Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 255411 |
|---|---|
| ensemblid | ENSG00000257987.6 |
| hgncid | 48628 |
| symbol | TEX49 |
| name | sperm microtubule inner protein 11 |
| refseq_nuc | NM_001351123.2 |
| refseq_prot | NP_001338052.1 |
| ensembl_nuc | ENST00000548380.6 |
| ensembl_prot | ENSP00000489652.1 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 48727435 |
| end | 48765790 |
| strand | + |
| ver | v1.2 |
| region | chr12:48727435-48765790 |
| region5000 | chr12:48722435-48770790 |
| regionname0 | TEX49_chr12_48727435_48765790 |
| regionname5000 | TEX49_chr12_48722435_48770790 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 131 | 319 | 82 | 64 | 118 | 14 | 39 | 90 | TEX49_chr12_48722435_48770790 | TEX49 | copy fasta | chr12 | 48722435 | 48770790 |
| a0002 | 0/0 | 131 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | copy fasta | chr12 | 48722435 | 48770790 |
| a0003 | 0/0 | 131 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | copy fasta | chr12 | 48722435 | 48770790 |
| chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 396 | 317 | 81 | 64 | 118 | 14 | 38 | TEX49_chr12_48722435_48770790 | TEX49 | copy fasta | chr12 | 48722435 | 48770790 |
| c0002 | 0/0 | 396 | 2 | 0 | 2 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | copy fasta | chr12 | 48722435 | 48770790 |
| c0003 | 0/0 | 396 | 1 | 0 | 0 | 0 | 0 | 1 | TEX49_chr12_48722435_48770790 | TEX49 | copy fasta | chr12 | 48722435 | 48770790 |
| c0004 | 0/0 | 396 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | copy fasta | chr12 | 48722435 | 48770790 |
| c0005 | 0/0 | 396 | 1 | 0 | 0 | 0 | 0 | 1 | TEX49_chr12_48722435_48770790 | TEX49 | copy fasta | chr12 | 48722435 | 48770790 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 182 | 308 | 82 | 66 | 106 | 14 | 38 | TEX49_chr12_48722435_48770790 | TEX49 | copy fasta | chr12 | 48722435 | 48770790 |
| t0002 | 0/0 | 182 | 11 | 0 | 0 | 10 | 0 | 1 | TEX49_chr12_48722435_48770790 | TEX49 | copy fasta | chr12 | 48722435 | 48770790 |
| t0003 | 0/0 | 182 | 2 | 0 | 0 | 2 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | copy fasta | chr12 | 48722435 | 48770790 |
| t0004 | 0/0 | 182 | 1 | 0 | 0 | 0 | 0 | 1 | TEX49_chr12_48722435_48770790 | TEX49 | copy fasta | chr12 | 48722435 | 48770790 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0002 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0006 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0007 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0031 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0059 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0201 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0205 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0285 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 396 | 317 | 81 | 64 | 118 | 14 | 38 | TEX49_chr12_48722435_48770790 | TEX49 | copy fasta | chr12 | 48722435 | 48770790 |
| a0001c0003 | 0/0 | 396 | 1 | 0 | 0 | 0 | 0 | 1 | TEX49_chr12_48722435_48770790 | TEX49 | copy fasta | chr12 | 48722435 | 48770790 |
| a0001c0004 | 0/0 | 396 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | copy fasta | chr12 | 48722435 | 48770790 |
| a0002c0002 | 0/0 | 396 | 2 | 0 | 2 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | copy fasta | chr12 | 48722435 | 48770790 |
| a0003c0005 | 0/0 | 396 | 1 | 0 | 0 | 0 | 0 | 1 | TEX49_chr12_48722435_48770790 | TEX49 | copy fasta | chr12 | 48722435 | 48770790 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 577 | 303 | 81 | 64 | 106 | 14 | 36 | TEX49_chr12_48722435_48770790 | TEX49 | copy fasta | chr12 | 48722435 | 48770790 |
| a0001c0001t0002 | 0/0 | 577 | 11 | 0 | 0 | 10 | 0 | 1 | TEX49_chr12_48722435_48770790 | TEX49 | copy fasta | chr12 | 48722435 | 48770790 |
| a0001c0001t0003 | 0/0 | 577 | 2 | 0 | 0 | 2 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | copy fasta | chr12 | 48722435 | 48770790 |
| a0001c0001t0004 | 0/0 | 577 | 1 | 0 | 0 | 0 | 0 | 1 | TEX49_chr12_48722435_48770790 | TEX49 | copy fasta | chr12 | 48722435 | 48770790 |
| a0001c0003t0001 | 0/0 | 577 | 1 | 0 | 0 | 0 | 0 | 1 | TEX49_chr12_48722435_48770790 | TEX49 | copy fasta | chr12 | 48722435 | 48770790 |
| a0001c0004t0001 | 0/0 | 577 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | copy fasta | chr12 | 48722435 | 48770790 |
| a0002c0002t0001 | 0/0 | 577 | 2 | 0 | 2 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | copy fasta | chr12 | 48722435 | 48770790 |
| a0003c0005t0001 | 0/0 | 577 | 1 | 0 | 0 | 0 | 0 | 1 | TEX49_chr12_48722435_48770790 | TEX49 | copy fasta | chr12 | 48722435 | 48770790 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0002 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0006 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0007 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0031 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0059 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0002g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0002g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0002g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0003g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0003g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0004g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0003t0001g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0004t0001g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0002c0002t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0002c0002t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0003c0005t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0124 | EUR | GBR | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0210 | EUR | GBR | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0046 | EUR | FIN | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0123 | EUR | FIN | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0201 | EUR | FIN | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0177 | EUR | FIN | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0189 | EAS | CHS | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | CHS | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | CHS | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | CHS | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | CHS | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | CHS | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | CHS | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | CHS | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0057 | AMR | PUR | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0284 | AMR | PUR | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0204 | AMR | PUR | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0224 | AMR | PUR | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | CHS | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | CHS | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0085 | AMR | PUR | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0193 | AMR | PUR | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | PUR | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0192 | AMR | PUR | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0079 | AMR | PUR | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0058 | AMR | PUR | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0187 | AMR | PUR | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0212 | AMR | PUR | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0091 | AMR | PUR | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0061 | AMR | PUR | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | PUR | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0060 | AMR | PUR | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0104 | AMR | PUR | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0291 | AMR | PUR | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0244 | AMR | PUR | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0052 | AMR | PUR | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0175 | AMR | PUR | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0047 | AMR | PUR | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0200 | AMR | PUR | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0184 | AMR | PUR | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0315 | AMR | PUR | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0126 | AMR | PUR | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0127 | AMR | PUR | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0139 | AMR | PUR | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0217 | AMR | PUR | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0068 | AMR | PUR | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0062 | AMR | PUR | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0173 | AMR | PUR | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0051 | AMR | PUR | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0170 | AMR | CLM | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0063 | AMR | CLM | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0213 | AMR | CLM | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0077 | AMR | CLM | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG01257 | hp1 | a0002 | c0002 | t0001 | g0171 | AMR | CLM | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0138 | AMR | CLM | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0206 | AMR | CLM | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG01258 | hp2 | a0002 | c0002 | t0001 | g0172 | AMR | CLM | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0119 | AMR | CLM | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0194 | AMR | CLM | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0050 | AMR | CLM | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0295 | AMR | CLM | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0207 | AMR | CLM | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | CLM | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0112 | AMR | CLM | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0211 | AMR | CLM | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0056 | AMR | CLM | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0181 | AMR | CLM | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0182 | AMR | CLM | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0243 | AMR | CLM | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0180 | EUR | IBS | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0065 | EUR | IBS | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0006 | EUR | IBS | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0285 | EUR | IBS | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0064 | EUR | IBS | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0007 | EUR | IBS | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0287 | AFR | ACB | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | ACB | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0078 | AFR | ACB | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0202 | AFR | ACB | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0255 | AMR | PEL | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0185 | AMR | PEL | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0270 | AMR | PEL | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PEL | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0102 | AMR | PEL | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0300 | EAS | KHV | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | KHV | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | ACB | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | KHV | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0273 | EAS | KHV | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG02071 | hp1 | a0001 | c0001 | t0003 | g0299 | EAS | KHV | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | KHV | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | KHV | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG02080 | hp2 | a0001 | c0001 | t0003 | g0298 | EAS | KHV | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | KHV | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | KHV | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | KHV | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0275 | EAS | KHV | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | CDX | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CDX | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | ACB | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0312 | AFR | ACB | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0264 | AFR | ACB | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0314 | AFR | ACB | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0122 | AMR | PEL | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0048 | AMR | PEL | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | ACB | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0261 | AFR | ACB | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0263 | AFR | GWD | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | GWD | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0168 | AFR | GWD | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0115 | AFR | GWD | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0110 | AFR | GWD | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG02630 | hp1 | a0001 | c0004 | t0001 | g0317 | AFR | GWD | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | GWD | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | GWD | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0262 | AFR | GWD | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0208 | SAS | PJL | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0044 | SAS | PJL | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0053 | SAS | PJL | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0043 | SAS | PJL | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0164 | AFR | GWD | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0125 | AFR | GWD | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0311 | AFR | GWD | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | GWD | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0159 | SAS | PJL | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0133 | SAS | PJL | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0290 | AFR | GWD | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0283 | AFR | GWD | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0158 | AFR | GWD | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0166 | AFR | GWD | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0276 | AFR | GWD | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0296 | AFR | GWD | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0190 | AFR | GWD | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | GWD | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0165 | AFR | ESN | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0088 | AFR | ESN | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0157 | AFR | ESN | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0108 | AFR | ESN | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | ESN | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | ESN | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | MSL | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | MSL | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0258 | AFR | ESN | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0259 | AFR | ESN | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | ESN | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0156 | AFR | ESN | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0257 | AFR | ESN | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | ESN | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | MSL | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0136 | AFR | MSL | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0049 | SAS | PJL | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0041 | SAS | PJL | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0147 | AFR | MSL | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | MSL | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0142 | SAS | PJL | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0054 | SAS | PJL | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | ESN | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | ESN | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0086 | AFR | GWD | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0167 | AFR | GWD | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0236 | AFR | MSL | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | MSL | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0169 | SAS | PJL | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0237 | SAS | PJL | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0246 | SAS | PJL | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0216 | SAS | PJL | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0045 | SAS | STU | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0174 | SAS | STU | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG03704 | hp1 | a0001 | c0003 | t0001 | g0288 | SAS | PJL | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0037 | SAS | PJL | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG03710 | hp1 | a0003 | c0005 | t0001 | g0203 | SAS | PJL | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0176 | SAS | PJL | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0271 | SAS | BEB | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0279 | SAS | BEB | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0095 | SAS | BEB | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0137 | SAS | BEB | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0280 | SAS | BEB | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0022 | SAS | BEB | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG04115 | hp1 | a0001 | c0001 | t0004 | g0219 | SAS | STU | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0221 | SAS | STU | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0218 | SAS | BEB | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0178 | SAS | BEB | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0272 | SAS | STU | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0188 | SAS | STU | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0132 | SAS | STU | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0266 | SAS | STU | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0067 | SAS | STU | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0247 | SAS | STU | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | YRI | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0289 | AFR | YRI | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | CHB | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | CHB | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | CHB | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHB | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0256 | AFR | YRI | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0109 | AFR | YRI | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0265 | EAS | JPT | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA18961 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0281 | EAS | JPT | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0294 | EAS | JPT | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA18984 | hp1 | a0001 | c0001 | t0002 | g0225 | EAS | JPT | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA18993 | hp2 | a0001 | c0001 | t0002 | g0254 | EAS | JPT | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0267 | EAS | JPT | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0307 | EAS | JPT | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0293 | AFR | LWK | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0055 | AFR | LWK | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0310 | EAS | JPT | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0286 | EAS | JPT | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0308 | EAS | JPT | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0305 | EAS | JPT | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | YRI | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0066 | AFR | YRI | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0135 | AFR | ASW | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | ASW | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0205 | EUR | TSI | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0069 | EUR | TSI | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0252 | SAS | GIH | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0209 | SAS | GIH | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0183 | AMR | CLM | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0269 | AMR | CLM | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0179 | AFR | ACB | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0313 | AFR | ACB | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0143 | AFR | ACB | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | ACB | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0120 | AFR | ACB | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0297 | AFR | ACB | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | MSL | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0260 | AFR | MSL | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0144 | AFR | USA | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | USA | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | USA | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0215 | AFR | USA | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0131 | AFR | LWK | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0316 | AFR | LWK | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0059 | REF | REF | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0031 | REF | REF | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:48759271
|
G | A | 1 | a0002 | 2 | HG01257.hp1 HG01258.hp2 |
missense_variant | MODERATE | c.142G>A | p.Val48Met | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 2/4 | 188/577 | 142/396 | 48/131 | chr12 | 48759271 | ||
| chr12:48764916
|
G | T | 1 | a0003 | 1 | HG03710.hp1 | missense_variant | MODERATE | c.268G>T | p.Asp90Tyr | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 3/4 | 314/577 | 268/396 | 90/131 | chr12 | 48764916 |
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:48759322
|
T | C | 1 | a0001c0003 | 1 | HG03704.hp1 | synonymous_variant | LOW | c.193T>C | p.Leu65Leu | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 2/4 | 239/577 | 193/396 | 65/131 | chr12 | 48759322 | ||
| chr12:48764987
|
G | C | 1 | a0001c0004 | 1 | HG02630.hp1 | synonymous_variant | LOW | c.339G>C | p.Ala113Ala | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 3/4 | 385/577 | 339/396 | 113/131 | chr12 | 48764987 |
| chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:48727447
|
T | C | 1 | a0001c0001t0003 | 2 | HG02071.hp1 HG02080.hp2 |
5_prime_UTR_variant | MODIFIER | c.-34T>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/4 | 34 | chr12 | 48727447 | |||||
| chr12:48765743
|
A | G | 1 | a0001c0001t0004 | 1 | HG04115.hp1 | 3_prime_UTR_variant | MODIFIER | c.*88A>G | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 4/4 | 88 | chr12 | 48765743 | |||||
| chr12:48765752
|
A | C | 1 | a0001c0001t0002 | 11 | HG00423.hp1 HG03654.hp2 NA18952.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*97A>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 4/4 | 97 | chr12 | 48765752 |
| chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:48727560
|
G | A | 2 | a0001c0001t0001g0006a0001c0001t0001g0007 | 2 | HG01516.hp1 HG01517.hp2 |
splice_donor_variant&intron_variant | HIGH | c.79+1G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48727560 | ||||||
| chr12:48727733
|
C | A | 1 | a0001c0001t0001g0008 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.79+174C>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48727733 | ||||||
| chr12:48727737
|
T | A | 1 | a0001c0001t0001g0009 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.79+178T>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48727737 | ||||||
| chr12:48727895
|
A | G | 7 | a0001c0001t0001g0311a0001c0001t0001g0312a0001c0001t0001g0313others(4): Show | 7 | HG01109.hp2 HG02109.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.79+336A>G | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48727895 | ||||||
| chr12:48728038
|
G | A | 1 | a0001c0001t0001g0010 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.79+479G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48728038 | ||||||
| chr12:48728048
|
CA | C | 188 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(185): Show | 191 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(188): Show |
intron_variant | MODIFIER | c.79+502delA | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr12 | 48728048 | |||||
| chr12:48728078
|
A | C | 1 | a0001c0004t0001g0317 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.79+519A>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48728078 | ||||||
| chr12:48728109
|
G | T | 187 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(184): Show | 190 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(187): Show |
intron_variant | MODIFIER | c.79+550G>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48728109 | ||||||
| chr12:48728170
|
C | CT | 11 | a0001c0001t0001g0300a0001c0001t0001g0301a0001c0001t0001g0302others(8): Show | 11 | HG02027.hp1 NA18970.hp1 NA18984.hp2 others(8): Show |
intron_variant | MODIFIER | c.79+612dupT | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr12 | 48728170 | |||||
| chr12:48728237
|
C | T | 2 | a0001c0001t0001g0137a0001c0001t0001g0138 | 2 | HG01257.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.79+678C>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48728237 | ||||||
| chr12:48728239
|
A | G | 2 | a0001c0001t0003g0298a0001c0001t0003g0299 | 2 | HG02071.hp1 HG02080.hp2 |
intron_variant | MODIFIER | c.79+680A>G | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48728239 | ||||||
| chr12:48728404
|
T | C | 1 | a0001c0001t0001g0140 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.79+845T>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48728404 | ||||||
| chr12:48728614
|
A | G | 7 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0132others(4): Show | 7 | HG02055.hp2 HG02735.hp2 HG03209.hp2 others(4): Show |
intron_variant | MODIFIER | c.79+1055A>G | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48728614 | ||||||
| chr12:48728633
|
G | A | 1 | a0001c0001t0001g0011 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.79+1074G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48728633 | ||||||
| chr12:48728653
|
A | T | 1 | a0001c0001t0001g0297 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.79+1094A>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48728653 | ||||||
| chr12:48728661
|
T | G | 1 | a0001c0001t0001g0297 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.79+1102T>G | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48728661 | ||||||
| chr12:48728662
|
C | T | 1 | a0001c0001t0001g0297 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.79+1103C>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48728662 | ||||||
| chr12:48728707
|
C | CA | 8 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(5): Show | 8 | HG01978.hp2 HG02055.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.79+1172dupA | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr12 | 48728707 | |||||
| chr12:48728707
|
CA | C | 157 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(154): Show | 160 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(157): Show |
intron_variant | MODIFIER | c.79+1172delA | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr12 | 48728707 | |||||
| chr12:48728707
|
CAA | C | 10 | a0001c0001t0001g0007a0001c0001t0001g0289a0001c0001t0001g0290others(7): Show | 10 | HG01081.hp1 HG01346.hp2 HG01517.hp2 others(7): Show |
intron_variant | MODIFIER | c.79+1171_79+1172del others(2): Show |
TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr12 | 48728707 | |||||
| chr12:48728707
|
CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0001g0316 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.79+1162_79+1172del others(11): Show |
TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr12 | 48728707 | |||||
| chr12:48728806
|
T | C | 1 | a0001c0001t0001g0159 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.79+1247T>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48728806 | ||||||
| chr12:48728994
|
G | A | 2 | a0001c0001t0001g0160a0001c0001t0001g0161 | 2 | HG00621.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.79+1435G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48728994 | ||||||
| chr12:48729046
|
A | G | 6 | a0001c0001t0001g0311a0001c0001t0001g0312a0001c0001t0001g0313others(3): Show | 6 | HG01109.hp2 HG02109.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.79+1487A>G | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48729046 | ||||||
| chr12:48729123
|
C | T | 1 | a0001c0003t0001g0288 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.79+1564C>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48729123 | ||||||
| chr12:48729130
|
T | A | 188 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(185): Show | 191 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(188): Show |
intron_variant | MODIFIER | c.79+1571T>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48729130 | ||||||
| chr12:48729140
|
G | A | 1 | a0001c0001t0001g0297 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.79+1581G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48729140 | ||||||
| chr12:48729175
|
G | A | 2 | a0001c0001t0001g0162a0001c0001t0001g0289 | 2 | HG02970.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.79+1616G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48729175 | ||||||
| chr12:48729244
|
A | G | 1 | a0001c0001t0001g0010 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.79+1685A>G | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48729244 | ||||||
| chr12:48729254
|
A | T | 6 | a0001c0001t0001g0311a0001c0001t0001g0312a0001c0001t0001g0313others(3): Show | 6 | HG01109.hp2 HG02109.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.79+1695A>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48729254 | ||||||
| chr12:48729257
|
C | T | 1 | a0001c0001t0001g0125 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.79+1698C>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48729257 | ||||||
| chr12:48729263
|
C | T | 3 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0158 | 3 | HG02818.hp1 HG02965.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.79+1704C>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48729263 | ||||||
| chr12:48729318
|
A | G | 7 | a0001c0001t0001g0311a0001c0001t0001g0312a0001c0001t0001g0313others(4): Show | 7 | HG01109.hp2 HG02109.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.79+1759A>G | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48729318 | ||||||
| chr12:48729526
|
T | G | 1 | a0001c0001t0001g0163 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.79+1967T>G | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48729526 | ||||||
| chr12:48729533
|
C | CA | 28 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0012others(25): Show | 28 | HG00323.hp2 HG01099.hp2 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.79+1984dupA | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr12 | 48729533 | |||||
| chr12:48729576
|
G | A | 1 | a0001c0001t0001g0186 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.79+2017G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48729576 | ||||||
| chr12:48729624
|
C | T | 2 | a0001c0001t0001g0123a0001c0001t0001g0124 | 2 | HG00099.hp1 HG00280.hp2 |
intron_variant | MODIFIER | c.79+2065C>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48729624 | ||||||
| chr12:48729707
|
T | TA | 12 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(9): Show | 12 | HG00741.hp2 HG01175.hp2 HG01358.hp2 others(9): Show |
intron_variant | MODIFIER | c.79+2168dupA | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr12 | 48729707 | |||||
| chr12:48729707
|
TA | T | 94 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(91): Show | 95 | HG00099.hp1 HG00323.hp2 HG00544.hp1 others(92): Show |
intron_variant | MODIFIER | c.79+2168delA | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr12 | 48729707 | |||||
| chr12:48729707
|
TAA | T | 11 | a0001c0001t0001g0122a0001c0001t0001g0128a0001c0001t0001g0129others(8): Show | 11 | HG01109.hp2 HG01884.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.79+2167_79+2168del others(2): Show |
TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr12 | 48729707 | |||||
| chr12:48729738
|
A | C | 1 | a0001c0004t0001g0317 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.79+2179A>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48729738 | ||||||
| chr12:48729874
|
T | A | 1 | a0001c0001t0001g0188 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.79+2315T>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48729874 | ||||||
| chr12:48730260
|
G | A | 1 | a0001c0001t0002g0189 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.79+2701G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48730260 | ||||||
| chr12:48730308
|
G | A | 1 | a0001c0001t0001g0190 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.79+2749G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48730308 | ||||||
| chr12:48730397
|
C | T | 1 | a0001c0001t0001g0069 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.79+2838C>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48730397 | ||||||
| chr12:48730429
|
C | G | 2 | a0001c0001t0001g0282a0001c0001t0002g0281 | 2 | NA18942.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.79+2870C>G | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48730429 | ||||||
| chr12:48730551
|
G | A | 1 | a0001c0001t0001g0156 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.79+2992G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48730551 | ||||||
| chr12:48730712
|
T | C | 1 | a0001c0001t0001g0191 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.79+3153T>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48730712 | ||||||
| chr12:48730724
|
G | A | 1 | a0001c0001t0001g0316 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.79+3165G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48730724 | ||||||
| chr12:48730892
|
C | T | 1 | a0001c0001t0001g0068 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.79+3333C>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48730892 | ||||||
| chr12:48731092
|
C | G | 1 | a0001c0001t0001g0287 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.79+3533C>G | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48731092 | ||||||
| chr12:48731141
|
C | A | 1 | a0001c0001t0001g0144 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.79+3582C>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48731141 | ||||||
| chr12:48731244
|
G | A | 42 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0012others(39): Show | 42 | HG00323.hp2 HG01099.hp2 HG01109.hp1 others(39): Show |
intron_variant | MODIFIER | c.79+3685G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48731244 | ||||||
| chr12:48731261
|
C | G | 51 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(48): Show | 51 | HG00323.hp2 HG01099.hp2 HG01109.hp1 others(48): Show |
intron_variant | MODIFIER | c.79+3702C>G | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48731261 | ||||||
| chr12:48731360
|
A | G | 189 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(186): Show | 192 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(189): Show |
intron_variant | MODIFIER | c.79+3801A>G | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48731360 | ||||||
| chr12:48731451
|
A | G | 2 | a0001c0001t0001g0162a0001c0001t0001g0289 | 2 | HG02970.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.79+3892A>G | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48731451 | ||||||
| chr12:48731490
|
C | CA | 10 | a0001c0001t0001g0192a0001c0001t0001g0193a0001c0001t0001g0194others(7): Show | 10 | HG00733.hp2 HG00735.hp2 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.79+3944dupA | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr12 | 48731490 | |||||
| chr12:48731631
|
A | C | 8 | a0001c0001t0001g0010a0001c0001t0001g0311a0001c0001t0001g0312others(5): Show | 8 | HG01109.hp2 HG02109.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.79+4072A>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48731631 | ||||||
| chr12:48731674
|
T | A | 1 | a0001c0001t0001g0297 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.79+4115T>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48731674 | ||||||
| chr12:48731919
|
C | T | 2 | a0001c0001t0001g0297a0001c0001t0001g0312 | 2 | HG02257.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.79+4360C>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48731919 | ||||||
| chr12:48732010
|
G | A | 11 | a0001c0001t0001g0019a0001c0001t0001g0023a0001c0001t0001g0024others(8): Show | 11 | HG01167.hp2 HG01169.hp1 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.79+4451G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48732010 | ||||||
