Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 7294 |
|---|---|
| ensemblid | ENSG00000074966.11 |
| hgncid | 12434 |
| symbol | TXK |
| name | TXK tyrosine kinase |
| refseq_nuc | NM_003328.3 |
| refseq_prot | NP_003319.2 |
| ensembl_nuc | ENST00000264316.9 |
| ensembl_prot | ENSP00000264316.4 |
| mane_status | MANE Select |
| chr | chr4 |
| start | 48066393 |
| end | 48134250 |
| strand | - |
| ver | v1.2 |
| region | chr4:48066393-48134250 |
| region5000 | chr4:48061393-48139250 |
| regionname0 | TXK_chr4_48066393_48134250 |
| regionname5000 | TXK_chr4_48061393_48139250 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 527 | 299 | 89 | 38 | 132 | 4 | 34 | 99 | TXK_chr4_48061393_48139250 | TXK | copy fasta | chr4 | 48061393 | 48139250 |
| a0002 | 0/0 | 527 | 49 | 3 | 20 | 14 | 5 | 7 | 9 | TXK_chr4_48061393_48139250 | TXK | copy fasta | chr4 | 48061393 | 48139250 |
| a0003 | 0/0 | 527 | 11 | 0 | 6 | 0 | 4 | 1 | 0 | TXK_chr4_48061393_48139250 | TXK | copy fasta | chr4 | 48061393 | 48139250 |
| a0004 | 0/0 | 527 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | TXK_chr4_48061393_48139250 | TXK | copy fasta | chr4 | 48061393 | 48139250 |
| a0005 | 0/0 | 527 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | copy fasta | chr4 | 48061393 | 48139250 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 1584 | 169 | 41 | 24 | 78 | 2 | 22 | TXK_chr4_48061393_48139250 | TXK | copy fasta | chr4 | 48061393 | 48139250 |
| c0002 | 0/0 | 1584 | 97 | 22 | 12 | 50 | 2 | 11 | TXK_chr4_48061393_48139250 | TXK | copy fasta | chr4 | 48061393 | 48139250 |
| c0003 | 0/0 | 1584 | 47 | 3 | 19 | 13 | 5 | 7 | TXK_chr4_48061393_48139250 | TXK | copy fasta | chr4 | 48061393 | 48139250 |
| c0004 | 0/0 | 1584 | 11 | 0 | 6 | 0 | 4 | 1 | TXK_chr4_48061393_48139250 | TXK | copy fasta | chr4 | 48061393 | 48139250 |
| c0005 | 0/0 | 1584 | 8 | 8 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | copy fasta | chr4 | 48061393 | 48139250 |
| c0006 | 0/0 | 1584 | 7 | 7 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | copy fasta | chr4 | 48061393 | 48139250 |
| c0007 | 0/0 | 1584 | 6 | 4 | 1 | 0 | 0 | 1 | TXK_chr4_48061393_48139250 | TXK | copy fasta | chr4 | 48061393 | 48139250 |
| c0008 | 0/0 | 1584 | 4 | 4 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | copy fasta | chr4 | 48061393 | 48139250 |
| c0009 | 0/0 | 1584 | 4 | 0 | 0 | 4 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | copy fasta | chr4 | 48061393 | 48139250 |
| c0010 | 0/0 | 1584 | 2 | 2 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | copy fasta | chr4 | 48061393 | 48139250 |
| c0011 | 0/0 | 1584 | 2 | 0 | 0 | 2 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | copy fasta | chr4 | 48061393 | 48139250 |
| c0012 | 0/0 | 1584 | 1 | 0 | 1 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | copy fasta | chr4 | 48061393 | 48139250 |
| c0013 | 0/0 | 1584 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | copy fasta | chr4 | 48061393 | 48139250 |
| c0014 | 0/0 | 1584 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | copy fasta | chr4 | 48061393 | 48139250 |
| c0015 | 0/0 | 1584 | 1 | 0 | 1 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | copy fasta | chr4 | 48061393 | 48139250 |
| c0016 | 0/0 | 1584 | 1 | 0 | 0 | 0 | 1 | 0 | TXK_chr4_48061393_48139250 | TXK | copy fasta | chr4 | 48061393 | 48139250 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/1 | 1325 | 236 | 53 | 39 | 112 | 9 | 22 | TXK_chr4_48061393_48139250 | TXK | copy fasta | chr4 | 48061393 | 48139250 |
| t0002 | 0/0 | 1325 | 63 | 1 | 18 | 35 | 1 | 8 | TXK_chr4_48061393_48139250 | TXK | copy fasta | chr4 | 48061393 | 48139250 |
| t0003 | 0/0 | 1325 | 34 | 13 | 6 | 0 | 4 | 11 | TXK_chr4_48061393_48139250 | TXK | copy fasta | chr4 | 48061393 | 48139250 |
| t0004 | 1/0 | 1325 | 19 | 17 | 1 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | copy fasta | chr4 | 48061393 | 48139250 |
| t0005 | 0/0 | 1325 | 5 | 5 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | copy fasta | chr4 | 48061393 | 48139250 |
| t0006 | 0/0 | 1325 | 2 | 2 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | copy fasta | chr4 | 48061393 | 48139250 |
| t0007 | 0/0 | 1325 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | copy fasta | chr4 | 48061393 | 48139250 |
| t0008 | 0/0 | 1325 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | copy fasta | chr4 | 48061393 | 48139250 |
| t0009 | 0/0 | 1325 | 1 | 0 | 0 | 0 | 0 | 1 | TXK_chr4_48061393_48139250 | TXK | copy fasta | chr4 | 48061393 | 48139250 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 4 | 0 | 3 | 0 | 1 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0003 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0004 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0005 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0007 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0008 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0009 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0010 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0014 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0140 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0227 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0249 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0250 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0330 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1584 | 169 | 41 | 24 | 78 | 2 | 22 | TXK_chr4_48061393_48139250 | TXK | copy fasta | chr4 | 48061393 | 48139250 |
| a0001c0002 | 0/0 | 1584 | 97 | 22 | 12 | 50 | 2 | 11 | TXK_chr4_48061393_48139250 | TXK | copy fasta | chr4 | 48061393 | 48139250 |
| a0001c0005 | 0/0 | 1584 | 8 | 8 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | copy fasta | chr4 | 48061393 | 48139250 |
| a0001c0006 | 0/0 | 1584 | 7 | 7 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | copy fasta | chr4 | 48061393 | 48139250 |
| a0001c0007 | 0/0 | 1584 | 6 | 4 | 1 | 0 | 0 | 1 | TXK_chr4_48061393_48139250 | TXK | copy fasta | chr4 | 48061393 | 48139250 |
| a0001c0008 | 0/0 | 1584 | 4 | 4 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | copy fasta | chr4 | 48061393 | 48139250 |
| a0001c0009 | 0/0 | 1584 | 4 | 0 | 0 | 4 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | copy fasta | chr4 | 48061393 | 48139250 |
| a0001c0010 | 0/0 | 1584 | 2 | 2 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | copy fasta | chr4 | 48061393 | 48139250 |
| a0001c0014 | 0/0 | 1584 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | copy fasta | chr4 | 48061393 | 48139250 |
| a0001c0015 | 0/0 | 1584 | 1 | 0 | 1 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | copy fasta | chr4 | 48061393 | 48139250 |
| a0002c0003 | 0/0 | 1584 | 47 | 3 | 19 | 13 | 5 | 7 | TXK_chr4_48061393_48139250 | TXK | copy fasta | chr4 | 48061393 | 48139250 |
| a0002c0012 | 0/0 | 1584 | 1 | 0 | 1 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | copy fasta | chr4 | 48061393 | 48139250 |
| a0002c0013 | 0/0 | 1584 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | copy fasta | chr4 | 48061393 | 48139250 |
| a0003c0004 | 0/0 | 1584 | 11 | 0 | 6 | 0 | 4 | 1 | TXK_chr4_48061393_48139250 | TXK | copy fasta | chr4 | 48061393 | 48139250 |
| a0004c0011 | 0/0 | 1584 | 2 | 0 | 0 | 2 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | copy fasta | chr4 | 48061393 | 48139250 |
| a0005c0016 | 0/0 | 1584 | 1 | 0 | 0 | 0 | 1 | 0 | TXK_chr4_48061393_48139250 | TXK | copy fasta | chr4 | 48061393 | 48139250 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 2908 | 60 | 6 | 6 | 43 | 1 | 3 | TXK_chr4_48061393_48139250 | TXK | copy fasta | chr4 | 48061393 | 48139250 |
| a0001c0001t0002 | 0/0 | 2908 | 62 | 1 | 17 | 35 | 1 | 8 | TXK_chr4_48061393_48139250 | TXK | copy fasta | chr4 | 48061393 | 48139250 |
| a0001c0001t0003 | 0/0 | 2908 | 20 | 10 | 0 | 0 | 0 | 10 | TXK_chr4_48061393_48139250 | TXK | copy fasta | chr4 | 48061393 | 48139250 |
| a0001c0001t0004 | 1/0 | 2908 | 19 | 17 | 1 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | copy fasta | chr4 | 48061393 | 48139250 |
| a0001c0001t0005 | 0/0 | 2908 | 5 | 5 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | copy fasta | chr4 | 48061393 | 48139250 |
| a0001c0001t0006 | 0/0 | 2908 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | copy fasta | chr4 | 48061393 | 48139250 |
| a0001c0001t0007 | 0/0 | 2908 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | copy fasta | chr4 | 48061393 | 48139250 |
| a0001c0001t0009 | 0/0 | 2908 | 1 | 0 | 0 | 0 | 0 | 1 | TXK_chr4_48061393_48139250 | TXK | copy fasta | chr4 | 48061393 | 48139250 |
| a0001c0002t0001 | 0/0 | 2908 | 96 | 22 | 12 | 49 | 2 | 11 | TXK_chr4_48061393_48139250 | TXK | copy fasta | chr4 | 48061393 | 48139250 |
| a0001c0002t0008 | 0/0 | 2908 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | copy fasta | chr4 | 48061393 | 48139250 |
| a0001c0005t0001 | 0/0 | 2908 | 8 | 8 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | copy fasta | chr4 | 48061393 | 48139250 |
| a0001c0006t0001 | 0/0 | 2908 | 7 | 7 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | copy fasta | chr4 | 48061393 | 48139250 |
| a0001c0007t0001 | 0/0 | 2908 | 6 | 4 | 1 | 0 | 0 | 1 | TXK_chr4_48061393_48139250 | TXK | copy fasta | chr4 | 48061393 | 48139250 |
| a0001c0008t0003 | 0/0 | 2908 | 3 | 3 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | copy fasta | chr4 | 48061393 | 48139250 |
| a0001c0008t0006 | 0/0 | 2908 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | copy fasta | chr4 | 48061393 | 48139250 |
| a0001c0009t0001 | 0/0 | 2908 | 4 | 0 | 0 | 4 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | copy fasta | chr4 | 48061393 | 48139250 |
| a0001c0010t0001 | 0/0 | 2908 | 2 | 2 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | copy fasta | chr4 | 48061393 | 48139250 |
| a0001c0014t0001 | 0/0 | 2908 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | copy fasta | chr4 | 48061393 | 48139250 |
| a0001c0015t0001 | 0/0 | 2908 | 1 | 0 | 1 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | copy fasta | chr4 | 48061393 | 48139250 |
| a0002c0003t0001 | 0/0 | 2908 | 47 | 3 | 19 | 13 | 5 | 7 | TXK_chr4_48061393_48139250 | TXK | copy fasta | chr4 | 48061393 | 48139250 |
| a0002c0012t0002 | 0/0 | 2908 | 1 | 0 | 1 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | copy fasta | chr4 | 48061393 | 48139250 |
| a0002c0013t0001 | 0/0 | 2908 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | copy fasta | chr4 | 48061393 | 48139250 |
| a0003c0004t0003 | 0/0 | 2908 | 11 | 0 | 6 | 0 | 4 | 1 | TXK_chr4_48061393_48139250 | TXK | copy fasta | chr4 | 48061393 | 48139250 |
| a0004c0011t0001 | 0/0 | 2908 | 2 | 0 | 0 | 2 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | copy fasta | chr4 | 48061393 | 48139250 |
| a0005c0016t0001 | 0/0 | 2908 | 1 | 0 | 0 | 0 | 1 | 0 | TXK_chr4_48061393_48139250 | TXK | copy fasta | chr4 | 48061393 | 48139250 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0005 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0001g0140 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0002g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0002g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0002g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0002g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0002g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0002g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0002g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0002g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0002g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0002g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0002g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0002g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0002g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0002g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0002g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0002g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0002g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0002g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0002g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0002g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0002g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0002g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0002g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0002g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0002g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0002g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0002g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0002g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0002g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0002g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0002g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0002g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0002g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0002g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0002g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0002g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0003g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0003g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0003g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0003g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0003g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0003g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0003g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0003g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0003g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0003g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0003g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0003g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0003g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0003g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0003g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0003g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0003g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0003g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0003g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0003g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0004g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0004g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0004g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0004g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0004g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0004g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0004g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0004g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0004g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0004g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0004g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0004g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0004g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0004g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0004g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0004g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0004g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0004g0227 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0004g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0005g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0005g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0005g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0005g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0006g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0007g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0009g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0002t0001g0003 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0002t0001g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0002t0001g0010 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0002t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0002t0001g0014 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0002t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0002t0001g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0002t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0002t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0002t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0002t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0002t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0002t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0002t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0002t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0002t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0002t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0002t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0002t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0002t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0002t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0002t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0002t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0002t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0002t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0002t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0002t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0002t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0002t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0002t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0002t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0002t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0002t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0002t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0002t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0002t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0002t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0002t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0002t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0002t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0002t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0002t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0002t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0002t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0002t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0002t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0002t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0002t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0002t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0002t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0002t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0002t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0002t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0002t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0002t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0002t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0002t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0002t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0002t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0002t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0002t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0002t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0002t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0002t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0002t0008g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0005t0001g0004 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0005t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0005t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0005t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0005t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0005t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0006t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0006t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0006t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0006t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0006t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0006t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0006t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0007t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0007t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0007t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0007t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0007t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0007t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0008t0003g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0008t0003g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0008t0003g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0008t0006g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0009t0001g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0010t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0010t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0014t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0015t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0002c0003t0001g0007 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0002c0003t0001g0008 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0002c0003t0001g0009 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0002c0003t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0002c0003t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0002c0003t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0002c0003t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0002c0003t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0002c0003t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0002c0003t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0002c0003t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0002c0003t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0002c0003t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0002c0003t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0002c0003t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0002c0003t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0002c0003t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0002c0003t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0002c0003t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0002c0003t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0002c0003t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0002c0003t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0002c0003t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0002c0003t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0002c0003t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0002c0003t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0002c0003t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0002c0003t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0002c0003t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0002c0003t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0002c0003t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0002c0003t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0002c0003t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0002c0003t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0002c0003t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0002c0003t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0002c0003t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0002c0003t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0002c0003t0001g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0002c0003t0001g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0002c0003t0001g0330 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0002c0003t0001g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0002c0012t0002g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0002c0013t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0003c0004t0003g0001 | 0/0 | 4 | 0 | 3 | 0 | 1 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0003c0004t0003g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0003c0004t0003g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0003c0004t0003g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0003c0004t0003g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0003c0004t0003g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0003c0004t0003g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0003c0004t0003g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0004c0011t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0005c0016t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0138 | EUR | GBR | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG00140 | hp2 | a0002 | c0003 | t0001 | g0007 | EUR | GBR | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0153 | EUR | FIN | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG00280 | hp2 | a0002 | c0003 | t0001 | g0249 | EUR | FIN | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG00323 | hp1 | a0003 | c0004 | t0003 | g0116 | EUR | FIN | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG00323 | hp2 | a0001 | c0002 | t0001 | g0099 | EUR | FIN | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | CHS | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG00408 | hp2 | a0001 | c0002 | t0001 | g0326 | EAS | CHS | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG00438 | hp1 | a0001 | c0002 | t0001 | g0282 | EAS | CHS | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0293 | EAS | CHS | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0305 | EAS | CHS | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG00544 | hp2 | a0001 | c0002 | t0001 | g0171 | EAS | CHS | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | CHS | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG00558 | hp2 | a0001 | c0002 | t0001 | g0067 | EAS | CHS | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG00597 | hp1 | a0001 | c0002 | t0001 | g0037 | EAS | CHS | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0313 | EAS | CHS | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | CHS | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0302 | EAS | CHS | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | CHS | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG00621 | hp2 | a0001 | c0002 | t0001 | g0063 | EAS | CHS | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG00639 | hp1 | a0002 | c0003 | t0001 | g0008 | AMR | PUR | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG00639 | hp2 | a0003 | c0004 | t0003 | g0137 | AMR | PUR | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG00642 | hp1 | a0002 | c0012 | t0002 | g0252 | AMR | PUR | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG00642 | hp2 | a0001 | c0002 | t0001 | g0271 | AMR | PUR | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | CHS | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0308 | EAS | CHS | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG00733 | hp1 | a0001 | c0001 | t0002 | g0197 | AMR | PUR | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG00733 | hp2 | a0002 | c0003 | t0001 | g0008 | AMR | PUR | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG00735 | hp1 | a0002 | c0003 | t0001 | g0254 | AMR | PUR | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0224 | AMR | PUR | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0212 | AMR | PUR | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG00738 | hp2 | a0002 | c0003 | t0001 | g0008 | AMR | PUR | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG01071 | hp1 | a0002 | c0003 | t0001 | g0265 | AMR | PUR | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG01071 | hp2 | a0001 | c0002 | t0001 | g0003 | AMR | PUR | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG01099 | hp1 | a0001 | c0002 | t0001 | g0083 | AMR | PUR | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0207 | AMR | PUR | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG01109 | hp1 | a0003 | c0004 | t0003 | g0001 | AMR | PUR | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG01109 | hp2 | a0001 | c0002 | t0001 | g0236 | AMR | PUR | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG01167 | hp1 | a0001 | c0002 | t0001 | g0062 | AMR | PUR | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0016 | AMR | PUR | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG01168 | hp1 | a0001 | c0001 | t0002 | g0196 | AMR | PUR | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG01168 | hp2 | a0002 | c0003 | t0001 | g0267 | AMR | PUR | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0016 | AMR | PUR | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG01169 | hp2 | a0002 | c0003 | t0001 | g0253 | AMR | PUR | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0228 | AMR | PUR | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG01175 | hp2 | a0002 | c0003 | t0001 | g0238 | AMR | PUR | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG01192 | hp1 | a0002 | c0003 | t0001 | g0329 | AMR | PUR | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG01192 | hp2 | a0002 | c0003 | t0001 | g0235 | AMR | PUR | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0198 | AMR | PUR | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG01243 | hp2 | a0001 | c0015 | t0001 | g0033 | AMR | PUR | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG01255 | hp1 | a0001 | c0007 | t0001 | g0107 | AMR | CLM | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG01255 | hp2 | a0001 | c0001 | t0004 | g0094 | AMR | CLM | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0205 | AMR | CLM | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG01256 | hp2 | a0002 | c0003 | t0001 | g0042 | AMR | CLM | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0154 | AMR | CLM | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0208 | AMR | CLM | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG01346 | hp1 | a0001 | c0002 | t0001 | g0091 | AMR | CLM | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG01346 | hp2 | a0001 | c0002 | t0001 | g0229 | AMR | CLM | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG01358 | hp1 | a0002 | c0003 | t0001 | g0049 | AMR | CLM | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG01358 | hp2 | a0003 | c0004 | t0003 | g0001 | AMR | CLM | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0226 | AMR | CLM | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG01361 | hp2 | a0003 | c0004 | t0003 | g0001 | AMR | CLM | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG01496 | hp1 | a0001 | c0002 | t0001 | g0090 | AMR | CLM | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0214 | AMR | CLM | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG01515 | hp1 | a0002 | c0003 | t0001 | g0009 | EUR | IBS | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG01515 | hp2 | a0005 | c0016 | t0001 | g0176 | EUR | IBS | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG01516 | hp1 | a0003 | c0004 | t0003 | g0109 | EUR | IBS | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG01516 | hp2 | a0002 | c0003 | t0001 | g0250 | EUR | IBS | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG01517 | hp1 | a0002 | c0003 | t0001 | g0009 | EUR | IBS | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG01517 | hp2 | a0003 | c0004 | t0003 | g0001 | EUR | IBS | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG01884 | hp1 | a0001 | c0006 | t0001 | g0125 | AFR | ACB | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG01884 | hp2 | a0001 | c0001 | t0005 | g0332 | AFR | ACB | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG01891 | hp1 | a0001 | c0001 | t0003 | g0322 | AFR | ACB | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG01891 | hp2 | a0001 | c0002 | t0001 | g0258 | AFR | ACB | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG01928 | hp1 | a0001 | c0002 | t0001 | g0003 | AMR | PEL | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG01928 | hp2 | a0002 | c0003 | t0001 | g0242 | AMR | PEL | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG01943 | hp1 | a0001 | c0002 | t0001 | g0092 | AMR | PEL | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG01943 | hp2 | a0002 | c0003 | t0001 | g0087 | AMR | PEL | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG01952 | hp1 | a0002 | c0003 | t0001 | g0243 | AMR | PEL | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0148 | AMR | PEL | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG01978 | hp1 | a0002 | c0003 | t0001 | g0043 | AMR | PEL | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG01978 | hp2 | a0002 | c0003 | t0001 | g0007 | AMR | PEL | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0149 | AMR | PEL | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0309 | AMR | PEL | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0151 | AMR | PEL | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG01993 | hp2 | a0002 | c0003 | t0001 | g0251 | AMR | PEL | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG02004 | hp1 | a0002 | c0003 | t0001 | g0007 | AMR | PEL | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0211 | AMR | PEL | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0294 | EAS | KHV | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | KHV | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0209 | EAS | KHV | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG02027 | hp2 | a0002 | c0003 | t0001 | g0055 | EAS | KHV | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG02040 | hp1 | a0001 | c0002 | t0001 | g0204 | EAS | KHV | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG02040 | hp2 | a0002 | c0003 | t0001 | g0056 | EAS | KHV | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG02055 | hp1 | a0001 | c0002 | t0001 | g0237 | AFR | ACB | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG02055 | hp2 | a0002 | c0003 | t0001 | g0331 | AFR | ACB | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | KHV | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG02056 | hp2 | a0002 | c0003 | t0001 | g0246 | EAS | KHV | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG02071 | hp1 | a0002 | c0003 | t0001 | g0058 | EAS | KHV | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0283 | EAS | KHV | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG02129 | hp1 | a0001 | c0002 | t0001 | g0096 | EAS | KHV | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | KHV | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0064 | EAS | KHV | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG02132 | hp2 | a0002 | c0003 | t0001 | g0173 | EAS | KHV | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG02145 | hp1 | a0001 | c0007 | t0001 | g0122 | AFR | ACB | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG02145 | hp2 | a0001 | c0006 | t0001 | g0030 | AFR | ACB | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0150 | AMR | PEL | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG02148 | hp2 | a0001 | c0002 | t0001 | g0044 | AMR | PEL | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG02155 | hp1 | a0001 | c0002 | t0001 | g0066 | EAS | CDX | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | CDX | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG02257 | hp1 | a0001 | c0014 | t0001 | g0025 | AFR | ACB | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG02257 | hp2 | a0001 | c0001 | t0004 | g0192 | AFR | ACB | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG02258 | hp1 | a0001 | c0001 | t0003 | g0289 | AFR | ACB | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0169 | AFR | ACB | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0161 | AMR | PEL | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG02273 | hp2 | a0001 | c0002 | t0001 | g0089 | AMR | PEL | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG02280 | hp1 | a0001 | c0002 | t0001 | g0278 | AFR | ACB | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0210 | AFR | ACB | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0272 | AMR | PEL | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG02300 | hp2 | a0003 | c0004 | t0003 | g0110 | AMR | PEL | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG02451 | hp1 | a0001 | c0006 | t0001 | g0029 | AFR | ACB | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG02451 | hp2 | a0001 | c0001 | t0004 | g0257 | AFR | ACB | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG02523 | hp1 | a0001 | c0002 | t0001 | g0121 | EAS | KHV | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0301 | EAS | KHV | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG02572 | hp1 | a0001 | c0001 | t0005 | g0018 | AFR | GWD | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG02572 | hp2 | a0001 | c0005 | t0001 | g0004 | AFR | GWD | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0273 | SAS | PJL | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG02602 | hp2 | a0001 | c0002 | t0001 | g0069 | SAS | PJL | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG02615 | hp1 | a0001 | c0002 | t0001 | g0080 | AFR | GWD | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG02615 | hp2 | a0001 | c0002 | t0001 | g0270 | AFR | GWD | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG02622 | hp1 | a0001 | c0001 | t0004 | g0189 | AFR | GWD | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG02622 | hp2 | a0001 | c0002 | t0001 | g0256 | AFR | GWD | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0115 | AFR | GWD | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG02630 | hp2 | a0001 | c0001 | t0005 | g0018 | AFR | GWD | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG02647 | hp1 | a0001 | c0002 | t0001 | g0259 | AFR | GWD | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG02647 | hp2 | a0001 | c0005 | t0001 | g0023 | AFR | GWD | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG02698 | hp1 | a0001 | c0001 | t0009 | g0220 | SAS | PJL | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG02698 | hp2 | a0002 | c0003 | t0001 | g0240 | SAS | PJL | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG02717 | hp1 | a0001 | c0002 | t0001 | g0260 | AFR | GWD | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG02717 | hp2 | a0001 | c0010 | t0001 | g0117 | AFR | GWD | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG02723 | hp1 | a0001 | c0001 | t0003 | g0323 | AFR | GWD | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG02723 | hp2 | a0001 | c0001 | t0004 | g0183 | AFR | GWD | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG02735 | hp1 | a0001 | c0002 | t0001 | g0071 | SAS | PJL | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0156 | SAS | PJL | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG02738 | hp1 | a0001 | c0001 | t0003 | g0114 | SAS | PJL | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG02738 | hp2 | a0002 | c0003 | t0001 | g0093 | SAS | PJL | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG02809 | hp1 | a0001 | c0001 | t0004 | g0194 | AFR | GWD | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG02809 | hp2 | a0001 | c0002 | t0001 | g0234 | AFR | GWD | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG02818 | hp1 | a0001 | c0001 | t0004 | g0185 | AFR | GWD | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG02818 | hp2 | a0001 | c0005 | t0001 | g0026 | AFR | GWD | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG02886 | hp1 | a0001 | c0002 | t0001 | g0079 | AFR | GWD | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG02886 | hp2 | a0001 | c0008 | t0006 | g0232 | AFR | GWD | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG02895 | hp1 | a0001 | c0002 | t0001 | g0097 | AFR | GWD | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG02895 | hp2 | a0001 | c0006 | t0001 | g0292 | AFR | GWD | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG02897 | hp1 | a0001 | c0008 | t0003 | g0230 | AFR | GWD | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG02897 | hp2 | a0001 | c0002 | t0001 | g0078 | AFR | GWD | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG02922 | hp1 | a0001 | c0010 | t0001 | g0217 | AFR | ESN | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0178 | AFR | ESN | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG02965 | hp1 | a0001 | c0001 | t0004 | g0182 | AFR | ESN | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG02965 | hp2 | a0001 | c0001 | t0005 | g0039 | AFR | ESN | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG02970 | hp1 | a0001 | c0002 | t0001 | g0261 | AFR | ESN | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG02970 | hp2 | a0001 | c0001 | t0004 | g0188 | AFR | ESN | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG02976 | hp1 | a0001 | c0002 | t0001 | g0248 | AFR | ESN | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG02976 | hp2 | a0001 | c0002 | t0001 | g0263 | AFR | ESN | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG03017 | hp1 | a0001 | c0001 | t0003 | g0108 | SAS | PJL | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0216 | SAS | PJL | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG03041 | hp1 | a0001 | c0001 | t0004 | g0193 | AFR | GWD | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG03041 | hp2 | a0001 | c0001 | t0003 | g0291 | AFR | GWD | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG03098 | hp1 | a0001 | c0006 | t0001 | g0028 | AFR | MSL | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG03098 | hp2 | a0001 | c0006 | t0001 | g0095 | AFR | MSL | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG03130 | hp1 | a0001 | c0005 | t0001 | g0024 | AFR | ESN | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG03130 | hp2 | a0001 | c0001 | t0005 | g0333 | AFR | ESN | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG03139 | hp1 | a0001 | c0005 | t0001 | g0022 | AFR | ESN | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG03139 | hp2 | a0001 | c0006 | t0001 | g0031 | AFR | ESN | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG03209 | hp1 | a0001 | c0001 | t0004 | g0184 | AFR | MSL | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG03209 | hp2 | a0001 | c0001 | t0003 | g0288 | AFR | MSL | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG03225 | hp1 | a0001 | c0002 | t0001 | g0269 | AFR | MSL | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG03225 | hp2 | a0001 | c0001 | t0004 | g0187 | AFR | MSL | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG03239 | hp1 | a0003 | c0004 | t0003 | g0112 | SAS | PJL | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG03239 | hp2 | a0001 | c0007 | t0001 | g0167 | SAS | PJL | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG03486 | hp1 | a0001 | c0001 | t0003 | g0281 | AFR | MSL | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG03486 | hp2 | a0001 | c0001 | t0004 | g0124 | AFR | MSL | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG03491 | hp1 | a0001 | c0001 | t0003 | g0215 | SAS | PJL | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG03491 | hp2 | a0001 | c0002 | t0001 | g0060 | SAS | PJL | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG03492 | hp1 | a0002 | c0003 | t0001 | g0330 | SAS | PJL | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG03492 | hp2 | a0001 | c0002 | t0001 | g0061 | SAS | PJL | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG03516 | hp1 | a0001 | c0001 | t0003 | g0290 | AFR | ESN | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG03516 | hp2 | a0001 | c0001 | t0004 | g0191 | AFR | ESN | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG03540 | hp1 | a0001 | c0002 | t0001 | g0077 | AFR | GWD | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG03540 | hp2 | a0001 | c0002 | t0001 | g0081 | AFR | GWD | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG03579 | hp1 | a0001 | c0002 | t0001 | g0076 | AFR | MSL | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG03579 | hp2 | a0001 | c0001 | t0003 | g0277 | AFR | MSL | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG03654 | hp1 | a0001 | c0001 | t0003 | g0102 | SAS | PJL | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG03654 | hp2 | a0001 | c0001 | t0003 | g0104 | SAS | PJL | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG03669 | hp1 | a0001 | c0002 | t0001 | g0010 | SAS | PJL | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0274 | SAS | STU | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG03688 | hp2 | a0001 | c0002 | t0001 | g0019 | SAS | STU | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0233 | SAS | PJL | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0206 | SAS | PJL | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0127 | SAS | BEB | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG03831 | hp2 | a0002 | c0003 | t0001 | g0244 | SAS | BEB | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG03834 | hp1 | a0001 | c0001 | t0003 | g0103 | SAS | BEB | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG03834 | hp2 | a0001 | c0002 | t0001 | g0035 | SAS | BEB | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG03927 | hp1 | a0001 | c0002 | t0001 | g0068 | SAS | BEB | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0213 | SAS | BEB | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG03942 | hp1 | a0001 | c0001 | t0003 | g0105 | SAS | BEB | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG03942 | hp2 | a0001 | c0002 | t0001 | g0010 | SAS | BEB | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG04184 | hp1 | a0002 | c0003 | t0001 | g0054 | SAS | BEB | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0219 | SAS | BEB | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG04199 | hp1 | a0002 | c0003 | t0001 | g0268 | SAS | STU | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG04199 | hp2 | a0001 | c0002 | t0001 | g0038 | SAS | STU | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG04204 | hp1 | a0001 | c0001 | t0003 | g0111 | SAS | STU | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG04204 | hp2 | a0002 | c0003 | t0001 | g0241 | SAS | STU | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0218 | SAS | STU | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG04228 | hp2 | a0001 | c0001 | t0003 | g0136 | SAS | STU | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | CHB | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA18612 | hp2 | a0001 | c0002 | t0001 | g0170 | EAS | CHB | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA18747 | hp1 | a0001 | c0002 | t0001 | g0200 | EAS | CHB | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | CHB | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA18906 | hp1 | a0001 | c0002 | t0001 | g0264 | AFR | YRI | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA18906 | hp2 | a0001 | c0001 | t0004 | g0190 | AFR | YRI | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA18939 | hp2 | a0001 | c0001 | t0002 | g0296 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA18940 | hp2 | a0001 | c0002 | t0001 | g0017 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA18942 | hp1 | a0004 | c0011 | t0001 | g0013 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA18942 | hp2 | a0001 | c0002 | t0001 | g0084 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA18944 | hp1 | a0001 | c0002 | t0001 | g0040 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA18944 | hp2 | a0001 | c0001 | t0002 | g0295 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA18945 | hp1 | a0001 | c0001 | t0002 | g0298 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA18945 | hp2 | a0001 | c0002 | t0001 | g0318 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA18949 | hp1 | a0002 | c0013 | t0001 | g0045 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA18957 | hp1 | a0001 | c0009 | t0001 | g0002 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA18957 | hp2 | a0001 | c0002 | t0001 | g0065 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA18960 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA18960 | hp2 | a0002 | c0003 | t0001 | g0046 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA18962 | hp1 | a0001 | c0002 | t0001 | g0100 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA18965 | hp1 | a0001 | c0002 | t0001 | g0098 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA18967 | hp1 | a0002 | c0003 | t0001 | g0036 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA18969 | hp1 | a0001 | c0002 | t0001 | g0006 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA18969 | hp2 | a0004 | c0011 | t0001 | g0013 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0299 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA18970 | hp2 | a0001 | c0009 | t0001 | g0002 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA18971 | hp2 | a0001 | c0002 | t0001 | g0020 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA18973 | hp1 | a0001 | c0001 | t0002 | g0306 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA18973 | hp2 | a0001 | c0002 | t0001 | g0073 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA18974 | hp1 | a0001 | c0001 | t0002 | g0279 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA18974 | hp2 | a0001 | c0002 | t0001 | g0034 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA18977 | hp1 | a0001 | c0002 | t0001 | g0131 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA18979 | hp1 | a0001 | c0002 | t0001 | g0006 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA18979 | hp2 | a0001 | c0001 | t0002 | g0287 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA18981 | hp1 | a0001 | c0001 | t0002 | g0297 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA18982 | hp1 | a0001 | c0002 | t0001 | g0285 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0307 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA18984 | hp2 | a0001 | c0001 | t0002 | g0310 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA18985 | hp1 | a0001 | c0002 | t0001 | g0276 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA18989 | hp2 | a0001 | c0002 | t0001 | g0006 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA18992 | hp1 | a0001 | c0002 | t0001 | g0017 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA18993 | hp2 | a0001 | c0001 | t0002 | g0316 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0280 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA18994 | hp2 | a0001 | c0002 | t0001 | g0202 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA18997 | hp1 | a0001 | c0002 | t0001 | g0319 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA18997 | hp2 | a0001 | c0001 | t0002 | g0312 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA19001 | hp1 | a0002 | c0003 | t0001 | g0052 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA19001 | hp2 | a0001 | c0002 | t0001 | g0082 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA19003 | hp1 | a0001 | c0002 | t0001 | g0088 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA19003 | hp2 | a0001 | c0001 | t0002 | g0327 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0328 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA19005 | hp1 | a0001 | c0002 | t0008 | g0041 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA19006 | hp1 | a0001 | c0001 | t0002 | g0303 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA19006 | hp2 | a0001 | c0002 | t0001 | g0317 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA19007 | hp1 | a0001 | c0002 | t0001 | g0201 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA19009 | hp2 | a0001 | c0002 | t0001 | g0314 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0321 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA19011 | hp1 | a0001 | c0009 | t0001 | g0002 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA19011 | hp2 | a0001 | c0002 | t0001 | g0011 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA19030 | hp1 | a0001 | c0001 | t0004 | g0186 | AFR | LWK | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA19030 | hp2 | a0001 | c0007 | t0001 | g0032 | AFR | LWK | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA19043 | hp1 | a0001 | c0001 | t0007 | g0119 | AFR | LWK | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA19043 | hp2 | a0001 | c0001 | t0003 | g0320 | AFR | LWK | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA19054 | hp2 | a0001 | c0001 | t0002 | g0311 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA19056 | hp1 | a0001 | c0002 | t0001 | g0072 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA19057 | hp2 | a0001 | c0002 | t0001 | g0074 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA19062 | hp1 | a0001 | c0002 | t0001 | g0059 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA19063 | hp1 | a0001 | c0001 | t0002 | g0300 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA19063 | hp2 | a0002 | c0003 | t0001 | g0085 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA19064 | hp1 | a0002 | c0003 | t0001 | g0047 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA19065 | hp2 | a0001 | c0002 | t0001 | g0011 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA19066 | hp2 | a0001 | c0002 | t0001 | g0286 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0325 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA19075 | hp1 | a0001 | c0001 | t0002 | g0172 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA19075 | hp2 | a0002 | c0003 | t0001 | g0057 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA19078 | hp2 | a0001 | c0001 | t0002 | g0315 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA19079 | hp1 | a0001 | c0009 | t0001 | g0002 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA19079 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA19080 | hp1 | a0001 | c0002 | t0001 | g0203 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA19080 | hp2 | a0002 | c0003 | t0001 | g0051 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA19082 | hp1 | a0002 | c0003 | t0001 | g0053 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA19082 | hp2 | a0001 | c0001 | t0002 | g0199 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA19083 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA19083 | hp2 | a0001 | c0002 | t0001 | g0075 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA19087 | hp1 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA19087 | hp2 | a0001 | c0002 | t0001 | g0070 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA19088 | hp1 | a0001 | c0002 | t0001 | g0275 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0304 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA19090 | hp2 | a0001 | c0002 | t0001 | g0284 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA19240 | hp1 | a0001 | c0005 | t0001 | g0004 | AFR | YRI | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0120 | AFR | YRI | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0163 | AFR | ASW | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0101 | AFR | ASW | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA20752 | hp1 | a0001 | c0002 | t0001 | g0014 | EUR | TSI | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA20752 | hp2 | a0003 | c0004 | t0003 | g0106 | EUR | TSI | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA20905 | hp1 | a0001 | c0001 | t0003 | g0113 | SAS | GIH | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA20905 | hp2 | a0001 | c0002 | t0001 | g0014 | SAS | GIH | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG01123 | hp1 | a0003 | c0004 | t0003 | g0239 | AMR | CLM | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0225 | AMR | CLM | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG02109 | hp1 | a0001 | c0001 | t0004 | g0180 | AFR | ACB | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG02109 | hp2 | a0001 | c0007 | t0001 | g0123 | AFR | ACB | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG02486 | hp1 | a0001 | c0002 | t0001 | g0266 | AFR | ACB | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG02486 | hp2 | a0001 | c0005 | t0001 | g0027 | AFR | ACB | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG02559 | hp1 | a0001 | c0008 | t0003 | g0221 | AFR | ACB | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG02559 | hp2 | a0001 | c0001 | t0003 | g0324 | AFR | ACB | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG03471 | hp1 | a0001 | c0001 | t0004 | g0181 | AFR | MSL | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG03471 | hp2 | a0001 | c0005 | t0001 | g0004 | AFR | MSL | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG06807 | hp1 | a0001 | c0001 | t0006 | g0247 | AFR | USA | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG06807 | hp2 | a0001 | c0002 | t0001 | g0262 | AFR | USA | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA20300 | hp1 | a0002 | c0003 | t0001 | g0245 | AFR | USA | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA20300 | hp2 | a0001 | c0008 | t0003 | g0231 | AFR | USA | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA21309 | hp1 | a0002 | c0003 | t0001 | g0255 | AFR | LWK | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA21309 | hp2 | a0001 | c0007 | t0001 | g0118 | AFR | LWK | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0140 | REF | REF | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0004 | g0227 | REF | REF | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:48080078
|
C | T | 1 | a0003 | 11 | HG00323.hp1 HG00639.hp2 HG01109.hp1 others(8): Show |
missense_variant | MODERATE | c.1007G>A | p.Arg336Gln | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 11/15 | 1087/2908 | 1007/1584 | 336/527 | chr4 | 48080078 | ||
| chr4:48094151
|
T | C | 1 | a0004 | 2 | NA18942.hp1 NA18969.hp2 |
missense_variant | MODERATE | c.635A>G | p.Gln212Arg | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 8/15 | 715/2908 | 635/1584 | 212/527 | chr4 | 48094151 | ||
| chr4:48112500
|
G | A | 1 | a0005 | 1 | HG01515.hp2 | missense_variant | MODERATE | c.187C>T | p.Arg63Cys | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 4/15 | 267/2908 | 187/1584 | 63/527 | chr4 | 48112500 | ||
| chr4:48113247
|
C | T | 1 | a0002 | 49 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(46): Show |
missense_variant | MODERATE | c.134G>A | p.Arg45His | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 3/15 | 214/2908 | 134/1584 | 45/527 | chr4 | 48113247 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:48067658
|
T | A | 1 | a0002c0013 | 1 | NA18949.hp1 | synonymous_variant | LOW | c.1563A>T | p.Thr521Thr | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 15/15 | 1643/2908 | 1563/1584 | 521/527 | chr4 | 48067658 | ||
| chr4:48067667
|
C | A | 1 | a0002c0013 | 1 | NA18949.hp1 | synonymous_variant | LOW | c.1554G>T | p.Arg518Arg | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 15/15 | 1634/2908 | 1554/1584 | 518/527 | chr4 | 48067667 | ||
| chr4:48067679
|
G | C | 5 | a0001c0002a0001c0010a0001c0014others(2): Show | 148 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(145): Show |
synonymous_variant | LOW | c.1542C>G | p.Ala514Ala | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 15/15 | 1622/2908 | 1542/1584 | 514/527 | chr4 | 48067679 | ||
| chr4:48089751
|
G | A | 1 | a0001c0007 | 6 | HG01255.hp1 HG02109.hp2 HG02145.hp1 others(3): Show |
splice_region_variant&synonymous_variant | LOW | c.783C>T | p.Tyr261Tyr | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 9/15 | 863/2908 | 783/1584 | 261/527 | chr4 | 48089751 | ||
| chr4:48094084
|
A | G | 3 | a0001c0005a0001c0006a0001c0014 | 16 | HG01884.hp1 HG02145.hp2 HG02257.hp1 others(13): Show |
synonymous_variant | LOW | c.702T>C | p.Asn234Asn | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 8/15 | 782/2908 | 702/1584 | 234/527 | chr4 | 48094084 | ||
| chr4:48095163
|
G | A | 1 | a0001c0015 | 1 | HG01243.hp2 | synonymous_variant | LOW | c.561C>T | p.Ser187Ser | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 7/15 | 641/2908 | 561/1584 | 187/527 | chr4 | 48095163 | ||
| chr4:48095163
|
G | T | 2 | a0001c0008a0001c0010 | 6 | HG02559.hp1 HG02717.hp2 HG02886.hp2 others(3): Show |
synonymous_variant | LOW | c.561C>A | p.Ser187Ser | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 7/15 | 641/2908 | 561/1584 | 187/527 | chr4 | 48095163 | ||
| chr4:48110594
|
G | A | 1 | a0001c0009 | 4 | NA18957.hp1 NA18970.hp2 NA19011.hp1 others(1): Show |
synonymous_variant | LOW | c.390C>T | p.Gly130Gly | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 5/15 | 470/2908 | 390/1584 | 130/527 | chr4 | 48110594 | ||
| chr4:48112489
|
C | T | 2 | a0001c0005a0001c0014 | 9 | HG02257.hp1 HG02486.hp2 HG02572.hp2 others(6): Show |
synonymous_variant | LOW | c.198G>A | p.Pro66Pro | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 4/15 | 278/2908 | 198/1584 | 66/527 | chr4 | 48112489 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:48066429
|
T | C | 1 | a0001c0002t0008 | 1 | NA19005.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1208A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 15/15 | 1208 | chr4 | 48066429 | |||||
| chr4:48066608
|
T | C | 24 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(21): Show | 343 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(340): Show |
3_prime_UTR_variant | MODIFIER | c.*1029A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 15/15 | 1029 | chr4 | 48066608 | |||||
| chr4:48066610
|
A | T | 18 | a0001c0001t0001a0001c0001t0002a0001c0001t0007others(15): Show | 302 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(299): Show |
3_prime_UTR_variant | MODIFIER | c.*1027T>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 15/15 | 1027 | chr4 | 48066610 | |||||
| chr4:48066766
|
G | A | 3 | a0001c0001t0002a0001c0001t0009a0002c0012t0002 | 64 | HG00140.hp1 HG00438.hp2 HG00597.hp2 others(61): Show |
3_prime_UTR_variant | MODIFIER | c.*871C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 15/15 | 871 | chr4 | 48066766 | |||||
| chr4:48067270
|
T | A | 18 | a0001c0001t0001a0001c0001t0002a0001c0001t0007others(15): Show | 302 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(299): Show |
3_prime_UTR_variant | MODIFIER | c.*367A>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 15/15 | 367 | chr4 | 48067270 | |||||
| chr4:48067275
|
C | T | 1 | a0001c0001t0007 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*362G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 15/15 | 362 | chr4 | 48067275 | |||||
| chr4:48067304
|
T | C | 1 | a0001c0001t0005 | 5 | HG01884.hp2 HG02572.hp1 HG02630.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*333A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 15/15 | 333 | chr4 | 48067304 | |||||
| chr4:48067371
|
G | A | 1 | a0001c0001t0009 | 1 | HG02698.hp1 | 3_prime_UTR_variant | MODIFIER | c.*266C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 15/15 | 266 | chr4 | 48067371 | |||||
| chr4:48067445
|
A | G | 2 | a0001c0001t0006a0001c0008t0006 | 2 | HG02886.hp2 HG06807.hp1 |
3_prime_UTR_variant | MODIFIER | c.*192T>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 15/15 | 192 | chr4 | 48067445 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:48067708
|
G | A | 134 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0010others(131): Show | 148 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(145): Show |
splice_region_variant&intron_variant | LOW | c.1516-3C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 14/14 | chr4 | 48067708 | ||||||
| chr4:48067720
|
T | G | 1 | a0001c0001t0005g0333 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1516-15A>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 14/14 | chr4 | 48067720 | ||||||
| chr4:48067883
|
C | G | 1 | a0002c0003t0001g0056 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1516-178G>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 14/14 | chr4 | 48067883 | ||||||
| chr4:48067936
|
A | T | 1 | a0002c0013t0001g0045 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1516-231T>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 14/14 | chr4 | 48067936 | ||||||
| chr4:48068056
|
C | T | 1 | a0002c0003t0001g0173 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1516-351G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 14/14 | chr4 | 48068056 | ||||||
| chr4:48068213
|
C | T | 1 | a0001c0001t0003g0323 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1516-508G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 14/14 | chr4 | 48068213 | ||||||
| chr4:48068838
|
G | A | 314 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0021others(311): Show | 343 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(340): Show |
intron_variant | MODIFIER | c.1516-1133C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 14/14 | chr4 | 48068838 | ||||||
| chr4:48068913
|
G | GCTCTGTG others(130): Show |
79 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0010others(76): Show | 87 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.1516-1209_1516-120 others(141): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 14/14 | chr4 | 48068913 | ||||||
| chr4:48068934
|
T | C | 46 | a0001c0002t0001g0014a0001c0002t0001g0090a0001c0002t0001g0229others(43): Show | 52 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(49): Show |
intron_variant | MODIFIER | c.1516-1229A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 14/14 | chr4 | 48068934 | ||||||
| chr4:48068936
|
C | T | 277 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0021others(274): Show | 302 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(299): Show |
intron_variant | MODIFIER | c.1516-1231G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 14/14 | chr4 | 48068936 | ||||||
| chr4:48069173
|
A | G | 277 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0021others(274): Show | 302 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(299): Show |
intron_variant | MODIFIER | c.1516-1468T>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 14/14 | chr4 | 48069173 | ||||||
| chr4:48069218
|
C | T | 277 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0021others(274): Show | 302 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(299): Show |
intron_variant | MODIFIER | c.1516-1513G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 14/14 | chr4 | 48069218 | ||||||
| chr4:48069321
|
C | A | 1 | a0001c0001t0002g0315 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1516-1616G>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 14/14 | chr4 | 48069321 | ||||||
| chr4:48069322
|
T | A | 1 | a0001c0001t0002g0315 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1516-1617A>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 14/14 | chr4 | 48069322 | ||||||
| chr4:48069323
|
T | A | 1 | a0001c0001t0002g0315 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1516-1618A>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 14/14 | chr4 | 48069323 | ||||||
| chr4:48069324
|
T | G | 1 | a0001c0001t0002g0315 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1516-1619A>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 14/14 | chr4 | 48069324 | ||||||
| chr4:48069325
|
T | A | 1 | a0001c0001t0002g0315 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1516-1620A>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 14/14 | chr4 | 48069325 | ||||||
| chr4:48069326
|
C | A | 1 | a0001c0001t0002g0315 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1516-1621G>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 14/14 | chr4 | 48069326 | ||||||
| chr4:48069326
|
C | CTT | 15 | a0001c0001t0003g0277a0001c0001t0003g0281a0001c0001t0003g0288others(12): Show | 15 | HG01891.hp1 HG02258.hp1 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.1516-1623_1516-162 others(6): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 14/14 | chr4 | 48069326 | ||||||
| chr4:48069327
|
T | A | 1 | a0001c0001t0002g0315 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1516-1622A>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 14/14 | chr4 | 48069327 | ||||||
| chr4:48069327
|
T | TTTTC | 51 | a0001c0002t0001g0014a0001c0002t0001g0090a0001c0002t0001g0200others(48): Show | 57 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(54): Show |
intron_variant | MODIFIER | c.1516-1623_1516-162 others(8): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 14/14 | chr4 | 48069327 | ||||||
| chr4:48069328
|
T | A | 1 | a0001c0001t0002g0315 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1516-1623A>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 14/14 | chr4 | 48069328 | ||||||
| chr4:48069328
|
T | TTTC | 221 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0021others(218): Show | 240 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(237): Show |
intron_variant | MODIFIER | c.1516-1624_1516-162 others(7): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 14/14 | chr4 | 48069328 | ||||||
| chr4:48069329
|
T | A | 1 | a0001c0001t0002g0315 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1516-1624A>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 14/14 | chr4 | 48069329 | ||||||
| chr4:48069330
|
T | A | 1 | a0001c0001t0002g0315 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1516-1625A>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 14/14 | chr4 | 48069330 | ||||||
| chr4:48069331
|
T | G | 1 | a0001c0001t0002g0315 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1516-1626A>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 14/14 | chr4 | 48069331 | ||||||
| chr4:48069332
|
T | A | 1 | a0001c0001t0002g0315 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1516-1627A>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 14/14 | chr4 | 48069332 | ||||||
| chr4:48069332
|
T | C | 51 | a0001c0002t0001g0014a0001c0002t0001g0090a0001c0002t0001g0200others(48): Show | 57 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(54): Show |
intron_variant | MODIFIER | c.1516-1627A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 14/14 | chr4 | 48069332 | ||||||
| chr4:48069333
|
T | C | 223 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0021others(220): Show | 242 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(239): Show |
intron_variant | MODIFIER | c.1516-1628A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 14/14 | chr4 | 48069333 | ||||||
| chr4:48069335
|
T | G | 1 | a0001c0001t0002g0315 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1516-1630A>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 14/14 | chr4 | 48069335 | ||||||
| chr4:48069336
|
T | A | 1 | a0001c0001t0002g0315 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1516-1631A>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 14/14 | chr4 | 48069336 | ||||||
| chr4:48069340
|
T | A | 1 | a0001c0001t0002g0315 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1516-1635A>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 14/14 | chr4 | 48069340 | ||||||
| chr4:48069356
|
G | T | 1 | a0001c0001t0002g0315 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1516-1651C>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 14/14 | chr4 | 48069356 | ||||||
| chr4:48069365
|
A | T | 1 | a0001c0001t0002g0315 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1516-1660T>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 14/14 | chr4 | 48069365 | ||||||
