| geneid | 23118 |
|---|---|
| ensemblid | ENSG00000055208.20 |
| hgncid | 17075 |
| symbol | TAB2 |
| name | TGF-beta activated kinase 1 (MAP3K7) binding protein 2 |
| refseq_nuc | NM_001292034.3 |
| refseq_prot | NP_001278963.1 |
| ensembl_nuc | ENST00000637181.2 |
| ensembl_prot | ENSP00000490618.1 |
| mane_status | MANE Select |
| chr | chr6 |
| start | 149317712 |
| end | 149411607 |
| strand | + |
| ver | v1.2 |
| region | chr6:149317712-149411607 |
| region5000 | chr6:149312712-149416607 |
| regionname0 | TAB2_chr6_149317712_149411607 |
| regionname5000 | TAB2_chr6_149312712_149416607 |
| 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 | 693 | 366 | 98 | 70 | 150 | 12 | 34 | 116 | TAB2_chr6_149312712_149416607 | TAB2 | copy fasta | chr6 | 149312712 | 149416607 |
| 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 | 2082 | 275 | 95 | 55 | 85 | 10 | 28 | TAB2_chr6_149312712_149416607 | TAB2 | copy fasta | chr6 | 149312712 | 149416607 |
| c0002 | 0/0 | 2082 | 84 | 3 | 12 | 61 | 2 | 6 | TAB2_chr6_149312712_149416607 | TAB2 | copy fasta | chr6 | 149312712 | 149416607 |
| c0003 | 0/0 | 2082 | 2 | 0 | 2 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | copy fasta | chr6 | 149312712 | 149416607 |
| c0004 | 0/0 | 2082 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | copy fasta | chr6 | 149312712 | 149416607 |
| c0005 | 0/0 | 2082 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | copy fasta | chr6 | 149312712 | 149416607 |
| c0006 | 0/0 | 2082 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | copy fasta | chr6 | 149312712 | 149416607 |
| c0007 | 0/0 | 2082 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | copy fasta | chr6 | 149312712 | 149416607 |
| c0008 | 0/0 | 2082 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | copy fasta | chr6 | 149312712 | 149416607 |
| 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 | 0/0 | 2279 | 131 | 39 | 28 | 49 | 5 | 10 | TAB2_chr6_149312712_149416607 | TAB2 | copy fasta | chr6 | 149312712 | 149416607 |
| t0002 | 0/0 | 2279 | 78 | 3 | 13 | 54 | 2 | 6 | TAB2_chr6_149312712_149416607 | TAB2 | copy fasta | chr6 | 149312712 | 149416607 |
| t0003 | 0/1 | 2279 | 61 | 19 | 19 | 10 | 3 | 9 | TAB2_chr6_149312712_149416607 | TAB2 | copy fasta | chr6 | 149312712 | 149416607 |
| t0004 | 1/0 | 2282 | 47 | 13 | 7 | 22 | 1 | 3 | TAB2_chr6_149312712_149416607 | TAB2 | copy fasta | chr6 | 149312712 | 149416607 |
| t0005 | 0/0 | 2279 | 9 | 3 | 1 | 0 | 0 | 5 | TAB2_chr6_149312712_149416607 | TAB2 | copy fasta | chr6 | 149312712 | 149416607 |
| t0006 | 0/0 | 2279 | 5 | 0 | 0 | 5 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | copy fasta | chr6 | 149312712 | 149416607 |
| t0007 | 0/0 | 2301 | 5 | 5 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | copy fasta | chr6 | 149312712 | 149416607 |
| t0008 | 0/0 | 2279 | 4 | 4 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | copy fasta | chr6 | 149312712 | 149416607 |
| t0009 | 0/0 | 2279 | 4 | 4 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | copy fasta | chr6 | 149312712 | 149416607 |
| t0010 | 0/0 | 2279 | 3 | 0 | 0 | 3 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | copy fasta | chr6 | 149312712 | 149416607 |
| t0011 | 0/0 | 2279 | 3 | 0 | 1 | 0 | 1 | 1 | TAB2_chr6_149312712_149416607 | TAB2 | copy fasta | chr6 | 149312712 | 149416607 |
| t0012 | 0/0 | 2279 | 2 | 0 | 0 | 2 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | copy fasta | chr6 | 149312712 | 149416607 |
| t0013 | 0/0 | 2279 | 2 | 2 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | copy fasta | chr6 | 149312712 | 149416607 |
| t0014 | 0/0 | 2282 | 2 | 0 | 0 | 2 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | copy fasta | chr6 | 149312712 | 149416607 |
| t0015 | 0/0 | 2279 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | copy fasta | chr6 | 149312712 | 149416607 |
| t0016 | 0/0 | 2267 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | copy fasta | chr6 | 149312712 | 149416607 |
| t0017 | 0/0 | 2279 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | copy fasta | chr6 | 149312712 | 149416607 |
| t0018 | 0/0 | 2279 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | copy fasta | chr6 | 149312712 | 149416607 |
| t0019 | 0/0 | 2279 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | copy fasta | chr6 | 149312712 | 149416607 |
| t0020 | 0/0 | 2282 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | copy fasta | chr6 | 149312712 | 149416607 |
| t0021 | 0/0 | 2282 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | copy fasta | chr6 | 149312712 | 149416607 |
| t0022 | 0/0 | 2282 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | copy fasta | chr6 | 149312712 | 149416607 |
| t0023 | 0/0 | 2301 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | copy fasta | chr6 | 149312712 | 149416607 |
| t0024 | 0/0 | 2302 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | copy fasta | chr6 | 149312712 | 149416607 |
| 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 | 2 | 0 | 0 | 2 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0003 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0051 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0246 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0257 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0266 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0285 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0288 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0319 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0334 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0335 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0341 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0350 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0351 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0353 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0360 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0361 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0362 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| g0363 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| 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 | 2082 | 275 | 95 | 55 | 85 | 10 | 28 | TAB2_chr6_149312712_149416607 | TAB2 | copy fasta | chr6 | 149312712 | 149416607 |
| a0001c0002 | 0/0 | 2082 | 84 | 3 | 12 | 61 | 2 | 6 | TAB2_chr6_149312712_149416607 | TAB2 | copy fasta | chr6 | 149312712 | 149416607 |
| a0001c0003 | 0/0 | 2082 | 2 | 0 | 2 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | copy fasta | chr6 | 149312712 | 149416607 |
| a0001c0004 | 0/0 | 2082 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | copy fasta | chr6 | 149312712 | 149416607 |
| a0001c0005 | 0/0 | 2082 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | copy fasta | chr6 | 149312712 | 149416607 |
| a0001c0006 | 0/0 | 2082 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | copy fasta | chr6 | 149312712 | 149416607 |
| a0001c0007 | 0/0 | 2082 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | copy fasta | chr6 | 149312712 | 149416607 |
| a0001c0008 | 0/0 | 2082 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | copy fasta | chr6 | 149312712 | 149416607 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 4360 | 129 | 39 | 26 | 49 | 5 | 10 | TAB2_chr6_149312712_149416607 | TAB2 | copy fasta | chr6 | 149312712 | 149416607 |
| a0001c0001t0003 | 0/1 | 4360 | 61 | 19 | 19 | 10 | 3 | 9 | TAB2_chr6_149312712_149416607 | TAB2 | copy fasta | chr6 | 149312712 | 149416607 |
| a0001c0001t0004 | 1/0 | 4363 | 46 | 13 | 7 | 21 | 1 | 3 | TAB2_chr6_149312712_149416607 | TAB2 | copy fasta | chr6 | 149312712 | 149416607 |
| a0001c0001t0005 | 0/0 | 4360 | 9 | 3 | 1 | 0 | 0 | 5 | TAB2_chr6_149312712_149416607 | TAB2 | copy fasta | chr6 | 149312712 | 149416607 |
| a0001c0001t0007 | 0/0 | 4382 | 5 | 5 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | copy fasta | chr6 | 149312712 | 149416607 |
| a0001c0001t0008 | 0/0 | 4360 | 4 | 4 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | copy fasta | chr6 | 149312712 | 149416607 |
| a0001c0001t0009 | 0/0 | 4360 | 4 | 4 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | copy fasta | chr6 | 149312712 | 149416607 |
| a0001c0001t0010 | 0/0 | 4360 | 3 | 0 | 0 | 3 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | copy fasta | chr6 | 149312712 | 149416607 |
| a0001c0001t0011 | 0/0 | 4360 | 3 | 0 | 1 | 0 | 1 | 1 | TAB2_chr6_149312712_149416607 | TAB2 | copy fasta | chr6 | 149312712 | 149416607 |
| a0001c0001t0013 | 0/0 | 4360 | 2 | 2 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | copy fasta | chr6 | 149312712 | 149416607 |
| a0001c0001t0015 | 0/0 | 4360 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | copy fasta | chr6 | 149312712 | 149416607 |
| a0001c0001t0016 | 0/0 | 4348 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | copy fasta | chr6 | 149312712 | 149416607 |
| a0001c0001t0017 | 0/0 | 4360 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | copy fasta | chr6 | 149312712 | 149416607 |
| a0001c0001t0019 | 0/0 | 4360 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | copy fasta | chr6 | 149312712 | 149416607 |
| a0001c0001t0020 | 0/0 | 4363 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | copy fasta | chr6 | 149312712 | 149416607 |
| a0001c0001t0021 | 0/0 | 4363 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | copy fasta | chr6 | 149312712 | 149416607 |
| a0001c0001t0022 | 0/0 | 4363 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | copy fasta | chr6 | 149312712 | 149416607 |
| a0001c0001t0023 | 0/0 | 4382 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | copy fasta | chr6 | 149312712 | 149416607 |
| a0001c0001t0024 | 0/0 | 4383 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | copy fasta | chr6 | 149312712 | 149416607 |
| a0001c0002t0002 | 0/0 | 4360 | 75 | 3 | 12 | 52 | 2 | 6 | TAB2_chr6_149312712_149416607 | TAB2 | copy fasta | chr6 | 149312712 | 149416607 |
| a0001c0002t0006 | 0/0 | 4360 | 5 | 0 | 0 | 5 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | copy fasta | chr6 | 149312712 | 149416607 |
| a0001c0002t0012 | 0/0 | 4360 | 2 | 0 | 0 | 2 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | copy fasta | chr6 | 149312712 | 149416607 |
| a0001c0002t0014 | 0/0 | 4363 | 2 | 0 | 0 | 2 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | copy fasta | chr6 | 149312712 | 149416607 |
| a0001c0003t0001 | 0/0 | 4360 | 2 | 0 | 2 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | copy fasta | chr6 | 149312712 | 149416607 |
| a0001c0004t0002 | 0/0 | 4360 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | copy fasta | chr6 | 149312712 | 149416607 |
| a0001c0005t0002 | 0/0 | 4360 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | copy fasta | chr6 | 149312712 | 149416607 |
| a0001c0006t0004 | 0/0 | 4363 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | copy fasta | chr6 | 149312712 | 149416607 |
| a0001c0007t0002 | 0/0 | 4360 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | copy fasta | chr6 | 149312712 | 149416607 |
| a0001c0008t0018 | 0/0 | 4360 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | copy fasta | chr6 | 149312712 | 149416607 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0360 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0361 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0362 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0363 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0003g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0003g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0003g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0003g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0003g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0003g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0003g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0003g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0003g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0003g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0003g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0003g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0003g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0003g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0003g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0003g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0003g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0003g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0003g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0003g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0003g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0003g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0003g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0003g0319 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0003g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0003g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0003g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0003g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0003g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0003g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0003g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0003g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0003g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0003g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0003g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0003g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0003g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0003g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0003g0334 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0003g0335 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0003g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0003g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0003g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0003g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0003g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0003g0341 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0003g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0003g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0003g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0003g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0003g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0003g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0003g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0003g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0003g0350 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0003g0351 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0003g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0003g0353 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0003g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0003g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0003g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0004g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0004g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0004g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0004g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0004g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0004g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0004g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0004g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0004g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0004g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0004g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0004g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0004g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0004g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0004g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0004g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0004g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0004g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0004g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0004g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0004g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0004g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0004g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0004g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0004g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0004g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0004g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0004g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0004g0051 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0004g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0004g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0004g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0004g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0004g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0004g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0004g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0004g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0004g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0004g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0004g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0004g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0004g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0004g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0004g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0004g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0004g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0005g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0005g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0005g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0005g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0005g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0005g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0005g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0005g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0005g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0007g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0007g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0007g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0007g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0007g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0008g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0008g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0008g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0008g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0009g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0009g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0009g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0009g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0010g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0010g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0010g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0011g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0011g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0011g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0013g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0013g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0015g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0016g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0017g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0019g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0020g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0021g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0022g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0023g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0024g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0002t0002g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0002t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0002t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0002t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0002t0002g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0002t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0002t0002g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0002t0002g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0002t0002g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0002t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0002t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0002t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0002t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0002t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0002t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0002t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0002t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0002t0002g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0002t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0002t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0002t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0002t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0002t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0002t0002g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0002t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0002t0002g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0002t0002g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0002t0002g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0002t0002g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0002t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0002t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0002t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0002t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0002t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0002t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0002t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0002t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0002t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0002t0002g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0002t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0002t0002g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0002t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0002t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0002t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0002t0002g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0002t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0002t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0002t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0002t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0002t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0002t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0002t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0002t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0002t0002g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0002t0002g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0002t0002g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0002t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0002t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0002t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0002t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0002t0002g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0002t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0002t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0002t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0002t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0002t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0002t0002g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0002t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0002t0002g0246 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0002t0002g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0002t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0002t0002g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0002t0002g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0002t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0002t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0002t0006g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0002t0006g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0002t0006g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0002t0006g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0002t0006g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0002t0012g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0002t0012g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0002t0014g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0002t0014g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0003t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0003t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0004t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0005t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0006t0004g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0007t0002g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0008t0018g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0266 | EUR | GBR | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG00099 | hp2 | a0001 | c0001 | t0003 | g0341 | EUR | GBR | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0137 | EUR | GBR | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG00140 | hp2 | a0001 | c0001 | t0003 | g0319 | EUR | GBR | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG00423 | hp1 | a0001 | c0002 | t0002 | g0190 | EAS | CHS | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0290 | EAS | CHS | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG00558 | hp1 | a0001 | c0002 | t0006 | g0240 | EAS | CHS | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0280 | EAS | CHS | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | CHS | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG00597 | hp2 | a0001 | c0002 | t0002 | g0101 | EAS | CHS | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG00609 | hp1 | a0001 | c0002 | t0002 | g0207 | EAS | CHS | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG00609 | hp2 | a0001 | c0001 | t0003 | g0307 | EAS | CHS | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG00621 | hp1 | a0001 | c0002 | t0002 | g0097 | EAS | CHS | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG00621 | hp2 | a0001 | c0002 | t0002 | g0245 | EAS | CHS | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG00639 | hp1 | a0001 | c0001 | t0003 | g0171 | AMR | PUR | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG00639 | hp2 | a0001 | c0002 | t0002 | g0198 | AMR | PUR | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG00642 | hp1 | a0001 | c0003 | t0001 | g0259 | AMR | PUR | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0133 | AMR | PUR | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0303 | EAS | CHS | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG00673 | hp2 | a0001 | c0002 | t0002 | g0099 | EAS | CHS | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0292 | AMR | PUR | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG00735 | hp1 | a0001 | c0001 | t0004 | g0066 | AMR | PUR | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0151 | AMR | PUR | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG00738 | hp1 | a0001 | c0001 | t0004 | g0065 | AMR | PUR | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG00738 | hp2 | a0001 | c0001 | t0003 | g0005 | AMR | PUR | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG00741 | hp1 | a0001 | c0001 | t0003 | g0344 | AMR | PUR | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG00741 | hp2 | a0001 | c0007 | t0002 | g0108 | AMR | PUR | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0287 | AMR | PUR | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG01069 | hp2 | a0001 | c0001 | t0004 | g0050 | AMR | PUR | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0152 | AMR | PUR | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG01070 | hp2 | a0001 | c0001 | t0003 | g0346 | AMR | PUR | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG01071 | hp1 | a0001 | c0001 | t0003 | g0339 | AMR | PUR | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG01071 | hp2 | a0001 | c0001 | t0004 | g0045 | AMR | PUR | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0296 | AMR | PUR | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0294 | AMR | PUR | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG01099 | hp1 | a0001 | c0001 | t0003 | g0338 | AMR | PUR | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG01099 | hp2 | a0001 | c0001 | t0004 | g0038 | AMR | PUR | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG01109 | hp1 | a0001 | c0001 | t0003 | g0170 | AMR | PUR | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0175 | AMR | PUR | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG01167 | hp1 | a0001 | c0002 | t0002 | g0230 | AMR | PUR | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG01167 | hp2 | a0001 | c0001 | t0003 | g0168 | AMR | PUR | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0273 | AMR | PUR | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG01168 | hp2 | a0001 | c0001 | t0003 | g0318 | AMR | PUR | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG01175 | hp1 | a0001 | c0001 | t0021 | g0095 | AMR | PUR | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG01175 | hp2 | a0001 | c0001 | t0003 | g0322 | AMR | PUR | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG01192 | hp1 | a0001 | c0001 | t0003 | g0314 | AMR | PUR | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG01192 | hp2 | a0001 | c0001 | t0003 | g0333 | AMR | PUR | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0187 | AMR | PUR | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG01243 | hp2 | a0001 | c0001 | t0005 | g0118 | AMR | PUR | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG01255 | hp1 | a0001 | c0002 | t0002 | g0244 | AMR | CLM | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG01255 | hp2 | a0001 | c0001 | t0003 | g0167 | AMR | CLM | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0362 | AMR | CLM | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG01256 | hp2 | a0001 | c0001 | t0003 | g0351 | AMR | CLM | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG01257 | hp1 | a0001 | c0002 | t0002 | g0199 | AMR | CLM | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG01257 | hp2 | a0001 | c0001 | t0003 | g0345 | AMR | CLM | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0363 | AMR | CLM | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG01258 | hp2 | a0001 | c0002 | t0002 | g0197 | AMR | CLM | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG01261 | hp1 | a0001 | c0002 | t0002 | g0102 | AMR | CLM | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0261 | AMR | CLM | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0064 | AMR | CLM | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG01346 | hp2 | a0001 | c0003 | t0001 | g0260 | AMR | CLM | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0360 | AMR | CLM | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0150 | AMR | CLM | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG01361 | hp1 | a0001 | c0001 | t0003 | g0342 | AMR | CLM | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0267 | AMR | CLM | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG01433 | hp1 | a0001 | c0001 | t0011 | g0134 | AMR | CLM | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG01433 | hp2 | a0001 | c0002 | t0002 | g0195 | AMR | CLM | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0302 | AMR | CLM | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG01496 | hp2 | a0001 | c0001 | t0003 | g0340 | AMR | CLM | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG01515 | hp1 | a0001 | c0001 | t0011 | g0135 | EUR | IBS | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG01515 | hp2 | a0001 | c0002 | t0002 | g0247 | EUR | IBS | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0285 | EUR | IBS | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG01516 | hp2 | a0001 | c0001 | t0004 | g0046 | EUR | IBS | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG01517 | hp1 | a0001 | c0002 | t0002 | g0246 | EUR | IBS | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0288 | EUR | IBS | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0145 | AFR | ACB | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0068 | AFR | ACB | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0089 | AFR | ACB | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG01891 | hp2 | a0001 | c0001 | t0003 | g0329 | AFR | ACB | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG01934 | hp1 | a0001 | c0001 | t0004 | g0119 | AMR | PEL | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0149 | AMR | PEL | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0153 | AMR | PEL | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG01943 | hp2 | a0001 | c0002 | t0002 | g0249 | AMR | PEL | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG02004 | hp1 | a0001 | c0001 | t0003 | g0172 | AMR | PEL | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0284 | AMR | PEL | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | KHV | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG02015 | hp2 | a0001 | c0002 | t0002 | g0224 | EAS | KHV | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG02040 | hp1 | a0001 | c0002 | t0002 | g0115 | EAS | KHV | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG02040 | hp2 | a0001 | c0001 | t0004 | g0033 | EAS | KHV | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG02055 | hp1 | a0001 | c0001 | t0009 | g0081 | AFR | ACB | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0087 | AFR | ACB | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0281 | EAS | KHV | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG02056 | hp2 | a0001 | c0002 | t0006 | g0357 | EAS | KHV | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG02080 | hp1 | a0001 | c0008 | t0018 | g0293 | EAS | KHV | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG02080 | hp2 | a0001 | c0002 | t0002 | g0217 | EAS | KHV | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | KHV | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG02083 | hp2 | a0001 | c0002 | t0002 | g0220 | EAS | KHV | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG02129 | hp1 | a0001 | c0001 | t0003 | g0309 | EAS | KHV | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG02129 | hp2 | a0001 | c0002 | t0002 | g0234 | EAS | KHV | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | KHV | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG02132 | hp2 | a0001 | c0002 | t0002 | g0098 | EAS | KHV | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG02135 | hp1 | a0001 | c0001 | t0003 | g0310 | EAS | KHV | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG02135 | hp2 | a0001 | c0002 | t0002 | g0107 | EAS | KHV | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG02145 | hp2 | a0001 | c0001 | t0009 | g0080 | AFR | ACB | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG02148 | hp1 | a0001 | c0002 | t0002 | g0100 | AMR | PEL | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0139 | AMR | PEL | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | CDX | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG02155 | hp2 | a0001 | c0002 | t0002 | g0112 | EAS | CDX | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0070 | AFR | ACB | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG02257 | hp2 | a0001 | c0001 | t0003 | g0317 | AFR | ACB | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG02258 | hp1 | a0001 | c0001 | t0004 | g0023 | AFR | ACB | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0300 | AFR | ACB | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0282 | AMR | PEL | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG02273 | hp2 | a0001 | c0002 | t0002 | g0229 | AMR | PEL | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG02280 | hp1 | a0001 | c0001 | t0008 | g0164 | AFR | ACB | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG02280 | hp2 | a0001 | c0001 | t0003 | g0328 | AFR | ACB | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0138 | AMR | PEL | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG02293 | hp2 | a0001 | c0002 | t0002 | g0214 | AMR | PEL | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG02300 | hp1 | a0001 | c0002 | t0002 | g0219 | AMR | PEL | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG02300 | hp2 | a0001 | c0001 | t0003 | g0347 | AMR | PEL | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG02451 | hp2 | a0001 | c0001 | t0003 | g0343 | AFR | ACB | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG02523 | hp1 | a0001 | c0002 | t0002 | g0243 | EAS | KHV | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | KHV | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | GWD | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG02572 | hp2 | a0001 | c0001 | t0009 | g0079 | AFR | GWD | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0276 | SAS | PJL | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG02602 | hp2 | a0001 | c0001 | t0005 | g0182 | SAS | PJL | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG02615 | hp1 | a0001 | c0001 | t0004 | g0031 | AFR | GWD | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG02615 | hp2 | a0001 | c0001 | t0013 | g0177 | AFR | GWD | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG02622 | hp1 | a0001 | c0001 | t0003 | g0332 | AFR | GWD | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | GWD | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG02630 | hp1 | a0001 | c0001 | t0004 | g0035 | AFR | GWD | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG02630 | hp2 | a0001 | c0001 | t0007 | g0075 | AFR | GWD | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG02647 | hp1 | a0001 | c0001 | t0003 | g0325 | AFR | GWD | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG02647 | hp2 | a0001 | c0002 | t0002 | g0096 | AFR | GWD | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG02683 | hp1 | a0001 | c0001 | t0005 | g0180 | SAS | PJL | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG02683 | hp2 | a0001 | c0001 | t0003 | g0350 | SAS | PJL | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG02698 | hp1 | a0001 | c0002 | t0002 | g0250 | SAS | PJL | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG02698 | hp2 | a0001 | c0001 | t0004 | g0026 | SAS | PJL | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG02717 | hp1 | a0001 | c0001 | t0004 | g0183 | AFR | GWD | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG02717 | hp2 | a0001 | c0001 | t0008 | g0163 | AFR | GWD | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0262 | SAS | PJL | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG02735 | hp2 | a0001 | c0002 | t0002 | g0200 | SAS | PJL | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0088 | AFR | GWD | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0258 | AFR | GWD | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG02818 | hp1 | a0001 | c0001 | t0005 | g0358 | AFR | GWD | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG02886 | hp1 | a0001 | c0001 | t0004 | g0184 | AFR | GWD | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | GWD | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG02896 | hp2 | a0001 | c0001 | t0003 | g0356 | AFR | GWD | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG02897 | hp2 | a0001 | c0001 | t0003 | g0355 | AFR | GWD | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG02922 | hp1 | a0001 | c0001 | t0003 | g0173 | AFR | ESN | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | ESN | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG02965 | hp1 | a0001 | c0001 | t0004 | g0034 | AFR | ESN | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG02965 | hp2 | a0001 | c0001 | t0003 | g0337 | AFR | ESN | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG02970 | hp1 | a0001 | c0001 | t0003 | g0305 | AFR | ESN | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG02970 | hp2 | a0001 | c0001 | t0004 | g0025 | AFR | ESN | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG02976 | hp1 | a0001 | c0001 | t0004 | g0037 | AFR | ESN | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0162 | AFR | ESN | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG03041 | hp1 | a0001 | c0001 | t0003 | g0327 | AFR | GWD | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG03041 | hp2 | a0001 | c0001 | t0004 | g0029 | AFR | GWD | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG03098 | hp1 | a0001 | c0001 | t0005 | g0359 | AFR | MSL | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG03098 | hp2 | a0001 | c0001 | t0003 | g0331 | AFR | MSL | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG03130 | hp1 | a0001 | c0001 | t0003 | g0349 | AFR | ESN | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | ESN | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0298 | AFR | ESN | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | ESN | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG03195 | hp2 | a0001 | c0001 | t0004 | g0032 | AFR | ESN | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | MSL | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | MSL | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG03225 | hp1 | a0001 | c0001 | t0007 | g0077 | AFR | MSL | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | MSL | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | MSL | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG03453 | hp2 | a0001 | c0001 | t0008 | g0021 | AFR | MSL | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0144 | AFR | MSL | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG03486 | hp2 | a0001 | c0001 | t0007 | g0083 | AFR | MSL | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG03490 | hp1 | a0001 | c0001 | t0003 | g0316 | SAS | PJL | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG03490 | hp2 | a0001 | c0001 | t0003 | g0353 | SAS | PJL | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG03491 | hp2 | a0001 | c0001 | t0003 | g0320 | SAS | PJL | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG03492 | hp1 | a0001 | c0001 | t0003 | g0315 | SAS | PJL | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG03516 | hp1 | a0001 | c0001 | t0009 | g0082 | AFR | ESN | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG03516 | hp2 | a0001 | c0001 | t0008 | g0165 | AFR | ESN | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0073 | AFR | GWD | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG03579 | hp1 | a0001 | c0001 | t0007 | g0074 | AFR | MSL | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | MSL | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG03704 | hp1 | a0001 | c0001 | t0003 | g0174 | SAS | PJL | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG03704 | hp2 | a0001 | c0001 | t0005 | g0117 | SAS | PJL | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0361 | SAS | PJL | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG03710 | hp2 | a0001 | c0002 | t0002 | g0212 | SAS | PJL | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG03831 | hp1 | a0001 | c0002 | t0002 | g0116 | SAS | BEB | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0283 | SAS | BEB | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG03927 | hp1 | a0001 | c0001 | t0003 | g0169 | SAS | BEB | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0141 | SAS | BEB | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG03942 | hp1 | a0001 | c0001 | t0004 | g0027 | SAS | BEB | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG03942 | hp2 | a0001 | c0001 | t0005 | g0179 | SAS | BEB | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG04115 | hp1 | a0001 | c0001 | t0005 | g0181 | SAS | STU | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0268 | SAS | STU | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG04184 | hp1 | a0001 | c0001 | t0003 | g0323 | SAS | BEB | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG04184 | hp2 | a0001 | c0001 | t0011 | g0140 | SAS | BEB | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG04199 | hp1 | a0001 | c0001 | t0004 | g0067 | SAS | STU | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG04199 | hp2 | a0001 | c0001 | t0003 | g0304 | SAS | STU | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG04204 | hp1 | a0001 | c0002 | t0002 | g0104 | SAS | STU | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0274 | SAS | STU | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0275 | SAS | STU | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG04228 | hp2 | a0001 | c0002 | t0002 | g0105 | SAS | STU | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0299 | AFR | YRI | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0092 | AFR | YRI | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | CHB | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA18612 | hp2 | a0001 | c0002 | t0002 | g0227 | EAS | CHB | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA18906 | hp1 | a0001 | c0001 | t0023 | g0071 | AFR | YRI | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | YRI | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA18941 | hp1 | a0001 | c0002 | t0002 | g0204 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA18942 | hp1 | a0001 | c0001 | t0004 | g0039 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA18942 | hp2 | a0001 | c0002 | t0002 | g0239 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA18943 | hp2 | a0001 | c0001 | t0004 | g0040 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA18944 | hp1 | a0001 | c0002 | t0002 | g0202 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA18944 | hp2 | a0001 | c0001 | t0004 | g0055 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA18947 | hp2 | a0001 | c0002 | t0012 | g0193 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA18949 | hp1 | a0001 | c0001 | t0015 | g0154 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA18949 | hp2 | a0001 | c0001 | t0004 | g0030 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA18950 | hp1 | a0001 | c0001 | t0003 | g0311 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA18950 | hp2 | a0001 | c0001 | t0004 | g0042 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA18952 | hp1 | a0001 | c0002 | t0002 | g0252 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA18953 | hp1 | a0001 | c0002 | t0002 | g0248 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA18956 | hp2 | a0001 | c0006 | t0004 | g0043 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA18957 | hp1 | a0001 | c0002 | t0002 | g0205 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA18957 | hp2 | a0001 | c0001 | t0004 | g0053 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA18962 | hp1 | a0001 | c0002 | t0006 | g0211 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA18962 | hp2 | a0001 | c0001 | t0004 | g0063 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA18963 | hp1 | a0001 | c0001 | t0003 | g0352 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA18963 | hp2 | a0001 | c0001 | t0004 | g0049 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA18964 | hp1 | a0001 | c0002 | t0002 | g0222 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA18966 | hp1 | a0001 | c0001 | t0003 | g0336 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA18968 | hp1 | a0001 | c0001 | t0004 | g0056 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA18973 | hp1 | a0001 | c0001 | t0004 | g0044 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA18973 | hp2 | a0001 | c0002 | t0014 | g0103 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA18975 | hp1 | a0001 | c0001 | t0004 | g0059 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA18975 | hp2 | a0001 | c0002 | t0002 | g0111 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA18977 | hp1 | a0001 | c0002 | t0002 | g0241 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA18977 | hp2 | a0001 | c0001 | t0003 | g0308 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA18978 | hp1 | a0001 | c0001 | t0003 | g0313 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA18978 | hp2 | a0001 | c0002 | t0002 | g0109 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA18979 | hp1 | a0001 | c0002 | t0002 | g0114 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA18980 | hp2 | a0001 | c0002 | t0002 | g0216 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA18985 | hp1 | a0001 | c0002 | t0002 | g0206 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA18985 | hp2 | a0001 | c0001 | t0004 | g0048 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA18987 | hp1 | a0001 | c0002 | t0002 | g0237 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA18989 | hp2 | a0001 | c0002 | t0014 | g0110 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA18990 | hp2 | a0001 | c0002 | t0002 | g0209 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA18993 | hp2 | a0001 | c0002 | t0002 | g0225 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA18994 | hp2 | a0001 | c0002 | t0002 | g0191 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA18995 | hp1 | a0001 | c0002 | t0002 | g0208 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA18998 | hp1 | a0001 | c0002 | t0002 | g0188 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA18999 | hp1 | a0001 | c0001 | t0003 | g0354 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA18999 | hp2 | a0001 | c0002 | t0012 | g0194 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA19000 | hp2 | a0001 | c0004 | t0002 | g0218 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA19001 | hp1 | a0001 | c0002 | t0002 | g0106 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA19001 | hp2 | a0001 | c0001 | t0004 | g0062 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA19002 | hp1 | a0001 | c0002 | t0002 | g0221 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA19002 | hp2 | a0001 | c0001 | t0010 | g0157 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA19004 | hp1 | a0001 | c0002 | t0002 | g0226 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA19005 | hp2 | a0001 | c0002 | t0002 | g0113 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA19009 | hp1 | a0001 | c0002 | t0002 | g0213 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA19009 | hp2 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA19011 | hp1 | a0001 | c0001 | t0003 | g0312 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA19011 | hp2 | a0001 | c0002 | t0002 | g0231 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA19030 | hp1 | a0001 | c0001 | t0003 | g0321 | AFR | LWK | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA19030 | hp2 | a0001 | c0001 | t0024 | g0078 | AFR | LWK | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA19043 | hp1 | a0001 | c0001 | t0022 | g0176 | AFR | LWK | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA19043 | hp2 | a0001 | c0001 | t0016 | g0084 | AFR | LWK | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA19059 | hp1 | a0001 | c0002 | t0002 | g0251 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA19059 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA19060 | hp2 | a0001 | c0002 | t0002 | g0232 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA19062 | hp1 | a0001 | c0002 | t0006 | g0210 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA19063 | hp1 | a0001 | c0002 | t0002 | g0203 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA19063 | hp2 | a0001 | c0001 | t0004 | g0058 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA19066 | hp1 | a0001 | c0001 | t0004 | g0061 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA19067 | hp1 | a0001 | c0001 | t0004 | g0060 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA19067 | hp2 | a0001 | c0002 | t0002 | g0235 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA19068 | hp1 | a0001 | c0002 | t0006 | g0238 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA19070 | hp1 | a0001 | c0002 | t0002 | g0189 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA19072 | hp1 | a0001 | c0001 | t0004 | g0052 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA19078 | hp1 | a0001 | c0002 | t0002 | g0192 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA19078 | hp2 | a0001 | c0001 | t0020 | g0054 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA19079 | hp1 | a0001 | c0002 | t0002 | g0242 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA19080 | hp1 | a0001 | c0002 | t0002 | g0215 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA19080 | hp2 | a0001 | c0001 | t0004 | g0041 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA19083 | hp1 | a0001 | c0005 | t0002 | g0233 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA19085 | hp2 | a0001 | c0002 | t0002 | g0196 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA19086 | hp1 | a0001 | c0002 | t0002 | g0201 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA19086 | hp2 | a0001 | c0001 | t0004 | g0047 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA19087 | hp2 | a0001 | c0002 | t0002 | g0223 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA19088 | hp2 | a0001 | c0001 | t0010 | g0158 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA19091 | hp1 | a0001 | c0001 | t0010 | g0156 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA19240 | hp1 | a0001 | c0001 | t0019 | g0306 | AFR | YRI | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA19240 | hp2 | a0001 | c0001 | t0017 | g0022 | AFR | YRI | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA20129 | hp1 | a0001 | c0002 | t0002 | g0236 | AFR | ASW | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA20129 | hp2 | a0001 | c0001 | t0003 | g0326 | AFR | ASW | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0257 | EUR | TSI | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA20805 | hp2 | a0001 | c0001 | t0003 | g0335 | EUR | TSI | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0277 | AMR | CLM | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG01123 | hp2 | a0001 | c0001 | t0004 | g0057 | AMR | CLM | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG02109 | hp1 | a0001 | c0001 | t0013 | g0178 | AFR | ACB | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0090 | AFR | ACB | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG02486 | hp2 | a0001 | c0001 | t0003 | g0324 | AFR | ACB | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG02559 | hp1 | a0001 | c0001 | t0003 | g0330 | AFR | ACB | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG02559 | hp2 | a0001 | c0001 | t0004 | g0024 | AFR | ACB | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | MSL | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG03471 | hp2 | a0001 | c0001 | t0004 | g0036 | AFR | MSL | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG06807 | hp1 | a0001 | c0001 | t0007 | g0076 | AFR | USA | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG06807 | hp2 | a0001 | c0001 | t0004 | g0028 | AFR | USA | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA20300 | hp1 | a0001 | c0002 | t0002 | g0228 | AFR | USA | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA20300 | hp2 | a0001 | c0001 | t0003 | g0348 | AFR | USA | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA21309 | hp1 | a0001 | c0001 | t0005 | g0253 | AFR | LWK | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0072 | AFR | LWK | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0003 | g0334 | REF | REF | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0004 | g0051 | REF | REF | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| 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 |
|---|
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:149370018
|
A | G | 1 | a0001c0008 | 1 | HG02080.hp1 | synonymous_variant | LOW | c.21A>G | p.Gln7Gln | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 2/7 | 414/4363 | 21/2082 | 7/693 | chr6 | 149370018 | ||
| chr6:149378197
|
A | G | 1 | a0001c0003 | 2 | HG00642.hp1 HG01346.hp2 |
synonymous_variant | LOW | c.282A>G | p.Gly94Gly | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/7 | 675/4363 | 282/2082 | 94/693 | chr6 | 149378197 | ||
| chr6:149378290
|
G | A | 2 | a0001c0004a0001c0005 | 2 | NA19000.hp2 NA19083.hp1 |
synonymous_variant | LOW | c.375G>A | p.Glu125Glu | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/7 | 768/4363 | 375/2082 | 125/693 | chr6 | 149378290 | ||
| chr6:149378686
|
T | C | 1 | a0001c0006 | 1 | NA18956.hp2 | synonymous_variant | LOW | c.771T>C | p.Thr257Thr | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/7 | 1164/4363 | 771/2082 | 257/693 | chr6 | 149378686 | ||
| chr6:149379043
|
G | A | 1 | a0001c0007 | 1 | HG00741.hp2 | synonymous_variant | LOW | c.1128G>A | p.Thr376Thr | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/7 | 1521/4363 | 1128/2082 | 376/693 | chr6 | 149379043 | ||
| chr6:149379067
|
A | G | 1 | a0001c0005 | 1 | NA19083.hp1 | synonymous_variant | LOW | c.1152A>G | p.Gln384Gln | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/7 | 1545/4363 | 1152/2082 | 384/693 | chr6 | 149379067 | ||
| chr6:149379355
|
G | A | 4 | a0001c0002a0001c0004a0001c0005others(1): Show | 87 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(84): Show |
synonymous_variant | LOW | c.1440G>A | p.Val480Val | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/7 | 1833/4363 | 1440/2082 | 480/693 | chr6 | 149379355 | ||
| chr6:149409710
|
G | A | 4 | a0001c0002a0001c0004a0001c0005others(1): Show | 87 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(84): Show |
synonymous_variant | LOW | c.2073G>A | p.Arg691Arg | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 7/7 | 2466/4363 | 2073/2082 | 691/693 | chr6 | 149409710 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:149317834
|
A | AGGGGGCT others(15): Show |
2 | a0001c0001t0007a0001c0001t0023 | 6 | HG02630.hp2 HG03225.hp1 HG03486.hp2 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-269_-248dupGGGGCT others(16): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/7 | 52140 | INFO_REALIGN_3_PRIME | chr6 | 149317834 | ||||
| chr6:149317834
|
A | AGGGGGCT others(16): Show |
1 | a0001c0001t0024 | 1 | NA19030.hp2 | 5_prime_UTR_variant | MODIFIER | c.-270_-248dupGGGGGC others(17): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/7 | 52140 | INFO_REALIGN_3_PRIME | chr6 | 149317834 | ||||
| chr6:149317891
|
G | A | 1 | a0001c0001t0015 | 1 | NA18949.hp1 | 5_prime_UTR_variant | MODIFIER | c.-214G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/7 | 52107 | chr6 | 149317891 | |||||
| chr6:149317896
|
CGGCGGCG others(5): Show |
C | 1 | a0001c0001t0016 | 1 | NA19043.hp2 | 5_prime_UTR_variant | MODIFIER | c.-199_-188delGCTGGC others(6): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/7 | 52081 | INFO_REALIGN_3_PRIME | chr6 | 149317896 | ||||
| chr6:149317962
|
AGGC | A | 23 | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(20): Show | 314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
5_prime_UTR_variant | MODIFIER | c.-127_-125delGGC | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/7 | 52018 | INFO_REALIGN_3_PRIME | chr6 | 149317962 | ||||
| chr6:149318000
|
G | A | 1 | a0001c0002t0012 | 2 | NA18947.hp2 NA18999.hp2 |
5_prime_UTR_variant | MODIFIER | c.-105G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/7 | 51998 | chr6 | 149318000 | |||||
| chr6:149410005
|
A | C | 2 | a0001c0001t0013a0001c0001t0022 | 3 | HG02109.hp1 HG02615.hp2 NA19043.hp1 |
3_prime_UTR_variant | MODIFIER | c.*286A>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 7/7 | 286 | chr6 | 149410005 | |||||
| chr6:149410309
|
A | G | 1 | a0001c0001t0019 | 1 | NA19240.hp1 | 3_prime_UTR_variant | MODIFIER | c.*590A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 7/7 | 590 | chr6 | 149410309 | |||||
| chr6:149410340
|
C | G | 3 | a0001c0001t0003a0001c0001t0019a0001c0001t0021 | 63 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(60): Show |
3_prime_UTR_variant | MODIFIER | c.*621C>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 7/7 | 621 | chr6 | 149410340 | |||||
| chr6:149410420
|
A | G | 1 | a0001c0001t0011 | 3 | HG01433.hp1 HG01515.hp1 HG04184.hp2 |
3_prime_UTR_variant | MODIFIER | c.*701A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 7/7 | 701 | chr6 | 149410420 | |||||
| chr6:149410523
|
C | A | 2 | a0001c0001t0013a0001c0001t0022 | 3 | HG02109.hp1 HG02615.hp2 NA19043.hp1 |
3_prime_UTR_variant | MODIFIER | c.*804C>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 7/7 | 804 | chr6 | 149410523 | |||||
| chr6:149410655
|
G | T | 1 | a0001c0001t0005 | 9 | HG01243.hp2 HG02602.hp2 HG02683.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*936G>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 7/7 | 936 | chr6 | 149410655 | |||||
| chr6:149410658
|
A | G | 4 | a0001c0001t0007a0001c0001t0009a0001c0001t0016others(1): Show | 11 | HG02055.hp1 HG02145.hp2 HG02572.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*939A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 7/7 | 939 | chr6 | 149410658 | |||||
| chr6:149410658
|
A | T | 1 | a0001c0001t0005 | 9 | HG01243.hp2 HG02602.hp2 HG02683.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*939A>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 7/7 | 939 | chr6 | 149410658 | |||||
| chr6:149410767
|
C | A | 1 | a0001c0001t0020 | 1 | NA19078.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1048C>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 7/7 | 1048 | chr6 | 149410767 | |||||
| chr6:149410768
|
C | T | 7 | a0001c0002t0002a0001c0002t0006a0001c0002t0012others(4): Show | 87 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(84): Show |
3_prime_UTR_variant | MODIFIER | c.*1049C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 7/7 | 1049 | chr6 | 149410768 | |||||
| chr6:149411096
|
A | G | 1 | a0001c0002t0006 | 5 | HG00558.hp1 HG02056.hp2 NA18962.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1377A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 7/7 | 1377 | chr6 | 149411096 | |||||
| chr6:149411383
|
C | T | 1 | a0001c0001t0008 | 4 | HG02280.hp1 HG02717.hp2 HG03453.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1664C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 7/7 | 1664 | chr6 | 149411383 | |||||
| chr6:149411404
|
G | A | 1 | a0001c0001t0017 | 1 | NA19240.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1685G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 7/7 | 1685 | chr6 | 149411404 | |||||
| chr6:149411468
|
G | A | 1 | a0001c0001t0010 | 3 | NA19002.hp2 NA19088.hp2 NA19091.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1749G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 7/7 | 1749 | chr6 | 149411468 | |||||
| chr6:149411507
|
G | A | 1 | a0001c0008t0018 | 1 | HG02080.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1788G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 7/7 | 1788 | chr6 | 149411507 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:149318152
|
T | C | 1 | a0001c0001t0001g0004 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.-90+137T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149318152 | ||||||
| chr6:149318177
|
C | T | 2 | a0001c0001t0001g0362a0001c0001t0001g0363 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.-90+162C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149318177 | ||||||
| chr6:149318264
|
G | C | 1 | a0001c0001t0003g0005 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-90+249G>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149318264 | ||||||
| chr6:149318273
|
C | CG | 179 | a0001c0001t0001g0185a0001c0001t0001g0186a0001c0001t0001g0187others(176): Show | 179 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.-90+266dupG | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149318273 | |||||
| chr6:149318276
|
G | A | 1 | a0001c0001t0001g0006 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-90+261G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149318276 | ||||||
| chr6:149318278
|
G | T | 1 | a0001c0001t0001g0361 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-90+263G>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149318278 | ||||||
| chr6:149318380
|
C | G | 2 | a0001c0001t0004g0183a0001c0001t0004g0184 | 2 | HG02717.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.-90+365C>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149318380 | ||||||
| chr6:149318400
|
G | A | 15 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(12): Show | 15 | HG00733.hp2 HG02145.hp1 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.-90+385G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149318400 | ||||||
| chr6:149318490
|
G | T | 3 | a0001c0001t0001g0360a0001c0001t0001g0362a0001c0001t0001g0363 | 3 | HG01256.hp1 HG01258.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.-90+475G>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149318490 | ||||||
| chr6:149318616
|
A | T | 177 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(174): Show | 178 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(175): Show |
intron_variant | MODIFIER | c.-90+601A>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149318616 | ||||||
| chr6:149318762
|
C | T | 1 | a0001c0001t0004g0119 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-90+747C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149318762 | ||||||
| chr6:149318956
|
C | T | 1 | a0001c0001t0005g0118 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-90+941C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149318956 | ||||||
| chr6:149319055
|
G | A | 1 | a0001c0001t0017g0022 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-90+1040G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149319055 | ||||||
| chr6:149319177
|
G | T | 9 | a0001c0001t0005g0117a0001c0001t0005g0118a0001c0001t0005g0179others(6): Show | 9 | HG01243.hp2 HG02602.hp2 HG02683.hp1 others(6): Show |
intron_variant | MODIFIER | c.-90+1162G>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149319177 | ||||||
| chr6:149319366
|
G | A | 1 | a0001c0001t0004g0023 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-90+1351G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149319366 | ||||||
| chr6:149319538
|
A | T | 297 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(294): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.-90+1523A>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149319538 | ||||||
| chr6:149319839
|
A | G | 3 | a0001c0001t0013g0177a0001c0001t0013g0178a0001c0001t0022g0176 | 3 | HG02109.hp1 HG02615.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-90+1824A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149319839 | ||||||
| chr6:149319972
|
A | G | 8 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(5): Show | 8 | HG02895.hp1 HG02895.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.-90+1957A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149319972 | ||||||
| chr6:149319982
|
C | T | 1 | a0001c0001t0001g0175 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-90+1967C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149319982 | ||||||
| chr6:149320047
|
G | A | 1 | a0001c0001t0022g0176 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-90+2032G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149320047 | ||||||
| chr6:149320064
|
A | T | 87 | a0001c0002t0002g0096a0001c0002t0002g0097a0001c0002t0002g0098others(84): Show | 87 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.-90+2049A>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149320064 | ||||||
| chr6:149320090
|
T | C | 1 | a0001c0002t0002g0188 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.-90+2075T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149320090 | ||||||
| chr6:149320136
|
G | C | 17 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0070others(14): Show | 17 | HG01884.hp2 HG02055.hp1 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.-90+2121G>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149320136 | ||||||
| chr6:149320324
|
G | T | 1 | a0001c0001t0001g0003 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.-90+2309G>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149320324 | ||||||
| chr6:149320346
|
A | G | 9 | a0001c0001t0005g0117a0001c0001t0005g0118a0001c0001t0005g0179others(6): Show | 9 | HG01243.hp2 HG02602.hp2 HG02683.hp1 others(6): Show |
intron_variant | MODIFIER | c.-90+2331A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149320346 | ||||||
| chr6:149320372
|
G | A | 1 | a0001c0001t0001g0175 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-90+2357G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149320372 | ||||||
| chr6:149320491
|
T | C | 116 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(113): Show | 118 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.-90+2476T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149320491 | ||||||
| chr6:149320501
|
ATTTTCCC others(15): Show |
A | 116 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(113): Show | 118 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.-90+2495_-90+2516d others(24): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149320501 | |||||
| chr6:149320662
|
C | G | 1 | a0001c0002t0002g0252 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.-90+2647C>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149320662 | ||||||
| chr6:149320672
|
A | AT | 64 | a0001c0001t0001g0303a0001c0001t0003g0005a0001c0001t0003g0167others(61): Show | 64 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(61): Show |
intron_variant | MODIFIER | c.-90+2666dupT | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149320672 | |||||
| chr6:149320683
|
A | C | 3 | a0001c0001t0013g0177a0001c0001t0013g0178a0001c0001t0022g0176 | 3 | HG02109.hp1 HG02615.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-90+2668A>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149320683 | ||||||
| chr6:149320754
|
A | G | 2 | a0001c0001t0003g0355a0001c0001t0003g0356 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-90+2739A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149320754 | ||||||
| chr6:149321471
|
A | C | 11 | a0001c0001t0007g0074a0001c0001t0007g0075a0001c0001t0007g0076others(8): Show | 11 | HG02055.hp1 HG02145.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.-90+3456A>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149321471 | ||||||
| chr6:149321536
|
C | T | 1 | a0001c0001t0005g0182 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-90+3521C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149321536 | ||||||
| chr6:149321721
|
A | G | 3 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0020 | 3 | HG03209.hp1 HG03453.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-90+3706A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149321721 | ||||||
| chr6:149321733
|
G | C | 2 | a0001c0001t0001g0257a0001c0001t0001g0258 | 2 | HG02809.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.-90+3718G>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149321733 | ||||||
| chr6:149321953
|
A | G | 17 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0070others(14): Show | 17 | HG01884.hp2 HG02055.hp1 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.-90+3938A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149321953 | ||||||
| chr6:149322050
|
A | T | 1 | a0001c0001t0001g0302 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-90+4035A>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149322050 | ||||||
| chr6:149322150
|
T | A | 63 | a0001c0001t0003g0005a0001c0001t0003g0167a0001c0001t0003g0168others(60): Show | 63 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.-90+4135T>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149322150 | ||||||
| chr6:149322151
|
G | T | 63 | a0001c0001t0003g0005a0001c0001t0003g0167a0001c0001t0003g0168others(60): Show | 63 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.-90+4136G>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149322151 | ||||||
| chr6:149322152
|
C | G | 63 | a0001c0001t0003g0005a0001c0001t0003g0167a0001c0001t0003g0168others(60): Show | 63 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.-90+4137C>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149322152 | ||||||
| chr6:149322213
|
G | A | 3 | a0001c0001t0013g0177a0001c0001t0013g0178a0001c0001t0022g0176 | 3 | HG02109.hp1 HG02615.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-90+4198G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149322213 | ||||||
| chr6:149322289
|
A | G | 18 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0070others(15): Show | 18 | HG01884.hp2 HG02055.hp1 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.-90+4274A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149322289 | ||||||
| chr6:149322423
|
A | G | 1 | a0001c0001t0003g0354 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.-90+4408A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149322423 | ||||||
| chr6:149322467
|
G | A | 1 | a0001c0001t0005g0179 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-90+4452G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149322467 | ||||||
| chr6:149322475
|
A | G | 1 | a0001c0001t0001g0301 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.-90+4460A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149322475 | ||||||
| chr6:149322478
|
G | C | 1 | a0001c0001t0001g0013 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-90+4463G>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149322478 | ||||||
| chr6:149322548
|
A | G | 2 | a0001c0001t0001g0299a0001c0001t0001g0300 | 2 | HG02258.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-90+4533A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149322548 | ||||||
| chr6:149322573
|
T | C | 63 | a0001c0001t0003g0005a0001c0001t0003g0167a0001c0001t0003g0168others(60): Show | 63 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.-90+4558T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149322573 | ||||||
| chr6:149322615
|
T | G | 3 | a0001c0001t0001g0261a0001c0003t0001g0259a0001c0003t0001g0260 | 3 | HG00642.hp1 HG01261.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.-90+4600T>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149322615 | ||||||
| chr6:149322826
|
T | A | 87 | a0001c0002t0002g0096a0001c0002t0002g0097a0001c0002t0002g0098others(84): Show | 87 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.-90+4811T>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149322826 | ||||||
| chr6:149322924
|
A | G | 1 | a0001c0001t0017g0022 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-90+4909A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149322924 | ||||||
| chr6:149322942
|
A | G | 1 | a0001c0002t0002g0251 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.-90+4927A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149322942 | ||||||
| chr6:149323203
|
T | C | 1 | a0001c0001t0003g0304 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-90+5188T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149323203 | ||||||
| chr6:149323497
|
C | T | 1 | a0001c0001t0001g0166 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.-90+5482C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149323497 | ||||||
| chr6:149323538
|
G | A | 1 | a0001c0001t0001g0120 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.-90+5523G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149323538 | ||||||
| chr6:149323562
|
G | A | 86 | a0001c0002t0002g0096a0001c0002t0002g0097a0001c0002t0002g0098others(83): Show | 86 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(83): Show |
intron_variant | MODIFIER | c.-90+5547G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149323562 | ||||||
| chr6:149323568
|
C | G | 6 | a0001c0001t0001g0161a0001c0001t0001g0162a0001c0001t0001g0298others(3): Show | 6 | HG02280.hp1 HG02622.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.-90+5553C>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149323568 | ||||||
| chr6:149323625
|
T | G | 6 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(3): Show | 6 | HG00733.hp2 HG02145.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.-90+5610T>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149323625 | ||||||
| chr6:149323648
|
G | A | 63 | a0001c0001t0003g0005a0001c0001t0003g0167a0001c0001t0003g0168others(60): Show | 63 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.-90+5633G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149323648 | ||||||
| chr6:149323676
|
A | C | 2 | a0001c0001t0001g0159a0001c0001t0001g0160 | 2 | NA18987.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.-90+5661A>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149323676 | ||||||
| chr6:149323742
|
A | G | 1 | a0001c0001t0001g0297 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-90+5727A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149323742 | ||||||
| chr6:149323783
|
G | A | 1 | a0001c0001t0001g0004 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.-90+5768G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149323783 | ||||||
| chr6:149323918
|
A | AT | 296 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(293): Show | 298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.-90+5911dupT | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149323918 | |||||
| chr6:149324033
|
G | C | 1 | a0001c0001t0004g0024 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-90+6018G>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149324033 | ||||||
| chr6:149324280
|
C | T | 3 | a0001c0001t0010g0156a0001c0001t0010g0157a0001c0001t0010g0158 | 3 | NA19002.hp2 NA19088.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.-90+6265C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149324280 | ||||||
| chr6:149324351
|
A | C | 1 | a0001c0001t0004g0067 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-90+6336A>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149324351 | ||||||
| chr6:149324405
|
A | G | 3 | a0001c0001t0013g0177a0001c0001t0013g0178a0001c0001t0022g0176 | 3 | HG02109.hp1 HG02615.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-90+6390A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149324405 | ||||||
| chr6:149324503
|
G | T | 1 | a0001c0001t0016g0084 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-90+6488G>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149324503 | ||||||
| chr6:149324685
|
A | G | 3 | a0001c0001t0013g0177a0001c0001t0013g0178a0001c0001t0022g0176 | 3 | HG02109.hp1 HG02615.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-90+6670A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149324685 | ||||||
| chr6:149324713
|
G | A | 3 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009 | 3 | HG00733.hp2 HG02145.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.-90+6698G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149324713 | ||||||
| chr6:149324826
|
C | CT | 75 | a0001c0001t0001g0155a0001c0001t0003g0005a0001c0001t0003g0168others(72): Show | 75 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(72): Show |
intron_variant | MODIFIER | c.-90+6829dupT | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149324826 | |||||
| chr6:149324826
|
C | CTTT | 17 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0070others(14): Show | 17 | HG01884.hp2 HG02055.hp1 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.-90+6827_-90+6829d others(5): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149324826 | |||||
| chr6:149325097
|
A | G | 6 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0150others(3): Show | 6 | HG00735.hp2 HG01070.hp1 HG01358.hp2 others(3): Show |
intron_variant | MODIFIER | c.-90+7082A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149325097 | ||||||
| chr6:149325172
|
C | T | 153 | a0001c0001t0003g0005a0001c0001t0003g0167a0001c0001t0003g0168others(150): Show | 153 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(150): Show |
intron_variant | MODIFIER | c.-90+7157C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149325172 | ||||||
| chr6:149325317
|
T | C | 1 | a0001c0002t0002g0097 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-90+7302T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149325317 | ||||||
| chr6:149325364
|
G | A | 116 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(113): Show | 118 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.-90+7349G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149325364 | ||||||
| chr6:149325385
|
A | G | 87 | a0001c0002t0002g0096a0001c0002t0002g0097a0001c0002t0002g0098others(84): Show | 87 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.-90+7370A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149325385 | ||||||
| chr6:149325582
|
T | C | 1 | a0001c0001t0001g0262 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-90+7567T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149325582 | ||||||
| chr6:149325694
|
C | T | 2 | a0001c0002t0002g0249a0001c0002t0002g0250 | 2 | HG01943.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.-90+7679C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149325694 | ||||||
| chr6:149325795
|
A | G | 63 | a0001c0001t0003g0005a0001c0001t0003g0167a0001c0001t0003g0168others(60): Show | 63 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.-90+7780A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149325795 | ||||||
| chr6:149325804
|
A | G | 63 | a0001c0001t0003g0005a0001c0001t0003g0167a0001c0001t0003g0168others(60): Show | 63 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.-90+7789A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149325804 | ||||||
| chr6:149325886
|
C | G | 1 | a0001c0001t0003g0353 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.-90+7871C>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149325886 | ||||||
| chr6:149325929
|
G | A | 1 | a0001c0001t0008g0021 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-90+7914G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149325929 | ||||||
| chr6:149325964
|
G | A | 297 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(294): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.-90+7949G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149325964 | ||||||
| chr6:149326236
|
A | G | 1 | a0001c0001t0001g0064 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.-90+8221A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149326236 | ||||||
| chr6:149326271
|
CA | C | 207 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(204): Show | 209 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(206): Show |
intron_variant | MODIFIER | c.-90+8275delA | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149326271 | |||||
| chr6:149326271
|
CAA | C | 10 | a0001c0001t0001g0017a0001c0001t0005g0117a0001c0001t0005g0118others(7): Show | 10 | HG01243.hp2 HG02602.hp2 HG02683.hp1 others(7): Show |
intron_variant | MODIFIER | c.-90+8274_-90+8275d others(4): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149326271 | |||||
| chr6:149326271
|
CAAAAAA | C | 63 | a0001c0001t0003g0005a0001c0001t0003g0167a0001c0001t0003g0168others(60): Show | 63 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.-90+8270_-90+8275d others(8): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149326271 | |||||
| chr6:149326295
|
G | A | 1 | a0001c0001t0005g0253 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-90+8280G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149326295 | ||||||
| chr6:149326389
|
T | C | 154 | a0001c0001t0003g0005a0001c0001t0003g0167a0001c0001t0003g0168others(151): Show | 154 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(151): Show |
intron_variant | MODIFIER | c.-90+8374T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149326389 | ||||||
| chr6:149326397
|
T | A | 1 | a0001c0001t0001g0006 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-90+8382T>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149326397 | ||||||
| chr6:149326425
|
C | G | 6 | a0001c0001t0001g0161a0001c0001t0001g0162a0001c0001t0001g0298others(3): Show | 6 | HG02280.hp1 HG02622.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.-90+8410C>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149326425 | ||||||
| chr6:149326546
|
G | A | 1 | a0001c0001t0008g0021 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-90+8531G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149326546 | ||||||
| chr6:149326551
|
TA | T | 82 | a0001c0001t0001g0147a0001c0002t0002g0096a0001c0002t0002g0097others(79): Show | 82 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.-90+8537delA | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149326551 | ||||||
| chr6:149326552
|
A | T | 5 | a0001c0002t0002g0113a0001c0002t0002g0114a0001c0002t0002g0115others(2): Show | 5 | HG02040.hp1 HG02056.hp2 NA18953.hp1 others(2): Show |
intron_variant | MODIFIER | c.-90+8537A>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149326552 | ||||||
| chr6:149326552
|
AT | A | 127 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(124): Show | 129 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(126): Show |
intron_variant | MODIFIER | c.-90+8550delT | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149326552 | |||||
| chr6:149326552
|
ATT | A | 79 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0070others(76): Show | 79 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(76): Show |
intron_variant | MODIFIER | c.-90+8549_-90+8550d others(4): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149326552 | |||||
| chr6:149326567
|
A | G | 3 | a0001c0001t0008g0163a0001c0001t0008g0164a0001c0001t0008g0165 | 3 | HG02280.hp1 HG02717.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-90+8552A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149326567 | ||||||
| chr6:149326622
|
A | G | 3 | a0001c0001t0013g0177a0001c0001t0013g0178a0001c0001t0022g0176 | 3 | HG02109.hp1 HG02615.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-90+8607A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149326622 | ||||||
| chr6:149326667
|
C | G | 9 | a0001c0001t0005g0117a0001c0001t0005g0118a0001c0001t0005g0179others(6): Show | 9 | HG01243.hp2 HG02602.hp2 HG02683.hp1 others(6): Show |
intron_variant | MODIFIER | c.-90+8652C>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149326667 | ||||||
| chr6:149326692
|
C | T | 1 | a0001c0001t0005g0253 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-90+8677C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149326692 | ||||||
| chr6:149326749
|
T | C | 1 | a0001c0002t0002g0190 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.-90+8734T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149326749 | ||||||
| chr6:149326752
|
T | C | 1 | a0001c0002t0002g0191 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.-90+8737T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149326752 | ||||||
| chr6:149326808
|
C | T | 153 | a0001c0001t0003g0005a0001c0001t0003g0167a0001c0001t0003g0168others(150): Show | 153 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(150): Show |
