| geneid | 135152 |
|---|---|
| ensemblid | ENSG00000112309.11 |
| hgncid | 922 |
| symbol | B3GAT2 |
| name | beta-1,3-glucuronyltransferase 2 |
| refseq_nuc | NM_080742.3 |
| refseq_prot | NP_542780.1 |
| ensembl_nuc | ENST00000230053.11 |
| ensembl_prot | ENSP00000230053.6 |
| mane_status | MANE Select |
| chr | chr6 |
| start | 70856679 |
| end | 70957060 |
| strand | - |
| ver | v1.2 |
| region | chr6:70856679-70957060 |
| region5000 | chr6:70851679-70962060 |
| regionname0 | B3GAT2_chr6_70856679_70957060 |
| regionname5000 | B3GAT2_chr6_70851679_70962060 |
| 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 | 323 | 315 | 86 | 54 | 128 | 8 | 37 | 92 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| a0002 | 0/0 | 323 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| 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 | 0/0 | 972 | 186 | 55 | 30 | 79 | 4 | 18 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| c0002 | 1/1 | 972 | 128 | 30 | 24 | 49 | 4 | 19 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| c0003 | 0/0 | 972 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| c0004 | 0/0 | 972 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| 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 | 5615 | 25 | 1 | 4 | 12 | 1 | 7 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| t0002 | 0/0 | 5616 | 22 | 0 | 0 | 22 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| t0003 | 0/0 | 5615 | 21 | 7 | 2 | 7 | 0 | 5 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| t0004 | 0/0 | 5616 | 14 | 11 | 1 | 1 | 1 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| t0005 | 0/0 | 5615 | 13 | 1 | 3 | 8 | 0 | 1 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| t0006 | 0/0 | 5616 | 10 | 6 | 0 | 3 | 0 | 1 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| t0007 | 0/0 | 5615 | 9 | 1 | 0 | 6 | 0 | 2 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| t0008 | 0/0 | 5615 | 8 | 0 | 6 | 0 | 0 | 2 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| t0009 | 0/0 | 5616 | 7 | 1 | 3 | 3 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| t0010 | 0/0 | 5615 | 7 | 1 | 2 | 3 | 0 | 1 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| t0011 | 0/0 | 5616 | 7 | 6 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| t0012 | 0/0 | 5616 | 6 | 2 | 0 | 4 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| t0013 | 0/0 | 5615 | 6 | 0 | 2 | 4 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| t0014 | 0/0 | 5615 | 6 | 0 | 5 | 0 | 0 | 1 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| t0015 | 0/0 | 5615 | 6 | 0 | 3 | 0 | 1 | 2 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| t0016 | 0/0 | 5615 | 5 | 0 | 0 | 3 | 0 | 2 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| t0017 | 0/0 | 5615 | 4 | 0 | 3 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| t0018 | 0/0 | 5615 | 4 | 1 | 3 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| t0019 | 0/0 | 5615 | 4 | 0 | 1 | 3 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| t0020 | 0/0 | 5615 | 4 | 0 | 2 | 0 | 1 | 1 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| t0021 | 0/0 | 5615 | 4 | 0 | 0 | 4 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| t0022 | 0/0 | 5616 | 4 | 0 | 1 | 3 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| t0023 | 0/0 | 5613 | 3 | 3 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| t0024 | 0/0 | 5617 | 3 | 3 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| t0025 | 0/0 | 5616 | 3 | 2 | 1 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| t0026 | 0/0 | 5617 | 3 | 0 | 0 | 3 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| t0027 | 1/0 | 5616 | 3 | 0 | 0 | 0 | 2 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| t0028 | 0/0 | 5616 | 3 | 2 | 0 | 0 | 0 | 1 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| t0029 | 0/0 | 5615 | 3 | 0 | 1 | 1 | 0 | 1 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| t0030 | 0/0 | 5615 | 3 | 0 | 0 | 3 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| t0031 | 0/1 | 5616 | 3 | 1 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| t0032 | 0/0 | 5617 | 2 | 0 | 0 | 2 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| t0033 | 0/0 | 5616 | 2 | 2 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| t0034 | 0/0 | 5614 | 2 | 1 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| t0035 | 0/0 | 5615 | 2 | 0 | 1 | 0 | 1 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| t0036 | 0/0 | 5613 | 2 | 2 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| t0037 | 0/0 | 5616 | 2 | 0 | 0 | 0 | 0 | 2 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| t0038 | 0/0 | 5615 | 2 | 0 | 0 | 2 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| t0039 | 0/0 | 5616 | 2 | 0 | 0 | 2 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| t0040 | 0/0 | 5617 | 2 | 0 | 1 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| t0041 | 0/0 | 5616 | 2 | 2 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| t0042 | 0/0 | 5616 | 2 | 2 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| t0043 | 0/0 | 5615 | 2 | 2 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| t0044 | 0/0 | 5615 | 2 | 0 | 2 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| t0045 | 0/0 | 5626 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| t0046 | 0/0 | 5615 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| t0047 | 0/0 | 5615 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| t0048 | 0/0 | 5615 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| t0049 | 0/0 | 5613 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| t0050 | 0/0 | 5616 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| t0051 | 0/0 | 5616 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| t0052 | 0/0 | 5620 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| t0053 | 0/0 | 5615 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| t0054 | 0/0 | 5615 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| t0055 | 0/0 | 5614 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| t0056 | 0/0 | 5616 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| t0057 | 0/0 | 5617 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| t0058 | 0/0 | 5614 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| t0059 | 0/0 | 5617 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| t0060 | 0/0 | 5617 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| t0061 | 0/0 | 5604 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| t0062 | 0/0 | 5615 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| t0063 | 0/0 | 5606 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| t0064 | 0/0 | 5614 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| t0065 | 0/0 | 5614 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| t0066 | 0/0 | 5617 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| t0067 | 0/0 | 5616 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| t0068 | 0/0 | 5612 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| t0069 | 0/0 | 5616 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| t0070 | 0/0 | 5612 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| t0071 | 0/0 | 5620 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| t0072 | 0/0 | 5619 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| t0073 | 0/0 | 5617 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| t0074 | 0/0 | 5617 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| t0075 | 0/0 | 5597 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| t0076 | 0/0 | 5615 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| t0077 | 0/0 | 5615 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| t0078 | 0/0 | 5616 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| t0079 | 0/0 | 5616 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| t0080 | 0/0 | 5613 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| t0081 | 0/0 | 5616 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| t0082 | 0/0 | 5615 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| t0083 | 0/0 | 5616 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| t0084 | 0/0 | 5606 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| t0085 | 0/0 | 5617 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| t0086 | 0/0 | 5614 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| t0087 | 0/0 | 5597 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| t0088 | 0/0 | 5615 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| t0089 | 0/0 | 5614 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| t0090 | 0/0 | 5616 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| t0091 | 0/0 | 5613 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| t0092 | 0/0 | 5617 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| t0093 | 0/0 | 5616 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| t0094 | 0/0 | 5614 | 1 | 0 | 0 | 0 | 1 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| t0095 | 0/0 | 5614 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| t0096 | 0/0 | 5617 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| t0097 | 0/0 | 5615 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| t0098 | 0/0 | 5616 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| t0099 | 0/0 | 5614 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| t0100 | 0/0 | 5613 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| t0101 | 0/0 | 5613 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| t0102 | 0/0 | 5616 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| t0103 | 0/0 | 5615 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| t0104 | 0/0 | 5616 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| t0105 | 0/0 | 5615 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| t0106 | 0/0 | 5615 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| t0107 | 0/0 | 5616 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| t0108 | 0/0 | 5617 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| t0109 | 0/0 | 5616 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| t0110 | 0/0 | 5615 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| t0111 | 0/0 | 5616 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| 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 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0200 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0213 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0275 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0281 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0282 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| 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 | 0/0 | 972 | 186 | 55 | 30 | 79 | 4 | 18 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| a0001c0002 | 1/1 | 972 | 128 | 30 | 24 | 49 | 4 | 19 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| a0001c0003 | 0/0 | 972 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| a0002c0004 | 0/0 | 972 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 6586 | 25 | 1 | 4 | 12 | 1 | 7 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| a0001c0001t0002 | 0/0 | 6587 | 22 | 0 | 0 | 22 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| a0001c0001t0003 | 0/0 | 6586 | 21 | 7 | 2 | 7 | 0 | 5 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| a0001c0001t0004 | 0/0 | 6587 | 14 | 11 | 1 | 1 | 1 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| a0001c0001t0009 | 0/0 | 6587 | 7 | 1 | 3 | 3 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| a0001c0001t0010 | 0/0 | 6586 | 7 | 1 | 2 | 3 | 0 | 1 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| a0001c0001t0012 | 0/0 | 6587 | 6 | 2 | 0 | 4 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| a0001c0001t0013 | 0/0 | 6586 | 6 | 0 | 2 | 4 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| a0001c0001t0017 | 0/0 | 6586 | 4 | 0 | 3 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| a0001c0001t0018 | 0/0 | 6586 | 4 | 1 | 3 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| a0001c0001t0019 | 0/0 | 6586 | 4 | 0 | 1 | 3 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| a0001c0001t0020 | 0/0 | 6586 | 4 | 0 | 2 | 0 | 1 | 1 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| a0001c0001t0023 | 0/0 | 6584 | 3 | 3 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| a0001c0001t0024 | 0/0 | 6588 | 3 | 3 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| a0001c0001t0025 | 0/0 | 6587 | 3 | 2 | 1 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| a0001c0001t0032 | 0/0 | 6588 | 2 | 0 | 0 | 2 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| a0001c0001t0033 | 0/0 | 6587 | 2 | 2 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| a0001c0001t0034 | 0/0 | 6585 | 2 | 1 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| a0001c0001t0035 | 0/0 | 6586 | 2 | 0 | 1 | 0 | 1 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| a0001c0001t0036 | 0/0 | 6584 | 2 | 2 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| a0001c0001t0037 | 0/0 | 6587 | 2 | 0 | 0 | 0 | 0 | 2 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| a0001c0001t0044 | 0/0 | 6586 | 2 | 0 | 2 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| a0001c0001t0045 | 0/0 | 6597 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| a0001c0001t0046 | 0/0 | 6586 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| a0001c0001t0047 | 0/0 | 6586 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| a0001c0001t0048 | 0/0 | 6586 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| a0001c0001t0049 | 0/0 | 6584 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| a0001c0001t0050 | 0/0 | 6587 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| a0001c0001t0051 | 0/0 | 6587 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| a0001c0001t0052 | 0/0 | 6591 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| a0001c0001t0053 | 0/0 | 6586 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| a0001c0001t0054 | 0/0 | 6586 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| a0001c0001t0055 | 0/0 | 6585 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| a0001c0001t0056 | 0/0 | 6587 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| a0001c0001t0057 | 0/0 | 6588 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| a0001c0001t0058 | 0/0 | 6585 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| a0001c0001t0059 | 0/0 | 6588 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| a0001c0001t0060 | 0/0 | 6588 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| a0001c0001t0061 | 0/0 | 6575 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| a0001c0001t0064 | 0/0 | 6585 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| a0001c0001t0065 | 0/0 | 6585 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| a0001c0001t0066 | 0/0 | 6588 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| a0001c0001t0067 | 0/0 | 6587 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| a0001c0001t0068 | 0/0 | 6583 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| a0001c0001t0069 | 0/0 | 6587 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| a0001c0001t0070 | 0/0 | 6583 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| a0001c0001t0071 | 0/0 | 6591 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| a0001c0001t0072 | 0/0 | 6590 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| a0001c0001t0073 | 0/0 | 6588 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| a0001c0001t0074 | 0/0 | 6588 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| a0001c0001t0075 | 0/0 | 6568 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| a0001c0001t0076 | 0/0 | 6586 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| a0001c0001t0102 | 0/0 | 6587 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| a0001c0001t0103 | 0/0 | 6586 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| a0001c0001t0104 | 0/0 | 6587 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| a0001c0001t0105 | 0/0 | 6586 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| a0001c0001t0107 | 0/0 | 6587 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| a0001c0001t0108 | 0/0 | 6588 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| a0001c0001t0109 | 0/0 | 6587 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| a0001c0001t0110 | 0/0 | 6586 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| a0001c0001t0111 | 0/0 | 6587 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| a0001c0002t0005 | 0/0 | 6586 | 13 | 1 | 3 | 8 | 0 | 1 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| a0001c0002t0006 | 0/0 | 6587 | 10 | 6 | 0 | 3 | 0 | 1 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| a0001c0002t0007 | 0/0 | 6586 | 9 | 1 | 0 | 6 | 0 | 2 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| a0001c0002t0008 | 0/0 | 6586 | 8 | 0 | 6 | 0 | 0 | 2 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| a0001c0002t0011 | 0/0 | 6587 | 7 | 6 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| a0001c0002t0014 | 0/0 | 6586 | 6 | 0 | 5 | 0 | 0 | 1 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| a0001c0002t0015 | 0/0 | 6586 | 6 | 0 | 3 | 0 | 1 | 2 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| a0001c0002t0016 | 0/0 | 6586 | 5 | 0 | 0 | 3 | 0 | 2 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| a0001c0002t0021 | 0/0 | 6586 | 4 | 0 | 0 | 4 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| a0001c0002t0022 | 0/0 | 6587 | 4 | 0 | 1 | 3 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| a0001c0002t0026 | 0/0 | 6588 | 3 | 0 | 0 | 3 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| a0001c0002t0027 | 1/0 | 6587 | 3 | 0 | 0 | 0 | 2 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| a0001c0002t0028 | 0/0 | 6587 | 3 | 2 | 0 | 0 | 0 | 1 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| a0001c0002t0029 | 0/0 | 6586 | 3 | 0 | 1 | 1 | 0 | 1 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| a0001c0002t0030 | 0/0 | 6586 | 3 | 0 | 0 | 3 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| a0001c0002t0031 | 0/1 | 6587 | 3 | 1 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| a0001c0002t0038 | 0/0 | 6586 | 2 | 0 | 0 | 2 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| a0001c0002t0039 | 0/0 | 6587 | 2 | 0 | 0 | 2 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| a0001c0002t0040 | 0/0 | 6588 | 2 | 0 | 1 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| a0001c0002t0041 | 0/0 | 6587 | 2 | 2 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| a0001c0002t0042 | 0/0 | 6587 | 2 | 2 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| a0001c0002t0043 | 0/0 | 6586 | 2 | 2 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| a0001c0002t0077 | 0/0 | 6586 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| a0001c0002t0078 | 0/0 | 6587 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| a0001c0002t0079 | 0/0 | 6587 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| a0001c0002t0080 | 0/0 | 6584 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| a0001c0002t0081 | 0/0 | 6587 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| a0001c0002t0082 | 0/0 | 6586 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| a0001c0002t0083 | 0/0 | 6587 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| a0001c0002t0084 | 0/0 | 6577 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| a0001c0002t0085 | 0/0 | 6588 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| a0001c0002t0086 | 0/0 | 6585 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| a0001c0002t0087 | 0/0 | 6568 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| a0001c0002t0088 | 0/0 | 6586 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| a0001c0002t0089 | 0/0 | 6585 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| a0001c0002t0090 | 0/0 | 6587 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| a0001c0002t0091 | 0/0 | 6584 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| a0001c0002t0092 | 0/0 | 6588 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| a0001c0002t0093 | 0/0 | 6587 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| a0001c0002t0094 | 0/0 | 6585 | 1 | 0 | 0 | 0 | 1 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| a0001c0002t0095 | 0/0 | 6585 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| a0001c0002t0096 | 0/0 | 6588 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| a0001c0002t0097 | 0/0 | 6586 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| a0001c0002t0098 | 0/0 | 6587 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| a0001c0002t0099 | 0/0 | 6585 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| a0001c0002t0100 | 0/0 | 6584 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| a0001c0002t0101 | 0/0 | 6584 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| a0001c0002t0106 | 0/0 | 6586 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| a0001c0003t0062 | 0/0 | 6586 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| a0002c0004t0063 | 0/0 | 6577 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | copy fasta | chr6 | 70851679 | 70962060 