| chr4:48069374
|
G | A | 1 | a0001c0001t0002g0315 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1516-1669C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 14/14 | chr4 | 48069374 | ||||||
| chr4:48069375
|
G | C | 1 | a0001c0001t0002g0315 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1516-1670C>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 14/14 | chr4 | 48069375 | ||||||
| chr4:48069385
|
G | T | 1 | a0001c0001t0002g0315 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1516-1680C>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 14/14 | chr4 | 48069385 | ||||||
| chr4:48069386
|
T | G | 1 | a0001c0001t0002g0315 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1516-1681A>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 14/14 | chr4 | 48069386 | ||||||
| chr4:48069388
|
G | C | 1 | a0001c0001t0002g0315 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1516-1683C>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 14/14 | chr4 | 48069388 | ||||||
| chr4:48069389
|
G | A | 1 | a0001c0001t0002g0315 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1516-1684C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 14/14 | chr4 | 48069389 | ||||||
| chr4:48069393
|
T | A | 1 | a0001c0001t0002g0315 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1516-1688A>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 14/14 | chr4 | 48069393 | ||||||
| chr4:48069406
|
A | G | 1 | a0001c0001t0002g0315 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1516-1701T>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 14/14 | chr4 | 48069406 | ||||||
| chr4:48069419
|
A | T | 1 | a0001c0001t0002g0315 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1516-1714T>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 14/14 | chr4 | 48069419 | ||||||
| chr4:48069422
|
T | G | 1 | a0001c0001t0002g0315 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1516-1717A>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 14/14 | chr4 | 48069422 | ||||||
| chr4:48069424
|
C | T | 1 | a0001c0001t0002g0315 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1516-1719G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 14/14 | chr4 | 48069424 | ||||||
| chr4:48069426
|
A | C | 1 | a0001c0001t0002g0315 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1516-1721T>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 14/14 | chr4 | 48069426 | ||||||
| chr4:48069432
|
T | C | 1 | a0001c0001t0002g0315 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1516-1727A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 14/14 | chr4 | 48069432 | ||||||
| chr4:48069434
|
T | G | 1 | a0001c0001t0002g0315 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1516-1729A>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 14/14 | chr4 | 48069434 | ||||||
| chr4:48069437
|
T | A | 1 | a0001c0001t0002g0315 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1516-1732A>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 14/14 | chr4 | 48069437 | ||||||
| chr4:48069453
|
G | A | 1 | a0001c0001t0002g0315 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1516-1748C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 14/14 | chr4 | 48069453 | ||||||
| chr4:48069463
|
T | C | 1 | a0001c0001t0002g0315 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1516-1758A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 14/14 | chr4 | 48069463 | ||||||
| chr4:48069562
|
G | A | 1 | a0001c0002t0001g0270 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1516-1857C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 14/14 | chr4 | 48069562 | ||||||
| chr4:48069569
|
G | A | 19 | a0001c0001t0003g0277a0001c0001t0003g0281a0001c0001t0003g0288others(16): Show | 20 | HG01884.hp2 HG01891.hp1 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.1516-1864C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 14/14 | chr4 | 48069569 | ||||||
| chr4:48069578
|
A | G | 276 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0021others(273): Show | 301 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(298): Show |
intron_variant | MODIFIER | c.1516-1873T>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 14/14 | chr4 | 48069578 | ||||||
| chr4:48069621
|
C | T | 1 | a0001c0001t0001g0050 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1515+1896G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 14/14 | chr4 | 48069621 | ||||||
| chr4:48070143
|
TC | T | 88 | a0001c0001t0001g0101a0001c0001t0001g0115a0001c0001t0001g0120others(85): Show | 93 | HG00140.hp1 HG00438.hp2 HG00597.hp2 others(90): Show |
intron_variant | MODIFIER | c.1515+1373delG | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 14/14 | chr4 | 48070143 | ||||||
| chr4:48070188
|
C | G | 296 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0021others(293): Show | 322 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(319): Show |
intron_variant | MODIFIER | c.1515+1329G>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 14/14 | chr4 | 48070188 | ||||||
| chr4:48070225
|
G | T | 1 | a0001c0001t0002g0219 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1515+1292C>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 14/14 | chr4 | 48070225 | ||||||
| chr4:48070264
|
GA | G | 4 | a0001c0002t0001g0234a0001c0002t0001g0270a0001c0010t0001g0117others(1): Show | 4 | HG02615.hp2 HG02717.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.1515+1252delT | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 14/14 | chr4 | 48070264 | ||||||
| chr4:48070349
|
T | A | 18 | a0001c0001t0003g0102a0001c0001t0003g0103a0001c0001t0003g0104others(15): Show | 21 | HG00323.hp1 HG00639.hp2 HG01109.hp1 others(18): Show |
intron_variant | MODIFIER | c.1515+1168A>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 14/14 | chr4 | 48070349 | ||||||
| chr4:48070429
|
C | T | 1 | a0001c0002t0001g0229 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1515+1088G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 14/14 | chr4 | 48070429 | ||||||
| chr4:48070590
|
A | T | 77 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0010others(74): Show | 85 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.1515+927T>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 14/14 | chr4 | 48070590 | ||||||
| chr4:48070623
|
G | C | 1 | a0001c0002t0001g0204 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1515+894C>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 14/14 | chr4 | 48070623 | ||||||
| chr4:48070639
|
C | T | 281 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0021others(278): Show | 307 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.1515+878G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 14/14 | chr4 | 48070639 | ||||||
| chr4:48070696
|
C | A | 296 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0021others(293): Show | 322 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(319): Show |
intron_variant | MODIFIER | c.1515+821G>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 14/14 | chr4 | 48070696 | ||||||
| chr4:48070796
|
C | G | 37 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0002g0048others(34): Show | 39 | HG00438.hp2 HG00597.hp2 HG00609.hp2 others(36): Show |
intron_variant | MODIFIER | c.1515+721G>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 14/14 | chr4 | 48070796 | ||||||
| chr4:48070831
|
G | A | 1 | a0001c0001t0002g0206 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1515+686C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 14/14 | chr4 | 48070831 | ||||||
| chr4:48070859
|
G | A | 1 | a0001c0002t0001g0066 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1515+658C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 14/14 | chr4 | 48070859 | ||||||
| chr4:48070893
|
C | CT | 9 | a0001c0001t0002g0209a0001c0001t0002g0224a0001c0001t0002g0315others(6): Show | 9 | HG00735.hp2 HG01123.hp1 HG01175.hp2 others(6): Show |
intron_variant | MODIFIER | c.1515+623dupA | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 14/14 | chr4 | 48070893 | ||||||
| chr4:48070893
|
CT | C | 96 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0021others(93): Show | 105 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(102): Show |
intron_variant | MODIFIER | c.1515+623delA | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 14/14 | chr4 | 48070893 | ||||||
| chr4:48070893
|
CTT | C | 5 | a0001c0001t0001g0120a0001c0001t0003g0324a0001c0001t0005g0018others(2): Show | 6 | HG01884.hp2 HG02559.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.1515+622_1515+623d others(4): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 14/14 | chr4 | 48070893 | ||||||
| chr4:48071056
|
C | T | 62 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0002g0048others(59): Show | 64 | HG00140.hp1 HG00438.hp2 HG00597.hp2 others(61): Show |
intron_variant | MODIFIER | c.1515+461G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 14/14 | chr4 | 48071056 | ||||||
| chr4:48071283
|
G | C | 222 | a0001c0001t0001g0101a0001c0001t0001g0115a0001c0001t0001g0120others(219): Show | 241 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(238): Show |
intron_variant | MODIFIER | c.1515+234C>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 14/14 | chr4 | 48071283 | ||||||
| chr4:48071284
|
A | G | 1 | a0001c0001t0002g0064 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1515+233T>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 14/14 | chr4 | 48071284 | ||||||
| chr4:48071297
|
A | C | 4 | a0001c0001t0005g0018a0001c0001t0005g0039a0001c0001t0005g0332others(1): Show | 5 | HG01884.hp2 HG02572.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1515+220T>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 14/14 | chr4 | 48071297 | ||||||
| chr4:48071339
|
A | T | 79 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0010others(76): Show | 87 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.1515+178T>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 14/14 | chr4 | 48071339 | ||||||
| chr4:48071356
|
T | C | 8 | a0001c0001t0003g0277a0001c0001t0003g0281a0001c0001t0003g0288others(5): Show | 8 | HG01891.hp1 HG02258.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.1515+161A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 14/14 | chr4 | 48071356 | ||||||
| chr4:48071484
|
G | T | 281 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0021others(278): Show | 307 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.1515+33C>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 14/14 | chr4 | 48071484 | ||||||
| chr4:48071919
|
C | T | 15 | a0001c0001t0003g0277a0001c0001t0003g0281a0001c0001t0003g0288others(12): Show | 15 | HG01891.hp1 HG02258.hp1 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.1358-245G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 13/14 | chr4 | 48071919 | ||||||
| chr4:48071920
|
T | C | 222 | a0001c0001t0001g0101a0001c0001t0001g0115a0001c0001t0001g0120others(219): Show | 241 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(238): Show |
intron_variant | MODIFIER | c.1358-246A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 13/14 | chr4 | 48071920 | ||||||
| chr4:48071956
|
C | CT | 220 | a0001c0001t0001g0101a0001c0001t0001g0115a0001c0001t0001g0120others(217): Show | 239 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(236): Show |
intron_variant | MODIFIER | c.1358-283dupA | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 13/14 | chr4 | 48071956 | ||||||
| chr4:48071984
|
C | T | 1 | a0001c0001t0003g0290 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1358-310G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 13/14 | chr4 | 48071984 | ||||||
| chr4:48072118
|
T | G | 1 | a0002c0003t0001g0242 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1358-444A>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 13/14 | chr4 | 48072118 | ||||||
| chr4:48072155
|
C | G | 1 | a0001c0001t0003g0103 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1358-481G>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 13/14 | chr4 | 48072155 | ||||||
| chr4:48072669
|
T | C | 2 | a0001c0001t0006g0247a0001c0008t0006g0232 | 2 | HG02886.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1358-995A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 13/14 | chr4 | 48072669 | ||||||
| chr4:48072702
|
T | C | 1 | a0001c0001t0003g0277 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1358-1028A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 13/14 | chr4 | 48072702 | ||||||
| chr4:48073010
|
A | T | 1 | a0001c0002t0001g0082 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1357+925T>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 13/14 | chr4 | 48073010 | ||||||
| chr4:48073091
|
A | AT | 167 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0021others(164): Show | 180 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(177): Show |
intron_variant | MODIFIER | c.1357+843dupA | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 13/14 | chr4 | 48073091 | ||||||
| chr4:48073091
|
A | ATT | 59 | a0001c0001t0001g0148a0001c0001t0002g0206a0001c0001t0002g0287others(56): Show | 65 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(62): Show |
intron_variant | MODIFIER | c.1357+842_1357+843d others(4): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 13/14 | chr4 | 48073091 | ||||||
| chr4:48073091
|
A | ATTT | 77 | a0001c0001t0002g0064a0001c0002t0001g0003a0001c0002t0001g0006others(74): Show | 85 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.1357+841_1357+843d others(5): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 13/14 | chr4 | 48073091 | ||||||
| chr4:48073117
|
G | T | 2 | a0001c0002t0001g0069a0001c0002t0001g0071 | 2 | HG02602.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.1357+818C>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 13/14 | chr4 | 48073117 | ||||||
| chr4:48073582
|
T | C | 1 | a0001c0001t0007g0119 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1357+353A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 13/14 | chr4 | 48073582 | ||||||
| chr4:48073814
|
A | G | 1 | a0001c0007t0001g0123 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1357+121T>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 13/14 | chr4 | 48073814 | ||||||
| chr4:48074074
|
G | A | 20 | a0001c0001t0001g0115a0001c0001t0001g0120a0001c0001t0003g0102others(17): Show | 23 | HG00323.hp1 HG00639.hp2 HG01109.hp1 others(20): Show |
intron_variant | MODIFIER | c.1239-21C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 12/14 | chr4 | 48074074 | ||||||
| chr4:48074106
|
T | C | 1 | a0001c0001t0001g0115 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1239-53A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 12/14 | chr4 | 48074106 | ||||||
| chr4:48074231
|
A | G | 83 | a0001c0001t0001g0101a0001c0001t0001g0178a0001c0001t0002g0015others(80): Show | 88 | HG00140.hp1 HG00597.hp2 HG00609.hp2 others(85): Show |
intron_variant | MODIFIER | c.1239-178T>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 12/14 | chr4 | 48074231 | ||||||
| chr4:48074300
|
C | T | 1 | a0001c0002t0001g0080 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1239-247G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 12/14 | chr4 | 48074300 | ||||||
| chr4:48074376
|
TA | T | 3 | a0001c0002t0001g0010a0001c0002t0001g0035a0001c0002t0001g0038 | 4 | HG03669.hp1 HG03834.hp2 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.1239-324delT | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 12/14 | chr4 | 48074376 | ||||||
| chr4:48074468
|
C | T | 6 | a0001c0006t0001g0028a0001c0006t0001g0029a0001c0006t0001g0030others(3): Show | 6 | HG02109.hp2 HG02145.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.1239-415G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 12/14 | chr4 | 48074468 | ||||||
| chr4:48074469
|
G | A | 57 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0021others(54): Show | 64 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(61): Show |
intron_variant | MODIFIER | c.1239-416C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 12/14 | chr4 | 48074469 | ||||||
| chr4:48074545
|
T | A | 138 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0021others(135): Show | 150 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(147): Show |
intron_variant | MODIFIER | c.1239-492A>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 12/14 | chr4 | 48074545 | ||||||
| chr4:48074689
|
TGAG | T | 4 | a0001c0001t0001g0178a0001c0006t0001g0095a0001c0006t0001g0125others(1): Show | 4 | HG01884.hp1 HG02895.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1239-639_1239-637d others(5): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 12/14 | chr4 | 48074689 | ||||||
| chr4:48074707
|
A | G | 25 | a0001c0001t0003g0277a0001c0001t0003g0281a0001c0001t0003g0288others(22): Show | 27 | HG01891.hp1 HG02258.hp1 HG02486.hp2 others(24): Show |
intron_variant | MODIFIER | c.1239-654T>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 12/14 | chr4 | 48074707 | ||||||
| chr4:48074976
|
G | A | 1 | a0001c0001t0004g0188 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1239-923C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 12/14 | chr4 | 48074976 | ||||||
| chr4:48075070
|
C | T | 1 | a0002c0003t0001g0173 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1239-1017G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 12/14 | chr4 | 48075070 | ||||||
| chr4:48075089
|
G | A | 56 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0021others(53): Show | 63 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(60): Show |
intron_variant | MODIFIER | c.1239-1036C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 12/14 | chr4 | 48075089 | ||||||
| chr4:48075121
|
A | G | 1 | a0001c0001t0004g0190 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1239-1068T>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 12/14 | chr4 | 48075121 | ||||||
| chr4:48075247
|
C | T | 49 | a0001c0001t0002g0279a0001c0002t0001g0014a0001c0002t0001g0090others(46): Show | 55 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(52): Show |
intron_variant | MODIFIER | c.1238+1155G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 12/14 | chr4 | 48075247 | ||||||
| chr4:48075300
|
T | C | 1 | a0001c0001t0007g0119 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1238+1102A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 12/14 | chr4 | 48075300 | ||||||
| chr4:48075312
|
T | C | 54 | a0001c0001t0001g0101a0001c0001t0003g0320a0001c0002t0001g0014others(51): Show | 60 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(57): Show |
intron_variant | MODIFIER | c.1238+1090A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 12/14 | chr4 | 48075312 | ||||||
| chr4:48075367
|
C | T | 4 | a0003c0004t0003g0001a0003c0004t0003g0109a0003c0004t0003g0110others(1): Show | 7 | HG00323.hp1 HG01109.hp1 HG01358.hp2 others(4): Show |
intron_variant | MODIFIER | c.1238+1035G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 12/14 | chr4 | 48075367 | ||||||
| chr4:48075676
|
A | G | 1 | a0001c0001t0003g0105 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1238+726T>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 12/14 | chr4 | 48075676 | ||||||
| chr4:48075805
|
A | C | 301 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0021others(298): Show | 329 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(326): Show |
intron_variant | MODIFIER | c.1238+597T>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 12/14 | chr4 | 48075805 | ||||||
| chr4:48075827
|
G | A | 1 | a0001c0001t0003g0288 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1238+575C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 12/14 | chr4 | 48075827 | ||||||
| chr4:48075875
|
C | A | 1 | a0001c0001t0001g0101 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1238+527G>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 12/14 | chr4 | 48075875 | ||||||
| chr4:48075945
|
G | T | 1 | a0001c0015t0001g0033 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1238+457C>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 12/14 | chr4 | 48075945 | ||||||
| chr4:48076576
|
C | A | 226 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0021others(223): Show | 246 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(243): Show |
intron_variant | MODIFIER | c.1174-110G>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 11/14 | chr4 | 48076576 | ||||||
| chr4:48076968
|
A | G | 15 | a0001c0001t0001g0178a0001c0005t0001g0004a0001c0005t0001g0022others(12): Show | 17 | HG01884.hp1 HG02145.hp2 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.1174-502T>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 11/14 | chr4 | 48076968 | ||||||
| chr4:48077271
|
A | C | 8 | a0001c0002t0001g0037a0001c0002t0001g0060a0001c0002t0001g0061others(5): Show | 8 | HG00558.hp2 HG00597.hp1 HG02602.hp2 others(5): Show |
intron_variant | MODIFIER | c.1174-805T>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 11/14 | chr4 | 48077271 | ||||||
| chr4:48077273
|
G | GTAAAC | 309 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0021others(306): Show | 337 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(334): Show |
intron_variant | MODIFIER | c.1174-808_1174-807i others(7): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 11/14 | chr4 | 48077273 | ||||||
| chr4:48077519
|
G | GA | 309 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0021others(306): Show | 337 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(334): Show |
intron_variant | MODIFIER | c.1174-1054dupT | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 11/14 | chr4 | 48077519 | ||||||
| chr4:48077579
|
G | A | 2 | a0001c0001t0004g0124a0001c0001t0004g0183 | 2 | HG02723.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1174-1113C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 11/14 | chr4 | 48077579 | ||||||
| chr4:48077907
|
G | A | 309 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0021others(306): Show | 337 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(334): Show |
intron_variant | MODIFIER | c.1174-1441C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 11/14 | chr4 | 48077907 | ||||||
| chr4:48078102
|
G | A | 9 | a0001c0001t0001g0012a0001c0001t0001g0126a0001c0001t0001g0141others(6): Show | 13 | NA18940.hp1 NA18949.hp2 NA18957.hp1 others(10): Show |
intron_variant | MODIFIER | c.1174-1636C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 11/14 | chr4 | 48078102 | ||||||
| chr4:48078178
|
G | A | 3 | a0001c0001t0001g0086a0001c0002t0001g0082a0001c0002t0001g0096 | 3 | HG02129.hp1 NA19001.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.1174-1712C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 11/14 | chr4 | 48078178 | ||||||
| chr4:48078204
|
T | C | 52 | a0001c0001t0002g0228a0001c0001t0006g0247a0001c0002t0001g0014others(49): Show | 58 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(55): Show |
intron_variant | MODIFIER | c.1173+1708A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 11/14 | chr4 | 48078204 | ||||||
| chr4:48078223
|
A | G | 1 | a0001c0001t0003g0320 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1173+1689T>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 11/14 | chr4 | 48078223 | ||||||
| chr4:48078445
|
G | A | 1 | a0001c0002t0001g0203 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.1173+1467C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 11/14 | chr4 | 48078445 | ||||||
| chr4:48078472
|
C | T | 1 | a0001c0015t0001g0033 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1173+1440G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 11/14 | chr4 | 48078472 | ||||||
| chr4:48078519
|
A | C | 287 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0021others(284): Show | 313 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(310): Show |
intron_variant | MODIFIER | c.1173+1393T>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 11/14 | chr4 | 48078519 | ||||||
| chr4:48078556
|
C | T | 51 | a0001c0001t0006g0247a0001c0002t0001g0014a0001c0002t0001g0090others(48): Show | 57 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(54): Show |
intron_variant | MODIFIER | c.1173+1356G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 11/14 | chr4 | 48078556 | ||||||
| chr4:48078590
|
A | G | 1 | a0001c0002t0001g0204 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1173+1322T>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 11/14 | chr4 | 48078590 | ||||||
| chr4:48078632
|
G | C | 58 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0021others(55): Show | 65 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(62): Show |
intron_variant | MODIFIER | c.1173+1280C>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 11/14 | chr4 | 48078632 | ||||||
| chr4:48079099
|
C | A | 8 | a0001c0001t0001g0127a0001c0001t0001g0148a0001c0001t0001g0149others(5): Show | 8 | HG01515.hp2 HG01952.hp2 HG01981.hp1 others(5): Show |
intron_variant | MODIFIER | c.1173+813G>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 11/14 | chr4 | 48079099 | ||||||
| chr4:48079301
|
G | A | 5 | a0001c0001t0006g0247a0001c0002t0001g0256a0001c0002t0001g0269others(2): Show | 5 | HG00642.hp2 HG02615.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1173+611C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 11/14 | chr4 | 48079301 | ||||||
| chr4:48079385
|
C | T | 1 | a0001c0001t0001g0021 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1173+527G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 11/14 | chr4 | 48079385 | ||||||
| chr4:48079454
|
G | A | 1 | a0001c0002t0001g0270 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1173+458C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 11/14 | chr4 | 48079454 | ||||||
| chr4:48079528
|
T | C | 288 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0021others(285): Show | 314 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(311): Show |
intron_variant | MODIFIER | c.1173+384A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 11/14 | chr4 | 48079528 | ||||||
| chr4:48079879
|
CA | C | 124 | a0001c0001t0001g0305a0001c0001t0002g0015a0001c0001t0002g0016others(121): Show | 132 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(129): Show |
intron_variant | MODIFIER | c.1173+32delT | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 11/14 | chr4 | 48079879 | ||||||
| chr4:48080191
|
T | C | 309 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0021others(306): Show | 337 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(334): Show |
intron_variant | MODIFIER | c.957-63A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 10/14 | chr4 | 48080191 | ||||||
| chr4:48080357
|
A | G | 309 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0021others(306): Show | 337 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(334): Show |
intron_variant | MODIFIER | c.957-229T>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 10/14 | chr4 | 48080357 | ||||||
| chr4:48080662
|
T | TCA | 10 | a0001c0001t0001g0153a0001c0001t0007g0119a0001c0002t0001g0019others(7): Show | 10 | HG00280.hp1 HG01099.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.957-536_957-535dup others(2): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 10/14 | chr4 | 48080662 | ||||||
| chr4:48080662
|
T | TCACA | 66 | a0001c0001t0001g0086a0001c0001t0001g0178a0001c0001t0002g0048others(63): Show | 74 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(71): Show |
intron_variant | MODIFIER | c.957-538_957-535dup others(4): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 10/14 | chr4 | 48080662 | ||||||
| chr4:48080662
|
T | TCACACA | 49 | a0001c0001t0001g0115a0001c0001t0001g0305a0001c0001t0002g0015others(46): Show | 55 | HG00323.hp1 HG00544.hp1 HG00558.hp2 others(52): Show |
intron_variant | MODIFIER | c.957-540_957-535dup others(6): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 10/14 | chr4 | 48080662 | ||||||
| chr4:48080662
|
T | TCACACAC others(1): Show |
25 | a0001c0001t0002g0016a0001c0001t0002g0138a0001c0001t0002g0197others(22): Show | 26 | HG00140.hp1 HG00733.hp1 HG00735.hp2 others(23): Show |
intron_variant | MODIFIER | c.957-542_957-535dup others(8): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 10/14 | chr4 | 48080662 | ||||||
| chr4:48080662
|
T | TCACACAC others(3): Show |
20 | a0001c0001t0002g0214a0001c0001t0002g0293a0001c0001t0002g0294others(17): Show | 20 | HG00438.hp2 HG00597.hp2 HG00673.hp2 others(17): Show |
intron_variant | MODIFIER | c.957-544_957-535dup others(10): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 10/14 | chr4 | 48080662 | ||||||
| chr4:48080662
|
T | TCACACAC others(5): Show |
5 | a0001c0001t0001g0120a0001c0001t0002g0207a0001c0001t0002g0297others(2): Show | 5 | HG01099.hp2 HG03041.hp2 NA18981.hp1 others(2): Show |
intron_variant | MODIFIER | c.957-546_957-535dup others(12): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 10/14 | chr4 | 48080662 | ||||||
| chr4:48080662
|
T | TCACACAC others(7): Show |
1 | a0001c0001t0003g0114 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.957-548_957-535dup others(14): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 10/14 | chr4 | 48080662 | ||||||
| chr4:48080662
|
TCA | T | 21 | a0001c0001t0001g0144a0001c0001t0001g0146a0001c0001t0001g0155others(18): Show | 21 | HG00558.hp1 HG00642.hp2 HG00673.hp1 others(18): Show |
intron_variant | MODIFIER | c.957-536_957-535del others(2): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 10/14 | chr4 | 48080662 | ||||||
| chr4:48080662
|
TCACA | T | 56 | a0001c0001t0001g0050a0001c0001t0001g0143a0001c0001t0001g0145others(53): Show | 62 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(59): Show |
intron_variant | MODIFIER | c.957-538_957-535del others(4): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 10/14 | chr4 | 48080662 | ||||||
| chr4:48080662
|
TCACACAC others(1): Show |
T | 6 | a0001c0008t0003g0221a0001c0008t0003g0230a0001c0008t0003g0231others(3): Show | 6 | HG02559.hp1 HG02717.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.957-542_957-535del others(8): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 10/14 | chr4 | 48080662 | ||||||
| chr4:48080664
|
A | T | 2 | a0002c0003t0001g0241a0002c0003t0001g0244 | 2 | HG03831.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.957-536T>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 10/14 | chr4 | 48080664 | ||||||
| chr4:48080666
|
A | T | 5 | a0001c0002t0001g0271a0002c0003t0001g0049a0002c0003t0001g0087others(2): Show | 5 | HG00642.hp2 HG00735.hp1 HG01358.hp1 others(2): Show |
intron_variant | MODIFIER | c.957-538T>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 10/14 | chr4 | 48080666 | ||||||
| chr4:48080668
|
A | T | 46 | a0001c0001t0006g0247a0001c0002t0001g0014a0001c0002t0001g0090others(43): Show | 52 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(49): Show |
intron_variant | MODIFIER | c.957-540T>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 10/14 | chr4 | 48080668 | ||||||
| chr4:48080704
|
A | AC | 3 | a0001c0001t0001g0127a0001c0001t0001g0132a0001c0001t0001g0165 | 3 | HG03831.hp1 NA18993.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.957-577_957-576ins others(1): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 10/14 | chr4 | 48080704 | ||||||
| chr4:48080785
|
G | A | 1 | a0001c0007t0001g0118 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.957-657C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 10/14 | chr4 | 48080785 | ||||||
| chr4:48080864
|
T | C | 1 | a0003c0004t0003g0112 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.957-736A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 10/14 | chr4 | 48080864 | ||||||
| chr4:48080931
|
C | G | 4 | a0001c0001t0001g0178a0001c0006t0001g0095a0001c0006t0001g0125others(1): Show | 4 | HG01884.hp1 HG02895.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.957-803G>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 10/14 | chr4 | 48080931 | ||||||
| chr4:48080997
|
T | G | 1 | a0002c0003t0001g0238 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.957-869A>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 10/14 | chr4 | 48080997 | ||||||
| chr4:48081004
|
G | A | 55 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0021others(52): Show | 62 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(59): Show |
intron_variant | MODIFIER | c.957-876C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 10/14 | chr4 | 48081004 | ||||||
| chr4:48081112
|
T | C | 1 | a0001c0001t0001g0163 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.957-984A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 10/14 | chr4 | 48081112 | ||||||
| chr4:48081277
|
G | A | 1 | a0001c0001t0001g0115 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.957-1149C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 10/14 | chr4 | 48081277 | ||||||
| chr4:48081379
|
C | T | 18 | a0001c0001t0001g0115a0001c0001t0001g0120a0001c0001t0003g0102others(15): Show | 21 | HG00323.hp1 HG00639.hp2 HG01109.hp1 others(18): Show |
intron_variant | MODIFIER | c.957-1251G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 10/14 | chr4 | 48081379 | ||||||
| chr4:48081408
|
A | G | 1 | a0001c0015t0001g0033 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.957-1280T>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 10/14 | chr4 | 48081408 | ||||||
| chr4:48081637
|
G | A | 1 | a0001c0001t0004g0182 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.957-1509C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 10/14 | chr4 | 48081637 | ||||||
| chr4:48081715
|
T | C | 5 | a0001c0001t0003g0277a0001c0001t0003g0281a0001c0001t0003g0288others(2): Show | 5 | HG02258.hp1 HG02559.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.957-1587A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 10/14 | chr4 | 48081715 | ||||||
| chr4:48081868
|
C | T | 51 | a0001c0001t0006g0247a0001c0002t0001g0014a0001c0002t0001g0090others(48): Show | 57 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(54): Show |
intron_variant | MODIFIER | c.957-1740G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 10/14 | chr4 | 48081868 | ||||||
| chr4:48081929
|
G | A | 1 | a0002c0003t0001g0250 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.957-1801C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 10/14 | chr4 | 48081929 | ||||||
| chr4:48081971
|
T | G | 1 | a0001c0001t0003g0320 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.957-1843A>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 10/14 | chr4 | 48081971 | ||||||
| chr4:48082011
|
A | G | 1 | a0001c0001t0003g0289 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.957-1883T>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 10/14 | chr4 | 48082011 | ||||||
| chr4:48082321
|
C | A | 1 | a0001c0001t0007g0119 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.957-2193G>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 10/14 | chr4 | 48082321 | ||||||
| chr4:48082322
|
T | A | 1 | a0001c0001t0007g0119 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.957-2194A>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 10/14 | chr4 | 48082322 | ||||||
| chr4:48082343
|
T | C | 1 | a0001c0001t0006g0247 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.957-2215A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 10/14 | chr4 | 48082343 | ||||||
| chr4:48082345
|
T | A | 1 | a0001c0001t0004g0124 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.957-2217A>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 10/14 | chr4 | 48082345 | ||||||
| chr4:48082365
|