intron_variant | MODIFIER | c.-90+8793C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149326808 | ||||||
| chr6:149327107
|
A | G | 6 | a0001c0001t0001g0161a0001c0001t0001g0162a0001c0001t0001g0298others(3): Show | 6 | HG02280.hp1 HG02622.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.-90+9092A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149327107 | ||||||
| chr6:149327119
|
T | C | 8 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(5): Show | 8 | HG02895.hp1 HG02895.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.-90+9104T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149327119 | ||||||
| chr6:149327245
|
G | A | 86 | a0001c0002t0002g0096a0001c0002t0002g0097a0001c0002t0002g0098others(83): Show | 86 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(83): Show |
intron_variant | MODIFIER | c.-90+9230G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149327245 | ||||||
| chr6:149327260
|
AAGAC | A | 3 | a0001c0001t0013g0177a0001c0001t0013g0178a0001c0001t0022g0176 | 3 | HG02109.hp1 HG02615.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-90+9249_-90+9252d others(6): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149327260 | |||||
| chr6:149327276
|
T | C | 2 | a0001c0001t0004g0026a0001c0001t0004g0027 | 2 | HG02698.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.-90+9261T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149327276 | ||||||
| chr6:149327304
|
T | A | 153 | a0001c0001t0003g0005a0001c0001t0003g0167a0001c0001t0003g0168others(150): Show | 153 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(150): Show |
intron_variant | MODIFIER | c.-90+9289T>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149327304 | ||||||
| chr6:149327363
|
C | T | 1 | a0001c0001t0003g0351 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.-90+9348C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149327363 | ||||||
| chr6:149327459
|
G | A | 92 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(89): Show | 93 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(90): Show |
intron_variant | MODIFIER | c.-90+9444G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149327459 | ||||||
| chr6:149327763
|
T | A | 87 | a0001c0002t0002g0096a0001c0002t0002g0097a0001c0002t0002g0098others(84): Show | 87 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.-90+9748T>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149327763 | ||||||
| chr6:149327860
|
T | C | 5 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0018others(2): Show | 5 | HG02895.hp2 HG02897.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.-90+9845T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149327860 | ||||||
| chr6:149328046
|
T | G | 1 | a0001c0001t0001g0086 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-90+10031T>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149328046 | ||||||
| chr6:149328128
|
C | G | 1 | a0001c0001t0005g0253 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-90+10113C>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149328128 | ||||||
| chr6:149328169
|
T | C | 1 | a0001c0001t0005g0253 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-90+10154T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149328169 | ||||||
| chr6:149328254
|
A | G | 1 | a0001c0002t0002g0251 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.-90+10239A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149328254 | ||||||
| chr6:149328276
|
A | G | 1 | a0001c0001t0003g0350 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-90+10261A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149328276 | ||||||
| chr6:149328293
|
C | T | 45 | a0001c0001t0003g0005a0001c0001t0003g0171a0001c0001t0003g0172others(42): Show | 45 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.-90+10278C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149328293 | ||||||
| chr6:149328357
|
G | T | 1 | a0001c0001t0005g0253 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-90+10342G>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149328357 | ||||||
| chr6:149328559
|
T | C | 1 | a0001c0001t0001g0161 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-90+10544T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149328559 | ||||||
| chr6:149328585
|
C | T | 86 | a0001c0002t0002g0096a0001c0002t0002g0097a0001c0002t0002g0098others(83): Show | 86 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(83): Show |
intron_variant | MODIFIER | c.-90+10570C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149328585 | ||||||
| chr6:149328625
|
A | C | 6 | a0001c0001t0001g0161a0001c0001t0001g0162a0001c0001t0001g0298others(3): Show | 6 | HG02280.hp1 HG02622.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.-90+10610A>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149328625 | ||||||
| chr6:149328647
|
C | T | 3 | a0001c0001t0013g0177a0001c0001t0013g0178a0001c0001t0022g0176 | 3 | HG02109.hp1 HG02615.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-90+10632C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149328647 | ||||||
| chr6:149328677
|
G | C | 1 | a0001c0002t0002g0192 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.-90+10662G>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149328677 | ||||||
| chr6:149328744
|
T | C | 296 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(293): Show | 298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.-90+10729T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149328744 | ||||||
| chr6:149328808
|
C | T | 63 | a0001c0001t0003g0005a0001c0001t0003g0167a0001c0001t0003g0168others(60): Show | 63 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.-90+10793C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149328808 | ||||||
| chr6:149328964
|
G | C | 86 | a0001c0002t0002g0096a0001c0002t0002g0097a0001c0002t0002g0098others(83): Show | 86 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(83): Show |
intron_variant | MODIFIER | c.-90+10949G>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149328964 | ||||||
| chr6:149329024
|
A | G | 3 | a0001c0001t0013g0177a0001c0001t0013g0178a0001c0001t0022g0176 | 3 | HG02109.hp1 HG02615.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-90+11009A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149329024 | ||||||
| chr6:149329030
|
A | T | 2 | a0001c0002t0002g0246a0001c0002t0002g0247 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.-90+11015A>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149329030 | ||||||
| chr6:149329248
|
G | T | 1 | a0001c0001t0001g0142 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-90+11233G>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149329248 | ||||||
| chr6:149329325
|
A | G | 2 | a0001c0002t0002g0249a0001c0002t0002g0250 | 2 | HG01943.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.-90+11310A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149329325 | ||||||
| chr6:149329344
|
TA | T | 296 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(293): Show | 298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.-90+11331delA | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149329344 | |||||
| chr6:149329492
|
G | A | 1 | a0001c0001t0003g0171 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-90+11477G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149329492 | ||||||
| chr6:149329723
|
G | A | 2 | a0001c0001t0004g0028a0001c0001t0004g0029 | 2 | HG03041.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.-90+11708G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149329723 | ||||||
| chr6:149329728
|
T | C | 2 | a0001c0001t0005g0180a0001c0001t0005g0181 | 2 | HG02683.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.-90+11713T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149329728 | ||||||
| chr6:149330070
|
G | A | 294 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(291): Show | 296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.-90+12055G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149330070 | ||||||
| chr6:149330072
|
G | GA | 17 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0070others(14): Show | 17 | HG01884.hp2 HG02055.hp1 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.-90+12058dupA | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149330072 | |||||
| chr6:149330095
|
C | CT | 86 | a0001c0002t0002g0096a0001c0002t0002g0097a0001c0002t0002g0098others(83): Show | 86 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(83): Show |
intron_variant | MODIFIER | c.-90+12090dupT | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149330095 | |||||
| chr6:149330128
|
G | A | 152 | a0001c0001t0003g0005a0001c0001t0003g0167a0001c0001t0003g0168others(149): Show | 152 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(149): Show |
intron_variant | MODIFIER | c.-90+12113G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149330128 | ||||||
| chr6:149330279
|
G | A | 2 | a0001c0001t0001g0147a0001c0001t0015g0154 | 2 | NA18949.hp1 NA19059.hp2 |
intron_variant | MODIFIER | c.-90+12264G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149330279 | ||||||
| chr6:149330637
|
T | C | 2 | a0001c0001t0003g0305a0001c0001t0019g0306 | 2 | HG02970.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-90+12622T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149330637 | ||||||
| chr6:149330927
|
G | C | 1 | a0001c0001t0017g0022 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-90+12912G>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149330927 | ||||||
| chr6:149330961
|
G | C | 1 | a0001c0001t0022g0176 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-90+12946G>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149330961 | ||||||
| chr6:149331071
|
T | C | 3 | a0001c0001t0003g0317a0001c0001t0003g0318a0001c0001t0003g0319 | 3 | HG00140.hp2 HG01168.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.-90+13056T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149331071 | ||||||
| chr6:149331148
|
G | A | 63 | a0001c0001t0003g0005a0001c0001t0003g0167a0001c0001t0003g0168others(60): Show | 63 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.-90+13133G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149331148 | ||||||
| chr6:149331150
|
G | A | 86 | a0001c0002t0002g0096a0001c0002t0002g0097a0001c0002t0002g0098others(83): Show | 86 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(83): Show |
intron_variant | MODIFIER | c.-90+13135G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149331150 | ||||||
| chr6:149331222
|
C | A | 1 | a0001c0001t0008g0021 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-90+13207C>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149331222 | ||||||
| chr6:149331370
|
A | G | 6 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0070others(3): Show | 6 | HG01884.hp2 HG02257.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.-90+13355A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149331370 | ||||||
| chr6:149331469
|
G | A | 3 | a0001c0001t0013g0177a0001c0001t0013g0178a0001c0001t0022g0176 | 3 | HG02109.hp1 HG02615.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-90+13454G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149331469 | ||||||
| chr6:149331599
|
C | T | 1 | a0001c0001t0003g0171 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-90+13584C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149331599 | ||||||
| chr6:149331730
|
T | A | 1 | a0001c0001t0004g0030 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.-90+13715T>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149331730 | ||||||
| chr6:149331749
|
A | G | 5 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0013g0177others(2): Show | 5 | HG02109.hp1 HG02615.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.-90+13734A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149331749 | ||||||
| chr6:149331854
|
G | A | 2 | a0001c0002t0012g0193a0001c0002t0012g0194 | 2 | NA18947.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.-90+13839G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149331854 | ||||||
| chr6:149332153
|
A | C | 9 | a0001c0001t0005g0117a0001c0001t0005g0118a0001c0001t0005g0179others(6): Show | 9 | HG01243.hp2 HG02602.hp2 HG02683.hp1 others(6): Show |
intron_variant | MODIFIER | c.-90+14138A>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149332153 | ||||||
| chr6:149332288
|
G | A | 5 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0131others(2): Show | 5 | NA18943.hp1 NA18956.hp1 NA18968.hp2 others(2): Show |
intron_variant | MODIFIER | c.-90+14273G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149332288 | ||||||
| chr6:149332379
|
A | G | 1 | a0001c0001t0008g0021 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-90+14364A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149332379 | ||||||
| chr6:149332448
|
T | C | 1 | a0001c0001t0003g0320 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.-90+14433T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149332448 | ||||||
| chr6:149332449
|
A | G | 1 | a0001c0001t0001g0153 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.-90+14434A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149332449 | ||||||
| chr6:149332615
|
G | T | 1 | a0001c0001t0008g0021 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-90+14600G>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149332615 | ||||||
| chr6:149332656
|
G | A | 87 | a0001c0002t0002g0096a0001c0002t0002g0097a0001c0002t0002g0098others(84): Show | 87 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.-90+14641G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149332656 | ||||||
| chr6:149332662
|
G | C | 4 | a0001c0001t0013g0177a0001c0001t0013g0178a0001c0001t0017g0022others(1): Show | 4 | HG02109.hp1 HG02615.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.-90+14647G>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149332662 | ||||||
| chr6:149332667
|
A | C | 1 | a0001c0001t0001g0295 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.-90+14652A>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149332667 | ||||||
| chr6:149332692
|
C | T | 297 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(294): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.-90+14677C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149332692 | ||||||
| chr6:149332694
|
G | A | 1 | a0001c0002t0002g0195 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-90+14679G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149332694 | ||||||
| chr6:149332749
|
A | C | 1 | a0001c0001t0001g0294 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-90+14734A>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149332749 | ||||||
| chr6:149332898
|
T | C | 8 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(5): Show | 8 | HG02895.hp1 HG02895.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.-90+14883T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149332898 | ||||||
| chr6:149332899
|
A | G | 1 | a0001c0001t0001g0073 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-90+14884A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149332899 | ||||||
| chr6:149332984
|
G | A | 63 | a0001c0001t0003g0005a0001c0001t0003g0167a0001c0001t0003g0168others(60): Show | 63 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.-90+14969G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149332984 | ||||||
| chr6:149333074
|
C | T | 3 | a0001c0001t0010g0156a0001c0001t0010g0157a0001c0001t0010g0158 | 3 | NA19002.hp2 NA19088.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.-90+15059C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149333074 | ||||||
| chr6:149333094
|
G | A | 3 | a0001c0001t0013g0177a0001c0001t0013g0178a0001c0001t0022g0176 | 3 | HG02109.hp1 HG02615.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-90+15079G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149333094 | ||||||
| chr6:149333276
|
A | G | 1 | a0001c0001t0013g0178 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-90+15261A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149333276 | ||||||
| chr6:149333493
|
T | C | 1 | a0001c0001t0001g0129 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-90+15478T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149333493 | ||||||
| chr6:149333708
|
A | AGT | 103 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0064others(100): Show | 103 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(100): Show |
intron_variant | MODIFIER | c.-90+15730_-90+1573 others(6): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149333708 | |||||
| chr6:149333708
|
A | AGTGT | 36 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0258others(33): Show | 36 | HG00099.hp2 HG00558.hp1 HG00738.hp2 others(33): Show |
intron_variant | MODIFIER | c.-90+15728_-90+1573 others(8): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149333708 | |||||
| chr6:149333708
|
A | AGTGTGT | 10 | a0001c0001t0001g0292a0001c0001t0003g0347a0001c0001t0003g0348others(7): Show | 10 | HG00621.hp1 HG00621.hp2 HG00733.hp1 others(7): Show |
intron_variant | MODIFIER | c.-90+15726_-90+1573 others(10): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149333708 | |||||
| chr6:149333708
|
A | AGTGTGTG others(3): Show |
1 | a0001c0001t0003g0171 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-90+15722_-90+1573 others(14): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149333708 | |||||
| chr6:149333708
|
AGT | A | 29 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(26): Show | 29 | HG00609.hp2 HG00642.hp1 HG00642.hp2 others(26): Show |
intron_variant | MODIFIER | c.-90+15730_-90+1573 others(6): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149333708 | |||||
| chr6:149333708
|
AGTGT | A | 29 | a0001c0001t0001g0073a0001c0001t0001g0143a0001c0001t0001g0144others(26): Show | 29 | HG00099.hp1 HG01081.hp1 HG01109.hp2 others(26): Show |
intron_variant | MODIFIER | c.-90+15728_-90+1573 others(8): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149333708 | |||||
| chr6:149333708
|
AGTGTGT | A | 11 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(8): Show | 11 | HG00733.hp2 HG01884.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.-90+15726_-90+1573 others(10): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149333708 | |||||
| chr6:149333708
|
AGTGTGTG others(1): Show |
A | 3 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0001g0263 | 3 | HG02523.hp2 NA19070.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.-90+15724_-90+1573 others(12): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149333708 | |||||
| chr6:149333708
|
AGTGTGTG others(3): Show |
A | 11 | a0001c0001t0001g0002a0001c0001t0001g0086a0001c0001t0001g0087others(8): Show | 12 | HG01243.hp1 HG01891.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.-90+15722_-90+1573 others(14): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149333708 | |||||
| chr6:149333741
|
G | GTGTGTGT others(13): Show |
2 | a0001c0002t0002g0111a0001c0002t0002g0112 | 2 | HG02155.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.-90+15731_-90+1573 others(24): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149333741 | |||||
| chr6:149333749
|
A | G | 6 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0070others(3): Show | 6 | HG01884.hp2 HG02257.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.-90+15734A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149333749 | ||||||
| chr6:149333812
|
A | G | 87 | a0001c0002t0002g0096a0001c0002t0002g0097a0001c0002t0002g0098others(84): Show | 87 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.-90+15797A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149333812 | ||||||
| chr6:149334072
|
T | G | 1 | a0001c0001t0005g0179 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-90+16057T>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149334072 | ||||||
| chr6:149334125
|
G | A | 18 | a0001c0001t0003g0167a0001c0001t0003g0168a0001c0001t0003g0169others(15): Show | 18 | HG00609.hp2 HG01109.hp1 HG01167.hp2 others(15): Show |
intron_variant | MODIFIER | c.-90+16110G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149334125 | ||||||
| chr6:149334210
|
A | C | 1 | a0001c0001t0001g0094 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-90+16195A>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149334210 | ||||||
| chr6:149334300
|
A | G | 1 | a0001c0001t0017g0022 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-90+16285A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149334300 | ||||||
| chr6:149334337
|
C | T | 297 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(294): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.-90+16322C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149334337 | ||||||
| chr6:149334387
|
T | C | 63 | a0001c0001t0003g0005a0001c0001t0003g0167a0001c0001t0003g0168others(60): Show | 63 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.-90+16372T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149334387 | ||||||
| chr6:149334422
|
G | A | 1 | a0001c0001t0001g0087 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-90+16407G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149334422 | ||||||
| chr6:149334462
|
T | C | 87 | a0001c0002t0002g0096a0001c0002t0002g0097a0001c0002t0002g0098others(84): Show | 87 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.-90+16447T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149334462 | ||||||
| chr6:149334477
|
G | C | 9 | a0001c0001t0005g0117a0001c0001t0005g0118a0001c0001t0005g0179others(6): Show | 9 | HG01243.hp2 HG02602.hp2 HG02683.hp1 others(6): Show |
intron_variant | MODIFIER | c.-90+16462G>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149334477 | ||||||
| chr6:149334585
|
GAGGATCA others(16): Show |
G | 1 | a0001c0002t0002g0237 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.-90+16571_-90+1659 others(27): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149334585 | ||||||
| chr6:149334612
|
G | C | 18 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0070others(15): Show | 18 | HG01884.hp2 HG02055.hp1 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.-90+16597G>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149334612 | ||||||
| chr6:149334622
|
CTA | C | 3 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012 | 3 | HG02818.hp2 HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-90+16609_-90+1661 others(6): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149334622 | |||||
| chr6:149334676
|
TA | T | 6 | a0001c0001t0001g0256a0001c0001t0001g0287a0001c0001t0001g0288others(3): Show | 6 | HG01069.hp1 HG01070.hp2 HG01517.hp2 others(3): Show |
intron_variant | MODIFIER | c.-90+16675delA | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149334676 | |||||
| chr6:149334776
|
A | G | 87 | a0001c0002t0002g0096a0001c0002t0002g0097a0001c0002t0002g0098others(84): Show | 87 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.-90+16761A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149334776 | ||||||
| chr6:149334824
|
G | A | 1 | a0001c0001t0013g0178 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-90+16809G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149334824 | ||||||
| chr6:149334914
|
A | G | 87 | a0001c0002t0002g0096a0001c0002t0002g0097a0001c0002t0002g0098others(84): Show | 87 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.-90+16899A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149334914 | ||||||
| chr6:149335473
|
A | ACCTCCCA others(6): Show |
1 | a0001c0001t0003g0352 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.-90+17466_-90+1747 others(17): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149335473 | |||||
| chr6:149335555
|
G | T | 3 | a0001c0001t0013g0177a0001c0001t0013g0178a0001c0001t0022g0176 | 3 | HG02109.hp1 HG02615.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-90+17540G>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149335555 | ||||||
| chr6:149335558
|
G | A | 1 | a0001c0001t0001g0266 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-90+17543G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149335558 | ||||||
| chr6:149335950
|
A | G | 63 | a0001c0001t0003g0005a0001c0001t0003g0167a0001c0001t0003g0168others(60): Show | 63 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.-90+17935A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149335950 | ||||||
| chr6:149336077
|
C | T | 63 | a0001c0001t0003g0005a0001c0001t0003g0167a0001c0001t0003g0168others(60): Show | 63 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.-90+18062C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149336077 | ||||||
| chr6:149336079
|
G | A | 18 | a0001c0001t0001g0002a0001c0001t0001g0086a0001c0001t0001g0087others(15): Show | 19 | HG01081.hp1 HG01109.hp2 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.-90+18064G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149336079 | ||||||
| chr6:149336091
|
G | A | 153 | a0001c0001t0003g0005a0001c0001t0003g0167a0001c0001t0003g0168others(150): Show | 153 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(150): Show |
intron_variant | MODIFIER | c.-90+18076G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149336091 | ||||||
| chr6:149336142
|
G | C | 1 | a0001c0001t0004g0031 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-90+18127G>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149336142 | ||||||
| chr6:149336288
|
T | C | 1 | a0001c0001t0004g0028 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-90+18273T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149336288 | ||||||
| chr6:149336291
|
A | G | 1 | a0001c0001t0003g0304 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-90+18276A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149336291 | ||||||
| chr6:149336293
|
G | C | 1 | a0001c0001t0016g0084 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-90+18278G>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149336293 | ||||||
| chr6:149336635
|
G | A | 2 | a0001c0002t0002g0201a0001c0002t0002g0248 | 2 | NA18953.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.-90+18620G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149336635 | ||||||
| chr6:149336922
|
T | TA | 61 | a0001c0001t0003g0005a0001c0001t0003g0167a0001c0001t0003g0168others(58): Show | 61 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(58): Show |
intron_variant | MODIFIER | c.-90+18919dupA | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149336922 | |||||
| chr6:149336922
|
TA | T | 232 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(229): Show | 234 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(231): Show |
intron_variant | MODIFIER | c.-90+18919delA | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149336922 | |||||
| chr6:149336965
|
A | T | 116 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(113): Show | 118 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.-90+18950A>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149336965 | ||||||
| chr6:149336982
|
A | C | 298 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(295): Show | 300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.-90+18967A>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149336982 | ||||||
| chr6:149337223
|
CTG | C | 90 | a0001c0001t0013g0177a0001c0001t0013g0178a0001c0001t0022g0176others(87): Show | 90 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(87): Show |
intron_variant | MODIFIER | c.-90+19210_-90+1921 others(6): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149337223 | |||||
| chr6:149337256
|
A | ATATTT | 297 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(294): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.-90+19245_-90+1924 others(9): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149337256 | |||||
| chr6:149337290
|
C | CAATT | 310 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(307): Show | 312 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(309): Show |
intron_variant | MODIFIER | c.-90+19277_-90+1927 others(8): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149337290 | |||||
| chr6:149337658
|
C | T | 297 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(294): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.-90+19643C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149337658 | ||||||
| chr6:149337673
|
C | T | 1 | a0001c0002t0002g0250 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-90+19658C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149337673 | ||||||
| chr6:149337699
|
T | G | 2 | a0001c0001t0003g0315a0001c0001t0003g0316 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.-90+19684T>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149337699 | ||||||
| chr6:149337842
|
T | G | 153 | a0001c0001t0003g0005a0001c0001t0003g0167a0001c0001t0003g0168others(150): Show | 153 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(150): Show |
intron_variant | MODIFIER | c.-90+19827T>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149337842 | ||||||
| chr6:149338020
|
T | A | 3 | a0001c0001t0003g0320a0001c0001t0003g0322a0001c0001t0003g0323 | 3 | HG01175.hp2 HG03491.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.-90+20005T>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149338020 | ||||||
| chr6:149338050
|
C | T | 1 | a0001c0001t0001g0291 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.-90+20035C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149338050 | ||||||
| chr6:149338060
|
A | G | 1 | a0001c0001t0004g0066 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-90+20045A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149338060 | ||||||
| chr6:149338123
|
C | T | 1 | a0001c0001t0001g0286 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.-90+20108C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149338123 | ||||||
| chr6:149338451
|
G | C | 2 | a0001c0001t0001g0269a0001c0001t0001g0303 | 2 | HG00673.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.-90+20436G>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149338451 | ||||||
| chr6:149338467
|
G | T | 6 | a0001c0001t0007g0074a0001c0001t0007g0075a0001c0001t0007g0076others(3): Show | 6 | HG02630.hp2 HG03225.hp1 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.-90+20452G>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149338467 | ||||||
| chr6:149338512
|
T | C | 87 | a0001c0002t0002g0096a0001c0002t0002g0097a0001c0002t0002g0098others(84): Show | 87 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.-90+20497T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149338512 | ||||||
| chr6:149338559
|
T | TTAAGTTT others(5): Show |
1 | a0001c0002t0002g0237 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.-90+20550_-90+2056 others(16): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149338559 | |||||
| chr6:149338563
|
G | T | 18 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0070others(15): Show | 18 | HG01884.hp2 HG02055.hp1 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.-90+20548G>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149338563 | ||||||
| chr6:149338873
|
T | C | 2 | a0001c0001t0004g0028a0001c0001t0004g0029 | 2 | HG03041.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.-90+20858T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149338873 | ||||||
| chr6:149338889
|
A | T | 2 | a0001c0001t0003g0336a0001c0001t0003g0350 | 2 | HG02683.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.-90+20874A>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149338889 | ||||||
| chr6:149338973
|
C | T | 63 | a0001c0001t0003g0005a0001c0001t0003g0167a0001c0001t0003g0168others(60): Show | 63 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.-90+20958C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149338973 | ||||||
| chr6:149339039
|
G | A | 8 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(5): Show | 8 | HG02895.hp1 HG02895.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.-90+21024G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149339039 | ||||||
| chr6:149339132
|
G | A | 88 | a0001c0001t0008g0021a0001c0002t0002g0096a0001c0002t0002g0097others(85): Show | 88 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(85): Show |
intron_variant | MODIFIER | c.-90+21117G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149339132 | ||||||
| chr6:149339233
|
C | T | 1 | a0001c0001t0001g0093 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-90+21218C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149339233 | ||||||
| chr6:149339272
|
A | G | 8 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(5): Show | 8 | HG02895.hp1 HG02895.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.-90+21257A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149339272 | ||||||
| chr6:149339301
|
G | A | 63 | a0001c0001t0003g0005a0001c0001t0003g0167a0001c0001t0003g0168others(60): Show | 63 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.-90+21286G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149339301 | ||||||
| chr6:149339312
|
T | A | 1 | a0001c0001t0001g0006 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-90+21297T>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149339312 | ||||||
| chr6:149339362
|
C | T | 87 | a0001c0002t0002g0096a0001c0002t0002g0097a0001c0002t0002g0098others(84): Show | 87 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.-90+21347C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149339362 | ||||||
| chr6:149339367
|
C | CA | 8 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0070others(5): Show | 8 | HG01256.hp1 HG01258.hp1 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.-90+21360dupA | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149339367 | |||||
| chr6:149339376
|
T | G | 2 | a0001c0001t0001g0362a0001c0001t0001g0363 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.-90+21361T>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149339376 | ||||||
| chr6:149339385
|
GA | G | 87 | a0001c0002t0002g0096a0001c0002t0002g0097a0001c0002t0002g0098others(84): Show | 87 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.-90+21378delA | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149339385 | |||||
| chr6:149339512
|
A | G | 3 | a0001c0001t0001g0141a0001c0001t0001g0285a0001c0001t0001g0288 | 3 | HG01516.hp1 HG01517.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.-90+21497A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149339512 | ||||||
| chr6:149339585
|
TTTTATTT others(5): Show |
T | 106 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(103): Show | 108 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.-90+21582_-90+2159 others(16): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149339585 | |||||
| chr6:149339589
|
A | AT | 12 | a0001c0001t0001g0068a0001c0001t0007g0074a0001c0001t0007g0075others(9): Show | 12 | HG01884.hp2 HG02055.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.-90+21577dupT | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149339589 | |||||
| chr6:149339590
|
T | TTTTA | 5 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0072others(2): Show | 5 | HG02257.hp1 HG02886.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.-90+21577_-90+2157 others(8): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149339590 | |||||
| chr6:149339590
|
TTTA | T | 63 | a0001c0001t0003g0005a0001c0001t0003g0167a0001c0001t0003g0168others(60): Show | 63 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.-90+21578_-90+2158 others(7): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149339590 | |||||
| chr6:149339590
|
TTTATTTA others(4): Show |
T | 6 | a0001c0001t0001g0160a0001c0001t0001g0294a0001c0001t0008g0164others(3): Show | 6 | HG01081.hp2 HG02280.hp1 HG04184.hp2 others(3): Show |
intron_variant | MODIFIER | c.-90+21578_-90+2158 others(15): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149339590 | |||||
| chr6:149339591
|
TTATTTAT others(3): Show |
T | 7 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(4): Show | 7 | HG01081.hp1 HG01884.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.-90+21578_-90+2158 others(14): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149339591 | |||||
| chr6:149339592
|
TA | T | 87 | a0001c0002t0002g0096a0001c0002t0002g0097a0001c0002t0002g0098others(84): Show | 87 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.-90+21578delA | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149339592 | ||||||
| chr6:149339592
|
TATTTATT others(6): Show |
T | 2 | a0001c0001t0001g0147a0001c0001t0001g0270 | 2 | NA18952.hp2 NA19059.hp2 |
intron_variant | MODIFIER | c.-90+21578_-90+2159 others(17): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149339592 | ||||||
| chr6:149339593
|
A | T | 6 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0072others(3): Show | 6 | HG02257.hp1 HG02886.hp2 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.-90+21578A>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149339593 | ||||||
| chr6:149339597
|
A | T | 81 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0070others(78): Show | 81 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(78): Show |
intron_variant | MODIFIER | c.-90+21582A>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149339597 | ||||||
| chr6:149339597
|
ATTTATTT others(4): Show |
A | 1 | a0001c0001t0005g0253 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-90+21586_-90+2159 others(15): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149339597 | |||||
| chr6:149339597
|
ATTTATTT others(5): Show |
A | 7 | a0001c0001t0005g0117a0001c0001t0005g0179a0001c0001t0005g0180others(4): Show | 7 | HG02602.hp2 HG02683.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.-90+21586_-90+2159 others(16): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149339597 | |||||
| chr6:149339601
|
A | T | 17 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0070others(14): Show | 17 | HG01884.hp2 HG02055.hp1 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.-90+21586A>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149339601 | ||||||
| chr6:149339603
|
TTA | T | 17 | a0001c0001t0003g0167a0001c0001t0003g0168a0001c0001t0003g0169others(14): Show | 17 | HG00609.hp2 HG01109.hp1 HG01167.hp2 others(14): Show |
intron_variant | MODIFIER | c.-90+21590_-90+2159 others(6): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149339603 | |||||
| chr6:149339604
|
T | TTTTA | 11 | a0001c0001t0007g0074a0001c0001t0007g0075a0001c0001t0007g0076others(8): Show | 11 | HG02055.hp1 HG02145.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.-90+21589_-90+2159 others(8): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149339604 | ||||||
| chr6:149339604
|
TA | T | 44 | a0001c0001t0003g0005a0001c0001t0003g0171a0001c0001t0003g0172others(41): Show | 44 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(41): Show |
intron_variant | MODIFIER | c.-90+21590delA | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149339604 | ||||||
| chr6:149339605
|
A | AT | 9 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(6): Show | 9 | HG02895.hp1 HG02895.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.-90+21605dupT | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149339605 | |||||
| chr6:149339605
|
A | T | 130 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(127): Show | 132 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(129): Show |
intron_variant | MODIFIER | c.-90+21590A>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149339605 | ||||||
| chr6:149339605
|
ATT | A | 91 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(88): Show | 91 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(88): Show |
intron_variant | MODIFIER | c.-90+21604_-90+2160 others(6): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149339605 | |||||
| chr6:149339609
|
T | A | 1 | a0001c0001t0001g0254 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.-90+21594T>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149339609 | ||||||
| chr6:149339788
|
G | A | 18 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0070others(15): Show | 18 | HG01884.hp2 HG02055.hp1 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.-90+21773G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149339788 | ||||||
| chr6:149339844
|
C | A | 1 | a0001c0002t0002g0107 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.-90+21829C>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149339844 | ||||||
| chr6:149339974
|
T | C | 3 | a0001c0001t0013g0177a0001c0001t0013g0178a0001c0001t0022g0176 | 3 | HG02109.hp1 HG02615.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-90+21959T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149339974 | ||||||
| chr6:149339977
|
TAATG | T | 9 | a0001c0001t0005g0117a0001c0001t0005g0118a0001c0001t0005g0179others(6): Show | 9 | HG01243.hp2 HG02602.hp2 HG02683.hp1 others(6): Show |
intron_variant | MODIFIER | c.-90+21963_-90+2196 others(8): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149339977 | ||||||
| chr6:149340017
|
C | T | 18 | a0001c0001t0001g0002a0001c0001t0001g0086a0001c0001t0001g0087others(15): Show | 19 | HG01081.hp1 HG01109.hp2 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.-90+22002C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149340017 | ||||||
| chr6:149340049
|
C | G | 3 | a0001c0001t0010g0156a0001c0001t0010g0157a0001c0001t0010g0158 | 3 | NA19002.hp2 NA19088.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.-90+22034C>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149340049 | ||||||
| chr6:149340089
|
C | G | 1 | a0001c0001t0003g0171 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-90+22074C>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149340089 | ||||||
| chr6:149340102
|
A | G | 63 | a0001c0001t0003g0005a0001c0001t0003g0167a0001c0001t0003g0168others(60): Show | 63 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.-90+22087A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149340102 | ||||||
| chr6:149340190
|
G | A | 6 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(3): Show | 6 | HG01081.hp1 HG01884.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.-90+22175G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149340190 | ||||||
| chr6:149340667
|
C | G | 2 | a0001c0001t0013g0177a0001c0001t0013g0178 | 2 | HG02109.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.-90+22652C>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149340667 | ||||||
| chr6:149340693
|
A | G | 3 | a0001c0001t0013g0177a0001c0001t0013g0178a0001c0001t0022g0176 | 3 | HG02109.hp1 HG02615.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-90+22678A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149340693 | ||||||
| chr6:149340868
|
A | T | 18 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0070others(15): Show | 18 | HG01884.hp2 HG02055.hp1 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.-90+22853A>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149340868 | ||||||
| chr6:149341021
|
T | C | 1 | a0001c0002t0002g0202 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.-90+23006T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149341021 | ||||||
| chr6:149341278
|
A | G | 1 | a0001c0001t0004g0031 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-90+23263A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149341278 | ||||||
| chr6:149341354
|
C | T | 1 | a0001c0001t0017g0022 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-90+23339C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149341354 | ||||||
| chr6:149341813
|
A | G | 87 | a0001c0002t0002g0096a0001c0002t0002g0097a0001c0002t0002g0098others(84): Show | 87 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.-90+23798A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149341813 | ||||||