| chr12:48732110
|
C | G | 7 | a0001c0001t0001g0311a0001c0001t0001g0312a0001c0001t0001g0313others(4): Show | 7 | HG01109.hp2 HG02109.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.79+4551C>G | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48732110 | ||||||
| chr12:48732127
|
C | T | 102 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(99): Show | 104 | HG00423.hp1 HG00544.hp2 HG00621.hp1 others(101): Show |
intron_variant | MODIFIER | c.79+4568C>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48732127 | ||||||
| chr12:48732146
|
C | CA | 6 | a0001c0001t0001g0010a0001c0001t0001g0070a0001c0001t0001g0071others(3): Show | 6 | HG00544.hp1 HG00673.hp2 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.79+4603dupA | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr12 | 48732146 | |||||
| chr12:48732146
|
CA | C | 8 | a0001c0001t0001g0144a0001c0001t0001g0145a0001c0001t0001g0146others(5): Show | 8 | HG02818.hp1 HG02965.hp1 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.79+4603delA | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr12 | 48732146 | |||||
| chr12:48732146
|
CAA | C | 7 | a0001c0001t0001g0311a0001c0001t0001g0312a0001c0001t0001g0313others(4): Show | 7 | HG01109.hp2 HG02109.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.79+4602_79+4603del others(2): Show |
TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr12 | 48732146 | |||||
| chr12:48732362
|
G | C | 1 | a0001c0001t0001g0075 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.79+4803G>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48732362 | ||||||
| chr12:48732643
|
G | A | 7 | a0001c0001t0001g0144a0001c0001t0001g0145a0001c0001t0001g0146others(4): Show | 7 | HG02818.hp1 HG02965.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.79+5084G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48732643 | ||||||
| chr12:48732685
|
G | A | 1 | a0001c0001t0001g0076 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.79+5126G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48732685 | ||||||
| chr12:48732825
|
G | A | 15 | a0001c0001t0001g0144a0001c0001t0001g0145a0001c0001t0001g0146others(12): Show | 15 | HG01109.hp2 HG02109.hp2 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.79+5266G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48732825 | ||||||
| chr12:48732979
|
G | A | 1 | a0001c0001t0001g0312 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.79+5420G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48732979 | ||||||
| chr12:48733072
|
C | CT | 212 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(209): Show | 215 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(212): Show |
intron_variant | MODIFIER | c.79+5534dupT | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr12 | 48733072 | |||||
| chr12:48733072
|
C | CTT | 76 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0018others(73): Show | 77 | HG00099.hp1 HG00544.hp1 HG00544.hp2 others(74): Show |
intron_variant | MODIFIER | c.79+5533_79+5534dup others(2): Show |
TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr12 | 48733072 | |||||
| chr12:48733072
|
C | CTTT | 26 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0012others(23): Show | 26 | HG00323.hp2 HG00621.hp2 HG01099.hp2 others(23): Show |
intron_variant | MODIFIER | c.79+5532_79+5534dup others(3): Show |
TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr12 | 48733072 | |||||
| chr12:48733123
|
G | A | 6 | a0001c0001t0001g0191a0001c0001t0001g0195a0001c0001t0001g0196others(3): Show | 6 | HG00423.hp2 HG00558.hp1 HG02135.hp1 others(3): Show |
intron_variant | MODIFIER | c.79+5564G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48733123 | ||||||
| chr12:48733230
|
C | A | 1 | a0001c0001t0001g0032 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.79+5671C>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48733230 | ||||||
| chr12:48733381
|
G | A | 1 | a0001c0001t0001g0010 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.79+5822G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48733381 | ||||||
| chr12:48733424
|
C | T | 189 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(186): Show | 192 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(189): Show |
intron_variant | MODIFIER | c.79+5865C>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48733424 | ||||||
| chr12:48733606
|
T | C | 1 | a0001c0001t0001g0316 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.79+6047T>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48733606 | ||||||
| chr12:48733764
|
C | CT | 173 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(170): Show | 177 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(174): Show |
intron_variant | MODIFIER | c.79+6228dupT | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr12 | 48733764 | |||||
| chr12:48733764
|
C | CTT | 28 | a0001c0001t0001g0068a0001c0001t0001g0074a0001c0001t0001g0113others(25): Show | 28 | HG00621.hp1 HG00621.hp2 HG01069.hp1 others(25): Show |
intron_variant | MODIFIER | c.79+6227_79+6228dup others(2): Show |
TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr12 | 48733764 | |||||
| chr12:48733764
|
CT | C | 36 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0012others(33): Show | 36 | HG00323.hp2 HG01070.hp2 HG01099.hp2 others(33): Show |
intron_variant | MODIFIER | c.79+6228delT | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr12 | 48733764 | |||||
| chr12:48733852
|
C | A | 1 | a0001c0001t0001g0010 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.79+6293C>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48733852 | ||||||
| chr12:48733914
|
G | A | 1 | a0001c0001t0001g0010 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.79+6355G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48733914 | ||||||
| chr12:48733924
|
C | G | 2 | a0001c0001t0001g0162a0001c0001t0001g0289 | 2 | HG02970.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.79+6365C>G | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48733924 | ||||||
| chr12:48734150
|
G | A | 1 | a0001c0001t0001g0156 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.79+6591G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48734150 | ||||||
| chr12:48734478
|
A | G | 29 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0012others(26): Show | 29 | HG00323.hp2 HG01099.hp2 HG01109.hp1 others(26): Show |
intron_variant | MODIFIER | c.79+6919A>G | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48734478 | ||||||
| chr12:48734739
|
C | T | 2 | a0001c0001t0001g0269a0001c0001t0001g0279 | 2 | HG01123.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.79+7180C>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48734739 | ||||||
| chr12:48734796
|
G | C | 2 | a0001c0001t0001g0010a0001c0001t0001g0080 | 2 | HG03516.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.79+7237G>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48734796 | ||||||
| chr12:48734799
|
C | A | 1 | a0001c0001t0001g0081 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.79+7240C>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48734799 | ||||||
| chr12:48734833
|
C | A | 1 | a0001c0001t0001g0130 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.79+7274C>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48734833 | ||||||
| chr12:48734998
|
T | C | 1 | a0001c0001t0001g0143 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.79+7439T>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48734998 | ||||||
| chr12:48735003
|
C | CA | 126 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0013others(123): Show | 127 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(124): Show |
intron_variant | MODIFIER | c.79+7464dupA | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr12 | 48735003 | |||||
| chr12:48735003
|
C | CAA | 40 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0012others(37): Show | 40 | HG00323.hp2 HG00558.hp1 HG00558.hp2 others(37): Show |
intron_variant | MODIFIER | c.79+7463_79+7464dup others(2): Show |
TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr12 | 48735003 | |||||
| chr12:48735003
|
C | CAAA | 131 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(128): Show | 134 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(131): Show |
intron_variant | MODIFIER | c.79+7462_79+7464dup others(3): Show |
TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr12 | 48735003 | |||||
| chr12:48735003
|
C | CAAAA | 16 | a0001c0001t0001g0008a0001c0001t0001g0148a0001c0001t0001g0154others(13): Show | 16 | HG00642.hp2 HG00673.hp1 HG01106.hp2 others(13): Show |
intron_variant | MODIFIER | c.79+7461_79+7464dup others(4): Show |
TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr12 | 48735003 | |||||
| chr12:48735024
|
G | A | 6 | a0001c0001t0001g0311a0001c0001t0001g0312a0001c0001t0001g0313others(3): Show | 6 | HG01109.hp2 HG02109.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.79+7465G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48735024 | ||||||
| chr12:48735025
|
A | C | 1 | a0001c0001t0001g0211 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.79+7466A>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48735025 | ||||||
| chr12:48735330
|
G | A | 1 | a0001c0001t0001g0287 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.79+7771G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48735330 | ||||||
| chr12:48735456
|
G | A | 2 | a0001c0001t0001g0295a0001c0001t0001g0296 | 2 | HG01346.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.79+7897G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48735456 | ||||||
| chr12:48735534
|
G | C | 4 | a0001c0001t0001g0010a0001c0001t0001g0283a0001c0001t0001g0295others(1): Show | 4 | HG01346.hp2 HG02809.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.79+7975G>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48735534 | ||||||
| chr12:48735582
|
T | C | 7 | a0001c0001t0001g0125a0001c0001t0001g0311a0001c0001t0001g0312others(4): Show | 7 | HG01109.hp2 HG02109.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.79+8023T>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48735582 | ||||||
| chr12:48735587
|
A | AAAAT | 12 | a0001c0001t0001g0010a0001c0001t0001g0125a0001c0001t0001g0283others(9): Show | 12 | HG01109.hp2 HG01346.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.79+8042_79+8045dup others(4): Show |
TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr12 | 48735587 | |||||
| chr12:48735666
|
G | A | 28 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0012others(25): Show | 28 | HG00323.hp2 HG01099.hp2 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.79+8107G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48735666 | ||||||
| chr12:48735713
|
G | A | 14 | a0001c0001t0001g0003a0001c0001t0001g0186a0001c0001t0001g0226others(11): Show | 15 | HG02056.hp1 HG02080.hp1 HG02129.hp2 others(12): Show |
intron_variant | MODIFIER | c.79+8154G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48735713 | ||||||
| chr12:48735831
|
C | T | 1 | a0001c0001t0001g0287 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.79+8272C>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48735831 | ||||||
| chr12:48735863
|
G | A | 1 | a0001c0001t0001g0084 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.79+8304G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48735863 | ||||||
| chr12:48736126
|
C | A | 1 | a0001c0001t0001g0297 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.79+8567C>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48736126 | ||||||
| chr12:48736156
|
G | A | 2 | a0001c0001t0001g0162a0001c0001t0001g0289 | 2 | HG02970.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.79+8597G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48736156 | ||||||
| chr12:48736208
|
A | T | 5 | a0001c0001t0001g0010a0001c0001t0001g0283a0001c0001t0001g0295others(2): Show | 5 | HG01346.hp2 HG02809.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.79+8649A>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48736208 | ||||||
| chr12:48736244
|
G | C | 52 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(49): Show | 52 | HG00323.hp2 HG01099.hp2 HG01109.hp1 others(49): Show |
intron_variant | MODIFIER | c.79+8685G>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48736244 | ||||||
| chr12:48736413
|
C | CA | 23 | a0001c0001t0001g0013a0001c0001t0001g0034a0001c0001t0001g0063others(20): Show | 23 | HG00621.hp2 HG00733.hp1 HG00735.hp2 others(20): Show |
intron_variant | MODIFIER | c.79+8876dupA | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr12 | 48736413 | |||||
| chr12:48736413
|
CA | C | 42 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0012others(39): Show | 42 | HG00323.hp2 HG01099.hp2 HG01109.hp1 others(39): Show |
intron_variant | MODIFIER | c.79+8876delA | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr12 | 48736413 | |||||
| chr12:48736695
|
G | A | 1 | a0001c0001t0001g0137 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.79+9136G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48736695 | ||||||
| chr12:48736699
|
G | GT | 152 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(149): Show | 155 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(152): Show |
intron_variant | MODIFIER | c.79+9153dupT | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr12 | 48736699 | |||||
| chr12:48736758
|
T | C | 4 | a0001c0001t0001g0311a0001c0001t0001g0313a0001c0001t0001g0314others(1): Show | 4 | HG01109.hp2 HG02109.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.79+9199T>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48736758 | ||||||
| chr12:48737012
|
A | C | 52 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(49): Show | 52 | HG00323.hp2 HG01099.hp2 HG01109.hp1 others(49): Show |
intron_variant | MODIFIER | c.79+9453A>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48737012 | ||||||
| chr12:48737053
|
G | A | 1 | a0001c0001t0001g0196 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.79+9494G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48737053 | ||||||
| chr12:48737100
|
C | G | 29 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0012others(26): Show | 29 | HG00323.hp2 HG01099.hp2 HG01109.hp1 others(26): Show |
intron_variant | MODIFIER | c.79+9541C>G | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48737100 | ||||||
| chr12:48737243
|
G | A | 1 | a0001c0001t0001g0035 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.79+9684G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48737243 | ||||||
| chr12:48737281
|
G | A | 3 | a0001c0001t0001g0079a0001c0001t0001g0086a0001c0001t0001g0115 | 3 | HG00738.hp1 HG02615.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.79+9722G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48737281 | ||||||
| chr12:48737415
|
A | AT | 13 | a0001c0001t0001g0010a0001c0001t0001g0061a0001c0001t0001g0062others(10): Show | 13 | HG00642.hp2 HG01070.hp1 HG01109.hp2 others(10): Show |
intron_variant | MODIFIER | c.79+9872dupT | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr12 | 48737415 | |||||
| chr12:48737415
|
AT | A | 6 | a0001c0001t0001g0018a0001c0001t0001g0162a0001c0001t0001g0268others(3): Show | 6 | HG01884.hp1 HG02970.hp1 NA18522.hp2 others(3): Show |
intron_variant | MODIFIER | c.79+9872delT | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr12 | 48737415 | |||||
| chr12:48737483
|
C | T | 1 | a0001c0001t0001g0156 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.79+9924C>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48737483 | ||||||
| chr12:48737544
|
A | T | 3 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0182 | 3 | HG01433.hp2 HG01496.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.79+9985A>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48737544 | ||||||
| chr12:48737568
|
C | A | 28 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0012others(25): Show | 28 | HG00323.hp2 HG01099.hp2 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.79+10009C>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48737568 | ||||||
| chr12:48737575
|
T | C | 190 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(187): Show | 193 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(190): Show |
intron_variant | MODIFIER | c.79+10016T>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48737575 | ||||||
| chr12:48737616
|
T | C | 1 | a0001c0001t0001g0070 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.79+10057T>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48737616 | ||||||
| chr12:48737677
|
A | C | 7 | a0001c0001t0001g0125a0001c0001t0001g0311a0001c0001t0001g0312others(4): Show | 7 | HG01109.hp2 HG02109.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.79+10118A>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48737677 | ||||||
| chr12:48737697
|
G | A | 7 | a0001c0001t0001g0144a0001c0001t0001g0145a0001c0001t0001g0146others(4): Show | 7 | HG02818.hp1 HG02965.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.79+10138G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48737697 | ||||||
| chr12:48737702
|
A | T | 2 | a0001c0001t0001g0162a0001c0001t0001g0289 | 2 | HG02970.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.79+10143A>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48737702 | ||||||
| chr12:48737831
|
C | T | 12 | a0001c0001t0001g0010a0001c0001t0001g0125a0001c0001t0001g0283others(9): Show | 12 | HG01109.hp2 HG01346.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.79+10272C>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48737831 | ||||||
| chr12:48737888
|
T | A | 4 | a0001c0001t0001g0010a0001c0001t0001g0283a0001c0001t0001g0295others(1): Show | 4 | HG01346.hp2 HG02809.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.79+10329T>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48737888 | ||||||
| chr12:48737906
|
C | T | 12 | a0001c0001t0001g0010a0001c0001t0001g0125a0001c0001t0001g0283others(9): Show | 12 | HG01109.hp2 HG01346.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.79+10347C>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48737906 | ||||||
| chr12:48737925
|
C | T | 2 | a0001c0001t0001g0158a0001c0001t0001g0303 | 2 | HG02818.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.79+10366C>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48737925 | ||||||
| chr12:48738013
|
C | T | 1 | a0001c0001t0001g0010 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.79+10454C>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48738013 | ||||||
| chr12:48738014
|
G | A | 7 | a0001c0001t0001g0125a0001c0001t0001g0311a0001c0001t0001g0312others(4): Show | 7 | HG01109.hp2 HG02109.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.79+10455G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48738014 | ||||||
| chr12:48738028
|