T | C | 1 | a0001c0002t0001g0088 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.957-2237A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 10/14 | chr4 | 48082365 | ||||||
| chr4:48082607
|
T | A | 1 | a0001c0008t0006g0232 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.957-2479A>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 10/14 | chr4 | 48082607 | ||||||
| chr4:48082718
|
C | T | 1 | a0001c0015t0001g0033 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.957-2590G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 10/14 | chr4 | 48082718 | ||||||
| chr4:48082733
|
A | G | 1 | a0001c0002t0001g0072 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.957-2605T>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 10/14 | chr4 | 48082733 | ||||||
| chr4:48082735
|
C | T | 1 | a0002c0003t0001g0043 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.957-2607G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 10/14 | chr4 | 48082735 | ||||||
| chr4:48082736
|
G | A | 1 | a0001c0002t0001g0100 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.957-2608C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 10/14 | chr4 | 48082736 | ||||||
| chr4:48082776
|
C | T | 46 | a0001c0002t0001g0014a0001c0002t0001g0090a0001c0002t0001g0248others(43): Show | 52 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(49): Show |
intron_variant | MODIFIER | c.957-2648G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 10/14 | chr4 | 48082776 | ||||||
| chr4:48082820
|
C | T | 6 | a0001c0007t0001g0032a0001c0007t0001g0107a0001c0007t0001g0118others(3): Show | 6 | HG01255.hp1 HG02109.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.957-2692G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 10/14 | chr4 | 48082820 | ||||||
| chr4:48083206
|
C | T | 1 | a0001c0006t0001g0031 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.957-3078G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 10/14 | chr4 | 48083206 | ||||||
| chr4:48083456
|
G | A | 1 | a0001c0001t0001g0150 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.956+3010C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 10/14 | chr4 | 48083456 | ||||||
| chr4:48083467
|
G | A | 1 | a0001c0001t0001g0120 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.956+2999C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 10/14 | chr4 | 48083467 | ||||||
| chr4:48084110
|
G | T | 19 | a0001c0001t0001g0115a0001c0001t0001g0120a0001c0001t0003g0102others(16): Show | 22 | HG00323.hp1 HG00639.hp2 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.956+2356C>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 10/14 | chr4 | 48084110 | ||||||
| chr4:48084232
|
G | A | 162 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0021others(159): Show | 180 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(177): Show |
intron_variant | MODIFIER | c.956+2234C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 10/14 | chr4 | 48084232 | ||||||
| chr4:48084287
|
T | A | 1 | a0001c0015t0001g0033 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.956+2179A>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 10/14 | chr4 | 48084287 | ||||||
| chr4:48084290
|
C | T | 1 | a0001c0002t0001g0314 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.956+2176G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 10/14 | chr4 | 48084290 | ||||||
| chr4:48084341
|
A | G | 2 | a0001c0010t0001g0117a0001c0010t0001g0217 | 2 | HG02717.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.956+2125T>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 10/14 | chr4 | 48084341 | ||||||
| chr4:48084687
|
G | A | 19 | a0001c0001t0001g0115a0001c0001t0001g0120a0001c0001t0003g0102others(16): Show | 22 | HG00323.hp1 HG00639.hp2 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.956+1779C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 10/14 | chr4 | 48084687 | ||||||
| chr4:48084737
|
T | C | 1 | a0001c0015t0001g0033 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.956+1729A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 10/14 | chr4 | 48084737 | ||||||
| chr4:48084819
|
C | T | 1 | a0001c0001t0001g0142 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.956+1647G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 10/14 | chr4 | 48084819 | ||||||
| chr4:48084823
|
A | AGAGAATG others(13): Show |
11 | a0001c0001t0001g0195a0001c0001t0001g0222a0001c0001t0002g0196others(8): Show | 11 | HG01168.hp1 HG02015.hp2 HG02056.hp2 others(8): Show |
intron_variant | MODIFIER | c.956+1623_956+1642d others(22): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 10/14 | chr4 | 48084823 | ||||||
| chr4:48084823
|
A | AGAGAATG others(33): Show |
54 | a0001c0001t0002g0197a0001c0001t0002g0198a0001c0001t0002g0205others(51): Show | 60 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(57): Show |
intron_variant | MODIFIER | c.956+1603_956+1642d others(42): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 10/14 | chr4 | 48084823 | ||||||
| chr4:48084823
|
A | AGAGAATG others(53): Show |
69 | a0001c0001t0001g0305a0001c0001t0002g0015a0001c0001t0002g0016others(66): Show | 71 | HG00140.hp1 HG00438.hp2 HG00544.hp1 others(68): Show |
intron_variant | MODIFIER | c.956+1583_956+1642d others(62): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 10/14 | chr4 | 48084823 | ||||||
| chr4:48084823
|
AGAGAATG others(13): Show |
A | 58 | a0001c0001t0001g0086a0001c0001t0001g0161a0001c0001t0002g0064others(55): Show | 66 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(63): Show |
intron_variant | MODIFIER | c.956+1623_956+1642d others(22): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 10/14 | chr4 | 48084823 | ||||||
| chr4:48084842
|
T | TCGAGAAT others(33): Show |
1 | a0002c0003t0001g0255 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.956+1623_956+1624i others(42): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 10/14 | chr4 | 48084842 | ||||||
| chr4:48084844
|
G | GAGAATGG others(33): Show |
15 | a0001c0001t0001g0178a0001c0005t0001g0004a0001c0005t0001g0022others(12): Show | 17 | HG01884.hp1 HG02145.hp2 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.956+1621_956+1622i others(42): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 10/14 | chr4 | 48084844 | ||||||
| chr4:48084942
|
C | T | 2 | a0001c0008t0003g0230a0001c0008t0003g0231 | 2 | HG02897.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.956+1524G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 10/14 | chr4 | 48084942 | ||||||
| chr4:48084989
|
C | T | 1 | a0001c0002t0001g0248 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.956+1477G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 10/14 | chr4 | 48084989 | ||||||
| chr4:48085203
|
C | T | 2 | a0001c0007t0001g0107a0001c0007t0001g0167 | 2 | HG01255.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.956+1263G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 10/14 | chr4 | 48085203 | ||||||
| chr4:48085231
|
T | C | 289 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0021others(286): Show | 315 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(312): Show |
intron_variant | MODIFIER | c.956+1235A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 10/14 | chr4 | 48085231 | ||||||
| chr4:48085407
|
G | GA | 9 | a0001c0001t0001g0130a0001c0001t0001g0132a0001c0001t0001g0133others(6): Show | 9 | HG02602.hp2 HG02735.hp1 HG03491.hp2 others(6): Show |
intron_variant | MODIFIER | c.956+1058dupT | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 10/14 | chr4 | 48085407 | ||||||
| chr4:48085678
|
CAG | C | 51 | a0001c0001t0006g0247a0001c0002t0001g0014a0001c0002t0001g0090others(48): Show | 57 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(54): Show |
intron_variant | MODIFIER | c.956+786_956+787del others(2): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 10/14 | chr4 | 48085678 | ||||||
| chr4:48085705
|
A | G | 3 | a0002c0003t0001g0250a0002c0003t0001g0251a0002c0012t0002g0252 | 3 | HG00642.hp1 HG01516.hp2 HG01993.hp2 |
intron_variant | MODIFIER | c.956+761T>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 10/14 | chr4 | 48085705 | ||||||
| chr4:48085763
|
C | G | 6 | a0003c0004t0003g0001a0003c0004t0003g0106a0003c0004t0003g0109others(3): Show | 9 | HG00323.hp1 HG01109.hp1 HG01358.hp2 others(6): Show |
intron_variant | MODIFIER | c.956+703G>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 10/14 | chr4 | 48085763 | ||||||
| chr4:48085838
|
G | A | 288 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0021others(285): Show | 314 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(311): Show |
intron_variant | MODIFIER | c.956+628C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 10/14 | chr4 | 48085838 | ||||||
| chr4:48085950
|
G | A | 1 | a0002c0003t0001g0043 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.956+516C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 10/14 | chr4 | 48085950 | ||||||
| chr4:48086052
|
C | T | 288 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0021others(285): Show | 314 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(311): Show |
intron_variant | MODIFIER | c.956+414G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 10/14 | chr4 | 48086052 | ||||||
| chr4:48086105
|
C | T | 2 | a0001c0002t0001g0035a0001c0002t0001g0038 | 2 | HG03834.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.956+361G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 10/14 | chr4 | 48086105 | ||||||
| chr4:48086163
|
A | G | 310 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0021others(307): Show | 338 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(335): Show |
intron_variant | MODIFIER | c.956+303T>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 10/14 | chr4 | 48086163 | ||||||
| chr4:48086310
|
C | T | 1 | a0001c0002t0001g0083 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.956+156G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 10/14 | chr4 | 48086310 | ||||||
| chr4:48086402
|
C | T | 161 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0021others(158): Show | 179 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(176): Show |
intron_variant | MODIFIER | c.956+64G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 10/14 | chr4 | 48086402 | ||||||
| chr4:48086405
|
A | G | 15 | a0001c0001t0001g0178a0001c0005t0001g0004a0001c0005t0001g0022others(12): Show | 17 | HG01884.hp1 HG02145.hp2 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.956+61T>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 10/14 | chr4 | 48086405 | ||||||
| chr4:48086429
|
A | G | 288 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0021others(285): Show | 314 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(311): Show |
intron_variant | MODIFIER | c.956+37T>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 10/14 | chr4 | 48086429 | ||||||
| chr4:48086799
|
C | T | 2 | a0001c0001t0001g0162a0001c0001t0001g0175 | 2 | HG00558.hp1 HG00673.hp1 |
intron_variant | MODIFIER | c.785-162G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 9/14 | chr4 | 48086799 | ||||||
| chr4:48086874
|
C | T | 1 | a0001c0002t0001g0131 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.785-237G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 9/14 | chr4 | 48086874 | ||||||
| chr4:48086985
|
G | GT | 238 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0021others(235): Show | 258 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(255): Show |
intron_variant | MODIFIER | c.785-349dupA | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 9/14 | chr4 | 48086985 | ||||||
| chr4:48087075
|
C | T | 2 | a0001c0010t0001g0117a0001c0010t0001g0217 | 2 | HG02717.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.785-438G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 9/14 | chr4 | 48087075 | ||||||
| chr4:48087092
|
T | C | 1 | a0002c0003t0001g0265 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.785-455A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 9/14 | chr4 | 48087092 | ||||||
| chr4:48087241
|
CTG | C | 75 | a0001c0001t0001g0305a0001c0001t0002g0015a0001c0001t0002g0016others(72): Show | 77 | HG00140.hp1 HG00438.hp2 HG00544.hp1 others(74): Show |
intron_variant | MODIFIER | c.785-606_785-605del others(2): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 9/14 | chr4 | 48087241 | ||||||
| chr4:48087359
|
A | G | 6 | a0001c0008t0003g0221a0001c0008t0003g0230a0001c0008t0003g0231others(3): Show | 6 | HG02559.hp1 HG02717.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.785-722T>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 9/14 | chr4 | 48087359 | ||||||
| chr4:48087438
|
A | T | 2 | a0001c0001t0002g0310a0001c0015t0001g0033 | 2 | HG01243.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.785-801T>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 9/14 | chr4 | 48087438 | ||||||
| chr4:48087441
|
A | T | 83 | a0001c0001t0001g0223a0001c0001t0001g0305a0001c0001t0002g0015others(80): Show | 87 | HG00140.hp1 HG00438.hp2 HG00544.hp1 others(84): Show |
intron_variant | MODIFIER | c.785-804T>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 9/14 | chr4 | 48087441 | ||||||
| chr4:48087444
|
T | A | 50 | a0001c0001t0005g0018a0001c0001t0005g0039a0001c0001t0005g0332others(47): Show | 56 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(53): Show |
intron_variant | MODIFIER | c.785-807A>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 9/14 | chr4 | 48087444 | ||||||
| chr4:48087750
|
A | C | 14 | a0001c0005t0001g0004a0001c0005t0001g0022a0001c0005t0001g0023others(11): Show | 16 | HG01884.hp1 HG02145.hp2 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.785-1113T>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 9/14 | chr4 | 48087750 | ||||||
| chr4:48087843
|
A | G | 9 | a0001c0001t0003g0277a0001c0001t0003g0281a0001c0001t0003g0288others(6): Show | 9 | HG01891.hp1 HG02258.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.785-1206T>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 9/14 | chr4 | 48087843 | ||||||
| chr4:48088023
|
T | C | 56 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0021others(53): Show | 63 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(60): Show |
intron_variant | MODIFIER | c.785-1386A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 9/14 | chr4 | 48088023 | ||||||
| chr4:48088118
|
C | T | 238 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0021others(235): Show | 258 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(255): Show |
intron_variant | MODIFIER | c.785-1481G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 9/14 | chr4 | 48088118 | ||||||
| chr4:48088135
|
T | A | 1 | a0001c0010t0001g0217 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.785-1498A>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 9/14 | chr4 | 48088135 | ||||||
| chr4:48088152
|
C | A | 6 | a0001c0008t0003g0221a0001c0008t0003g0230a0001c0008t0003g0231others(3): Show | 6 | HG02559.hp1 HG02717.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.785-1515G>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 9/14 | chr4 | 48088152 | ||||||
| chr4:48088425
|
G | GC | 7 | a0001c0001t0001g0144a0001c0001t0001g0146a0001c0001t0001g0157others(4): Show | 7 | HG00408.hp1 HG02071.hp2 NA18747.hp2 others(4): Show |
intron_variant | MODIFIER | c.784+1324dupG | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 9/14 | chr4 | 48088425 | ||||||
| chr4:48088537
|
G | A | 1 | a0001c0001t0002g0213 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.784+1213C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 9/14 | chr4 | 48088537 | ||||||
| chr4:48088630
|
T | C | 1 | a0001c0001t0005g0039 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.784+1120A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 9/14 | chr4 | 48088630 | ||||||
| chr4:48088807
|
C | T | 2 | a0003c0004t0003g0137a0003c0004t0003g0239 | 2 | HG00639.hp2 HG01123.hp1 |
intron_variant | MODIFIER | c.784+943G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 9/14 | chr4 | 48088807 | ||||||
| chr4:48088811
|
C | T | 1 | a0001c0001t0002g0199 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.784+939G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 9/14 | chr4 | 48088811 | ||||||
| chr4:48088857
|
C | T | 4 | a0001c0001t0005g0018a0001c0001t0005g0039a0001c0001t0005g0332others(1): Show | 5 | HG01884.hp2 HG02572.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.784+893G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 9/14 | chr4 | 48088857 | ||||||
| chr4:48089289
|
C | T | 2 | a0001c0002t0001g0069a0001c0002t0001g0071 | 2 | HG02602.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.784+461G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 9/14 | chr4 | 48089289 | ||||||
| chr4:48089385
|
C | CT | 54 | a0001c0001t0006g0247a0001c0002t0001g0014a0001c0002t0001g0090others(51): Show | 60 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(57): Show |
intron_variant | MODIFIER | c.784+364dupA | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 9/14 | chr4 | 48089385 | ||||||
| chr4:48089399
|
C | CT | 6 | a0001c0007t0001g0032a0001c0007t0001g0107a0001c0007t0001g0118others(3): Show | 6 | HG01255.hp1 HG02109.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.784+350dupA | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 9/14 | chr4 | 48089399 | ||||||
| chr4:48089416
|
A | G | 1 | a0002c0003t0001g0058 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.784+334T>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 9/14 | chr4 | 48089416 | ||||||
| chr4:48089550
|
C | G | 1 | a0001c0002t0001g0068 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.784+200G>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 9/14 | chr4 | 48089550 | ||||||
| chr4:48089841
|
A | G | 1 | a0001c0001t0004g0257 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.710-17T>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 8/14 | chr4 | 48089841 | ||||||
| chr4:48089960
|
C | T | 2 | a0001c0002t0001g0006a0001c0002t0001g0201 | 4 | NA18969.hp1 NA18979.hp1 NA18989.hp2 others(1): Show |
intron_variant | MODIFIER | c.710-136G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 8/14 | chr4 | 48089960 | ||||||
| chr4:48089988
|
AT | A | 75 | a0001c0001t0001g0305a0001c0001t0002g0015a0001c0001t0002g0016others(72): Show | 77 | HG00140.hp1 HG00438.hp2 HG00544.hp1 others(74): Show |
intron_variant | MODIFIER | c.710-165delA | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 8/14 | chr4 | 48089988 | ||||||
| chr4:48090215
|
T | C | 2 | a0001c0001t0004g0124a0001c0001t0004g0183 | 2 | HG02723.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.710-391A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 8/14 | chr4 | 48090215 | ||||||
| chr4:48090277
|
A | G | 1 | a0001c0001t0001g0130 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.710-453T>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 8/14 | chr4 | 48090277 | ||||||
| chr4:48090280
|
T | A | 2 | a0001c0002t0001g0080a0001c0002t0001g0081 | 2 | HG02615.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.710-456A>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 8/14 | chr4 | 48090280 | ||||||
| chr4:48090463
|
T | C | 1 | a0001c0001t0001g0145 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.710-639A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 8/14 | chr4 | 48090463 | ||||||
| chr4:48090659
|
T | C | 1 | a0001c0002t0001g0270 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.710-835A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 8/14 | chr4 | 48090659 | ||||||
| chr4:48090772
|
G | A | 1 | a0001c0001t0001g0128 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.710-948C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 8/14 | chr4 | 48090772 | ||||||
| chr4:48091380
|
A | G | 1 | a0001c0002t0001g0099 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.710-1556T>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 8/14 | chr4 | 48091380 | ||||||
| chr4:48091415
|
C | T | 1 | a0001c0001t0007g0119 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.710-1591G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 8/14 | chr4 | 48091415 | ||||||
| chr4:48091510
|
CT | C | 26 | a0001c0001t0004g0094a0001c0001t0004g0124a0001c0001t0004g0180others(23): Show | 26 | HG01255.hp2 HG02109.hp1 HG02257.hp2 others(23): Show |
intron_variant | MODIFIER | c.710-1687delA | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 8/14 | chr4 | 48091510 | ||||||
| chr4:48091565
|
G | A | 52 | a0001c0001t0006g0247a0001c0002t0001g0014a0001c0002t0001g0090others(49): Show | 58 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(55): Show |
intron_variant | MODIFIER | c.710-1741C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 8/14 | chr4 | 48091565 | ||||||
| chr4:48091749
|
C | G | 1 | a0001c0002t0001g0082 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.710-1925G>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 8/14 | chr4 | 48091749 | ||||||
| chr4:48091751
|
C | A | 17 | a0001c0002t0001g0062a0001c0002t0001g0076a0001c0002t0001g0077others(14): Show | 17 | HG01167.hp1 HG01891.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.710-1927G>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 8/14 | chr4 | 48091751 | ||||||
| chr4:48091756
|
T | C | 1 | a0001c0001t0004g0181 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.710-1932A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 8/14 | chr4 | 48091756 | ||||||
| chr4:48091787
|
G | A | 1 | a0001c0001t0002g0325 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.710-1963C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 8/14 | chr4 | 48091787 | ||||||
| chr4:48092009
|
G | A | 1 | a0002c0003t0001g0085 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.709+2068C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 8/14 | chr4 | 48092009 | ||||||
| chr4:48092088
|
T | C | 18 | a0001c0001t0001g0115a0001c0001t0003g0102a0001c0001t0003g0103others(15): Show | 21 | HG00323.hp1 HG00639.hp2 HG01109.hp1 others(18): Show |
intron_variant | MODIFIER | c.709+1989A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 8/14 | chr4 | 48092088 | ||||||
| chr4:48092144
|
C | A | 6 | a0001c0007t0001g0032a0001c0007t0001g0107a0001c0007t0001g0118others(3): Show | 6 | HG01255.hp1 HG02109.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.709+1933G>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 8/14 | chr4 | 48092144 | ||||||
| chr4:48092258
|
C | T | 72 | a0001c0001t0006g0247a0001c0002t0001g0014a0001c0002t0001g0090others(69): Show | 80 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(77): Show |
intron_variant | MODIFIER | c.709+1819G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 8/14 | chr4 | 48092258 | ||||||
| chr4:48092517
|
A | C | 155 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0021others(152): Show | 173 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(170): Show |
intron_variant | MODIFIER | c.709+1560T>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 8/14 | chr4 | 48092517 | ||||||
| chr4:48092517
|
A | T | 1 | a0001c0001t0002g0064 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.709+1560T>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 8/14 | chr4 | 48092517 | ||||||
| chr4:48092553
|
TGGACACA others(60): Show |
T | 58 | a0001c0001t0006g0247a0001c0002t0001g0014a0001c0002t0001g0090others(55): Show | 64 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(61): Show |
intron_variant | MODIFIER | c.709+1457_709+1523d others(69): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 8/14 | chr4 | 48092553 | ||||||
| chr4:48092573
|
T | C | 22 | a0001c0001t0004g0094a0001c0001t0004g0124a0001c0001t0004g0180others(19): Show | 23 | HG01255.hp2 HG01884.hp2 HG02109.hp1 others(20): Show |
intron_variant | MODIFIER | c.709+1504A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 8/14 | chr4 | 48092573 | ||||||
| chr4:48092640
|
T | C | 46 | a0001c0002t0001g0014a0001c0002t0001g0090a0002c0003t0001g0007others(43): Show | 52 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(49): Show |
intron_variant | MODIFIER | c.709+1437A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 8/14 | chr4 | 48092640 | ||||||
| chr4:48092690
|
G | A | 1 | a0001c0007t0001g0122 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.709+1387C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 8/14 | chr4 | 48092690 | ||||||
| chr4:48092790
|
T | C | 3 | a0001c0002t0001g0237a0001c0002t0001g0258a0001c0002t0001g0260 | 3 | HG01891.hp2 HG02055.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.709+1287A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 8/14 | chr4 | 48092790 | ||||||
| chr4:48093110
|
T | C | 18 | a0001c0001t0004g0094a0001c0001t0004g0124a0001c0001t0004g0180others(15): Show | 18 | HG01255.hp2 HG02109.hp1 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.709+967A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 8/14 | chr4 | 48093110 | ||||||
| chr4:48093394
|
G | A | 1 | a0001c0001t0003g0114 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.709+683C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 8/14 | chr4 | 48093394 | ||||||
| chr4:48093592
|
C | T | 6 | a0001c0007t0001g0032a0001c0007t0001g0107a0001c0007t0001g0118others(3): Show | 6 | HG01255.hp1 HG02109.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.709+485G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 8/14 | chr4 | 48093592 | ||||||
| chr4:48093732
|
A | G | 1 | a0002c0003t0001g0053 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.709+345T>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 8/14 | chr4 | 48093732 | ||||||
| chr4:48093971
|
T | C | 6 | a0001c0008t0003g0221a0001c0008t0003g0230a0001c0008t0003g0231others(3): Show | 6 | HG02559.hp1 HG02717.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.709+106A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 8/14 | chr4 | 48093971 | ||||||
| chr4:48094284
|
C | A | 1 | a0001c0001t0001g0159 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.582-80G>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 7/14 | chr4 | 48094284 | ||||||
| chr4:48094588
|
A | G | 3 | a0001c0001t0001g0086a0001c0002t0001g0082a0001c0002t0001g0096 | 3 | HG02129.hp1 NA19001.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.582-384T>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 7/14 | chr4 | 48094588 | ||||||
| chr4:48094764
|
T | C | 243 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0021others(240): Show | 268 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(265): Show |
intron_variant | MODIFIER | c.581+379A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 7/14 | chr4 | 48094764 | ||||||
| chr4:48094772
|
G | A | 1 | a0001c0001t0002g0015 | 2 | NA18950.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.581+371C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 7/14 | chr4 | 48094772 | ||||||
| chr4:48094777
|
G | C | 243 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0021others(240): Show | 268 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(265): Show |
intron_variant | MODIFIER | c.581+366C>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 7/14 | chr4 | 48094777 | ||||||
| chr4:48094963
|
G | A | 79 | a0001c0001t0001g0086a0001c0001t0002g0064a0001c0002t0001g0003others(76): Show | 87 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.581+180C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 7/14 | chr4 | 48094963 | ||||||
| chr4:48095383
|
T | A | 52 | a0001c0001t0006g0247a0001c0002t0001g0014a0001c0002t0001g0090others(49): Show | 58 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(55): Show |
intron_variant | MODIFIER | c.502-161A>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48095383 | ||||||
| chr4:48095463
|
A | G | 162 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0021others(159): Show | 180 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(177): Show |
intron_variant | MODIFIER | c.502-241T>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48095463 | ||||||
| chr4:48095596
|
G | A | 1 | a0001c0008t0006g0232 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.502-374C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48095596 | ||||||
| chr4:48095817
|
T | C | 1 | a0001c0002t0001g0090 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.502-595A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48095817 | ||||||
| chr4:48095829
|
G | A | 1 | a0003c0004t0003g0106 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.502-607C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48095829 | ||||||
| chr4:48095869
|
T | C | 1 | a0001c0001t0001g0128 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.502-647A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48095869 | ||||||
| chr4:48095876
|
C | T | 1 | a0001c0008t0003g0221 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.502-654G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48095876 | ||||||
| chr4:48095922
|
A | C | 1 | a0001c0007t0001g0118 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.502-700T>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48095922 | ||||||
| chr4:48096060
|
G | A | 1 | a0001c0008t0006g0232 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.502-838C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48096060 | ||||||
| chr4:48096353
|
T | C | 52 | a0001c0001t0006g0247a0001c0002t0001g0014a0001c0002t0001g0090others(49): Show | 58 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(55): Show |
intron_variant | MODIFIER | c.502-1131A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48096353 | ||||||
| chr4:48096370
|
G | T | 1 | a0001c0005t0001g0022 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.502-1148C>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48096370 | ||||||
| chr4:48096557
|
G | A | 162 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0021others(159): Show | 180 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(177): Show |
intron_variant | MODIFIER | c.502-1335C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48096557 | ||||||
| chr4:48096573
|
T | C | 1 | a0001c0002t0001g0040 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.502-1351A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48096573 | ||||||
| chr4:48096582
|
A | G | 1 | a0001c0001t0003g0290 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.502-1360T>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48096582 | ||||||
| chr4:48096590
|
G | A | 6 | a0001c0008t0003g0221a0001c0008t0003g0230a0001c0008t0003g0231others(3): Show | 6 | HG02559.hp1 HG02717.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.502-1368C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48096590 | ||||||
| chr4:48096607
|
A | C | 6 | a0001c0002t0001g0090a0002c0003t0001g0007a0002c0003t0001g0042others(3): Show | 8 | HG00140.hp2 HG01256.hp2 HG01496.hp1 others(5): Show |
intron_variant | MODIFIER | c.502-1385T>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48096607 | ||||||
| chr4:48096825
|
G | A | 1 | a0001c0006t0001g0292 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.502-1603C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48096825 | ||||||
| chr4:48096873
|
C | T | 4 | a0001c0006t0001g0095a0001c0006t0001g0125a0001c0006t0001g0292others(1): Show | 4 | HG01243.hp2 HG01884.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.502-1651G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48096873 | ||||||
| chr4:48096883
|
C | A | 1 | a0001c0001t0003g0320 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.502-1661G>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48096883 | ||||||
| chr4:48096925
|
A | G | 1 | a0001c0015t0001g0033 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.502-1703T>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48096925 | ||||||
| chr4:48096952
|
T | C | 1 | a0001c0001t0001g0120 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.502-1730A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48096952 | ||||||
| chr4:48096960
|
T | A | 22 | a0001c0001t0004g0094a0001c0001t0004g0124a0001c0001t0004g0180others(19): Show | 23 | HG01255.hp2 HG01884.hp2 HG02109.hp1 others(20): Show |
intron_variant | MODIFIER | c.502-1738A>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48096960 | ||||||
| chr4:48097056
|
A | C | 2 | a0001c0002t0001g0078a0001c0002t0001g0097 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.502-1834T>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48097056 | ||||||
| chr4:48097208
|
C | A | 2 | a0001c0010t0001g0117a0001c0010t0001g0217 | 2 | HG02717.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.502-1986G>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48097208 | ||||||
| chr4:48097343
|
A | G | 22 | a0001c0001t0004g0094a0001c0001t0004g0124a0001c0001t0004g0180others(19): Show | 23 | HG01255.hp2 HG01884.hp2 HG02109.hp1 others(20): Show |
intron_variant | MODIFIER | c.502-2121T>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48097343 | ||||||
| chr4:48097422
|
C | CT | 31 | a0001c0001t0004g0094a0001c0001t0004g0124a0001c0001t0004g0180others(28): Show | 32 | HG01255.hp2 HG01516.hp2 HG01884.hp2 others(29): Show |
intron_variant | MODIFIER | c.502-2201dupA | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48097422 | ||||||
| chr4:48097422
|
C | CTT | 151 | a0001c0001t0001g0086a0001c0001t0001g0115a0001c0001t0001g0120others(148): Show | 168 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.502-2202_502-2201d others(4): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48097422 | ||||||
| chr4:48097422
|
C | CTTT | 72 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0021others(69): Show | 81 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.502-2203_502-2201d others(5): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48097422 | ||||||
| chr4:48097627
|
A | G | 243 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0021others(240): Show | 268 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(265): Show |
intron_variant | MODIFIER | c.502-2405T>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48097627 | ||||||
| chr4:48097640
|
G | A | 2 | a0001c0001t0006g0247a0001c0002t0001g0248 | 2 | HG02976.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.502-2418C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48097640 | ||||||
| chr4:48097748
|
A | AT | 11 | a0001c0001t0001g0126a0001c0001t0001g0223a0001c0001t0002g0210others(8): Show | 11 | HG00738.hp1 HG01243.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.502-2527dupA | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48097748 | ||||||
| chr4:48097748
|
A | G | 1 | a0001c0002t0001g0075 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.502-2526T>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48097748 | ||||||
| chr4:48097748
|
AT | A | 26 | a0001c0001t0001g0120a0001c0001t0005g0018a0001c0001t0005g0039others(23): Show | 29 | HG01884.hp1 HG01884.hp2 HG02145.hp2 others(26): Show |
intron_variant | MODIFIER | c.502-2527delA | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48097748 | ||||||
| chr4:48097894
|
C | A | 6 | a0001c0008t0003g0221a0001c0008t0003g0230a0001c0008t0003g0231others(3): Show | 6 | HG02559.hp1 HG02717.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.502-2672G>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48097894 | ||||||
| chr4:48097991
|
C | T | 1 | a0001c0001t0001g0128 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.502-2769G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48097991 | ||||||
| chr4:48098433
|
C | G | 1 | a0001c0006t0001g0031 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.502-3211G>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48098433 | ||||||