| chr6:149341855
|
G | C | 126 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(123): Show | 128 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(125): Show |
intron_variant | MODIFIER | c.-90+23840G>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149341855 | ||||||
| chr6:149341977
|
A | G | 2 | a0001c0001t0003g0347a0001c0001t0003g0348 | 2 | HG02300.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-90+23962A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149341977 | ||||||
| chr6:149342044
|
A | AT | 149 | a0001c0001t0003g0005a0001c0001t0003g0167a0001c0001t0003g0168others(146): Show | 149 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(146): Show |
intron_variant | MODIFIER | c.-90+24031dupT | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149342044 | |||||
| chr6:149342046
|
TA | T | 115 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(112): Show | 117 | HG00140.hp1 HG00423.hp2 HG00558.hp2 others(114): Show |
intron_variant | MODIFIER | c.-90+24044delA | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149342046 | |||||
| chr6:149342047
|
A | T | 4 | a0001c0002t0002g0111a0001c0002t0002g0112a0001c0002t0002g0236others(1): Show | 4 | HG02155.hp2 NA18975.hp2 NA18989.hp2 others(1): Show |
intron_variant | MODIFIER | c.-90+24032A>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149342047 | ||||||
| chr6:149342240
|
G | T | 324 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(321): Show | 326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
intron_variant | MODIFIER | c.-90+24225G>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149342240 | ||||||
| chr6:149342826
|
A | G | 1 | a0001c0002t0002g0243 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-90+24811A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149342826 | ||||||
| chr6:149342995
|
A | G | 3 | a0001c0001t0001g0261a0001c0003t0001g0259a0001c0003t0001g0260 | 3 | HG00642.hp1 HG01261.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.-90+24980A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149342995 | ||||||
| chr6:149343097
|
C | T | 17 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0070others(14): Show | 17 | HG01884.hp2 HG02055.hp1 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.-90+25082C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149343097 | ||||||
| chr6:149343276
|
T | C | 1 | a0001c0001t0001g0009 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.-90+25261T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149343276 | ||||||
| chr6:149343289
|
C | T | 1 | a0001c0001t0001g0361 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-90+25274C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149343289 | ||||||
| chr6:149343314
|
CA | C | 63 | a0001c0001t0003g0005a0001c0001t0003g0167a0001c0001t0003g0168others(60): Show | 63 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.-90+25306delA | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149343314 | |||||
| chr6:149343404
|
G | A | 125 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(122): Show | 127 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(124): Show |
intron_variant | MODIFIER | c.-90+25389G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149343404 | ||||||
| chr6:149343471
|
C | CA | 7 | a0001c0001t0001g0006a0001c0001t0003g0308a0001c0001t0004g0060others(4): Show | 7 | HG02109.hp1 HG02135.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.-90+25471dupA | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149343471 | |||||
| chr6:149343471
|
CA | C | 8 | a0001c0001t0001g0152a0001c0001t0003g0319a0001c0001t0009g0079others(5): Show | 8 | HG00140.hp2 HG01070.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.-90+25471delA | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149343471 | |||||
| chr6:149343532
|
G | A | 1 | a0001c0001t0001g0148 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.-90+25517G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149343532 | ||||||
| chr6:149343693
|
A | G | 297 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(294): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.-90+25678A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149343693 | ||||||
| chr6:149343745
|
G | C | 17 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0070others(14): Show | 17 | HG01884.hp2 HG02055.hp1 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.-90+25730G>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149343745 | ||||||
| chr6:149344274
|
T | C | 1 | a0001c0002t0002g0099 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.-89-25635T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149344274 | ||||||
| chr6:149344716
|
C | T | 63 | a0001c0001t0003g0005a0001c0001t0003g0167a0001c0001t0003g0168others(60): Show | 63 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.-89-25193C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149344716 | ||||||
| chr6:149344801
|
C | T | 150 | a0001c0001t0003g0005a0001c0001t0003g0167a0001c0001t0003g0168others(147): Show | 150 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(147): Show |
intron_variant | MODIFIER | c.-89-25108C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149344801 | ||||||
| chr6:149344837
|
A | G | 1 | a0001c0001t0001g0142 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-89-25072A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149344837 | ||||||
| chr6:149345285
|
A | G | 4 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(1): Show | 4 | HG01081.hp1 HG01884.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.-89-24624A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149345285 | ||||||
| chr6:149345327
|
A | G | 1 | a0001c0001t0003g0336 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.-89-24582A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149345327 | ||||||
| chr6:149345332
|
G | A | 3 | a0001c0001t0013g0177a0001c0001t0013g0178a0001c0001t0022g0176 | 3 | HG02109.hp1 HG02615.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-89-24577G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149345332 | ||||||
| chr6:149345346
|
G | C | 2 | a0001c0001t0003g0174a0001c0001t0003g0351 | 2 | HG01256.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.-89-24563G>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149345346 | ||||||
| chr6:149345484
|
T | A | 63 | a0001c0001t0003g0005a0001c0001t0003g0167a0001c0001t0003g0168others(60): Show | 63 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.-89-24425T>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149345484 | ||||||
| chr6:149345507
|
T | A | 1 | a0001c0002t0002g0196 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.-89-24402T>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149345507 | ||||||
| chr6:149345508
|
A | G | 305 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(302): Show | 307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.-89-24401A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149345508 | ||||||
| chr6:149345551
|
AAT | A | 87 | a0001c0002t0002g0096a0001c0002t0002g0097a0001c0002t0002g0098others(84): Show | 87 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.-89-24355_-89-2435 others(6): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149345551 | |||||
| chr6:149345841
|
G | A | 168 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0070others(165): Show | 168 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(165): Show |
intron_variant | MODIFIER | c.-89-24068G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149345841 | ||||||
| chr6:149345845
|
A | G | 2 | a0001c0001t0003g0170a0001c0001t0003g0314 | 2 | HG01109.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.-89-24064A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149345845 | ||||||
| chr6:149345899
|
T | G | 1 | a0001c0002t0002g0192 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.-89-24010T>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149345899 | ||||||
| chr6:149345993
|
A | T | 63 | a0001c0001t0003g0005a0001c0001t0003g0167a0001c0001t0003g0168others(60): Show | 63 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.-89-23916A>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149345993 | ||||||
| chr6:149346112
|
A | G | 63 | a0001c0001t0003g0005a0001c0001t0003g0167a0001c0001t0003g0168others(60): Show | 63 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.-89-23797A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149346112 | ||||||
| chr6:149346124
|
A | C | 87 | a0001c0002t0002g0096a0001c0002t0002g0097a0001c0002t0002g0098others(84): Show | 87 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.-89-23785A>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149346124 | ||||||
| chr6:149346253
|
C | T | 2 | a0001c0001t0013g0177a0001c0001t0013g0178 | 2 | HG02109.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.-89-23656C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149346253 | ||||||
| chr6:149346257
|
C | CACGCATG others(27): Show |
1 | a0001c0001t0001g0147 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.-89-23651_-89-2361 others(38): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149346257 | |||||
| chr6:149346260
|
G | A | 1 | a0001c0002t0006g0238 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.-89-23649G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149346260 | ||||||
| chr6:149346323
|
G | A | 1 | a0001c0001t0001g0147 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.-89-23586G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149346323 | ||||||
| chr6:149346374
|
A | G | 2 | a0001c0001t0004g0052a0001c0001t0004g0053 | 2 | NA18957.hp2 NA19072.hp1 |
intron_variant | MODIFIER | c.-89-23535A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149346374 | ||||||
| chr6:149346426
|
G | A | 3 | a0001c0001t0001g0271a0001c0001t0001g0272a0001c0001t0001g0291 | 3 | NA18990.hp1 NA19005.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.-89-23483G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149346426 | ||||||
| chr6:149346448
|
C | CT | 127 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(124): Show | 129 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(126): Show |
intron_variant | MODIFIER | c.-89-23439dupT | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149346448 | |||||
| chr6:149346448
|
C | CTT | 8 | a0001c0001t0001g0155a0001c0001t0001g0161a0001c0001t0001g0162others(5): Show | 8 | HG02280.hp1 HG02622.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.-89-23440_-89-2343 others(6): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149346448 | |||||
| chr6:149346448
|
CT | C | 48 | a0001c0001t0003g0172a0001c0001t0003g0173a0001c0001t0003g0305others(45): Show | 48 | HG00140.hp2 HG01099.hp2 HG01168.hp2 others(45): Show |
intron_variant | MODIFIER | c.-89-23439delT | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149346448 | |||||
| chr6:149346448
|
CTT | C | 100 | a0001c0001t0003g0167a0001c0001t0003g0168a0001c0001t0003g0169others(97): Show | 100 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(97): Show |
intron_variant | MODIFIER | c.-89-23440_-89-2343 others(6): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149346448 | |||||
| chr6:149346448
|
CTTT | C | 15 | a0001c0001t0003g0005a0001c0001t0003g0171a0001c0001t0003g0174others(12): Show | 15 | HG00099.hp2 HG00639.hp1 HG00738.hp2 others(12): Show |
intron_variant | MODIFIER | c.-89-23441_-89-2343 others(7): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149346448 | |||||
| chr6:149346457
|
T | G | 9 | a0001c0001t0005g0117a0001c0001t0005g0118a0001c0001t0005g0179others(6): Show | 9 | HG01243.hp2 HG02602.hp2 HG02683.hp1 others(6): Show |
intron_variant | MODIFIER | c.-89-23452T>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149346457 | ||||||
| chr6:149346540
|
G | A | 63 | a0001c0001t0003g0005a0001c0001t0003g0167a0001c0001t0003g0168others(60): Show | 63 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.-89-23369G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149346540 | ||||||
| chr6:149346667
|
T | C | 1 | a0001c0001t0001g0068 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-89-23242T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149346667 | ||||||
| chr6:149346777
|
C | T | 4 | a0001c0001t0013g0177a0001c0001t0013g0178a0001c0001t0017g0022others(1): Show | 4 | HG02109.hp1 HG02615.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.-89-23132C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149346777 | ||||||
| chr6:149346833
|
C | T | 1 | a0001c0002t0002g0196 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.-89-23076C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149346833 | ||||||
| chr6:149347002
|
C | G | 17 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0070others(14): Show | 17 | HG01884.hp2 HG02055.hp1 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.-89-22907C>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149347002 | ||||||
| chr6:149347048
|
T | A | 4 | a0001c0001t0004g0023a0001c0001t0004g0024a0001c0001t0004g0034others(1): Show | 4 | HG02258.hp1 HG02559.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.-89-22861T>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149347048 | ||||||
| chr6:149347076
|
T | C | 88 | a0001c0001t0004g0040a0001c0002t0002g0096a0001c0002t0002g0097others(85): Show | 88 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(85): Show |
intron_variant | MODIFIER | c.-89-22833T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149347076 | ||||||
| chr6:149347091
|
A | G | 6 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(3): Show | 6 | HG00733.hp2 HG02145.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.-89-22818A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149347091 | ||||||
| chr6:149347129
|
A | G | 1 | a0001c0001t0001g0092 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-89-22780A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149347129 | ||||||
| chr6:149347369
|
T | C | 1 | a0001c0001t0022g0176 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-89-22540T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149347369 | ||||||
| chr6:149347391
|
A | G | 87 | a0001c0002t0002g0096a0001c0002t0002g0097a0001c0002t0002g0098others(84): Show | 87 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.-89-22518A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149347391 | ||||||
| chr6:149347450
|
CAT | C | 9 | a0001c0001t0005g0117a0001c0001t0005g0118a0001c0001t0005g0179others(6): Show | 9 | HG01243.hp2 HG02602.hp2 HG02683.hp1 others(6): Show |
intron_variant | MODIFIER | c.-89-22457_-89-2245 others(6): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149347450 | |||||
| chr6:149347543
|
G | A | 1 | a0001c0002t0014g0110 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.-89-22366G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149347543 | ||||||
| chr6:149347851
|
T | A | 1 | a0001c0001t0001g0147 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.-89-22058T>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149347851 | ||||||
| chr6:149347899
|
T | C | 1 | a0001c0001t0001g0147 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.-89-22010T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149347899 | ||||||
| chr6:149347967
|
A | C | 1 | a0001c0001t0001g0284 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-89-21942A>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149347967 | ||||||
| chr6:149348046
|
A | T | 1 | a0001c0002t0002g0251 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.-89-21863A>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149348046 | ||||||
| chr6:149348056
|
G | T | 1 | a0001c0002t0002g0251 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.-89-21853G>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149348056 | ||||||
| chr6:149348058
|
T | C | 1 | a0001c0002t0002g0251 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.-89-21851T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149348058 | ||||||
| chr6:149348060
|
A | G | 1 | a0001c0002t0002g0251 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.-89-21849A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149348060 | ||||||
| chr6:149348062
|
G | A | 1 | a0001c0002t0002g0251 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.-89-21847G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149348062 | ||||||
| chr6:149348070
|
A | T | 1 | a0001c0002t0002g0251 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.-89-21839A>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149348070 | ||||||
| chr6:149348072
|
T | A | 1 | a0001c0002t0002g0251 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.-89-21837T>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149348072 | ||||||
| chr6:149348088
|
T | C | 2 | a0001c0001t0003g0317a0001c0001t0003g0319 | 2 | HG00140.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.-89-21821T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149348088 | ||||||
| chr6:149348137
|
T | A | 324 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(321): Show | 326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
intron_variant | MODIFIER | c.-89-21772T>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149348137 | ||||||
| chr6:149348218
|
G | T | 324 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(321): Show | 326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
intron_variant | MODIFIER | c.-89-21691G>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149348218 | ||||||
| chr6:149348265
|
G | A | 297 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(294): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.-89-21644G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149348265 | ||||||
| chr6:149348282
|
A | G | 1 | a0001c0002t0002g0234 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-89-21627A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149348282 | ||||||
| chr6:149348291
|
G | A | 311 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(308): Show | 313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
intron_variant | MODIFIER | c.-89-21618G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149348291 | ||||||
| chr6:149348407
|
A | G | 1 | a0001c0001t0001g0302 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-89-21502A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149348407 | ||||||
| chr6:149348443
|
A | C | 87 | a0001c0002t0002g0096a0001c0002t0002g0097a0001c0002t0002g0098others(84): Show | 87 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.-89-21466A>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149348443 | ||||||
| chr6:149348455
|
C | T | 1 | a0001c0001t0008g0021 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-89-21454C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149348455 | ||||||
| chr6:149348501
|
T | C | 297 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(294): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.-89-21408T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149348501 | ||||||
| chr6:149348614
|
G | GA | 97 | a0001c0001t0001g0160a0001c0001t0005g0117a0001c0001t0005g0118others(94): Show | 97 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(94): Show |
intron_variant | MODIFIER | c.-89-21285dupA | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149348614 | |||||
| chr6:149348715
|
G | A | 63 | a0001c0001t0003g0005a0001c0001t0003g0167a0001c0001t0003g0168others(60): Show | 63 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.-89-21194G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149348715 | ||||||
| chr6:149348818
|
T | G | 1 | a0001c0001t0017g0022 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-89-21091T>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149348818 | ||||||
| chr6:149348857
|
G | C | 297 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(294): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.-89-21052G>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149348857 | ||||||
| chr6:149348931
|
A | C | 297 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(294): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.-89-20978A>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149348931 | ||||||
| chr6:149348935
|
C | T | 18 | a0001c0001t0003g0167a0001c0001t0003g0168a0001c0001t0003g0169others(15): Show | 18 | HG00609.hp2 HG01109.hp1 HG01167.hp2 others(15): Show |
intron_variant | MODIFIER | c.-89-20974C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149348935 | ||||||
| chr6:149348975
|
T | TA | 4 | a0001c0001t0013g0177a0001c0001t0013g0178a0001c0001t0022g0176others(1): Show | 4 | HG02109.hp1 HG02615.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.-89-20934_-89-2093 others(5): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149348975 | ||||||
| chr6:149348976
|
T | A | 297 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(294): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.-89-20933T>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149348976 | ||||||
| chr6:149349042
|
A | G | 17 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0070others(14): Show | 17 | HG01884.hp2 HG02055.hp1 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.-89-20867A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149349042 | ||||||
| chr6:149349186
|
T | C | 297 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(294): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.-89-20723T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149349186 | ||||||
| chr6:149349248
|
G | A | 87 | a0001c0002t0002g0096a0001c0002t0002g0097a0001c0002t0002g0098others(84): Show | 87 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.-89-20661G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149349248 | ||||||
| chr6:149349378
|
C | G | 1 | a0001c0002t0002g0195 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-89-20531C>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149349378 | ||||||
| chr6:149349419
|
C | CA | 65 | a0001c0001t0001g0160a0001c0001t0001g0264a0001c0001t0001g0265others(62): Show | 65 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(62): Show |
intron_variant | MODIFIER | c.-89-20472dupA | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149349419 | |||||
| chr6:149349419
|
CA | C | 7 | a0001c0001t0001g0012a0001c0001t0001g0283a0001c0001t0004g0063others(4): Show | 7 | HG01243.hp2 HG03540.hp2 HG03704.hp2 others(4): Show |
intron_variant | MODIFIER | c.-89-20472delA | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149349419 | |||||
| chr6:149349572
|
C | T | 1 | a0001c0001t0004g0058 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.-89-20337C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149349572 | ||||||
| chr6:149349607
|
TA | T | 17 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0070others(14): Show | 17 | HG01884.hp2 HG02055.hp1 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.-89-20301delA | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149349607 | ||||||
| chr6:149349658
|
G | A | 17 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0070others(14): Show | 17 | HG01884.hp2 HG02055.hp1 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.-89-20251G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149349658 | ||||||
| chr6:149349696
|
T | G | 1 | a0001c0001t0001g0147 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.-89-20213T>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149349696 | ||||||
| chr6:149349742
|
C | T | 90 | a0001c0001t0013g0177a0001c0001t0013g0178a0001c0001t0022g0176others(87): Show | 90 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(87): Show |
intron_variant | MODIFIER | c.-89-20167C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149349742 | ||||||
| chr6:149349898
|
T | C | 1 | a0001c0001t0017g0022 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-89-20011T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149349898 | ||||||
| chr6:149349941
|
A | T | 63 | a0001c0001t0003g0005a0001c0001t0003g0167a0001c0001t0003g0168others(60): Show | 63 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.-89-19968A>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149349941 | ||||||
| chr6:149349980
|
A | G | 116 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(113): Show | 118 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.-89-19929A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149349980 | ||||||
| chr6:149350041
|
T | C | 153 | a0001c0001t0003g0005a0001c0001t0003g0167a0001c0001t0003g0168others(150): Show | 153 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(150): Show |
intron_variant | MODIFIER | c.-89-19868T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149350041 | ||||||
| chr6:149350057
|
G | A | 30 | a0001c0001t0003g0172a0001c0001t0003g0173a0001c0001t0003g0305others(27): Show | 30 | HG00140.hp2 HG01168.hp2 HG01175.hp2 others(27): Show |
intron_variant | MODIFIER | c.-89-19852G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149350057 | ||||||
| chr6:149350220
|
C | T | 1 | a0001c0002t0002g0204 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.-89-19689C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149350220 | ||||||
| chr6:149350224
|
G | A | 116 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(113): Show | 118 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.-89-19685G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149350224 | ||||||
| chr6:149350249
|
C | T | 63 | a0001c0001t0003g0005a0001c0001t0003g0167a0001c0001t0003g0168others(60): Show | 63 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.-89-19660C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149350249 | ||||||
| chr6:149350270
|
C | G | 63 | a0001c0001t0003g0005a0001c0001t0003g0167a0001c0001t0003g0168others(60): Show | 63 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.-89-19639C>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149350270 | ||||||
| chr6:149350319
|
G | A | 2 | a0001c0001t0001g0274a0001c0001t0001g0302 | 2 | HG01496.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.-89-19590G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149350319 | ||||||
| chr6:149350365
|
T | A | 3 | a0001c0001t0013g0177a0001c0001t0013g0178a0001c0001t0022g0176 | 3 | HG02109.hp1 HG02615.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-89-19544T>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149350365 | ||||||
| chr6:149350562
|
G | T | 171 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0070others(168): Show | 171 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(168): Show |
intron_variant | MODIFIER | c.-89-19347G>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149350562 | ||||||
| chr6:149350617
|
C | CT | 57 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(54): Show | 57 | HG00099.hp2 HG00609.hp2 HG00639.hp1 others(54): Show |
intron_variant | MODIFIER | c.-89-19268dupT | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149350617 | |||||
| chr6:149350617
|
C | CTT | 22 | a0001c0001t0001g0072a0001c0001t0003g0169a0001c0001t0003g0172others(19): Show | 22 | HG00140.hp2 HG01168.hp2 HG01175.hp1 others(19): Show |
intron_variant | MODIFIER | c.-89-19269_-89-1926 others(6): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149350617 | |||||
| chr6:149350617
|
CT | C | 95 | a0001c0001t0001g0087a0001c0001t0001g0255a0001c0001t0001g0283others(92): Show | 95 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(92): Show |
intron_variant | MODIFIER | c.-89-19268delT | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149350617 | |||||
| chr6:149350617
|
CTT | C | 114 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(111): Show | 116 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(113): Show |
intron_variant | MODIFIER | c.-89-19269_-89-1926 others(6): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149350617 | |||||
| chr6:149350617
|
CTTT | C | 8 | a0001c0001t0001g0086a0001c0001t0001g0130a0001c0001t0001g0147others(5): Show | 8 | HG01496.hp1 HG03098.hp1 HG03225.hp2 others(5): Show |
intron_variant | MODIFIER | c.-89-19270_-89-1926 others(7): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149350617 | |||||
| chr6:149350632
|
T | C | 1 | a0001c0002t0002g0203 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-89-19277T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149350632 | ||||||
| chr6:149350664
|
G | T | 1 | a0001c0001t0008g0021 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-89-19245G>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149350664 | ||||||
| chr6:149350685
|
G | A | 3 | a0001c0001t0001g0161a0001c0001t0001g0162a0001c0001t0001g0298 | 3 | HG02622.hp2 HG02976.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-89-19224G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149350685 | ||||||
| chr6:149350714
|
A | G | 8 | a0001c0001t0005g0117a0001c0001t0005g0118a0001c0001t0005g0179others(5): Show | 8 | HG01243.hp2 HG02602.hp2 HG02683.hp1 others(5): Show |
intron_variant | MODIFIER | c.-89-19195A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149350714 | ||||||
| chr6:149350762
|
G | A | 3 | a0001c0001t0013g0177a0001c0001t0013g0178a0001c0001t0022g0176 | 3 | HG02109.hp1 HG02615.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-89-19147G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149350762 | ||||||
| chr6:149350827
|
G | A | 9 | a0001c0001t0005g0117a0001c0001t0005g0118a0001c0001t0005g0179others(6): Show | 9 | HG01243.hp2 HG02602.hp2 HG02683.hp1 others(6): Show |
intron_variant | MODIFIER | c.-89-19082G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149350827 | ||||||
| chr6:149350888
|
T | C | 1 | a0001c0002t0002g0113 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.-89-19021T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149350888 | ||||||
| chr6:149350889
|
T | C | 1 | a0001c0001t0001g0013 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-89-19020T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149350889 | ||||||
| chr6:149350993
|
T | A | 6 | a0001c0001t0007g0074a0001c0001t0007g0075a0001c0001t0007g0076others(3): Show | 6 | HG02630.hp2 HG03225.hp1 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.-89-18916T>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149350993 | ||||||
| chr6:149351080
|
C | A | 1 | a0001c0001t0001g0068 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-89-18829C>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149351080 | ||||||
| chr6:149351130
|
GC | G | 87 | a0001c0002t0002g0096a0001c0002t0002g0097a0001c0002t0002g0098others(84): Show | 87 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.-89-18776delC | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149351130 | |||||
| chr6:149351187
|
A | G | 27 | a0001c0001t0001g0085a0001c0001t0001g0121a0001c0001t0001g0122others(24): Show | 27 | HG00597.hp1 HG00735.hp2 HG01070.hp1 others(24): Show |
intron_variant | MODIFIER | c.-89-18722A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149351187 | ||||||
| chr6:149351239
|
C | G | 126 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(123): Show | 128 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(125): Show |
intron_variant | MODIFIER | c.-89-18670C>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149351239 | ||||||
| chr6:149351261
|
C | T | 1 | a0001c0001t0017g0022 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-89-18648C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149351261 | ||||||
| chr6:149351262
|
G | A | 3 | a0001c0001t0013g0177a0001c0001t0013g0178a0001c0001t0022g0176 | 3 | HG02109.hp1 HG02615.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-89-18647G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149351262 | ||||||
| chr6:149351529
|
T | C | 87 | a0001c0002t0002g0096a0001c0002t0002g0097a0001c0002t0002g0098others(84): Show | 87 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.-89-18380T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149351529 | ||||||
| chr6:149351579
|
A | T | 9 | a0001c0001t0005g0117a0001c0001t0005g0118a0001c0001t0005g0179others(6): Show | 9 | HG01243.hp2 HG02602.hp2 HG02683.hp1 others(6): Show |
intron_variant | MODIFIER | c.-89-18330A>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149351579 | ||||||
| chr6:149351669
|
A | G | 297 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(294): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.-89-18240A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149351669 | ||||||
| chr6:149351705
|
A | AAAT | 3 | a0001c0001t0013g0177a0001c0001t0013g0178a0001c0001t0022g0176 | 3 | HG02109.hp1 HG02615.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-89-18202_-89-1820 others(7): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149351705 | |||||
| chr6:149351920
|
A | G | 1 | a0001c0001t0005g0358 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-89-17989A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149351920 | ||||||
| chr6:149351937
|
A | G | 3 | a0001c0001t0013g0177a0001c0001t0013g0178a0001c0001t0022g0176 | 3 | HG02109.hp1 HG02615.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-89-17972A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149351937 | ||||||
| chr6:149352129
|
GT | G | 3 | a0001c0002t0002g0206a0001c0002t0002g0207a0001c0002t0002g0208 | 3 | HG00609.hp1 NA18985.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.-89-17778delT | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149352129 | |||||
| chr6:149352246
|
A | C | 1 | a0001c0001t0003g0173 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-89-17663A>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149352246 | ||||||
| chr6:149352455
|
C | T | 297 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(294): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.-89-17454C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149352455 | ||||||
| chr6:149352598
|
A | G | 2 | a0001c0002t0002g0104a0001c0002t0002g0105 | 2 | HG04204.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.-89-17311A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149352598 | ||||||
| chr6:149352678
|
C | A | 363 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(360): Show | 365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.-89-17231C>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149352678 | ||||||
| chr6:149352720
|
T | A | 63 | a0001c0001t0003g0005a0001c0001t0003g0167a0001c0001t0003g0168others(60): Show | 63 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.-89-17189T>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149352720 | ||||||
| chr6:149352728
|
G | A | 1 | a0001c0001t0017g0022 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-89-17181G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149352728 | ||||||
| chr6:149352748
|
C | T | 8 | a0001c0001t0005g0117a0001c0001t0005g0118a0001c0001t0005g0179others(5): Show | 8 | HG01243.hp2 HG02602.hp2 HG02683.hp1 others(5): Show |
intron_variant | MODIFIER | c.-89-17161C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149352748 | ||||||
| chr6:149352783
|
A | C | 1 | a0001c0001t0008g0021 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-89-17126A>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149352783 | ||||||
| chr6:149352920
|
G | C | 2 | a0001c0002t0002g0188a0001c0002t0002g0203 | 2 | NA18998.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.-89-16989G>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149352920 | ||||||
| chr6:149353040
|
T | C | 9 | a0001c0001t0005g0117a0001c0001t0005g0118a0001c0001t0005g0179others(6): Show | 9 | HG01243.hp2 HG02602.hp2 HG02683.hp1 others(6): Show |
intron_variant | MODIFIER | c.-89-16869T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149353040 | ||||||
| chr6:149353228
|
G | GTGC | 21 | a0001c0001t0001g0002a0001c0001t0001g0086a0001c0001t0001g0087others(18): Show | 22 | HG01081.hp1 HG01109.hp2 HG01243.hp1 others(19): Show |
intron_variant | MODIFIER | c.-89-16663_-89-1666 others(7): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149353228 | |||||
| chr6:149353228
|
GTGCTGCT others(22): Show |
G | 1 | a0001c0001t0001g0166 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.-89-16664_-89-1663 others(33): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149353228 | |||||
| chr6:149353306
|
C | T | 11 | a0001c0001t0007g0074a0001c0001t0007g0075a0001c0001t0007g0076others(8): Show | 11 | HG02055.hp1 HG02145.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.-89-16603C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149353306 | ||||||
| chr6:149353456
|
C | A | 1 | a0001c0002t0002g0209 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.-89-16453C>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149353456 | ||||||
| chr6:149353652
|
A | G | 2 | a0001c0001t0003g0324a0001c0001t0003g0337 | 2 | HG02486.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.-89-16257A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149353652 | ||||||
| chr6:149353678
|
C | T | 63 | a0001c0001t0003g0005a0001c0001t0003g0167a0001c0001t0003g0168others(60): Show | 63 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.-89-16231C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149353678 | ||||||
| chr6:149353925
|
C | T | 4 | a0001c0001t0003g0339a0001c0001t0003g0344a0001c0001t0003g0346others(1): Show | 4 | HG00741.hp1 HG01070.hp2 HG01071.hp1 others(1): Show |
intron_variant | MODIFIER | c.-89-15984C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149353925 | ||||||
| chr6:149353927
|
T | C | 2 | a0001c0001t0001g0007a0001c0001t0001g0008 | 2 | HG02145.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.-89-15982T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149353927 | ||||||
| chr6:149353968
|
T | C | 297 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(294): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.-89-15941T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149353968 | ||||||
| chr6:149354136
|
T | G | 87 | a0001c0002t0002g0096a0001c0002t0002g0097a0001c0002t0002g0098others(84): Show | 87 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.-89-15773T>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149354136 | ||||||
| chr6:149354531
|
A | T | 3 | a0001c0002t0002g0201a0001c0002t0002g0231a0001c0002t0002g0248 | 3 | NA18953.hp1 NA19011.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.-89-15378A>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149354531 | ||||||
| chr6:149354608
|
G | A | 1 | a0001c0001t0017g0022 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-89-15301G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149354608 | ||||||
| chr6:149354727
|
T | C | 1 | a0001c0001t0017g0022 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-89-15182T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149354727 | ||||||
| chr6:149354755
|
T | A | 297 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(294): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.-89-15154T>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149354755 | ||||||
| chr6:149354992
|
T | C | 6 | a0001c0001t0003g0308a0001c0001t0003g0309a0001c0001t0003g0311others(3): Show | 6 | HG02129.hp1 NA18950.hp1 NA18977.hp2 others(3): Show |
intron_variant | MODIFIER | c.-89-14917T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149354992 | ||||||
| chr6:149355176
|
C | T | 1 | a0001c0001t0023g0071 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-89-14733C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149355176 | ||||||
| chr6:149355181
|
G | A | 9 | a0001c0001t0005g0117a0001c0001t0005g0118a0001c0001t0005g0179others(6): Show | 9 | HG01243.hp2 HG02602.hp2 HG02683.hp1 others(6): Show |
intron_variant | MODIFIER | c.-89-14728G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149355181 | ||||||
| chr6:149355415
|
C | T | 2 | a0001c0001t0004g0028a0001c0001t0004g0029 | 2 | HG03041.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.-89-14494C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149355415 | ||||||
| chr6:149355464
|
G | C | 92 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(89): Show | 93 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(90): Show |
intron_variant | MODIFIER | c.-89-14445G>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149355464 | ||||||
| chr6:149355667
|
C | CA | 13 | a0001c0001t0001g0009a0001c0001t0001g0141a0001c0001t0001g0271others(10): Show | 13 | HG00733.hp2 HG02055.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.-89-14225dupA | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149355667 | |||||
| chr6:149355667
|
CA | C | 104 | a0001c0001t0001g0002a0001c0001t0001g0086a0001c0001t0001g0087others(101): Show | 105 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(102): Show |
intron_variant | MODIFIER | c.-89-14225delA | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149355667 | |||||
| chr6:149355667
|
CAA | C | 83 | a0001c0001t0005g0253a0001c0002t0002g0096a0001c0002t0002g0097others(80): Show | 83 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(80): Show |
intron_variant | MODIFIER | c.-89-14226_-89-1422 others(6): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149355667 | |||||
| chr6:149355860
|
C | G | 2 | a0001c0001t0001g0007a0001c0001t0001g0008 | 2 | HG02145.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.-89-14049C>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149355860 | ||||||
| chr6:149355860
|
C | T | 1 | a0001c0001t0001g0273 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.-89-14049C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149355860 | ||||||
| chr6:149355955
|
CA | C | 8 | a0001c0001t0005g0117a0001c0001t0005g0118a0001c0001t0005g0179others(5): Show | 8 | HG01243.hp2 HG02602.hp2 HG02683.hp1 others(5): Show |
intron_variant | MODIFIER | c.-89-13944delA | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149355955 | |||||
| chr6:149355965
|
A | C | 2 | a0001c0001t0005g0180a0001c0001t0005g0181 | 2 | HG02683.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.-89-13944A>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149355965 | ||||||
| chr6:149356053
|
G | A | 1 | a0001c0001t0008g0021 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-89-13856G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149356053 | ||||||
| chr6:149356097
|
C | G | 1 | a0001c0001t0003g0322 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-89-13812C>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149356097 | ||||||
| chr6:149356136
|
A | C | 3 | a0001c0001t0008g0163a0001c0001t0008g0164a0001c0001t0008g0165 | 3 | HG02280.hp1 HG02717.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-89-13773A>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149356136 | ||||||
| chr6:149356324
|
C | T | 1 | a0001c0001t0004g0067 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-89-13585C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149356324 | ||||||
| chr6:149356361
|
A | G | 63 | a0001c0001t0003g0005a0001c0001t0003g0167a0001c0001t0003g0168others(60): Show | 63 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.-89-13548A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149356361 | ||||||
| chr6:149356563
|
C | T | 1 | a0001c0001t0004g0055 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.-89-13346C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149356563 | ||||||
| chr6:149356594
|
G | A | 1 | a0001c0001t0001g0187 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-89-13315G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149356594 | ||||||
| chr6:149356678
|