T | C | 1 | a0001c0004t0001g0317 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.79+10469T>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48738028 | ||||||
| chr12:48738350
|
T | C | 185 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(182): Show | 188 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(185): Show |
intron_variant | MODIFIER | c.79+10791T>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48738350 | ||||||
| chr12:48738369
|
CATATAAT others(8): Show |
C | 7 | a0001c0001t0001g0125a0001c0001t0001g0311a0001c0001t0001g0312others(4): Show | 7 | HG01109.hp2 HG02109.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.79+10813_79+10827d others(17): Show |
TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr12 | 48738369 | |||||
| chr12:48738512
|
T | C | 1 | a0001c0001t0004g0219 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.79+10953T>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48738512 | ||||||
| chr12:48738539
|
CT | C | 138 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(135): Show | 141 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(138): Show |
intron_variant | MODIFIER | c.79+10993delT | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr12 | 48738539 | |||||
| chr12:48738620
|
C | T | 1 | a0001c0001t0001g0112 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.79+11061C>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48738620 | ||||||
| chr12:48738858
|
C | T | 2 | a0001c0001t0001g0033a0001c0001t0001g0060 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.79+11299C>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48738858 | ||||||
| chr12:48738924
|
C | CT | 175 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(172): Show | 178 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(175): Show |
intron_variant | MODIFIER | c.79+11377dupT | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr12 | 48738924 | |||||
| chr12:48738974
|
C | T | 139 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(136): Show | 142 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(139): Show |
intron_variant | MODIFIER | c.79+11415C>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48738974 | ||||||
| chr12:48739015
|
C | T | 2 | a0001c0001t0001g0153a0001c0001t0001g0307 | 2 | NA18967.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.79+11456C>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48739015 | ||||||
| chr12:48739084
|
C | T | 1 | a0001c0001t0001g0301 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.79+11525C>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48739084 | ||||||
| chr12:48739339
|
G | A | 4 | a0001c0001t0001g0311a0001c0001t0001g0313a0001c0001t0001g0314others(1): Show | 4 | HG01109.hp2 HG02109.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.79+11780G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48739339 | ||||||
| chr12:48739366
|
A | T | 3 | a0001c0001t0001g0192a0001c0001t0001g0193a0001c0001t0001g0194 | 3 | HG00733.hp2 HG00735.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.79+11807A>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48739366 | ||||||
| chr12:48739499
|
A | C | 3 | a0001c0001t0001g0079a0001c0001t0001g0086a0001c0001t0001g0115 | 3 | HG00738.hp1 HG02615.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.79+11940A>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48739499 | ||||||
| chr12:48739500
|
ATTAC | A | 3 | a0001c0001t0001g0079a0001c0001t0001g0086a0001c0001t0001g0115 | 3 | HG00738.hp1 HG02615.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.79+11942_79+11945d others(6): Show |
TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48739500 | ||||||
| chr12:48739505
|
C | A | 3 | a0001c0001t0001g0079a0001c0001t0001g0086a0001c0001t0001g0115 | 3 | HG00738.hp1 HG02615.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.79+11946C>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48739505 | ||||||
| chr12:48739567
|
G | A | 1 | a0001c0001t0001g0316 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.79+12008G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48739567 | ||||||
| chr12:48739571
|
G | A | 2 | a0001c0001t0001g0238a0001c0001t0002g0286 | 2 | NA19065.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.79+12012G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48739571 | ||||||
| chr12:48739574
|
T | C | 14 | a0001c0001t0001g0010a0001c0001t0001g0032a0001c0001t0001g0036others(11): Show | 14 | HG01346.hp2 HG02559.hp2 HG02647.hp1 others(11): Show |
intron_variant | MODIFIER | c.79+12015T>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48739574 | ||||||
| chr12:48739578
|
C | A | 189 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(186): Show | 192 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(189): Show |
intron_variant | MODIFIER | c.79+12019C>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48739578 | ||||||
| chr12:48739595
|
A | C | 1 | a0001c0001t0001g0150 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.79+12036A>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48739595 | ||||||
| chr12:48739708
|
A | G | 1 | a0001c0001t0002g0265 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.79+12149A>G | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48739708 | ||||||
| chr12:48739734
|
A | G | 3 | a0001c0001t0001g0283a0001c0001t0001g0295a0001c0001t0001g0296 | 3 | HG01346.hp2 HG02809.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.79+12175A>G | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48739734 | ||||||
| chr12:48739735
|
C | T | 1 | a0001c0001t0001g0163 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.79+12176C>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48739735 | ||||||
| chr12:48739822
|
C | T | 10 | a0001c0001t0001g0186a0001c0001t0001g0226a0001c0001t0001g0227others(7): Show | 10 | HG02129.hp2 NA18944.hp2 NA18962.hp1 others(7): Show |
intron_variant | MODIFIER | c.79+12263C>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48739822 | ||||||
| chr12:48739901
|
C | G | 4 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0179others(1): Show | 4 | HG01175.hp1 HG01516.hp1 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.79+12342C>G | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48739901 | ||||||
| chr12:48739942
|
C | T | 150 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(147): Show | 153 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(150): Show |
intron_variant | MODIFIER | c.79+12383C>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48739942 | ||||||
| chr12:48740051
|
T | C | 4 | a0001c0001t0001g0010a0001c0001t0001g0283a0001c0001t0001g0295others(1): Show | 4 | HG01346.hp2 HG02809.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.79+12492T>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48740051 | ||||||
| chr12:48740451
|
A | G | 1 | a0001c0001t0001g0316 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.79+12892A>G | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48740451 | ||||||
| chr12:48740493
|
CT | C | 14 | a0001c0001t0001g0032a0001c0001t0001g0084a0001c0001t0001g0087others(11): Show | 14 | HG00323.hp1 HG01256.hp1 HG02647.hp1 others(11): Show |
intron_variant | MODIFIER | c.79+12951delT | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr12 | 48740493 | |||||
| chr12:48740495
|
T | C | 88 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(85): Show | 90 | HG00423.hp1 HG00544.hp2 HG00621.hp1 others(87): Show |
intron_variant | MODIFIER | c.79+12936T>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48740495 | ||||||
| chr12:48740496
|
T | C | 4 | a0001c0001t0001g0032a0001c0001t0001g0239a0001c0001t0001g0240others(1): Show | 4 | HG02647.hp1 NA18950.hp1 NA18954.hp1 others(1): Show |
intron_variant | MODIFIER | c.79+12937T>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48740496 | ||||||
| chr12:48740521
|
C | T | 1 | a0001c0001t0001g0111 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.79+12962C>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48740521 | ||||||
| chr12:48740549
|
T | C | 1 | a0001c0001t0001g0280 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.79+12990T>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48740549 | ||||||
| chr12:48740660
|
C | CT | 6 | a0001c0001t0001g0144a0001c0001t0001g0156a0001c0001t0001g0157others(3): Show | 6 | HG00741.hp2 HG02818.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.79+13116dupT | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr12 | 48740660 | |||||
| chr12:48740703
|
G | A | 1 | a0001c0001t0001g0089 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.79+13144G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48740703 | ||||||
| chr12:48740881
|
T | C | 292 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(289): Show | 296 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(293): Show |
intron_variant | MODIFIER | c.79+13322T>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48740881 | ||||||
| chr12:48740917
|
G | A | 2 | a0001c0001t0001g0162a0001c0001t0001g0289 | 2 | HG02970.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.79+13358G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48740917 | ||||||
| chr12:48741069
|
C | CT | 13 | a0001c0001t0001g0034a0001c0001t0001g0114a0001c0001t0001g0140others(10): Show | 13 | HG00423.hp2 HG00741.hp1 HG01261.hp2 others(10): Show |
intron_variant | MODIFIER | c.79+13531dupT | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr12 | 48741069 | |||||
| chr12:48741069
|
CT | C | 50 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0037others(47): Show | 50 | HG00323.hp1 HG00323.hp2 HG01069.hp2 others(47): Show |
intron_variant | MODIFIER | c.79+13531delT | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr12 | 48741069 | |||||
| chr12:48741183
|
C | T | 138 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(135): Show | 141 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(138): Show |
intron_variant | MODIFIER | c.79+13624C>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48741183 | ||||||
| chr12:48741468
|
C | CCGATATG others(3): Show |
8 | a0001c0001t0001g0010a0001c0001t0001g0162a0001c0001t0001g0163others(5): Show | 8 | HG01346.hp2 HG01884.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.79+13909_79+13910i others(12): Show |
TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48741468 | ||||||
| chr12:48741469
|
G | A | 27 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0012others(24): Show | 27 | HG00323.hp2 HG01099.hp2 HG01109.hp1 others(24): Show |
intron_variant | MODIFIER | c.79+13910G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48741469 | ||||||
| chr12:48741619
|
T | C | 1 | a0001c0001t0001g0062 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.79+14060T>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48741619 | ||||||
| chr12:48741647
|
C | CT | 11 | a0001c0001t0001g0008a0001c0001t0001g0017a0001c0001t0001g0088others(8): Show | 11 | HG02257.hp1 HG02559.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.79+14105dupT | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr12 | 48741647 | |||||
| chr12:48741775
|
G | A | 6 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0147others(3): Show | 6 | HG02109.hp2 HG02258.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.79+14216G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48741775 | ||||||
| chr12:48741886
|
G | A | 5 | a0001c0001t0001g0144a0001c0001t0001g0156a0001c0001t0001g0157others(2): Show | 5 | HG02818.hp1 HG02965.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.79+14327G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48741886 | ||||||
| chr12:48741987
|
T | C | 6 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0001t0001g0166others(3): Show | 6 | HG02615.hp1 HG02717.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.79+14428T>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48741987 | ||||||
| chr12:48742021
|
T | C | 2 | a0001c0001t0001g0035a0001c0001t0001g0038 | 2 | HG02572.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.79+14462T>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48742021 | ||||||
| chr12:48742081
|
T | A | 11 | a0001c0001t0001g0019a0001c0001t0001g0023a0001c0001t0001g0024others(8): Show | 11 | HG01167.hp2 HG01169.hp1 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.79+14522T>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48742081 | ||||||
| chr12:48742082
|
T | A | 18 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0019others(15): Show | 18 | HG01167.hp2 HG01169.hp1 HG01192.hp1 others(15): Show |
intron_variant | MODIFIER | c.79+14523T>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48742082 | ||||||
| chr12:48742204
|
A | C | 1 | a0001c0001t0001g0316 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.79+14645A>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48742204 | ||||||
| chr12:48742276
|
TC | T | 11 | a0001c0001t0001g0019a0001c0001t0001g0023a0001c0001t0001g0077others(8): Show | 11 | HG01167.hp2 HG01169.hp1 HG01256.hp2 others(8): Show |
intron_variant | MODIFIER | c.79+14719delC | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr12 | 48742276 | |||||
| chr12:48742277
|
C | CT | 14 | a0001c0001t0001g0119a0001c0001t0001g0145a0001c0001t0001g0146others(11): Show | 14 | HG00642.hp2 HG01256.hp1 HG01261.hp1 others(11): Show |
intron_variant | MODIFIER | c.79+14718_79+14719i others(3): Show |
TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48742277 | ||||||
| chr12:48742277
|
C | CTT | 118 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(115): Show | 121 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(118): Show |
intron_variant | MODIFIER | c.79+14718_79+14719i others(4): Show |
TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48742277 | ||||||
| chr12:48742277
|
C | CTTT | 7 | a0001c0001t0001g0140a0001c0001t0001g0155a0001c0001t0001g0211others(4): Show | 7 | HG01361.hp2 HG02080.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.79+14718_79+14719i others(5): Show |
TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48742277 | ||||||
| chr12:48742278
|
C | T | 305 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(302): Show | 309 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(306): Show |
intron_variant | MODIFIER | c.79+14719C>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48742278 | ||||||
| chr12:48742281
|
T | TC | 3 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0001t0001g0289 | 3 | HG02486.hp2 HG02970.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.79+14722_79+14723i others(3): Show |
TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48742281 | ||||||
| chr12:48742282
|
T | C | 6 | a0001c0001t0001g0024a0001c0001t0001g0026a0001c0001t0001g0027others(3): Show | 6 | HG01884.hp2 HG02451.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.79+14723T>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48742282 | ||||||
| chr12:48742285
|
T | C | 1 | a0001c0001t0001g0011 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.79+14726T>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48742285 | ||||||
| chr12:48742285
|
T | TTC | 7 | a0001c0001t0001g0187a0001c0001t0001g0212a0001c0001t0001g0215others(4): Show | 7 | HG00639.hp2 HG00741.hp2 HG01069.hp1 others(4): Show |
intron_variant | MODIFIER | c.79+14727_79+14728i others(4): Show |
TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr12 | 48742285 | |||||
| chr12:48742358
|
C | T | 3 | a0001c0001t0001g0032a0001c0001t0001g0036a0001c0001t0001g0297 | 3 | HG02559.hp2 HG02647.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.79+14799C>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48742358 | ||||||
| chr12:48742442
|
C | T | 2 | a0001c0001t0001g0192a0001c0001t0001g0193 | 2 | HG00733.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.79+14883C>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48742442 | ||||||
| chr12:48742478
|
T | C | 1 | a0001c0001t0001g0142 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.79+14919T>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48742478 | ||||||
| chr12:48742522
|
T | A | 1 | a0001c0001t0001g0093 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.79+14963T>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48742522 | ||||||
| chr12:48742568
|
G | A | 3 | a0001c0001t0001g0012a0001c0001t0001g0169a0001c0001t0001g0170 | 3 | HG01255.hp1 HG03654.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.79+15009G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48742568 | ||||||
| chr12:48742682
|
G | C | 3 | a0001c0001t0001g0311a0001c0001t0001g0313a0001c0001t0001g0314 | 3 | HG02109.hp2 HG02258.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.79+15123G>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48742682 | ||||||
| chr12:48742986
|
C | T | 1 | a0001c0004t0001g0317 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.79+15427C>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48742986 | ||||||
| chr12:48743154
|
T | C | 6 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0147others(3): Show | 6 | HG02109.hp2 HG02258.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.79+15595T>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48743154 | ||||||
| chr12:48743180
|
G | C | 3 | a0001c0001t0001g0283a0001c0001t0001g0295a0001c0001t0001g0296 | 3 | HG01346.hp2 HG02809.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.79+15621G>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48743180 | ||||||
| chr12:48743230
|
T | TA | 7 | a0001c0001t0001g0114a0001c0001t0001g0118a0001c0001t0001g0187others(4): Show | 7 | HG00741.hp2 HG01346.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.79+15688dupA | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr12 | 48743230 | |||||
| chr12:48743255
|
G | A | 58 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0009others(55): Show | 59 | HG00423.hp1 HG00544.hp2 HG00621.hp1 others(56): Show |
intron_variant | MODIFIER | c.79+15696G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48743255 | ||||||
| chr12:48743591
|
G | A | 6 | a0001c0001t0001g0009a0001c0001t0001g0243a0001c0001t0001g0253others(3): Show | 6 | HG01496.hp2 HG01978.hp1 HG02004.hp1 others(3): Show |
intron_variant | MODIFIER | c.80-15618G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48743591 | ||||||
| chr12:48743669
|
C | T | 8 | a0001c0001t0001g0144a0001c0001t0001g0156a0001c0001t0001g0157others(5): Show | 8 | HG01346.hp2 HG02809.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.80-15540C>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48743669 | ||||||
| chr12:48743792
|
C | A | 13 | a0001c0001t0001g0144a0001c0001t0001g0156a0001c0001t0001g0157others(10): Show | 13 | HG01346.hp2 HG01884.hp1 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.80-15417C>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48743792 | ||||||