| chr4:48098469
|
T | C | 1 | a0003c0004t0003g0112 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.502-3247A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48098469 | ||||||
| chr4:48098480
|
A | C | 184 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0021others(181): Show | 203 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(200): Show |
intron_variant | MODIFIER | c.502-3258T>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48098480 | ||||||
| chr4:48098556
|
T | TTTTTTTT others(453): Show |
1 | a0001c0015t0001g0033 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.502-3335_502-3334i others(462): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48098556 | ||||||
| chr4:48098559
|
A | T | 1 | a0001c0015t0001g0033 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.502-3337T>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48098559 | ||||||
| chr4:48098561
|
A | G | 1 | a0001c0015t0001g0033 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.502-3339T>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48098561 | ||||||
| chr4:48098563
|
T | C | 1 | a0001c0015t0001g0033 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.502-3341A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48098563 | ||||||
| chr4:48098565
|
T | G | 1 | a0001c0015t0001g0033 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.502-3343A>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48098565 | ||||||
| chr4:48098576
|
G | C | 1 | a0001c0015t0001g0033 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.502-3354C>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48098576 | ||||||
| chr4:48098578
|
A | T | 1 | a0001c0015t0001g0033 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.502-3356T>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48098578 | ||||||
| chr4:48098579
|
A | G | 1 | a0001c0015t0001g0033 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.502-3357T>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48098579 | ||||||
| chr4:48098583
|
G | A | 1 | a0001c0015t0001g0033 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.502-3361C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48098583 | ||||||
| chr4:48098589
|
A | C | 1 | a0001c0015t0001g0033 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.502-3367T>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48098589 | ||||||
| chr4:48098590
|
C | T | 1 | a0001c0015t0001g0033 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.502-3368G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48098590 | ||||||
| chr4:48098593
|
C | T | 3 | a0002c0003t0001g0329a0002c0003t0001g0330a0002c0003t0001g0331 | 3 | HG01192.hp1 HG02055.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.502-3371G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48098593 | ||||||
| chr4:48098595
|
T | A | 1 | a0001c0015t0001g0033 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.502-3373A>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48098595 | ||||||
| chr4:48098598
|
A | G | 1 | a0001c0015t0001g0033 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.502-3376T>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48098598 | ||||||
| chr4:48098601
|
C | G | 1 | a0001c0015t0001g0033 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.502-3379G>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48098601 | ||||||
| chr4:48098602
|
A | C | 1 | a0001c0015t0001g0033 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.502-3380T>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48098602 | ||||||
| chr4:48098603
|
A | ATGATTTA others(968): Show |
1 | a0001c0015t0001g0033 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.502-3382_502-3381i others(977): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48098603 | ||||||
| chr4:48098607
|
C | G | 1 | a0001c0015t0001g0033 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.502-3385G>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48098607 | ||||||
| chr4:48098609
|
C | T | 1 | a0001c0015t0001g0033 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.502-3387G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48098609 | ||||||
| chr4:48098640
|
T | G | 22 | a0001c0001t0004g0094a0001c0001t0004g0124a0001c0001t0004g0180others(19): Show | 23 | HG01255.hp2 HG01884.hp2 HG02109.hp1 others(20): Show |
intron_variant | MODIFIER | c.502-3418A>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48098640 | ||||||
| chr4:48098716
|
C | CT | 52 | a0001c0001t0006g0247a0001c0002t0001g0014a0001c0002t0001g0090others(49): Show | 58 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(55): Show |
intron_variant | MODIFIER | c.502-3495dupA | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48098716 | ||||||
| chr4:48098858
|
G | A | 1 | a0001c0001t0001g0021 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.502-3636C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48098858 | ||||||
| chr4:48098923
|
A | G | 1 | a0001c0006t0001g0031 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.502-3701T>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48098923 | ||||||
| chr4:48098945
|
A | G | 1 | a0001c0001t0002g0206 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.502-3723T>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48098945 | ||||||
| chr4:48098947
|
CA | C | 242 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0021others(239): Show | 267 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(264): Show |
intron_variant | MODIFIER | c.502-3726delT | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48098947 | ||||||
| chr4:48098957
|
A | T | 1 | a0002c0003t0001g0052 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.502-3735T>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48098957 | ||||||
| chr4:48098958
|
T | G | 1 | a0002c0003t0001g0052 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.502-3736A>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48098958 | ||||||
| chr4:48098961
|
G | A | 1 | a0002c0003t0001g0052 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.502-3739C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48098961 | ||||||
| chr4:48098971
|
A | G | 6 | a0001c0008t0003g0221a0001c0008t0003g0230a0001c0008t0003g0231others(3): Show | 6 | HG02559.hp1 HG02717.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.502-3749T>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48098971 | ||||||
| chr4:48099204
|
G | A | 5 | a0001c0008t0003g0221a0001c0008t0003g0230a0001c0008t0003g0231others(2): Show | 5 | HG02559.hp1 HG02717.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.502-3982C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48099204 | ||||||
| chr4:48099343
|
C | T | 1 | a0001c0001t0005g0039 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.502-4121G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48099343 | ||||||
| chr4:48099549
|
G | A | 1 | a0002c0003t0001g0052 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.502-4327C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48099549 | ||||||
| chr4:48099550
|
A | AT | 5 | a0001c0007t0001g0032a0001c0007t0001g0107a0001c0007t0001g0122others(2): Show | 5 | HG01255.hp1 HG02109.hp2 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.502-4329dupA | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48099550 | ||||||
| chr4:48099550
|
A | G | 1 | a0002c0003t0001g0052 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.502-4328T>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48099550 | ||||||
| chr4:48099551
|
T | A | 1 | a0002c0003t0001g0052 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.502-4329A>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48099551 | ||||||
| chr4:48100025
|
A | G | 11 | a0001c0005t0001g0004a0001c0005t0001g0022a0001c0005t0001g0023others(8): Show | 13 | HG02145.hp2 HG02257.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.502-4803T>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48100025 | ||||||
| chr4:48100077
|
C | T | 6 | a0001c0007t0001g0032a0001c0007t0001g0107a0001c0007t0001g0118others(3): Show | 6 | HG01255.hp1 HG02109.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.501+4824G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48100077 | ||||||
| chr4:48100089
|
G | A | 3 | a0001c0006t0001g0095a0001c0006t0001g0125a0001c0006t0001g0292 | 3 | HG01884.hp1 HG02895.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.501+4812C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48100089 | ||||||
| chr4:48100158
|
A | C | 243 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0021others(240): Show | 268 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(265): Show |
intron_variant | MODIFIER | c.501+4743T>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48100158 | ||||||
| chr4:48100171
|
C | CA | 43 | a0001c0001t0001g0115a0001c0001t0003g0102a0001c0001t0003g0103others(40): Show | 48 | HG00323.hp1 HG00621.hp2 HG00639.hp2 others(45): Show |
intron_variant | MODIFIER | c.501+4729dupT | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48100171 | ||||||
| chr4:48100171
|
C | CAA | 21 | a0001c0001t0003g0113a0001c0001t0003g0114a0001c0001t0004g0180others(18): Show | 21 | HG02055.hp1 HG02109.hp1 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.501+4728_501+4729d others(4): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48100171 | ||||||
| chr4:48100171
|
C | CAAA | 30 | a0001c0001t0001g0120a0001c0001t0004g0094a0001c0001t0004g0124others(27): Show | 36 | HG00140.hp2 HG00639.hp1 HG00733.hp2 others(33): Show |
intron_variant | MODIFIER | c.501+4727_501+4729d others(5): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48100171 | ||||||
| chr4:48100171
|
C | CAAAA | 16 | a0001c0001t0006g0247a0001c0002t0001g0090a0001c0002t0001g0248others(13): Show | 16 | HG00280.hp2 HG00642.hp1 HG01192.hp2 others(13): Show |
intron_variant | MODIFIER | c.501+4726_501+4729d others(6): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48100171 | ||||||
| chr4:48100171
|
CA | C | 101 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0021others(98): Show | 110 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(107): Show |
intron_variant | MODIFIER | c.501+4729delT | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48100171 | ||||||
| chr4:48100171
|
CAA | C | 9 | a0001c0001t0002g0211a0001c0001t0002g0272a0001c0001t0002g0273others(6): Show | 9 | HG02004.hp2 HG02258.hp1 HG02300.hp1 others(6): Show |
intron_variant | MODIFIER | c.501+4728_501+4729d others(4): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48100171 | ||||||
| chr4:48100397
|
T | C | 1 | a0001c0001t0002g0328 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.501+4504A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48100397 | ||||||
| chr4:48100496
|
A | C | 1 | a0001c0015t0001g0033 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.501+4405T>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48100496 | ||||||
| chr4:48100506
|
G | A | 1 | a0002c0003t0001g0043 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.501+4395C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48100506 | ||||||
| chr4:48100635
|
C | T | 52 | a0001c0001t0006g0247a0001c0002t0001g0014a0001c0002t0001g0090others(49): Show | 58 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(55): Show |
intron_variant | MODIFIER | c.501+4266G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48100635 | ||||||
| chr4:48100717
|
G | A | 1 | a0001c0015t0001g0033 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.501+4184C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48100717 | ||||||
| chr4:48100874
|
T | A | 1 | a0001c0002t0001g0071 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.501+4027A>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48100874 | ||||||
| chr4:48100923
|
T | A | 3 | a0001c0001t0004g0193a0002c0003t0001g0254a0002c0003t0001g0255 | 3 | HG00735.hp1 HG03041.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.501+3978A>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48100923 | ||||||
| chr4:48101056
|
T | G | 1 | a0001c0001t0001g0151 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.501+3845A>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48101056 | ||||||
| chr4:48101082
|
A | G | 1 | a0001c0015t0001g0033 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.501+3819T>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48101082 | ||||||
| chr4:48101113
|
C | T | 2 | a0001c0002t0001g0080a0001c0002t0001g0081 | 2 | HG02615.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.501+3788G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48101113 | ||||||
| chr4:48101202
|
T | C | 1 | a0001c0001t0001g0160 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.501+3699A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48101202 | ||||||
| chr4:48101600
|
A | G | 3 | a0001c0002t0001g0256a0001c0002t0001g0269a0001c0002t0001g0271 | 3 | HG00642.hp2 HG02622.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.501+3301T>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48101600 | ||||||
| chr4:48101657
|
T | G | 1 | a0001c0001t0003g0108 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.501+3244A>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48101657 | ||||||
| chr4:48101662
|
T | A | 1 | a0001c0001t0004g0257 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.501+3239A>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48101662 | ||||||
| chr4:48101815
|
A | T | 14 | a0001c0005t0001g0004a0001c0005t0001g0022a0001c0005t0001g0023others(11): Show | 16 | HG01884.hp1 HG02145.hp2 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.501+3086T>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48101815 | ||||||
| chr4:48101924
|
A | C | 2 | a0001c0001t0001g0153a0001c0001t0001g0154 | 2 | HG00280.hp1 HG01257.hp1 |
intron_variant | MODIFIER | c.501+2977T>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48101924 | ||||||
| chr4:48102186
|
C | A | 1 | a0002c0003t0001g0238 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.501+2715G>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48102186 | ||||||
| chr4:48102235
|
T | C | 47 | a0001c0001t0006g0247a0001c0002t0001g0014a0001c0002t0001g0090others(44): Show | 53 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(50): Show |
intron_variant | MODIFIER | c.501+2666A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48102235 | ||||||
| chr4:48102239
|
G | A | 257 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0021others(254): Show | 284 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(281): Show |
intron_variant | MODIFIER | c.501+2662C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48102239 | ||||||
| chr4:48102274
|
C | A | 1 | a0003c0004t0003g0106 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.501+2627G>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48102274 | ||||||
| chr4:48102290
|
A | C | 1 | a0001c0001t0002g0064 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.501+2611T>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48102290 | ||||||
| chr4:48102293
|
T | C | 22 | a0001c0001t0004g0094a0001c0001t0004g0124a0001c0001t0004g0180others(19): Show | 23 | HG01255.hp2 HG01884.hp2 HG02109.hp1 others(20): Show |
intron_variant | MODIFIER | c.501+2608A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48102293 | ||||||
| chr4:48102493
|
C | T | 1 | a0001c0001t0001g0153 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.501+2408G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48102493 | ||||||
| chr4:48102635
|
C | G | 162 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0021others(159): Show | 180 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(177): Show |
intron_variant | MODIFIER | c.501+2266G>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48102635 | ||||||
| chr4:48102811
|
G | A | 1 | a0001c0002t0001g0318 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.501+2090C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48102811 | ||||||
| chr4:48103204
|
C | T | 52 | a0001c0001t0006g0247a0001c0002t0001g0014a0001c0002t0001g0090others(49): Show | 58 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(55): Show |
intron_variant | MODIFIER | c.501+1697G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48103204 | ||||||
| chr4:48103244
|
A | G | 6 | a0001c0008t0003g0221a0001c0008t0003g0230a0001c0008t0003g0231others(3): Show | 6 | HG02559.hp1 HG02717.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.501+1657T>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48103244 | ||||||
| chr4:48103346
|
G | A | 1 | a0001c0001t0002g0172 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.501+1555C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48103346 | ||||||
| chr4:48103358
|
G | A | 2 | a0001c0002t0001g0078a0001c0002t0001g0097 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.501+1543C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48103358 | ||||||
| chr4:48103455
|
C | T | 1 | a0001c0002t0001g0098 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.501+1446G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48103455 | ||||||
| chr4:48103478
|
A | G | 1 | a0001c0015t0001g0033 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.501+1423T>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48103478 | ||||||
| chr4:48103974
|
G | A | 53 | a0001c0001t0006g0247a0001c0002t0001g0014a0001c0002t0001g0090others(50): Show | 59 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(56): Show |
intron_variant | MODIFIER | c.501+927C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48103974 | ||||||
| chr4:48104115
|
T | C | 1 | a0001c0002t0001g0084 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.501+786A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104115 | ||||||
| chr4:48104205
|
AAT | A | 233 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0021others(230): Show | 259 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(256): Show |
intron_variant | MODIFIER | c.501+694_501+695del others(2): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104205 | ||||||
| chr4:48104212
|
A | ATATATAT others(30): Show |
1 | a0001c0008t0003g0230 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.501+688_501+689ins others(37): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104212 | ||||||
| chr4:48104214
|
ATATATAT others(7): Show |
A | 22 | a0001c0001t0004g0094a0001c0001t0004g0124a0001c0001t0004g0180others(19): Show | 23 | HG01255.hp2 HG01884.hp2 HG02109.hp1 others(20): Show |
intron_variant | MODIFIER | c.501+673_501+686del others(14): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104214 | ||||||
| chr4:48104222
|
T | A | 1 | a0001c0008t0003g0230 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.501+679A>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104222 | ||||||
| chr4:48104223
|
A | T | 1 | a0001c0001t0001g0120 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.501+678T>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104223 | ||||||
| chr4:48104229
|
T | A | 234 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0021others(231): Show | 260 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(257): Show |
intron_variant | MODIFIER | c.501+672A>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104229 | ||||||
| chr4:48104234
|
T | A | 1 | a0001c0001t0001g0120 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.501+667A>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104234 | ||||||
| chr4:48104234
|
TATATATA others(20): Show |
T | 14 | a0001c0001t0001g0305a0001c0001t0002g0172a0001c0001t0002g0199others(11): Show | 14 | HG00544.hp1 HG00597.hp2 HG02015.hp1 others(11): Show |
intron_variant | MODIFIER | c.501+640_501+666del others(27): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104234 | ||||||
| chr4:48104234
|
TATATATA others(48): Show |
T | 5 | a0001c0001t0002g0015a0001c0001t0002g0302a0001c0001t0002g0311others(2): Show | 6 | HG00609.hp2 NA18950.hp1 NA18997.hp2 others(3): Show |
intron_variant | MODIFIER | c.501+612_501+666del others(55): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104234 | ||||||
| chr4:48104241
|
A | T | 22 | a0001c0001t0004g0094a0001c0001t0004g0124a0001c0001t0004g0180others(19): Show | 23 | HG01255.hp2 HG01884.hp2 HG02109.hp1 others(20): Show |
intron_variant | MODIFIER | c.501+660T>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104241 | ||||||
| chr4:48104243
|
T | A | 1 | a0001c0002t0001g0035 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.501+658A>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104243 | ||||||
| chr4:48104245
|
T | C | 1 | a0001c0001t0004g0181 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.501+656A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104245 | ||||||
| chr4:48104245
|
T | TA | 17 | a0001c0001t0002g0048a0001c0001t0002g0287a0001c0001t0002g0293others(14): Show | 17 | HG00438.hp2 HG00673.hp2 HG02523.hp2 others(14): Show |
intron_variant | MODIFIER | c.501+655dupT | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104245 | ||||||
| chr4:48104248
|
ATTTTATA others(286): Show |
A | 1 | a0001c0001t0001g0120 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.501+360_501+652del | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104248 | ||||||
| chr4:48104250
|
T | A | 17 | a0001c0001t0002g0048a0001c0001t0002g0287a0001c0001t0002g0293others(14): Show | 17 | HG00438.hp2 HG00673.hp2 HG02523.hp2 others(14): Show |
intron_variant | MODIFIER | c.501+651A>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104250 | ||||||
| chr4:48104250
|
TTTATATA others(245): Show |
T | 7 | a0001c0006t0001g0028a0001c0006t0001g0029a0001c0006t0001g0030others(4): Show | 7 | HG01884.hp1 HG02145.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.501+399_501+650del | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104250 | ||||||
| chr4:48104252
|
T | A | 17 | a0001c0001t0002g0048a0001c0001t0002g0287a0001c0001t0002g0293others(14): Show | 17 | HG00438.hp2 HG00673.hp2 HG02523.hp2 others(14): Show |
intron_variant | MODIFIER | c.501+649A>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104252 | ||||||
| chr4:48104252
|
T | TATATATA others(21): Show |
1 | a0001c0001t0002g0138 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.501+621_501+648dup others(28): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104252 | ||||||
| chr4:48104252
|
T | TATATATA others(84): Show |
1 | a0001c0001t0002g0216 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.501+648_501+649ins others(91): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104252 | ||||||
| chr4:48104252
|
TATATATA others(21): Show |
T | 4 | a0001c0001t0002g0016a0001c0001t0002g0198a0001c0001t0002g0219others(1): Show | 5 | HG01167.hp2 HG01169.hp1 HG01243.hp1 others(2): Show |
intron_variant | MODIFIER | c.501+621_501+648del others(28): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104252 | ||||||
| chr4:48104261
|
A | T | 1 | a0001c0008t0006g0232 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.501+640T>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104261 | ||||||
| chr4:48104261
|
AATATATA others(117): Show |
A | 1 | a0002c0003t0001g0255 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.501+516_501+639del | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104261 | ||||||
| chr4:48104268
|
AATATAAT others(259): Show |
A | 4 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0150others(1): Show | 4 | HG01952.hp2 HG01981.hp1 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.501+367_501+632del | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104268 | ||||||
| chr4:48104270
|
T | A | 155 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0021others(152): Show | 173 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(170): Show |
intron_variant | MODIFIER | c.501+631A>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104270 | ||||||
| chr4:48104270
|
TATAATAT others(115): Show |
T | 1 | a0001c0015t0001g0033 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.501+509_501+630del | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104270 | ||||||
| chr4:48104271
|
ATAATATA others(225): Show |
A | 1 | a0002c0003t0001g0240 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.501+398_501+629del | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104271 | ||||||
| chr4:48104272
|
TA | T | 152 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0021others(149): Show | 170 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(167): Show |
intron_variant | MODIFIER | c.501+628delT | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104272 | ||||||
| chr4:48104272
|
TAATATAT others(1): Show |
T | 42 | a0001c0001t0006g0247a0001c0002t0001g0014a0001c0002t0001g0090others(39): Show | 48 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(45): Show |
intron_variant | MODIFIER | c.501+621_501+628del others(8): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104272 | ||||||
| chr4:48104272
|
TAATATAT others(85): Show |
T | 1 | a0002c0003t0001g0085 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.501+537_501+628del others(92): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104272 | ||||||
| chr4:48104272
|
TAATATAT others(113): Show |
T | 4 | a0001c0002t0001g0256a0001c0002t0001g0269a0001c0002t0001g0270others(1): Show | 4 | HG00642.hp2 HG02615.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.501+509_501+628del | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104272 | ||||||
| chr4:48104272
|
TAATATAT others(141): Show |
T | 2 | a0002c0003t0001g0251a0002c0003t0001g0331 | 2 | HG01993.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.501+481_501+628del | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104272 | ||||||
| chr4:48104272
|
TAATATAT others(178): Show |
T | 4 | a0001c0001t0001g0147a0001c0002t0001g0202a0001c0007t0001g0122others(1): Show | 4 | HG02109.hp2 HG02145.hp1 HG02155.hp2 others(1): Show |
intron_variant | MODIFIER | c.501+444_501+628del | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104272 | ||||||
| chr4:48104273
|
A | T | 35 | a0001c0001t0004g0094a0001c0001t0004g0124a0001c0001t0004g0180others(32): Show | 38 | HG01255.hp2 HG01884.hp2 HG02109.hp1 others(35): Show |
intron_variant | MODIFIER | c.501+628T>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104273 | ||||||
| chr4:48104273
|
AATATATA others(142): Show |
A | 1 | a0002c0003t0001g0245 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.501+479_501+627del | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104273 | ||||||
| chr4:48104280
|
A | AATATATA others(4): Show |
2 | a0001c0008t0003g0221a0001c0008t0003g0231 | 2 | HG02559.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.501+620_501+621ins others(11): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104280 | ||||||
| chr4:48104280
|
A | T | 1 | a0001c0001t0001g0161 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.501+621T>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104280 | ||||||
| chr4:48104283
|
ATATATAA others(122): Show |
A | 12 | a0001c0001t0004g0094a0001c0001t0004g0124a0001c0001t0004g0180others(9): Show | 12 | HG01255.hp2 HG02109.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.501+489_501+617del | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104283 | ||||||
| chr4:48104283
|
ATATATAA others(206): Show |
A | 7 | a0001c0005t0001g0004a0001c0005t0001g0022a0001c0005t0001g0023others(4): Show | 9 | HG02257.hp1 HG02486.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.501+405_501+617del | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104283 | ||||||
| chr4:48104284
|
TATATAAT others(10): Show |
T | 1 | a0001c0001t0004g0191 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.501+600_501+616del others(17): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104284 | ||||||
| chr4:48104284
|
TATATAAT others(66): Show |
T | 3 | a0001c0001t0004g0189a0001c0001t0004g0194a0001c0001t0004g0257 | 3 | HG02451.hp2 HG02622.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.501+544_501+616del others(73): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104284 | ||||||
| chr4:48104289
|
A | AATATATA others(77): Show |
1 | a0001c0010t0001g0117 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.501+611_501+612ins others(84): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104289 | ||||||
| chr4:48104289
|
A | T | 200 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0021others(197): Show | 225 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(222): Show |
intron_variant | MODIFIER | c.501+612T>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104289 | ||||||
| chr4:48104290
|
A | T | 157 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0021others(154): Show | 176 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(173): Show |
intron_variant | MODIFIER | c.501+611T>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104290 | ||||||
| chr4:48104295
|
TA | T | 156 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0021others(153): Show | 175 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(172): Show |
intron_variant | MODIFIER | c.501+605delT | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104295 | ||||||
| chr4:48104296
|
AATATAAT others(231): Show |
A | 1 | a0001c0001t0001g0161 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.501+367_501+604del | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104296 | ||||||
| chr4:48104301
|
A | T | 48 | a0001c0001t0006g0247a0001c0002t0001g0014a0001c0002t0001g0090others(45): Show | 54 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(51): Show |
intron_variant | MODIFIER | c.501+600T>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104301 | ||||||
| chr4:48104306
|
A | T | 1 | a0001c0001t0004g0191 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.501+595T>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104306 | ||||||
| chr4:48104308
|
A | T | 1 | a0001c0001t0004g0191 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.501+593T>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104308 | ||||||
| chr4:48104308
|
AATATATA others(53): Show |
A | 1 | a0001c0001t0004g0190 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.501+533_501+592del others(60): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104308 | ||||||
| chr4:48104309
|
A | T | 4 | a0001c0001t0005g0018a0001c0001t0005g0039a0001c0001t0005g0332others(1): Show | 5 | HG01884.hp2 HG02572.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.501+592T>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104309 | ||||||
| chr4:48104315
|
ATAATATA others(219): Show |
A | 145 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0021others(142): Show | 163 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(160): Show |
intron_variant | MODIFIER | c.501+360_501+585del | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104315 | ||||||
| chr4:48104316
|
TAATATAT others(239): Show |
T | 1 | a0001c0002t0001g0079 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.501+339_501+584del | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104316 | ||||||
| chr4:48104317
|
A | T | 50 | a0001c0001t0001g0101a0001c0001t0004g0188a0001c0001t0005g0039others(47): Show | 56 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(53): Show |
intron_variant | MODIFIER | c.501+584T>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104317 | ||||||
| chr4:48104318
|
A | T | 1 | a0001c0001t0004g0188 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.501+583T>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104318 | ||||||
| chr4:48104318
|
ATATATAA others(171): Show |
A | 1 | a0001c0001t0005g0039 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.501+405_501+582del | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104318 | ||||||
| chr4:48104321
|
TATA | T | 6 | a0001c0001t0001g0101a0001c0002t0001g0072a0001c0002t0001g0073others(3): Show | 6 | NA18965.hp1 NA18973.hp2 NA19056.hp1 others(3): Show |
intron_variant | MODIFIER | c.501+577_501+579del others(3): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104321 | ||||||
| chr4:48104325
|
A | T | 3 | a0001c0001t0005g0018a0001c0001t0005g0332a0001c0001t0005g0333 | 4 | HG01884.hp2 HG02572.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.501+576T>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104325 | ||||||
| chr4:48104327
|
A | T | 3 | a0001c0001t0005g0018a0001c0001t0005g0332a0001c0001t0005g0333 | 4 | HG01884.hp2 HG02572.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.501+574T>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104327 | ||||||
| chr4:48104329
|
A | AT | 3 | a0001c0001t0005g0018a0001c0001t0005g0332a0001c0001t0005g0333 | 4 | HG01884.hp2 HG02572.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.501+571_501+572ins others(1): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104329 | ||||||
| chr4:48104329
|
A | T | 49 | a0001c0001t0004g0191a0001c0001t0006g0247a0001c0002t0001g0014others(46): Show | 55 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(52): Show |
intron_variant | MODIFIER | c.501+572T>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104329 | ||||||
| chr4:48104337
|
ATATATAT others(124): Show |
A | 42 | a0001c0001t0006g0247a0001c0002t0001g0014a0001c0002t0001g0090others(39): Show | 48 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(45): Show |
intron_variant | MODIFIER | c.501+433_501+563del | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104337 | ||||||
| chr4:48104342
|
TATAATAT others(136): Show |
T | 1 | a0001c0001t0004g0188 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.501+416_501+558del | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104342 | ||||||
| chr4:48104343
|
ATAATATA others(128): Show |
A | 3 | a0001c0001t0005g0018a0001c0001t0005g0332a0001c0001t0005g0333 | 4 | HG01884.hp2 HG02572.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.501+423_501+557del | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104343 | ||||||
| chr4:48104343
|
ATAATATA others(191): Show |
A | 4 | a0001c0002t0001g0072a0001c0002t0001g0073a0001c0002t0001g0074others(1): Show | 4 | NA18973.hp2 NA19056.hp1 NA19057.hp2 others(1): Show |
intron_variant | MODIFIER | c.501+360_501+557del | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104343 | ||||||
| chr4:48104345
|
A | T | 3 | a0001c0001t0001g0101a0001c0001t0004g0191a0001c0002t0001g0098 | 3 | HG03516.hp2 NA18965.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.501+556T>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104345 | ||||||
| chr4:48104346
|
A | T | 1 | a0001c0001t0004g0191 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.501+555T>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104346 | ||||||
| chr4:48104349
|
TATA | T | 4 | a0001c0001t0001g0101a0001c0001t0002g0048a0001c0001t0002g0303others(1): Show | 4 | NA18965.hp1 NA19006.hp1 NA19087.hp1 others(1): Show |
intron_variant | MODIFIER | c.501+549_501+551del others(3): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104349 | ||||||
| chr4:48104357
|
A | AATATATA others(161): Show |
1 | a0001c0001t0003g0288 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.501+543_501+544ins others(168): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104357 | ||||||
| chr4:48104357
|
A | AATATATA others(77): Show |
1 | a0001c0001t0003g0323 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.501+460_501+543dup others(84): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104357 | ||||||
| chr4:48104357
|
A | AATATATA others(105): Show |
2 | a0001c0001t0003g0289a0001c0001t0003g0324 | 2 | HG02258.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.501+432_501+543dup others(112): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104357 | ||||||
