.hp2 others(72): Show |
intron_variant | MODIFIER | c.58+1331_58+1332dup others(2): Show |
TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156961808 | ||||||
| chr5:156961808
|
C | CAAA | 42 | a0001c0001t0001g0013a0001c0001t0001g0016a0001c0001t0001g0188others(39): Show | 43 | HG00099.hp1 HG00323.hp1 HG00423.hp2 others(40): Show |
intron_variant | MODIFIER | c.58+1330_58+1332dup others(3): Show |
TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156961808 | ||||||
| chr5:156961808
|
C | CAAAA | 15 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0224others(12): Show | 15 | HG01069.hp2 HG01071.hp2 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.58+1329_58+1332dup others(4): Show |
TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156961808 | ||||||
| chr5:156961808
|
C | CAAAAA | 10 | a0001c0001t0001g0019a0001c0001t0001g0233a0001c0001t0001g0284others(7): Show | 10 | HG01346.hp1 HG02257.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.58+1328_58+1332dup others(5): Show |
TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156961808 | ||||||
| chr5:156961808
|
CA | C | 7 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0057others(4): Show | 9 | HG01099.hp1 HG01256.hp1 HG01258.hp2 others(6): Show |
intron_variant | MODIFIER | c.58+1332delT | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156961808 | ||||||
| chr5:156961808
|
CAAA | C | 34 | a0001c0001t0001g0030a0001c0001t0001g0033a0001c0001t0001g0051others(31): Show | 39 | HG00408.hp2 HG00423.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.58+1330_58+1332del others(3): Show |
TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156961808 | ||||||
| chr5:156961808
|
CAAAAAAA others(7): Show |
C | 1 | a0001c0001t0001g0056 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.58+1319_58+1332del others(14): Show |
TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156961808 | ||||||
| chr5:156961808
|
CAAAAAAA others(8): Show |
C | 2 | a0001c0001t0001g0049a0001c0001t0001g0050 | 2 | HG02027.hp1 NA18950.hp2 |
intron_variant | MODIFIER | c.58+1318_58+1332del others(15): Show |
TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156961808 | ||||||
| chr5:156961808
|
CAAAAAAA others(11): Show |
C | 5 | a0002c0003t0001g0048a0002c0003t0001g0235a0002c0003t0001g0236others(2): Show | 5 | HG01070.hp2 HG01167.hp2 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.58+1315_58+1332del others(18): Show |
TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156961808 | ||||||
| chr5:156961819
|
A | G | 1 | a0001c0008t0001g0234 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.58+1322T>C | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156961819 | ||||||
| chr5:156961822
|
A | G | 34 | a0001c0001t0001g0030a0001c0001t0001g0033a0001c0001t0001g0051others(31): Show | 39 | HG00408.hp2 HG00423.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.58+1319T>C | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156961822 | ||||||
| chr5:156961833
|
A | G | 1 | a0001c0008t0001g0234 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.58+1308T>C | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156961833 | ||||||
| chr5:156961837
|
G | A | 2 | a0001c0001t0001g0293a0001c0001t0001g0294 | 2 | HG03195.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.58+1304C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156961837 | ||||||
| chr5:156961841
|
G | A | 1 | a0001c0001t0001g0294 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.58+1300C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156961841 | ||||||
| chr5:156961841
|
GA | G | 12 | a0001c0001t0001g0047a0001c0001t0001g0286a0001c0001t0001g0287others(9): Show | 12 | HG01358.hp2 HG02257.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.58+1299delT | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156961841 | ||||||
| chr5:156961848
|
A | G | 16 | a0001c0001t0001g0030a0001c0001t0001g0033a0001c0001t0002g0004others(13): Show | 19 | HG01884.hp2 HG02451.hp2 HG02615.hp1 others(16): Show |
intron_variant | MODIFIER | c.58+1293T>C | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156961848 | ||||||
| chr5:156961849
|
A | G | 1 | a0005c0006t0001g0239 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.58+1292T>C | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156961849 | ||||||
| chr5:156962081
|
G | A | 1 | a0001c0001t0003g0285 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.58+1060C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156962081 | ||||||
| chr5:156962143
|
G | A | 1 | a0001c0008t0001g0234 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.58+998C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156962143 | ||||||
| chr5:156962224
|
T | C | 4 | a0002c0003t0001g0235a0002c0003t0001g0236a0002c0003t0001g0237others(1): Show | 4 | HG01070.hp2 HG01167.hp2 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.58+917A>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156962224 | ||||||
| chr5:156962332
|
TC | T | 7 | a0003c0004t0001g0023a0003c0004t0001g0024a0003c0004t0001g0025others(4): Show | 7 | HG02451.hp1 HG02559.hp2 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.58+808delG | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156962332 | ||||||
| chr5:156962408
|
TA | T | 234 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(231): Show | 250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.58+732delT | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156962408 | ||||||
| chr5:156962480
|
G | A | 9 | a0001c0001t0001g0286a0001c0001t0001g0287a0001c0001t0001g0288others(6): Show | 9 | HG02257.hp2 HG02572.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.58+661C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156962480 | ||||||
| chr5:156962552
|
C | T | 2 | a0001c0001t0001g0020a0001c0001t0001g0021 | 2 | HG03041.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.58+589G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156962552 | ||||||
| chr5:156962571
|
C | T | 3 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019 | 3 | HG01081.hp1 HG01257.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.58+570G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156962571 | ||||||
| chr5:156962612
|
A | G | 1 | a0001c0001t0001g0016 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.58+529T>C | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156962612 |