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0002g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0003g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0003g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0003g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0003g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0003g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0003g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0003g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0003g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0003g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0003g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0003g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0003g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0003g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0003g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0003g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0003g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0003g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0003g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0003g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0003g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0003g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0004g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0004g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0004g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0004g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0004g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0004g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0004g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0004g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0004g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0004g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0004g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0004g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0004g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0004g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0009g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0009g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0009g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0009g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0009g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0009g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0009g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0010g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0010g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0010g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0010g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0010g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0010g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0010g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0012g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0012g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0012g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0012g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0012g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0012g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0013g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0013g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0013g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0013g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0013g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0013g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0017g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0017g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0017g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0017g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0018g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0018g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0018g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0018g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0019g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0019g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0019g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0019g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0020g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0020g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0020g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0020g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0023g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0023g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0023g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0024g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0024g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0024g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0025g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0025g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0025g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0032g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0032g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0033g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0033g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0034g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0034g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0035g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0035g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0036g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0036g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0037g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0037g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0044g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0044g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0045g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0046g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0047g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0048g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0049g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0050g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0051g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0052g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0053g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0054g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0055g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0056g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0057g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0058g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0059g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0060g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0061g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0064g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0065g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0066g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0067g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0068g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0069g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0070g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0071g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0072g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0073g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0074g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0075g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0076g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0102g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0103g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0104g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0105g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0107g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0108g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0109g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0110g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0001t0111g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0002t0005g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0002t0005g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0002t0005g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0002t0005g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0002t0005g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0002t0005g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0002t0005g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0002t0005g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0002t0005g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0002t0005g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0002t0005g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0002t0005g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0002t0005g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0002t0006g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0002t0006g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0002t0006g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0002t0006g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0002t0006g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0002t0006g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0002t0006g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0002t0006g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0002t0006g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0002t0006g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0002t0007g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0002t0007g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0002t0007g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0002t0007g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0002t0007g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0002t0007g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0002t0007g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0002t0007g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0002t0007g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0002t0008g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0002t0008g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0002t0008g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0002t0008g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0002t0008g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0002t0008g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0002t0008g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0002t0011g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0002t0011g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0002t0011g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0002t0011g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0002t0011g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0002t0011g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0002t0011g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0002t0014g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0002t0014g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0002t0014g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0002t0014g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0002t0014g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0002t0014g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0002t0015g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0002t0015g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0002t0015g0281 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0002t0015g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0002t0015g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0002t0015g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0002t0016g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0002t0016g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0002t0016g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0002t0016g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0002t0016g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0002t0021g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0002t0021g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0002t0021g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0002t0021g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0002t0022g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0002t0022g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0002t0022g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0002t0022g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0002t0026g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0002t0026g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0002t0026g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0002t0027g0200 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0002t0027g0213 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0002t0027g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0002t0028g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0002t0028g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0002t0028g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0002t0029g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0002t0029g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0002t0029g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0002t0030g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0002t0030g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0002t0030g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0002t0031g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0002t0031g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0002t0031g0282 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0002t0038g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0002t0038g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0002t0039g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0002t0039g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0002t0040g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0002t0040g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0002t0041g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0002t0041g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0002t0042g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0002t0042g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0002t0043g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0002t0043g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0002t0077g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0002t0078g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0002t0079g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0002t0080g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0002t0081g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0002t0082g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0002t0083g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0002t0084g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0002t0085g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0002t0086g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0002t0087g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0002t0088g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0002t0089g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0002t0090g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0002t0091g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0002t0092g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0002t0093g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0002t0094g0275 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0002t0095g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0002t0096g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0002t0097g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0002t0098g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0002t0099g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0002t0100g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0002t0101g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0002t0106g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0001c0003t0062g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| a0002c0004t0063g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0094 | g0275 | EUR | GBR | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0054 | EUR | GBR | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG00323 | hp1 | a0001 | c0002 | t0015 | g0281 | EUR | FIN | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG00323 | hp2 | a0001 | c0001 | t0004 | g0098 | EUR | FIN | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG00408 | hp1 | a0001 | c0001 | t0002 | g0151 | EAS | CHS | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG00408 | hp2 | a0001 | c0001 | t0010 | g0122 | EAS | CHS | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG00423 | hp1 | a0001 | c0001 | t0003 | g0143 | EAS | CHS | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG00423 | hp2 | a0001 | c0002 | t0078 | g0207 | EAS | CHS | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0153 | EAS | CHS | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG00544 | hp2 | a0001 | c0001 | t0009 | g0159 | EAS | CHS | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG00597 | hp1 | a0001 | c0001 | t0013 | g0049 | EAS | CHS | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG00597 | hp2 | a0001 | c0002 | t0016 | g0237 | EAS | CHS | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG00621 | hp1 | a0001 | c0002 | t0087 | g0236 | EAS | CHS | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG00621 | hp2 | a0001 | c0002 | t0007 | g0204 | EAS | CHS | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG00642 | hp1 | a0001 | c0002 | t0014 | g0290 | AMR | PUR | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG00642 | hp2 | a0001 | c0002 | t0040 | g0224 | AMR | PUR | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | CHS | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG00673 | hp2 | a0001 | c0001 | t0012 | g0030 | EAS | CHS | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG00735 | hp1 | a0001 | c0001 | t0044 | g0304 | AMR | PUR | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG00735 | hp2 | a0001 | c0002 | t0008 | g0221 | AMR | PUR | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG00738 | hp1 | a0001 | c0002 | t0008 | g0002 | AMR | PUR | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG00738 | hp2 | a0001 | c0002 | t0014 | g0293 | AMR | PUR | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG00741 | hp1 | a0001 | c0001 | t0004 | g0124 | AMR | PUR | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG00741 | hp2 | a0001 | c0002 | t0014 | g0279 | AMR | PUR | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG01069 | hp1 | a0001 | c0001 | t0025 | g0109 | AMR | PUR | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG01069 | hp2 | a0001 | c0002 | t0095 | g0284 | AMR | PUR | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG01071 | hp1 | a0001 | c0002 | t0014 | g0285 | AMR | PUR | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG01071 | hp2 | a0001 | c0002 | t0005 | g0226 | AMR | PUR | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG01074 | hp1 | a0001 | c0001 | t0019 | g0012 | AMR | PUR | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG01074 | hp2 | a0001 | c0002 | t0099 | g0292 | AMR | PUR | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG01099 | hp1 | a0001 | c0002 | t0015 | g0278 | AMR | PUR | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG01099 | hp2 | a0001 | c0002 | t0082 | g0239 | AMR | PUR | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG01167 | hp1 | a0001 | c0001 | t0003 | g0102 | AMR | PUR | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG01167 | hp2 | a0001 | c0002 | t0014 | g0289 | AMR | PUR | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG01168 | hp1 | a0001 | c0001 | t0035 | g0166 | AMR | PUR | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG01168 | hp2 | a0001 | c0002 | t0008 | g0219 | AMR | PUR | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG01169 | hp1 | a0001 | c0001 | t0003 | g0125 | AMR | PUR | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG01169 | hp2 | a0001 | c0001 | t0064 | g0165 | AMR | PUR | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG01192 | hp1 | a0001 | c0002 | t0084 | g0244 | AMR | PUR | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0046 | AMR | PUR | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG01255 | hp1 | a0001 | c0001 | t0017 | g0013 | AMR | CLM | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG01255 | hp2 | a0001 | c0002 | t0008 | g0002 | AMR | CLM | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG01256 | hp1 | a0001 | c0001 | t0013 | g0096 | AMR | CLM | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG01256 | hp2 | a0001 | c0001 | t0018 | g0025 | AMR | CLM | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG01257 | hp1 | a0001 | c0001 | t0018 | g0027 | AMR | CLM | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG01257 | hp2 | a0001 | c0001 | t0044 | g0306 | AMR | CLM | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG01261 | hp1 | a0001 | c0001 | t0010 | g0084 | AMR | CLM | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG01261 | hp2 | a0001 | c0001 | t0103 | g0308 | AMR | CLM | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG01346 | hp1 | a0001 | c0002 | t0015 | g0287 | AMR | CLM | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG01346 | hp2 | a0001 | c0001 | t0018 | g0026 | AMR | CLM | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG01433 | hp1 | a0001 | c0001 | t0020 | g0053 | AMR | CLM | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG01433 | hp2 | a0001 | c0002 | t0029 | g0280 | AMR | CLM | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG01496 | hp1 | a0001 | c0002 | t0005 | g0199 | AMR | CLM | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG01496 | hp2 | a0001 | c0002 | t0008 | g0216 | AMR | CLM | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG01517 | hp1 | a0001 | c0001 | t0035 | g0045 | EUR | IBS | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG01517 | hp2 | a0001 | c0002 | t0027 | g0220 | EUR | IBS | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG01884 | hp1 | a0001 | c0002 | t0011 | g0272 | AFR | ACB | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG01884 | hp2 | a0001 | c0001 | t0003 | g0133 | AFR | ACB | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG01891 | hp1 | a0001 | c0002 | t0005 | g0201 | AFR | ACB | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG01891 | hp2 | a0001 | c0001 | t0010 | g0051 | AFR | ACB | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0048 | AMR | PEL | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG01934 | hp2 | a0001 | c0002 | t0022 | g0283 | AMR | PEL | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0160 | AMR | PEL | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG01952 | hp2 | a0001 | c0001 | t0013 | g0085 | AMR | PEL | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG01975 | hp1 | a0001 | c0001 | t0010 | g0071 | AMR | PEL | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG01975 | hp2 | a0001 | c0001 | t0020 | g0097 | AMR | PEL | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG01978 | hp1 | a0001 | c0001 | t0009 | g0047 | AMR | PEL | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG01978 | hp2 | a0001 | c0002 | t0005 | g0182 | AMR | PEL | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG01981 | hp1 | a0001 | c0002 | t0008 | g0228 | AMR | PEL | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG01981 | hp2 | a0001 | c0001 | t0017 | g0014 | AMR | PEL | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG01993 | hp1 | a0001 | c0001 | t0065 | g0067 | AMR | PEL | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0121 | AMR | PEL | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG02004 | hp1 | a0001 | c0001 | t0009 | g0083 | AMR | PEL | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG02004 | hp2 | a0001 | c0001 | t0017 | g0023 | AMR | PEL | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG02015 | hp1 | a0001 | c0001 | t0010 | g0094 | EAS | KHV | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG02015 | hp2 | a0001 | c0001 | t0002 | g0058 | EAS | KHV | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG02027 | hp1 | a0001 | c0001 | t0012 | g0017 | EAS | KHV | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG02027 | hp2 | a0001 | c0002 | t0021 | g0238 | EAS | KHV | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG02040 | hp1 | a0001 | c0002 | t0026 | g0209 | EAS | KHV | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | KHV | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG02055 | hp1 | a0001 | c0001 | t0024 | g0127 | AFR | ACB | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG02055 | hp2 | a0001 | c0001 | t0009 | g0095 | AFR | ACB | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG02056 | hp1 | a0001 | c0001 | t0013 | g0033 | EAS | KHV | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | KHV | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG02071 | hp1 | a0001 | c0001 | t0111 | g0314 | EAS | KHV | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG02071 | hp2 | a0001 | c0002 | t0007 | g0212 | EAS | KHV | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG02129 | hp1 | a0001 | c0001 | t0003 | g0146 | EAS | KHV | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG02129 | hp2 | a0001 | c0002 | t0021 | g0231 | EAS | KHV | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG02132 | hp1 | a0001 | c0002 | t0030 | g0302 | EAS | KHV | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG02132 | hp2 | a0001 | c0002 | t0079 | g0202 | EAS | KHV | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG02135 | hp1 | a0001 | c0002 | t0022 | g0266 | EAS | KHV | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG02135 | hp2 | a0001 | c0001 | t0004 | g0149 | EAS | KHV | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG02145 | hp1 | a0001 | c0002 | t0031 | g0277 | AFR | ACB | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG02145 | hp2 | a0001 | c0001 | t0024 | g0040 | AFR | ACB | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG02155 | hp1 | a0001 | c0002 | t0021 | g0249 | EAS | CDX | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG02155 | hp2 | a0001 | c0001 | t0012 | g0022 | EAS | CDX | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG02165 | hp1 | a0001 | c0002 | t0006 | g0235 | EAS | CDX | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG02165 | hp2 | a0001 | c0001 | t0060 | g0118 | EAS | CDX | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG02258 | hp1 | a0001 | c0001 | t0024 | g0123 | AFR | ACB | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG02258 | hp2 | a0001 | c0001 | t0004 | g0056 | AFR | ACB | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG02280 | hp1 | a0001 | c0001 | t0051 | g0005 | AFR | ACB | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG02280 | hp2 | a0001 | c0001 | t0004 | g0131 | AFR | ACB | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG02300 | hp1 | a0001 | c0001 | t0009 | g0092 | AMR | PEL | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG02300 | hp2 | a0001 | c0002 | t0015 | g0253 | AMR | PEL | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG02451 | hp1 | a0001 | c0001 | t0018 | g0006 | AFR | ACB | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG02451 | hp2 | a0001 | c0001 | t0003 | g0126 | AFR | ACB | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG02523 | hp1 | a0001 | c0001 | t0010 | g0039 | EAS | KHV | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG02523 | hp2 | a0001 | c0001 | t0012 | g0020 | EAS | KHV | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG02572 | hp1 | a0001 | c0002 | t0080 | g0194 | AFR | GWD | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG02572 | hp2 | a0001 | c0001 | t0003 | g0129 | AFR | GWD | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG02602 | hp1 | a0001 | c0002 | t0106 | g0309 | SAS | PJL | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG02602 | hp2 | a0001 | c0002 | t0081 | g0240 | SAS | PJL | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG02622 | hp1 | a0001 | c0002 | t0006 | g0189 | AFR | GWD | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG02622 | hp2 | a0001 | c0001 | t0102 | g0303 | AFR | GWD | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG02630 | hp1 | a0001 | c0002 | t0006 | g0188 | AFR | GWD | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG02630 | hp2 | a0001 | c0001 | t0012 | g0010 | AFR | GWD | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG02647 | hp1 | a0001 | c0002 | t0041 | g0196 | AFR | GWD | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG02647 | hp2 | a0001 | c0002 | t0100 | g0258 | AFR | GWD | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG02683 | hp1 | a0001 | c0001 | t0010 | g0157 | SAS | PJL | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0079 | SAS | PJL | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0044 | SAS | PJL | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG02698 | hp2 | a0002 | c0004 | t0063 | g0176 | SAS | PJL | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG02717 | hp1 | a0001 | c0001 | t0069 | g0103 | AFR | GWD | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG02717 | hp2 | a0001 | c0002 | t0011 | g0256 | AFR | GWD | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG02723 | hp1 | a0001 | c0002 | t0041 | g0190 | AFR | GWD | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG02723 | hp2 | a0001 | c0001 | t0049 | g0011 | AFR | GWD | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG02735 | hp1 | a0001 | c0002 | t0008 | g0248 | SAS | PJL | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG02735 | hp2 | a0001 | c0002 | t0015 | g0288 | SAS | PJL | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG02738 | hp1 | a0001 | c0002 | t0088 | g0298 | SAS | PJL | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG02738 | hp2 | a0001 | c0002 | t0028 | g0252 | SAS | PJL | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG02809 | hp1 | a0001 | c0001 | t0004 | g0164 | AFR | GWD | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG02809 | hp2 | a0001 | c0002 | t0028 | g0195 | AFR | GWD | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG02818 | hp1 | a0001 | c0001 | t0053 | g0032 | AFR | GWD | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG02818 | hp2 | a0001 | c0001 | t0034 | g0106 | AFR | GWD | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG02886 | hp1 | a0001 | c0002 | t0028 | g0222 | AFR | GWD | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG02886 | hp2 | a0001 | c0001 | t0067 | g0113 | AFR | GWD | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG02895 | hp1 | a0001 | c0001 | t0003 | g0135 | AFR | GWD | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG02895 | hp2 | a0001 | c0002 | t0101 | g0257 | AFR | GWD | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG02896 | hp1 | a0001 | c0001 | t0048 | g0008 | AFR | GWD | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG02896 | hp2 | a0001 | c0001 | t0004 | g0163 | AFR | GWD | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG02965 | hp1 | a0001 | c0002 | t0011 | g0262 | AFR | ESN | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG02965 | hp2 | a0001 | c0001 | t0004 | g0112 | AFR | ESN | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG02970 | hp1 | a0001 | c0002 | t0006 | g0191 | AFR | ESN | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG02970 | hp2 | a0001 | c0001 | t0056 | g0115 | AFR | ESN | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG02976 | hp1 | a0001 | c0002 | t0091 | g0260 | AFR | ESN | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG02976 | hp2 | a0001 | c0001 | t0073 | g0107 | AFR | ESN | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG03041 | hp1 | a0001 | c0001 | t0003 | g0142 | AFR | GWD | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG03041 | hp2 | a0001 | c0001 | t0036 | g0104 | AFR | GWD | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG03098 | hp1 | a0001 | c0002 | t0042 | g0295 | AFR | MSL | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG03098 | hp2 | a0001 | c0002 | t0011 | g0255 | AFR | MSL | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG03130 | hp1 | a0001 | c0002 | t0096 | g0261 | AFR | ESN | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG03130 | hp2 | a0001 | c0001 | t0004 | g0137 | AFR | ESN | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG03139 | hp1 | a0001 | c0002 | t0011 | g0259 | AFR | ESN | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG03139 | hp2 | a0001 | c0001 | t0023 | g0077 | AFR | ESN | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG03195 | hp1 | a0001 | c0001 | t0055 | g0128 | AFR | ESN | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG03195 | hp2 | a0001 | c0001 | t0054 | g0031 | AFR | ESN | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG03209 | hp1 | a0001 | c0001 | t0004 | g0161 | AFR | MSL | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG03209 | hp2 | a0001 | c0001 | t0070 | g0111 | AFR | MSL | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG03225 | hp1 | a0001 | c0002 | t0043 | g0273 | AFR | MSL | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG03225 | hp2 | a0001 | c0001 | t0033 | g0075 | AFR | MSL | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG03239 | hp1 | a0001 | c0001 | t0037 | g0061 | SAS | PJL | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG03239 | hp2 | a0001 | c0002 | t0008 | g0250 | SAS | PJL | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG03453 | hp1 | a0001 | c0002 | t0042 | g0254 | AFR | MSL | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG03453 | hp2 | a0001 | c0001 | t0004 | g0136 | AFR | MSL | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG03486 | hp1 | a0001 | c0003 | t0062 | g0105 | AFR | MSL | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG03486 | hp2 | a0001 | c0002 | t0043 | g0274 | AFR | MSL | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG03490 | hp1 | a0001 | c0001 | t0003 | g0168 | SAS | PJL | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0169 | SAS | PJL | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG03491 | hp1 | a0001 | c0001 | t0020 | g0078 | SAS | PJL | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG03491 | hp2 | a0001 | c0002 | t0016 | g0229 | SAS | PJL | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0170 | SAS | PJL | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG03492 | hp2 | a0001 | c0002 | t0016 | g0227 | SAS | PJL | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG03516 | hp1 | a0001 | c0001 | t0033 | g0114 | AFR | ESN | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG03516 | hp2 | a0001 | c0002 | t0006 | g0197 | AFR | ESN | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG03540 | hp1 | a0001 | c0002 | t0007 | g0185 | AFR | GWD | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG03540 | hp2 | a0001 | c0001 | t0025 | g0134 | AFR | GWD | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG03579 | hp1 | a0001 | c0001 | t0003 | g0132 | AFR | MSL | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG03579 | hp2 | a0001 | c0002 | t0006 | g0187 | AFR | MSL | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG03654 | hp1 | a0001 | c0002 | t0005 | g0241 | SAS | PJL | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG03654 | hp2 | a0001 | c0002 | t0029 | g0276 | SAS | PJL | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG03669 | hp1 | a0001 | c0001 | t0074 | g0087 | SAS | PJL | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG03669 | hp2 | a0001 | c0001 | t0003 | g0099 | SAS | PJL | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG03688 | hp1 | a0001 | c0001 | t0003 | g0100 | SAS | STU | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0042 | SAS | STU | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0172 | SAS | PJL | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG03710 | hp2 | a0001 | c0001 | t0037 | g0088 | SAS | PJL | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG03831 | hp1 | a0001 | c0002 | t0014 | g0291 | SAS | BEB | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG03831 | hp2 | a0001 | c0002 | t0006 | g0246 | SAS | BEB | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG03834 | hp1 | a0001 | c0002 | t0007 | g0192 | SAS | BEB | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG03834 | hp2 | a0001 | c0002 | t0086 | g0184 | SAS | BEB | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG03927 | hp1 | a0001 | c0002 | t0097 | g0296 | SAS | BEB | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0171 | SAS | BEB | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG04184 | hp1 | a0001 | c0002 | t0015 | g0286 | SAS | BEB | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG04184 | hp2 | a0001 | c0001 | t0003 | g0080 | SAS | BEB | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG04199 | hp1 | a0001 | c0001 | t0047 | g0028 | SAS | STU | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG04199 | hp2 | a0001 | c0002 | t0007 | g0251 | SAS | STU | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG04204 | hp1 | a0001 | c0001 | t0003 | g0154 | SAS | STU | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG04204 | hp2 | a0001 | c0002 | t0098 | g0294 | SAS | STU | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| NA18747 | hp1 | a0001 | c0002 | t0026 | g0181 | EAS | CHB | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| NA18747 | hp2 | a0001 | c0001 | t0046 | g0029 | EAS | CHB | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| NA18906 | hp1 | a0001 | c0002 | t0085 | g0198 | AFR | YRI | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| NA18906 | hp2 | a0001 | c0001 | t0023 | g0086 | AFR | YRI | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| NA18940 | hp1 | a0001 | c0001 | t0003 | g0091 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| NA18940 | hp2 | a0001 | c0001 | t0002 | g0050 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| NA18945 | hp1 | a0001 | c0001 | t0019 | g0019 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| NA18945 | hp2 | a0001 | c0001 | t0071 | g0038 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0037 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0120 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| NA18949 | hp1 | a0001 | c0002 | t0005 | g0232 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| NA18949 | hp2 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0150 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| NA18951 | hp1 | a0001 | c0002 | t0092 | g0265 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| NA18960 | hp1 | a0001 | c0001 | t0104 | g0305 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| NA18960 | hp2 | a0001 | c0002 | t0005 | g0233 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| NA18962 | hp1 | a0001 | c0001 | t0003 | g0090 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| NA18962 | hp2 | a0001 | c0002 | t0030 | g0263 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| NA18963 | hp1 | a0001 | c0002 | t0005 | g0217 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| NA18963 | hp2 | a0001 | c0001 | t0019 | g0018 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| NA18964 | hp1 | a0001 | c0001 | t0050 | g0016 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| NA18964 | hp2 | a0001 | c0001 | t0108 | g0313 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| NA18965 | hp1 | a0001 | c0002 | t0093 | g0268 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| NA18965 | hp2 | a0001 | c0001 | t0002 | g0144 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| NA18967 | hp1 | a0001 | c0001 | t0013 | g0140 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| NA18967 | hp2 | a0001 | c0001 | t0002 | g0072 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0152 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| NA18969 | hp2 | a0001 | c0002 | t0006 | g0208 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| NA18974 | hp1 | a0001 | c0002 | t0026 | g0243 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| NA18974 | hp2 | a0001 | c0002 | t0031 | g0267 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| NA18975 | hp2 | a0001 | c0002 | t0038 | g0178 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| NA18980 | hp1 | a0001 | c0002 | t0040 | g0186 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| NA18980 | hp2 | a0001 | c0001 | t0034 | g0148 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| NA18981 | hp1 | a0001 | c0001 | t0032 | g0004 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| NA18981 | hp2 | a0001 | c0002 | t0090 | g0301 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| NA18984 | hp1 | a0001 | c0002 | t0030 | g0264 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0070 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| NA18994 | hp2 | a0001 | c0002 | t0005 | g0211 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| NA18997 | hp1 | a0001 | c0001 | t0052 | g0015 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| NA18997 | hp2 | a0001 | c0001 | t0013 | g0141 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| NA18999 | hp2 | a0001 | c0001 | t0003 | g0035 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| NA19000 | hp1 | a0001 | c0002 | t0083 | g0210 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| NA19000 | hp2 | a0001 | c0001 | t0003 | g0147 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| NA19002 | hp1 | a0001 | c0001 | t0009 | g0116 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| NA19002 | hp2 | a0001 | c0002 | t0007 | g0242 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| NA19005 | hp2 | a0001 | c0002 | t0005 | g0203 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| NA19006 | hp1 | a0001 | c0001 | t0003 | g0089 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| NA19006 | hp2 | a0001 | c0001 | t0107 | g0312 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0175 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| NA19007 | hp2 | a0001 | c0002 | t0006 | g0230 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| NA19009 | hp1 | a0001 | c0001 | t0061 | g0093 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| NA19009 | hp2 | a0001 | c0002 | t0022 | g0299 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| NA19010 | hp1 | a0001 | c0002 | t0011 | g0270 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0043 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0119 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| NA19011 | hp2 | a0001 | c0002 | t0007 | g0225 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| NA19012 | hp1 | a0001 | c0002 | t0029 | g0300 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| NA19012 | hp2 | a0001 | c0001 | t0072 | g0036 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| NA19030 | hp1 | a0001 | c0001 | t0004 | g0074 | AFR | LWK | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| NA19030 | hp2 | a0001 | c0001 | t0066 | g0139 | AFR | LWK | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| NA19043 | hp1 | a0001 | c0001 | t0025 | g0110 | AFR | LWK | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| NA19043 | hp2 | a0001 | c0002 | t0011 | g0271 | AFR | LWK | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| NA19056 | hp1 | a0001 | c0002 | t0038 | g0180 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| NA19056 | hp2 | a0001 | c0002 | t0039 | g0247 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| NA19057 | hp1 | a0001 | c0001 | t0058 | g0082 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| NA19057 | hp2 | a0001 | c0002 | t0005 | g0234 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| NA19058 | hp1 | a0001 | c0002 | t0039 | g0205 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| NA19058 | hp2 | a0001 | c0001 | t0076 | g0177 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| NA19062 | hp1 | a0001 | c0001 | t0002 | g0065 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| NA19062 | hp2 | a0001 | c0002 | t0007 | g0223 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| NA19064 | hp1 | a0001 | c0001 | t0057 | g0073 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| NA19064 | hp2 | a0001 | c0002 | t0005 | g0218 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| NA19065 | hp2 | a0001 | c0001 | t0032 | g0021 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| NA19066 | hp1 | a0001 | c0002 | t0007 | g0214 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| NA19066 | hp2 | a0001 | c0001 | t0110 | g0311 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| NA19070 | hp2 | a0001 | c0002 | t0021 | g0183 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| NA19078 | hp1 | a0001 | c0001 | t0017 | g0007 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| NA19078 | hp2 | a0001 | c0001 | t0002 | g0158 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| NA19081 | hp1 | a0001 | c0001 | t0009 | g0155 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| NA19081 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| NA19082 | hp1 | a0001 | c0001 | t0019 | g0024 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| NA19082 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| NA19083 | hp1 | a0001 | c0002 | t0022 | g0269 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| NA19083 | hp2 | a0001 | c0002 | t0005 | g0215 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| NA19084 | hp1 | a0001 | c0002 | t0077 | g0179 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| NA19084 | hp2 | a0001 | c0001 | t0002 | g0069 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| NA19085 | hp1 | a0001 | c0002 | t0016 | g0206 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0059 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| NA20752 | hp1 | a0001 | c0001 | t0020 | g0066 | EUR | TSI | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| NA20752 | hp2 | a0001 | c0002 | t0027 | g0213 | EUR | TSI | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG02109 | hp1 | a0001 | c0001 | t0059 | g0162 | AFR | ACB | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG02109 | hp2 | a0001 | c0001 | t0036 | g0138 | AFR | ACB | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | ACB | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG02486 | hp2 | a0001 | c0001 | t0004 | g0108 | AFR | ACB | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG02559 | hp1 | a0001 | c0001 | t0045 | g0003 | AFR | ACB | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG02559 | hp2 | a0001 | c0002 | t0006 | g0193 | AFR | ACB | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG03471 | hp1 | a0001 | c0001 | t0003 | g0081 | AFR | MSL | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG03471 | hp2 | a0001 | c0001 | t0012 | g0009 | AFR | MSL | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG06807 | hp1 | a0001 | c0001 | t0023 | g0076 | AFR | USA | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| HG06807 | hp2 | a0001 | c0001 | t0068 | g0167 | AFR | USA | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| NA18955 | hp1 | a0001 | c0001 | t0109 | g0310 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| NA18955 | hp2 | a0001 | c0002 | t0016 | g0245 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| NA20300 | hp1 | a0001 | c0001 | t0105 | g0307 | AFR | USA | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| NA20300 | hp2 | a0001 | c0001 | t0004 | g0052 | AFR | USA | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| NA21309 | hp1 | a0001 | c0001 | t0075 | g0130 | AFR | LWK | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| NA21309 | hp2 | a0001 | c0002 | t0089 | g0297 | AFR | LWK | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0002 | t0031 | g0282 | REF | REF | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| homoSapiens_grch38 | hp1 | a0001 | c0002 | t0027 | g0200 | REF | REF | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:70956279
|
G | C | 1 | a0002 | 1 | HG02698.hp2 | missense_variant | MODERATE | c.151C>G | p.Arg51Gly | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/4 | 782/6587 | 151/972 | 51/323 | chr6 | 70956279 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:70861893
|
A | G | 1 | a0001c0003 | 1 | HG03486.hp1 | synonymous_variant | LOW | c.822T>C | p.Ser274Ser | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 3/4 | 1453/6587 | 822/972 | 274/323 | chr6 | 70861893 | ||
| chr6:70956283
|
G | A | 3 | a0001c0001a0001c0003a0002c0004 | 188 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(185): Show |
synonymous_variant | LOW | c.147C>T | p.Gly49Gly | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/4 | 778/6587 | 147/972 | 49/323 | chr6 | 70956283 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:70856766
|
A | G | 1 | a0001c0002t0042 | 2 | HG03098.hp1 HG03453.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4897T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 4/4 | 4897 | chr6 | 70856766 | |||||
| chr6:70856944
|
C | G | 1 | a0001c0002t0100 | 1 | HG02647.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4719G>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 4/4 | 4719 | chr6 | 70856944 | |||||
| chr6:70857845
|
A | G | 2 | a0001c0001t0045a0001c0002t0042 | 3 | HG02559.hp1 HG03098.hp1 HG03453.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3818T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 4/4 | 3818 | chr6 | 70857845 | |||||
| chr6:70857887
|
GCT | G | 4 | a0001c0001t0036a0001c0001t0068a0001c0002t0100others(1): Show | 5 | HG02109.hp2 HG02647.hp2 HG02895.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3774_*3775delAG | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 4/4 | 3774 | chr6 | 70857887 | |||||
| chr6:70857946
|
T | C | 1 | a0001c0002t0093 | 1 | NA18965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3717A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 4/4 | 3717 | chr6 | 70857946 | |||||
| chr6:70858014
|
G | C | 1 | a0001c0002t0083 | 1 | NA19000.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3649C>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 4/4 | 3649 | chr6 | 70858014 | |||||
| chr6:70858287
|
C | CT | 13 | a0001c0001t0024a0001c0001t0032a0001c0001t0057others(10): Show | 19 | HG00642.hp2 HG02040.hp1 HG02055.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*3375dupA | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 4/4 | 3375 | chr6 | 70858287 | |||||
| chr6:70858287
|
C | CTTTTTTT others(3): Show |
1 | a0001c0001t0045 | 1 | HG02559.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3366_*3375dupAAAA others(6): Show |
B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 4/4 | 3375 | chr6 | 70858287 | |||||
| chr6:70858287
|
CT | C | 42 | a0001c0001t0001a0001c0001t0003a0001c0001t0010others(39): Show | 162 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(159): Show |
3_prime_UTR_variant | MODIFIER | c.*3375delA | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 4/4 | 3375 | chr6 | 70858287 | |||||
| chr6:70858287
|
CTT | C | 11 | a0001c0001t0034a0001c0001t0055a0001c0001t0058others(8): Show | 12 | HG00099.hp1 HG01069.hp2 HG01074.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*3374_*3375delAA | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 4/4 | 3374 | chr6 | 70858287 | |||||
| chr6:70858287
|
CTTTT | C | 5 | a0001c0001t0023a0001c0001t0049a0001c0001t0070others(2): Show | 7 | HG02572.hp1 HG02723.hp2 HG02976.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3372_*3375delAAAA | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 4/4 | 3372 | chr6 | 70858287 | |||||
| chr6:70858287
|
CTTTTTTT others(3): Show |
C | 2 | a0001c0002t0084a0002c0004t0063 | 2 | HG01192.hp1 HG02698.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3366_*3375delAAAA others(6): Show |
B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 4/4 | 3366 | chr6 | 70858287 | |||||
| chr6:70858287
|
CTTTTTTT others(5): Show |
C | 1 | a0001c0001t0061 | 1 | NA19009.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3364_*3375delAAAA others(8): Show |
B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 4/4 | 3364 | chr6 | 70858287 | |||||
| chr6:70858299
|
T | G | 9 | a0001c0001t0010a0001c0001t0019a0001c0001t0103others(6): Show | 22 | HG00408.hp2 HG01074.hp1 HG01099.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*3364A>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 4/4 | 3364 | chr6 | 70858299 | |||||
| chr6:70858338
|
G | A | 4 | a0001c0001t0023a0001c0001t0049a0001c0002t0080others(1): Show | 6 | HG02572.hp1 HG02723.hp2 HG02976.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3325C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 4/4 | 3325 | chr6 | 70858338 | |||||
| chr6:70858427
|
G | C | 98 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(95): Show | 273 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(270): Show |
3_prime_UTR_variant | MODIFIER | c.*3236C>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 4/4 | 3236 | chr6 | 70858427 | |||||
| chr6:70858714
|
A | G | 36 | a0001c0001t0001a0001c0001t0009a0001c0001t0010others(33): Show | 110 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(107): Show |
3_prime_UTR_variant | MODIFIER | c.*2949T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 4/4 | 2949 | chr6 | 70858714 | |||||
| chr6:70858976
|
A | G | 2 | a0001c0002t0084a0002c0004t0063 | 2 | HG01192.hp1 HG02698.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2687T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 4/4 | 2687 | chr6 | 70858976 | |||||
| chr6:70859049
|
G | A | 2 | a0001c0001t0069a0001c0001t0070 | 2 | HG02717.hp1 HG03209.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2614C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 4/4 | 2614 | chr6 | 70859049 | |||||
| chr6:70859138
|
T | C | 23 | a0001c0001t0001a0001c0001t0009a0001c0001t0010others(20): Show | 77 | HG00099.hp2 HG00408.hp2 HG00544.hp2 others(74): Show |
3_prime_UTR_variant | MODIFIER | c.*2525A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 4/4 | 2525 | chr6 | 70859138 | |||||
| chr6:70859204
|
G | A | 1 | a0001c0002t0080 | 1 | HG02572.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2459C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 4/4 | 2459 | chr6 | 70859204 | |||||
| chr6:70859210
|
A | T | 1 | a0001c0001t0050 | 1 | NA18964.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2453T>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 4/4 | 2453 | chr6 | 70859210 | |||||
| chr6:70859232
|
A | G | 23 | a0001c0001t0001a0001c0001t0009a0001c0001t0010others(20): Show | 77 | HG00099.hp2 HG00408.hp2 HG00544.hp2 others(74): Show |
3_prime_UTR_variant | MODIFIER | c.*2431T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 4/4 | 2431 | chr6 | 70859232 | |||||
| chr6:70859303
|
G | C | 1 | a0001c0002t0080 | 1 | HG02572.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2360C>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 4/4 | 2360 | chr6 | 70859303 | |||||
| chr6:70859379
|
C | T | 1 | a0001c0003t0062 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2284G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 4/4 | 2284 | chr6 | 70859379 | |||||
| chr6:70859387
|
T | C | 56 | a0001c0001t0001a0001c0001t0009a0001c0001t0010others(53): Show | 135 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(132): Show |
3_prime_UTR_variant | MODIFIER | c.*2276A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 4/4 | 2276 | chr6 | 70859387 | |||||
| chr6:70859426
|
C | T | 22 | a0001c0001t0002a0001c0001t0012a0001c0001t0032others(19): Show | 58 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(55): Show |
3_prime_UTR_variant | MODIFIER | c.*2237G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 4/4 | 2237 | chr6 | 70859426 | |||||
| chr6:70859483
|
C | T | 2 | a0001c0001t0103a0001c0002t0082 | 2 | HG01099.hp2 HG01261.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2180G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 4/4 | 2180 | chr6 | 70859483 | |||||
| chr6:70859545
|
T | TGTAA | 3 | a0001c0001t0052a0001c0001t0071a0001c0001t0072 | 3 | NA18945.hp2 NA18997.hp1 NA19012.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2114_*2117dupTTAC | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 4/4 | 2117 | chr6 | 70859545 | |||||
| chr6:70860115
|
A | G | 1 | a0001c0002t0081 | 1 | HG02602.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1548T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 4/4 | 1548 | chr6 | 70860115 | |||||
| chr6:70860310
|
T | A | 1 | a0001c0001t0045 | 1 | HG02559.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1353A>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 4/4 | 1353 | chr6 | 70860310 | |||||
| chr6:70860420
|
A | AT | 5 | a0001c0001t0023a0001c0001t0049a0001c0001t0059others(2): Show | 7 | HG02109.hp1 HG02572.hp1 HG02723.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1242dupA | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 4/4 | 1242 | chr6 | 70860420 | |||||
| chr6:70860773
|
T | C | 1 | a0001c0002t0077 | 1 | NA19084.hp1 | 3_prime_UTR_variant | MODIFIER | c.*890A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 4/4 | 890 | chr6 | 70860773 | |||||
| chr6:70860938
|
A | G | 16 | a0001c0001t0001a0001c0001t0009a0001c0001t0044others(13): Show | 58 | HG00099.hp2 HG00544.hp2 HG00621.hp2 others(55): Show |
3_prime_UTR_variant | MODIFIER | c.*725T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 4/4 | 725 | chr6 | 70860938 | |||||
| chr6:70860956
|
T | C | 1 | a0001c0001t0073 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*707A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 4/4 | 707 | chr6 | 70860956 | |||||
| chr6:70861042
|
C | T | 1 | a0001c0001t0056 | 1 | HG02970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*621G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 4/4 | 621 | chr6 | 70861042 | |||||
| chr6:70861177
|
T | A | 2 | a0001c0001t0037a0001c0001t0074 | 3 | HG03239.hp1 HG03669.hp1 HG03710.hp2 |
3_prime_UTR_variant | MODIFIER | c.*486A>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 4/4 | 486 | chr6 | 70861177 | |||||
| chr6:70861178
|
T | C | 2 | a0001c0001t0111a0001c0002t0078 | 2 | HG00423.hp2 HG02071.hp1 |
3_prime_UTR_variant | MODIFIER | c.*485A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 4/4 | 485 | chr6 | 70861178 | |||||
| chr6:70861262
|
C | T | 1 | a0001c0001t0055 | 1 | HG03195.hp1 | 3_prime_UTR_variant | MODIFIER | c.*401G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 4/4 | 401 | chr6 | 70861262 | |||||
| chr6:70861294
|
AAACCTGT others(11): Show |
A | 2 | a0001c0001t0075a0001c0002t0087 | 2 | HG00621.hp1 NA21309.hp1 |
3_prime_UTR_variant | MODIFIER | c.*351_*368delGGTAGA others(12): Show |
B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 4/4 | 351 | chr6 | 70861294 | |||||
| chr6:70861511
|
C | G | 1 | a0001c0002t0078 | 1 | HG00423.hp2 | 3_prime_UTR_variant | MODIFIER | c.*152G>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 4/4 | 152 | chr6 | 70861511 | |||||
| chr6:70861593
|
C | G | 2 | a0001c0002t0088a0001c0002t0089 | 2 | HG02738.hp1 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*70G>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 4/4 | 70 | chr6 | 70861593 | |||||
| chr6:70861617
|
A | T | 1 | a0001c0001t0033 | 2 | HG03225.hp2 HG03516.hp1 |
3_prime_UTR_variant | MODIFIER | c.*46T>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 4/4 | 46 | chr6 | 70861617 | |||||
| chr6:70861626
|
C | T | 1 | a0001c0001t0046 | 1 | NA18747.hp2 | 3_prime_UTR_variant | MODIFIER | c.*37G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 4/4 | 37 | chr6 | 70861626 | |||||
| chr6:70861646
|
C | T | 1 | a0001c0001t0053 | 1 | HG02818.hp1 | 3_prime_UTR_variant | MODIFIER | c.*17G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 4/4 | 17 | chr6 | 70861646 | |||||
| chr6:70956443
|
T | C | 87 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(84): Show | 239 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(236): Show |
5_prime_UTR_variant | MODIFIER | c.-14A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/4 | 14 | chr6 | 70956443 | |||||
| chr6:70956511
|
G | A | 2 | a0001c0001t0053a0001c0001t0054 | 2 | HG02818.hp1 HG03195.hp2 |
5_prime_UTR_variant | MODIFIER | c.-82C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/4 | 82 | chr6 | 70956511 | |||||
| chr6:70956524
|
G | A | 63 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(60): Show | 188 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(185): Show |
5_prime_UTR_variant | MODIFIER | c.-95C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/4 | 95 | chr6 | 70956524 | |||||
| chr6:70956676
|
A | C | 2 | a0001c0002t0038a0001c0002t0077 | 3 | NA18975.hp2 NA19056.hp1 NA19084.hp1 |
5_prime_UTR_variant | MODIFIER | c.-247T>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/4 | 247 | chr6 | 70956676 | |||||
| chr6:70956697
|
G | A | 1 | a0001c0001t0076 | 1 | NA19058.hp2 | 5_prime_UTR_variant | MODIFIER | c.-268C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/4 | 268 | chr6 | 70956697 | |||||
| chr6:70956842
|
C | G | 63 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(60): Show | 188 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(185): Show |
5_prime_UTR_variant | MODIFIER | c.-413G>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/4 | 413 | chr6 | 70956842 | |||||
| chr6:70956906
|
C | T | 14 | a0001c0001t0012a0001c0001t0017a0001c0001t0018others(11): Show | 29 | HG00673.hp2 HG01074.hp1 HG01255.hp1 others(26): Show |
5_prime_UTR_variant | MODIFIER | c.-477G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/4 | 477 | chr6 | 70956906 | |||||
| chr6:70956937
|
C | A | 1 | a0001c0001t0102 | 1 | HG02622.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-508G>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/4 | chr6 | 70956937 | ||||||
| chr6:70956942
|
T | G | 4 | a0001c0001t0044a0001c0001t0103a0001c0001t0104others(1): Show | 5 | HG00735.hp1 HG01257.hp2 HG01261.hp2 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-513A>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/4 | 513 | chr6 | 70956942 | |||||
| chr6:70956954
|
G | T | 1 | a0001c0001t0045 | 1 | HG02559.hp1 | 5_prime_UTR_variant | MODIFIER | c.-525C>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/4 | 525 | chr6 | 70956954 | |||||
| chr6:70956987
|
T | G | 1 | a0001c0002t0106 | 1 | HG02602.hp1 | 5_prime_UTR_variant | MODIFIER | c.-558A>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/4 | 558 | chr6 | 70956987 | |||||
| chr6:70957039
|
G | C | 5 | a0001c0001t0107a0001c0001t0108a0001c0001t0109others(2): Show | 5 | HG02071.hp1 NA18955.hp1 NA18964.hp2 others(2): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-610C>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/4 | chr6 | 70957039 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:70861778
|
C | T | 1 | a0001c0001t0109g0310 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.886-29G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 3/3 | chr6 | 70861778 | ||||||
| chr6:70862002
|
A | G | 2 | a0001c0001t0002g0058a0001c0001t0012g0022 | 2 | HG02015.hp2 HG02155.hp2 |
intron_variant | MODIFIER | c.737-24T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70862002 | ||||||
| chr6:70862061
|
A | G | 1 | a0001c0001t0055g0128 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.737-83T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70862061 | ||||||