G | T | 1 | a0001c0008t0018g0293 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-89-13231G>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149356678 | ||||||
| chr6:149356958
|
T | G | 1 | a0001c0001t0001g0012 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-89-12951T>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149356958 | ||||||
| chr6:149357191
|
G | T | 63 | a0001c0001t0003g0005a0001c0001t0003g0167a0001c0001t0003g0168others(60): Show | 63 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.-89-12718G>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149357191 | ||||||
| chr6:149357230
|
A | G | 6 | a0001c0001t0001g0161a0001c0001t0001g0162a0001c0001t0001g0298others(3): Show | 6 | HG02280.hp1 HG02622.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.-89-12679A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149357230 | ||||||
| chr6:149357277
|
G | A | 6 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0070others(3): Show | 6 | HG01884.hp2 HG02257.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.-89-12632G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149357277 | ||||||
| chr6:149357286
|
T | C | 299 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(296): Show | 301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.-89-12623T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149357286 | ||||||
| chr6:149357287
|
G | C | 1 | a0001c0001t0008g0021 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-89-12622G>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149357287 | ||||||
| chr6:149357298
|
C | G | 63 | a0001c0001t0003g0005a0001c0001t0003g0167a0001c0001t0003g0168others(60): Show | 63 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.-89-12611C>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149357298 | ||||||
| chr6:149357306
|
C | T | 6 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0070others(3): Show | 6 | HG01884.hp2 HG02257.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.-89-12603C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149357306 | ||||||
| chr6:149357323
|
G | A | 3 | a0001c0001t0013g0177a0001c0001t0013g0178a0001c0001t0022g0176 | 3 | HG02109.hp1 HG02615.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-89-12586G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149357323 | ||||||
| chr6:149357354
|
T | G | 1 | a0001c0001t0021g0095 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-89-12555T>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149357354 | ||||||
| chr6:149357410
|
C | T | 1 | a0001c0001t0005g0179 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-89-12499C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149357410 | ||||||
| chr6:149357411
|
G | A | 17 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0070others(14): Show | 17 | HG01884.hp2 HG02055.hp1 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.-89-12498G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149357411 | ||||||
| chr6:149357419
|
G | GA | 3 | a0001c0001t0013g0177a0001c0001t0013g0178a0001c0001t0022g0176 | 3 | HG02109.hp1 HG02615.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-89-12489dupA | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149357419 | |||||
| chr6:149357421
|
G | A | 152 | a0001c0001t0003g0005a0001c0001t0003g0167a0001c0001t0003g0168others(149): Show | 152 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(149): Show |
intron_variant | MODIFIER | c.-89-12488G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149357421 | ||||||
| chr6:149357426
|
A | AAC | 7 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(4): Show | 7 | HG00733.hp2 HG02145.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.-89-12482_-89-1248 others(6): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149357426 | |||||
| chr6:149357426
|
A | C | 1 | a0001c0001t0009g0080 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-89-12483A>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149357426 | ||||||
| chr6:149357428
|
A | AC | 4 | a0001c0001t0004g0058a0001c0001t0007g0074a0001c0001t0007g0075others(1): Show | 4 | HG02630.hp2 HG03579.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.-89-12481_-89-1248 others(5): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149357428 | ||||||
| chr6:149357428
|
A | C | 17 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(14): Show | 17 | HG00733.hp2 HG02055.hp1 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.-89-12481A>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149357428 | ||||||
| chr6:149357430
|
A | AAAAAAAA others(5): Show |
1 | a0001c0002t0002g0212 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-89-12478_-89-1247 others(16): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149357430 | |||||
| chr6:149357430
|
A | AAAAAAAA others(4): Show |
1 | a0001c0002t0006g0210 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.-89-12478_-89-1247 others(15): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149357430 | |||||
| chr6:149357430
|
A | AAAAAAAA others(3): Show |
4 | a0001c0002t0002g0101a0001c0002t0002g0107a0001c0002t0002g0205others(1): Show | 4 | HG00597.hp2 HG00621.hp2 HG02135.hp2 others(1): Show |
intron_variant | MODIFIER | c.-89-12478_-89-1247 others(14): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149357430 | |||||
| chr6:149357430
|
A | AAAAAAAA others(5): Show |
15 | a0001c0002t0002g0100a0001c0002t0002g0105a0001c0002t0002g0189others(12): Show | 15 | HG01258.hp2 HG02080.hp2 HG02148.hp1 others(12): Show |
intron_variant | MODIFIER | c.-89-12478_-89-1247 others(16): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149357430 | |||||
| chr6:149357430
|
A | AAAAAAAA others(7): Show |
3 | a0001c0002t0002g0104a0001c0002t0002g0192a0001c0002t0002g0213 | 3 | HG04204.hp1 NA19009.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.-89-12478_-89-1247 others(18): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149357430 | |||||
| chr6:149357430
|
A | AAAAAAAA others(13): Show |
1 | a0001c0001t0003g0325 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-89-12478_-89-1247 others(24): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149357430 | |||||
| chr6:149357430
|
A | AAAAAAAA others(4): Show |
31 | a0001c0002t0002g0096a0001c0002t0002g0112a0001c0002t0002g0114others(28): Show | 31 | HG00423.hp1 HG00558.hp1 HG00639.hp2 others(28): Show |
intron_variant | MODIFIER | c.-89-12478_-89-1247 others(15): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149357430 | |||||
| chr6:149357430
|
A | AAAAAAAA others(6): Show |
11 | a0001c0002t0002g0102a0001c0002t0002g0191a0001c0002t0002g0203others(8): Show | 11 | HG00609.hp1 HG01255.hp1 HG01261.hp1 others(8): Show |
intron_variant | MODIFIER | c.-89-12478_-89-1247 others(17): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149357430 | |||||
| chr6:149357430
|
A | AAAAAAAA others(8): Show |
3 | a0001c0002t0002g0099a0001c0002t0002g0109a0001c0002t0002g0188 | 3 | HG00673.hp2 NA18978.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.-89-12478_-89-1247 others(19): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149357430 | |||||
| chr6:149357430
|
A | AAAAAAAA others(12): Show |
3 | a0001c0001t0003g0326a0001c0001t0003g0327a0001c0002t0002g0106 | 3 | HG03041.hp1 NA19001.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-89-12478_-89-1247 others(23): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149357430 | |||||
| chr6:149357430
|
A | AAAAAAAA others(3): Show |
1 | a0001c0001t0017g0022 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-89-12478_-89-1247 others(14): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149357430 | |||||
| chr6:149357430
|
A | AAAAAAAA others(5): Show |
4 | a0001c0001t0005g0359a0001c0002t0002g0097a0001c0002t0002g0208others(1): Show | 4 | HG00621.hp1 HG02129.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.-89-12478_-89-1247 others(16): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149357430 | |||||
| chr6:149357430
|
A | AAAAAAAA others(7): Show |
1 | a0001c0001t0005g0181 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-89-12478_-89-1247 others(18): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149357430 | |||||
| chr6:149357430
|
A | AAAAAAAA others(9): Show |
1 | a0001c0001t0003g0005 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-89-12478_-89-1247 others(20): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149357430 | |||||
| chr6:149357430
|
A | AAAAAAAA others(11): Show |
1 | a0001c0001t0003g0305 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-89-12478_-89-1247 others(22): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149357430 | |||||
| chr6:149357430
|
A | AAAAAAAA others(13): Show |
1 | a0001c0001t0003g0334 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.-89-12478_-89-1247 others(24): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149357430 | |||||
| chr6:149357430
|
A | AAAAAAAA others(15): Show |
2 | a0001c0001t0003g0331a0001c0001t0003g0332 | 2 | HG02622.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-89-12478_-89-1247 others(26): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149357430 | |||||
| chr6:149357430
|
A | AAAAAAAA others(17): Show |
2 | a0001c0001t0003g0330a0001c0001t0003g0333 | 2 | HG01192.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.-89-12478_-89-1247 others(28): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149357430 | |||||
| chr6:149357430
|
A | AAAAAAAA others(19): Show |
1 | a0001c0001t0003g0321 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-89-12478_-89-1247 others(30): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149357430 | |||||
| chr6:149357430
|
A | AAAAAAAA others(21): Show |
1 | a0001c0001t0003g0329 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-89-12478_-89-1247 others(32): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149357430 | |||||
| chr6:149357430
|
A | AAAAAAAA others(29): Show |
1 | a0001c0001t0003g0328 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-89-12478_-89-1247 others(40): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149357430 | |||||
| chr6:149357430
|
A | AAAAAAAC others(4): Show |
5 | a0001c0002t0002g0098a0001c0002t0002g0115a0001c0002t0002g0237others(2): Show | 5 | HG00741.hp2 HG02040.hp1 HG02132.hp2 others(2): Show |
intron_variant | MODIFIER | c.-89-12478_-89-1247 others(15): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149357430 | |||||
| chr6:149357430
|
A | AAAAAAAC others(6): Show |
5 | a0001c0001t0003g0348a0001c0001t0005g0118a0001c0001t0005g0182others(2): Show | 5 | HG01243.hp2 HG02602.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.-89-12478_-89-1247 others(17): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149357430 | |||||
| chr6:149357430
|
A | AAAAAAAC others(8): Show |
7 | a0001c0001t0003g0342a0001c0001t0003g0343a0001c0001t0003g0345others(4): Show | 7 | HG01256.hp2 HG01257.hp2 HG01361.hp1 others(4): Show |
intron_variant | MODIFIER | c.-89-12478_-89-1247 others(19): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149357430 | |||||
| chr6:149357430
|
A | AAAAAAAC others(10): Show |
12 | a0001c0001t0003g0170a0001c0001t0003g0173a0001c0001t0003g0174others(9): Show | 12 | HG00099.hp2 HG01070.hp2 HG01071.hp1 others(9): Show |
intron_variant | MODIFIER | c.-89-12478_-89-1247 others(21): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149357430 | |||||
| chr6:149357430
|
A | AAAAAAAC others(12): Show |
4 | a0001c0001t0003g0171a0001c0001t0003g0319a0001c0001t0003g0335others(1): Show | 4 | HG00140.hp2 HG00639.hp1 HG00741.hp1 others(1): Show |
intron_variant | MODIFIER | c.-89-12478_-89-1247 others(23): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149357430 | |||||
| chr6:149357430
|
A | AAAAAAAC others(14): Show |
7 | a0001c0001t0003g0317a0001c0001t0003g0318a0001c0001t0003g0322others(4): Show | 7 | HG01168.hp2 HG01175.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.-89-12478_-89-1247 others(25): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149357430 | |||||
| chr6:149357430
|
A | AAAAAAAC others(16): Show |
2 | a0001c0001t0003g0172a0001c0001t0003g0337 | 2 | HG02004.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.-89-12478_-89-1247 others(27): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149357430 | |||||
| chr6:149357430
|
A | AAAAAAAC others(18): Show |
1 | a0001c0001t0003g0350 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-89-12478_-89-1247 others(29): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149357430 | |||||
| chr6:149357430
|
A | AAAAAACA others(5): Show |
1 | a0001c0002t0002g0248 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.-89-12478_-89-1247 others(16): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149357430 | |||||
| chr6:149357430
|
A | AAAAAACA others(11): Show |
2 | a0001c0001t0003g0307a0001c0001t0003g0320 | 2 | HG00609.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.-89-12478_-89-1247 others(22): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149357430 | |||||
| chr6:149357430
|
A | AAAAAACA others(13): Show |
1 | a0001c0001t0021g0095 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-89-12478_-89-1247 others(24): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149357430 | |||||
| chr6:149357430
|
A | AAAAAACA others(15): Show |
1 | a0001c0001t0003g0349 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-89-12478_-89-1247 others(26): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149357430 | |||||
| chr6:149357430
|
A | AAAAACAC others(6): Show |
1 | a0001c0002t0002g0201 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.-89-12478_-89-1247 others(17): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149357430 | |||||
| chr6:149357430
|
A | AAAAACAC others(8): Show |
1 | a0001c0001t0003g0316 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.-89-12478_-89-1247 others(19): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149357430 | |||||
| chr6:149357430
|
A | AAAAACAC others(10): Show |
6 | a0001c0001t0003g0167a0001c0001t0003g0169a0001c0001t0003g0309others(3): Show | 6 | HG01255.hp2 HG02129.hp1 HG03492.hp1 others(3): Show |
intron_variant | MODIFIER | c.-89-12478_-89-1247 others(21): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149357430 | |||||
| chr6:149357430
|
A | AAAAACAC others(12): Show |
3 | a0001c0001t0003g0308a0001c0001t0003g0311a0001c0001t0003g0313 | 3 | NA18950.hp1 NA18977.hp2 NA18978.hp1 |
intron_variant | MODIFIER | c.-89-12478_-89-1247 others(23): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149357430 | |||||
| chr6:149357430
|
A | AAAAACAC others(14): Show |
1 | a0001c0001t0003g0323 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-89-12478_-89-1247 others(25): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149357430 | |||||
| chr6:149357430
|
A | AAAACACA others(11): Show |
1 | a0001c0001t0003g0312 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.-89-12478_-89-1247 others(22): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149357430 | |||||
| chr6:149357430
|
A | AAACACAC others(6): Show |
1 | a0001c0001t0003g0352 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.-89-12478_-89-1247 others(17): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149357430 | |||||
| chr6:149357430
|
A | AAACACAC others(8): Show |
1 | a0001c0001t0003g0168 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.-89-12478_-89-1247 others(19): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149357430 | |||||
| chr6:149357430
|
A | AAACACAC others(10): Show |
1 | a0001c0001t0003g0310 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-89-12478_-89-1247 others(21): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149357430 | |||||
| chr6:149357430
|
A | AAC | 28 | a0001c0001t0001g0002a0001c0001t0001g0064a0001c0001t0001g0086others(25): Show | 29 | HG00642.hp1 HG00642.hp2 HG01123.hp1 others(26): Show |
intron_variant | MODIFIER | c.-89-12443_-89-1244 others(6): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149357430 | |||||
| chr6:149357430
|
A | AACAC | 9 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(6): Show | 9 | HG01081.hp1 HG01099.hp2 HG01109.hp2 others(6): Show |
intron_variant | MODIFIER | c.-89-12445_-89-1244 others(8): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149357430 | |||||
| chr6:149357430
|
A | ACAC | 4 | a0001c0001t0001g0092a0001c0001t0001g0120a0001c0001t0001g0299others(1): Show | 4 | HG02258.hp2 NA18522.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.-89-12479_-89-1247 others(7): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149357430 | ||||||
| chr6:149357430
|
A | ACACACAC others(2): Show |
4 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0073others(1): Show | 4 | HG02257.hp1 HG02886.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.-89-12479_-89-1247 others(13): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149357430 | ||||||
| chr6:149357430
|
A | ACACACAC others(6): Show |
1 | a0001c0001t0001g0072 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-89-12479_-89-1247 others(17): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149357430 | ||||||
| chr6:149357430
|
A | C | 44 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(41): Show | 44 | HG00733.hp2 HG01496.hp1 HG01884.hp2 others(41): Show |
intron_variant | MODIFIER | c.-89-12479A>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149357430 | ||||||
| chr6:149357432
|
C | A | 5 | a0001c0001t0013g0177a0001c0001t0013g0178a0001c0001t0022g0176others(2): Show | 5 | HG01433.hp2 HG02080.hp1 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.-89-12477C>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149357432 | ||||||
| chr6:149357434
|
C | A | 4 | a0001c0001t0013g0177a0001c0001t0013g0178a0001c0001t0022g0176others(1): Show | 4 | HG01433.hp2 HG02109.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.-89-12475C>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149357434 | ||||||
| chr6:149357436
|
C | A | 4 | a0001c0001t0013g0177a0001c0001t0013g0178a0001c0001t0022g0176others(1): Show | 4 | HG01433.hp2 HG02109.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.-89-12473C>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149357436 | ||||||
| chr6:149357438
|
C | A | 4 | a0001c0001t0013g0177a0001c0001t0013g0178a0001c0001t0022g0176others(1): Show | 4 | HG01433.hp2 HG02109.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.-89-12471C>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149357438 | ||||||
| chr6:149357440
|
C | A | 3 | a0001c0001t0013g0177a0001c0001t0013g0178a0001c0001t0022g0176 | 3 | HG02109.hp1 HG02615.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-89-12469C>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149357440 | ||||||
| chr6:149357464
|
C | T | 16 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0070others(13): Show | 16 | HG01884.hp2 HG02055.hp1 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.-89-12445C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149357464 | ||||||
| chr6:149357502
|
ACT | A | 63 | a0001c0001t0003g0005a0001c0001t0003g0167a0001c0001t0003g0168others(60): Show | 63 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.-89-12404_-89-1240 others(6): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149357502 | |||||
| chr6:149357639
|
T | C | 1 | a0001c0002t0014g0110 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.-89-12270T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149357639 | ||||||
| chr6:149357708
|
C | CT | 10 | a0001c0001t0001g0133a0001c0001t0001g0147a0001c0001t0005g0117others(7): Show | 10 | HG00642.hp2 HG01243.hp2 HG02602.hp2 others(7): Show |
intron_variant | MODIFIER | c.-89-12192dupT | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149357708 | |||||
| chr6:149357799
|
A | G | 2 | a0001c0001t0005g0358a0001c0001t0005g0359 | 2 | HG02818.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-89-12110A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149357799 | ||||||
| chr6:149357921
|
G | A | 18 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0070others(15): Show | 18 | HG01884.hp2 HG02055.hp1 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.-89-11988G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149357921 | ||||||
| chr6:149358073
|
G | A | 8 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(5): Show | 8 | HG02895.hp1 HG02895.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.-89-11836G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149358073 | ||||||
| chr6:149358235
|
A | G | 153 | a0001c0001t0003g0005a0001c0001t0003g0167a0001c0001t0003g0168others(150): Show | 153 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(150): Show |
intron_variant | MODIFIER | c.-89-11674A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149358235 | ||||||
| chr6:149358254
|
A | G | 3 | a0001c0001t0007g0074a0001c0001t0007g0076a0001c0001t0007g0077 | 3 | HG03225.hp1 HG03579.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-89-11655A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149358254 | ||||||
| chr6:149358329
|
TG | T | 18 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0070others(15): Show | 18 | HG01884.hp2 HG02055.hp1 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.-89-11579delG | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149358329 | ||||||
| chr6:149358364
|
G | A | 2 | a0001c0001t0003g0347a0001c0001t0003g0348 | 2 | HG02300.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-89-11545G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149358364 | ||||||
| chr6:149358640
|
C | CTG | 6 | a0001c0001t0004g0042a0001c0001t0004g0058a0001c0001t0013g0177others(3): Show | 6 | HG02109.hp1 HG02615.hp2 NA18950.hp2 others(3): Show |
intron_variant | MODIFIER | c.-89-11237_-89-1123 others(6): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149358640 | |||||
| chr6:149358640
|
C | CTGTG | 8 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(5): Show | 8 | HG00733.hp2 HG01099.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.-89-11239_-89-1123 others(8): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149358640 | |||||
| chr6:149358640
|
C | CTGTGTG | 17 | a0001c0001t0003g0167a0001c0001t0003g0168a0001c0001t0003g0307others(14): Show | 17 | HG00609.hp2 HG01167.hp2 HG01175.hp1 others(14): Show |
intron_variant | MODIFIER | c.-89-11241_-89-1123 others(10): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149358640 | |||||
| chr6:149358640
|
C | CTGTGTGT others(1): Show |
15 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0003g0170others(12): Show | 15 | HG01109.hp1 HG02055.hp1 HG02129.hp1 others(12): Show |
intron_variant | MODIFIER | c.-89-11243_-89-1123 others(12): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149358640 | |||||
| chr6:149358640
|
C | CTGTGTGT others(3): Show |
4 | a0001c0001t0003g0313a0001c0001t0003g0337a0001c0001t0007g0076others(1): Show | 4 | HG02965.hp2 HG06807.hp1 NA18978.hp1 others(1): Show |
intron_variant | MODIFIER | c.-89-11245_-89-1123 others(14): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149358640 | |||||
| chr6:149358640
|
C | CTGTGTGT others(5): Show |
3 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0003g0322 | 3 | HG01175.hp2 HG03540.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-89-11247_-89-1123 others(16): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149358640 | |||||
| chr6:149358640
|
C | CTGTGTGT others(7): Show |
14 | a0001c0001t0001g0068a0001c0001t0001g0145a0001c0001t0001g0285others(11): Show | 14 | HG01243.hp2 HG01516.hp1 HG01517.hp2 others(11): Show |
intron_variant | MODIFIER | c.-89-11249_-89-1123 others(18): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149358640 | |||||
| chr6:149358640
|
C | CTGTGTGT others(9): Show |
15 | a0001c0001t0001g0137a0001c0001t0001g0139a0001c0001t0001g0141others(12): Show | 15 | HG00140.hp1 HG01496.hp1 HG02080.hp1 others(12): Show |
intron_variant | MODIFIER | c.-89-11251_-89-1123 others(20): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149358640 | |||||
| chr6:149358640
|
C | CTGTGTGT others(11): Show |
23 | a0001c0001t0001g0006a0001c0001t0001g0159a0001c0001t0001g0261others(20): Show | 23 | HG00140.hp2 HG00733.hp1 HG00738.hp2 others(20): Show |
intron_variant | MODIFIER | c.-89-11253_-89-1123 others(22): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149358640 | |||||
| chr6:149358640
|
C | CTGTGTGT others(13): Show |
36 | a0001c0001t0001g0091a0001c0001t0001g0121a0001c0001t0001g0122others(33): Show | 36 | HG00099.hp2 HG00735.hp2 HG00741.hp1 others(33): Show |
intron_variant | MODIFIER | c.-89-11255_-89-1123 others(24): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149358640 | |||||
| chr6:149358640
|
C | CTGTGTGT others(15): Show |
37 | a0001c0001t0001g0002a0001c0001t0001g0090a0001c0001t0001g0124others(34): Show | 38 | HG00423.hp2 HG00558.hp2 HG00639.hp1 others(35): Show |
intron_variant | MODIFIER | c.-89-11257_-89-1123 others(26): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149358640 | |||||
| chr6:149358640
|
C | CTGTGTGT others(17): Show |
28 | a0001c0001t0001g0004a0001c0001t0001g0085a0001c0001t0001g0087others(25): Show | 28 | HG00597.hp1 HG00642.hp2 HG01243.hp1 others(25): Show |
intron_variant | MODIFIER | c.-89-11259_-89-1123 others(28): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149358640 | |||||
| chr6:149358640
|
C | CTGTGTGT others(19): Show |
32 | a0001c0001t0001g0003a0001c0001t0001g0086a0001c0001t0001g0088others(29): Show | 33 | HG00099.hp1 HG00621.hp1 HG00642.hp1 others(30): Show |
intron_variant | MODIFIER | c.-89-11261_-89-1123 others(30): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149358640 | |||||
| chr6:149358640
|
C | CTGTGTGT others(21): Show |
24 | a0001c0001t0001g0123a0001c0001t0003g0331a0001c0001t0015g0154others(21): Show | 24 | HG00639.hp2 HG00741.hp2 HG01257.hp1 others(21): Show |
intron_variant | MODIFIER | c.-89-11263_-89-1123 others(32): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149358640 | |||||
| chr6:149358640
|
C | CTGTGTGT others(23): Show |
14 | a0001c0002t0002g0101a0001c0002t0002g0197a0001c0002t0002g0208others(11): Show | 14 | HG00597.hp2 HG01258.hp2 HG02015.hp2 others(11): Show |
intron_variant | MODIFIER | c.-89-11265_-89-1123 others(34): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149358640 | |||||
| chr6:149358640
|
C | CTGTGTGT others(25): Show |
7 | a0001c0001t0001g0142a0001c0002t0002g0113a0001c0002t0002g0196others(4): Show | 7 | HG00558.hp1 HG00621.hp2 HG02083.hp1 others(4): Show |
intron_variant | MODIFIER | c.-89-11267_-89-1123 others(36): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149358640 | |||||
| chr6:149358640
|
C | CTGTGTGT others(27): Show |
2 | a0001c0001t0001g0146a0001c0005t0002g0233 | 2 | HG02132.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.-89-11236_-89-1123 others(38): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149358640 | |||||
| chr6:149358640
|
C | CTGTGTGT others(29): Show |
1 | a0001c0002t0002g0204 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.-89-11236_-89-1123 others(40): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149358640 | |||||
| chr6:149358640
|
C | CTGTGTGT others(31): Show |
1 | a0001c0002t0002g0207 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-89-11236_-89-1123 others(42): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149358640 | |||||
| chr6:149358640
|
CTG | C | 3 | a0001c0001t0001g0015a0001c0001t0004g0035a0001c0002t0002g0190 | 3 | HG00423.hp1 HG02630.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-89-11237_-89-1123 others(6): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149358640 | |||||
| chr6:149358673
|
T | TGTGTGTG others(12): Show |
1 | a0001c0001t0001g0160 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.-89-11236_-89-1123 others(23): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149358673 | ||||||
| chr6:149358673
|
T | TGTGTGTG others(14): Show |
1 | a0001c0001t0003g0328 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-89-11236_-89-1123 others(25): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149358673 | ||||||
| chr6:149358673
|
T | TGTGTGTG others(16): Show |
3 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0002t0002g0105 | 3 | HG02572.hp1 HG04228.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-89-11236_-89-1123 others(27): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149358673 | ||||||
| chr6:149358673
|
T | TGTGTGTG others(18): Show |
2 | a0001c0001t0001g0094a0001c0001t0001g0155 | 2 | HG03579.hp2 NA18956.hp1 |
intron_variant | MODIFIER | c.-89-11236_-89-1123 others(29): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149358673 | ||||||
| chr6:149358673
|
T | TGTGTGTG others(20): Show |
3 | a0001c0001t0001g0120a0001c0002t0002g0114a0001c0002t0002g0232 | 3 | NA18947.hp1 NA18979.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.-89-11236_-89-1123 others(31): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149358673 | ||||||
| chr6:149358673
|
T | TGTGTGTG others(22): Show |
1 | a0001c0002t0002g0115 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-89-11236_-89-1123 others(33): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149358673 | ||||||
| chr6:149358673
|
T | TGTGTGTG others(24): Show |
1 | a0001c0002t0002g0244 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-89-11236_-89-1123 others(35): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149358673 | ||||||
| chr6:149358674
|
T | G | 2 | a0001c0001t0001g0299a0001c0001t0017g0022 | 2 | NA18522.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-89-11235T>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149358674 | ||||||
| chr6:149358675
|
T | G | 1 | a0001c0001t0001g0092 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-89-11234T>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149358675 | ||||||
| chr6:149358896
|
A | G | 305 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(302): Show | 307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.-89-11013A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149358896 | ||||||
| chr6:149358927
|
T | G | 3 | a0001c0001t0007g0075a0001c0001t0007g0083a0001c0001t0024g0078 | 3 | HG02630.hp2 HG03486.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-89-10982T>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149358927 | ||||||
| chr6:149359145
|
G | C | 4 | a0001c0001t0009g0079a0001c0001t0009g0080a0001c0001t0009g0081others(1): Show | 4 | HG02055.hp1 HG02145.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.-89-10764G>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149359145 | ||||||
| chr6:149359276
|
T | C | 2 | a0001c0001t0004g0026a0001c0001t0004g0027 | 2 | HG02698.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.-89-10633T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149359276 | ||||||
| chr6:149359288
|
C | T | 2 | a0001c0002t0002g0217a0001c0002t0002g0241 | 2 | HG02080.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.-89-10621C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149359288 | ||||||
| chr6:149359307
|
A | G | 1 | a0001c0001t0003g0353 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.-89-10602A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149359307 | ||||||
| chr6:149359370
|
G | A | 6 | a0001c0001t0003g0308a0001c0001t0003g0309a0001c0001t0003g0311others(3): Show | 6 | HG02129.hp1 NA18950.hp1 NA18977.hp2 others(3): Show |
intron_variant | MODIFIER | c.-89-10539G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149359370 | ||||||
| chr6:149359680
|
C | T | 11 | a0001c0001t0007g0074a0001c0001t0007g0075a0001c0001t0007g0076others(8): Show | 11 | HG02055.hp1 HG02145.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.-89-10229C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149359680 | ||||||
| chr6:149359682
|
C | G | 1 | a0001c0002t0002g0228 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-89-10227C>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149359682 | ||||||
| chr6:149360056
|
T | C | 63 | a0001c0001t0003g0005a0001c0001t0003g0167a0001c0001t0003g0168others(60): Show | 63 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.-89-9853T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149360056 | ||||||
| chr6:149360100
|
G | T | 18 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0070others(15): Show | 18 | HG01884.hp2 HG02055.hp1 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.-89-9809G>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149360100 | ||||||
| chr6:149360253
|
C | T | 2 | a0001c0001t0001g0185a0001c0001t0001g0186 | 2 | NA18966.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.-89-9656C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149360253 | ||||||
| chr6:149360381
|
C | T | 73 | a0001c0002t0002g0100a0001c0002t0002g0101a0001c0002t0002g0102others(70): Show | 73 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(70): Show |
intron_variant | MODIFIER | c.-89-9528C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149360381 | ||||||
| chr6:149360420
|
C | G | 2 | a0001c0001t0004g0183a0001c0001t0004g0184 | 2 | HG02717.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.-89-9489C>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149360420 | ||||||
| chr6:149360432
|
A | G | 1 | a0001c0001t0001g0127 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.-89-9477A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149360432 | ||||||
| chr6:149360529
|
A | G | 1 | a0001c0001t0003g0350 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-89-9380A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149360529 | ||||||
| chr6:149360816
|
T | C | 18 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0070others(15): Show | 18 | HG01884.hp2 HG02055.hp1 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.-89-9093T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149360816 | ||||||
| chr6:149360944
|
A | C | 1 | a0001c0001t0005g0253 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-89-8965A>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149360944 | ||||||
| chr6:149361264
|
TTC | T | 3 | a0001c0001t0007g0074a0001c0001t0007g0076a0001c0001t0007g0077 | 3 | HG03225.hp1 HG03579.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-89-8642_-89-8641d others(4): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149361264 | |||||
| chr6:149361703
|
C | T | 2 | a0001c0001t0008g0164a0001c0001t0008g0165 | 2 | HG02280.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-89-8206C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149361703 | ||||||
| chr6:149361828
|
T | G | 11 | a0001c0001t0007g0074a0001c0001t0007g0075a0001c0001t0007g0076others(8): Show | 11 | HG02055.hp1 HG02145.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.-89-8081T>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149361828 | ||||||
| chr6:149361884
|
G | A | 8 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(5): Show | 8 | HG02895.hp1 HG02895.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.-89-8025G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149361884 | ||||||
| chr6:149362087
|
C | T | 1 | a0001c0002t0002g0230 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-89-7822C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149362087 | ||||||
| chr6:149362479
|
A | G | 1 | a0001c0001t0001g0254 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.-89-7430A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149362479 | ||||||
| chr6:149362602
|
TA | T | 18 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0070others(15): Show | 18 | HG01884.hp2 HG02055.hp1 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.-89-7304delA | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149362602 | |||||
| chr6:149362646
|
T | A | 1 | a0001c0001t0003g0169 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-89-7263T>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149362646 | ||||||
| chr6:149362663
|
TA | T | 297 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(294): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.-89-7244delA | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149362663 | |||||
| chr6:149362733
|
A | G | 3 | a0001c0002t0006g0210a0001c0002t0006g0211a0001c0002t0006g0238 | 3 | NA18962.hp1 NA19062.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.-89-7176A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149362733 | ||||||
| chr6:149363429
|
A | G | 1 | a0001c0003t0001g0259 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-89-6480A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149363429 | ||||||
| chr6:149363504
|
A | T | 1 | a0001c0002t0002g0096 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-89-6405A>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149363504 | ||||||
| chr6:149363655
|
G | A | 5 | a0001c0001t0001g0002a0001c0001t0001g0086a0001c0001t0001g0090others(2): Show | 6 | HG02109.hp2 HG02451.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.-89-6254G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149363655 | ||||||
| chr6:149363719
|
C | T | 3 | a0001c0001t0001g0360a0001c0001t0001g0362a0001c0001t0001g0363 | 3 | HG01256.hp1 HG01258.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.-89-6190C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149363719 | ||||||
| chr6:149363734
|
G | T | 1 | a0001c0001t0001g0124 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.-89-6175G>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149363734 | ||||||
| chr6:149363743
|
A | G | 1 | a0001c0001t0001g0013 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-89-6166A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149363743 | ||||||
| chr6:149363769
|
C | T | 1 | a0001c0001t0001g0266 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-89-6140C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149363769 | ||||||
| chr6:149363791
|
C | T | 1 | a0001c0001t0001g0009 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.-89-6118C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149363791 | ||||||
| chr6:149363820
|
A | G | 1 | a0001c0001t0005g0253 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-89-6089A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149363820 | ||||||
| chr6:149363941
|
G | A | 1 | a0001c0002t0002g0114 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.-89-5968G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149363941 | ||||||
| chr6:149364195
|
G | A | 2 | a0001c0001t0003g0005a0001c0001t0003g0340 | 2 | HG00738.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.-89-5714G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149364195 | ||||||
| chr6:149364209
|
C | A | 1 | a0001c0002t0002g0212 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-89-5700C>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149364209 | ||||||
| chr6:149364212
|
G | C | 1 | a0001c0001t0001g0094 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-89-5697G>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149364212 | ||||||
| chr6:149364451
|
T | C | 15 | a0001c0001t0007g0074a0001c0001t0007g0075a0001c0001t0007g0076others(12): Show | 15 | HG02055.hp1 HG02109.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.-89-5458T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149364451 | ||||||
| chr6:149364481
|
C | T | 184 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0070others(181): Show | 184 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(181): Show |
intron_variant | MODIFIER | c.-89-5428C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149364481 | ||||||
| chr6:149364488
|
A | G | 1 | a0001c0001t0001g0297 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-89-5421A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149364488 | ||||||
| chr6:149364520
|
T | C | 1 | a0001c0001t0001g0280 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.-89-5389T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149364520 | ||||||
| chr6:149364577
|
G | C | 63 | a0001c0001t0003g0005a0001c0001t0003g0167a0001c0001t0003g0168others(60): Show | 63 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.-89-5332G>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149364577 | ||||||
| chr6:149364633
|
A | G | 2 | a0001c0002t0002g0189a0001c0002t0002g0227 | 2 | NA18612.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.-89-5276A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149364633 | ||||||
| chr6:149364851
|
A | G | 4 | a0001c0001t0001g0159a0001c0001t0001g0160a0001c0001t0001g0264others(1): Show | 4 | NA18969.hp1 NA18987.hp2 NA18995.hp2 others(1): Show |
intron_variant | MODIFIER | c.-89-5058A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149364851 | ||||||
| chr6:149364984
|
A | G | 1 | a0001c0001t0017g0022 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-89-4925A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149364984 | ||||||
| chr6:149365049
|
T | C | 1 | a0001c0001t0001g0294 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-89-4860T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149365049 | ||||||
| chr6:149365102
|
G | T | 1 | a0001c0001t0001g0266 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-89-4807G>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149365102 | ||||||
| chr6:149365124
|
T | C | 4 | a0001c0001t0008g0021a0001c0001t0008g0163a0001c0001t0008g0164others(1): Show | 4 | HG02280.hp1 HG02717.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.-89-4785T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149365124 | ||||||
| chr6:149365124
|
T | G | 3 | a0001c0001t0013g0177a0001c0001t0013g0178a0001c0001t0022g0176 | 3 | HG02109.hp1 HG02615.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-89-4785T>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149365124 | ||||||
| chr6:149365291
|
A | G | 2 | a0001c0001t0003g0305a0001c0001t0019g0306 | 2 | HG02970.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-89-4618A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149365291 | ||||||
| chr6:149365327
|
A | G | 2 | a0001c0001t0001g0269a0001c0001t0001g0303 | 2 | HG00673.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.-89-4582A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149365327 | ||||||
| chr6:149365353
|
A | G | 2 | a0001c0001t0001g0120a0001c0001t0001g0290 | 2 | HG00423.hp2 NA18947.hp1 |
intron_variant | MODIFIER | c.-89-4556A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149365353 | ||||||
| chr6:149365382
|
T | G | 113 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(110): Show | 115 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(112): Show |
intron_variant | MODIFIER | c.-89-4527T>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149365382 | ||||||
| chr6:149365455
|
A | G | 3 | a0001c0001t0013g0177a0001c0001t0013g0178a0001c0001t0022g0176 | 3 | HG02109.hp1 HG02615.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-89-4454A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149365455 | ||||||
| chr6:149365561
|
T | C | 1 | a0001c0001t0001g0284 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-89-4348T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149365561 | ||||||
| chr6:149365641
|
C | A | 1 | a0001c0001t0004g0052 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.-89-4268C>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149365641 | ||||||
| chr6:149365826
|
C | T | 1 | a0001c0001t0001g0009 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.-89-4083C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149365826 | ||||||
| chr6:149365897
|
T | C | 1 | a0001c0002t0002g0214 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.-89-4012T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149365897 | ||||||
| chr6:149365991
|