| chr12:48743909
|
G | A | 1 | a0001c0001t0001g0014 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.80-15300G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48743909 | ||||||
| chr12:48743933
|
C | CA | 24 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0021others(21): Show | 24 | HG00323.hp1 HG00741.hp1 HG01106.hp1 others(21): Show |
intron_variant | MODIFIER | c.80-15246dupA | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr12 | 48743933 | |||||
| chr12:48743933
|
C | CAA | 12 | a0001c0001t0001g0010a0001c0001t0001g0040a0001c0001t0001g0046others(9): Show | 12 | HG00280.hp1 HG01167.hp1 HG01175.hp1 others(9): Show |
intron_variant | MODIFIER | c.80-15247_80-15246d others(4): Show |
TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr12 | 48743933 | |||||
| chr12:48743933
|
C | CAAAAAAA others(5): Show |
1 | a0001c0001t0001g0289 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.80-15257_80-15246d others(14): Show |
TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr12 | 48743933 | |||||
| chr12:48743933
|
C | CAAAAAAA others(6): Show |
1 | a0001c0001t0001g0312 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.80-15258_80-15246d others(15): Show |
TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr12 | 48743933 | |||||
| chr12:48743933
|
C | CAAAAAAA others(10): Show |
1 | a0001c0001t0001g0163 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.80-15262_80-15246d others(19): Show |
TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr12 | 48743933 | |||||
| chr12:48743933
|
C | CAAAAAAA others(11): Show |
1 | a0001c0001t0001g0125 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.80-15263_80-15246d others(20): Show |
TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr12 | 48743933 | |||||
| chr12:48743933
|
C | CAAAAAAA others(12): Show |
1 | a0001c0001t0001g0162 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.80-15264_80-15246d others(21): Show |
TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr12 | 48743933 | |||||
| chr12:48743933
|
CA | C | 162 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(159): Show | 166 | HG00099.hp1 HG00099.hp2 HG00544.hp1 others(163): Show |
intron_variant | MODIFIER | c.80-15246delA | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr12 | 48743933 | |||||
| chr12:48743933
|
CAA | C | 10 | a0001c0001t0001g0065a0001c0001t0001g0074a0001c0001t0001g0080others(7): Show | 10 | HG01346.hp2 HG01515.hp2 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.80-15247_80-15246d others(4): Show |
TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr12 | 48743933 | |||||
| chr12:48743990
|
G | A | 3 | a0001c0001t0001g0032a0001c0001t0001g0036a0001c0001t0001g0297 | 3 | HG02559.hp2 HG02647.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.80-15219G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48743990 | ||||||
| chr12:48744014
|
G | A | 3 | a0001c0001t0001g0283a0001c0001t0001g0295a0001c0001t0001g0296 | 3 | HG01346.hp2 HG02809.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.80-15195G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48744014 | ||||||
| chr12:48744248
|
CA | C | 175 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(172): Show | 178 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(175): Show |
intron_variant | MODIFIER | c.80-14942delA | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr12 | 48744248 | |||||
| chr12:48744248
|
CAA | C | 7 | a0001c0001t0001g0144a0001c0001t0001g0156a0001c0001t0001g0157others(4): Show | 7 | HG01978.hp1 HG02818.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.80-14943_80-14942d others(4): Show |
TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr12 | 48744248 | |||||
| chr12:48744283
|
G | A | 2 | a0001c0001t0001g0162a0001c0001t0001g0289 | 2 | HG02970.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.80-14926G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48744283 | ||||||
| chr12:48744385
|
G | A | 1 | a0001c0001t0001g0094 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.80-14824G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48744385 | ||||||
| chr12:48744435
|
G | C | 5 | a0001c0001t0001g0035a0001c0001t0001g0038a0001c0001t0001g0040others(2): Show | 5 | HG01167.hp1 HG02572.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.80-14774G>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48744435 | ||||||
| chr12:48744590
|
T | C | 1 | a0001c0001t0001g0287 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.80-14619T>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48744590 | ||||||
| chr12:48744650
|
C | A | 2 | a0001c0001t0001g0125a0001c0001t0001g0312 | 2 | HG02257.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.80-14559C>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48744650 | ||||||
| chr12:48744663
|
C | G | 3 | a0001c0001t0001g0032a0001c0001t0001g0036a0001c0001t0001g0297 | 3 | HG02559.hp2 HG02647.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.80-14546C>G | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48744663 | ||||||
| chr12:48744698
|
G | A | 173 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(170): Show | 176 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(173): Show |
intron_variant | MODIFIER | c.80-14511G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48744698 | ||||||
| chr12:48744739
|
T | A | 2 | a0001c0001t0001g0216a0001c0003t0001g0288 | 2 | HG03669.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.80-14470T>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48744739 | ||||||
| chr12:48744740
|
A | G | 2 | a0001c0001t0001g0216a0001c0003t0001g0288 | 2 | HG03669.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.80-14469A>G | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48744740 | ||||||
| chr12:48744813
|
GGAA | G | 34 | a0001c0001t0001g0002a0001c0001t0001g0187a0001c0001t0001g0190others(31): Show | 35 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(32): Show |
intron_variant | MODIFIER | c.80-14383_80-14381d others(5): Show |
TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr12 | 48744813 | |||||
| chr12:48744817
|
G | A | 6 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0147others(3): Show | 6 | HG02109.hp2 HG02258.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.80-14392G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48744817 | ||||||
| chr12:48744838
|
A | G | 1 | a0001c0001t0001g0010 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.80-14371A>G | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48744838 | ||||||
| chr12:48744993
|
G | A | 37 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(34): Show | 37 | HG00323.hp2 HG01099.hp2 HG01109.hp1 others(34): Show |
intron_variant | MODIFIER | c.80-14216G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48744993 | ||||||
| chr12:48745008
|
C | T | 1 | a0001c0001t0001g0143 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.80-14201C>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48745008 | ||||||
| chr12:48745033
|
A | G | 16 | a0001c0001t0001g0032a0001c0001t0001g0036a0001c0001t0001g0144others(13): Show | 16 | HG01346.hp2 HG01884.hp1 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.80-14176A>G | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48745033 | ||||||
| chr12:48745041
|
C | T | 3 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0111 | 3 | NA18975.hp1 NA18977.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.80-14168C>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48745041 | ||||||
| chr12:48745140
|
G | C | 1 | a0001c0001t0001g0287 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.80-14069G>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48745140 | ||||||
| chr12:48745144
|
G | A | 1 | a0001c0001t0001g0131 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.80-14065G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48745144 | ||||||
| chr12:48745175
|
G | A | 37 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(34): Show | 37 | HG00323.hp2 HG01099.hp2 HG01109.hp1 others(34): Show |
intron_variant | MODIFIER | c.80-14034G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48745175 | ||||||
| chr12:48745220
|
G | C | 3 | a0001c0001t0001g0032a0001c0001t0001g0036a0001c0001t0001g0297 | 3 | HG02559.hp2 HG02647.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.80-13989G>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48745220 | ||||||
| chr12:48745222
|
G | A | 3 | a0001c0001t0001g0283a0001c0001t0001g0295a0001c0001t0001g0296 | 3 | HG01346.hp2 HG02809.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.80-13987G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48745222 | ||||||
| chr12:48745462
|
C | T | 1 | a0001c0001t0001g0159 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.80-13747C>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48745462 | ||||||
| chr12:48745477
|
C | A | 3 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0147 | 3 | HG02970.hp2 HG03453.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.80-13732C>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48745477 | ||||||
| chr12:48745493
|
C | G | 5 | a0001c0001t0001g0009a0001c0001t0001g0243a0001c0001t0001g0253others(2): Show | 5 | HG01496.hp2 HG01978.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.80-13716C>G | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48745493 | ||||||
| chr12:48745538
|
G | A | 1 | a0001c0001t0001g0214 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.80-13671G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48745538 | ||||||
| chr12:48745646
|
C | T | 6 | a0001c0001t0001g0088a0001c0001t0001g0107a0001c0001t0001g0108others(3): Show | 6 | HG02257.hp1 HG02559.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.80-13563C>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48745646 | ||||||
| chr12:48745731
|
T | A | 252 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(249): Show | 256 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(253): Show |
intron_variant | MODIFIER | c.80-13478T>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48745731 | ||||||
| chr12:48745908
|
G | A | 1 | a0001c0001t0001g0244 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.80-13301G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48745908 | ||||||
| chr12:48745922
|
T | C | 4 | a0001c0001t0001g0144a0001c0001t0001g0156a0001c0001t0001g0157others(1): Show | 4 | HG02818.hp1 HG02965.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.80-13287T>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48745922 | ||||||
| chr12:48746029
|
C | T | 2 | a0001c0001t0001g0162a0001c0001t0001g0289 | 2 | HG02970.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.80-13180C>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48746029 | ||||||
| chr12:48746168
|
A | G | 1 | a0001c0001t0001g0249 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.80-13041A>G | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48746168 | ||||||
| chr12:48746360
|
C | CT | 20 | a0001c0001t0001g0009a0001c0001t0001g0016a0001c0001t0001g0017others(17): Show | 20 | HG01175.hp2 HG01192.hp2 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.80-12825dupT | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr12 | 48746360 | |||||
| chr12:48746360
|
CT | C | 36 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(33): Show | 36 | HG00323.hp1 HG01099.hp1 HG01099.hp2 others(33): Show |
intron_variant | MODIFIER | c.80-12825delT | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr12 | 48746360 | |||||
| chr12:48746397
|
C | T | 1 | a0001c0001t0001g0079 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.80-12812C>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48746397 | ||||||
| chr12:48746565
|
C | T | 1 | a0001c0001t0001g0123 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.80-12644C>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48746565 | ||||||
| chr12:48746660
|
C | T | 1 | a0001c0001t0001g0210 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.80-12549C>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48746660 | ||||||
| chr12:48746691
|
T | C | 4 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0001t0001g0287others(1): Show | 4 | HG01884.hp1 HG02486.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.80-12518T>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48746691 | ||||||
| chr12:48746747
|
C | T | 1 | a0001c0001t0001g0198 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.80-12462C>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48746747 | ||||||
| chr12:48746817
|
G | A | 7 | a0001c0001t0001g0032a0001c0001t0001g0036a0001c0001t0001g0144others(4): Show | 7 | HG02559.hp2 HG02647.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.80-12392G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48746817 | ||||||
| chr12:48746857
|
T | G | 7 | a0001c0001t0001g0032a0001c0001t0001g0036a0001c0001t0001g0144others(4): Show | 7 | HG02559.hp2 HG02647.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.80-12352T>G | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48746857 | ||||||
| chr12:48746868
|
C | G | 1 | a0001c0001t0001g0240 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.80-12341C>G | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48746868 | ||||||
| chr12:48746933
|
A | T | 3 | a0001c0001t0001g0227a0001c0001t0001g0233a0001c0001t0001g0234 | 3 | NA18944.hp2 NA18975.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.80-12276A>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48746933 | ||||||
| chr12:48746951
|
T | C | 9 | a0001c0001t0001g0032a0001c0001t0001g0036a0001c0001t0001g0144others(6): Show | 9 | HG02559.hp2 HG02630.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.80-12258T>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48746951 | ||||||
| chr12:48747001
|
C | A | 4 | a0001c0001t0001g0090a0001c0001t0001g0095a0001c0001t0001g0098others(1): Show | 4 | HG03834.hp1 NA18950.hp2 NA18951.hp1 others(1): Show |
intron_variant | MODIFIER | c.80-12208C>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48747001 | ||||||
| chr12:48747056
|
A | G | 2 | a0001c0001t0001g0316a0001c0004t0001g0317 | 2 | HG02630.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.80-12153A>G | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48747056 | ||||||
| chr12:48747057
|
T | A | 1 | a0001c0001t0001g0316 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.80-12152T>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48747057 | ||||||
| chr12:48747058
|
T | C | 3 | a0001c0001t0001g0283a0001c0001t0001g0295a0001c0001t0001g0296 | 3 | HG01346.hp2 HG02809.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.80-12151T>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48747058 | ||||||
| chr12:48747076
|
A | G | 190 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(187): Show | 193 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(190): Show |
intron_variant | MODIFIER | c.80-12133A>G | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48747076 | ||||||
| chr12:48747231
|
C | G | 2 | a0001c0001t0001g0316a0001c0004t0001g0317 | 2 | HG02630.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.80-11978C>G | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48747231 | ||||||
| chr12:48747407
|
A | C | 1 | a0001c0001t0001g0263 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.80-11802A>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48747407 | ||||||
| chr12:48747412
|
T | C | 182 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(179): Show | 185 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(182): Show |
intron_variant | MODIFIER | c.80-11797T>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48747412 | ||||||
| chr12:48747431
|
A | G | 1 | a0001c0001t0001g0306 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.80-11778A>G | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48747431 | ||||||
| chr12:48747445
|
T | G | 4 | a0001c0001t0001g0144a0001c0001t0001g0156a0001c0001t0001g0157others(1): Show | 4 | HG02818.hp1 HG02965.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.80-11764T>G | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48747445 | ||||||
| chr12:48747581
|
T | C | 1 | a0001c0001t0001g0245 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.80-11628T>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48747581 | ||||||
| chr12:48747596
|
T | C | 3 | a0001c0001t0001g0283a0001c0001t0001g0295a0001c0001t0001g0296 | 3 | HG01346.hp2 HG02809.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.80-11613T>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48747596 | ||||||
| chr12:48747647
|
CTTGGCTA others(13): Show |
C | 2 | a0001c0001t0001g0163a0001c0001t0003g0298 | 2 | HG02080.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.80-11539_80-11520d others(22): Show |
TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr12 | 48747647 | |||||
| chr12:48747803
|
G | A | 1 | a0001c0001t0001g0069 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.80-11406G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48747803 | ||||||
| chr12:48747830
|
T | C | 7 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0147others(4): Show | 7 | HG02109.hp2 HG02257.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.80-11379T>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48747830 | ||||||
| chr12:48747860
|
C | T | 1 | a0001c0001t0001g0086 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.80-11349C>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48747860 | ||||||
| chr12:48747947
|
G | A | 5 | a0001c0001t0001g0035a0001c0001t0001g0038a0001c0001t0001g0040others(2): Show | 5 | HG01167.hp1 HG02572.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.80-11262G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48747947 | ||||||
| chr12:48748271
|
A | G | 4 | a0001c0001t0001g0088a0001c0001t0001g0107a0001c0001t0001g0110others(1): Show | 4 | HG02257.hp1 HG02559.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.80-10938A>G | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48748271 | ||||||
| chr12:48748314
|
C | T | 1 | a0001c0001t0001g0068 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.80-10895C>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48748314 | ||||||
| chr12:48748469
|
G | A | 143 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(140): Show | 146 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(143): Show |
intron_variant | MODIFIER | c.80-10740G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48748469 | ||||||
| chr12:48748488
|
C | T | 141 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(138): Show | 144 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(141): Show |
intron_variant | MODIFIER | c.80-10721C>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48748488 | ||||||