| chr4:48104357
|
A | AATATATA others(133): Show |
3 | a0001c0001t0003g0277a0001c0001t0003g0291a0001c0001t0003g0322 | 3 | HG01891.hp1 HG03041.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.501+543_501+544ins others(140): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104357 | ||||||
| chr4:48104357
|
A | T | 12 | a0001c0001t0002g0048a0001c0001t0002g0218a0001c0001t0002g0303others(9): Show | 12 | HG02559.hp1 HG02717.hp2 HG02886.hp2 others(9): Show |
intron_variant | MODIFIER | c.501+544T>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104357 | ||||||
| chr4:48104357
|
AATATATA others(21): Show |
A | 1 | a0001c0001t0002g0206 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.501+516_501+543del others(28): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104357 | ||||||
| chr4:48104362
|
A | T | 3 | a0001c0001t0004g0189a0001c0001t0004g0194a0001c0001t0004g0257 | 3 | HG02451.hp2 HG02622.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.501+539T>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104362 | ||||||
| chr4:48104364
|
A | T | 3 | a0001c0001t0004g0189a0001c0001t0004g0194a0001c0001t0004g0257 | 3 | HG02451.hp2 HG02622.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.501+537T>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104364 | ||||||
| chr4:48104371
|
ATAATATA others(163): Show |
A | 1 | a0001c0002t0001g0098 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.501+360_501+529del | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104371 | ||||||
| chr4:48104373
|
A | T | 3 | a0001c0001t0004g0190a0001c0010t0001g0217a0002c0003t0001g0085 | 3 | HG02922.hp1 NA18906.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.501+528T>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104373 | ||||||
| chr4:48104377
|
TATA | T | 4 | a0001c0001t0002g0048a0001c0001t0002g0303a0001c0001t0002g0321others(1): Show | 4 | NA19003.hp2 NA19006.hp1 NA19010.hp2 others(1): Show |
intron_variant | MODIFIER | c.501+521_501+523del others(3): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104377 | ||||||
| chr4:48104380
|
A | AATATTAT others(18): Show |
1 | a0001c0002t0001g0314 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.501+496_501+520dup others(25): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104380 | ||||||
| chr4:48104380
|
A | AATATTAT others(102): Show |
1 | a0001c0001t0003g0290 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.501+520_501+521ins others(109): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104380 | ||||||
| chr4:48104385
|
T | A | 4 | a0001c0001t0002g0293a0001c0001t0002g0308a0001c0001t0002g0311others(1): Show | 4 | HG00438.hp2 HG00673.hp2 NA18997.hp2 others(1): Show |
intron_variant | MODIFIER | c.501+516A>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104385 | ||||||
| chr4:48104390
|
A | T | 2 | a0001c0001t0004g0190a0001c0001t0004g0191 | 2 | HG03516.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.501+511T>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104390 | ||||||
| chr4:48104392
|
A | T | 3 | a0001c0001t0001g0101a0001c0001t0004g0190a0001c0001t0004g0191 | 3 | HG03516.hp2 NA18906.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.501+509T>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104392 | ||||||
| chr4:48104401
|
A | T | 10 | a0001c0001t0004g0189a0001c0001t0004g0194a0001c0001t0004g0257others(7): Show | 10 | HG00642.hp2 HG01243.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.501+500T>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104401 | ||||||
| chr4:48104402
|
A | T | 3 | a0001c0001t0004g0189a0001c0001t0004g0194a0001c0001t0004g0257 | 3 | HG02451.hp2 HG02622.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.501+499T>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104402 | ||||||
| chr4:48104405
|
TATA | T | 29 | a0001c0001t0001g0305a0001c0001t0002g0015a0001c0001t0002g0048others(26): Show | 30 | HG00544.hp1 HG00597.hp2 HG00609.hp2 others(27): Show |
intron_variant | MODIFIER | c.501+493_501+495del others(3): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104405 | ||||||
| chr4:48104407
|
TA | T | 3 | a0001c0001t0004g0189a0001c0001t0004g0194a0001c0001t0004g0257 | 3 | HG02451.hp2 HG02622.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.501+493delT | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104407 | ||||||
| chr4:48104408
|
A | AATATTAT others(18): Show |
2 | a0001c0001t0002g0293a0001c0001t0002g0308 | 2 | HG00438.hp2 HG00673.hp2 |
intron_variant | MODIFIER | c.501+468_501+492dup others(25): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104408 | ||||||
| chr4:48104413
|
T | A | 3 | a0001c0001t0004g0189a0001c0001t0004g0194a0001c0001t0004g0257 | 3 | HG02451.hp2 HG02622.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.501+488A>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104413 | ||||||
| chr4:48104418
|
A | T | 12 | a0001c0001t0004g0094a0001c0001t0004g0124a0001c0001t0004g0180others(9): Show | 12 | HG01255.hp2 HG02109.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.501+483T>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104418 | ||||||
| chr4:48104419
|
T | A | 1 | a0001c0001t0002g0310 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.501+482A>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104419 | ||||||
| chr4:48104420
|
A | T | 14 | a0001c0001t0001g0101a0001c0001t0002g0310a0001c0001t0004g0094others(11): Show | 14 | HG01255.hp2 HG02109.hp1 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.501+481T>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104420 | ||||||
| chr4:48104426
|
TATA | T | 3 | a0001c0001t0004g0189a0001c0001t0004g0194a0001c0001t0004g0257 | 3 | HG02451.hp2 HG02622.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.501+472_501+474del others(3): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104426 | ||||||
| chr4:48104429
|
A | T | 13 | a0001c0001t0002g0310a0001c0001t0004g0190a0001c0001t0004g0191others(10): Show | 13 | HG00642.hp2 HG01993.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.501+472T>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104429 | ||||||
| chr4:48104430
|
A | T | 2 | a0001c0001t0004g0190a0001c0001t0004g0191 | 2 | HG03516.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.501+471T>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104430 | ||||||
| chr4:48104439
|
AT | A | 4 | a0001c0001t0002g0310a0001c0001t0004g0189a0001c0001t0004g0194others(1): Show | 4 | HG02451.hp2 HG02622.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.501+461delA | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104439 | ||||||
| chr4:48104441
|
T | A | 2 | a0001c0001t0004g0190a0001c0001t0004g0191 | 2 | HG03516.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.501+460A>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104441 | ||||||
| chr4:48104446
|
A | T | 3 | a0001c0001t0004g0189a0001c0001t0004g0194a0001c0001t0004g0257 | 3 | HG02451.hp2 HG02622.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.501+455T>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104446 | ||||||
| chr4:48104448
|
A | T | 7 | a0001c0001t0002g0216a0001c0001t0002g0303a0001c0001t0002g0327others(4): Show | 7 | HG02451.hp2 HG02622.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.501+453T>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104448 | ||||||
| chr4:48104449
|
A | T | 1 | a0001c0015t0001g0033 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.501+452T>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104449 | ||||||
| chr4:48104449
|
ATATATAT others(12): Show |
A | 2 | a0002c0003t0001g0085a0002c0003t0001g0255 | 2 | NA19063.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.501+433_501+451del others(19): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104449 | ||||||
| chr4:48104449
|
ATATATAT others(40): Show |
A | 1 | a0001c0001t0001g0101 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.501+405_501+451del others(47): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104449 | ||||||
| chr4:48104457
|
A | T | 19 | a0001c0001t0004g0094a0001c0001t0004g0124a0001c0001t0004g0180others(16): Show | 19 | HG00642.hp2 HG01255.hp2 HG01993.hp2 others(16): Show |
intron_variant | MODIFIER | c.501+444T>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104457 | ||||||
| chr4:48104458
|
A | T | 16 | a0001c0001t0004g0094a0001c0001t0004g0124a0001c0001t0004g0180others(13): Show | 16 | HG00642.hp2 HG01255.hp2 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.501+443T>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104458 | ||||||
| chr4:48104463
|
TA | T | 12 | a0001c0001t0004g0094a0001c0001t0004g0124a0001c0001t0004g0180others(9): Show | 12 | HG01255.hp2 HG02109.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.501+437delT | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104463 | ||||||
| chr4:48104464
|
AATAT | A | 4 | a0001c0002t0001g0256a0001c0002t0001g0269a0001c0002t0001g0270others(1): Show | 4 | HG00642.hp2 HG02615.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.501+433_501+436del others(4): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104464 | ||||||
| chr4:48104467
|
AT | A | 7 | a0001c0001t0001g0147a0001c0001t0002g0300a0001c0001t0004g0190others(4): Show | 7 | HG02109.hp2 HG02145.hp1 HG02155.hp2 others(4): Show |
intron_variant | MODIFIER | c.501+433delA | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104467 | ||||||
| chr4:48104467
|
ATTATATA others(1): Show |
A | 4 | a0001c0001t0004g0189a0001c0001t0004g0194a0001c0001t0004g0257others(1): Show | 4 | HG01243.hp2 HG02451.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.501+426_501+433del others(8): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104467 | ||||||
| chr4:48104469
|
T | A | 12 | a0001c0001t0004g0094a0001c0001t0004g0124a0001c0001t0004g0180others(9): Show | 12 | HG01255.hp2 HG02109.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.501+432A>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104469 | ||||||
| chr4:48104474
|
A | T | 6 | a0001c0001t0001g0147a0001c0001t0004g0190a0001c0001t0004g0191others(3): Show | 6 | HG02109.hp2 HG02145.hp1 HG02155.hp2 others(3): Show |
intron_variant | MODIFIER | c.501+427T>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104474 | ||||||
| chr4:48104476
|
T | A | 34 | a0001c0001t0003g0215a0001c0001t0003g0277a0001c0001t0003g0281others(31): Show | 34 | HG00642.hp2 HG01255.hp2 HG01891.hp1 others(31): Show |
intron_variant | MODIFIER | c.501+425A>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104476 | ||||||
| chr4:48104477
|
A | T | 44 | a0001c0001t0006g0247a0001c0002t0001g0014a0001c0002t0001g0090others(41): Show | 50 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(47): Show |
intron_variant | MODIFIER | c.501+424T>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104477 | ||||||
| chr4:48104479
|
A | ATATATAA others(49): Show |
1 | a0001c0001t0003g0281 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.501+421_501+422ins others(56): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104479 | ||||||
| chr4:48104482
|
TATA | T | 16 | a0001c0001t0004g0094a0001c0001t0004g0124a0001c0001t0004g0180others(13): Show | 16 | HG00642.hp2 HG01255.hp2 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.501+416_501+418del others(3): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104482 | ||||||
| chr4:48104483
|
A | T | 1 | a0002c0003t0001g0251 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.501+418T>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104483 | ||||||
| chr4:48104484
|
T | A | 2 | a0001c0008t0003g0221a0001c0008t0003g0230 | 2 | HG02559.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.501+417A>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104484 | ||||||
| chr4:48104484
|
TA | T | 3 | a0001c0001t0005g0018a0001c0001t0005g0332a0001c0001t0005g0333 | 4 | HG01884.hp2 HG02572.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.501+416delT | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104484 | ||||||
| chr4:48104485
|
A | T | 7 | a0001c0008t0003g0221a0001c0008t0003g0230a0001c0008t0006g0232others(4): Show | 7 | HG01993.hp2 HG02055.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.501+416T>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104485 | ||||||
| chr4:48104486
|
A | T | 2 | a0002c0003t0001g0245a0002c0003t0001g0331 | 2 | HG02055.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.501+415T>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104486 | ||||||
| chr4:48104486
|
ATATATAA others(3): Show |
A | 1 | a0001c0015t0001g0033 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.501+405_501+414del others(10): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104486 | ||||||
| chr4:48104488
|
ATATAATA others(1): Show |
A | 3 | a0001c0001t0004g0189a0001c0001t0004g0194a0001c0001t0004g0257 | 3 | HG02451.hp2 HG02622.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.501+405_501+412del others(8): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104488 | ||||||
| chr4:48104493
|
ATAT | A | 8 | a0001c0001t0001g0147a0001c0002t0001g0202a0001c0002t0001g0256others(5): Show | 8 | HG00642.hp2 HG02109.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.501+405_501+407del others(3): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104493 | ||||||
| chr4:48104495
|
AT | A | 17 | a0001c0001t0004g0094a0001c0001t0004g0124a0001c0001t0004g0180others(14): Show | 18 | HG01255.hp2 HG01884.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.501+405delA | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104495 | ||||||
| chr4:48104495
|
ATTATATA others(1): Show |
A | 44 | a0001c0001t0006g0247a0001c0002t0001g0014a0001c0002t0001g0090others(41): Show | 50 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(47): Show |
intron_variant | MODIFIER | c.501+398_501+405del others(8): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104495 | ||||||
| chr4:48104495
|
ATTATATA others(40): Show |
A | 1 | a0001c0001t0004g0191 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.501+359_501+405del others(47): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104495 | ||||||
| chr4:48104496
|
T | A | 2 | a0002c0003t0001g0245a0002c0003t0001g0331 | 2 | HG02055.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.501+405A>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104496 | ||||||
| chr4:48104497
|
T | A | 1 | a0002c0003t0001g0251 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.501+404A>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104497 | ||||||
| chr4:48104502
|
A | T | 28 | a0001c0001t0004g0094a0001c0001t0004g0124a0001c0001t0004g0180others(25): Show | 31 | HG01255.hp2 HG01884.hp2 HG02109.hp1 others(28): Show |
intron_variant | MODIFIER | c.501+399T>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104502 | ||||||
| chr4:48104503
|
T | A | 2 | a0002c0003t0001g0245a0002c0003t0001g0331 | 2 | HG02055.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.501+398A>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104503 | ||||||
| chr4:48104503
|
T | TAATATAT others(22): Show |
1 | a0001c0001t0002g0327 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.501+397_501+398ins others(29): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104503 | ||||||
| chr4:48104504
|
T | A | 16 | a0001c0001t0002g0216a0001c0001t0003g0277a0001c0001t0003g0281others(13): Show | 16 | HG01891.hp1 HG02258.hp1 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.501+397A>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104504 | ||||||
| chr4:48104504
|
T | TATATATA others(21): Show |
3 | a0001c0001t0002g0207a0001c0001t0002g0211a0001c0001t0002g0214 | 3 | HG01099.hp2 HG01496.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.501+396_501+397ins others(28): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104504 | ||||||
| chr4:48104505
|
A | T | 5 | a0001c0002t0001g0256a0001c0002t0001g0269a0001c0002t0001g0270others(2): Show | 5 | HG00642.hp2 HG01243.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.501+396T>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104505 | ||||||
| chr4:48104513
|
A | AATATATA others(68): Show |
1 | a0001c0008t0003g0231 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.501+387_501+388ins others(75): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104513 | ||||||
| chr4:48104513
|
A | T | 2 | a0001c0008t0006g0232a0001c0010t0001g0117 | 2 | HG02717.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.501+388T>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104513 | ||||||
| chr4:48104519
|
TA | T | 47 | a0001c0001t0006g0247a0001c0002t0001g0014a0001c0002t0001g0090others(44): Show | 53 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(50): Show |
intron_variant | MODIFIER | c.501+381delT | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104519 | ||||||
| chr4:48104521
|
A | T | 2 | a0001c0007t0001g0122a0001c0007t0001g0123 | 2 | HG02109.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.501+380T>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104521 | ||||||
| chr4:48104523
|
A | T | 48 | a0001c0001t0006g0247a0001c0002t0001g0014a0001c0002t0001g0090others(45): Show | 54 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(51): Show |
intron_variant | MODIFIER | c.501+378T>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104523 | ||||||
| chr4:48104523
|
AT | A | 4 | a0001c0001t0001g0101a0001c0001t0001g0147a0001c0007t0001g0123others(1): Show | 4 | HG01243.hp2 HG02109.hp2 HG02155.hp2 others(1): Show |
intron_variant | MODIFIER | c.501+377delA | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104523 | ||||||
| chr4:48104524
|
T | TA | 27 | a0001c0001t0004g0094a0001c0001t0004g0124a0001c0001t0004g0180others(24): Show | 28 | HG00642.hp2 HG01255.hp2 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.501+376_501+377ins others(1): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104524 | ||||||
| chr4:48104532
|
T | A | 160 | a0001c0001t0001g0101a0001c0001t0001g0147a0001c0001t0001g0305others(157): Show | 171 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(168): Show |
intron_variant | MODIFIER | c.501+369A>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104532 | ||||||
| chr4:48104532
|
T | TATATATA others(12): Show |
2 | a0001c0008t0003g0221a0001c0008t0003g0230 | 2 | HG02559.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.501+368_501+369ins others(19): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104532 | ||||||
| chr4:48104532
|
T | TATATATA others(21): Show |
1 | a0001c0001t0002g0196 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.501+368_501+369ins others(28): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104532 | ||||||
| chr4:48104532
|
T | TATATATA others(49): Show |
2 | a0001c0001t0002g0210a0001c0001t0002g0212 | 2 | HG00738.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.501+368_501+369ins others(56): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104532 | ||||||
| chr4:48104539
|
ATT | A | 5 | a0001c0001t0001g0101a0001c0001t0001g0147a0001c0002t0001g0202others(2): Show | 5 | HG02109.hp2 HG02145.hp1 HG02155.hp2 others(2): Show |
intron_variant | MODIFIER | c.501+360_501+361del others(2): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104539 | ||||||
| chr4:48104540
|
T | TAATATAT others(14): Show |
1 | a0001c0001t0003g0215 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.501+360_501+361ins others(21): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104540 | ||||||
| chr4:48104541
|
T | A | 9 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0150others(6): Show | 9 | HG00642.hp2 HG01952.hp2 HG01981.hp1 others(6): Show |
intron_variant | MODIFIER | c.501+360A>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104541 | ||||||
| chr4:48104542
|
T | A | 3 | a0001c0001t0003g0215a0001c0008t0006g0232a0001c0010t0001g0217 | 3 | HG02886.hp2 HG02922.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.501+359A>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104542 | ||||||
| chr4:48104545
|
TATATATA | T | 52 | a0001c0001t0006g0247a0001c0002t0001g0014a0001c0002t0001g0090others(49): Show | 58 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(55): Show |
intron_variant | MODIFIER | c.501+349_501+355del others(7): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104545 | ||||||
| chr4:48104547
|
T | TAATATTA others(107): Show |
1 | a0001c0010t0001g0217 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.501+353_501+354ins others(114): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104547 | ||||||
| chr4:48104552
|
A | T | 5 | a0001c0008t0003g0221a0001c0008t0003g0230a0001c0008t0006g0232others(2): Show | 5 | HG02559.hp1 HG02717.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.501+349T>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104552 | ||||||
| chr4:48104559
|
AAT | A | 39 | a0001c0001t0001g0305a0001c0001t0002g0015a0001c0001t0002g0016others(36): Show | 41 | HG00438.hp2 HG00544.hp1 HG00597.hp2 others(38): Show |
intron_variant | MODIFIER | c.501+340_501+341del others(2): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104559 | ||||||
| chr4:48104560
|
A | T | 2 | a0001c0001t0004g0191a0001c0008t0003g0231 | 2 | HG03516.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.501+341T>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104560 | ||||||
| chr4:48104562
|
A | T | 1 | a0001c0001t0004g0191 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.501+339T>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104562 | ||||||
| chr4:48104570
|
ATAAT | A | 11 | a0001c0005t0001g0004a0001c0005t0001g0022a0001c0005t0001g0023others(8): Show | 13 | HG01884.hp1 HG02257.hp1 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.501+327_501+330del others(4): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104570 | ||||||
| chr4:48104572
|
AAT | A | 204 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0021others(201): Show | 228 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(225): Show |
intron_variant | MODIFIER | c.501+327_501+328del others(2): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104572 | ||||||
| chr4:48104573
|
A | T | 2 | a0001c0001t0004g0191a0003c0004t0003g0137 | 2 | HG00639.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.501+328T>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104573 | ||||||
| chr4:48104574
|
T | A | 2 | a0001c0001t0004g0191a0003c0004t0003g0137 | 2 | HG00639.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.501+327A>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104574 | ||||||
| chr4:48104581
|
A | T | 35 | a0001c0001t0004g0094a0001c0001t0004g0124a0001c0001t0004g0180others(32): Show | 36 | HG00642.hp1 HG01192.hp1 HG01243.hp2 others(33): Show |
intron_variant | MODIFIER | c.501+320T>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104581 | ||||||
| chr4:48104584
|
A | T | 66 | a0001c0001t0004g0182a0001c0001t0004g0191a0001c0001t0006g0247others(63): Show | 74 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(71): Show |
intron_variant | MODIFIER | c.501+317T>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104584 | ||||||
| chr4:48104586
|
A | T | 45 | a0001c0001t0006g0247a0001c0002t0001g0014a0001c0002t0001g0090others(42): Show | 51 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(48): Show |
intron_variant | MODIFIER | c.501+315T>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104586 | ||||||
| chr4:48104591
|
T | G | 1 | a0001c0001t0003g0136 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.501+310A>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104591 | ||||||
| chr4:48104591
|
TATATAG | T | 4 | a0002c0003t0001g0268a0002c0003t0001g0329a0002c0003t0001g0330others(1): Show | 4 | HG01192.hp1 HG02055.hp2 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.501+304_501+309del others(6): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104591 | ||||||
| chr4:48104593
|
T | G | 24 | a0001c0001t0001g0129a0001c0001t0001g0162a0001c0001t0001g0163others(21): Show | 24 | HG00673.hp1 HG00738.hp1 HG01109.hp2 others(21): Show |
intron_variant | MODIFIER | c.501+308A>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104593 | ||||||
| chr4:48104595
|
T | G | 184 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0021others(181): Show | 200 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(197): Show |
intron_variant | MODIFIER | c.501+306A>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104595 | ||||||
| chr4:48104595
|
TAG | T | 24 | a0001c0001t0004g0094a0001c0001t0004g0124a0001c0001t0004g0180others(21): Show | 25 | HG00642.hp1 HG01243.hp2 HG01255.hp2 others(22): Show |
intron_variant | MODIFIER | c.501+304_501+305del others(2): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104595 | ||||||
| chr4:48104597
|
G | T | 41 | a0001c0001t0002g0225a0001c0001t0002g0226a0001c0001t0002g0272others(38): Show | 46 | HG00323.hp1 HG00408.hp2 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.501+304C>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104597 | ||||||
| chr4:48104599
|
G | T | 27 | a0001c0001t0002g0225a0001c0001t0002g0272a0001c0001t0003g0290others(24): Show | 32 | HG01109.hp1 HG01123.hp2 HG01243.hp2 others(29): Show |
intron_variant | MODIFIER | c.501+302C>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104599 | ||||||
| chr4:48104601
|
G | T | 3 | a0001c0006t0001g0029a0001c0006t0001g0030a0001c0006t0001g0031 | 3 | HG02145.hp2 HG02451.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.501+300C>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104601 | ||||||
| chr4:48104679
|
CT | C | 22 | a0001c0001t0004g0094a0001c0001t0004g0124a0001c0001t0004g0180others(19): Show | 23 | HG01255.hp2 HG01884.hp2 HG02109.hp1 others(20): Show |
intron_variant | MODIFIER | c.501+221delA | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104679 | ||||||
| chr4:48104797
|
T | C | 1 | a0001c0001t0002g0316 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.501+104A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104797 | ||||||
| chr4:48104957
|
T | G | 1 | a0001c0001t0005g0039 | 1 | HG02965.hp2 | splice_acceptor_variant&intron_variant | HIGH | c.447-2A>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 5/14 | chr4 | 48104957 | ||||||
| chr4:48105070
|
G | C | 4 | a0001c0002t0001g0256a0001c0002t0001g0269a0001c0002t0001g0270others(1): Show | 4 | HG00642.hp2 HG02615.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.447-115C>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 5/14 | chr4 | 48105070 | ||||||
| chr4:48105079
|
T | A | 53 | a0001c0001t0006g0247a0001c0002t0001g0014a0001c0002t0001g0090others(50): Show | 59 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(56): Show |
intron_variant | MODIFIER | c.447-124A>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 5/14 | chr4 | 48105079 | ||||||
| chr4:48105080
|
A | T | 1 | a0001c0001t0002g0316 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.447-125T>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 5/14 | chr4 | 48105080 | ||||||
| chr4:48105109
|
T | C | 80 | a0001c0001t0001g0086a0001c0001t0001g0101a0001c0001t0002g0064others(77): Show | 88 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(85): Show |
intron_variant | MODIFIER | c.447-154A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 5/14 | chr4 | 48105109 | ||||||
| chr4:48105287
|
C | G | 48 | a0001c0001t0006g0247a0001c0002t0001g0014a0001c0002t0001g0090others(45): Show | 54 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(51): Show |
intron_variant | MODIFIER | c.447-332G>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 5/14 | chr4 | 48105287 | ||||||
| chr4:48105293
|
G | A | 251 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0021others(248): Show | 278 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(275): Show |
intron_variant | MODIFIER | c.447-338C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 5/14 | chr4 | 48105293 | ||||||
| chr4:48105478
|
G | T | 14 | a0001c0005t0001g0004a0001c0005t0001g0022a0001c0005t0001g0023others(11): Show | 16 | HG01884.hp1 HG02145.hp2 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.447-523C>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 5/14 | chr4 | 48105478 | ||||||
| chr4:48105547
|
G | A | 14 | a0001c0005t0001g0004a0001c0005t0001g0022a0001c0005t0001g0023others(11): Show | 16 | HG01884.hp1 HG02145.hp2 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.447-592C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 5/14 | chr4 | 48105547 | ||||||
| chr4:48105572
|
G | C | 19 | a0001c0001t0001g0115a0001c0001t0001g0120a0001c0001t0003g0102others(16): Show | 22 | HG00323.hp1 HG00639.hp2 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.447-617C>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 5/14 | chr4 | 48105572 | ||||||
| chr4:48105588
|
A | G | 22 | a0001c0001t0004g0094a0001c0001t0004g0124a0001c0001t0004g0180others(19): Show | 23 | HG01255.hp2 HG01884.hp2 HG02109.hp1 others(20): Show |
intron_variant | MODIFIER | c.447-633T>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 5/14 | chr4 | 48105588 | ||||||
| chr4:48105620
|
C | T | 1 | a0001c0001t0003g0215 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.447-665G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 5/14 | chr4 | 48105620 | ||||||
| chr4:48105624
|
C | T | 14 | a0001c0005t0001g0004a0001c0005t0001g0022a0001c0005t0001g0023others(11): Show | 16 | HG01884.hp1 HG02145.hp2 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.447-669G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 5/14 | chr4 | 48105624 | ||||||
| chr4:48105663
|
G | A | 1 | a0001c0015t0001g0033 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.447-708C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 5/14 | chr4 | 48105663 | ||||||
| chr4:48105694
|
A | T | 1 | a0001c0001t0005g0039 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.447-739T>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 5/14 | chr4 | 48105694 | ||||||
| chr4:48105702
|
A | G | 14 | a0001c0005t0001g0004a0001c0005t0001g0022a0001c0005t0001g0023others(11): Show | 16 | HG01884.hp1 HG02145.hp2 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.447-747T>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 5/14 | chr4 | 48105702 | ||||||
| chr4:48105741
|
C | T | 22 | a0001c0001t0004g0094a0001c0001t0004g0124a0001c0001t0004g0180others(19): Show | 23 | HG01255.hp2 HG01884.hp2 HG02109.hp1 others(20): Show |
intron_variant | MODIFIER | c.447-786G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 5/14 | chr4 | 48105741 | ||||||
| chr4:48106041
|
A | G | 1 | a0002c0003t0001g0173 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.447-1086T>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 5/14 | chr4 | 48106041 | ||||||
| chr4:48106121
|
C | T | 2 | a0001c0001t0004g0094a0001c0001t0004g0189 | 2 | HG01255.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.447-1166G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 5/14 | chr4 | 48106121 | ||||||
| chr4:48106185
|
G | A | 1 | a0001c0015t0001g0033 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.447-1230C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 5/14 | chr4 | 48106185 | ||||||
| chr4:48106210
|
A | C | 214 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0021others(211): Show | 238 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(235): Show |
intron_variant | MODIFIER | c.447-1255T>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 5/14 | chr4 | 48106210 | ||||||
| chr4:48106388
|
G | GT | 128 | a0001c0001t0001g0086a0001c0001t0001g0101a0001c0001t0001g0129others(125): Show | 139 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(136): Show |
intron_variant | MODIFIER | c.447-1434dupA | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 5/14 | chr4 | 48106388 | ||||||
| chr4:48106392
|
T | G | 1 | a0001c0002t0001g0319 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.447-1437A>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 5/14 | chr4 | 48106392 | ||||||
| chr4:48106548
|
G | C | 2 | a0001c0001t0001g0164a0001c0001t0001g0165 | 2 | NA18992.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.447-1593C>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 5/14 | chr4 | 48106548 | ||||||
| chr4:48106598
|
A | G | 1 | a0001c0001t0001g0120 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.447-1643T>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 5/14 | chr4 | 48106598 | ||||||
| chr4:48106642
|
T | C | 1 | a0001c0001t0003g0289 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.447-1687A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 5/14 | chr4 | 48106642 | ||||||
| chr4:48106805
|
A | G | 12 | a0001c0007t0001g0032a0001c0007t0001g0107a0001c0007t0001g0118others(9): Show | 12 | HG01255.hp1 HG02109.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.447-1850T>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 5/14 | chr4 | 48106805 | ||||||
| chr4:48106901
|
T | A | 16 | a0001c0001t0003g0102a0001c0001t0003g0103a0001c0001t0003g0104others(13): Show | 19 | HG00323.hp1 HG00639.hp2 HG01109.hp1 others(16): Show |
intron_variant | MODIFIER | c.447-1946A>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 5/14 | chr4 | 48106901 | ||||||
| chr4:48106914
|
A | G | 1 | a0001c0001t0001g0120 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.447-1959T>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 5/14 | chr4 | 48106914 | ||||||
| chr4:48106960
|
A | C | 1 | a0002c0003t0001g0330 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.447-2005T>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 5/14 | chr4 | 48106960 | ||||||
| chr4:48107303
|
C | A | 17 | a0001c0002t0001g0062a0001c0002t0001g0076a0001c0002t0001g0077others(14): Show | 17 | HG01167.hp1 HG01891.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.447-2348G>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 5/14 | chr4 | 48107303 | ||||||
| chr4:48107373
|
A | T | 1 | a0001c0001t0002g0316 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.447-2418T>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 5/14 | chr4 | 48107373 | ||||||
| chr4:48107386
|
C | G | 1 | a0001c0001t0002g0316 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.447-2431G>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 5/14 | chr4 | 48107386 | ||||||
| chr4:48107387
|
T | C | 1 | a0001c0001t0002g0316 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.447-2432A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 5/14 | chr4 | 48107387 | ||||||
| chr4:48107388
|
C | T | 1 | a0001c0001t0002g0316 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.447-2433G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 5/14 | chr4 | 48107388 | ||||||
| chr4:48107393
|
C | G | 1 | a0001c0001t0009g0220 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.447-2438G>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 5/14 | chr4 | 48107393 | ||||||
| chr4:48107438
|
C | T | 48 | a0001c0001t0006g0247a0001c0002t0001g0014a0001c0002t0001g0090others(45): Show | 54 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(51): Show |
intron_variant | MODIFIER | c.447-2483G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 5/14 | chr4 | 48107438 | ||||||
| chr4:48107574
|
G | A | 2 | a0001c0001t0001g0164a0001c0001t0001g0165 | 2 | NA18992.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.447-2619C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 5/14 | chr4 | 48107574 | ||||||
| chr4:48107723
|
A | C | 257 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0021others(254): Show | 284 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(281): Show |