T | A | 4 | a0001c0001t0008g0021a0001c0001t0008g0163a0001c0001t0008g0164others(1): Show | 4 | HG02280.hp1 HG02717.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.-89-3918T>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149365991 | ||||||
| chr6:149366342
|
A | G | 1 | a0001c0001t0003g0307 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.-89-3567A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149366342 | ||||||
| chr6:149366395
|
T | G | 2 | a0001c0001t0001g0016a0001c0001t0001g0017 | 2 | HG02895.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.-89-3514T>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149366395 | ||||||
| chr6:149366587
|
C | A | 1 | a0001c0002t0002g0249 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.-89-3322C>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149366587 | ||||||
| chr6:149366607
|
A | G | 6 | a0001c0001t0007g0074a0001c0001t0007g0075a0001c0001t0007g0076others(3): Show | 6 | HG02630.hp2 HG03225.hp1 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.-89-3302A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149366607 | ||||||
| chr6:149366720
|
G | A | 1 | a0001c0001t0005g0180 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-89-3189G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149366720 | ||||||
| chr6:149366953
|
A | AC | 43 | a0001c0001t0003g0005a0001c0001t0003g0171a0001c0001t0003g0172others(40): Show | 43 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.-89-2956_-89-2955i others(3): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149366953 | ||||||
| chr6:149366954
|
A | C | 2 | a0001c0001t0003g0320a0001c0001t0003g0323 | 2 | HG03491.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.-89-2955A>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149366954 | ||||||
| chr6:149366955
|
A | AT | 138 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(135): Show | 138 | HG00558.hp1 HG00597.hp2 HG00609.hp1 others(135): Show |
intron_variant | MODIFIER | c.-89-2943dupT | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149366955 | |||||
| chr6:149366955
|
A | T | 43 | a0001c0001t0003g0005a0001c0001t0003g0171a0001c0001t0003g0172others(40): Show | 43 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.-89-2954A>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149366955 | ||||||
| chr6:149367060
|
A | G | 297 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(294): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.-89-2849A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149367060 | ||||||
| chr6:149367400
|
T | A | 2 | a0001c0001t0004g0183a0001c0001t0004g0184 | 2 | HG02717.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.-89-2509T>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149367400 | ||||||
| chr6:149367490
|
A | C | 63 | a0001c0001t0003g0005a0001c0001t0003g0167a0001c0001t0003g0168others(60): Show | 63 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.-89-2419A>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149367490 | ||||||
| chr6:149367578
|
C | T | 2 | a0001c0001t0005g0180a0001c0001t0005g0181 | 2 | HG02683.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.-89-2331C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149367578 | ||||||
| chr6:149368106
|
C | A | 1 | a0001c0001t0004g0029 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-89-1803C>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149368106 | ||||||
| chr6:149368170
|
T | C | 3 | a0001c0001t0013g0177a0001c0001t0013g0178a0001c0001t0022g0176 | 3 | HG02109.hp1 HG02615.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-89-1739T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149368170 | ||||||
| chr6:149368196
|
T | C | 63 | a0001c0001t0003g0005a0001c0001t0003g0167a0001c0001t0003g0168others(60): Show | 63 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.-89-1713T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149368196 | ||||||
| chr6:149368305
|
T | C | 4 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(1): Show | 4 | HG01081.hp1 HG01884.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.-89-1604T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149368305 | ||||||
| chr6:149368321
|
A | G | 153 | a0001c0001t0003g0005a0001c0001t0003g0167a0001c0001t0003g0168others(150): Show | 153 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(150): Show |
intron_variant | MODIFIER | c.-89-1588A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149368321 | ||||||
| chr6:149368329
|
A | G | 2 | a0001c0002t0002g0249a0001c0002t0002g0250 | 2 | HG01943.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.-89-1580A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149368329 | ||||||
| chr6:149368430
|
TACGTATA others(3): Show |
T | 1 | a0001c0001t0008g0021 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-89-1477_-89-1468d others(12): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149368430 | |||||
| chr6:149368592
|
T | C | 1 | a0001c0001t0017g0022 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-89-1317T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149368592 | ||||||
| chr6:149368612
|
A | C | 1 | a0001c0001t0001g0010 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-89-1297A>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149368612 | ||||||
| chr6:149368618
|
A | G | 1 | a0001c0001t0001g0122 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.-89-1291A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149368618 | ||||||
| chr6:149368631
|
T | C | 1 | a0001c0001t0017g0022 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-89-1278T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149368631 | ||||||
| chr6:149368645
|
T | TTG | 52 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0009others(49): Show | 53 | HG00140.hp2 HG00673.hp1 HG00733.hp2 others(50): Show |
intron_variant | MODIFIER | c.-89-1230_-89-1229d others(4): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149368645 | |||||
| chr6:149368645
|
T | TTGTG | 33 | a0001c0001t0001g0068a0001c0001t0001g0072a0001c0001t0001g0073others(30): Show | 33 | HG00423.hp2 HG00558.hp2 HG00639.hp1 others(30): Show |
intron_variant | MODIFIER | c.-89-1232_-89-1229d others(6): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149368645 | |||||
| chr6:149368645
|
T | TTGTGTG | 18 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0003g0005others(15): Show | 18 | HG00099.hp2 HG00738.hp2 HG01099.hp1 others(15): Show |
intron_variant | MODIFIER | c.-89-1234_-89-1229d others(8): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149368645 | |||||
| chr6:149368645
|
T | TTGTGTGT others(1): Show |
27 | a0001c0001t0003g0167a0001c0001t0003g0168a0001c0001t0003g0169others(24): Show | 27 | HG00609.hp2 HG00741.hp1 HG01070.hp2 others(24): Show |
intron_variant | MODIFIER | c.-89-1236_-89-1229d others(10): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149368645 | |||||
| chr6:149368645
|
T | TTGTGTGT others(3): Show |
2 | a0001c0001t0003g0172a0001c0001t0003g0304 | 2 | HG02004.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.-89-1238_-89-1229d others(12): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149368645 | |||||
| chr6:149368645
|
T | TTGTGTGT others(5): Show |
6 | a0001c0001t0003g0308a0001c0001t0003g0311a0001c0001t0003g0312others(3): Show | 6 | HG02109.hp1 HG02615.hp2 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.-89-1240_-89-1229d others(14): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149368645 | |||||
| chr6:149368645
|
T | TTGTGTGT others(7): Show |
1 | a0001c0001t0022g0176 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-89-1242_-89-1229d others(16): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149368645 | |||||
| chr6:149368645
|
TTG | T | 3 | a0001c0001t0001g0269a0001c0001t0017g0022a0001c0002t0002g0198 | 3 | HG00639.hp2 NA18989.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-89-1230_-89-1229d others(4): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149368645 | |||||
| chr6:149368645
|
TTGTG | T | 27 | a0001c0001t0001g0001a0001c0001t0004g0001a0001c0001t0004g0041others(24): Show | 27 | HG00609.hp1 HG00673.hp2 HG01257.hp1 others(24): Show |
intron_variant | MODIFIER | c.-89-1232_-89-1229d others(6): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149368645 | |||||
| chr6:149368645
|
TTGTGTG | T | 69 | a0001c0001t0005g0253a0001c0002t0002g0096a0001c0002t0002g0100others(66): Show | 69 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(66): Show |
intron_variant | MODIFIER | c.-89-1234_-89-1229d others(8): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149368645 | |||||
| chr6:149368906
|
T | A | 1 | a0001c0001t0003g0311 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.-89-1003T>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149368906 | ||||||
| chr6:149369020
|
T | C | 4 | a0001c0001t0008g0021a0001c0001t0008g0163a0001c0001t0008g0164others(1): Show | 4 | HG02280.hp1 HG02717.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.-89-889T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149369020 | ||||||
| chr6:149369294
|
C | T | 1 | a0001c0001t0005g0117 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-89-615C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149369294 | ||||||
| chr6:149369589
|
A | C | 87 | a0001c0002t0002g0096a0001c0002t0002g0097a0001c0002t0002g0098others(84): Show | 87 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.-89-320A>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149369589 | ||||||
| chr6:149369601
|
A | G | 17 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0070others(14): Show | 17 | HG01884.hp2 HG02055.hp1 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.-89-308A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149369601 | ||||||
| chr6:149369671
|
G | A | 4 | a0001c0001t0004g0023a0001c0001t0004g0024a0001c0001t0004g0034others(1): Show | 4 | HG02258.hp1 HG02559.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.-89-238G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149369671 | ||||||
| chr6:149369729
|
A | C | 3 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0020 | 3 | HG03209.hp1 HG03453.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-89-180A>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149369729 | ||||||
| chr6:149369876
|
T | C | 1 | a0001c0001t0001g0271 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.-89-33T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149369876 | ||||||
| chr6:149370155
|
AT | A | 87 | a0001c0002t0002g0096a0001c0002t0002g0097a0001c0002t0002g0098others(84): Show | 87 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.102+58delT | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr6 | 149370155 | |||||
| chr6:149370219
|
T | G | 116 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(113): Show | 118 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.102+120T>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 2/6 | chr6 | 149370219 | ||||||
| chr6:149370254
|
C | T | 1 | a0001c0001t0001g0068 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.102+155C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 2/6 | chr6 | 149370254 | ||||||
| chr6:149370316
|
G | A | 1 | a0001c0001t0001g0147 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.102+217G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 2/6 | chr6 | 149370316 | ||||||
| chr6:149370466
|
A | G | 87 | a0001c0002t0002g0096a0001c0002t0002g0097a0001c0002t0002g0098others(84): Show | 87 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.102+367A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 2/6 | chr6 | 149370466 | ||||||
| chr6:149370678
|
T | C | 1 | a0001c0001t0001g0088 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.102+579T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 2/6 | chr6 | 149370678 | ||||||
| chr6:149370723
|
G | A | 116 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(113): Show | 118 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.102+624G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 2/6 | chr6 | 149370723 | ||||||
| chr6:149370902
|
C | A | 63 | a0001c0001t0003g0005a0001c0001t0003g0167a0001c0001t0003g0168others(60): Show | 63 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.102+803C>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 2/6 | chr6 | 149370902 | ||||||
| chr6:149370986
|
A | C | 1 | a0001c0001t0001g0268 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.102+887A>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 2/6 | chr6 | 149370986 | ||||||
| chr6:149371007
|
A | G | 30 | a0001c0001t0003g0172a0001c0001t0003g0173a0001c0001t0003g0305others(27): Show | 30 | HG00140.hp2 HG01168.hp2 HG01175.hp2 others(27): Show |
intron_variant | MODIFIER | c.102+908A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 2/6 | chr6 | 149371007 | ||||||
| chr6:149371054
|
AG | A | 9 | a0001c0001t0005g0117a0001c0001t0005g0118a0001c0001t0005g0179others(6): Show | 9 | HG01243.hp2 HG02602.hp2 HG02683.hp1 others(6): Show |
intron_variant | MODIFIER | c.102+956delG | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 2/6 | chr6 | 149371054 | ||||||
| chr6:149371065
|
C | CA | 105 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(102): Show | 107 | HG00099.hp1 HG00558.hp2 HG00597.hp1 others(104): Show |
intron_variant | MODIFIER | c.102+991dupA | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr6 | 149371065 | |||||
| chr6:149371065
|
C | CAA | 6 | a0001c0001t0001g0087a0001c0001t0001g0137a0001c0001t0001g0153others(3): Show | 6 | HG00140.hp1 HG00423.hp2 HG01943.hp1 others(3): Show |
intron_variant | MODIFIER | c.102+990_102+991dup others(2): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr6 | 149371065 | |||||
| chr6:149371065
|
C | CAAA | 8 | a0001c0001t0005g0117a0001c0001t0005g0118a0001c0001t0005g0253others(5): Show | 8 | HG01243.hp2 HG02109.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.102+989_102+991dup others(3): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr6 | 149371065 | |||||
| chr6:149371065
|
CA | C | 90 | a0001c0001t0001g0013a0001c0001t0001g0015a0001c0001t0001g0016others(87): Show | 90 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(87): Show |
intron_variant | MODIFIER | c.102+991delA | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr6 | 149371065 | |||||
| chr6:149371065
|
CAA | C | 78 | a0001c0001t0001g0014a0001c0001t0003g0338a0001c0002t0002g0096others(75): Show | 78 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(75): Show |
intron_variant | MODIFIER | c.102+990_102+991del others(2): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr6 | 149371065 | |||||
| chr6:149371093
|
G | A | 150 | a0001c0001t0003g0005a0001c0001t0003g0167a0001c0001t0003g0168others(147): Show | 150 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(147): Show |
intron_variant | MODIFIER | c.102+994G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 2/6 | chr6 | 149371093 | ||||||
| chr6:149371097
|
G | A | 1 | a0001c0002t0002g0097 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.102+998G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 2/6 | chr6 | 149371097 | ||||||
| chr6:149371108
|
A | G | 4 | a0001c0001t0003g0005a0001c0001t0003g0340a0001c0001t0003g0342others(1): Show | 4 | HG00738.hp2 HG01257.hp2 HG01361.hp1 others(1): Show |
intron_variant | MODIFIER | c.102+1009A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 2/6 | chr6 | 149371108 | ||||||
| chr6:149371278
|
C | T | 1 | a0001c0001t0004g0065 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.102+1179C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 2/6 | chr6 | 149371278 | ||||||
| chr6:149371721
|
A | G | 1 | a0001c0001t0001g0123 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.102+1622A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 2/6 | chr6 | 149371721 | ||||||
| chr6:149371799
|
G | A | 168 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0070others(165): Show | 168 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(165): Show |
intron_variant | MODIFIER | c.102+1700G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 2/6 | chr6 | 149371799 | ||||||
| chr6:149371901
|
A | G | 1 | a0001c0001t0005g0118 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.102+1802A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 2/6 | chr6 | 149371901 | ||||||
| chr6:149371927
|
C | T | 9 | a0001c0001t0005g0117a0001c0001t0005g0118a0001c0001t0005g0179others(6): Show | 9 | HG01243.hp2 HG02602.hp2 HG02683.hp1 others(6): Show |
intron_variant | MODIFIER | c.102+1828C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 2/6 | chr6 | 149371927 | ||||||
| chr6:149372001
|
C | G | 63 | a0001c0001t0003g0005a0001c0001t0003g0167a0001c0001t0003g0168others(60): Show | 63 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.102+1902C>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 2/6 | chr6 | 149372001 | ||||||
| chr6:149372022
|
A | G | 4 | a0001c0001t0013g0177a0001c0001t0013g0178a0001c0001t0017g0022others(1): Show | 4 | HG02109.hp1 HG02615.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.102+1923A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 2/6 | chr6 | 149372022 | ||||||
| chr6:149372131
|
G | A | 2 | a0001c0001t0013g0177a0001c0001t0013g0178 | 2 | HG02109.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.102+2032G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 2/6 | chr6 | 149372131 | ||||||
| chr6:149372131
|
G | C | 150 | a0001c0001t0003g0005a0001c0001t0003g0167a0001c0001t0003g0168others(147): Show | 150 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(147): Show |
intron_variant | MODIFIER | c.102+2032G>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 2/6 | chr6 | 149372131 | ||||||
| chr6:149372182
|
T | A | 1 | a0001c0002t0002g0111 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.102+2083T>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 2/6 | chr6 | 149372182 | ||||||
| chr6:149372183
|
C | A | 87 | a0001c0002t0002g0096a0001c0002t0002g0097a0001c0002t0002g0098others(84): Show | 87 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.102+2084C>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 2/6 | chr6 | 149372183 | ||||||
| chr6:149372263
|
A | C | 18 | a0001c0001t0001g0002a0001c0001t0001g0086a0001c0001t0001g0087others(15): Show | 19 | HG01081.hp1 HG01109.hp2 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.102+2164A>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 2/6 | chr6 | 149372263 | ||||||
| chr6:149372476
|
T | C | 297 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(294): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.102+2377T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 2/6 | chr6 | 149372476 | ||||||
| chr6:149372556
|
A | T | 1 | a0001c0001t0003g0350 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.102+2457A>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 2/6 | chr6 | 149372556 | ||||||
| chr6:149372648
|
C | A | 63 | a0001c0001t0003g0005a0001c0001t0003g0167a0001c0001t0003g0168others(60): Show | 63 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.102+2549C>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 2/6 | chr6 | 149372648 | ||||||
| chr6:149373269
|
T | A | 1 | a0001c0001t0001g0257 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.102+3170T>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 2/6 | chr6 | 149373269 | ||||||
| chr6:149373270
|
T | A | 1 | a0001c0001t0001g0257 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.102+3171T>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 2/6 | chr6 | 149373270 | ||||||
| chr6:149373271
|
T | A | 1 | a0001c0001t0001g0257 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.102+3172T>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 2/6 | chr6 | 149373271 | ||||||
| chr6:149373272
|
T | A | 1 | a0001c0001t0001g0257 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.102+3173T>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 2/6 | chr6 | 149373272 | ||||||
| chr6:149373512
|
T | TG | 21 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0070others(18): Show | 21 | HG01884.hp2 HG02055.hp1 HG02145.hp2 others(18): Show |
intron_variant | MODIFIER | c.102+3414dupG | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr6 | 149373512 | |||||
| chr6:149373894
|
T | A | 1 | a0001c0001t0005g0179 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.102+3795T>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 2/6 | chr6 | 149373894 | ||||||
| chr6:149374051
|
C | T | 8 | a0001c0001t0005g0117a0001c0001t0005g0118a0001c0001t0005g0179others(5): Show | 8 | HG01243.hp2 HG02602.hp2 HG02683.hp1 others(5): Show |
intron_variant | MODIFIER | c.102+3952C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 2/6 | chr6 | 149374051 | ||||||
| chr6:149374052
|
T | C | 18 | a0001c0001t0003g0167a0001c0001t0003g0168a0001c0001t0003g0169others(15): Show | 18 | HG00609.hp2 HG01109.hp1 HG01167.hp2 others(15): Show |
intron_variant | MODIFIER | c.102+3953T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 2/6 | chr6 | 149374052 | ||||||
| chr6:149374079
|
G | A | 1 | a0001c0001t0001g0138 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.103-3939G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 2/6 | chr6 | 149374079 | ||||||
| chr6:149374208
|
T | C | 63 | a0001c0001t0003g0005a0001c0001t0003g0167a0001c0001t0003g0168others(60): Show | 63 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.103-3810T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 2/6 | chr6 | 149374208 | ||||||
| chr6:149374224
|
T | C | 1 | a0001c0001t0017g0022 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.103-3794T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 2/6 | chr6 | 149374224 | ||||||
| chr6:149374914
|
C | T | 2 | a0001c0001t0001g0016a0001c0001t0001g0017 | 2 | HG02895.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.103-3104C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 2/6 | chr6 | 149374914 | ||||||
| chr6:149375030
|
T | C | 63 | a0001c0001t0003g0005a0001c0001t0003g0167a0001c0001t0003g0168others(60): Show | 63 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.103-2988T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 2/6 | chr6 | 149375030 | ||||||
| chr6:149375118
|
A | G | 6 | a0001c0001t0003g0308a0001c0001t0003g0309a0001c0001t0003g0311others(3): Show | 6 | HG02129.hp1 NA18950.hp1 NA18977.hp2 others(3): Show |
intron_variant | MODIFIER | c.103-2900A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 2/6 | chr6 | 149375118 | ||||||
| chr6:149375139
|
T | C | 4 | a0001c0001t0013g0177a0001c0001t0013g0178a0001c0001t0017g0022others(1): Show | 4 | HG02109.hp1 HG02615.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.103-2879T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 2/6 | chr6 | 149375139 | ||||||
| chr6:149375145
|
C | T | 11 | a0001c0001t0007g0074a0001c0001t0007g0075a0001c0001t0007g0076others(8): Show | 11 | HG02055.hp1 HG02145.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.103-2873C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 2/6 | chr6 | 149375145 | ||||||
| chr6:149375404
|
G | C | 1 | a0001c0001t0004g0063 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.103-2614G>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 2/6 | chr6 | 149375404 | ||||||
| chr6:149375414
|
A | G | 1 | a0001c0002t0002g0235 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.103-2604A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 2/6 | chr6 | 149375414 | ||||||
| chr6:149375507
|
G | A | 3 | a0001c0002t0006g0210a0001c0002t0006g0211a0001c0002t0006g0238 | 3 | NA18962.hp1 NA19062.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.103-2511G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 2/6 | chr6 | 149375507 | ||||||
| chr6:149375841
|
G | A | 6 | a0001c0001t0007g0074a0001c0001t0007g0075a0001c0001t0007g0076others(3): Show | 6 | HG02630.hp2 HG03225.hp1 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.103-2177G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 2/6 | chr6 | 149375841 | ||||||
| chr6:149375970
|
C | G | 63 | a0001c0001t0003g0005a0001c0001t0003g0167a0001c0001t0003g0168others(60): Show | 63 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.103-2048C>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 2/6 | chr6 | 149375970 | ||||||
| chr6:149376196
|
C | T | 2 | a0001c0002t0002g0249a0001c0002t0002g0250 | 2 | HG01943.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.103-1822C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 2/6 | chr6 | 149376196 | ||||||
| chr6:149376428
|
A | G | 63 | a0001c0001t0003g0005a0001c0001t0003g0167a0001c0001t0003g0168others(60): Show | 63 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.103-1590A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 2/6 | chr6 | 149376428 | ||||||
| chr6:149376558
|
T | C | 3 | a0001c0001t0013g0177a0001c0001t0013g0178a0001c0001t0022g0176 | 3 | HG02109.hp1 HG02615.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.103-1460T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 2/6 | chr6 | 149376558 | ||||||
| chr6:149376624
|
C | T | 87 | a0001c0002t0002g0096a0001c0002t0002g0097a0001c0002t0002g0098others(84): Show | 87 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.103-1394C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 2/6 | chr6 | 149376624 | ||||||
| chr6:149376886
|
T | TC | 64 | a0001c0001t0003g0005a0001c0001t0003g0167a0001c0001t0003g0168others(61): Show | 64 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(61): Show |
intron_variant | MODIFIER | c.103-1122dupC | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr6 | 149376886 | |||||
| chr6:149376886
|
TC | T | 27 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(24): Show | 27 | HG02145.hp1 HG02155.hp1 HG02258.hp1 others(24): Show |
intron_variant | MODIFIER | c.103-1122delC | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr6 | 149376886 | |||||
| chr6:149376888
|
C | A | 1 | a0001c0002t0002g0097 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.103-1130C>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 2/6 | chr6 | 149376888 | ||||||
| chr6:149376920
|
G | A | 6 | a0001c0001t0007g0074a0001c0001t0007g0075a0001c0001t0007g0076others(3): Show | 6 | HG02630.hp2 HG03225.hp1 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.103-1098G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 2/6 | chr6 | 149376920 | ||||||
| chr6:149376996
|
G | A | 1 | a0001c0001t0005g0253 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.103-1022G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 2/6 | chr6 | 149376996 | ||||||
| chr6:149377067
|
CTT | C | 62 | a0001c0001t0003g0005a0001c0001t0003g0167a0001c0001t0003g0168others(59): Show | 62 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.103-950_103-949del others(2): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 2/6 | chr6 | 149377067 | ||||||
| chr6:149377070
|
A | AT | 10 | a0001c0001t0001g0008a0001c0001t0001g0069a0001c0001t0001g0159others(7): Show | 10 | HG00733.hp1 HG02145.hp1 HG02273.hp1 others(7): Show |
intron_variant | MODIFIER | c.103-931dupT | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr6 | 149377070 | |||||
| chr6:149377070
|
A | ATT | 15 | a0001c0001t0001g0068a0001c0001t0001g0070a0001c0001t0001g0072others(12): Show | 15 | HG01884.hp2 HG02257.hp1 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.103-932_103-931dup others(2): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr6 | 149377070 | |||||
| chr6:149377070
|
AT | A | 87 | a0001c0001t0001g0017a0001c0001t0004g0028a0001c0001t0013g0178others(84): Show | 87 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.103-931delT | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr6 | 149377070 | |||||
| chr6:149377071
|
T | A | 1 | a0001c0001t0003g0318 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.103-947T>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 2/6 | chr6 | 149377071 | ||||||
| chr6:149377143
|
C | A | 9 | a0001c0001t0004g0023a0001c0001t0004g0024a0001c0001t0004g0025others(6): Show | 9 | HG02258.hp1 HG02559.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.103-875C>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 2/6 | chr6 | 149377143 | ||||||
| chr6:149377163
|
A | G | 153 | a0001c0001t0003g0005a0001c0001t0003g0167a0001c0001t0003g0168others(150): Show | 153 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(150): Show |
intron_variant | MODIFIER | c.103-855A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 2/6 | chr6 | 149377163 | ||||||
| chr6:149377163
|
A | GGGTTCAC others(471): Show |
5 | a0001c0001t0009g0079a0001c0001t0009g0080a0001c0001t0009g0081others(2): Show | 5 | HG02055.hp1 HG02145.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.103-856_103-855ins others(478): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 2/6 | chr6 | 149377163 | ||||||
| chr6:149377168
|
C | T | 6 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0070others(3): Show | 6 | HG01884.hp2 HG02257.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.103-850C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 2/6 | chr6 | 149377168 | ||||||
| chr6:149377245
|
T | G | 9 | a0001c0001t0005g0117a0001c0001t0005g0118a0001c0001t0005g0179others(6): Show | 9 | HG01243.hp2 HG02602.hp2 HG02683.hp1 others(6): Show |
intron_variant | MODIFIER | c.103-773T>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 2/6 | chr6 | 149377245 | ||||||
| chr6:149377265
|
A | G | 297 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(294): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.103-753A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 2/6 | chr6 | 149377265 | ||||||
| chr6:149377295
|
G | A | 1 | a0001c0001t0004g0031 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.103-723G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 2/6 | chr6 | 149377295 | ||||||
| chr6:149377485
|
G | T | 1 | a0001c0001t0001g0281 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.103-533G>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 2/6 | chr6 | 149377485 | ||||||
| chr6:149377508
|
T | A | 1 | a0001c0001t0017g0022 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.103-510T>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 2/6 | chr6 | 149377508 | ||||||
| chr6:149377677
|
T | G | 21 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0070others(18): Show | 21 | HG01884.hp2 HG02055.hp1 HG02145.hp2 others(18): Show |
intron_variant | MODIFIER | c.103-341T>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 2/6 | chr6 | 149377677 | ||||||
| chr6:149377766
|
G | T | 313 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(310): Show | 315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.103-252G>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 2/6 | chr6 | 149377766 | ||||||
| chr6:149377814
|
TAGTC | T | 63 | a0001c0001t0003g0005a0001c0001t0003g0167a0001c0001t0003g0168others(60): Show | 63 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.103-201_103-198del others(4): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr6 | 149377814 | |||||
| chr6:149377873
|
A | G | 1 | a0001c0002t0002g0096 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.103-145A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 2/6 | chr6 | 149377873 | ||||||
| chr6:149377880
|
A | T | 297 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(294): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.103-138A>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 2/6 | chr6 | 149377880 | ||||||
| chr6:149379569
|
G | T | 1 | a0001c0001t0004g0060 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.1603+51G>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149379569 | ||||||
| chr6:149379669
|
G | A | 297 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(294): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.1603+151G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149379669 | ||||||
| chr6:149379733
|
T | G | 1 | a0001c0001t0001g0274 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1603+215T>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149379733 | ||||||
| chr6:149379737
|
A | T | 63 | a0001c0001t0003g0005a0001c0001t0003g0167a0001c0001t0003g0168others(60): Show | 63 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.1603+219A>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149379737 | ||||||
| chr6:149379806
|
C | G | 63 | a0001c0001t0003g0005a0001c0001t0003g0167a0001c0001t0003g0168others(60): Show | 63 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.1603+288C>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149379806 | ||||||
| chr6:149379915
|
A | G | 1 | a0001c0001t0003g0350 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1603+397A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149379915 | ||||||
| chr6:149380045
|
G | A | 1 | a0001c0001t0001g0301 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1603+527G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149380045 | ||||||
| chr6:149380115
|
C | T | 4 | a0001c0001t0008g0021a0001c0001t0013g0177a0001c0001t0013g0178others(1): Show | 4 | HG02109.hp1 HG02615.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1603+597C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149380115 | ||||||
| chr6:149380333
|
C | T | 63 | a0001c0001t0003g0005a0001c0001t0003g0167a0001c0001t0003g0168others(60): Show | 63 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.1603+815C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149380333 | ||||||
| chr6:149380399
|
A | T | 63 | a0001c0001t0003g0005a0001c0001t0003g0167a0001c0001t0003g0168others(60): Show | 63 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.1603+881A>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149380399 | ||||||
| chr6:149380475
|
CTA | C | 147 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(144): Show | 149 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(146): Show |
intron_variant | MODIFIER | c.1603+959_1603+960d others(4): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr6 | 149380475 | |||||
| chr6:149380766
|
T | C | 4 | a0001c0001t0013g0177a0001c0001t0013g0178a0001c0001t0017g0022others(1): Show | 4 | HG02109.hp1 HG02615.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.1603+1248T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149380766 | ||||||
| chr6:149380857
|
T | TTTGCCTT others(2102): Show |
1 | a0001c0001t0003g0321 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1603+1358_1603+135 others(2113): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr6 | 149380857 | |||||
| chr6:149380901
|
G | A | 3 | a0001c0001t0003g0317a0001c0001t0003g0318a0001c0001t0003g0319 | 3 | HG00140.hp2 HG01168.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.1603+1383G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149380901 | ||||||
| chr6:149380938
|
C | G | 21 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0070others(18): Show | 21 | HG01884.hp2 HG02055.hp1 HG02145.hp2 others(18): Show |
intron_variant | MODIFIER | c.1603+1420C>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149380938 | ||||||
| chr6:149380990
|
C | A | 13 | a0001c0001t0003g0172a0001c0001t0003g0317a0001c0001t0003g0318others(10): Show | 13 | HG00140.hp2 HG01168.hp2 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.1603+1472C>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149380990 | ||||||
| chr6:149381032
|
A | G | 1 | a0001c0002t0002g0098 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1603+1514A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149381032 | ||||||
| chr6:149381057
|
C | T | 1 | a0001c0002t0006g0240 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1603+1539C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149381057 | ||||||
| chr6:149381090
|
C | T | 18 | a0001c0001t0003g0167a0001c0001t0003g0168a0001c0001t0003g0169others(15): Show | 18 | HG00609.hp2 HG01109.hp1 HG01167.hp2 others(15): Show |
intron_variant | MODIFIER | c.1603+1572C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149381090 | ||||||
| chr6:149381110
|
G | A | 1 | a0001c0001t0001g0008 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1603+1592G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149381110 | ||||||
| chr6:149381168
|
G | A | 1 | a0001c0001t0022g0176 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1603+1650G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149381168 | ||||||
| chr6:149381434
|
A | G | 4 | a0001c0001t0013g0177a0001c0001t0013g0178a0001c0001t0017g0022others(1): Show | 4 | HG02109.hp1 HG02615.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.1603+1916A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149381434 | ||||||
| chr6:149381514
|
A | G | 17 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0070others(14): Show | 17 | HG01884.hp2 HG02055.hp1 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.1603+1996A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149381514 | ||||||
| chr6:149381547
|
T | A | 1 | a0001c0001t0004g0039 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1603+2029T>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149381547 | ||||||
| chr6:149381569
|
C | CT | 79 | a0001c0001t0001g0132a0001c0001t0001g0148a0001c0001t0001g0265others(76): Show | 79 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(76): Show |
intron_variant | MODIFIER | c.1603+2073dupT | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr6 | 149381569 | |||||
| chr6:149381569
|
C | CTT | 9 | a0001c0001t0003g0308a0001c0001t0003g0310a0001c0001t0003g0313others(6): Show | 9 | HG01891.hp2 HG02135.hp1 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.1603+2072_1603+207 others(6): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr6 | 149381569 | |||||
| chr6:149381569
|
CT | C | 95 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(92): Show | 96 | HG00733.hp1 HG00733.hp2 HG00735.hp1 others(93): Show |
intron_variant | MODIFIER | c.1603+2073delT | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr6 | 149381569 | |||||
| chr6:149381569
|
CTT | C | 10 | a0001c0001t0007g0074a0001c0001t0007g0075a0001c0001t0007g0076others(7): Show | 10 | HG02055.hp1 HG02145.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.1603+2072_1603+207 others(6): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr6 | 149381569 | |||||
| chr6:149381591
|
T | G | 1 | a0001c0008t0018g0293 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1603+2073T>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149381591 | ||||||
| chr6:149381591
|
T | TG | 70 | a0001c0002t0002g0100a0001c0002t0002g0101a0001c0002t0002g0102others(67): Show | 70 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(67): Show |
intron_variant | MODIFIER | c.1603+2076dupG | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr6 | 149381591 | |||||
| chr6:149381613
|
G | A | 1 | a0001c0002t0002g0102 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1603+2095G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149381613 | ||||||
| chr6:149381729
|
C | T | 1 | a0001c0001t0004g0055 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1603+2211C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149381729 | ||||||
| chr6:149381743
|
T | C | 2 | a0001c0001t0001g0274a0001c0001t0001g0302 | 2 | HG01496.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.1603+2225T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149381743 | ||||||
| chr6:149381762
|
A | G | 2 | a0001c0001t0001g0159a0001c0001t0001g0160 | 2 | NA18987.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.1603+2244A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149381762 | ||||||
| chr6:149381786
|
TG | T | 4 | a0001c0001t0013g0177a0001c0001t0013g0178a0001c0001t0017g0022others(1): Show | 4 | HG02109.hp1 HG02615.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.1603+2270delG | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr6 | 149381786 | |||||
| chr6:149381812
|
A | T | 9 | a0001c0001t0005g0117a0001c0001t0005g0118a0001c0001t0005g0179others(6): Show | 9 | HG01243.hp2 HG02602.hp2 HG02683.hp1 others(6): Show |
intron_variant | MODIFIER | c.1603+2294A>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149381812 | ||||||
| chr6:149381999
|
C | A | 2 | a0001c0001t0001g0018a0001c0001t0001g0019 | 2 | HG03209.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1603+2481C>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149381999 | ||||||
| chr6:149382307
|
C | G | 5 | a0001c0001t0003g0305a0001c0001t0003g0325a0001c0001t0003g0326others(2): Show | 5 | HG02647.hp1 HG02970.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1603+2789C>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149382307 | ||||||
| chr6:149382335
|
C | T | 1 | a0001c0001t0017g0022 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1603+2817C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149382335 | ||||||
| chr6:149382412
|
A | G | 87 | a0001c0002t0002g0096a0001c0002t0002g0097a0001c0002t0002g0098others(84): Show | 87 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1603+2894A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149382412 | ||||||
| chr6:149382597
|
GA | G | 13 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0007g0074others(10): Show | 13 | HG02055.hp1 HG02145.hp2 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.1603+3092delA | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr6 | 149382597 | |||||
| chr6:149382640
|
A | G | 1 | a0001c0001t0003g0349 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1603+3122A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149382640 | ||||||
| chr6:149382650
|
C | T | 2 | a0001c0001t0001g0130a0001c0001t0001g0131 | 2 | NA18968.hp2 NA19072.hp2 |
intron_variant | MODIFIER | c.1603+3132C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149382650 | ||||||
| chr6:149382690
|
C | A | 1 | a0001c0002t0014g0110 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.1603+3172C>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149382690 | ||||||
| chr6:149382707
|
T | C | 2 | a0001c0001t0003g0315a0001c0001t0003g0316 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1603+3189T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149382707 | ||||||
| chr6:149382752
|
G | C | 1 | a0001c0002t0002g0096 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1603+3234G>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149382752 | ||||||
| chr6:149382785
|
T | A | 87 | a0001c0002t0002g0096a0001c0002t0002g0097a0001c0002t0002g0098others(84): Show | 87 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1603+3267T>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149382785 | ||||||
| chr6:149382822
|
T | C | 1 | a0001c0001t0008g0163 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1603+3304T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149382822 | ||||||
| chr6:149383024
|
G | C | 18 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0070others(15): Show | 18 | HG01884.hp2 HG02055.hp1 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.1603+3506G>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149383024 | ||||||
| chr6:149383104
|
G | A | 63 | a0001c0001t0003g0005a0001c0001t0003g0167a0001c0001t0003g0168others(60): Show | 63 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.1603+3586G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149383104 | ||||||
| chr6:149383174
|
A | G | 7 | a0001c0001t0003g0321a0001c0001t0003g0328a0001c0001t0003g0329others(4): Show | 7 | HG01192.hp2 HG01891.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.1603+3656A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149383174 | ||||||
| chr6:149383356
|
T | A | 1 | a0001c0001t0004g0183 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1603+3838T>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149383356 | ||||||