| chr6:70862404
|
T | A | 7 | a0001c0001t0023g0076a0001c0001t0023g0077a0001c0001t0066g0139others(4): Show | 7 | HG02572.hp1 HG02647.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.737-426A>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70862404 | ||||||
| chr6:70862789
|
A | G | 1 | a0001c0002t0042g0254 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.737-811T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70862789 | ||||||
| chr6:70862863
|
G | A | 1 | a0001c0002t0006g0197 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.737-885C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70862863 | ||||||
| chr6:70862903
|
T | C | 1 | a0001c0001t0003g0143 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.737-925A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70862903 | ||||||
| chr6:70862965
|
G | A | 1 | a0001c0002t0029g0276 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.737-987C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70862965 | ||||||
| chr6:70863068
|
C | T | 2 | a0001c0002t0084g0244a0002c0004t0063g0176 | 2 | HG01192.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.737-1090G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70863068 | ||||||
| chr6:70863107
|
G | C | 1 | a0001c0001t0066g0139 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.737-1129C>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70863107 | ||||||
| chr6:70863406
|
G | A | 113 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0046others(110): Show | 114 | HG00099.hp2 HG00323.hp1 HG00544.hp2 others(111): Show |
intron_variant | MODIFIER | c.737-1428C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70863406 | ||||||
| chr6:70863672
|
T | C | 5 | a0001c0001t0024g0040a0001c0001t0024g0123a0001c0001t0024g0127others(2): Show | 5 | HG02055.hp1 HG02109.hp1 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.737-1694A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70863672 | ||||||
| chr6:70863853
|
G | A | 3 | a0001c0001t0045g0003a0001c0002t0042g0254a0001c0002t0042g0295 | 3 | HG02559.hp1 HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.737-1875C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70863853 | ||||||
| chr6:70864053
|
G | C | 1 | a0001c0001t0001g0171 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.737-2075C>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70864053 | ||||||
| chr6:70864061
|
C | CT | 22 | a0001c0001t0020g0053a0001c0001t0020g0066a0001c0001t0020g0097others(19): Show | 23 | HG00323.hp1 HG00735.hp2 HG00738.hp1 others(20): Show |
intron_variant | MODIFIER | c.737-2084dupA | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70864061 | ||||||
| chr6:70864061
|
CT | C | 35 | a0001c0001t0002g0037a0001c0001t0002g0058a0001c0001t0002g0120others(32): Show | 35 | HG00741.hp1 HG01169.hp1 HG01255.hp1 others(32): Show |
intron_variant | MODIFIER | c.737-2084delA | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70864061 | ||||||
| chr6:70864061
|
CTT | C | 62 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0046others(59): Show | 62 | HG00099.hp2 HG00544.hp2 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.737-2085_737-2084d others(4): Show |
B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70864061 | ||||||
| chr6:70864061
|
CTTT | C | 20 | a0001c0001t0001g0145a0001c0001t0001g0156a0001c0001t0010g0094others(17): Show | 20 | HG00408.hp2 HG01074.hp1 HG01257.hp2 others(17): Show |
intron_variant | MODIFIER | c.737-2086_737-2084d others(5): Show |
B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70864061 | ||||||
| chr6:70864666
|
A | G | 62 | a0001c0001t0003g0035a0001c0001t0003g0080a0001c0001t0003g0081others(59): Show | 62 | HG00323.hp2 HG00423.hp1 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.737-2688T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70864666 | ||||||
| chr6:70864895
|
C | T | 1 | a0001c0001t0055g0128 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.737-2917G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70864895 | ||||||
| chr6:70864938
|
A | G | 1 | a0001c0002t0014g0289 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.737-2960T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70864938 | ||||||
| chr6:70865092
|
A | G | 128 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0046others(125): Show | 129 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.737-3114T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70865092 | ||||||
| chr6:70865252
|
G | A | 3 | a0001c0001t0045g0003a0001c0002t0042g0254a0001c0002t0042g0295 | 3 | HG02559.hp1 HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.737-3274C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70865252 | ||||||
| chr6:70865282
|
C | G | 1 | a0001c0001t0004g0052 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.737-3304G>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70865282 | ||||||
| chr6:70865406
|
C | T | 1 | a0001c0002t0043g0274 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.737-3428G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70865406 | ||||||
| chr6:70865483
|
G | C | 1 | a0001c0001t0009g0095 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.737-3505C>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70865483 | ||||||
| chr6:70865498
|
G | A | 77 | a0001c0001t0002g0001a0001c0001t0002g0034a0001c0001t0002g0037others(74): Show | 78 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(75): Show |
intron_variant | MODIFIER | c.737-3520C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70865498 | ||||||
| chr6:70865536
|
A | G | 1 | a0001c0002t0006g0191 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.737-3558T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70865536 | ||||||
| chr6:70865764
|
C | T | 3 | a0001c0001t0045g0003a0001c0002t0042g0254a0001c0002t0042g0295 | 3 | HG02559.hp1 HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.737-3786G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70865764 | ||||||
| chr6:70865784
|
A | G | 274 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0046others(271): Show | 276 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(273): Show |
intron_variant | MODIFIER | c.737-3806T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70865784 | ||||||
| chr6:70865849
|
A | C | 11 | a0001c0001t0023g0076a0001c0001t0023g0077a0001c0001t0023g0086others(8): Show | 11 | HG02572.hp1 HG02647.hp1 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.737-3871T>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70865849 | ||||||
| chr6:70865869
|
G | A | 1 | a0001c0002t0011g0255 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.737-3891C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70865869 | ||||||
| chr6:70866006
|
G | C | 1 | a0001c0001t0019g0024 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.737-4028C>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70866006 | ||||||
| chr6:70866165
|
G | A | 3 | a0001c0002t0008g0248a0001c0002t0028g0252a0001c0002t0098g0294 | 3 | HG02735.hp1 HG02738.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.737-4187C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70866165 | ||||||
| chr6:70866349
|
A | G | 1 | a0001c0001t0070g0111 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.737-4371T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70866349 | ||||||
| chr6:70866439
|
A | G | 1 | a0001c0001t0104g0305 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.737-4461T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70866439 | ||||||
| chr6:70866566
|
G | A | 1 | a0001c0001t0067g0113 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.737-4588C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70866566 | ||||||
| chr6:70866626
|
T | C | 115 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0046others(112): Show | 116 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.737-4648A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70866626 | ||||||
| chr6:70866721
|
A | C | 3 | a0001c0001t0045g0003a0001c0002t0042g0254a0001c0002t0042g0295 | 3 | HG02559.hp1 HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.737-4743T>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70866721 | ||||||
| chr6:70866894
|
C | T | 2 | a0001c0001t0023g0086a0001c0001t0049g0011 | 2 | HG02723.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.737-4916G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70866894 | ||||||
| chr6:70866911
|
T | C | 2 | a0001c0002t0016g0227a0001c0002t0016g0229 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.737-4933A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70866911 | ||||||
| chr6:70866964
|
T | C | 1 | a0001c0001t0024g0127 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.737-4986A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70866964 | ||||||
| chr6:70867150
|
G | A | 1 | a0001c0001t0002g0120 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.737-5172C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70867150 | ||||||
| chr6:70867289
|
A | G | 22 | a0001c0001t0010g0039a0001c0001t0010g0051a0001c0001t0010g0071others(19): Show | 22 | HG00408.hp2 HG01074.hp1 HG01099.hp2 others(19): Show |
intron_variant | MODIFIER | c.737-5311T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70867289 | ||||||
| chr6:70867411
|
A | C | 7 | a0001c0001t0023g0076a0001c0001t0023g0077a0001c0001t0055g0128others(4): Show | 7 | HG02572.hp1 HG02647.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.737-5433T>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70867411 | ||||||
| chr6:70867567
|
C | A | 2 | a0001c0002t0084g0244a0002c0004t0063g0176 | 2 | HG01192.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.737-5589G>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70867567 | ||||||
| chr6:70867653
|
T | A | 1 | a0001c0002t0084g0244 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.737-5675A>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70867653 | ||||||
| chr6:70868100
|
C | A | 85 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0046others(82): Show | 86 | HG00099.hp2 HG00323.hp1 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.737-6122G>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70868100 | ||||||
| chr6:70868172
|
A | G | 273 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0046others(270): Show | 275 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(272): Show |
intron_variant | MODIFIER | c.737-6194T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70868172 | ||||||
| chr6:70868288
|
G | T | 1 | a0001c0001t0001g0068 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.737-6310C>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70868288 | ||||||
| chr6:70868324
|
C | T | 1 | a0001c0001t0076g0177 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.737-6346G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70868324 | ||||||
| chr6:70868460
|
A | G | 1 | a0001c0001t0002g0153 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.737-6482T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70868460 | ||||||
| chr6:70868828
|
G | C | 1 | a0001c0002t0093g0268 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.737-6850C>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70868828 | ||||||
| chr6:70868944
|
T | A | 1 | a0001c0002t0084g0244 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.737-6966A>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70868944 | ||||||
| chr6:70869273
|
C | T | 72 | a0001c0001t0002g0001a0001c0001t0002g0034a0001c0001t0002g0037others(69): Show | 73 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(70): Show |
intron_variant | MODIFIER | c.737-7295G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70869273 | ||||||
| chr6:70869319
|
A | G | 126 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0046others(123): Show | 127 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.737-7341T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70869319 | ||||||
| chr6:70869327
|
G | A | 3 | a0001c0001t0045g0003a0001c0002t0042g0254a0001c0002t0042g0295 | 3 | HG02559.hp1 HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.737-7349C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70869327 | ||||||
| chr6:70869905
|
G | A | 1 | a0001c0001t0012g0020 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.737-7927C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70869905 | ||||||
| chr6:70869958
|
A | T | 4 | a0001c0001t0024g0040a0001c0001t0024g0123a0001c0001t0024g0127others(1): Show | 4 | HG02055.hp1 HG02109.hp1 HG02145.hp2 others(1): Show |
intron_variant | MODIFIER | c.737-7980T>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70869958 | ||||||
| chr6:70869959
|
A | C | 4 | a0001c0001t0024g0040a0001c0001t0024g0123a0001c0001t0024g0127others(1): Show | 4 | HG02055.hp1 HG02109.hp1 HG02145.hp2 others(1): Show |
intron_variant | MODIFIER | c.737-7981T>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70869959 | ||||||
| chr6:70869984
|
G | A | 1 | a0001c0002t0084g0244 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.737-8006C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70869984 | ||||||
| chr6:70870273
|
C | A | 44 | a0001c0001t0003g0035a0001c0001t0003g0080a0001c0001t0003g0081others(41): Show | 44 | HG00323.hp2 HG00423.hp1 HG00597.hp2 others(41): Show |
intron_variant | MODIFIER | c.737-8295G>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70870273 | ||||||
| chr6:70870284
|
C | T | 2 | a0001c0002t0084g0244a0002c0004t0063g0176 | 2 | HG01192.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.737-8306G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70870284 | ||||||
| chr6:70870285
|
G | A | 2 | a0001c0001t0073g0107a0001c0002t0096g0261 | 2 | HG02976.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.737-8307C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70870285 | ||||||
| chr6:70870307
|
C | T | 1 | a0001c0002t0043g0273 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.737-8329G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70870307 | ||||||
| chr6:70870433
|
C | T | 1 | a0001c0001t0047g0028 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.737-8455G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70870433 | ||||||
| chr6:70870631
|
A | AAAAC | 11 | a0001c0001t0010g0094a0001c0001t0010g0122a0001c0001t0010g0157others(8): Show | 11 | HG00408.hp2 HG01074.hp1 HG02015.hp1 others(8): Show |
intron_variant | MODIFIER | c.737-8657_737-8654d others(6): Show |
B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70870631 | ||||||
| chr6:70870840
|
C | T | 1 | a0001c0002t0006g0193 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.737-8862G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70870840 | ||||||
| chr6:70871050
|
T | C | 15 | a0001c0001t0010g0094a0001c0001t0010g0122a0001c0001t0010g0157others(12): Show | 15 | HG00408.hp2 HG01074.hp1 HG02015.hp1 others(12): Show |
intron_variant | MODIFIER | c.737-9072A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70871050 | ||||||
| chr6:70871108
|
A | G | 2 | a0001c0002t0084g0244a0002c0004t0063g0176 | 2 | HG01192.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.737-9130T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70871108 | ||||||
| chr6:70871154
|
AT | A | 52 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0046others(49): Show | 52 | HG00099.hp2 HG00544.hp2 HG00621.hp2 others(49): Show |
intron_variant | MODIFIER | c.737-9177delA | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70871154 | ||||||
| chr6:70871215
|
TTTTTTTG | T | 17 | a0001c0001t0001g0145a0001c0001t0001g0156a0001c0001t0009g0083others(14): Show | 17 | HG01069.hp1 HG01975.hp2 HG02004.hp1 others(14): Show |
intron_variant | MODIFIER | c.737-9244_737-9238d others(9): Show |
B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70871215 | ||||||
| chr6:70871216
|
TTTTTTG | T | 71 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0046others(68): Show | 72 | HG00099.hp2 HG00323.hp1 HG00544.hp2 others(69): Show |
intron_variant | MODIFIER | c.737-9244_737-9239d others(8): Show |
B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70871216 | ||||||
| chr6:70871217
|
TTTTTG | T | 16 | a0001c0001t0001g0060a0001c0001t0010g0122a0001c0001t0010g0157others(13): Show | 16 | HG00408.hp2 HG01074.hp1 HG02027.hp2 others(13): Show |
intron_variant | MODIFIER | c.737-9244_737-9240d others(7): Show |
B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70871217 | ||||||
| chr6:70871220
|
TTG | T | 6 | a0001c0001t0045g0003a0001c0001t0055g0128a0001c0001t0069g0103others(3): Show | 6 | HG02559.hp1 HG02717.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.737-9244_737-9243d others(4): Show |
B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70871220 | ||||||
| chr6:70871221
|
TG | T | 5 | a0001c0001t0023g0086a0001c0001t0049g0011a0001c0001t0066g0139others(2): Show | 5 | HG02572.hp1 HG02647.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.737-9244delC | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70871221 | ||||||
| chr6:70871222
|
G | T | 2 | a0001c0001t0002g0050a0001c0001t0032g0004 | 2 | NA18940.hp2 NA18981.hp1 |
intron_variant | MODIFIER | c.737-9244C>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70871222 | ||||||
| chr6:70871222
|
GT | G | 69 | a0001c0001t0002g0001a0001c0001t0002g0034a0001c0001t0002g0037others(66): Show | 70 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(67): Show |
intron_variant | MODIFIER | c.737-9245delA | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70871222 | ||||||
| chr6:70871223
|
T | G | 2 | a0001c0001t0002g0050a0001c0001t0032g0004 | 2 | NA18940.hp2 NA18981.hp1 |
intron_variant | MODIFIER | c.737-9245A>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70871223 | ||||||
| chr6:70871227
|
T | G | 1 | a0001c0002t0016g0206 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.737-9249A>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70871227 | ||||||
| chr6:70871441
|
C | T | 2 | a0001c0001t0023g0086a0001c0001t0049g0011 | 2 | HG02723.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.737-9463G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70871441 | ||||||
| chr6:70871680
|
G | T | 116 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0046others(113): Show | 117 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.737-9702C>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70871680 | ||||||
| chr6:70871937
|
T | C | 106 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0046others(103): Show | 107 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(104): Show |
intron_variant | MODIFIER | c.737-9959A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70871937 | ||||||
| chr6:70871989
|
T | C | 1 | a0001c0003t0062g0105 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.737-10011A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70871989 | ||||||
| chr6:70872037
|
C | T | 87 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0046others(84): Show | 88 | HG00099.hp2 HG00323.hp1 HG00544.hp2 others(85): Show |
intron_variant | MODIFIER | c.737-10059G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70872037 | ||||||
| chr6:70872160
|
C | T | 1 | a0002c0004t0063g0176 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.737-10182G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70872160 | ||||||
| chr6:70872161
|
G | A | 5 | a0001c0001t0025g0109a0001c0001t0025g0110a0001c0001t0025g0134others(2): Show | 5 | HG01069.hp1 HG02809.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.737-10183C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70872161 | ||||||
| chr6:70872190
|
T | C | 2 | a0001c0001t0023g0086a0001c0001t0049g0011 | 2 | HG02723.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.737-10212A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70872190 | ||||||
| chr6:70872459
|
G | A | 1 | a0001c0001t0070g0111 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.737-10481C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70872459 | ||||||
| chr6:70872504
|
CT | C | 19 | a0001c0001t0002g0065a0001c0001t0023g0076a0001c0001t0023g0077others(16): Show | 19 | HG01192.hp1 HG02559.hp1 HG02572.hp1 others(16): Show |
intron_variant | MODIFIER | c.737-10527delA | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70872504 | ||||||
| chr6:70872504
|
CTT | C | 100 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0046others(97): Show | 101 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.737-10528_737-1052 others(6): Show |
B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70872504 | ||||||
| chr6:70872522
|
G | T | 2 | a0001c0002t0014g0285a0001c0002t0095g0284 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.737-10544C>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70872522 | ||||||
| chr6:70872729
|
T | C | 6 | a0001c0001t0003g0081a0001c0001t0003g0132a0001c0001t0003g0133others(3): Show | 6 | HG01884.hp2 HG02280.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.737-10751A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70872729 | ||||||
| chr6:70872986
|
T | G | 114 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0046others(111): Show | 115 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(112): Show |