| chr12:48748497
|
GA | G | 6 | a0001c0001t0001g0142a0001c0001t0001g0156a0001c0001t0001g0157others(3): Show | 6 | HG02818.hp1 HG02965.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.80-10698delA | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr12 | 48748497 | |||||
| chr12:48748555
|
A | G | 6 | a0001c0001t0001g0013a0001c0001t0001g0016a0001c0001t0001g0017others(3): Show | 6 | HG01891.hp1 HG02055.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.80-10654A>G | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48748555 | ||||||
| chr12:48748622
|
G | T | 4 | a0001c0001t0001g0013a0001c0001t0001g0016a0001c0001t0001g0017others(1): Show | 4 | HG01891.hp1 HG02055.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.80-10587G>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48748622 | ||||||
| chr12:48748669
|
C | A | 1 | a0001c0001t0001g0068 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.80-10540C>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48748669 | ||||||
| chr12:48748889
|
A | G | 1 | a0001c0001t0001g0262 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.80-10320A>G | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48748889 | ||||||
| chr12:48748902
|
T | C | 6 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0147others(3): Show | 6 | HG02109.hp2 HG02258.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.80-10307T>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48748902 | ||||||
| chr12:48748919
|
C | T | 1 | a0001c0001t0001g0216 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.80-10290C>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48748919 | ||||||
| chr12:48749177
|
G | A | 50 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0012others(47): Show | 50 | HG00280.hp1 HG00323.hp2 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.80-10032G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48749177 | ||||||
| chr12:48749261
|
C | CA | 132 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(129): Show | 134 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(131): Show |
intron_variant | MODIFIER | c.80-9933dupA | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr12 | 48749261 | |||||
| chr12:48749313
|
T | C | 51 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0012others(48): Show | 51 | HG00280.hp1 HG00323.hp2 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.80-9896T>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48749313 | ||||||
| chr12:48749323
|
G | A | 1 | a0001c0001t0001g0061 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.80-9886G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48749323 | ||||||
| chr12:48749333
|
G | C | 1 | a0001c0001t0001g0300 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.80-9876G>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48749333 | ||||||
| chr12:48749356
|
C | T | 1 | a0001c0001t0001g0207 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.80-9853C>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48749356 | ||||||
| chr12:48749496
|
C | T | 1 | a0001c0001t0001g0304 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.80-9713C>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48749496 | ||||||
| chr12:48749497
|
G | A | 1 | a0001c0001t0001g0100 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.80-9712G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48749497 | ||||||
| chr12:48749603
|
C | G | 143 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(140): Show | 146 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(143): Show |
intron_variant | MODIFIER | c.80-9606C>G | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48749603 | ||||||
| chr12:48749629
|
C | T | 5 | a0001c0001t0001g0196a0001c0001t0001g0248a0001c0001t0001g0302others(2): Show | 5 | NA18953.hp1 NA19058.hp1 NA19060.hp1 others(2): Show |
intron_variant | MODIFIER | c.80-9580C>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48749629 | ||||||
| chr12:48749635
|
CA | C | 8 | a0001c0001t0001g0052a0001c0001t0001g0116a0001c0001t0001g0131others(5): Show | 8 | HG00735.hp2 HG01099.hp1 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.80-9548delA | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr12 | 48749635 | |||||
| chr12:48749635
|
CAA | C | 47 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0020others(44): Show | 47 | HG00544.hp1 HG00621.hp2 HG00642.hp2 others(44): Show |
intron_variant | MODIFIER | c.80-9549_80-9548del others(2): Show |
TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr12 | 48749635 | |||||
| chr12:48749635
|
CAAA | C | 202 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(199): Show | 206 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.80-9550_80-9548del others(3): Show |
TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr12 | 48749635 | |||||
| chr12:48749635
|
CAAAA | C | 6 | a0001c0001t0001g0099a0001c0001t0001g0118a0001c0001t0001g0127others(3): Show | 6 | HG01169.hp1 HG02451.hp2 NA18999.hp1 others(3): Show |
intron_variant | MODIFIER | c.80-9551_80-9548del others(4): Show |
TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr12 | 48749635 | |||||
| chr12:48749635
|
CAAAAAAA | C | 46 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0012others(43): Show | 46 | HG00280.hp1 HG00323.hp2 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.80-9554_80-9548del others(7): Show |
TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr12 | 48749635 | |||||
| chr12:48749635
|
CAAAAAAA others(5): Show |
C | 1 | a0001c0001t0001g0117 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.80-9559_80-9548del others(12): Show |
TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr12 | 48749635 | |||||
| chr12:48749683
|
G | GTTC | 42 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0012others(39): Show | 42 | HG00280.hp1 HG00323.hp2 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.80-9514_80-9512dup others(3): Show |
TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr12 | 48749683 | |||||
| chr12:48749695
|
C | CTTCT | 7 | a0001c0001t0001g0013a0001c0001t0001g0016a0001c0001t0001g0017others(4): Show | 7 | HG01891.hp1 HG02055.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.80-9512_80-9511ins others(4): Show |
TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr12 | 48749695 | |||||
| chr12:48749753
|
C | G | 317 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(314): Show | 321 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(318): Show |
intron_variant | MODIFIER | c.80-9456C>G | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48749753 | ||||||
| chr12:48749841
|
G | A | 1 | a0001c0001t0001g0053 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.80-9368G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48749841 | ||||||
| chr12:48749849
|
G | A | 1 | a0001c0001t0001g0068 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.80-9360G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48749849 | ||||||
| chr12:48749933
|
C | T | 16 | a0001c0001t0001g0125a0001c0001t0001g0144a0001c0001t0001g0145others(13): Show | 16 | HG02109.hp2 HG02257.hp2 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.80-9276C>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48749933 | ||||||
| chr12:48750118
|
G | A | 1 | a0001c0001t0001g0099 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.80-9091G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48750118 | ||||||
| chr12:48750196
|
C | A | 136 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(133): Show | 139 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(136): Show |
intron_variant | MODIFIER | c.80-9013C>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48750196 | ||||||
| chr12:48750220
|
G | A | 1 | a0001c0001t0001g0101 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.80-8989G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48750220 | ||||||
| chr12:48750620
|
C | T | 4 | a0001c0001t0001g0144a0001c0001t0001g0156a0001c0001t0001g0157others(1): Show | 4 | HG02818.hp1 HG02965.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.80-8589C>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48750620 | ||||||
| chr12:48750696
|
C | G | 1 | a0001c0001t0001g0158 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.80-8513C>G | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48750696 | ||||||
| chr12:48750749
|
C | A | 1 | a0001c0004t0001g0317 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.80-8460C>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48750749 | ||||||
| chr12:48750851
|
C | T | 6 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0147others(3): Show | 6 | HG02109.hp2 HG02258.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.80-8358C>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48750851 | ||||||
| chr12:48751349
|
C | A | 1 | a0001c0001t0001g0036 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.80-7860C>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48751349 | ||||||
| chr12:48751354
|
C | T | 51 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0012others(48): Show | 51 | HG00280.hp1 HG00323.hp2 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.80-7855C>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48751354 | ||||||
| chr12:48751367
|
A | G | 50 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0012others(47): Show | 50 | HG00280.hp1 HG00323.hp2 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.80-7842A>G | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48751367 | ||||||
| chr12:48751372
|
G | A | 51 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0012others(48): Show | 51 | HG00280.hp1 HG00323.hp2 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.80-7837G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48751372 | ||||||
| chr12:48751383
|
G | A | 1 | a0001c0001t0001g0163 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.80-7826G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48751383 | ||||||
| chr12:48751562
|
C | T | 51 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0012others(48): Show | 51 | HG00280.hp1 HG00323.hp2 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.80-7647C>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48751562 | ||||||
| chr12:48751736
|
A | G | 1 | a0001c0001t0001g0115 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.80-7473A>G | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48751736 | ||||||
| chr12:48751796
|
G | T | 1 | a0001c0001t0001g0311 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.80-7413G>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48751796 | ||||||
| chr12:48751963
|
A | C | 1 | a0001c0001t0001g0215 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.80-7246A>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48751963 | ||||||
| chr12:48751975
|
G | A | 2 | a0001c0001t0001g0023a0001c0001t0001g0127 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.80-7234G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48751975 | ||||||
| chr12:48751985
|
C | T | 15 | a0001c0001t0001g0125a0001c0001t0001g0144a0001c0001t0001g0145others(12): Show | 15 | HG02109.hp2 HG02257.hp2 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.80-7224C>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48751985 | ||||||
| chr12:48752002
|
G | A | 51 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0012others(48): Show | 51 | HG00280.hp1 HG00323.hp2 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.80-7207G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48752002 | ||||||
| chr12:48752066
|
C | CA | 37 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0012others(34): Show | 37 | HG00280.hp1 HG00323.hp2 HG00639.hp2 others(34): Show |
intron_variant | MODIFIER | c.80-7130dupA | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr12 | 48752066 | |||||
| chr12:48752066
|
C | CAA | 7 | a0001c0001t0001g0047a0001c0001t0001g0059a0001c0001t0001g0169others(4): Show | 7 | HG01106.hp1 HG01175.hp1 HG01257.hp1 others(4): Show |
intron_variant | MODIFIER | c.80-7131_80-7130dup others(2): Show |
TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr12 | 48752066 | |||||
| chr12:48752076
|
A | C | 1 | a0001c0001t0001g0300 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.80-7133A>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48752076 | ||||||
| chr12:48752079
|
AC | A | 12 | a0001c0001t0001g0125a0001c0001t0001g0144a0001c0001t0001g0146others(9): Show | 12 | HG02257.hp2 HG02258.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.80-7129delC | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48752079 | ||||||
| chr12:48752080
|
C | A | 54 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0012others(51): Show | 54 | HG00280.hp1 HG00323.hp2 HG00639.hp2 others(51): Show |
intron_variant | MODIFIER | c.80-7129C>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48752080 | ||||||
| chr12:48752084
|
C | A | 1 | a0001c0004t0001g0317 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.80-7125C>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48752084 | ||||||
| chr12:48752257
|
G | A | 15 | a0001c0001t0001g0125a0001c0001t0001g0144a0001c0001t0001g0145others(12): Show | 15 | HG02109.hp2 HG02257.hp2 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.80-6952G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48752257 | ||||||
| chr12:48752269
|
A | G | 10 | a0001c0001t0001g0125a0001c0001t0001g0145a0001c0001t0001g0146others(7): Show | 10 | HG02109.hp2 HG02257.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.80-6940A>G | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48752269 | ||||||
| chr12:48752338
|
G | T | 50 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0012others(47): Show | 50 | HG00280.hp1 HG00323.hp2 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.80-6871G>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48752338 | ||||||
| chr12:48752396
|
A | G | 1 | a0001c0001t0001g0287 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.80-6813A>G | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48752396 | ||||||
| chr12:48752477
|
A | C | 1 | a0001c0001t0001g0287 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.80-6732A>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48752477 | ||||||
| chr12:48752669
|
CT | C | 31 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0033others(28): Show | 31 | HG00323.hp1 HG00639.hp2 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.80-6519delT | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr12 | 48752669 | |||||
| chr12:48752669
|
CTT | C | 117 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(114): Show | 120 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(117): Show |
intron_variant | MODIFIER | c.80-6520_80-6519del others(2): Show |
TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr12 | 48752669 | |||||
| chr12:48752669
|
CTTT | C | 6 | a0001c0001t0001g0144a0001c0001t0001g0156a0001c0001t0001g0157others(3): Show | 6 | HG02683.hp1 HG02818.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.80-6521_80-6519del others(3): Show |
TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr12 | 48752669 | |||||
| chr12:48752767
|
G | A | 15 | a0001c0001t0001g0125a0001c0001t0001g0144a0001c0001t0001g0145others(12): Show | 15 | HG02109.hp2 HG02257.hp2 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.80-6442G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48752767 | ||||||
| chr12:48752872
|
G | A | 1 | a0001c0001t0001g0124 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.80-6337G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48752872 | ||||||
| chr12:48752883
|
G | T | 50 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0012others(47): Show | 50 | HG00280.hp1 HG00323.hp2 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.80-6326G>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48752883 | ||||||
| chr12:48752913
|
C | T | 1 | a0001c0001t0001g0255 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.80-6296C>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48752913 | ||||||
| chr12:48752967
|
A | C | 203 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(200): Show | 206 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(203): Show |
intron_variant | MODIFIER | c.80-6242A>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48752967 | ||||||
| chr12:48752970
|
C | T | 15 | a0001c0001t0001g0125a0001c0001t0001g0144a0001c0001t0001g0145others(12): Show | 15 | HG02109.hp2 HG02257.hp2 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.80-6239C>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48752970 | ||||||
| chr12:48753063
|
C | A | 2 | a0001c0001t0001g0064a0001c0001t0001g0065 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.80-6146C>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48753063 | ||||||
| chr12:48753152
|
T | C | 1 | a0001c0001t0001g0141 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.80-6057T>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48753152 | ||||||
| chr12:48753164
|
G | A | 135 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(132): Show | 138 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(135): Show |
intron_variant | MODIFIER | c.80-6045G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48753164 | ||||||
| chr12:48753544
|
C | A | 3 | a0001c0001t0001g0311a0001c0001t0001g0313a0001c0001t0001g0314 | 3 | HG02109.hp2 HG02258.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.80-5665C>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48753544 | ||||||
| chr12:48753547
|
G | A | 2 | a0001c0001t0001g0018a0001c0001t0001g0096 | 2 | NA18974.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.80-5662G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48753547 | ||||||
| chr12:48753566
|
T | C | 2 | a0001c0001t0001g0021a0001c0001t0001g0034 | 2 | HG00741.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.80-5643T>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48753566 | ||||||
| chr12:48753664
|
G | T | 58 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0044others(55): Show | 59 | HG00544.hp1 HG00558.hp2 HG00621.hp2 others(56): Show |
intron_variant | MODIFIER | c.80-5545G>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48753664 | ||||||
| chr12:48753672
|
T | G | 1 | a0001c0004t0001g0317 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.80-5537T>G | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48753672 | ||||||
| chr12:48753691
|
T | C | 1 | a0001c0001t0001g0264 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.80-5518T>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48753691 | ||||||
| chr12:48753691
|
TC | T | 7 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0025others(4): Show | 7 | HG01891.hp1 HG02559.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.80-5517delC | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48753691 | ||||||