intron_variant | MODIFIER | c.447-2768T>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 5/14 | chr4 | 48107723 | ||||||
| chr4:48107753
|
C | A | 1 | a0001c0015t0001g0033 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.446+2785G>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 5/14 | chr4 | 48107753 | ||||||
| chr4:48107758
|
C | A | 3 | a0001c0008t0003g0221a0001c0008t0003g0230a0001c0008t0003g0231 | 3 | HG02559.hp1 HG02897.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.446+2780G>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 5/14 | chr4 | 48107758 | ||||||
| chr4:48107800
|
C | T | 1 | a0001c0001t0003g0102 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.446+2738G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 5/14 | chr4 | 48107800 | ||||||
| chr4:48107838
|
G | A | 1 | a0002c0003t0001g0058 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.446+2700C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 5/14 | chr4 | 48107838 | ||||||
| chr4:48107899
|
T | TA | 32 | a0001c0001t0002g0198a0001c0001t0002g0213a0001c0001t0002g0214others(29): Show | 33 | HG00597.hp2 HG00735.hp2 HG01243.hp1 others(30): Show |
intron_variant | MODIFIER | c.446+2638dupT | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 5/14 | chr4 | 48107899 | ||||||
| chr4:48107899
|
T | TAA | 6 | a0001c0001t0002g0316a0001c0001t0003g0290a0001c0007t0001g0032others(3): Show | 6 | HG01255.hp1 HG02145.hp1 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.446+2637_446+2638d others(4): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 5/14 | chr4 | 48107899 | ||||||
| chr4:48107899
|
TA | T | 8 | a0001c0005t0001g0022a0001c0005t0001g0023a0001c0005t0001g0024others(5): Show | 8 | HG01884.hp1 HG02257.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.446+2638delT | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 5/14 | chr4 | 48107899 | ||||||
| chr4:48107899
|
TAAAAAAA others(5): Show |
T | 4 | a0001c0001t0001g0166a0001c0001t0001g0169a0001c0001t0001g0178others(1): Show | 4 | HG02258.hp2 HG02922.hp2 NA18967.hp1 others(1): Show |
intron_variant | MODIFIER | c.446+2627_446+2638d others(14): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 5/14 | chr4 | 48107899 | ||||||
| chr4:48107899
|
TAAAAAAA others(6): Show |
T | 204 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0021others(201): Show | 228 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(225): Show |
intron_variant | MODIFIER | c.446+2626_446+2638d others(15): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 5/14 | chr4 | 48107899 | ||||||
| chr4:48107939
|
C | T | 1 | a0001c0001t0004g0182 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.446+2599G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 5/14 | chr4 | 48107939 | ||||||
| chr4:48107945
|
C | G | 208 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0021others(205): Show | 232 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(229): Show |
intron_variant | MODIFIER | c.446+2593G>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 5/14 | chr4 | 48107945 | ||||||
| chr4:48107965
|
G | A | 1 | a0001c0015t0001g0033 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.446+2573C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 5/14 | chr4 | 48107965 | ||||||
| chr4:48108072
|
AAAAT | A | 12 | a0001c0007t0001g0032a0001c0007t0001g0107a0001c0007t0001g0118others(9): Show | 12 | HG01255.hp1 HG02109.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.446+2462_446+2465d others(6): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 5/14 | chr4 | 48108072 | ||||||
| chr4:48108199
|
G | T | 1 | a0001c0002t0001g0082 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.446+2339C>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 5/14 | chr4 | 48108199 | ||||||
| chr4:48108227
|
A | T | 1 | a0002c0003t0001g0235 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.446+2311T>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 5/14 | chr4 | 48108227 | ||||||
| chr4:48108280
|
T | C | 1 | a0001c0015t0001g0033 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.446+2258A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 5/14 | chr4 | 48108280 | ||||||
| chr4:48108323
|
TTTCATAG others(6): Show |
T | 1 | a0001c0002t0001g0121 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.446+2202_446+2214d others(15): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 5/14 | chr4 | 48108323 | ||||||
| chr4:48108324
|
T | G | 79 | a0001c0001t0001g0086a0001c0001t0001g0101a0001c0001t0002g0064others(76): Show | 87 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.446+2214A>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 5/14 | chr4 | 48108324 | ||||||
| chr4:48108337
|
A | C | 1 | a0001c0002t0001g0121 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.446+2201T>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 5/14 | chr4 | 48108337 | ||||||
| chr4:48108338
|
A | C | 1 | a0001c0002t0001g0121 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.446+2200T>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 5/14 | chr4 | 48108338 | ||||||
| chr4:48108381
|
C | T | 245 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0021others(242): Show | 272 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(269): Show |
intron_variant | MODIFIER | c.446+2157G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 5/14 | chr4 | 48108381 | ||||||
| chr4:48108394
|
T | C | 1 | a0001c0006t0001g0292 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.446+2144A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 5/14 | chr4 | 48108394 | ||||||
| chr4:48108404
|
T | C | 14 | a0001c0005t0001g0004a0001c0005t0001g0022a0001c0005t0001g0023others(11): Show | 16 | HG01884.hp1 HG02145.hp2 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.446+2134A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 5/14 | chr4 | 48108404 | ||||||
| chr4:48108832
|
C | T | 14 | a0001c0005t0001g0004a0001c0005t0001g0022a0001c0005t0001g0023others(11): Show | 16 | HG01884.hp1 HG02145.hp2 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.446+1706G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 5/14 | chr4 | 48108832 | ||||||
| chr4:48109148
|
G | A | 1 | a0001c0015t0001g0033 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.446+1390C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 5/14 | chr4 | 48109148 | ||||||
| chr4:48109181
|
C | CT | 142 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0115others(139): Show | 159 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(156): Show |
intron_variant | MODIFIER | c.446+1356dupA | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 5/14 | chr4 | 48109181 | ||||||
| chr4:48109181
|
C | CTT | 11 | a0001c0001t0001g0021a0001c0001t0001g0050a0001c0001t0001g0128others(8): Show | 11 | HG02129.hp2 NA18612.hp1 NA18949.hp1 others(8): Show |
intron_variant | MODIFIER | c.446+1355_446+1356d others(4): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 5/14 | chr4 | 48109181 | ||||||
| chr4:48109181
|
CT | C | 15 | a0001c0002t0001g0081a0001c0005t0001g0004a0001c0005t0001g0022others(12): Show | 17 | HG01884.hp1 HG02145.hp2 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.446+1356delA | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 5/14 | chr4 | 48109181 | ||||||
| chr4:48109200
|
C | CT | 14 | a0001c0005t0001g0004a0001c0005t0001g0022a0001c0005t0001g0023others(11): Show | 16 | HG01884.hp1 HG02145.hp2 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.446+1337dupA | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 5/14 | chr4 | 48109200 | ||||||
| chr4:48109216
|
A | C | 1 | a0001c0001t0001g0012 | 2 | NA18949.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.446+1322T>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 5/14 | chr4 | 48109216 | ||||||
| chr4:48109401
|
C | T | 47 | a0001c0001t0006g0247a0001c0002t0001g0014a0001c0002t0001g0090others(44): Show | 53 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(50): Show |
intron_variant | MODIFIER | c.446+1137G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 5/14 | chr4 | 48109401 | ||||||
| chr4:48109402
|
G | A | 14 | a0001c0005t0001g0004a0001c0005t0001g0022a0001c0005t0001g0023others(11): Show | 16 | HG01884.hp1 HG02145.hp2 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.446+1136C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 5/14 | chr4 | 48109402 | ||||||
| chr4:48109506
|
T | C | 1 | a0002c0003t0001g0056 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.446+1032A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 5/14 | chr4 | 48109506 | ||||||
| chr4:48109670
|
A | C | 1 | a0001c0001t0007g0119 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.446+868T>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 5/14 | chr4 | 48109670 | ||||||
| chr4:48109874
|
G | C | 5 | a0002c0003t0001g0249a0002c0003t0001g0268a0002c0003t0001g0329others(2): Show | 5 | HG00280.hp2 HG01192.hp1 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.446+664C>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 5/14 | chr4 | 48109874 | ||||||
| chr4:48110057
|
A | G | 1 | a0001c0007t0001g0118 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.446+481T>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 5/14 | chr4 | 48110057 | ||||||
| chr4:48110088
|
C | T | 1 | a0001c0001t0006g0247 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.446+450G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 5/14 | chr4 | 48110088 | ||||||
| chr4:48110219
|
C | A | 19 | a0001c0001t0004g0094a0001c0001t0004g0124a0001c0001t0004g0180others(16): Show | 19 | HG01255.hp2 HG02055.hp1 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.446+319G>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 5/14 | chr4 | 48110219 | ||||||
| chr4:48110274
|
A | T | 195 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0021others(192): Show | 212 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(209): Show |
intron_variant | MODIFIER | c.446+264T>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 5/14 | chr4 | 48110274 | ||||||
| chr4:48110365
|
A | T | 233 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0021others(230): Show | 253 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(250): Show |
intron_variant | MODIFIER | c.446+173T>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 5/14 | chr4 | 48110365 | ||||||
| chr4:48110442
|
CT | C | 7 | a0001c0005t0001g0004a0001c0005t0001g0022a0001c0005t0001g0023others(4): Show | 9 | HG02257.hp1 HG02486.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.446+95delA | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 5/14 | chr4 | 48110442 | ||||||
| chr4:48110619
|
A | G | 3 | a0001c0006t0001g0028a0001c0006t0001g0029a0001c0006t0001g0030 | 3 | HG02145.hp2 HG02451.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.381-16T>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 4/14 | chr4 | 48110619 | ||||||
| chr4:48110931
|
A | G | 1 | a0001c0001t0003g0136 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.381-328T>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 4/14 | chr4 | 48110931 | ||||||
| chr4:48111070
|
G | A | 11 | a0001c0005t0001g0004a0001c0005t0001g0022a0001c0005t0001g0023others(8): Show | 13 | HG02145.hp2 HG02257.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.381-467C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 4/14 | chr4 | 48111070 | ||||||
| chr4:48111128
|
T | C | 1 | a0001c0001t0003g0215 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.381-525A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 4/14 | chr4 | 48111128 | ||||||
| chr4:48111202
|
C | G | 58 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0021others(55): Show | 65 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(62): Show |
intron_variant | MODIFIER | c.381-599G>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 4/14 | chr4 | 48111202 | ||||||
| chr4:48111374
|
T | C | 50 | a0001c0001t0006g0247a0001c0002t0001g0248a0001c0002t0001g0256others(47): Show | 55 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(52): Show |
intron_variant | MODIFIER | c.381-771A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 4/14 | chr4 | 48111374 | ||||||
| chr4:48111724
|
T | C | 58 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0021others(55): Show | 65 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(62): Show |
intron_variant | MODIFIER | c.380+583A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 4/14 | chr4 | 48111724 | ||||||
| chr4:48111792
|
G | C | 1 | a0001c0001t0002g0216 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.380+515C>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 4/14 | chr4 | 48111792 | ||||||
| chr4:48111803
|
C | G | 30 | a0001c0001t0004g0094a0001c0001t0004g0124a0001c0001t0004g0180others(27): Show | 32 | HG01255.hp2 HG02055.hp1 HG02109.hp1 others(29): Show |
intron_variant | MODIFIER | c.380+504G>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 4/14 | chr4 | 48111803 | ||||||
| chr4:48111806
|
T | C | 1 | a0001c0001t0001g0135 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.380+501A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 4/14 | chr4 | 48111806 | ||||||
| chr4:48111821
|
T | C | 3 | a0001c0006t0001g0095a0001c0006t0001g0125a0001c0006t0001g0292 | 3 | HG01884.hp1 HG02895.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.380+486A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 4/14 | chr4 | 48111821 | ||||||
| chr4:48111841
|
G | A | 5 | a0001c0001t0005g0018a0001c0001t0005g0039a0001c0001t0005g0332others(2): Show | 6 | HG01243.hp2 HG01884.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.380+466C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 4/14 | chr4 | 48111841 | ||||||
| chr4:48111913
|
C | T | 1 | a0001c0002t0001g0089 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.380+394G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 4/14 | chr4 | 48111913 | ||||||
| chr4:48112010
|
C | G | 145 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0021others(142): Show | 157 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.380+297G>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 4/14 | chr4 | 48112010 | ||||||
| chr4:48112193
|
G | A | 1 | a0001c0001t0001g0115 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.380+114C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 4/14 | chr4 | 48112193 | ||||||
| chr4:48112677
|
C | T | 63 | a0001c0001t0001g0086a0001c0001t0001g0101a0001c0001t0002g0064others(60): Show | 65 | HG00323.hp2 HG00544.hp2 HG00558.hp2 others(62): Show |
intron_variant | MODIFIER | c.175-165G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 3/14 | chr4 | 48112677 | ||||||
| chr4:48112685
|
T | G | 6 | a0001c0008t0003g0221a0001c0008t0003g0230a0001c0008t0003g0231others(3): Show | 6 | HG02559.hp1 HG02717.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.175-173A>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 3/14 | chr4 | 48112685 | ||||||
| chr4:48112821
|
A | AT | 5 | a0001c0001t0003g0277a0001c0001t0005g0018a0001c0001t0005g0039others(2): Show | 6 | HG01884.hp2 HG02572.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.175-310dupA | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 3/14 | chr4 | 48112821 | ||||||
| chr4:48112858
|
T | C | 3 | a0001c0006t0001g0095a0001c0006t0001g0125a0001c0006t0001g0292 | 3 | HG01884.hp1 HG02895.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.175-346A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 3/14 | chr4 | 48112858 | ||||||
| chr4:48112869
|
G | C | 1 | a0001c0001t0002g0216 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.174+338C>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 3/14 | chr4 | 48112869 | ||||||
| chr4:48113486
|
T | C | 1 | a0001c0002t0001g0270 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.72-177A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 2/14 | chr4 | 48113486 | ||||||
| chr4:48113495
|
C | T | 3 | a0001c0002t0001g0017a0001c0002t0001g0317a0001c0002t0001g0318 | 4 | NA18940.hp2 NA18945.hp2 NA18992.hp1 others(1): Show |
intron_variant | MODIFIER | c.72-186G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 2/14 | chr4 | 48113495 | ||||||
| chr4:48113656
|
C | T | 16 | a0001c0001t0003g0102a0001c0001t0003g0103a0001c0001t0003g0104others(13): Show | 19 | HG00323.hp1 HG00639.hp2 HG01109.hp1 others(16): Show |
intron_variant | MODIFIER | c.72-347G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 2/14 | chr4 | 48113656 | ||||||
| chr4:48113717
|
A | T | 233 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0021others(230): Show | 253 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(250): Show |
intron_variant | MODIFIER | c.72-408T>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 2/14 | chr4 | 48113717 | ||||||
| chr4:48113976
|
G | T | 1 | a0001c0001t0003g0103 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.71+372C>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 2/14 | chr4 | 48113976 | ||||||
| chr4:48114046
|
A | G | 1 | a0001c0001t0001g0115 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.71+302T>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 2/14 | chr4 | 48114046 | ||||||
| chr4:48114118
|
G | A | 3 | a0001c0006t0001g0095a0001c0006t0001g0125a0001c0006t0001g0292 | 3 | HG01884.hp1 HG02895.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.71+230C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 2/14 | chr4 | 48114118 | ||||||
| chr4:48114261
|
G | A | 1 | a0001c0001t0002g0272 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.71+87C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 2/14 | chr4 | 48114261 | ||||||
| chr4:48114664
|
G | A | 1 | a0001c0001t0001g0168 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.17-262C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48114664 | ||||||
| chr4:48114700
|
G | A | 1 | a0001c0001t0003g0323 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.17-298C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48114700 | ||||||
| chr4:48114835
|
C | T | 4 | a0001c0002t0001g0256a0001c0002t0001g0269a0001c0002t0001g0270others(1): Show | 4 | HG00642.hp2 HG02615.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.17-433G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48114835 | ||||||
| chr4:48114865
|
T | G | 1 | a0001c0007t0001g0032 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.17-463A>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48114865 | ||||||
| chr4:48114869
|
G | T | 183 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0021others(180): Show | 198 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(195): Show |
intron_variant | MODIFIER | c.17-467C>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48114869 | ||||||
| chr4:48114976
|
A | G | 1 | a0001c0001t0003g0108 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.17-574T>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48114976 | ||||||
| chr4:48114992
|
A | T | 7 | a0001c0002t0001g0237a0001c0002t0001g0258a0001c0002t0001g0259others(4): Show | 7 | HG01891.hp2 HG02055.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.17-590T>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48114992 | ||||||
| chr4:48115033
|
CT | C | 183 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0021others(180): Show | 198 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(195): Show |
intron_variant | MODIFIER | c.17-632delA | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48115033 | ||||||
| chr4:48115070
|
A | G | 1 | a0002c0003t0001g0173 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.17-668T>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48115070 | ||||||
| chr4:48115385
|
C | T | 1 | a0001c0001t0001g0128 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.17-983G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48115385 | ||||||
| chr4:48115436
|
T | C | 1 | a0001c0002t0001g0079 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.17-1034A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48115436 | ||||||
| chr4:48115478
|
A | G | 1 | a0001c0001t0004g0183 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.17-1076T>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48115478 | ||||||
| chr4:48115601
|
C | T | 3 | a0001c0006t0001g0095a0001c0006t0001g0125a0001c0006t0001g0292 | 3 | HG01884.hp1 HG02895.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.17-1199G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48115601 | ||||||
| chr4:48115612
|
C | T | 2 | a0001c0001t0001g0140a0001c0001t0001g0141 | 2 | NA19066.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.17-1210G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48115612 | ||||||
| chr4:48115639
|
G | A | 4 | a0001c0001t0005g0018a0001c0001t0005g0039a0001c0001t0005g0332others(1): Show | 5 | HG01884.hp2 HG02572.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.17-1237C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48115639 | ||||||
| chr4:48115683
|
C | T | 1 | a0001c0001t0001g0283 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.17-1281G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48115683 | ||||||
| chr4:48115724
|
G | C | 2 | a0001c0002t0001g0263a0001c0002t0001g0264 | 2 | HG02976.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.17-1322C>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48115724 | ||||||
| chr4:48115749
|
G | T | 1 | a0001c0006t0001g0292 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.17-1347C>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48115749 | ||||||
| chr4:48115960
|
G | C | 4 | a0001c0001t0005g0018a0001c0001t0005g0039a0001c0001t0005g0332others(1): Show | 5 | HG01884.hp2 HG02572.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.17-1558C>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48115960 | ||||||
| chr4:48116185
|
T | C | 248 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0021others(245): Show | 268 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(265): Show |
intron_variant | MODIFIER | c.17-1783A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48116185 | ||||||
| chr4:48116257
|
C | T | 1 | a0001c0010t0001g0117 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.17-1855G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48116257 | ||||||
| chr4:48116583
|
C | T | 4 | a0001c0007t0001g0032a0001c0007t0001g0118a0001c0007t0001g0122others(1): Show | 4 | HG02109.hp2 HG02145.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.17-2181G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48116583 | ||||||
| chr4:48116794
|
A | G | 18 | a0001c0001t0004g0094a0001c0001t0004g0124a0001c0001t0004g0180others(15): Show | 18 | HG01255.hp2 HG02109.hp1 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.17-2392T>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48116794 | ||||||
| chr4:48116878
|
T | C | 1 | a0001c0001t0003g0290 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.17-2476A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48116878 | ||||||
| chr4:48117003
|
A | G | 1 | a0002c0003t0001g0240 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.17-2601T>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48117003 | ||||||
| chr4:48117177
|
C | T | 48 | a0001c0001t0006g0247a0001c0002t0001g0248a0001c0006t0001g0095others(45): Show | 53 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(50): Show |
intron_variant | MODIFIER | c.17-2775G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48117177 | ||||||
| chr4:48117178
|
G | A | 147 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0021others(144): Show | 159 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(156): Show |
intron_variant | MODIFIER | c.17-2776C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48117178 | ||||||
| chr4:48117258
|
C | T | 11 | a0001c0005t0001g0004a0001c0005t0001g0022a0001c0005t0001g0023others(8): Show | 13 | HG02145.hp2 HG02257.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.17-2856G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48117258 | ||||||
| chr4:48117494
|
C | T | 1 | a0001c0001t0003g0108 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.17-3092G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48117494 | ||||||
| chr4:48117646
|
C | G | 4 | a0001c0002t0001g0019a0001c0002t0001g0020a0001c0002t0001g0040others(1): Show | 4 | HG03688.hp2 NA18612.hp2 NA18944.hp1 others(1): Show |
intron_variant | MODIFIER | c.17-3244G>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48117646 | ||||||
| chr4:48117960
|
A | G | 2 | a0001c0002t0001g0060a0001c0002t0001g0061 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.17-3558T>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48117960 | ||||||
| chr4:48118002
|
T | C | 3 | a0001c0001t0005g0018a0001c0001t0005g0332a0001c0001t0005g0333 | 4 | HG01884.hp2 HG02572.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.17-3600A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48118002 | ||||||
| chr4:48118005
|
C | A | 2 | a0001c0002t0001g0080a0001c0002t0001g0081 | 2 | HG02615.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.17-3603G>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48118005 | ||||||
| chr4:48118109
|
T | C | 2 | a0001c0010t0001g0117a0001c0010t0001g0217 | 2 | HG02717.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.17-3707A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48118109 | ||||||
| chr4:48118185
|
T | G | 1 | a0001c0001t0007g0119 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.17-3783A>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48118185 | ||||||
| chr4:48118210
|
A | G | 2 | a0002c0003t0001g0036a0002c0003t0001g0051 | 2 | NA18967.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.17-3808T>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48118210 | ||||||
| chr4:48118767
|
T | C | 3 | a0001c0006t0001g0028a0001c0006t0001g0029a0001c0006t0001g0030 | 3 | HG02145.hp2 HG02451.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.17-4365A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48118767 | ||||||
| chr4:48118801
|
C | T | 1 | a0001c0001t0001g0139 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.17-4399G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48118801 | ||||||
| chr4:48118854
|
G | A | 8 | a0001c0001t0003g0277a0001c0001t0003g0281a0001c0001t0003g0288others(5): Show | 8 | HG01891.hp1 HG02258.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.17-4452C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48118854 | ||||||
| chr4:48119166
|
A | G | 5 | a0001c0001t0003g0277a0001c0001t0003g0281a0001c0001t0003g0288others(2): Show | 5 | HG02258.hp1 HG02559.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.17-4764T>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48119166 | ||||||
| chr4:48119210
|
G | A | 1 | a0001c0001t0001g0120 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.17-4808C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48119210 | ||||||
| chr4:48119296
|
A | G | 1 | a0002c0003t0001g0085 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.17-4894T>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48119296 | ||||||
| chr4:48119300
|
T | C | 3 | a0001c0006t0001g0095a0001c0006t0001g0125a0001c0006t0001g0292 | 3 | HG01884.hp1 HG02895.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.17-4898A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48119300 | ||||||
| chr4:48119873
|
T | G | 1 | a0002c0003t0001g0058 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.17-5471A>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48119873 | ||||||
| chr4:48119905
|
A | G | 19 | a0001c0001t0004g0094a0001c0001t0004g0124a0001c0001t0004g0180others(16): Show | 19 | HG01255.hp2 HG02055.hp1 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.17-5503T>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48119905 | ||||||
| chr4:48119924
|
T | C | 1 | a0001c0001t0007g0119 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.17-5522A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48119924 | ||||||
| chr4:48120078
|
TAC | T | 326 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0021others(323): Show | 355 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(352): Show |
intron_variant | MODIFIER | c.17-5678_17-5677del others(2): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48120078 | ||||||
| chr4:48120107
|
G | A | 18 | a0001c0001t0004g0094a0001c0001t0004g0124a0001c0001t0004g0180others(15): Show | 18 | HG01255.hp2 HG02109.hp1 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.17-5705C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48120107 | ||||||
| chr4:48120112
|
C | CAT | 4 | a0001c0001t0005g0018a0001c0001t0005g0039a0001c0001t0005g0332others(1): Show | 5 | HG01884.hp2 HG02572.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.17-5712_17-5711dup others(2): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48120112 | ||||||
| chr4:48120116
|
C | T | 1 | a0001c0001t0004g0182 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.17-5714G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48120116 | ||||||
| chr4:48120126
|
T | C | 282 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0021others(279): Show | 304 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(301): Show |
intron_variant | MODIFIER | c.17-5724A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48120126 | ||||||
| chr4:48120157
|
A | ATATGTAT others(1): Show |
246 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0021others(243): Show | 263 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(260): Show |
intron_variant | MODIFIER | c.17-5756_17-5755ins others(8): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48120157 | ||||||
| chr4:48120161
|
A | G | 36 | a0002c0003t0001g0007a0002c0003t0001g0008a0002c0003t0001g0009others(33): Show | 41 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(38): Show |
intron_variant | MODIFIER | c.17-5759T>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48120161 | ||||||
| chr4:48120164
|
TGTATATA others(55): Show |
T | 35 | a0002c0003t0001g0007a0002c0003t0001g0008a0002c0003t0001g0009others(32): Show | 40 | HG00140.hp2 HG00639.hp1 HG00733.hp2 others(37): Show |
intron_variant | MODIFIER | c.17-5824_17-5763del others(62): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48120164 | ||||||
| chr4:48120168
|
T | C | 168 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0021others(165): Show | 180 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(177): Show |
intron_variant | MODIFIER | c.17-5766A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48120168 | ||||||
| chr4:48120172
|
C | T | 1 | a0002c0003t0001g0249 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.17-5770G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48120172 | ||||||
| chr4:48120179
|
G | A | 1 | a0002c0003t0001g0249 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.17-5777C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48120179 | ||||||
| chr4:48120180
|
T | C | 1 | a0002c0003t0001g0249 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.17-5778A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48120180 | ||||||
| chr4:48120188
|
T | C | 4 | a0001c0001t0005g0018a0001c0001t0005g0039a0001c0001t0005g0332others(1): Show | 5 | HG01884.hp2 HG02572.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.17-5786A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48120188 | ||||||
| chr4:48120196
|
CACATATA others(13): Show |
C | 1 | a0001c0001t0001g0130 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.17-5814_17-5795del others(20): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48120196 | ||||||
| chr4:48120242
|
C | T | 1 | a0001c0001t0005g0039 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.17-5840G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48120242 | ||||||
| chr4:48120328
|
G | A | 49 | a0001c0001t0006g0247a0001c0002t0001g0248a0001c0002t0001g0256others(46): Show | 54 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(51): Show |
intron_variant | MODIFIER | c.17-5926C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48120328 | ||||||
| chr4:48120382
|
C | T | 1 | a0001c0015t0001g0033 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.17-5980G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48120382 | ||||||
| chr4:48120428
|
C | T | 1 | a0001c0001t0003g0324 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.17-6026G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48120428 | ||||||
| chr4:48120456
|
GCTCT | G | 3 | a0002c0003t0001g0250a0002c0003t0001g0251a0002c0012t0002g0252 | 3 | HG00642.hp1 HG01516.hp2 HG01993.hp2 |
intron_variant | MODIFIER | c.17-6058_17-6055del others(4): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48120456 | ||||||
| chr4:48120522
|
G | A | 164 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0021others(161): Show | 176 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(173): Show |
intron_variant | MODIFIER | c.17-6120C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48120522 | ||||||
| chr4:48120533
|
G | A | 18 | a0001c0001t0004g0094a0001c0001t0004g0124a0001c0001t0004g0180others(15): Show | 18 | HG01255.hp2 HG02109.hp1 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.17-6131C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48120533 | ||||||
| chr4:48120569
|
C | T | 1 | a0001c0006t0001g0028 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.17-6167G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48120569 | ||||||
| chr4:48120658
|
T | A | 4 | a0002c0003t0001g0253a0002c0003t0001g0254a0002c0003t0001g0255others(1): Show | 4 | HG00735.hp1 HG01168.hp2 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.17-6256A>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48120658 | ||||||
| chr4:48120677
|
G | A | 1 | a0001c0001t0005g0039 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.17-6275C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48120677 | ||||||
| chr4:48120818
|
T | A | 2 | a0001c0002t0001g0256a0001c0002t0001g0271 | 2 | HG00642.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.17-6416A>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48120818 | ||||||
| chr4:48120834
|
C | T | 5 | a0001c0001t0001g0101a0001c0006t0001g0095a0001c0006t0001g0125others(2): Show | 5 | HG01243.hp2 HG01884.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.17-6432G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48120834 | ||||||
| chr4:48120869
|
G | GA | 173 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0021others(170): Show | 186 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(183): Show |
intron_variant | MODIFIER | c.17-6468dupT | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48120869 | ||||||
| chr4:48120926
|
T | C | 1 | a0001c0001t0009g0220 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.17-6524A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48120926 | ||||||
| chr4:48120931
|
C | T | 165 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0021others(162): Show | 177 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(174): Show |
intron_variant | MODIFIER | c.17-6529G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48120931 | ||||||
| chr4:48121069
|
C | T | 1 | a0001c0002t0001g0059 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.17-6667G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48121069 | ||||||
| chr4:48121397
|
T | G | 1 | a0001c0002t0001g0082 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.17-6995A>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48121397 | ||||||
| chr4:48121398
|