| chr6:149383390
|
G | A | 297 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(294): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.1603+3872G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149383390 | ||||||
| chr6:149383506
|
A | G | 4 | a0001c0001t0008g0021a0001c0001t0008g0163a0001c0001t0008g0164others(1): Show | 4 | HG02280.hp1 HG02717.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1603+3988A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149383506 | ||||||
| chr6:149383616
|
A | T | 63 | a0001c0001t0003g0005a0001c0001t0003g0167a0001c0001t0003g0168others(60): Show | 63 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.1603+4098A>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149383616 | ||||||
| chr6:149383740
|
G | A | 8 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(5): Show | 8 | HG02895.hp1 HG02895.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.1603+4222G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149383740 | ||||||
| chr6:149383765
|
G | C | 174 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0070others(171): Show | 174 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(171): Show |
intron_variant | MODIFIER | c.1603+4247G>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149383765 | ||||||
| chr6:149383875
|
A | C | 8 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(5): Show | 8 | HG02895.hp1 HG02895.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.1603+4357A>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149383875 | ||||||
| chr6:149383926
|
G | A | 3 | a0001c0001t0004g0060a0001c0001t0004g0061a0001c0001t0004g0063 | 3 | NA18962.hp2 NA19066.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.1603+4408G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149383926 | ||||||
| chr6:149384226
|
A | G | 1 | a0001c0002t0002g0099 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1603+4708A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149384226 | ||||||
| chr6:149384442
|
C | T | 21 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0070others(18): Show | 21 | HG01884.hp2 HG02055.hp1 HG02145.hp2 others(18): Show |
intron_variant | MODIFIER | c.1603+4924C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149384442 | ||||||
| chr6:149384499
|
T | C | 63 | a0001c0001t0003g0005a0001c0001t0003g0167a0001c0001t0003g0168others(60): Show | 63 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.1603+4981T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149384499 | ||||||
| chr6:149384793
|
A | G | 87 | a0001c0002t0002g0096a0001c0002t0002g0097a0001c0002t0002g0098others(84): Show | 87 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1603+5275A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149384793 | ||||||
| chr6:149384795
|
C | T | 21 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0070others(18): Show | 21 | HG01884.hp2 HG02055.hp1 HG02145.hp2 others(18): Show |
intron_variant | MODIFIER | c.1603+5277C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149384795 | ||||||
| chr6:149384940
|
C | CT | 8 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(5): Show | 8 | HG02895.hp1 HG02895.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.1603+5427dupT | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr6 | 149384940 | |||||
| chr6:149384949
|
A | T | 21 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0070others(18): Show | 21 | HG01884.hp2 HG02055.hp1 HG02145.hp2 others(18): Show |
intron_variant | MODIFIER | c.1603+5431A>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149384949 | ||||||
| chr6:149385041
|
A | G | 4 | a0001c0001t0013g0177a0001c0001t0013g0178a0001c0001t0017g0022others(1): Show | 4 | HG02109.hp1 HG02615.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.1603+5523A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149385041 | ||||||
| chr6:149385388
|
G | T | 2 | a0001c0001t0005g0180a0001c0001t0005g0181 | 2 | HG02683.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.1603+5870G>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149385388 | ||||||
| chr6:149385418
|
T | C | 63 | a0001c0001t0003g0005a0001c0001t0003g0167a0001c0001t0003g0168others(60): Show | 63 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.1603+5900T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149385418 | ||||||
| chr6:149385473
|
G | A | 1 | a0001c0001t0004g0023 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1603+5955G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149385473 | ||||||
| chr6:149385570
|
A | C | 21 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0070others(18): Show | 21 | HG01884.hp2 HG02055.hp1 HG02145.hp2 others(18): Show |
intron_variant | MODIFIER | c.1603+6052A>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149385570 | ||||||
| chr6:149385748
|
T | C | 1 | a0001c0001t0001g0006 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1603+6230T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149385748 | ||||||
| chr6:149385761
|
G | A | 4 | a0001c0001t0013g0177a0001c0001t0013g0178a0001c0001t0017g0022others(1): Show | 4 | HG02109.hp1 HG02615.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.1603+6243G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149385761 | ||||||
| chr6:149386152
|
A | G | 150 | a0001c0001t0003g0005a0001c0001t0003g0167a0001c0001t0003g0168others(147): Show | 150 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(147): Show |
intron_variant | MODIFIER | c.1603+6634A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149386152 | ||||||
| chr6:149386240
|
G | A | 6 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0070others(3): Show | 6 | HG01884.hp2 HG02257.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1603+6722G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149386240 | ||||||
| chr6:149386248
|
A | G | 1 | a0001c0001t0001g0291 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1603+6730A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149386248 | ||||||
| chr6:149386254
|
C | A | 1 | a0001c0001t0003g0331 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1603+6736C>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149386254 | ||||||
| chr6:149386331
|
T | C | 4 | a0001c0001t0013g0177a0001c0001t0013g0178a0001c0001t0017g0022others(1): Show | 4 | HG02109.hp1 HG02615.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.1603+6813T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149386331 | ||||||
| chr6:149386453
|
AC | A | 64 | a0001c0001t0003g0005a0001c0001t0003g0167a0001c0001t0003g0168others(61): Show | 64 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(61): Show |
intron_variant | MODIFIER | c.1603+6941delC | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr6 | 149386453 | |||||
| chr6:149386515
|
A | G | 87 | a0001c0002t0002g0096a0001c0002t0002g0097a0001c0002t0002g0098others(84): Show | 87 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1603+6997A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149386515 | ||||||
| chr6:149386665
|
T | G | 1 | a0001c0002t0002g0102 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1603+7147T>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149386665 | ||||||
| chr6:149386668
|
T | G | 57 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(54): Show | 57 | HG00733.hp2 HG00735.hp1 HG01069.hp2 others(54): Show |
intron_variant | MODIFIER | c.1603+7150T>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149386668 | ||||||
| chr6:149386706
|
C | G | 2 | a0001c0001t0005g0180a0001c0001t0005g0181 | 2 | HG02683.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.1603+7188C>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149386706 | ||||||
| chr6:149386706
|
C | T | 1 | a0001c0001t0004g0037 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1603+7188C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149386706 | ||||||
| chr6:149386778
|
G | A | 1 | a0001c0001t0017g0022 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1603+7260G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149386778 | ||||||
| chr6:149387029
|
C | T | 2 | a0001c0001t0003g0305a0001c0001t0019g0306 | 2 | HG02970.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1603+7511C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149387029 | ||||||
| chr6:149387232
|
T | C | 65 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(62): Show | 65 | HG00733.hp2 HG00735.hp1 HG01069.hp2 others(62): Show |
intron_variant | MODIFIER | c.1603+7714T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149387232 | ||||||
| chr6:149387276
|
C | G | 5 | a0001c0001t0001g0267a0001c0001t0001g0273a0001c0001t0001g0277others(2): Show | 5 | HG01069.hp1 HG01123.hp1 HG01168.hp1 others(2): Show |
intron_variant | MODIFIER | c.1603+7758C>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149387276 | ||||||
| chr6:149387288
|
C | T | 6 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(3): Show | 6 | HG00733.hp2 HG02145.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.1603+7770C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149387288 | ||||||
| chr6:149387405
|
A | T | 1 | a0001c0001t0001g0187 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1603+7887A>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149387405 | ||||||
| chr6:149387449
|
A | G | 1 | a0001c0001t0001g0175 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1603+7931A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149387449 | ||||||
| chr6:149387494
|
G | A | 1 | a0001c0001t0008g0021 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1603+7976G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149387494 | ||||||
| chr6:149387631
|
A | G | 1 | a0001c0001t0005g0179 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1603+8113A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149387631 | ||||||
| chr6:149387642
|
A | T | 1 | a0001c0001t0001g0068 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1603+8124A>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149387642 | ||||||
| chr6:149387803
|
CT | C | 87 | a0001c0002t0002g0096a0001c0002t0002g0097a0001c0002t0002g0098others(84): Show | 87 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1603+8293delT | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr6 | 149387803 | |||||
| chr6:149387973
|
G | A | 18 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0070others(15): Show | 18 | HG01884.hp2 HG02055.hp1 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.1603+8455G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149387973 | ||||||
| chr6:149388015
|
T | C | 1 | a0001c0001t0003g0321 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1603+8497T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149388015 | ||||||
| chr6:149388077
|
G | T | 1 | a0001c0002t0002g0107 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1603+8559G>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149388077 | ||||||
| chr6:149388197
|
C | T | 1 | a0001c0001t0001g0153 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1603+8679C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149388197 | ||||||
| chr6:149388243
|
C | T | 1 | a0001c0001t0003g0336 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1603+8725C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149388243 | ||||||
| chr6:149388675
|
T | C | 3 | a0001c0002t0002g0215a0001c0002t0002g0234a0001c0002t0002g0235 | 3 | HG02129.hp2 NA19067.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.1604-8929T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149388675 | ||||||
| chr6:149388765
|
C | T | 1 | a0001c0001t0001g0127 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1604-8839C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149388765 | ||||||
| chr6:149388851
|
A | G | 1 | a0001c0002t0002g0111 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1604-8753A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149388851 | ||||||
| chr6:149388954
|
C | CT | 18 | a0001c0001t0001g0141a0001c0001t0001g0258a0001c0001t0001g0268others(15): Show | 18 | HG02055.hp1 HG02145.hp2 HG02280.hp1 others(15): Show |
intron_variant | MODIFIER | c.1604-8631dupT | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr6 | 149388954 | |||||
| chr6:149388954
|
CT | C | 214 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(211): Show | 214 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(211): Show |
intron_variant | MODIFIER | c.1604-8631delT | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr6 | 149388954 | |||||
| chr6:149389066
|
C | T | 87 | a0001c0002t0002g0096a0001c0002t0002g0097a0001c0002t0002g0098others(84): Show | 87 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1604-8538C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149389066 | ||||||
| chr6:149389167
|
G | A | 1 | a0001c0001t0001g0302 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1604-8437G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149389167 | ||||||
| chr6:149389171
|
G | A | 21 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0070others(18): Show | 21 | HG01884.hp2 HG02055.hp1 HG02145.hp2 others(18): Show |
intron_variant | MODIFIER | c.1604-8433G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149389171 | ||||||
| chr6:149389261
|
T | C | 1 | a0001c0001t0001g0013 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1604-8343T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149389261 | ||||||
| chr6:149389361
|
T | C | 150 | a0001c0001t0003g0005a0001c0001t0003g0167a0001c0001t0003g0168others(147): Show | 150 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(147): Show |
intron_variant | MODIFIER | c.1604-8243T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149389361 | ||||||
| chr6:149389527
|
T | C | 237 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(234): Show | 237 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(234): Show |
intron_variant | MODIFIER | c.1604-8077T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149389527 | ||||||
| chr6:149389645
|
C | CA | 35 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0072others(32): Show | 35 | HG01261.hp1 HG01496.hp1 HG02145.hp2 others(32): Show |
intron_variant | MODIFIER | c.1604-7939dupA | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr6 | 149389645 | |||||
| chr6:149389645
|
CA | C | 8 | a0001c0001t0001g0147a0001c0001t0003g0325a0001c0001t0008g0021others(5): Show | 8 | HG02109.hp1 HG02280.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.1604-7939delA | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr6 | 149389645 | |||||
| chr6:149389645
|
CAA | C | 62 | a0001c0001t0003g0005a0001c0001t0003g0167a0001c0001t0003g0168others(59): Show | 62 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.1604-7940_1604-793 others(6): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr6 | 149389645 | |||||
| chr6:149389679
|
CT | C | 87 | a0001c0002t0002g0096a0001c0002t0002g0097a0001c0002t0002g0098others(84): Show | 87 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1604-7924delT | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149389679 | ||||||
| chr6:149389703
|
G | A | 5 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0018others(2): Show | 5 | HG02895.hp2 HG02897.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.1604-7901G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149389703 | ||||||
| chr6:149389712
|
C | T | 250 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(247): Show | 250 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(247): Show |
intron_variant | MODIFIER | c.1604-7892C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149389712 | ||||||
| chr6:149389902
|
T | G | 1 | a0001c0001t0001g0269 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1604-7702T>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149389902 | ||||||
| chr6:149389905
|
A | G | 1 | a0001c0001t0001g0257 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1604-7699A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149389905 | ||||||
| chr6:149389935
|
A | G | 5 | a0001c0001t0009g0079a0001c0001t0009g0080a0001c0001t0009g0081others(2): Show | 5 | HG02055.hp1 HG02145.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.1604-7669A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149389935 | ||||||
| chr6:149389975
|
A | G | 17 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0070others(14): Show | 17 | HG01884.hp2 HG02055.hp1 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.1604-7629A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149389975 | ||||||
| chr6:149390141
|
T | C | 1 | a0001c0001t0022g0176 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1604-7463T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149390141 | ||||||
| chr6:149390151
|
A | G | 1 | a0001c0001t0001g0280 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1604-7453A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149390151 | ||||||
| chr6:149390485
|
T | C | 3 | a0001c0001t0007g0075a0001c0001t0007g0083a0001c0001t0024g0078 | 3 | HG02630.hp2 HG03486.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1604-7119T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149390485 | ||||||
| chr6:149390668
|
G | T | 1 | a0001c0001t0008g0021 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1604-6936G>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149390668 | ||||||
| chr6:149390686
|
T | C | 1 | a0001c0001t0001g0273 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1604-6918T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149390686 | ||||||
| chr6:149390718
|
A | G | 2 | a0001c0001t0013g0177a0001c0001t0013g0178 | 2 | HG02109.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.1604-6886A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149390718 | ||||||
| chr6:149390726
|
A | C | 150 | a0001c0001t0003g0005a0001c0001t0003g0167a0001c0001t0003g0168others(147): Show | 150 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(147): Show |
intron_variant | MODIFIER | c.1604-6878A>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149390726 | ||||||
| chr6:149390726
|
A | T | 121 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(118): Show | 122 | HG00733.hp2 HG00735.hp1 HG00738.hp1 others(119): Show |
intron_variant | MODIFIER | c.1604-6878A>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149390726 | ||||||
| chr6:149390847
|
G | C | 87 | a0001c0002t0002g0096a0001c0002t0002g0097a0001c0002t0002g0098others(84): Show | 87 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1604-6757G>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149390847 | ||||||
| chr6:149390859
|
A | G | 1 | a0001c0002t0002g0235 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.1604-6745A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149390859 | ||||||
| chr6:149390902
|
C | G | 6 | a0001c0001t0001g0161a0001c0001t0001g0162a0001c0001t0001g0298others(3): Show | 6 | HG02280.hp1 HG02622.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1604-6702C>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149390902 | ||||||
| chr6:149391274
|
A | G | 2 | a0001c0001t0001g0275a0001c0008t0018g0293 | 2 | HG02080.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.1604-6330A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149391274 | ||||||
| chr6:149391282
|
C | G | 1 | a0001c0001t0008g0021 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1604-6322C>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149391282 | ||||||
| chr6:149391362
|
C | T | 11 | a0001c0001t0007g0074a0001c0001t0007g0075a0001c0001t0007g0076others(8): Show | 11 | HG02055.hp1 HG02145.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.1604-6242C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149391362 | ||||||
| chr6:149391409
|
T | C | 6 | a0001c0001t0001g0092a0001c0001t0001g0143a0001c0001t0001g0144others(3): Show | 6 | HG01081.hp1 HG01884.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.1604-6195T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149391409 | ||||||
| chr6:149391419
|
T | C | 3 | a0001c0001t0011g0134a0001c0001t0011g0135a0001c0001t0011g0140 | 3 | HG01433.hp1 HG01515.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.1604-6185T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149391419 | ||||||
| chr6:149391493
|
A | G | 5 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0018others(2): Show | 5 | HG02895.hp2 HG02897.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.1604-6111A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149391493 | ||||||
| chr6:149391563
|
G | A | 87 | a0001c0002t0002g0096a0001c0002t0002g0097a0001c0002t0002g0098others(84): Show | 87 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1604-6041G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149391563 | ||||||
| chr6:149391689
|
G | A | 6 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(3): Show | 6 | HG00733.hp2 HG02145.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.1604-5915G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149391689 | ||||||
| chr6:149391800
|
G | A | 1 | a0001c0002t0014g0110 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.1604-5804G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149391800 | ||||||
| chr6:149391837
|
G | C | 1 | a0001c0001t0008g0163 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1604-5767G>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149391837 | ||||||
| chr6:149391954
|
T | C | 87 | a0001c0002t0002g0096a0001c0002t0002g0097a0001c0002t0002g0098others(84): Show | 87 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1604-5650T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149391954 | ||||||
| chr6:149392113
|
C | T | 11 | a0001c0001t0007g0074a0001c0001t0007g0075a0001c0001t0007g0076others(8): Show | 11 | HG02055.hp1 HG02145.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.1604-5491C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149392113 | ||||||
| chr6:149392145
|
C | CG | 75 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0016others(72): Show | 75 | HG00597.hp1 HG00673.hp1 HG01070.hp1 others(72): Show |
intron_variant | MODIFIER | c.1604-5452dupG | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr6 | 149392145 | |||||
| chr6:149392156
|
G | C | 1 | a0001c0001t0004g0065 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1604-5448G>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149392156 | ||||||
| chr6:149392179
|
C | T | 1 | a0001c0001t0001g0268 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1604-5425C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149392179 | ||||||
| chr6:149392248
|
C | T | 1 | a0001c0001t0022g0176 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1604-5356C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149392248 | ||||||
| chr6:149392290
|
G | A | 1 | a0001c0001t0001g0155 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1604-5314G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149392290 | ||||||
| chr6:149392640
|
TTCATTCA others(4): Show |
T | 8 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(5): Show | 8 | HG02895.hp1 HG02895.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.1604-4958_1604-494 others(15): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr6 | 149392640 | |||||
| chr6:149392727
|
G | A | 63 | a0001c0001t0003g0005a0001c0001t0003g0167a0001c0001t0003g0168others(60): Show | 63 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.1604-4877G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149392727 | ||||||
| chr6:149392759
|
C | A | 3 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009 | 3 | HG00733.hp2 HG02145.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.1604-4845C>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149392759 | ||||||
| chr6:149392940
|
AAACTCAC | A | 11 | a0001c0001t0007g0074a0001c0001t0007g0075a0001c0001t0007g0076others(8): Show | 11 | HG02055.hp1 HG02145.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.1604-4662_1604-465 others(11): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr6 | 149392940 | |||||
| chr6:149392988
|
GA | G | 18 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0070others(15): Show | 18 | HG01884.hp2 HG02055.hp1 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.1604-4615delA | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149392988 | ||||||
| chr6:149392990
|
T | C | 18 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0070others(15): Show | 18 | HG01884.hp2 HG02055.hp1 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.1604-4614T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149392990 | ||||||
| chr6:149393013
|
C | T | 50 | a0001c0001t0001g0001a0001c0001t0001g0064a0001c0001t0001g0254others(47): Show | 50 | HG00735.hp1 HG00738.hp1 HG01069.hp2 others(47): Show |
intron_variant | MODIFIER | c.1604-4591C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149393013 | ||||||
| chr6:149393026
|
A | G | 1 | a0001c0001t0001g0360 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1604-4578A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149393026 | ||||||
| chr6:149393084
|
A | T | 1 | a0001c0001t0004g0048 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.1604-4520A>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149393084 | ||||||
| chr6:149393129
|
A | T | 1 | a0001c0001t0001g0123 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1604-4475A>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149393129 | ||||||
| chr6:149393183
|
C | G | 87 | a0001c0002t0002g0096a0001c0002t0002g0097a0001c0002t0002g0098others(84): Show | 87 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1604-4421C>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149393183 | ||||||
| chr6:149393186
|
T | C | 63 | a0001c0001t0003g0005a0001c0001t0003g0167a0001c0001t0003g0168others(60): Show | 63 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.1604-4418T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149393186 | ||||||
| chr6:149393457
|
T | C | 63 | a0001c0001t0003g0005a0001c0001t0003g0167a0001c0001t0003g0168others(60): Show | 63 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.1604-4147T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149393457 | ||||||
| chr6:149393468
|
C | G | 3 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0020 | 3 | HG03209.hp1 HG03453.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1604-4136C>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149393468 | ||||||
| chr6:149393506
|
C | T | 8 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(5): Show | 8 | HG02895.hp1 HG02895.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.1604-4098C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149393506 | ||||||
| chr6:149393654
|
G | T | 87 | a0001c0002t0002g0096a0001c0002t0002g0097a0001c0002t0002g0098others(84): Show | 87 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1604-3950G>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149393654 | ||||||
| chr6:149393718
|
G | A | 63 | a0001c0001t0003g0005a0001c0001t0003g0167a0001c0001t0003g0168others(60): Show | 63 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.1604-3886G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149393718 | ||||||
| chr6:149393727
|
G | C | 1 | a0001c0001t0017g0022 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1604-3877G>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149393727 | ||||||
| chr6:149393798
|
TAAGTA | T | 10 | a0001c0001t0005g0117a0001c0001t0005g0118a0001c0001t0005g0179others(7): Show | 10 | HG01243.hp2 HG02602.hp2 HG02683.hp1 others(7): Show |
intron_variant | MODIFIER | c.1604-3802_1604-379 others(9): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr6 | 149393798 | |||||
| chr6:149393821
|
A | G | 6 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(3): Show | 6 | HG01243.hp1 HG01891.hp1 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.1604-3783A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149393821 | ||||||
| chr6:149393843
|
AT | A | 66 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(63): Show | 66 | HG00733.hp2 HG00735.hp1 HG00738.hp1 others(63): Show |
intron_variant | MODIFIER | c.1604-3754delT | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr6 | 149393843 | |||||
| chr6:149393873
|
T | C | 63 | a0001c0001t0003g0005a0001c0001t0003g0167a0001c0001t0003g0168others(60): Show | 63 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.1604-3731T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149393873 | ||||||
| chr6:149393969
|
G | A | 1 | a0001c0002t0006g0240 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1604-3635G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149393969 | ||||||
| chr6:149394107
|
G | GT | 11 | a0001c0001t0007g0074a0001c0001t0007g0075a0001c0001t0007g0076others(8): Show | 11 | HG02055.hp1 HG02145.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.1604-3489dupT | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr6 | 149394107 | |||||
| chr6:149394314
|
A | C | 1 | a0001c0001t0004g0119 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1604-3290A>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149394314 | ||||||
| chr6:149394436
|
G | T | 1 | a0001c0001t0017g0022 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1604-3168G>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149394436 | ||||||
| chr6:149394551
|
T | C | 9 | a0001c0001t0005g0117a0001c0001t0005g0118a0001c0001t0005g0179others(6): Show | 9 | HG01243.hp2 HG02602.hp2 HG02683.hp1 others(6): Show |
intron_variant | MODIFIER | c.1604-3053T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149394551 | ||||||
| chr6:149394782
|
A | G | 1 | a0001c0001t0008g0021 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1604-2822A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149394782 | ||||||
| chr6:149395036
|
A | G | 66 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(63): Show | 66 | HG00733.hp2 HG00735.hp1 HG00738.hp1 others(63): Show |
intron_variant | MODIFIER | c.1604-2568A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149395036 | ||||||
| chr6:149395129
|
AT | A | 9 | a0001c0001t0005g0117a0001c0001t0005g0118a0001c0001t0005g0179others(6): Show | 9 | HG01243.hp2 HG02602.hp2 HG02683.hp1 others(6): Show |
intron_variant | MODIFIER | c.1604-2469delT | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr6 | 149395129 | |||||
| chr6:149395167
|
A | G | 1 | a0001c0001t0005g0179 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1604-2437A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149395167 | ||||||
| chr6:149395299
|
A | G | 1 | a0001c0001t0001g0013 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1604-2305A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149395299 | ||||||
| chr6:149395361
|
T | G | 1 | a0001c0001t0008g0021 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1604-2243T>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149395361 | ||||||
| chr6:149395705
|
CT | C | 11 | a0001c0001t0001g0130a0001c0001t0001g0141a0001c0001t0005g0117others(8): Show | 11 | HG01243.hp2 HG02602.hp2 HG02683.hp1 others(8): Show |
intron_variant | MODIFIER | c.1604-1888delT | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr6 | 149395705 | |||||
| chr6:149395883
|
T | G | 9 | a0001c0001t0005g0117a0001c0001t0005g0118a0001c0001t0005g0179others(6): Show | 9 | HG01243.hp2 HG02602.hp2 HG02683.hp1 others(6): Show |
intron_variant | MODIFIER | c.1604-1721T>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149395883 | ||||||
| chr6:149396110
|
C | T | 66 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(63): Show | 66 | HG00733.hp2 HG00735.hp1 HG00738.hp1 others(63): Show |
intron_variant | MODIFIER | c.1604-1494C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149396110 | ||||||
| chr6:149396130
|
G | A | 1 | a0001c0002t0002g0221 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1604-1474G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149396130 | ||||||
| chr6:149396183
|
A | G | 66 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(63): Show | 66 | HG00733.hp2 HG00735.hp1 HG00738.hp1 others(63): Show |
intron_variant | MODIFIER | c.1604-1421A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149396183 | ||||||
| chr6:149396206
|
C | T | 87 | a0001c0002t0002g0096a0001c0002t0002g0097a0001c0002t0002g0098others(84): Show | 87 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1604-1398C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149396206 | ||||||
| chr6:149396224
|
G | A | 6 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0070others(3): Show | 6 | HG01884.hp2 HG02257.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1604-1380G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149396224 | ||||||
| chr6:149396238
|
G | A | 2 | a0001c0002t0002g0111a0001c0002t0002g0112 | 2 | HG02155.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.1604-1366G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149396238 | ||||||
| chr6:149396289
|
A | G | 250 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(247): Show | 250 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(247): Show |
intron_variant | MODIFIER | c.1604-1315A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149396289 | ||||||
| chr6:149396340
|
C | A | 184 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0070others(181): Show | 184 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(181): Show |
intron_variant | MODIFIER | c.1604-1264C>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149396340 | ||||||
| chr6:149396393
|
A | G | 4 | a0001c0001t0013g0177a0001c0001t0013g0178a0001c0001t0017g0022others(1): Show | 4 | HG02109.hp1 HG02615.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.1604-1211A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149396393 | ||||||
| chr6:149396688
|
A | G | 1 | a0001c0002t0002g0251 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.1604-916A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149396688 | ||||||
| chr6:149396905
|
A | T | 1 | a0001c0001t0003g0173 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1604-699A>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149396905 | ||||||
| chr6:149396929
|
C | A | 1 | a0001c0001t0003g0349 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1604-675C>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149396929 | ||||||
| chr6:149397004
|
A | C | 1 | a0001c0001t0003g0349 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1604-600A>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149397004 | ||||||
| chr6:149397186
|
A | G | 1 | a0001c0001t0020g0054 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1604-418A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149397186 | ||||||
| chr6:149397360
|
G | A | 1 | a0001c0001t0007g0074 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1604-244G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149397360 | ||||||
| chr6:149397364
|
C | T | 1 | a0001c0001t0001g0266 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1604-240C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149397364 | ||||||
| chr6:149397414
|
C | T | 2 | a0001c0001t0013g0177a0001c0001t0013g0178 | 2 | HG02109.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.1604-190C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149397414 | ||||||
| chr6:149397441
|
CA | C | 14 | a0001c0001t0003g0328a0001c0001t0004g0058a0001c0001t0007g0074others(11): Show | 14 | HG01943.hp2 HG02055.hp1 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.1604-148delA | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr6 | 149397441 | |||||
| chr6:149397514
|
C | T | 250 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(247): Show | 250 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(247): Show |
intron_variant | MODIFIER | c.1604-90C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149397514 | ||||||
| chr6:149397840
|
A | G | 1 | a0001c0001t0001g0068 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1764+76A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 4/6 | chr6 | 149397840 | ||||||
| chr6:149398097
|
G | T | 1 | a0001c0001t0004g0046 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1858+35G>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 5/6 | chr6 | 149398097 | ||||||
| chr6:149398102
|
T | G | 1 | a0001c0001t0003g0173 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1858+40T>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 5/6 | chr6 | 149398102 | ||||||
| chr6:149398125
|
G | A | 1 | a0001c0001t0001g0266 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1858+63G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 5/6 | chr6 | 149398125 | ||||||
| chr6:149398218
|
C | A | 1 | a0001c0001t0001g0009 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1858+156C>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 5/6 | chr6 | 149398218 | ||||||
| chr6:149398264
|
G | A | 150 | a0001c0001t0003g0005a0001c0001t0003g0167a0001c0001t0003g0168others(147): Show | 150 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(147): Show |
intron_variant | MODIFIER | c.1858+202G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 5/6 | chr6 | 149398264 | ||||||
| chr6:149398289
|
T | C | 1 | a0001c0001t0003g0173 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1858+227T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 5/6 | chr6 | 149398289 | ||||||
| chr6:149398665
|
C | T | 1 | a0001c0001t0013g0177 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1859-439C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 5/6 | chr6 | 149398665 | ||||||
| chr6:149398767
|
C | T | 66 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(63): Show | 66 | HG00733.hp2 HG00735.hp1 HG00738.hp1 others(63): Show |
intron_variant | MODIFIER | c.1859-337C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 5/6 | chr6 | 149398767 | ||||||
| chr6:149398795
|
AT | A | 4 | a0001c0001t0008g0021a0001c0001t0008g0163a0001c0001t0008g0164others(1): Show | 4 | HG02280.hp1 HG02717.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1859-305delT | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr6 | 149398795 | |||||
| chr6:149398831
|
A | T | 63 | a0001c0001t0003g0005a0001c0001t0003g0167a0001c0001t0003g0168others(60): Show | 63 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.1859-273A>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 5/6 | chr6 | 149398831 | ||||||
| chr6:149398964
|
A | G | 6 | a0001c0001t0001g0133a0001c0001t0001g0141a0001c0001t0001g0262others(3): Show | 6 | HG00642.hp2 HG01516.hp1 HG01517.hp2 others(3): Show |
intron_variant | MODIFIER | c.1859-140A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 5/6 | chr6 | 149398964 | ||||||
| chr6:149398978
|
G | C | 4 | a0001c0001t0013g0177a0001c0001t0013g0178a0001c0001t0017g0022others(1): Show | 4 | HG02109.hp1 HG02615.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.1859-126G>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 5/6 | chr6 | 149398978 | ||||||
| chr6:149398998
|
A | G | 5 | a0001c0001t0003g0167a0001c0001t0003g0168a0001c0001t0003g0170others(2): Show | 5 | HG01109.hp1 HG01167.hp2 HG01175.hp1 others(2): Show |
intron_variant | MODIFIER | c.1859-106A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 5/6 | chr6 | 149398998 | ||||||
| chr6:149399056
|
T | A | 18 | a0001c0001t0003g0167a0001c0001t0003g0168a0001c0001t0003g0169others(15): Show | 18 | HG00609.hp2 HG01109.hp1 HG01167.hp2 others(15): Show |
intron_variant | MODIFIER | c.1859-48T>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 5/6 | chr6 | 149399056 | ||||||
| chr6:149399292
|
A | C | 2 | a0001c0001t0001g0016a0001c0001t0001g0017 | 2 | HG02895.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.1939+108A>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149399292 | ||||||
| chr6:149399370
|
A | G | 2 | a0001c0001t0001g0016a0001c0001t0001g0017 | 2 | HG02895.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.1939+186A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149399370 | ||||||
| chr6:149399530
|
T | C | 3 | a0001c0001t0001g0161a0001c0001t0001g0162a0001c0001t0001g0298 | 3 | HG02622.hp2 HG02976.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1939+346T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149399530 | ||||||
| chr6:149399530
|
T | TC | 87 | a0001c0001t0001g0126a0001c0001t0001g0186a0001c0001t0001g0281others(84): Show | 87 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1939+356dupC | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr6 | 149399530 | |||||
| chr6:149399530
|
TC | T | 63 | a0001c0001t0003g0005a0001c0001t0003g0167a0001c0001t0003g0168others(60): Show | 63 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.1939+356delC | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr6 | 149399530 | |||||
| chr6:149399545
|
G | A | 271 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(268): Show | 272 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(269): Show |
intron_variant | MODIFIER | c.1939+361G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149399545 | ||||||
| chr6:149399706
|
A | T | 1 | a0001c0001t0001g0261 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1939+522A>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149399706 | ||||||
| chr6:149399710
|
A | G | 63 | a0001c0001t0003g0005a0001c0001t0003g0167a0001c0001t0003g0168others(60): Show | 63 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.1939+526A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149399710 | ||||||
| chr6:149399822
|
A | G | 63 | a0001c0001t0003g0005a0001c0001t0003g0167a0001c0001t0003g0168others(60): Show | 63 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.1939+638A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149399822 | ||||||
| chr6:149399888
|
A | G | 87 | a0001c0002t0002g0096a0001c0002t0002g0097a0001c0002t0002g0098others(84): Show | 87 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1939+704A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149399888 | ||||||
| chr6:149399940
|
T | C | 1 | a0001c0002t0006g0238 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1939+756T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149399940 | ||||||
| chr6:149399987
|
C | T | 2 | a0001c0001t0001g0257a0001c0001t0001g0258 | 2 | HG02809.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.1939+803C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149399987 | ||||||
| chr6:149400018
|
G | A | 1 | a0001c0001t0004g0055 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1939+834G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149400018 | ||||||
| chr6:149400053
|
A | C | 1 | a0001c0001t0017g0022 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1939+869A>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149400053 | ||||||
| chr6:149400095
|
A | G | 1 | a0001c0001t0005g0180 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1939+911A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149400095 | ||||||
| chr6:149400139
|
A | T | 1 | a0001c0001t0003g0352 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1939+955A>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149400139 | ||||||
| chr6:149400339
|
G | A | 1 | a0001c0002t0002g0116 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1939+1155G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149400339 | ||||||
| chr6:149400355
|
T | C | 2 | a0001c0001t0003g0355a0001c0001t0003g0356 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1939+1171T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149400355 | ||||||
| chr6:149400392
|