intron_variant | MODIFIER | c.737-11008A>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70872986 | ||||||
| chr6:70873019
|
C | A | 1 | a0001c0001t0069g0103 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.737-11041G>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70873019 | ||||||
| chr6:70873174
|
C | G | 116 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0046others(113): Show | 117 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.737-11196G>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70873174 | ||||||
| chr6:70873176
|
G | A | 1 | a0001c0001t0002g0058 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.737-11198C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70873176 | ||||||
| chr6:70873311
|
A | G | 6 | a0001c0001t0023g0086a0001c0001t0049g0011a0001c0001t0055g0128others(3): Show | 6 | HG02572.hp1 HG02647.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.737-11333T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70873311 | ||||||
| chr6:70873497
|
T | G | 2 | a0001c0001t0004g0098a0001c0002t0040g0224 | 2 | HG00323.hp2 HG00642.hp2 |
intron_variant | MODIFIER | c.737-11519A>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70873497 | ||||||
| chr6:70873604
|
T | C | 1 | a0001c0001t0069g0103 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.737-11626A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70873604 | ||||||
| chr6:70873672
|
C | T | 3 | a0001c0002t0014g0290a0001c0002t0027g0220a0001c0002t0031g0282 | 3 | HG00642.hp1 HG01517.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.737-11694G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70873672 | ||||||
| chr6:70873735
|
G | A | 58 | a0001c0001t0001g0160a0001c0001t0002g0001a0001c0001t0002g0034others(55): Show | 59 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(56): Show |
intron_variant | MODIFIER | c.737-11757C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70873735 | ||||||
| chr6:70873762
|
G | A | 1 | a0001c0001t0001g0101 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.737-11784C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70873762 | ||||||
| chr6:70873896
|
A | T | 126 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0046others(123): Show | 127 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.737-11918T>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70873896 | ||||||
| chr6:70873945
|
C | T | 1 | a0001c0001t0069g0103 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.737-11967G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70873945 | ||||||
| chr6:70874101
|
C | T | 112 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0046others(109): Show | 113 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(110): Show |
intron_variant | MODIFIER | c.737-12123G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70874101 | ||||||
| chr6:70874243
|
CCTTGAAC others(3): Show |
C | 4 | a0001c0001t0055g0128a0001c0001t0066g0139a0001c0002t0041g0196others(1): Show | 4 | HG02572.hp1 HG02647.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.737-12275_737-1226 others(14): Show |
B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70874243 | ||||||
| chr6:70874609
|
A | G | 2 | a0001c0001t0023g0086a0001c0001t0049g0011 | 2 | HG02723.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.737-12631T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70874609 | ||||||
| chr6:70874733
|
A | G | 4 | a0001c0001t0036g0104a0001c0001t0036g0138a0001c0002t0100g0258others(1): Show | 4 | HG02109.hp2 HG02647.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.737-12755T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70874733 | ||||||
| chr6:70874871
|
A | G | 3 | a0001c0001t0012g0017a0001c0001t0012g0022a0001c0002t0039g0247 | 3 | HG02027.hp1 HG02155.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.737-12893T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70874871 | ||||||
| chr6:70874998
|
C | CT | 5 | a0001c0001t0025g0109a0001c0001t0025g0110a0001c0001t0025g0134others(2): Show | 5 | HG01069.hp1 HG02809.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.737-13021dupA | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70874998 | ||||||
| chr6:70875004
|
T | A | 3 | a0001c0001t0045g0003a0001c0002t0042g0254a0001c0002t0042g0295 | 3 | HG02559.hp1 HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.737-13026A>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70875004 | ||||||
| chr6:70875005
|
A | T | 103 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0046others(100): Show | 104 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(101): Show |
intron_variant | MODIFIER | c.737-13027T>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70875005 | ||||||
| chr6:70875006
|
A | T | 26 | a0001c0001t0009g0092a0001c0001t0010g0094a0001c0001t0020g0053others(23): Show | 27 | HG00323.hp1 HG00735.hp2 HG00738.hp1 others(24): Show |
intron_variant | MODIFIER | c.737-13028T>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70875006 | ||||||
| chr6:70875104
|
C | A | 9 | a0001c0001t0003g0102a0001c0001t0003g0125a0001c0001t0003g0142others(6): Show | 9 | HG00741.hp1 HG01167.hp1 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.737-13126G>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70875104 | ||||||
| chr6:70875192
|
C | T | 3 | a0001c0001t0045g0003a0001c0002t0042g0254a0001c0002t0042g0295 | 3 | HG02559.hp1 HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.737-13214G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70875192 | ||||||
| chr6:70875226
|
TGTAATGT others(3): Show |
T | 9 | a0001c0001t0013g0085a0001c0001t0013g0141a0001c0001t0017g0007others(6): Show | 9 | HG01255.hp1 HG01952.hp2 HG01978.hp2 others(6): Show |
intron_variant | MODIFIER | c.737-13258_737-1324 others(14): Show |
B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70875226 | ||||||
| chr6:70875290
|
C | A | 1 | a0001c0001t0003g0168 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.737-13312G>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70875290 | ||||||
| chr6:70875306
|
C | T | 4 | a0001c0001t0036g0104a0001c0001t0036g0138a0001c0002t0100g0258others(1): Show | 4 | HG02109.hp2 HG02647.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.737-13328G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70875306 | ||||||
| chr6:70875348
|
G | A | 15 | a0001c0001t0010g0094a0001c0001t0010g0122a0001c0001t0010g0157others(12): Show | 15 | HG00408.hp2 HG01074.hp1 HG02015.hp1 others(12): Show |
intron_variant | MODIFIER | c.737-13370C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70875348 | ||||||
| chr6:70875381
|
T | A | 1 | a0001c0001t0070g0111 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.737-13403A>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70875381 | ||||||
| chr6:70875436
|
C | A | 2 | a0001c0001t0003g0080a0001c0001t0003g0168 | 2 | HG03490.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.737-13458G>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70875436 | ||||||
| chr6:70875513
|
C | T | 1 | a0001c0002t0015g0278 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.737-13535G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70875513 | ||||||
| chr6:70875801
|
G | A | 1 | a0001c0001t0001g0068 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.737-13823C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70875801 | ||||||
| chr6:70875887
|
C | A | 15 | a0001c0001t0010g0094a0001c0001t0010g0122a0001c0001t0010g0157others(12): Show | 15 | HG00408.hp2 HG01074.hp1 HG02015.hp1 others(12): Show |
intron_variant | MODIFIER | c.737-13909G>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70875887 | ||||||
| chr6:70875978
|
G | C | 3 | a0001c0001t0045g0003a0001c0002t0042g0254a0001c0002t0042g0295 | 3 | HG02559.hp1 HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.737-14000C>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70875978 | ||||||
| chr6:70876118
|
T | A | 1 | a0001c0001t0001g0068 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.737-14140A>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70876118 | ||||||
| chr6:70876444
|
A | T | 2 | a0001c0002t0021g0183a0001c0002t0038g0180 | 2 | NA19056.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.737-14466T>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70876444 | ||||||
| chr6:70876549
|
C | T | 1 | a0001c0001t0070g0111 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.737-14571G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70876549 | ||||||
| chr6:70876670
|
T | C | 8 | a0001c0001t0023g0086a0001c0001t0049g0011a0001c0001t0055g0128others(5): Show | 8 | HG02572.hp1 HG02647.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.737-14692A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70876670 | ||||||
| chr6:70877021
|
A | T | 1 | a0001c0002t0031g0277 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.737-15043T>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70877021 | ||||||
| chr6:70877026
|
G | A | 1 | a0001c0001t0003g0099 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.737-15048C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70877026 | ||||||
| chr6:70877239
|
C | G | 1 | a0001c0002t0015g0253 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.737-15261G>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70877239 | ||||||
| chr6:70877301
|
A | G | 1 | a0001c0002t0005g0215 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.737-15323T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70877301 | ||||||
| chr6:70877898
|
C | T | 1 | a0001c0001t0003g0133 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.737-15920G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70877898 | ||||||
| chr6:70877911
|
C | A | 1 | a0001c0002t0014g0293 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.737-15933G>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70877911 | ||||||
| chr6:70878331
|
T | G | 1 | a0001c0002t0006g0235 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.736+15797A>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70878331 | ||||||
| chr6:70878458
|
G | A | 22 | a0001c0001t0010g0039a0001c0001t0010g0051a0001c0001t0010g0071others(19): Show | 22 | HG00408.hp2 HG01074.hp1 HG01099.hp2 others(19): Show |
intron_variant | MODIFIER | c.736+15670C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70878458 | ||||||
| chr6:70878480
|
T | C | 1 | a0001c0001t0045g0003 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.736+15648A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70878480 | ||||||
| chr6:70878506
|
TATAGTTT others(26): Show |
T | 1 | a0001c0001t0013g0141 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.736+15589_736+1562 others(37): Show |
B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70878506 | ||||||
| chr6:70878612
|
C | A | 2 | a0001c0001t0023g0086a0001c0001t0049g0011 | 2 | HG02723.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.736+15516G>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70878612 | ||||||
| chr6:70878681
|
C | T | 3 | a0001c0001t0020g0078a0001c0002t0015g0281a0001c0002t0028g0222 | 3 | HG00323.hp1 HG02886.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.736+15447G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70878681 | ||||||
| chr6:70878802
|
G | A | 1 | a0001c0001t0001g0068 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.736+15326C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70878802 | ||||||
| chr6:70878874
|
C | T | 2 | a0001c0002t0005g0233a0001c0002t0005g0234 | 2 | NA18960.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.736+15254G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70878874 | ||||||
| chr6:70878878
|
T | C | 2 | a0001c0001t0023g0086a0001c0001t0049g0011 | 2 | HG02723.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.736+15250A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70878878 | ||||||
| chr6:70878917
|
A | G | 1 | a0001c0001t0001g0060 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.736+15211T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70878917 | ||||||
| chr6:70878957
|
G | C | 116 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0046others(113): Show | 117 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.736+15171C>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70878957 | ||||||
| chr6:70878969
|
C | T | 2 | a0001c0001t0002g0150a0001c0001t0071g0038 | 2 | NA18945.hp2 NA18950.hp1 |
intron_variant | MODIFIER | c.736+15159G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70878969 | ||||||
| chr6:70879043
|
C | T | 3 | a0001c0001t0045g0003a0001c0002t0042g0254a0001c0002t0042g0295 | 3 | HG02559.hp1 HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.736+15085G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70879043 | ||||||
| chr6:70879103
|
C | T | 114 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0046others(111): Show | 115 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(112): Show |
intron_variant | MODIFIER | c.736+15025G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70879103 | ||||||
| chr6:70879158
|
G | T | 6 | a0001c0001t0023g0086a0001c0001t0049g0011a0001c0001t0055g0128others(3): Show | 6 | HG02572.hp1 HG02647.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.736+14970C>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70879158 | ||||||
| chr6:70879189
|
T | TTTG | 110 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0046others(107): Show | 111 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(108): Show |
intron_variant | MODIFIER | c.736+14936_736+1493 others(7): Show |
B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70879189 | ||||||
| chr6:70879434
|
G | A | 1 | a0001c0001t0012g0022 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.736+14694C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70879434 | ||||||
| chr6:70879480
|
G | GATTCATT others(1): Show |
10 | a0001c0001t0002g0069a0001c0001t0012g0030a0001c0001t0023g0076others(7): Show | 10 | HG00423.hp2 HG00673.hp2 HG01934.hp2 others(7): Show |
intron_variant | MODIFIER | c.736+14640_736+1464 others(12): Show |
B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70879480 | ||||||
| chr6:70879480
|
G | GATTCATT others(5): Show |
16 | a0001c0001t0002g0065a0001c0001t0002g0120a0001c0001t0002g0144others(13): Show | 16 | HG00544.hp1 HG01884.hp1 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.736+14636_736+1464 others(16): Show |
B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70879480 | ||||||
| chr6:70879480
|
G | GATTCATT others(9): Show |
45 | a0001c0001t0002g0001a0001c0001t0002g0034a0001c0001t0002g0037others(42): Show | 46 | HG00099.hp1 HG00408.hp1 HG01192.hp1 others(43): Show |
intron_variant | MODIFIER | c.736+14632_736+1464 others(20): Show |
B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70879480 | ||||||
| chr6:70879480
|
G | GATTCATT others(13): Show |
2 | a0001c0001t0004g0052a0001c0002t0092g0265 | 2 | NA18951.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.736+14628_736+1464 others(24): Show |
B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70879480 | ||||||
| chr6:70879505
|
A | C | 1 | a0001c0002t0096g0261 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.736+14623T>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70879505 | ||||||
| chr6:70879514
|
A | C | 1 | a0001c0001t0002g0059 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.736+14614T>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70879514 | ||||||
| chr6:70879517
|
C | T | 12 | a0001c0001t0002g0050a0001c0001t0002g0070a0001c0001t0002g0144others(9): Show | 12 | HG02040.hp1 HG02135.hp1 NA18747.hp1 others(9): Show |
intron_variant | MODIFIER | c.736+14611G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70879517 | ||||||
| chr6:70879806
|
G | A | 23 | a0001c0001t0010g0051a0001c0001t0010g0071a0001c0001t0010g0084others(20): Show | 23 | HG00408.hp2 HG01074.hp1 HG01099.hp2 others(20): Show |
intron_variant | MODIFIER | c.736+14322C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70879806 | ||||||
| chr6:70879819
|
C | T | 1 | a0001c0001t0072g0036 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.736+14309G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70879819 | ||||||
| chr6:70879874
|
G | A | 4 | a0001c0001t0036g0104a0001c0001t0036g0138a0001c0002t0100g0258others(1): Show | 4 | HG02109.hp2 HG02647.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.736+14254C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70879874 | ||||||
| chr6:70879898
|
G | A | 26 | a0001c0001t0004g0137a0001c0001t0010g0051a0001c0001t0010g0071others(23): Show | 26 | HG00408.hp2 HG01074.hp1 HG01099.hp2 others(23): Show |
intron_variant | MODIFIER | c.736+14230C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70879898 | ||||||
| chr6:70879918
|
T | C | 9 | a0001c0001t0002g0001a0001c0001t0002g0037a0001c0001t0002g0043others(6): Show | 10 | HG00423.hp2 HG02015.hp2 HG02071.hp1 others(7): Show |
intron_variant | MODIFIER | c.736+14210A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70879918 | ||||||
| chr6:70879991
|
G | A | 1 | a0001c0001t0069g0103 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.736+14137C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70879991 | ||||||
| chr6:70880079
|
C | CGTGGGGG others(5): Show |
1 | a0001c0003t0062g0105 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.736+14037_736+1404 others(16): Show |
B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70880079 | ||||||
| chr6:70880478
|
A | C | 5 | a0001c0001t0023g0086a0001c0001t0037g0061a0001c0001t0037g0088others(2): Show | 5 | HG02723.hp2 HG03239.hp1 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.736+13650T>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70880478 | ||||||
| chr6:70880507
|
T | C | 1 | a0002c0004t0063g0176 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.736+13621A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70880507 | ||||||
| chr6:70880654
|
A | AT | 9 | a0001c0001t0002g0001a0001c0001t0002g0043a0001c0001t0023g0086others(6): Show | 10 | HG02572.hp1 HG02723.hp2 HG03239.hp1 others(7): Show |
intron_variant | MODIFIER | c.736+13473dupA | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70880654 | ||||||
| chr6:70880921
|
C | T | 1 | a0001c0002t0043g0273 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.736+13207G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70880921 | ||||||
| chr6:70880986
|
T | G | 1 | a0001c0001t0013g0141 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.736+13142A>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70880986 | ||||||
| chr6:70881000
|
A | T | 1 | a0001c0001t0013g0141 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.736+13128T>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70881000 | ||||||
| chr6:70881368
|
A | G | 2 | a0001c0001t0004g0137a0001c0002t0080g0194 | 2 | HG02572.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.736+12760T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70881368 | ||||||
| chr6:70881507
|
T | C | 1 | a0001c0002t0027g0213 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.736+12621A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70881507 | ||||||
| chr6:70881521
|
G | A | 1 | a0001c0001t0010g0157 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.736+12607C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70881521 | ||||||
| chr6:70881563
|
C | T | 1 | a0001c0001t0061g0093 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.736+12565G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70881563 | ||||||
| chr6:70881574
|
C | G | 93 | a0001c0001t0001g0044a0001c0001t0001g0046a0001c0001t0001g0048others(90): Show | 94 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(91): Show |
intron_variant | MODIFIER | c.736+12554G>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70881574 | ||||||
| chr6:70881686
|
G | A | 6 | a0001c0001t0004g0136a0001c0001t0023g0086a0001c0001t0037g0061others(3): Show | 6 | HG02723.hp2 HG03239.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.736+12442C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70881686 | ||||||
| chr6:70881734
|
G | A | 1 | a0001c0001t0001g0160 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.736+12394C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70881734 | ||||||
| chr6:70881838
|
C | T | 1 | a0001c0002t0006g0188 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.736+12290G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70881838 | ||||||
| chr6:70881921
|
C | T | 1 | a0001c0001t0003g0081 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.736+12207G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70881921 | ||||||
| chr6:70882154
|
T | C | 1 | a0001c0001t0004g0052 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.736+11974A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70882154 | ||||||
| chr6:70882199
|
C | T | 1 | a0001c0002t0011g0271 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.736+11929G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70882199 | ||||||
| chr6:70882220
|
C | T | 5 | a0001c0001t0004g0137a0001c0001t0068g0167a0001c0002t0042g0254others(2): Show | 5 | HG02572.hp1 HG03098.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.736+11908G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70882220 | ||||||