C | T | 18 | a0001c0001t0004g0094a0001c0001t0004g0124a0001c0001t0004g0180others(15): Show | 18 | HG01255.hp2 HG02109.hp1 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.17-6996G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48121398 | ||||||
| chr4:48121558
|
A | G | 1 | a0001c0001t0001g0222 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.17-7156T>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48121558 | ||||||
| chr4:48121583
|
C | T | 56 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0021others(53): Show | 63 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(60): Show |
intron_variant | MODIFIER | c.17-7181G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48121583 | ||||||
| chr4:48121705
|
A | G | 8 | a0001c0001t0005g0018a0001c0001t0005g0039a0001c0001t0005g0332others(5): Show | 9 | HG01884.hp1 HG01884.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.17-7303T>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48121705 | ||||||
| chr4:48121906
|
C | G | 9 | a0001c0001t0003g0277a0001c0001t0003g0281a0001c0001t0003g0288others(6): Show | 9 | HG01891.hp1 HG02258.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.17-7504G>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48121906 | ||||||
| chr4:48122003
|
A | T | 1 | a0001c0015t0001g0033 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.17-7601T>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48122003 | ||||||
| chr4:48122004
|
T | C | 3 | a0001c0008t0003g0221a0001c0008t0003g0230a0001c0008t0003g0231 | 3 | HG02559.hp1 HG02897.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.17-7602A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48122004 | ||||||
| chr4:48122040
|
C | T | 49 | a0001c0001t0006g0247a0001c0002t0001g0248a0001c0002t0001g0256others(46): Show | 54 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(51): Show |
intron_variant | MODIFIER | c.17-7638G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48122040 | ||||||
| chr4:48122183
|
C | A | 1 | a0001c0001t0001g0120 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.17-7781G>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48122183 | ||||||
| chr4:48122205
|
A | T | 1 | a0001c0001t0007g0119 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.17-7803T>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48122205 | ||||||
| chr4:48122389
|
C | T | 1 | a0001c0002t0001g0121 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.17-7987G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48122389 | ||||||
| chr4:48122571
|
T | A | 1 | a0001c0015t0001g0033 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.17-8169A>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48122571 | ||||||
| chr4:48122821
|
C | T | 58 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0021others(55): Show | 65 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(62): Show |
intron_variant | MODIFIER | c.17-8419G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48122821 | ||||||
| chr4:48122829
|
T | G | 1 | a0001c0002t0001g0083 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.17-8427A>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48122829 | ||||||
| chr4:48122932
|
G | A | 4 | a0001c0001t0005g0018a0001c0001t0005g0039a0001c0001t0005g0332others(1): Show | 5 | HG01884.hp2 HG02572.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.17-8530C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48122932 | ||||||
| chr4:48123278
|
C | T | 1 | a0001c0008t0006g0232 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.17-8876G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48123278 | ||||||
| chr4:48123442
|
C | T | 1 | a0001c0015t0001g0033 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.17-9040G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48123442 | ||||||
| chr4:48123630
|
G | C | 1 | a0002c0003t0001g0331 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.17-9228C>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48123630 | ||||||
| chr4:48123785
|
G | T | 58 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0021others(55): Show | 65 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(62): Show |
intron_variant | MODIFIER | c.17-9383C>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48123785 | ||||||
| chr4:48123849
|
A | G | 278 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0021others(275): Show | 300 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(297): Show |
intron_variant | MODIFIER | c.17-9447T>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48123849 | ||||||
| chr4:48124060
|
G | T | 1 | a0003c0004t0003g0106 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.17-9658C>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48124060 | ||||||
| chr4:48124069
|
T | C | 278 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0021others(275): Show | 300 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(297): Show |
intron_variant | MODIFIER | c.17-9667A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48124069 | ||||||
| chr4:48124232
|
C | G | 1 | a0001c0015t0001g0033 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.17-9830G>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48124232 | ||||||
| chr4:48124374
|
C | T | 1 | a0001c0001t0004g0181 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.16+9781G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48124374 | ||||||
| chr4:48124384
|
T | C | 1 | a0001c0007t0001g0118 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.16+9771A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48124384 | ||||||
| chr4:48124420
|
C | CT | 7 | a0001c0005t0001g0004a0001c0005t0001g0022a0001c0005t0001g0023others(4): Show | 9 | HG02257.hp1 HG02486.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.16+9734dupA | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48124420 | ||||||
| chr4:48124522
|
C | T | 1 | a0003c0004t0003g0137 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.16+9633G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48124522 | ||||||
| chr4:48124560
|
C | CT | 6 | a0001c0001t0001g0120a0001c0001t0005g0018a0001c0001t0005g0039others(3): Show | 7 | HG01884.hp2 HG02572.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.16+9594dupA | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48124560 | ||||||
| chr4:48124563
|
C | T | 219 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0021others(216): Show | 238 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(235): Show |
intron_variant | MODIFIER | c.16+9592G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48124563 | ||||||
| chr4:48124577
|
A | G | 21 | a0001c0001t0004g0094a0001c0001t0004g0124a0001c0001t0004g0180others(18): Show | 21 | HG01255.hp2 HG02109.hp1 HG02109.hp2 others(18): Show |
intron_variant | MODIFIER | c.16+9578T>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48124577 | ||||||
| chr4:48124639
|
G | A | 1 | a0001c0001t0007g0119 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.16+9516C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48124639 | ||||||
| chr4:48124662
|
G | A | 50 | a0001c0001t0001g0305a0001c0001t0002g0015a0001c0001t0002g0016others(47): Show | 52 | HG00438.hp2 HG00544.hp1 HG00597.hp2 others(49): Show |
intron_variant | MODIFIER | c.16+9493C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48124662 | ||||||
| chr4:48124715
|
A | G | 11 | a0001c0005t0001g0004a0001c0005t0001g0022a0001c0005t0001g0023others(8): Show | 13 | HG02145.hp2 HG02257.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.16+9440T>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48124715 | ||||||
| chr4:48124884
|
G | A | 1 | a0002c0003t0001g0265 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.16+9271C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48124884 | ||||||
| chr4:48124980
|
T | C | 1 | a0001c0015t0001g0033 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.16+9175A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48124980 | ||||||
| chr4:48125107
|
C | A | 2 | a0001c0008t0003g0230a0001c0008t0003g0231 | 2 | HG02897.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.16+9048G>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48125107 | ||||||
| chr4:48125245
|
A | G | 45 | a0001c0001t0002g0272a0001c0001t0004g0257a0001c0001t0006g0247others(42): Show | 49 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(46): Show |
intron_variant | MODIFIER | c.16+8910T>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48125245 | ||||||
| chr4:48125520
|
C | T | 1 | a0001c0001t0002g0199 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.16+8635G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48125520 | ||||||
| chr4:48125521
|
G | A | 4 | a0001c0002t0001g0017a0001c0002t0001g0317a0001c0002t0001g0318others(1): Show | 5 | NA18940.hp2 NA18945.hp2 NA18992.hp1 others(2): Show |
intron_variant | MODIFIER | c.16+8634C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48125521 | ||||||
| chr4:48125584
|
A | G | 3 | a0001c0001t0002g0196a0001c0001t0002g0197a0001c0001t0002g0198 | 3 | HG00733.hp1 HG01168.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.16+8571T>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48125584 | ||||||
| chr4:48125684
|
C | T | 11 | a0001c0005t0001g0004a0001c0005t0001g0022a0001c0005t0001g0023others(8): Show | 13 | HG02145.hp2 HG02257.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.16+8471G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48125684 | ||||||
| chr4:48125794
|
T | C | 7 | a0001c0005t0001g0004a0001c0005t0001g0022a0001c0005t0001g0023others(4): Show | 9 | HG02257.hp1 HG02486.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.16+8361A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48125794 | ||||||
| chr4:48125959
|
G | T | 1 | a0001c0015t0001g0033 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.16+8196C>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48125959 | ||||||
| chr4:48126162
|
CCT | C | 63 | a0001c0001t0002g0272a0001c0001t0002g0273a0001c0001t0002g0274others(60): Show | 70 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(67): Show |
intron_variant | MODIFIER | c.16+7991_16+7992del others(2): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48126162 | ||||||
| chr4:48126174
|
CT | C | 131 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0021others(128): Show | 141 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(138): Show |
intron_variant | MODIFIER | c.16+7980delA | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48126174 | ||||||
| chr4:48126265
|
A | G | 1 | a0001c0001t0001g0195 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.16+7890T>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48126265 | ||||||
| chr4:48126281
|
T | G | 11 | a0001c0005t0001g0004a0001c0005t0001g0022a0001c0005t0001g0023others(8): Show | 13 | HG02145.hp2 HG02257.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.16+7874A>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48126281 | ||||||
| chr4:48126288
|
T | C | 1 | a0001c0015t0001g0033 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.16+7867A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48126288 | ||||||
| chr4:48126368
|
C | A | 4 | a0001c0001t0003g0102a0001c0001t0003g0103a0001c0001t0003g0104others(1): Show | 4 | HG03654.hp1 HG03654.hp2 HG03834.hp1 others(1): Show |
intron_variant | MODIFIER | c.16+7787G>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48126368 | ||||||
| chr4:48126395
|
C | G | 5 | a0001c0007t0001g0032a0001c0007t0001g0118a0001c0007t0001g0122others(2): Show | 5 | HG02109.hp2 HG02145.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.16+7760G>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48126395 | ||||||
| chr4:48126535
|
C | G | 11 | a0001c0005t0001g0004a0001c0005t0001g0022a0001c0005t0001g0023others(8): Show | 13 | HG02145.hp2 HG02257.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.16+7620G>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48126535 | ||||||
| chr4:48126550
|
G | T | 3 | a0002c0003t0001g0046a0002c0003t0001g0047a0002c0013t0001g0045 | 3 | NA18949.hp1 NA18960.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.16+7605C>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48126550 | ||||||
| chr4:48126667
|
A | AT | 103 | a0001c0001t0001g0283a0001c0001t0001g0305a0001c0001t0002g0015others(100): Show | 113 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(110): Show |
intron_variant | MODIFIER | c.16+7487dupA | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48126667 | ||||||
| chr4:48126723
|
C | T | 1 | a0001c0002t0001g0282 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.16+7432G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48126723 | ||||||
| chr4:48126833
|
T | G | 270 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0021others(267): Show | 295 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(292): Show |
intron_variant | MODIFIER | c.16+7322A>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48126833 | ||||||
| chr4:48126887
|
C | T | 1 | a0002c0003t0001g0238 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.16+7268G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48126887 | ||||||
| chr4:48127071
|
A | G | 1 | a0001c0001t0003g0136 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.16+7084T>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48127071 | ||||||
| chr4:48127095
|
T | A | 269 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0021others(266): Show | 294 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(291): Show |
intron_variant | MODIFIER | c.16+7060A>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48127095 | ||||||
| chr4:48127171
|
C | T | 154 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0021others(151): Show | 167 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.16+6984G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48127171 | ||||||
| chr4:48127207
|
T | G | 104 | a0001c0001t0001g0283a0001c0001t0001g0305a0001c0001t0002g0015others(101): Show | 114 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(111): Show |
intron_variant | MODIFIER | c.16+6948A>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48127207 | ||||||
| chr4:48127298
|
C | A | 1 | a0001c0001t0003g0320 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.16+6857G>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48127298 | ||||||
| chr4:48127523
|
G | T | 5 | a0001c0001t0001g0120a0001c0001t0005g0018a0001c0001t0005g0039others(2): Show | 6 | HG01884.hp2 HG02572.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.16+6632C>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48127523 | ||||||
| chr4:48127746
|
C | T | 3 | a0001c0002t0001g0044a0002c0003t0001g0042a0002c0003t0001g0043 | 3 | HG01256.hp2 HG01978.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.16+6409G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48127746 | ||||||
| chr4:48127763
|
G | A | 1 | a0001c0001t0001g0086 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.16+6392C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48127763 | ||||||
| chr4:48127784
|
A | G | 276 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0021others(273): Show | 302 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(299): Show |
intron_variant | MODIFIER | c.16+6371T>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48127784 | ||||||
| chr4:48127795
|
G | A | 2 | a0001c0001t0002g0273a0001c0001t0002g0274 | 2 | HG02602.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.16+6360C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48127795 | ||||||
| chr4:48127898
|
C | T | 58 | a0001c0001t0001g0283a0001c0001t0001g0305a0001c0001t0002g0015others(55): Show | 64 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.16+6257G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48127898 | ||||||
| chr4:48128116
|
A | C | 4 | a0001c0001t0001g0132a0001c0001t0001g0133a0001c0001t0001g0134others(1): Show | 4 | NA18985.hp2 NA19005.hp2 NA19065.hp1 others(1): Show |
intron_variant | MODIFIER | c.16+6039T>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48128116 | ||||||
| chr4:48128165
|
G | A | 1 | a0001c0001t0003g0281 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.16+5990C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48128165 | ||||||
| chr4:48128168
|
T | C | 154 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0021others(151): Show | 167 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.16+5987A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48128168 | ||||||
| chr4:48128308
|
T | C | 1 | a0001c0001t0007g0119 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.16+5847A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48128308 | ||||||
| chr4:48128373
|
T | G | 3 | a0001c0001t0001g0174a0001c0001t0001g0179a0001c0009t0001g0002 | 6 | NA18940.hp1 NA18957.hp1 NA18970.hp2 others(3): Show |
intron_variant | MODIFIER | c.16+5782A>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48128373 | ||||||
| chr4:48128483
|
T | A | 1 | a0001c0001t0002g0321 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.16+5672A>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48128483 | ||||||
| chr4:48128520
|
A | T | 154 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0021others(151): Show | 167 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.16+5635T>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48128520 | ||||||
| chr4:48128529
|
A | G | 276 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0021others(273): Show | 302 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(299): Show |
intron_variant | MODIFIER | c.16+5626T>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48128529 | ||||||
| chr4:48128561
|
C | CT | 123 | a0001c0001t0001g0050a0001c0001t0001g0086a0001c0001t0001g0101others(120): Show | 130 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(127): Show |
intron_variant | MODIFIER | c.16+5593dupA | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48128561 | ||||||
| chr4:48128561
|
C | CTT | 60 | a0001c0001t0001g0283a0001c0001t0001g0305a0001c0001t0002g0015others(57): Show | 68 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(65): Show |
intron_variant | MODIFIER | c.16+5592_16+5593dup others(2): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48128561 | ||||||
| chr4:48128561
|
C | CTTT | 7 | a0001c0001t0002g0279a0001c0001t0002g0280a0001c0001t0003g0277others(4): Show | 7 | HG02280.hp1 HG02559.hp2 HG03486.hp1 others(4): Show |
intron_variant | MODIFIER | c.16+5591_16+5593dup others(3): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48128561 | ||||||
| chr4:48128561
|
CT | C | 11 | a0001c0001t0001g0120a0001c0001t0001g0175a0001c0001t0004g0193others(8): Show | 11 | HG00323.hp1 HG00558.hp1 HG01515.hp2 others(8): Show |
intron_variant | MODIFIER | c.16+5593delA | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48128561 | ||||||
| chr4:48128666
|
G | A | 1 | a0001c0015t0001g0033 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.16+5489C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48128666 | ||||||
| chr4:48128757
|
C | T | 1 | a0001c0001t0007g0119 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.16+5398G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48128757 | ||||||
| chr4:48128846
|
C | T | 1 | a0001c0001t0007g0119 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.16+5309G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48128846 | ||||||
| chr4:48128858
|
C | T | 1 | a0001c0002t0001g0234 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.16+5297G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48128858 | ||||||
| chr4:48129013
|
G | T | 1 | a0001c0015t0001g0033 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.16+5142C>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48129013 | ||||||
| chr4:48129091
|
T | C | 149 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0021others(146): Show | 162 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(159): Show |
intron_variant | MODIFIER | c.16+5064A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48129091 | ||||||
| chr4:48129125
|
T | C | 5 | a0001c0001t0001g0120a0001c0001t0005g0018a0001c0001t0005g0039others(2): Show | 6 | HG01884.hp2 HG02572.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.16+5030A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48129125 | ||||||
| chr4:48129162
|
T | A | 4 | a0001c0002t0001g0089a0001c0002t0001g0090a0001c0002t0001g0091others(1): Show | 4 | HG01346.hp1 HG01496.hp1 HG01943.hp1 others(1): Show |
intron_variant | MODIFIER | c.16+4993A>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48129162 | ||||||
| chr4:48129222
|
T | A | 1 | a0001c0008t0006g0232 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.16+4933A>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48129222 | ||||||
| chr4:48129364
|
G | T | 6 | a0001c0001t0001g0120a0001c0001t0005g0018a0001c0001t0005g0039others(3): Show | 7 | HG01884.hp2 HG02572.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.16+4791C>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48129364 | ||||||
| chr4:48129374
|
AAAG | A | 11 | a0001c0005t0001g0004a0001c0005t0001g0022a0001c0005t0001g0023others(8): Show | 13 | HG02145.hp2 HG02257.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.16+4778_16+4780del others(3): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48129374 | ||||||
| chr4:48129412
|
G | A | 276 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0021others(273): Show | 302 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(299): Show |
intron_variant | MODIFIER | c.16+4743C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48129412 | ||||||
| chr4:48129474
|
T | C | 1 | a0002c0003t0001g0093 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.16+4681A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48129474 | ||||||
| chr4:48129548
|
T | A | 1 | a0001c0015t0001g0033 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.16+4607A>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48129548 | ||||||
| chr4:48129679
|
C | G | 1 | a0001c0001t0003g0102 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.16+4476G>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48129679 | ||||||
| chr4:48129785
|
C | T | 11 | a0001c0005t0001g0004a0001c0005t0001g0022a0001c0005t0001g0023others(8): Show | 13 | HG02145.hp2 HG02257.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.16+4370G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48129785 | ||||||
| chr4:48129840
|
A | G | 1 | a0001c0001t0001g0126 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.16+4315T>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48129840 | ||||||
| chr4:48129862
|
C | G | 74 | a0001c0001t0001g0050a0001c0001t0001g0086a0001c0001t0001g0101others(71): Show | 77 | HG00323.hp2 HG00558.hp2 HG00597.hp1 others(74): Show |
intron_variant | MODIFIER | c.16+4293G>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48129862 | ||||||
| chr4:48129928
|
G | A | 17 | a0001c0001t0003g0324a0001c0001t0004g0124a0001c0001t0004g0180others(14): Show | 17 | HG02109.hp1 HG02257.hp2 HG02559.hp2 others(14): Show |
intron_variant | MODIFIER | c.16+4227C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48129928 | ||||||
| chr4:48130153
|
C | A | 149 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0021others(146): Show | 162 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(159): Show |
intron_variant | MODIFIER | c.16+4002G>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48130153 | ||||||
| chr4:48130172
|
A | G | 46 | a0001c0001t0002g0272a0001c0001t0002g0273a0001c0001t0002g0274others(43): Show | 50 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(47): Show |
intron_variant | MODIFIER | c.16+3983T>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48130172 | ||||||
| chr4:48130321
|
G | A | 1 | a0001c0001t0002g0325 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.16+3834C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48130321 | ||||||
| chr4:48130330
|
T | C | 276 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0021others(273): Show | 302 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(299): Show |
intron_variant | MODIFIER | c.16+3825A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48130330 | ||||||
| chr4:48130376
|
C | G | 104 | a0001c0001t0001g0283a0001c0001t0001g0305a0001c0001t0002g0015others(101): Show | 114 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(111): Show |
intron_variant | MODIFIER | c.16+3779G>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48130376 | ||||||
| chr4:48130437
|
G | A | 1 | a0001c0002t0001g0266 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.16+3718C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48130437 | ||||||
| chr4:48130454
|
C | T | 70 | a0001c0001t0001g0050a0001c0001t0001g0086a0001c0001t0002g0048others(67): Show | 73 | HG00323.hp2 HG00558.hp2 HG00597.hp1 others(70): Show |
intron_variant | MODIFIER | c.16+3701G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48130454 | ||||||
| chr4:48130536
|
A | G | 1 | a0001c0015t0001g0033 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.16+3619T>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48130536 | ||||||
| chr4:48130541
|
T | C | 149 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0021others(146): Show | 162 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(159): Show |
intron_variant | MODIFIER | c.16+3614A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48130541 | ||||||
| chr4:48130602
|
A | T | 1 | a0001c0002t0001g0014 | 2 | NA20752.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.16+3553T>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48130602 | ||||||
| chr4:48130669
|
A | G | 104 | a0001c0001t0001g0283a0001c0001t0001g0305a0001c0001t0002g0015others(101): Show | 114 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(111): Show |
intron_variant | MODIFIER | c.16+3486T>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48130669 | ||||||
| chr4:48130682
|
C | G | 5 | a0001c0007t0001g0032a0001c0007t0001g0118a0001c0007t0001g0122others(2): Show | 5 | HG02109.hp2 HG02145.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.16+3473G>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48130682 | ||||||
| chr4:48130812
|
G | T | 1 | a0001c0015t0001g0033 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.16+3343C>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48130812 | ||||||
| chr4:48130874
|
G | A | 149 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0021others(146): Show | 162 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(159): Show |
intron_variant | MODIFIER | c.16+3281C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48130874 | ||||||
| chr4:48130923
|
C | T | 1 | a0001c0002t0001g0099 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.16+3232G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48130923 | ||||||
| chr4:48131317
|
CT | C | 23 | a0001c0001t0001g0120a0001c0001t0001g0127a0001c0001t0002g0327others(20): Show | 26 | HG00408.hp2 HG01168.hp2 HG01884.hp2 others(23): Show |
intron_variant | MODIFIER | c.16+2837delA | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48131317 | ||||||
| chr4:48131317
|
CTT | C | 141 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0021others(138): Show | 154 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(151): Show |
intron_variant | MODIFIER | c.16+2836_16+2837del others(2): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48131317 | ||||||
| chr4:48131317
|
CTTT | C | 6 | a0001c0001t0001g0177a0001c0001t0001g0178a0001c0001t0001g0179others(3): Show | 6 | HG00323.hp1 HG02129.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.16+2835_16+2837del others(3): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48131317 | ||||||
| chr4:48131443
|
TTTTG | T | 149 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0021others(146): Show | 162 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(159): Show |
intron_variant | MODIFIER | c.16+2708_16+2711del others(4): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48131443 | ||||||
| chr4:48131452
|
T | G | 1 | a0001c0002t0001g0121 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.16+2703A>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48131452 | ||||||
| chr4:48131632
|
C | T | 2 | a0001c0002t0001g0020a0001c0002t0001g0040 | 2 | NA18944.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.16+2523G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48131632 | ||||||
| chr4:48131680
|
C | T | 46 | a0001c0001t0002g0272a0001c0001t0002g0273a0001c0001t0002g0274others(43): Show | 50 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(47): Show |
intron_variant | MODIFIER | c.16+2475G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48131680 | ||||||
| chr4:48131681
|
G | A | 1 | a0001c0002t0001g0098 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.16+2474C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48131681 | ||||||
| chr4:48131713
|
A | G | 276 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0021others(273): Show | 302 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(299): Show |
intron_variant | MODIFIER | c.16+2442T>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48131713 | ||||||
| chr4:48131903
|
G | A | 2 | a0001c0007t0001g0122a0001c0007t0001g0123 | 2 | HG02109.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.16+2252C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48131903 | ||||||
| chr4:48131924
|
C | T | 1 | a0001c0002t0001g0275 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.16+2231G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48131924 | ||||||
| chr4:48131972
|
G | C | 1 | a0001c0008t0006g0232 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.16+2183C>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48131972 | ||||||
| chr4:48132040
|
A | AT | 66 | a0001c0001t0001g0050a0001c0001t0001g0086a0001c0001t0001g0126others(63): Show | 69 | HG00558.hp2 HG00621.hp2 HG01099.hp1 others(66): Show |
intron_variant | MODIFIER | c.16+2114dupA | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48132040 | ||||||
| chr4:48132040
|
A | ATT | 9 | a0001c0001t0005g0018a0001c0001t0005g0039a0001c0001t0005g0332others(6): Show | 10 | HG00597.hp1 HG01884.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.16+2113_16+2114dup others(2): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48132040 | ||||||
| chr4:48132040
|
AT | A | 18 | a0001c0001t0002g0328a0001c0001t0004g0124a0001c0001t0004g0180others(15): Show | 18 | HG02109.hp1 HG02257.hp2 HG02622.hp1 others(15): Show |
intron_variant | MODIFIER | c.16+2114delA | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48132040 | ||||||
| chr4:48132075
|
A | G | 40 | a0001c0001t0004g0257a0001c0001t0006g0247a0001c0002t0001g0234others(37): Show | 44 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(41): Show |
intron_variant | MODIFIER | c.16+2080T>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48132075 | ||||||
| chr4:48132092
|
G | A | 1 | a0001c0006t0001g0125 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.16+2063C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48132092 | ||||||
| chr4:48132101
|
G | A | 59 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0021others(56): Show | 66 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(63): Show |
intron_variant | MODIFIER | c.16+2054C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48132101 | ||||||
| chr4:48132186
|
A | G | 1 | a0001c0015t0001g0033 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.16+1969T>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48132186 | ||||||
| chr4:48132310
|
C | G | 1 | a0001c0015t0001g0033 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.16+1845G>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48132310 | ||||||
| chr4:48132425
|
T | C | 1 | a0001c0001t0002g0233 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.16+1730A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48132425 | ||||||
| chr4:48132698
|
C | T | 1 | a0001c0007t0001g0032 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.16+1457G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48132698 | ||||||
| chr4:48132944
|
T | TA | 15 | a0001c0001t0004g0180a0001c0001t0004g0181a0001c0001t0004g0182others(12): Show | 15 | HG02109.hp1 HG02257.hp2 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.16+1210dupT | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48132944 | ||||||
| chr4:48133164
|
A | C | 104 | a0001c0001t0001g0283a0001c0001t0001g0305a0001c0001t0002g0015others(101): Show | 114 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(111): Show |
intron_variant | MODIFIER | c.16+991T>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48133164 | ||||||
| chr4:48133204
|
A | G | 11 | a0001c0005t0001g0004a0001c0005t0001g0022a0001c0005t0001g0023others(8): Show | 13 | HG02145.hp2 HG02257.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.16+951T>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48133204 | ||||||
| chr4:48133224
|
TG | T | 223 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0021others(220): Show | 241 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(238): Show |
intron_variant | MODIFIER | c.16+930delC | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48133224 | ||||||
| chr4:48133225
|
GGT | G | 58 | a0001c0001t0001g0283a0001c0001t0001g0305a0001c0001t0002g0015others(55): Show | 64 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.16+928_16+929delAC | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48133225 | ||||||
| chr4:48133226
|
G | T | 11 | a0001c0005t0001g0004a0001c0005t0001g0022a0001c0005t0001g0023others(8): Show | 13 | HG02145.hp2 HG02257.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.16+929C>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48133226 | ||||||
| chr4:48133316
|
G | A | 11 | a0001c0005t0001g0004a0001c0005t0001g0022a0001c0005t0001g0023others(8): Show | 13 | HG02145.hp2 HG02257.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.16+839C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48133316 | ||||||
| chr4:48133591
|
C | T | 11 | a0001c0005t0001g0004a0001c0005t0001g0022a0001c0005t0001g0023others(8): Show | 13 | HG02145.hp2 HG02257.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.16+564G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48133591 | ||||||
| chr4:48133661
|
G | A | 3 | a0002c0003t0001g0329a0002c0003t0001g0330a0002c0003t0001g0331 | 3 | HG01192.hp1 HG02055.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.16+494C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48133661 | ||||||
| chr4:48133695
|
A | T | 1 | a0001c0001t0001g0021 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.16+460T>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48133695 | ||||||
| chr4:48133766
|
T | G | 104 | a0001c0001t0001g0283a0001c0001t0001g0305a0001c0001t0002g0015others(101): Show | 114 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(111): Show |
intron_variant | MODIFIER | c.16+389A>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48133766 | ||||||
| chr4:48133769
|
A | G | 1 | a0001c0002t0001g0020 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.16+386T>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48133769 | ||||||
| chr4:48133887
|
T | C | 3 | a0001c0001t0005g0018a0001c0001t0005g0332a0001c0001t0005g0333 | 4 | HG01884.hp2 HG02572.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.16+268A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48133887 | ||||||
| chr4:48134112
|
A | G | 1 | a0001c0002t0001g0019 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.16+43T>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48134112 |