| chr12:48753692
|
C | CT | 72 | a0001c0001t0001g0009a0001c0001t0001g0015a0001c0001t0001g0020others(69): Show | 72 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(69): Show |
intron_variant | MODIFIER | c.80-5497dupT | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr12 | 48753692 | |||||
| chr12:48753692
|
C | T | 14 | a0001c0001t0001g0013a0001c0001t0001g0125a0001c0001t0001g0145others(11): Show | 14 | HG02055.hp1 HG02109.hp2 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.80-5517C>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48753692 | ||||||
| chr12:48753692
|
CT | C | 6 | a0001c0001t0001g0061a0001c0001t0001g0063a0001c0001t0001g0064others(3): Show | 6 | HG00323.hp1 HG01070.hp1 HG01255.hp2 others(3): Show |
intron_variant | MODIFIER | c.80-5497delT | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr12 | 48753692 | |||||
| chr12:48753693
|
T | C | 13 | a0001c0001t0001g0013a0001c0001t0001g0125a0001c0001t0001g0145others(10): Show | 13 | HG02055.hp1 HG02109.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.80-5516T>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48753693 | ||||||
| chr12:48753694
|
T | C | 7 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0025others(4): Show | 7 | HG01891.hp1 HG02559.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.80-5515T>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48753694 | ||||||
| chr12:48753697
|
T | C | 7 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0147others(4): Show | 7 | HG02109.hp2 HG02257.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.80-5512T>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48753697 | ||||||
| chr12:48753698
|
T | C | 1 | a0001c0001t0001g0196 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.80-5511T>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48753698 | ||||||
| chr12:48753763
|
G | A | 1 | a0001c0001t0001g0125 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.80-5446G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48753763 | ||||||
| chr12:48753777
|
C | T | 1 | a0001c0001t0001g0287 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.80-5432C>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48753777 | ||||||
| chr12:48753796
|
G | A | 1 | a0001c0001t0001g0138 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.80-5413G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48753796 | ||||||
| chr12:48753891
|
C | G | 9 | a0001c0001t0001g0013a0001c0001t0001g0016a0001c0001t0001g0017others(6): Show | 9 | HG01891.hp1 HG02055.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.80-5318C>G | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48753891 | ||||||
| chr12:48753950
|
G | A | 1 | a0001c0001t0001g0218 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.80-5259G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48753950 | ||||||
| chr12:48753984
|
T | G | 2 | a0001c0001t0001g0108a0001c0001t0001g0109 | 2 | HG02965.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.80-5225T>G | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48753984 | ||||||
| chr12:48754017
|
A | G | 2 | a0001c0001t0001g0162a0001c0001t0001g0289 | 2 | HG02970.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.80-5192A>G | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48754017 | ||||||
| chr12:48754127
|
G | A | 50 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0012others(47): Show | 50 | HG00280.hp1 HG00323.hp2 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.80-5082G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48754127 | ||||||
| chr12:48754544
|
G | A | 139 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(136): Show | 142 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(139): Show |
intron_variant | MODIFIER | c.80-4665G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48754544 | ||||||
| chr12:48754697
|
G | A | 8 | a0001c0001t0001g0130a0001c0001t0001g0133a0001c0001t0001g0134others(5): Show | 8 | HG00642.hp2 HG02055.hp2 HG02735.hp2 others(5): Show |
intron_variant | MODIFIER | c.80-4512G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48754697 | ||||||
| chr12:48754700
|
T | C | 9 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0147others(6): Show | 9 | HG02109.hp2 HG02257.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.80-4509T>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48754700 | ||||||
| chr12:48754861
|
T | TTCAGCCT others(38): Show |
4 | a0001c0001t0001g0035a0001c0001t0001g0040a0001c0001t0001g0042others(1): Show | 4 | HG01167.hp1 HG02630.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.80-4337_80-4293dup others(45): Show |
TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr12 | 48754861 | |||||
| chr12:48754875
|
T | TA | 3 | a0001c0001t0001g0173a0001c0001t0001g0175a0001c0001t0001g0183 | 3 | HG01099.hp2 HG01123.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.80-4333dupA | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr12 | 48754875 | |||||
| chr12:48755126
|
G | A | 1 | a0001c0001t0001g0010 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.80-4083G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48755126 | ||||||
| chr12:48755127
|
G | C | 52 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0012others(49): Show | 52 | HG00280.hp1 HG00323.hp2 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.80-4082G>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48755127 | ||||||
| chr12:48755477
|
C | T | 1 | a0001c0001t0001g0163 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.80-3732C>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48755477 | ||||||
| chr12:48755498
|
C | A | 2 | a0001c0001t0001g0116a0001c0001t0001g0122 | 2 | HG02300.hp1 NA18967.hp2 |
intron_variant | MODIFIER | c.80-3711C>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48755498 | ||||||
| chr12:48755586
|
T | A | 5 | a0001c0001t0001g0258a0001c0001t0001g0260a0001c0001t0001g0261others(2): Show | 5 | HG02451.hp2 HG02572.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.80-3623T>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48755586 | ||||||
| chr12:48755638
|
G | C | 8 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0076others(5): Show | 9 | HG01361.hp1 HG02004.hp2 HG02027.hp2 others(6): Show |
intron_variant | MODIFIER | c.80-3571G>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48755638 | ||||||
| chr12:48755642
|
C | T | 190 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(187): Show | 193 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(190): Show |
intron_variant | MODIFIER | c.80-3567C>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48755642 | ||||||
| chr12:48755681
|
T | C | 7 | a0001c0001t0001g0013a0001c0001t0001g0016a0001c0001t0001g0017others(4): Show | 7 | HG01891.hp1 HG02055.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.80-3528T>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48755681 | ||||||
| chr12:48755769
|
C | T | 1 | a0001c0001t0001g0125 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.80-3440C>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48755769 | ||||||
| chr12:48755814
|
A | G | 51 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0012others(48): Show | 51 | HG00280.hp1 HG00323.hp2 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.80-3395A>G | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48755814 | ||||||
| chr12:48755875
|
C | CT | 15 | a0001c0001t0001g0021a0001c0001t0001g0023a0001c0001t0001g0058others(12): Show | 15 | HG00544.hp1 HG00738.hp2 HG01167.hp2 others(12): Show |
intron_variant | MODIFIER | c.80-3314dupT | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr12 | 48755875 | |||||
| chr12:48755875
|
CT | C | 174 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(171): Show | 177 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(174): Show |
intron_variant | MODIFIER | c.80-3314delT | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr12 | 48755875 | |||||
| chr12:48755880
|
T | C | 1 | a0001c0001t0001g0140 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.80-3329T>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48755880 | ||||||
| chr12:48756036
|
C | G | 1 | a0001c0001t0001g0163 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.80-3173C>G | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48756036 | ||||||
| chr12:48756124
|
C | A | 1 | a0001c0001t0001g0316 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.80-3085C>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48756124 | ||||||
| chr12:48756134
|
C | G | 130 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(127): Show | 133 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(130): Show |
intron_variant | MODIFIER | c.80-3075C>G | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48756134 | ||||||
| chr12:48756248
|
C | T | 1 | a0001c0001t0001g0255 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.80-2961C>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48756248 | ||||||
| chr12:48756320
|
G | A | 1 | a0001c0001t0001g0148 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.80-2889G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48756320 | ||||||
| chr12:48756404
|
G | A | 3 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0001t0001g0073 | 3 | HG00544.hp1 HG00673.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.80-2805G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48756404 | ||||||
| chr12:48756618
|
C | T | 1 | a0001c0001t0001g0045 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.80-2591C>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48756618 | ||||||
| chr12:48756757
|
A | G | 203 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(200): Show | 206 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(203): Show |
intron_variant | MODIFIER | c.80-2452A>G | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48756757 | ||||||
| chr12:48756771
|
C | CTT | 7 | a0001c0001t0001g0125a0001c0001t0001g0146a0001c0001t0001g0147others(4): Show | 7 | HG02109.hp2 HG02258.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.80-2432_80-2431dup others(2): Show |
TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr12 | 48756771 | |||||
| chr12:48756773
|
T | TTC | 38 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(35): Show | 39 | HG00280.hp1 HG00323.hp2 HG00639.hp2 others(36): Show |
intron_variant | MODIFIER | c.80-2435_80-2434ins others(2): Show |
TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr12 | 48756773 | |||||
| chr12:48756779
|
C | T | 50 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(47): Show | 51 | HG00280.hp1 HG00323.hp2 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.80-2430C>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48756779 | ||||||
| chr12:48757137
|
G | A | 5 | a0001c0001t0001g0018a0001c0001t0001g0076a0001c0001t0001g0096others(2): Show | 5 | HG01361.hp1 HG02004.hp2 HG02027.hp2 others(2): Show |
intron_variant | MODIFIER | c.80-2072G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48757137 | ||||||
| chr12:48757314
|
A | G | 194 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(191): Show | 197 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(194): Show |
intron_variant | MODIFIER | c.80-1895A>G | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48757314 | ||||||
| chr12:48757373
|
C | A | 134 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(131): Show | 136 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(133): Show |
intron_variant | MODIFIER | c.80-1836C>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48757373 | ||||||
| chr12:48757423
|
G | A | 2 | a0001c0001t0001g0108a0001c0001t0001g0109 | 2 | HG02965.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.80-1786G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48757423 | ||||||
| chr12:48757507
|
G | A | 7 | a0001c0001t0001g0014a0001c0001t0001g0055a0001c0001t0001g0144others(4): Show | 7 | HG02559.hp2 HG02622.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.80-1702G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48757507 | ||||||
| chr12:48757519
|
G | A | 1 | a0001c0001t0001g0162 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.80-1690G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48757519 | ||||||
| chr12:48757581
|
T | G | 158 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(155): Show | 160 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(157): Show |
intron_variant | MODIFIER | c.80-1628T>G | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48757581 | ||||||
| chr12:48757610
|
C | T | 2 | a0001c0001t0001g0162a0001c0001t0001g0316 | 2 | HG02970.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.80-1599C>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48757610 | ||||||
| chr12:48757651
|
AAT | A | 38 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(35): Show | 39 | HG00280.hp1 HG00323.hp2 HG00639.hp2 others(36): Show |
intron_variant | MODIFIER | c.80-1556_80-1555del others(2): Show |
TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr12 | 48757651 | |||||
| chr12:48757652
|
AT | A | 147 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(144): Show | 149 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(146): Show |
intron_variant | MODIFIER | c.80-1556delT | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48757652 | ||||||
| chr12:48757653
|
T | A | 13 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0025others(10): Show | 13 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.80-1556T>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48757653 | ||||||
| chr12:48757657
|
AAT | A | 6 | a0001c0001t0001g0201a0001c0001t0001g0202a0001c0001t0001g0204others(3): Show | 6 | HG00323.hp1 HG00642.hp1 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.80-1550_80-1549del others(2): Show |
TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr12 | 48757657 | |||||
| chr12:48757659
|
T | A | 1 | a0001c0001t0001g0273 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.80-1550T>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48757659 | ||||||
| chr12:48757659
|
TA | T | 151 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(148): Show | 153 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(150): Show |
intron_variant | MODIFIER | c.80-1545delA | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr12 | 48757659 | |||||
| chr12:48757660
|
A | T | 6 | a0001c0001t0001g0201a0001c0001t0001g0202a0001c0001t0001g0204others(3): Show | 6 | HG00323.hp1 HG00642.hp1 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.80-1549A>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48757660 | ||||||
| chr12:48757783
|
C | T | 1 | a0001c0001t0001g0268 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.80-1426C>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48757783 | ||||||
| chr12:48758053
|
G | A | 50 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(47): Show | 51 | HG00280.hp1 HG00323.hp2 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.80-1156G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48758053 | ||||||
| chr12:48758060
|
C | T | 5 | a0001c0001t0001g0144a0001c0001t0001g0156a0001c0001t0001g0157others(2): Show | 5 | HG02559.hp2 HG02818.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.80-1149C>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48758060 | ||||||
| chr12:48758065
|
C | T | 4 | a0001c0001t0001g0144a0001c0001t0001g0156a0001c0001t0001g0157others(1): Show | 4 | HG02818.hp1 HG02965.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.80-1144C>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48758065 | ||||||
| chr12:48758082
|
C | T | 8 | a0001c0001t0001g0013a0001c0001t0001g0016a0001c0001t0001g0017others(5): Show | 8 | HG01891.hp1 HG02055.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.80-1127C>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48758082 | ||||||
| chr12:48758253
|
A | G | 206 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(203): Show | 209 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(206): Show |
intron_variant | MODIFIER | c.80-956A>G | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48758253 | ||||||
| chr12:48758282
|
A | G | 1 | a0001c0001t0001g0038 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.80-927A>G | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48758282 | ||||||
| chr12:48758417
|
C | T | 1 | a0001c0001t0001g0261 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.80-792C>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48758417 | ||||||
| chr12:48758428
|
G | T | 1 | a0001c0001t0001g0163 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.80-781G>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48758428 | ||||||
| chr12:48758433
|
C | T | 1 | a0001c0001t0001g0234 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.80-776C>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48758433 | ||||||
| chr12:48758650
|
A | G | 25 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0016others(22): Show | 25 | HG01167.hp1 HG01167.hp2 HG01169.hp1 others(22): Show |
intron_variant | MODIFIER | c.80-559A>G | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48758650 | ||||||
| chr12:48758805
|
T | C | 1 | a0001c0001t0001g0131 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.80-404T>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48758805 | ||||||
| chr12:48759097
|
T | C | 1 | a0001c0001t0001g0053 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.80-112T>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48759097 | ||||||
| chr12:48759133
|
T | G | 6 | a0001c0001t0001g0014a0001c0001t0001g0030a0001c0001t0001g0125others(3): Show | 6 | HG02258.hp1 HG02622.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.80-76T>G | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48759133 | ||||||
| chr12:48759374
|
T | C | 13 | a0001c0001t0001g0013a0001c0001t0001g0016a0001c0001t0001g0017others(10): Show | 13 | HG02055.hp1 HG02257.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.202+43T>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 2/3 | chr12 | 48759374 | ||||||
| chr12:48759415
|
T | G | 21 | a0001c0001t0001g0011a0001c0001t0001g0023a0001c0001t0001g0055others(18): Show | 21 | HG01167.hp2 HG01169.hp1 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.202+84T>G | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 2/3 | chr12 | 48759415 | ||||||
| chr12:48759416
|
T | C | 21 | a0001c0001t0001g0011a0001c0001t0001g0023a0001c0001t0001g0055others(18): Show | 21 | HG01167.hp2 HG01169.hp1 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.202+85T>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 2/3 | chr12 | 48759416 | ||||||
| chr12:48759455
|