| chr6:70882229
|
T | C | 1 | a0001c0001t0003g0154 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.736+11899A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70882229 | ||||||
| chr6:70882277
|
A | G | 1 | a0001c0001t0068g0167 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.736+11851T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70882277 | ||||||
| chr6:70882298
|
C | G | 1 | a0001c0002t0011g0270 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.736+11830G>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70882298 | ||||||
| chr6:70882306
|
A | C | 2 | a0001c0002t0011g0256a0001c0002t0094g0275 | 2 | HG00099.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.736+11822T>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70882306 | ||||||
| chr6:70882379
|
T | C | 1 | a0001c0002t0021g0238 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.736+11749A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70882379 | ||||||
| chr6:70882425
|
C | T | 1 | a0001c0001t0076g0177 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.736+11703G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70882425 | ||||||
| chr6:70882502
|
A | G | 6 | a0001c0001t0004g0136a0001c0001t0023g0086a0001c0001t0037g0061others(3): Show | 6 | HG02723.hp2 HG03239.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.736+11626T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70882502 | ||||||
| chr6:70882504
|
A | C | 3 | a0001c0001t0066g0139a0001c0002t0041g0196a0001c0002t0043g0273 | 3 | HG02647.hp1 HG03225.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.736+11624T>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70882504 | ||||||
| chr6:70882785
|
A | G | 5 | a0001c0001t0023g0086a0001c0001t0037g0061a0001c0001t0037g0088others(2): Show | 5 | HG02723.hp2 HG03239.hp1 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.736+11343T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70882785 | ||||||
| chr6:70882923
|
AATGT | A | 76 | a0001c0001t0001g0044a0001c0001t0001g0046a0001c0001t0001g0048others(73): Show | 77 | HG00099.hp2 HG00323.hp2 HG00544.hp1 others(74): Show |
intron_variant | MODIFIER | c.736+11201_736+1120 others(8): Show |
B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70882923 | ||||||
| chr6:70883124
|
G | A | 76 | a0001c0001t0001g0044a0001c0001t0001g0046a0001c0001t0001g0048others(73): Show | 77 | HG00099.hp2 HG00323.hp2 HG00544.hp1 others(74): Show |
intron_variant | MODIFIER | c.736+11004C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70883124 | ||||||
| chr6:70883351
|
C | T | 1 | a0001c0002t0043g0273 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.736+10777G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70883351 | ||||||
| chr6:70883444
|
T | C | 1 | a0002c0004t0063g0176 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.736+10684A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70883444 | ||||||
| chr6:70883460
|
C | CA | 12 | a0001c0001t0036g0104a0001c0001t0036g0138a0001c0001t0066g0139others(9): Show | 12 | HG00642.hp2 HG01496.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.736+10667dupT | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70883460 | ||||||
| chr6:70883460
|
CA | C | 77 | a0001c0001t0002g0065a0001c0001t0002g0069a0001c0001t0003g0081others(74): Show | 77 | HG00408.hp2 HG00423.hp1 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.736+10667delT | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70883460 | ||||||
| chr6:70883475
|
A | G | 1 | a0001c0001t0045g0003 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.736+10653T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70883475 | ||||||
| chr6:70883503
|
G | A | 1 | a0002c0004t0063g0176 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.736+10625C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70883503 | ||||||
| chr6:70883621
|
G | A | 3 | a0001c0001t0003g0102a0001c0001t0003g0125a0001c0001t0004g0124 | 3 | HG00741.hp1 HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.736+10507C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70883621 | ||||||
| chr6:70883649
|
A | G | 5 | a0001c0001t0025g0109a0001c0001t0025g0110a0001c0001t0025g0134others(2): Show | 5 | HG01069.hp1 HG02809.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.736+10479T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70883649 | ||||||
| chr6:70883703
|
A | G | 1 | a0001c0002t0005g0233 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.736+10425T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70883703 | ||||||
| chr6:70883730
|
C | T | 5 | a0001c0001t0036g0104a0001c0001t0036g0138a0001c0002t0100g0258others(2): Show | 5 | HG02109.hp2 HG02647.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.736+10398G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70883730 | ||||||
| chr6:70883793
|
T | C | 1 | a0001c0001t0044g0306 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.736+10335A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70883793 | ||||||
| chr6:70883949
|
C | T | 1 | a0001c0002t0041g0190 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.736+10179G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70883949 | ||||||
| chr6:70884016
|
G | A | 1 | a0001c0001t0003g0154 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.736+10112C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70884016 | ||||||
| chr6:70884095
|
C | CA | 10 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0117others(7): Show | 10 | HG00621.hp2 HG00735.hp1 HG01433.hp2 others(7): Show |
intron_variant | MODIFIER | c.736+10032dupT | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70884095 | ||||||
| chr6:70884095
|
CA | C | 190 | a0001c0001t0001g0042a0001c0001t0001g0145a0001c0001t0002g0001others(187): Show | 191 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(188): Show |
intron_variant | MODIFIER | c.736+10032delT | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70884095 | ||||||
| chr6:70884100
|
AAAAAAAA others(7): Show |
A | 1 | a0001c0001t0004g0136 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.736+10014_736+1002 others(18): Show |
B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70884100 | ||||||
| chr6:70884102
|
A | C | 4 | a0001c0001t0055g0128a0001c0001t0066g0139a0001c0002t0041g0196others(1): Show | 4 | HG02647.hp1 HG03195.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.736+10026T>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70884102 | ||||||
| chr6:70884103
|
AAAAAAAA others(4): Show |
A | 4 | a0001c0001t0023g0086a0001c0001t0037g0061a0001c0001t0037g0088others(1): Show | 4 | HG02723.hp2 HG03239.hp1 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.736+10014_736+1002 others(15): Show |
B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70884103 | ||||||
| chr6:70884104
|
AAAAAAAA others(3): Show |
A | 1 | a0001c0001t0074g0087 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.736+10014_736+1002 others(14): Show |
B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70884104 | ||||||
| chr6:70884108
|
A | C | 4 | a0001c0001t0055g0128a0001c0001t0066g0139a0001c0002t0041g0196others(1): Show | 4 | HG02647.hp1 HG03195.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.736+10020T>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70884108 | ||||||
| chr6:70884113
|
A | C | 2 | a0001c0001t0004g0108a0001c0002t0077g0179 | 2 | HG02486.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.736+10015T>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70884113 | ||||||
| chr6:70884114
|
C | A | 4 | a0001c0001t0002g0072a0001c0001t0004g0108a0001c0001t0034g0106others(1): Show | 4 | HG02486.hp2 HG02818.hp2 NA18967.hp2 others(1): Show |
intron_variant | MODIFIER | c.736+10014G>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70884114 | ||||||
| chr6:70884142
|
C | T | 1 | a0001c0002t0028g0222 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.736+9986G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70884142 | ||||||
| chr6:70884171
|
T | A | 1 | a0001c0001t0068g0167 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.736+9957A>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70884171 | ||||||
| chr6:70884175
|
T | A | 1 | a0001c0001t0068g0167 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.736+9953A>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70884175 | ||||||
| chr6:70884179
|
C | T | 1 | a0001c0002t0011g0271 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.736+9949G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70884179 | ||||||
| chr6:70884203
|
G | A | 9 | a0001c0001t0010g0051a0001c0001t0010g0071a0001c0001t0010g0084others(6): Show | 9 | HG01099.hp2 HG01261.hp1 HG01261.hp2 others(6): Show |
intron_variant | MODIFIER | c.736+9925C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70884203 | ||||||
| chr6:70884263
|
C | G | 1 | a0001c0001t0045g0003 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.736+9865G>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70884263 | ||||||
| chr6:70884507
|
C | G | 156 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0046others(153): Show | 158 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(155): Show |
intron_variant | MODIFIER | c.736+9621G>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70884507 | ||||||
| chr6:70884580
|
A | G | 1 | a0001c0002t0008g0221 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.736+9548T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70884580 | ||||||
| chr6:70885059
|
C | T | 69 | a0001c0001t0001g0044a0001c0001t0001g0046a0001c0001t0001g0048others(66): Show | 70 | HG00099.hp2 HG00323.hp2 HG00544.hp1 others(67): Show |
intron_variant | MODIFIER | c.736+9069G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70885059 | ||||||
| chr6:70885082
|
A | C | 158 | a0001c0001t0001g0042a0001c0001t0001g0145a0001c0001t0002g0001others(155): Show | 159 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(156): Show |
intron_variant | MODIFIER | c.736+9046T>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70885082 | ||||||
| chr6:70885342
|
G | A | 5 | a0001c0001t0025g0109a0001c0001t0025g0110a0001c0001t0025g0134others(2): Show | 5 | HG01069.hp1 HG02809.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.736+8786C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70885342 | ||||||
| chr6:70885372
|
T | G | 157 | a0001c0001t0001g0042a0001c0001t0001g0145a0001c0001t0002g0001others(154): Show | 158 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(155): Show |
intron_variant | MODIFIER | c.736+8756A>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70885372 | ||||||
| chr6:70885405
|
T | A | 1 | a0001c0001t0004g0137 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.736+8723A>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70885405 | ||||||
| chr6:70885448
|
T | C | 157 | a0001c0001t0001g0042a0001c0001t0001g0145a0001c0001t0002g0001others(154): Show | 158 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(155): Show |
intron_variant | MODIFIER | c.736+8680A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70885448 | ||||||
| chr6:70885618
|
G | A | 157 | a0001c0001t0001g0042a0001c0001t0001g0145a0001c0001t0002g0001others(154): Show | 158 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(155): Show |
intron_variant | MODIFIER | c.736+8510C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70885618 | ||||||
| chr6:70885645
|
G | A | 2 | a0001c0001t0019g0024a0001c0002t0021g0238 | 2 | HG02027.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.736+8483C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70885645 | ||||||
| chr6:70885687
|
A | T | 1 | a0001c0002t0091g0260 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.736+8441T>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70885687 | ||||||
| chr6:70885723
|
C | A | 1 | a0001c0001t0104g0305 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.736+8405G>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70885723 | ||||||
| chr6:70885779
|
C | T | 1 | a0002c0004t0063g0176 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.736+8349G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70885779 | ||||||
| chr6:70885868
|
T | G | 77 | a0001c0001t0001g0044a0001c0001t0001g0046a0001c0001t0001g0048others(74): Show | 78 | HG00099.hp2 HG00323.hp2 HG00544.hp1 others(75): Show |
intron_variant | MODIFIER | c.736+8260A>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70885868 | ||||||
| chr6:70885886
|
A | G | 157 | a0001c0001t0001g0042a0001c0001t0001g0145a0001c0001t0002g0001others(154): Show | 158 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(155): Show |
intron_variant | MODIFIER | c.736+8242T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70885886 | ||||||
| chr6:70885922
|
A | G | 4 | a0001c0001t0003g0143a0001c0001t0003g0146a0001c0001t0003g0147others(1): Show | 4 | HG00423.hp1 HG02129.hp1 HG02135.hp2 others(1): Show |
intron_variant | MODIFIER | c.736+8206T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70885922 | ||||||
| chr6:70885941
|
T | G | 2 | a0001c0001t0037g0088a0001c0001t0074g0087 | 2 | HG03669.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.736+8187A>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70885941 | ||||||
| chr6:70885945
|
C | G | 157 | a0001c0001t0001g0042a0001c0001t0001g0145a0001c0001t0002g0001others(154): Show | 158 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(155): Show |
intron_variant | MODIFIER | c.736+8183G>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70885945 | ||||||
| chr6:70886013
|
G | A | 1 | a0001c0001t0045g0003 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.736+8115C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70886013 | ||||||
| chr6:70886044
|
G | C | 1 | a0002c0004t0063g0176 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.736+8084C>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70886044 | ||||||
| chr6:70886095
|
A | G | 22 | a0001c0001t0001g0145a0001c0001t0004g0052a0001c0001t0004g0056others(19): Show | 22 | HG00408.hp2 HG01884.hp1 HG02258.hp2 others(19): Show |
intron_variant | MODIFIER | c.736+8033T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70886095 | ||||||
| chr6:70886221
|
A | G | 157 | a0001c0001t0001g0042a0001c0001t0001g0145a0001c0001t0002g0001others(154): Show | 158 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(155): Show |
intron_variant | MODIFIER | c.736+7907T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70886221 | ||||||
| chr6:70886325
|
G | A | 157 | a0001c0001t0001g0042a0001c0001t0001g0145a0001c0001t0002g0001others(154): Show | 158 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(155): Show |
intron_variant | MODIFIER | c.736+7803C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70886325 | ||||||
| chr6:70886423
|
T | C | 157 | a0001c0001t0001g0042a0001c0001t0001g0145a0001c0001t0002g0001others(154): Show | 158 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(155): Show |
intron_variant | MODIFIER | c.736+7705A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70886423 | ||||||
| chr6:70886513
|
T | A | 1 | a0001c0001t0067g0113 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.736+7615A>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70886513 | ||||||
| chr6:70886560
|
G | C | 157 | a0001c0001t0001g0042a0001c0001t0001g0145a0001c0001t0002g0001others(154): Show | 158 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(155): Show |
intron_variant | MODIFIER | c.736+7568C>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70886560 | ||||||
| chr6:70886581
|
C | T | 1 | a0001c0001t0002g0065 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.736+7547G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70886581 | ||||||
| chr6:70886660
|
C | T | 1 | a0002c0004t0063g0176 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.736+7468G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70886660 | ||||||
| chr6:70886768
|
G | C | 1 | a0001c0001t0009g0047 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.736+7360C>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70886768 | ||||||
| chr6:70886782
|
CCTGCAAG others(8): Show |
C | 1 | a0001c0001t0002g0072 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.736+7331_736+7345d others(17): Show |
B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70886782 | ||||||
| chr6:70886983
|
C | T | 155 | a0001c0001t0001g0042a0001c0001t0001g0145a0001c0001t0002g0001others(152): Show | 156 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(153): Show |
intron_variant | MODIFIER | c.736+7145G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70886983 | ||||||
| chr6:70886992
|
G | C | 155 | a0001c0001t0001g0042a0001c0001t0001g0145a0001c0001t0002g0001others(152): Show | 156 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(153): Show |
intron_variant | MODIFIER | c.736+7136C>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70886992 | ||||||
| chr6:70887037
|
G | C | 234 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0046others(231): Show | 236 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(233): Show |
intron_variant | MODIFIER | c.736+7091C>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70887037 | ||||||
| chr6:70887350
|
C | T | 154 | a0001c0001t0001g0042a0001c0001t0001g0145a0001c0001t0002g0001others(151): Show | 155 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(152): Show |
intron_variant | MODIFIER | c.736+6778G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70887350 | ||||||
| chr6:70887379
|
C | G | 156 | a0001c0001t0001g0042a0001c0001t0001g0145a0001c0001t0002g0001others(153): Show | 157 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(154): Show |
intron_variant | MODIFIER | c.736+6749G>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70887379 | ||||||
| chr6:70887466
|
A | T | 7 | a0001c0001t0012g0009a0001c0001t0012g0010a0001c0001t0036g0104others(4): Show | 7 | HG02109.hp2 HG02630.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.736+6662T>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70887466 | ||||||
| chr6:70887485
|
C | T | 1 | a0001c0001t0003g0100 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.736+6643G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70887485 | ||||||
| chr6:70887563
|
G | T | 153 | a0001c0001t0001g0042a0001c0001t0001g0145a0001c0001t0002g0001others(150): Show | 154 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(151): Show |
intron_variant | MODIFIER | c.736+6565C>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70887563 | ||||||
| chr6:70887628
|
G | A | 154 | a0001c0001t0001g0042a0001c0001t0001g0145a0001c0001t0002g0001others(151): Show | 155 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(152): Show |
intron_variant | MODIFIER | c.736+6500C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70887628 | ||||||
| chr6:70887674
|
G | T | 1 | a0002c0004t0063g0176 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.736+6454C>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70887674 | ||||||
| chr6:70887688
|
G | C | 76 | a0001c0001t0001g0044a0001c0001t0001g0046a0001c0001t0001g0048others(73): Show | 77 | HG00099.hp2 HG00323.hp2 HG00544.hp1 others(74): Show |
intron_variant | MODIFIER | c.736+6440C>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70887688 | ||||||
| chr6:70887711
|
T | C | 6 | a0001c0001t0004g0137a0001c0001t0023g0086a0001c0001t0037g0061others(3): Show | 6 | HG02723.hp2 HG03130.hp2 HG03239.hp1 others(3): Show |
intron_variant | MODIFIER | c.736+6417A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70887711 | ||||||
| chr6:70887861
|
A | G | 3 | a0001c0001t0068g0167a0001c0002t0042g0254a0001c0002t0042g0295 | 3 | HG03098.hp1 HG03453.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.736+6267T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70887861 | ||||||
| chr6:70888115
|
C | T | 67 | a0001c0001t0001g0042a0001c0001t0001g0145a0001c0001t0002g0001others(64): Show | 68 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(65): Show |
intron_variant | MODIFIER | c.736+6013G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70888115 | ||||||
| chr6:70888125
|
C | T | 140 | a0001c0001t0001g0042a0001c0001t0001g0145a0001c0001t0002g0001others(137): Show | 141 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(138): Show |
intron_variant | MODIFIER | c.736+6003G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70888125 | ||||||
| chr6:70888207
|
T | C | 1 | a0001c0003t0062g0105 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.736+5921A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70888207 | ||||||
| chr6:70888224
|
AT | A | 77 | a0001c0001t0001g0042a0001c0001t0001g0145a0001c0001t0002g0001others(74): Show | 78 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(75): Show |
intron_variant | MODIFIER | c.736+5903delA | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70888224 | ||||||
| chr6:70888288
|
G | C | 1 | a0001c0002t0006g0189 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.736+5840C>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70888288 | ||||||
| chr6:70888359
|
C | T | 8 | a0001c0001t0004g0137a0001c0001t0023g0076a0001c0001t0023g0077others(5): Show | 8 | HG02723.hp2 HG03130.hp2 HG03139.hp2 others(5): Show |