A | G | 7 | a0001c0001t0003g0321a0001c0001t0003g0328a0001c0001t0003g0329others(4): Show | 7 | HG01192.hp2 HG01891.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.1939+1208A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149400392 | ||||||
| chr6:149400543
|
G | A | 2 | a0001c0001t0004g0028a0001c0001t0004g0029 | 2 | HG03041.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1939+1359G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149400543 | ||||||
| chr6:149400554
|
G | A | 250 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(247): Show | 250 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(247): Show |
intron_variant | MODIFIER | c.1939+1370G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149400554 | ||||||
| chr6:149400663
|
C | T | 2 | a0001c0001t0004g0028a0001c0001t0004g0029 | 2 | HG03041.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1939+1479C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149400663 | ||||||
| chr6:149400664
|
G | A | 1 | a0001c0002t0002g0196 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1939+1480G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149400664 | ||||||
| chr6:149400829
|
T | C | 271 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(268): Show | 272 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(269): Show |
intron_variant | MODIFIER | c.1939+1645T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149400829 | ||||||
| chr6:149400899
|
A | G | 5 | a0001c0001t0001g0009a0001c0001t0008g0021a0001c0001t0008g0163others(2): Show | 5 | HG00733.hp2 HG02280.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.1939+1715A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149400899 | ||||||
| chr6:149400904
|
A | G | 363 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(360): Show | 365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.1939+1720A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149400904 | ||||||
| chr6:149401050
|
C | T | 4 | a0001c0001t0005g0179a0001c0001t0005g0180a0001c0001t0005g0181others(1): Show | 4 | HG02602.hp2 HG02683.hp1 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.1939+1866C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149401050 | ||||||
| chr6:149401053
|
A | C | 64 | a0001c0001t0001g0004a0001c0001t0003g0005a0001c0001t0003g0167others(61): Show | 64 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(61): Show |
intron_variant | MODIFIER | c.1939+1869A>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149401053 | ||||||
| chr6:149401580
|
G | A | 1 | a0001c0001t0004g0062 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1939+2396G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149401580 | ||||||
| chr6:149401626
|
A | G | 87 | a0001c0002t0002g0096a0001c0002t0002g0097a0001c0002t0002g0098others(84): Show | 87 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1939+2442A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149401626 | ||||||
| chr6:149401682
|
C | T | 1 | a0001c0001t0001g0151 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1939+2498C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149401682 | ||||||
| chr6:149401686
|
C | T | 63 | a0001c0001t0003g0005a0001c0001t0003g0167a0001c0001t0003g0168others(60): Show | 63 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.1939+2502C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149401686 | ||||||
| chr6:149401753
|
G | A | 4 | a0001c0002t0002g0106a0001c0002t0002g0191a0001c0002t0002g0221others(1): Show | 4 | NA18964.hp1 NA18994.hp2 NA19001.hp1 others(1): Show |
intron_variant | MODIFIER | c.1939+2569G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149401753 | ||||||
| chr6:149401801
|
A | G | 9 | a0001c0001t0005g0117a0001c0001t0005g0118a0001c0001t0005g0179others(6): Show | 9 | HG01243.hp2 HG02602.hp2 HG02683.hp1 others(6): Show |
intron_variant | MODIFIER | c.1939+2617A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149401801 | ||||||
| chr6:149401998
|
TA | T | 142 | a0001c0001t0001g0001a0001c0001t0001g0064a0001c0001t0001g0068others(139): Show | 142 | HG00558.hp1 HG00597.hp2 HG00609.hp1 others(139): Show |
intron_variant | MODIFIER | c.1939+2827delA | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr6 | 149401998 | |||||
| chr6:149401999
|
A | G | 1 | a0001c0001t0001g0266 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1939+2815A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149401999 | ||||||
| chr6:149402249
|
G | A | 1 | a0001c0002t0002g0217 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1939+3065G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149402249 | ||||||
| chr6:149402372
|
T | G | 1 | a0001c0001t0003g0172 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1939+3188T>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149402372 | ||||||
| chr6:149402412
|
A | G | 153 | a0001c0001t0003g0005a0001c0001t0003g0167a0001c0001t0003g0168others(150): Show | 153 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(150): Show |
intron_variant | MODIFIER | c.1939+3228A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149402412 | ||||||
| chr6:149402535
|
A | G | 1 | a0001c0002t0002g0252 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1939+3351A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149402535 | ||||||
| chr6:149402553
|
CTCAAACA others(1): Show |
C | 66 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(63): Show | 66 | HG00733.hp2 HG00735.hp1 HG00738.hp1 others(63): Show |
intron_variant | MODIFIER | c.1939+3370_1939+337 others(12): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149402553 | ||||||
| chr6:149402695
|
A | G | 6 | a0001c0001t0007g0074a0001c0001t0007g0075a0001c0001t0007g0076others(3): Show | 6 | HG02630.hp2 HG03225.hp1 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.1939+3511A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149402695 | ||||||
| chr6:149402776
|
C | A | 3 | a0001c0001t0013g0177a0001c0001t0013g0178a0001c0001t0022g0176 | 3 | HG02109.hp1 HG02615.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1939+3592C>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149402776 | ||||||
| chr6:149402900
|
A | C | 9 | a0001c0001t0005g0117a0001c0001t0005g0118a0001c0001t0005g0179others(6): Show | 9 | HG01243.hp2 HG02602.hp2 HG02683.hp1 others(6): Show |
intron_variant | MODIFIER | c.1939+3716A>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149402900 | ||||||
| chr6:149403093
|
G | C | 87 | a0001c0002t0002g0096a0001c0002t0002g0097a0001c0002t0002g0098others(84): Show | 87 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1939+3909G>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149403093 | ||||||
| chr6:149403126
|
C | T | 58 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(55): Show | 58 | HG00733.hp2 HG00735.hp1 HG00738.hp1 others(55): Show |
intron_variant | MODIFIER | c.1939+3942C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149403126 | ||||||
| chr6:149403234
|
TA | T | 6 | a0001c0001t0001g0068a0001c0001t0001g0086a0001c0001t0001g0087others(3): Show | 6 | HG01884.hp2 HG02055.hp2 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.1939+4064delA | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr6 | 149403234 | |||||
| chr6:149403234
|
TAA | T | 24 | a0001c0001t0001g0006a0001c0001t0001g0120a0001c0001t0001g0121others(21): Show | 24 | HG01433.hp1 HG02015.hp1 HG02056.hp1 others(21): Show |
intron_variant | MODIFIER | c.1939+4063_1939+406 others(6): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr6 | 149403234 | |||||
| chr6:149403243
|
AAAAAATA others(5): Show |
A | 2 | a0001c0001t0001g0016a0001c0001t0001g0017 | 2 | HG02895.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.1939+4061_1939+407 others(16): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr6 | 149403243 | |||||
| chr6:149403243
|
AAAAAATA others(9): Show |
A | 1 | a0001c0001t0001g0275 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1939+4061_1939+407 others(20): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr6 | 149403243 | |||||
| chr6:149403244
|
AAAAATAT others(4): Show |
A | 4 | a0001c0002t0002g0197a0001c0002t0002g0198a0001c0002t0002g0199others(1): Show | 4 | HG00639.hp2 HG01257.hp1 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.1939+4062_1939+407 others(15): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr6 | 149403244 | |||||
| chr6:149403244
|
AAAAATAT others(8): Show |
A | 2 | a0001c0001t0003g0338a0001c0001t0003g0343 | 2 | HG01099.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.1939+4062_1939+407 others(19): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr6 | 149403244 | |||||
| chr6:149403245
|
A | AATATATA others(3): Show |
1 | a0001c0001t0001g0360 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1939+4062_1939+406 others(14): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr6 | 149403245 | |||||
| chr6:149403245
|
A | AT | 7 | a0001c0001t0001g0088a0001c0001t0001g0089a0001c0001t0001g0092others(4): Show | 7 | HG01243.hp1 HG01891.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.1939+4061_1939+406 others(5): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149403245 | ||||||
| chr6:149403245
|
A | T | 3 | a0001c0001t0001g0161a0001c0001t0001g0162a0001c0001t0001g0298 | 3 | HG02622.hp2 HG02976.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1939+4061A>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149403245 | ||||||
| chr6:149403245
|
AAAAT | A | 26 | a0001c0001t0001g0072a0001c0001t0001g0148a0001c0001t0001g0149others(23): Show | 26 | HG00099.hp1 HG00733.hp1 HG00735.hp2 others(23): Show |
intron_variant | MODIFIER | c.1939+4063_1939+406 others(8): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr6 | 149403245 | |||||
| chr6:149403246
|
AAATATAT others(4): Show |
A | 1 | a0001c0002t0002g0212 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1939+4064_1939+407 others(15): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr6 | 149403246 | |||||
| chr6:149403246
|
AAATATAT others(6): Show |
A | 5 | a0001c0002t0002g0101a0001c0002t0002g0102a0001c0002t0002g0189others(2): Show | 5 | HG00597.hp2 HG01261.hp1 HG02015.hp2 others(2): Show |
intron_variant | MODIFIER | c.1939+4064_1939+407 others(17): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr6 | 149403246 | |||||
| chr6:149403246
|
AAATATAT others(10): Show |
A | 9 | a0001c0001t0005g0117a0001c0001t0005g0118a0001c0001t0005g0179others(6): Show | 9 | HG01243.hp2 HG02602.hp2 HG02683.hp1 others(6): Show |
intron_variant | MODIFIER | c.1939+4064_1939+408 others(21): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr6 | 149403246 | |||||
| chr6:149403247
|
A | AAAAATAT others(4): Show |
1 | a0001c0001t0008g0021 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1939+4064_1939+406 others(15): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr6 | 149403247 | |||||
| chr6:149403247
|
A | ATATATAT others(4): Show |
1 | a0001c0001t0007g0083 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1939+4063_1939+406 others(15): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149403247 | ||||||
| chr6:149403247
|
A | T | 52 | a0001c0001t0001g0004a0001c0001t0001g0086a0001c0001t0001g0087others(49): Show | 52 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(49): Show |
intron_variant | MODIFIER | c.1939+4063A>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149403247 | ||||||
| chr6:149403247
|
AATATATA others(17): Show |
A | 2 | a0001c0001t0001g0362a0001c0001t0001g0363 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.1939+4077_1939+410 others(28): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr6 | 149403247 | |||||
| chr6:149403248
|
AT | A | 3 | a0001c0001t0001g0070a0001c0001t0003g0327a0001c0001t0007g0076 | 3 | HG02257.hp1 HG03041.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1939+4065delT | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149403248 | ||||||
| chr6:149403248
|
ATATATAT others(4): Show |
A | 6 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(3): Show | 6 | HG01346.hp1 HG01433.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.1939+4065_1939+407 others(15): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149403248 | ||||||
| chr6:149403248
|
ATATATAT others(6): Show |
A | 76 | a0001c0001t0004g0058a0001c0001t0004g0061a0001c0001t0004g0063others(73): Show | 76 | HG00423.hp1 HG00558.hp1 HG00609.hp1 others(73): Show |
intron_variant | MODIFIER | c.1939+4065_1939+407 others(17): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149403248 | ||||||
| chr6:149403248
|
ATATATAT others(40): Show |
A | 1 | a0001c0001t0017g0022 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1939+4065_1939+411 others(51): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149403248 | ||||||
| chr6:149403249
|
T | A | 60 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0014others(57): Show | 60 | HG00609.hp2 HG00733.hp2 HG00735.hp1 others(57): Show |
intron_variant | MODIFIER | c.1939+4065T>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149403249 | ||||||
| chr6:149403251
|
T | A | 4 | a0001c0001t0003g0307a0001c0001t0004g0028a0001c0001t0004g0030others(1): Show | 4 | HG00609.hp2 HG06807.hp2 NA18949.hp2 others(1): Show |
intron_variant | MODIFIER | c.1939+4067T>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149403251 | ||||||
| chr6:149403263
|
T | A | 2 | a0001c0001t0004g0061a0001c0001t0004g0063 | 2 | NA18962.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.1939+4079T>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149403263 | ||||||
| chr6:149403263
|
T | TACAC | 5 | a0001c0001t0009g0079a0001c0001t0009g0080a0001c0001t0009g0081others(2): Show | 5 | HG02055.hp1 HG02145.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.1939+4080_1939+408 others(8): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr6 | 149403263 | |||||
| chr6:149403265
|
T | TACACAC | 3 | a0001c0001t0008g0163a0001c0001t0008g0164a0001c0001t0008g0165 | 3 | HG02280.hp1 HG02717.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1939+4082_1939+408 others(10): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr6 | 149403265 | |||||
| chr6:149403265
|
TATATATA others(15): Show |
T | 5 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0018others(2): Show | 5 | HG02895.hp2 HG02897.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.1939+4083_1939+410 others(26): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr6 | 149403265 | |||||
| chr6:149403269
|
TATATATA others(13): Show |
T | 2 | a0001c0001t0004g0060a0001c0002t0002g0109 | 2 | NA18978.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.1939+4087_1939+410 others(24): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr6 | 149403269 | |||||
| chr6:149403271
|
T | C | 40 | a0001c0001t0003g0005a0001c0001t0003g0171a0001c0001t0003g0172others(37): Show | 40 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(37): Show |
intron_variant | MODIFIER | c.1939+4087T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149403271 | ||||||
| chr6:149403271
|
TATATATA others(9): Show |
T | 3 | a0001c0001t0001g0013a0001c0001t0004g0036a0001c0001t0020g0054 | 3 | HG03195.hp1 HG03471.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.1939+4089_1939+410 others(20): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr6 | 149403271 | |||||
| chr6:149403271
|
TATATATA others(11): Show |
T | 38 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(35): Show | 38 | HG00733.hp2 HG00735.hp1 HG00738.hp1 others(35): Show |
intron_variant | MODIFIER | c.1939+4089_1939+410 others(22): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr6 | 149403271 | |||||
| chr6:149403271
|
TATATATA others(13): Show |
T | 6 | a0001c0001t0004g0030a0001c0001t0004g0033a0001c0001t0004g0039others(3): Show | 6 | HG02040.hp2 NA18942.hp1 NA18943.hp2 others(3): Show |
intron_variant | MODIFIER | c.1939+4089_1939+410 others(24): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr6 | 149403271 | |||||
| chr6:149403273
|
T | C | 57 | a0001c0001t0003g0005a0001c0001t0003g0167a0001c0001t0003g0168others(54): Show | 57 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.1939+4089T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149403273 | ||||||
| chr6:149403273
|
TATATATA others(9): Show |
T | 3 | a0001c0001t0004g0028a0001c0001t0004g0031a0001c0001t0004g0035 | 3 | HG02615.hp1 HG02630.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1939+4091_1939+410 others(20): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr6 | 149403273 | |||||
| chr6:149403275
|
T | A | 3 | a0001c0001t0008g0163a0001c0001t0008g0164a0001c0001t0008g0165 | 3 | HG02280.hp1 HG02717.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1939+4091T>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149403275 | ||||||
| chr6:149403275
|
T | C | 19 | a0001c0001t0003g0167a0001c0001t0003g0168a0001c0001t0003g0169others(16): Show | 19 | HG00609.hp2 HG01109.hp1 HG01167.hp2 others(16): Show |
intron_variant | MODIFIER | c.1939+4091T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149403275 | ||||||
| chr6:149403275
|
TATATATA others(9): Show |
T | 3 | a0001c0001t0003g0339a0001c0001t0003g0344a0001c0001t0003g0346 | 3 | HG00741.hp1 HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.1939+4093_1939+410 others(20): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr6 | 149403275 | |||||
| chr6:149403277
|
T | C | 1 | a0001c0001t0003g0310 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1939+4093T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149403277 | ||||||
| chr6:149403281
|
T | C | 7 | a0001c0001t0001g0006a0001c0001t0001g0136a0001c0001t0001g0267others(4): Show | 7 | HG01069.hp1 HG01123.hp1 HG01361.hp2 others(4): Show |
intron_variant | MODIFIER | c.1939+4097T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149403281 | ||||||
| chr6:149403283
|
T | C | 54 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(51): Show | 55 | HG00558.hp2 HG00597.hp1 HG00673.hp1 others(52): Show |
intron_variant | MODIFIER | c.1939+4099T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149403283 | ||||||
| chr6:149403283
|
TACAC | T | 24 | a0001c0001t0005g0117a0001c0001t0005g0118a0001c0001t0005g0179others(21): Show | 24 | HG01243.hp2 HG01261.hp1 HG02015.hp2 others(21): Show |
intron_variant | MODIFIER | c.1939+4109_1939+411 others(8): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr6 | 149403283 | |||||
| chr6:149403283
|
TACACAC | T | 84 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0016others(81): Show | 84 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(81): Show |
intron_variant | MODIFIER | c.1939+4107_1939+411 others(10): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr6 | 149403283 | |||||
| chr6:149403285
|
C | T | 40 | a0001c0001t0001g0070a0001c0001t0001g0142a0001c0001t0001g0161others(37): Show | 40 | HG00609.hp2 HG01109.hp1 HG01109.hp2 others(37): Show |
intron_variant | MODIFIER | c.1939+4101C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149403285 | ||||||
| chr6:149403287
|
C | T | 14 | a0001c0001t0003g0310a0001c0001t0007g0074a0001c0001t0007g0075others(11): Show | 14 | HG02055.hp1 HG02135.hp1 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.1939+4103C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149403287 | ||||||
| chr6:149403289
|
C | T | 7 | a0001c0001t0007g0076a0001c0001t0007g0077a0001c0001t0008g0163others(4): Show | 7 | HG02280.hp1 HG02717.hp2 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.1939+4105C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149403289 | ||||||
| chr6:149403289
|
CACACACA others(1): Show |
C | 5 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0072others(2): Show | 5 | HG01884.hp2 HG02886.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.1939+4107_1939+411 others(12): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr6 | 149403289 | |||||
| chr6:149403291
|
C | T | 7 | a0001c0001t0001g0267a0001c0001t0001g0277a0001c0001t0001g0284others(4): Show | 7 | HG01069.hp1 HG01123.hp1 HG01361.hp2 others(4): Show |
intron_variant | MODIFIER | c.1939+4107C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149403291 | ||||||
| chr6:149403291
|
CACACATA others(15): Show |
C | 39 | a0001c0001t0003g0005a0001c0001t0003g0171a0001c0001t0003g0172others(36): Show | 39 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.1939+4113_1939+413 others(26): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr6 | 149403291 | |||||
| chr6:149403293
|
C | T | 32 | a0001c0001t0001g0267a0001c0001t0001g0273a0001c0001t0001g0277others(29): Show | 32 | HG00733.hp1 HG01069.hp1 HG01123.hp1 others(29): Show |
intron_variant | MODIFIER | c.1939+4109C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149403293 | ||||||
| chr6:149403293
|
CACATATA others(13): Show |
C | 1 | a0001c0001t0003g0351 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1939+4113_1939+413 others(24): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr6 | 149403293 | |||||
| chr6:149403295
|
C | CAT | 3 | a0001c0001t0001g0122a0001c0001t0001g0147a0001c0001t0001g0290 | 3 | HG00423.hp2 NA19059.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.1939+4129_1939+413 others(6): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr6 | 149403295 | |||||
| chr6:149403295
|
C | T | 226 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(223): Show | 227 | HG00423.hp1 HG00558.hp1 HG00558.hp2 others(224): Show |
intron_variant | MODIFIER | c.1939+4111C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149403295 | ||||||
| chr6:149403295
|
CAT | C | 3 | a0001c0001t0001g0151a0001c0001t0001g0152a0001c0001t0001g0162 | 3 | HG00735.hp2 HG01070.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1939+4129_1939+413 others(6): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr6 | 149403295 | |||||
| chr6:149403295
|
CATATATA others(9): Show |
C | 1 | a0001c0001t0003g0310 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1939+4115_1939+413 others(20): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr6 | 149403295 | |||||
| chr6:149403295
|
CATATATA others(11): Show |
C | 17 | a0001c0001t0003g0167a0001c0001t0003g0168a0001c0001t0003g0169others(14): Show | 17 | HG00609.hp2 HG01109.hp1 HG01167.hp2 others(14): Show |
intron_variant | MODIFIER | c.1939+4113_1939+413 others(22): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr6 | 149403295 | |||||
| chr6:149403297
|
T | A | 1 | a0001c0001t0017g0022 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1939+4113T>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149403297 | ||||||
| chr6:149403297
|
T | C | 2 | a0001c0001t0001g0142a0001c0001t0001g0360 | 2 | HG01358.hp1 HG02083.hp1 |
intron_variant | MODIFIER | c.1939+4113T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149403297 | ||||||
| chr6:149403299
|
T | A | 1 | a0001c0001t0008g0021 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1939+4115T>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149403299 | ||||||
| chr6:149403307
|
T | C | 5 | a0001c0001t0003g0338a0001c0001t0003g0339a0001c0001t0003g0343others(2): Show | 5 | HG00741.hp1 HG01070.hp2 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.1939+4123T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149403307 | ||||||
| chr6:149403307
|
TATATATA others(17): Show |
T | 1 | a0001c0001t0015g0154 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1939+4131_1939+415 others(28): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr6 | 149403307 | |||||
| chr6:149403309
|
T | C | 5 | a0001c0001t0003g0338a0001c0001t0003g0339a0001c0001t0003g0343others(2): Show | 5 | HG00741.hp1 HG01070.hp2 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.1939+4125T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149403309 | ||||||
| chr6:149403311
|
T | C | 6 | a0001c0001t0003g0338a0001c0001t0003g0339a0001c0001t0003g0343others(3): Show | 6 | HG00741.hp1 HG01070.hp2 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.1939+4127T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149403311 | ||||||
| chr6:149403313
|
T | C | 31 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(28): Show | 31 | HG00140.hp1 HG00733.hp2 HG00741.hp1 others(28): Show |
intron_variant | MODIFIER | c.1939+4129T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149403313 | ||||||
| chr6:149403315
|
C | T | 1 | a0001c0001t0001g0087 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1939+4131C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149403315 | ||||||
| chr6:149403319
|
C | T | 10 | a0001c0001t0007g0074a0001c0001t0007g0075a0001c0001t0007g0076others(7): Show | 10 | HG02055.hp1 HG02145.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.1939+4135C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149403319 | ||||||
| chr6:149403321
|
C | T | 13 | a0001c0001t0007g0074a0001c0001t0007g0075a0001c0001t0007g0076others(10): Show | 13 | HG02055.hp1 HG02145.hp2 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.1939+4137C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149403321 | ||||||
| chr6:149403323
|
T | C | 1 | a0001c0001t0001g0087 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1939+4139T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149403323 | ||||||
| chr6:149403329
|
T | TACACACA others(1): Show |
10 | a0001c0001t0007g0074a0001c0001t0007g0075a0001c0001t0007g0076others(7): Show | 10 | HG02055.hp1 HG02145.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.1939+4148_1939+414 others(12): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr6 | 149403329 | |||||
| chr6:149403329
|
T | TATACACA others(3): Show |
1 | a0001c0001t0007g0077 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1939+4146_1939+414 others(14): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr6 | 149403329 | |||||
| chr6:149403329
|
T | TATATATA others(5): Show |
1 | a0001c0001t0022g0176 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1939+4146_1939+414 others(16): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr6 | 149403329 | |||||
| chr6:149403329
|
T | TATATATA others(7): Show |
2 | a0001c0001t0013g0177a0001c0001t0013g0178 | 2 | HG02109.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.1939+4146_1939+414 others(18): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr6 | 149403329 | |||||
| chr6:149403331
|
C | CACATAT | 3 | a0001c0001t0008g0163a0001c0001t0008g0164a0001c0001t0008g0165 | 3 | HG02280.hp1 HG02717.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1939+4148_1939+414 others(10): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr6 | 149403331 | |||||
| chr6:149403331
|
C | T | 3 | a0001c0001t0001g0087a0001c0001t0001g0280a0001c0001t0008g0021 | 3 | HG00558.hp2 HG02055.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1939+4147C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149403331 | ||||||
| chr6:149403333
|
T | C | 1 | a0001c0001t0001g0087 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1939+4149T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149403333 | ||||||
| chr6:149403337
|
TATACACA others(1): Show |
T | 4 | a0001c0001t0003g0350a0001c0002t0002g0207a0001c0002t0002g0234others(1): Show | 4 | HG00609.hp1 HG02129.hp2 HG02683.hp2 others(1): Show |
intron_variant | MODIFIER | c.1939+4155_1939+416 others(12): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr6 | 149403337 | |||||
| chr6:149403337
|
TATACACA others(3): Show |
T | 69 | a0001c0001t0004g0119a0001c0002t0002g0100a0001c0002t0002g0101others(66): Show | 69 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(66): Show |
intron_variant | MODIFIER | c.1939+4155_1939+416 others(14): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr6 | 149403337 | |||||
| chr6:149403337
|
TATACACA others(7): Show |
T | 1 | a0001c0002t0002g0195 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1939+4155_1939+416 others(18): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr6 | 149403337 | |||||
| chr6:149403339
|
TAC | T | 49 | a0001c0001t0001g0003a0001c0001t0001g0086a0001c0001t0001g0088others(46): Show | 50 | HG00140.hp1 HG00423.hp2 HG00642.hp1 others(47): Show |
intron_variant | MODIFIER | c.1939+4189_1939+419 others(6): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr6 | 149403339 | |||||
| chr6:149403339
|
TACAC | T | 5 | a0001c0001t0001g0090a0001c0001t0001g0268a0001c0001t0001g0287others(2): Show | 5 | HG00733.hp1 HG01069.hp1 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.1939+4187_1939+419 others(8): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr6 | 149403339 | |||||
| chr6:149403339
|
TACACACA others(1): Show |
T | 67 | a0001c0001t0001g0161a0001c0001t0001g0162a0001c0001t0001g0298others(64): Show | 67 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(64): Show |
intron_variant | MODIFIER | c.1939+4183_1939+419 others(12): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr6 | 149403339 | |||||
| chr6:149403339
|
TACACACA others(3): Show |
T | 84 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(81): Show | 84 | HG00621.hp1 HG00673.hp2 HG00733.hp2 others(81): Show |
intron_variant | MODIFIER | c.1939+4181_1939+419 others(14): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr6 | 149403339 | |||||
| chr6:149403339
|
TACACACA others(5): Show |
T | 11 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0070others(8): Show | 11 | HG00609.hp2 HG01099.hp2 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.1939+4179_1939+419 others(16): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr6 | 149403339 | |||||
| chr6:149403341
|
C | CAT | 10 | a0001c0001t0007g0074a0001c0001t0007g0076a0001c0001t0007g0077others(7): Show | 10 | HG02055.hp1 HG02145.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.1939+4158_1939+415 others(6): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr6 | 149403341 | |||||
| chr6:149403341
|
C | T | 1 | a0001c0001t0001g0136 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1939+4157C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149403341 | ||||||
| chr6:149403343
|
C | T | 14 | a0001c0001t0007g0074a0001c0001t0007g0075a0001c0001t0007g0076others(11): Show | 14 | HG02055.hp1 HG02109.hp1 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.1939+4159C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149403343 | ||||||
| chr6:149403345
|
C | CACATATA others(13): Show |
1 | a0001c0001t0001g0280 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1939+4164_1939+416 others(24): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr6 | 149403345 | |||||
| chr6:149403345
|
C | T | 14 | a0001c0001t0007g0074a0001c0001t0007g0075a0001c0001t0007g0076others(11): Show | 14 | HG02055.hp1 HG02109.hp1 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.1939+4161C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149403345 | ||||||
| chr6:149403347
|
C | T | 14 | a0001c0001t0007g0074a0001c0001t0007g0075a0001c0001t0007g0076others(11): Show | 14 | HG02055.hp1 HG02109.hp1 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.1939+4163C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149403347 | ||||||
| chr6:149403349
|
C | T | 4 | a0001c0001t0007g0075a0001c0001t0013g0177a0001c0001t0013g0178others(1): Show | 4 | HG02109.hp1 HG02615.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.1939+4165C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149403349 | ||||||
| chr6:149403351
|
C | CATATATA others(9): Show |
3 | a0001c0001t0008g0163a0001c0001t0008g0164a0001c0001t0008g0165 | 3 | HG02280.hp1 HG02717.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1939+4168_1939+416 others(20): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr6 | 149403351 | |||||
| chr6:149403351
|
C | CATATATA others(11): Show |
1 | a0001c0001t0008g0021 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1939+4168_1939+416 others(22): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr6 | 149403351 | |||||
| chr6:149403351
|
C | T | 10 | a0001c0001t0001g0013a0001c0001t0005g0117a0001c0001t0005g0118others(7): Show | 10 | HG01243.hp2 HG02602.hp2 HG02683.hp1 others(7): Show |
intron_variant | MODIFIER | c.1939+4167C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149403351 | ||||||
| chr6:149403353
|
C | T | 4 | a0001c0001t0008g0163a0001c0001t0008g0164a0001c0001t0008g0165others(1): Show | 4 | HG02280.hp1 HG02717.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1939+4169C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149403353 | ||||||
| chr6:149403395
|
G | T | 66 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(63): Show | 66 | HG00733.hp2 HG00735.hp1 HG00738.hp1 others(63): Show |
intron_variant | MODIFIER | c.1939+4211G>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149403395 | ||||||
| chr6:149403655
|
C | G | 1 | a0001c0002t0002g0104 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1939+4471C>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149403655 | ||||||
| chr6:149403736
|
G | A | 63 | a0001c0001t0003g0005a0001c0001t0003g0167a0001c0001t0003g0168others(60): Show | 63 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.1939+4552G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149403736 | ||||||
| chr6:149403761
|
G | T | 1 | a0001c0001t0004g0049 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1939+4577G>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149403761 | ||||||
| chr6:149403825
|
A | G | 19 | a0001c0001t0001g0268a0001c0001t0003g0167a0001c0001t0003g0168others(16): Show | 19 | HG00609.hp2 HG01109.hp1 HG01167.hp2 others(16): Show |
intron_variant | MODIFIER | c.1939+4641A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149403825 | ||||||
| chr6:149403970
|
A | G | 87 | a0001c0002t0002g0096a0001c0002t0002g0097a0001c0002t0002g0098others(84): Show | 87 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1939+4786A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149403970 | ||||||
| chr6:149403972
|
A | G | 1 | a0001c0003t0001g0259 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1939+4788A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149403972 | ||||||
| chr6:149404126
|
A | T | 1 | a0001c0001t0003g0349 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1939+4942A>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149404126 | ||||||
| chr6:149404154
|
G | A | 184 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0070others(181): Show | 184 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(181): Show |
intron_variant | MODIFIER | c.1939+4970G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149404154 | ||||||
| chr6:149404273
|
A | C | 1 | a0001c0001t0005g0117 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1939+5089A>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149404273 | ||||||
| chr6:149404446
|
A | G | 87 | a0001c0002t0002g0096a0001c0002t0002g0097a0001c0002t0002g0098others(84): Show | 87 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1940-5131A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149404446 | ||||||
| chr6:149404894
|
A | T | 1 | a0001c0002t0002g0230 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1940-4683A>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149404894 | ||||||
| chr6:149405030
|
A | G | 1 | a0001c0001t0003g0304 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1940-4547A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149405030 | ||||||
| chr6:149405222
|
T | C | 11 | a0001c0001t0007g0074a0001c0001t0007g0075a0001c0001t0007g0076others(8): Show | 11 | HG02055.hp1 HG02145.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.1940-4355T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149405222 | ||||||
| chr6:149405409
|
A | G | 21 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0070others(18): Show | 21 | HG01884.hp2 HG02055.hp1 HG02145.hp2 others(18): Show |
intron_variant | MODIFIER | c.1940-4168A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149405409 | ||||||
| chr6:149405489
|
A | G | 87 | a0001c0002t0002g0096a0001c0002t0002g0097a0001c0002t0002g0098others(84): Show | 87 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1940-4088A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149405489 | ||||||
| chr6:149405830
|
G | A | 63 | a0001c0001t0003g0005a0001c0001t0003g0167a0001c0001t0003g0168others(60): Show | 63 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.1940-3747G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149405830 | ||||||
| chr6:149405928
|
G | A | 245 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(242): Show | 245 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(242): Show |
intron_variant | MODIFIER | c.1940-3649G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149405928 | ||||||
| chr6:149406129
|
A | T | 1 | a0001c0001t0004g0060 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.1940-3448A>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149406129 | ||||||
| chr6:149406169
|
A | G | 1 | a0001c0001t0005g0179 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1940-3408A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149406169 | ||||||
| chr6:149406209
|
T | A | 87 | a0001c0002t0002g0096a0001c0002t0002g0097a0001c0002t0002g0098others(84): Show | 87 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1940-3368T>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149406209 | ||||||
| chr6:149406423
|
A | G | 2 | a0001c0001t0001g0270a0001c0001t0001g0278 | 2 | NA18952.hp2 NA18980.hp1 |
intron_variant | MODIFIER | c.1940-3154A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149406423 | ||||||
| chr6:149406556
|
C | CT | 6 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0070others(3): Show | 6 | HG01884.hp2 HG02257.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1940-3020dupT | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr6 | 149406556 | |||||
| chr6:149406585
|
G | A | 1 | a0001c0001t0005g0118 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1940-2992G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149406585 | ||||||
| chr6:149406741
|
A | G | 4 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(1): Show | 4 | HG01081.hp1 HG01884.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1940-2836A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149406741 | ||||||
| chr6:149406860
|
G | A | 1 | a0001c0001t0001g0257 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1940-2717G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149406860 | ||||||
| chr6:149407042
|
T | C | 87 | a0001c0002t0002g0096a0001c0002t0002g0097a0001c0002t0002g0098others(84): Show | 87 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1940-2535T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149407042 | ||||||
| chr6:149407118
|
G | C | 250 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(247): Show | 250 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(247): Show |
intron_variant | MODIFIER | c.1940-2459G>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149407118 | ||||||
| chr6:149407258
|
CTGAA | C | 6 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0070others(3): Show | 6 | HG01884.hp2 HG02257.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1940-2315_1940-231 others(8): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr6 | 149407258 | |||||
| chr6:149407277
|
A | G | 1 | a0001c0002t0002g0206 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1940-2300A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149407277 | ||||||
| chr6:149407370
|
T | C | 1 | a0001c0001t0001g0150 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1940-2207T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149407370 | ||||||
| chr6:149407409
|
G | C | 5 | a0001c0001t0009g0079a0001c0001t0009g0080a0001c0001t0009g0081others(2): Show | 5 | HG02055.hp1 HG02145.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.1940-2168G>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149407409 | ||||||
| chr6:149407440
|
G | A | 2 | a0001c0001t0003g0355a0001c0001t0003g0356 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1940-2137G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149407440 | ||||||
| chr6:149407498
|
A | G | 2 | a0001c0001t0004g0052a0001c0001t0004g0053 | 2 | NA18957.hp2 NA19072.hp1 |
intron_variant | MODIFIER | c.1940-2079A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149407498 | ||||||
| chr6:149407613
|
A | G | 63 | a0001c0001t0003g0005a0001c0001t0003g0167a0001c0001t0003g0168others(60): Show | 63 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.1940-1964A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149407613 | ||||||
| chr6:149407723
|
C | A | 1 | a0001c0001t0008g0163 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1940-1854C>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149407723 | ||||||
| chr6:149407829
|
C | T | 1 | a0001c0001t0017g0022 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1940-1748C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149407829 | ||||||
| chr6:149407937
|
G | A | 1 | a0001c0001t0001g0120 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1940-1640G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149407937 | ||||||
| chr6:149407944
|
G | A | 5 | a0001c0001t0009g0079a0001c0001t0009g0080a0001c0001t0009g0081others(2): Show | 5 | HG02055.hp1 HG02145.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.1940-1633G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149407944 | ||||||
| chr6:149407947
|
A | G | 2 | a0001c0001t0003g0342a0001c0001t0003g0345 | 2 | HG01257.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.1940-1630A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149407947 | ||||||
| chr6:149408062
|
T | C | 250 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(247): Show | 250 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(247): Show |
intron_variant | MODIFIER | c.1940-1515T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149408062 | ||||||
| chr6:149408142
|
C | T | 1 | a0001c0002t0002g0116 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1940-1435C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149408142 | ||||||
| chr6:149408143
|
G | C | 1 | a0001c0001t0003g0173 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1940-1434G>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149408143 | ||||||
| chr6:149408146
|
G | A | 63 | a0001c0001t0003g0005a0001c0001t0003g0167a0001c0001t0003g0168others(60): Show | 63 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.1940-1431G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149408146 | ||||||
| chr6:149408155
|
CA | C | 171 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0070others(168): Show | 171 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(168): Show |
intron_variant | MODIFIER | c.1940-1418delA | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr6 | 149408155 | |||||
| chr6:149408224
|
G | C | 1 | a0001c0002t0006g0211 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1940-1353G>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149408224 | ||||||
| chr6:149408237
|
A | G | 1 | a0001c0001t0001g0272 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1940-1340A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149408237 | ||||||
| chr6:149408446
|
T | C | 1 | a0001c0001t0004g0024 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1940-1131T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149408446 | ||||||
| chr6:149408707
|
A | T | 1 | a0001c0001t0022g0176 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1940-870A>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149408707 | ||||||
| chr6:149408824
|
C | T | 87 | a0001c0002t0002g0096a0001c0002t0002g0097a0001c0002t0002g0098others(84): Show | 87 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1940-753C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149408824 | ||||||
| chr6:149409418
|
G | A | 1 | a0001c0002t0002g0237 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1940-159G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149409418 |