G | A | 1 | a0001c0001t0001g0279 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.202+124G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 2/3 | chr12 | 48759455 | ||||||
| chr12:48759493
|
C | T | 3 | a0001c0001t0001g0179a0001c0001t0001g0202a0001c0001t0001g0285 | 3 | HG01516.hp2 HG01891.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.202+162C>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 2/3 | chr12 | 48759493 | ||||||
| chr12:48759582
|
GA | G | 9 | a0001c0001t0001g0013a0001c0001t0001g0016a0001c0001t0001g0017others(6): Show | 9 | HG02055.hp1 HG02257.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.202+252delA | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 2/3 | chr12 | 48759582 | ||||||
| chr12:48759584
|
G | C | 9 | a0001c0001t0001g0013a0001c0001t0001g0016a0001c0001t0001g0017others(6): Show | 9 | HG02055.hp1 HG02257.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.202+253G>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 2/3 | chr12 | 48759584 | ||||||
| chr12:48759585
|
G | T | 9 | a0001c0001t0001g0013a0001c0001t0001g0016a0001c0001t0001g0017others(6): Show | 9 | HG02055.hp1 HG02257.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.202+254G>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 2/3 | chr12 | 48759585 | ||||||
| chr12:48759586
|
C | A | 9 | a0001c0001t0001g0013a0001c0001t0001g0016a0001c0001t0001g0017others(6): Show | 9 | HG02055.hp1 HG02257.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.202+255C>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 2/3 | chr12 | 48759586 | ||||||
| chr12:48759700
|
G | A | 2 | a0001c0001t0001g0023a0001c0001t0001g0127 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.202+369G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 2/3 | chr12 | 48759700 | ||||||
| chr12:48759716
|
A | C | 1 | a0001c0001t0001g0011 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.202+385A>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 2/3 | chr12 | 48759716 | ||||||
| chr12:48759725
|
G | A | 161 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(158): Show | 162 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(159): Show |
intron_variant | MODIFIER | c.202+394G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 2/3 | chr12 | 48759725 | ||||||
| chr12:48759817
|
T | A | 1 | a0001c0001t0001g0163 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.202+486T>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 2/3 | chr12 | 48759817 | ||||||
| chr12:48759820
|
T | C | 11 | a0001c0001t0001g0024a0001c0001t0001g0027a0001c0001t0001g0030others(8): Show | 11 | HG01884.hp2 HG02109.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.202+489T>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 2/3 | chr12 | 48759820 | ||||||
| chr12:48759867
|
G | C | 28 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0014others(25): Show | 28 | HG01167.hp2 HG01169.hp1 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.202+536G>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 2/3 | chr12 | 48759867 | ||||||
| chr12:48759953
|
C | T | 24 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0016others(21): Show | 24 | HG01167.hp2 HG01169.hp1 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.202+622C>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 2/3 | chr12 | 48759953 | ||||||
| chr12:48760232
|
G | A | 1 | a0001c0001t0001g0275 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.202+901G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 2/3 | chr12 | 48760232 | ||||||
| chr12:48760471
|
C | G | 9 | a0001c0001t0001g0094a0001c0001t0001g0096a0001c0001t0001g0196others(6): Show | 9 | NA18953.hp1 NA18953.hp2 NA19058.hp1 others(6): Show |
intron_variant | MODIFIER | c.202+1140C>G | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 2/3 | chr12 | 48760471 | ||||||
| chr12:48760599
|
C | T | 10 | a0001c0001t0001g0024a0001c0001t0001g0027a0001c0001t0001g0030others(7): Show | 10 | HG01884.hp2 HG02109.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.202+1268C>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 2/3 | chr12 | 48760599 | ||||||
| chr12:48760767
|
T | C | 6 | a0001c0001t0001g0186a0001c0001t0001g0230a0001c0001t0001g0232others(3): Show | 6 | HG02129.hp2 NA18944.hp2 NA18962.hp1 others(3): Show |
intron_variant | MODIFIER | c.202+1436T>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 2/3 | chr12 | 48760767 | ||||||
| chr12:48760792
|
G | A | 1 | a0001c0001t0001g0293 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.202+1461G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 2/3 | chr12 | 48760792 | ||||||
| chr12:48761365
|
C | T | 1 | a0001c0001t0001g0296 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.202+2034C>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 2/3 | chr12 | 48761365 | ||||||
| chr12:48761445
|
C | CA | 30 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0022others(27): Show | 30 | HG00621.hp2 HG01433.hp2 HG01928.hp1 others(27): Show |
intron_variant | MODIFIER | c.202+2132dupA | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr12 | 48761445 | |||||
| chr12:48761445
|
CA | C | 34 | a0001c0001t0001g0003a0001c0001t0001g0027a0001c0001t0001g0030others(31): Show | 35 | HG01891.hp1 HG02056.hp2 HG02071.hp1 others(32): Show |
intron_variant | MODIFIER | c.202+2132delA | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr12 | 48761445 | |||||
| chr12:48761445
|
CAA | C | 30 | a0001c0001t0001g0011a0001c0001t0001g0019a0001c0001t0001g0026others(27): Show | 30 | HG00558.hp2 HG00621.hp1 HG01109.hp2 others(27): Show |
intron_variant | MODIFIER | c.202+2131_202+2132d others(4): Show |
TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr12 | 48761445 | |||||
| chr12:48761594
|
A | G | 3 | a0001c0001t0001g0013a0001c0001t0001g0016a0001c0001t0001g0017 | 3 | HG02055.hp1 HG03516.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.202+2263A>G | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 2/3 | chr12 | 48761594 | ||||||
| chr12:48761612
|
T | A | 1 | a0001c0001t0001g0275 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.202+2281T>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 2/3 | chr12 | 48761612 | ||||||
| chr12:48761612
|
T | TA | 10 | a0001c0001t0001g0018a0001c0001t0001g0032a0001c0001t0001g0058others(7): Show | 10 | HG00738.hp1 HG00738.hp2 HG01192.hp1 others(7): Show |
intron_variant | MODIFIER | c.202+2296dupA | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr12 | 48761612 | |||||
| chr12:48761651
|
T | C | 6 | a0001c0001t0001g0025a0001c0001t0001g0032a0001c0001t0001g0036others(3): Show | 6 | HG02257.hp1 HG02647.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.202+2320T>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 2/3 | chr12 | 48761651 | ||||||
| chr12:48761719
|
C | CT | 49 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0022others(46): Show | 49 | HG00639.hp1 HG00735.hp1 HG00741.hp2 others(46): Show |
intron_variant | MODIFIER | c.202+2412dupT | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr12 | 48761719 | |||||
| chr12:48761719
|
C | CTT | 9 | a0001c0001t0001g0051a0001c0001t0001g0055a0001c0001t0001g0068others(6): Show | 9 | HG01192.hp1 HG01243.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.202+2411_202+2412d others(4): Show |
TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr12 | 48761719 | |||||
| chr12:48761719
|
CT | C | 9 | a0001c0001t0001g0016a0001c0001t0001g0139a0001c0001t0001g0148others(6): Show | 9 | HG00099.hp2 HG00642.hp2 HG01069.hp1 others(6): Show |
intron_variant | MODIFIER | c.202+2412delT | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr12 | 48761719 | |||||
| chr12:48761840
|
A | G | 1 | a0001c0001t0001g0316 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.202+2509A>G | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 2/3 | chr12 | 48761840 | ||||||
| chr12:48761904
|
A | T | 1 | a0001c0001t0001g0163 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.202+2573A>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 2/3 | chr12 | 48761904 | ||||||
| chr12:48761982
|
G | A | 1 | a0001c0001t0001g0190 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.202+2651G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 2/3 | chr12 | 48761982 | ||||||
| chr12:48762014
|
T | C | 1 | a0001c0001t0001g0252 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.202+2683T>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 2/3 | chr12 | 48762014 | ||||||
| chr12:48762047
|
C | CT | 81 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0014others(78): Show | 82 | HG00639.hp1 HG00642.hp1 HG00673.hp2 others(79): Show |
intron_variant | MODIFIER | c.202+2741dupT | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr12 | 48762047 | |||||
| chr12:48762047
|
C | CTT | 13 | a0001c0001t0001g0023a0001c0001t0001g0035a0001c0001t0001g0097others(10): Show | 13 | HG00621.hp2 HG00735.hp1 HG01167.hp2 others(10): Show |
intron_variant | MODIFIER | c.202+2740_202+2741d others(4): Show |
TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr12 | 48762047 | |||||
| chr12:48762047
|
CT | C | 6 | a0001c0001t0001g0006a0001c0001t0001g0061a0001c0001t0001g0175others(3): Show | 6 | HG00323.hp1 HG01069.hp1 HG01070.hp1 others(3): Show |
intron_variant | MODIFIER | c.202+2741delT | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr12 | 48762047 | |||||
| chr12:48762094
|
T | G | 1 | a0001c0001t0001g0270 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.203-2757T>G | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 2/3 | chr12 | 48762094 | ||||||
| chr12:48762122
|
G | A | 2 | a0001c0001t0001g0192a0001c0001t0001g0193 | 2 | HG00733.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.203-2729G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 2/3 | chr12 | 48762122 | ||||||
| chr12:48762159
|
T | C | 1 | a0001c0001t0001g0046 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.203-2692T>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 2/3 | chr12 | 48762159 | ||||||
| chr12:48762215
|
T | C | 4 | a0001c0001t0001g0055a0001c0001t0001g0108a0001c0001t0001g0147others(1): Show | 4 | HG02886.hp2 HG02965.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.203-2636T>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 2/3 | chr12 | 48762215 | ||||||
| chr12:48762338
|
G | A | 8 | a0001c0001t0001g0011a0001c0001t0001g0024a0001c0001t0001g0109others(5): Show | 8 | HG01884.hp2 HG02109.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.203-2513G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 2/3 | chr12 | 48762338 | ||||||
| chr12:48762356
|
C | CT | 74 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(71): Show | 76 | HG00280.hp2 HG00621.hp1 HG00621.hp2 others(73): Show |
intron_variant | MODIFIER | c.203-2466dupT | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr12 | 48762356 | |||||
| chr12:48762356
|
C | CTT | 18 | a0001c0001t0001g0016a0001c0001t0001g0023a0001c0001t0001g0025others(15): Show | 18 | HG00558.hp2 HG00735.hp2 HG01167.hp2 others(15): Show |
intron_variant | MODIFIER | c.203-2467_203-2466d others(4): Show |
TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr12 | 48762356 | |||||
| chr12:48762356
|
C | CTTT | 9 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0193others(6): Show | 9 | HG00733.hp2 HG02055.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.203-2468_203-2466d others(5): Show |
TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr12 | 48762356 | |||||
| chr12:48762356
|
C | CTTTT | 17 | a0001c0001t0001g0011a0001c0001t0001g0019a0001c0001t0001g0024others(14): Show | 17 | HG01243.hp2 HG01884.hp2 HG02056.hp2 others(14): Show |
intron_variant | MODIFIER | c.203-2469_203-2466d others(6): Show |
TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr12 | 48762356 | |||||
| chr12:48762356
|
C | CTTTTT | 8 | a0001c0001t0001g0030a0001c0001t0001g0108a0001c0001t0001g0125others(5): Show | 8 | HG01109.hp2 HG01884.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.203-2470_203-2466d others(7): Show |
TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr12 | 48762356 | |||||
| chr12:48762356
|
CT | C | 6 | a0001c0001t0001g0029a0001c0001t0001g0052a0001c0001t0001g0165others(3): Show | 6 | HG01099.hp1 HG02896.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.203-2466delT | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr12 | 48762356 | |||||
| chr12:48762357
|
T | C | 1 | a0001c0001t0001g0144 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.203-2494T>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 2/3 | chr12 | 48762357 | ||||||
| chr12:48762431
|
G | A | 1 | a0001c0001t0004g0219 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.203-2420G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 2/3 | chr12 | 48762431 | ||||||
| chr12:48762437
|
G | A | 21 | a0001c0001t0001g0019a0001c0001t0001g0026a0001c0001t0001g0030others(18): Show | 21 | HG01109.hp2 HG01243.hp2 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.203-2414G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 2/3 | chr12 | 48762437 | ||||||
| chr12:48762471
|
G | A | 12 | a0001c0001t0001g0022a0001c0001t0001g0045a0001c0001t0001g0082others(9): Show | 12 | HG00733.hp2 HG00735.hp2 HG01069.hp1 others(9): Show |
intron_variant | MODIFIER | c.203-2380G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 2/3 | chr12 | 48762471 | ||||||
| chr12:48762559
|
G | T | 1 | a0001c0001t0001g0131 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.203-2292G>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 2/3 | chr12 | 48762559 | ||||||
| chr12:48762621
|
G | C | 21 | a0001c0001t0001g0019a0001c0001t0001g0026a0001c0001t0001g0030others(18): Show | 21 | HG01109.hp2 HG01243.hp2 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.203-2230G>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 2/3 | chr12 | 48762621 | ||||||
| chr12:48762779
|
G | C | 21 | a0001c0001t0001g0019a0001c0001t0001g0026a0001c0001t0001g0030others(18): Show | 21 | HG01109.hp2 HG01243.hp2 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.203-2072G>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 2/3 | chr12 | 48762779 | ||||||
| chr12:48763318
|
C | T | 1 | a0001c0001t0001g0157 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.203-1533C>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 2/3 | chr12 | 48763318 | ||||||
| chr12:48763355
|
G | A | 8 | a0001c0001t0001g0011a0001c0001t0001g0024a0001c0001t0001g0109others(5): Show | 8 | HG01884.hp2 HG02109.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.203-1496G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 2/3 | chr12 | 48763355 | ||||||
| chr12:48763414
|
A | G | 4 | a0001c0001t0001g0055a0001c0001t0001g0108a0001c0001t0001g0147others(1): Show | 4 | HG02886.hp2 HG02965.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.203-1437A>G | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 2/3 | chr12 | 48763414 | ||||||
| chr12:48763561
|
A | T | 1 | a0001c0001t0001g0296 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.203-1290A>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 2/3 | chr12 | 48763561 | ||||||
| chr12:48763681
|
C | CT | 28 | a0001c0001t0001g0008a0001c0001t0001g0014a0001c0001t0001g0035others(25): Show | 28 | HG00673.hp1 HG00673.hp2 HG01346.hp2 others(25): Show |
intron_variant | MODIFIER | c.203-1153dupT | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr12 | 48763681 | |||||
| chr12:48763681
|
CT | C | 11 | a0001c0001t0001g0055a0001c0001t0001g0072a0001c0001t0001g0108others(8): Show | 11 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(8): Show |
intron_variant | MODIFIER | c.203-1153delT | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr12 | 48763681 | |||||
| chr12:48763710
|
G | A | 1 | a0001c0001t0001g0163 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.203-1141G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 2/3 | chr12 | 48763710 | ||||||
| chr12:48763813
|
C | T | 1 | a0001c0001t0001g0297 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.203-1038C>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 2/3 | chr12 | 48763813 | ||||||
| chr12:48763839
|
C | G | 8 | a0001c0001t0001g0011a0001c0001t0001g0024a0001c0001t0001g0109others(5): Show | 8 | HG01884.hp2 HG02109.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.203-1012C>G | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 2/3 | chr12 | 48763839 | ||||||
| chr12:48763946
|
G | A | 10 | a0001c0001t0001g0013a0001c0001t0001g0016a0001c0001t0001g0017others(7): Show | 10 | HG02055.hp1 HG02257.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.203-905G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 2/3 | chr12 | 48763946 | ||||||
| chr12:48764216
|
C | T | 22 | a0001c0001t0001g0019a0001c0001t0001g0026a0001c0001t0001g0030others(19): Show | 22 | HG01109.hp2 HG01243.hp2 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.203-635C>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 2/3 | chr12 | 48764216 | ||||||
| chr12:48764614
|
G | C | 1 | a0001c0001t0001g0039 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.203-237G>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 2/3 | chr12 | 48764614 | ||||||
| chr12:48764689
|
G | A | 1 | a0001c0001t0001g0131 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.203-162G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 2/3 | chr12 | 48764689 | ||||||
| chr12:48764707
|
G | A | 22 | a0001c0001t0001g0019a0001c0001t0001g0026a0001c0001t0001g0030others(19): Show | 22 | HG01109.hp2 HG01243.hp2 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.203-144G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 2/3 | chr12 | 48764707 | ||||||
| chr12:48764721
|
C | A | 1 | a0001c0001t0001g0302 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.203-130C>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 2/3 | chr12 | 48764721 | ||||||
| chr12:48764756
|
G | A | 1 | a0001c0001t0001g0074 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.203-95G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 2/3 | chr12 | 48764756 | ||||||
| chr12:48765151
|
A | G | 5 | a0001c0001t0001g0078a0001c0001t0001g0144a0001c0001t0001g0157others(2): Show | 5 | HG01891.hp1 HG02486.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.347+156A>G | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 3/3 | chr12 | 48765151 | ||||||
| chr12:48765346
|
A | C | 2 | a0001c0001t0001g0023a0001c0001t0001g0127 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.348-261A>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 3/3 | chr12 | 48765346 | ||||||
| chr12:48765482
|
G | A | 4 | a0001c0001t0001g0049a0001c0001t0001g0170a0001c0001t0001g0173others(1): Show | 4 | HG01099.hp2 HG01243.hp1 HG01255.hp1 others(1): Show |
intron_variant | MODIFIER | c.348-125G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 3/3 | chr12 | 48765482 |