intron_variant | MODIFIER | c.736+5769G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70888359 | ||||||
| chr6:70888378
|
A | C | 9 | a0001c0001t0004g0136a0001c0001t0004g0137a0001c0001t0023g0076others(6): Show | 9 | HG02723.hp2 HG03130.hp2 HG03139.hp2 others(6): Show |
intron_variant | MODIFIER | c.736+5750T>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70888378 | ||||||
| chr6:70888470
|
G | C | 8 | a0001c0001t0004g0137a0001c0001t0023g0076a0001c0001t0023g0077others(5): Show | 8 | HG02723.hp2 HG03130.hp2 HG03139.hp2 others(5): Show |
intron_variant | MODIFIER | c.736+5658C>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70888470 | ||||||
| chr6:70888493
|
AG | A | 3 | a0001c0001t0066g0139a0001c0002t0041g0196a0001c0002t0043g0273 | 3 | HG02647.hp1 HG03225.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.736+5634delC | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70888493 | ||||||
| chr6:70888505
|
C | G | 9 | a0001c0001t0004g0136a0001c0001t0004g0137a0001c0001t0023g0076others(6): Show | 9 | HG02723.hp2 HG03130.hp2 HG03139.hp2 others(6): Show |
intron_variant | MODIFIER | c.736+5623G>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70888505 | ||||||
| chr6:70888546
|
G | C | 68 | a0001c0001t0002g0065a0001c0001t0002g0069a0001c0001t0003g0081others(65): Show | 68 | HG00423.hp1 HG00597.hp2 HG00621.hp1 others(65): Show |
intron_variant | MODIFIER | c.736+5582C>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70888546 | ||||||
| chr6:70888599
|
A | G | 1 | a0001c0001t0055g0128 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.736+5529T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70888599 | ||||||
| chr6:70888664
|
G | A | 22 | a0001c0001t0019g0012a0001c0001t0019g0024a0001c0001t0020g0053others(19): Show | 22 | HG00323.hp1 HG01074.hp1 HG01074.hp2 others(19): Show |
intron_variant | MODIFIER | c.736+5464C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70888664 | ||||||
| chr6:70888736
|
T | G | 1 | a0001c0002t0005g0233 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.736+5392A>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70888736 | ||||||
| chr6:70888842
|
C | T | 152 | a0001c0001t0001g0042a0001c0001t0001g0145a0001c0001t0002g0001others(149): Show | 153 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(150): Show |
intron_variant | MODIFIER | c.736+5286G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70888842 | ||||||
| chr6:70888868
|
C | T | 80 | a0001c0001t0001g0044a0001c0001t0001g0046a0001c0001t0001g0048others(77): Show | 81 | HG00099.hp2 HG00323.hp2 HG00544.hp1 others(78): Show |
intron_variant | MODIFIER | c.736+5260G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70888868 | ||||||
| chr6:70888885
|
C | T | 1 | a0001c0001t0054g0031 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.736+5243G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70888885 | ||||||
| chr6:70888921
|
T | C | 3 | a0001c0001t0003g0102a0001c0001t0003g0125a0001c0001t0004g0124 | 3 | HG00741.hp1 HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.736+5207A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70888921 | ||||||
| chr6:70888956
|
G | C | 6 | a0001c0001t0017g0013a0001c0001t0020g0097a0001c0002t0008g0002others(3): Show | 7 | HG00735.hp2 HG00738.hp1 HG01255.hp1 others(4): Show |
intron_variant | MODIFIER | c.736+5172C>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70888956 | ||||||
| chr6:70888957
|
A | G | 1 | a0001c0001t0045g0003 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.736+5171T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70888957 | ||||||
| chr6:70889064
|
A | C | 20 | a0001c0001t0003g0089a0001c0001t0003g0090a0001c0001t0003g0099others(17): Show | 20 | HG00423.hp1 HG00597.hp2 HG00621.hp1 others(17): Show |
intron_variant | MODIFIER | c.736+5064T>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70889064 | ||||||
| chr6:70889294
|
ATTAAAGA others(2671): Show |
A | 1 | a0001c0001t0068g0167 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.736+2156_736+4833d others(2): Show |
B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70889294 | ||||||
| chr6:70889439
|
C | G | 3 | a0001c0001t0066g0139a0001c0002t0041g0196a0001c0002t0043g0273 | 3 | HG02647.hp1 HG03225.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.736+4689G>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70889439 | ||||||
| chr6:70889487
|
C | T | 1 | a0001c0002t0005g0241 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.736+4641G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70889487 | ||||||
| chr6:70889517
|
C | T | 5 | a0001c0001t0018g0006a0001c0001t0051g0005a0001c0002t0007g0214others(2): Show | 5 | HG02280.hp1 HG02451.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.736+4611G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70889517 | ||||||
| chr6:70889615
|
C | T | 46 | a0001c0001t0002g0065a0001c0001t0002g0069a0001c0001t0003g0081others(43): Show | 46 | HG00423.hp1 HG00597.hp2 HG00621.hp1 others(43): Show |
intron_variant | MODIFIER | c.736+4513G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70889615 | ||||||
| chr6:70889617
|
C | T | 1 | a0001c0001t0105g0307 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.736+4511G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70889617 | ||||||
| chr6:70889716
|
C | T | 43 | a0001c0001t0001g0042a0001c0001t0002g0001a0001c0001t0002g0034others(40): Show | 44 | HG00408.hp1 HG02015.hp2 HG02027.hp1 others(41): Show |
intron_variant | MODIFIER | c.736+4412G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70889716 | ||||||
| chr6:70889764
|
C | G | 3 | a0001c0001t0060g0118a0001c0002t0006g0246a0001c0002t0016g0245 | 3 | HG02165.hp2 HG03831.hp2 NA18955.hp2 |
intron_variant | MODIFIER | c.736+4364G>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70889764 | ||||||
| chr6:70889786
|
A | AT | 6 | a0001c0001t0003g0135a0001c0001t0004g0108a0001c0001t0034g0106others(3): Show | 6 | HG01884.hp1 HG02486.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.736+4341dupA | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70889786 | ||||||
| chr6:70889786
|
AT | A | 94 | a0001c0001t0001g0044a0001c0001t0001g0046a0001c0001t0001g0048others(91): Show | 95 | HG00099.hp2 HG00323.hp2 HG00544.hp1 others(92): Show |
intron_variant | MODIFIER | c.736+4341delA | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70889786 | ||||||
| chr6:70889787
|
T | C | 1 | a0001c0001t0108g0313 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.736+4341A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70889787 | ||||||
| chr6:70889803
|
G | T | 1 | a0001c0001t0073g0107 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.736+4325C>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70889803 | ||||||
| chr6:70889839
|
G | C | 1 | a0001c0001t0055g0128 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.736+4289C>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70889839 | ||||||
| chr6:70889852
|
G | A | 1 | a0001c0001t0076g0177 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.736+4276C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70889852 | ||||||
| chr6:70889961
|
T | C | 1 | a0001c0001t0004g0137 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.736+4167A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70889961 | ||||||
| chr6:70889970
|
C | T | 1 | a0001c0001t0059g0162 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.736+4158G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70889970 | ||||||
| chr6:70889993
|
G | A | 1 | a0001c0002t0005g0241 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.736+4135C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70889993 | ||||||
| chr6:70890028
|
T | G | 3 | a0001c0001t0069g0103a0001c0002t0042g0254a0001c0002t0042g0295 | 3 | HG02717.hp1 HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.736+4100A>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70890028 | ||||||
| chr6:70890077
|
C | T | 3 | a0001c0001t0010g0122a0001c0001t0019g0018a0001c0001t0019g0019 | 3 | HG00408.hp2 NA18945.hp1 NA18963.hp2 |
intron_variant | MODIFIER | c.736+4051G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70890077 | ||||||
| chr6:70890085
|
A | G | 8 | a0001c0001t0023g0076a0001c0001t0023g0077a0001c0001t0023g0086others(5): Show | 8 | HG02559.hp1 HG02723.hp2 HG03139.hp2 others(5): Show |
intron_variant | MODIFIER | c.736+4043T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70890085 | ||||||
| chr6:70890109
|
T | G | 1 | a0001c0001t0073g0107 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.736+4019A>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70890109 | ||||||
| chr6:70890123
|
T | C | 17 | a0001c0001t0020g0053a0001c0001t0020g0066a0001c0001t0020g0078others(14): Show | 17 | HG00323.hp1 HG01074.hp2 HG01099.hp1 others(14): Show |
intron_variant | MODIFIER | c.736+4005A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70890123 | ||||||
| chr6:70890184
|
A | G | 69 | a0001c0001t0001g0145a0001c0001t0002g0001a0001c0001t0002g0034others(66): Show | 70 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(67): Show |
intron_variant | MODIFIER | c.736+3944T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70890184 | ||||||
| chr6:70890304
|
T | C | 1 | a0002c0004t0063g0176 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.736+3824A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70890304 | ||||||
| chr6:70890588
|
T | C | 1 | a0002c0004t0063g0176 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.736+3540A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70890588 | ||||||
| chr6:70890632
|
T | C | 232 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0046others(229): Show | 234 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(231): Show |
intron_variant | MODIFIER | c.736+3496A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70890632 | ||||||
| chr6:70890916
|
T | C | 2 | a0001c0001t0003g0135a0001c0002t0006g0197 | 2 | HG02895.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.736+3212A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70890916 | ||||||
| chr6:70891019
|
C | A | 1 | a0001c0001t0001g0064 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.736+3109G>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70891019 | ||||||
| chr6:70891164
|
T | C | 36 | a0001c0001t0001g0060a0001c0001t0002g0065a0001c0001t0002g0069others(33): Show | 36 | HG00673.hp2 HG00741.hp1 HG01074.hp1 others(33): Show |
intron_variant | MODIFIER | c.736+2964A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70891164 | ||||||
| chr6:70891220
|
A | G | 254 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0046others(251): Show | 256 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(253): Show |
intron_variant | MODIFIER | c.736+2908T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70891220 | ||||||
| chr6:70891385
|
G | T | 1 | a0001c0001t0037g0061 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.736+2743C>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70891385 | ||||||
| chr6:70891529
|
T | G | 12 | a0001c0001t0010g0051a0001c0001t0010g0071a0001c0001t0010g0084others(9): Show | 12 | HG01074.hp1 HG01099.hp2 HG01261.hp1 others(9): Show |
intron_variant | MODIFIER | c.736+2599A>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70891529 | ||||||
| chr6:70891588
|
C | G | 1 | a0001c0002t0040g0224 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.736+2540G>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70891588 | ||||||
| chr6:70891620
|
A | T | 1 | a0001c0001t0009g0095 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.736+2508T>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70891620 | ||||||
| chr6:70891654
|
G | A | 1 | a0001c0002t0011g0272 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.736+2474C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70891654 | ||||||
| chr6:70891718
|
T | C | 7 | a0001c0001t0013g0140a0001c0002t0005g0215a0001c0002t0005g0217others(4): Show | 7 | NA18949.hp1 NA18960.hp2 NA18963.hp1 others(4): Show |
intron_variant | MODIFIER | c.736+2410A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70891718 | ||||||
| chr6:70891748
|
T | TTG | 50 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0002g0059others(47): Show | 50 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(47): Show |
intron_variant | MODIFIER | c.736+2378_736+2379d others(4): Show |
B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70891748 | ||||||
| chr6:70891748
|
T | TTGTG | 8 | a0001c0001t0003g0154a0001c0001t0004g0052a0001c0001t0004g0056others(5): Show | 8 | HG00642.hp2 HG02258.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.736+2376_736+2379d others(6): Show |
B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70891748 | ||||||
| chr6:70891748
|
T | TTGTGTGT others(1): Show |
10 | a0001c0001t0001g0171a0001c0001t0002g0065a0001c0001t0002g0069others(7): Show | 10 | HG00423.hp2 HG00673.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.736+2372_736+2379d others(10): Show |
B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70891748 | ||||||
| chr6:70891748
|
T | TTGTGTGT others(5): Show |
1 | a0001c0001t0010g0094 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.736+2368_736+2379d others(14): Show |
B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70891748 | ||||||
| chr6:70891748
|
TTG | T | 35 | a0001c0001t0001g0042a0001c0001t0003g0099a0001c0001t0003g0100others(32): Show | 35 | HG01069.hp1 HG01074.hp2 HG01099.hp1 others(32): Show |
intron_variant | MODIFIER | c.736+2378_736+2379d others(4): Show |
B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70891748 | ||||||
| chr6:70891748
|
TTGTG | T | 6 | a0001c0002t0005g0203a0001c0002t0021g0183a0001c0002t0092g0265others(3): Show | 6 | HG02647.hp2 HG02698.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.736+2376_736+2379d others(6): Show |
B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70891748 | ||||||
| chr6:70891748
|
TTGTGTG | T | 4 | a0001c0001t0013g0141a0001c0002t0026g0243a0001c0002t0042g0295others(1): Show | 4 | HG03098.hp1 HG03927.hp1 NA18974.hp1 others(1): Show |
intron_variant | MODIFIER | c.736+2374_736+2379d others(8): Show |
B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70891748 | ||||||
| chr6:70891748
|
TTGTGTGT others(1): Show |
T | 12 | a0001c0001t0010g0051a0001c0001t0010g0071a0001c0001t0010g0084others(9): Show | 12 | HG01074.hp1 HG01099.hp2 HG01261.hp1 others(9): Show |
intron_variant | MODIFIER | c.736+2372_736+2379d others(10): Show |
B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70891748 | ||||||
| chr6:70891748
|
TTGTGTGT others(7): Show |
T | 1 | a0001c0002t0081g0240 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.736+2366_736+2379d others(16): Show |
B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70891748 | ||||||
| chr6:70891807
|
T | C | 43 | a0001c0001t0001g0042a0001c0001t0003g0099a0001c0001t0003g0100others(40): Show | 43 | HG00642.hp1 HG01069.hp1 HG01074.hp2 others(40): Show |
intron_variant | MODIFIER | c.736+2321A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70891807 | ||||||
| chr6:70892195
|
A | G | 1 | a0001c0002t0015g0286 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.736+1933T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70892195 | ||||||
| chr6:70892326
|
G | A | 1 | a0001c0001t0003g0135 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.736+1802C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70892326 | ||||||
| chr6:70892338
|
C | A | 2 | a0001c0001t0001g0169a0001c0001t0001g0170 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.736+1790G>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70892338 | ||||||
| chr6:70892365
|
C | G | 18 | a0001c0001t0001g0042a0001c0001t0003g0099a0001c0001t0003g0100others(15): Show | 18 | HG00642.hp1 HG01074.hp2 HG01099.hp1 others(15): Show |
intron_variant | MODIFIER | c.736+1763G>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70892365 | ||||||
| chr6:70892466
|
G | A | 55 | a0001c0001t0001g0057a0001c0001t0002g0001a0001c0001t0002g0034others(52): Show | 56 | HG00099.hp1 HG00741.hp1 HG01167.hp1 others(53): Show |
intron_variant | MODIFIER | c.736+1662C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70892466 | ||||||
| chr6:70892470
|
T | G | 55 | a0001c0001t0001g0057a0001c0001t0002g0001a0001c0001t0002g0034others(52): Show | 56 | HG00099.hp1 HG00741.hp1 HG01167.hp1 others(53): Show |
intron_variant | MODIFIER | c.736+1658A>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70892470 | ||||||
| chr6:70892484
|
T | C | 1 | a0001c0001t0004g0136 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.736+1644A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70892484 | ||||||
| chr6:70892492
|
C | A | 1 | a0001c0001t0103g0308 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.736+1636G>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70892492 | ||||||
| chr6:70892717
|
C | T | 114 | a0001c0001t0001g0044a0001c0001t0001g0046a0001c0001t0001g0048others(111): Show | 115 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.736+1411G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70892717 | ||||||
| chr6:70892772
|
C | T | 3 | a0001c0001t0003g0135a0001c0001t0055g0128a0001c0001t0069g0103 | 3 | HG02717.hp1 HG02895.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.736+1356G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70892772 | ||||||
| chr6:70892816
|
C | G | 3 | a0001c0001t0003g0135a0001c0001t0055g0128a0001c0001t0069g0103 | 3 | HG02717.hp1 HG02895.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.736+1312G>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70892816 | ||||||
| chr6:70892825
|
C | T | 3 | a0001c0001t0004g0164a0001c0001t0036g0104a0001c0001t0036g0138 | 3 | HG02109.hp2 HG02809.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.736+1303G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70892825 | ||||||
| chr6:70892900
|
A | C | 3 | a0001c0001t0003g0135a0001c0001t0055g0128a0001c0001t0069g0103 | 3 | HG02717.hp1 HG02895.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.736+1228T>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70892900 | ||||||
| chr6:70893155
|
T | C | 1 | a0001c0002t0021g0238 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.736+973A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70893155 | ||||||
| chr6:70893268
|
C | T | 1 | a0001c0001t0002g0120 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.736+860G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70893268 | ||||||
| chr6:70893288
|
A | G | 1 | a0001c0002t0042g0254 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.736+840T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70893288 | ||||||
| chr6:70893379
|
T | A | 1 | a0001c0002t0042g0254 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.736+749A>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70893379 | ||||||
| chr6:70893404
|
A | AT | 119 | a0001c0001t0001g0044a0001c0001t0001g0046a0001c0001t0001g0048others(116): Show | 120 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(117): Show |
intron_variant | MODIFIER | c.736+723dupA | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70893404 | ||||||
| chr6:70893870
|
C | T | 1 | a0001c0001t0057g0073 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.736+258G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70893870 | ||||||
| chr6:70893898
|
G | A | 1 | a0001c0002t0042g0254 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.736+230C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70893898 | ||||||
| chr6:70894081
|
A | G | 2 | a0001c0002t0008g0248a0001c0002t0098g0294 | 2 | HG02735.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.736+47T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70894081 | ||||||
| chr6:70894406
|
C | A | 1 | a0001c0002t0080g0194 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.592-134G>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70894406 | ||||||
| chr6:70894531
|
A | G | 1 | a0001c0001t0069g0103 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.592-259T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70894531 | ||||||
| chr6:70894536
|
T | A | 1 | a0001c0001t0069g0103 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.592-264A>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70894536 | ||||||
| chr6:70894707
|
A | ACTTTTCT others(10): Show |
1 | a0001c0001t0001g0068 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.592-452_592-436dup others(17): Show |
B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70894707 | ||||||
| chr6:70894847
|
A | T | 3 | a0001c0001t0001g0171a0001c0001t0037g0061a0001c0001t0074g0087 | 3 | HG03239.hp1 HG03669.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.592-575T>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70894847 | ||||||
| chr6:70894875
|
C | T | 1 | a0001c0002t0091g0260 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.592-603G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70894875 | ||||||
| chr6:70894924
|
A | T | 1 | a0001c0001t0017g0007 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.592-652T>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70894924 | ||||||
| chr6:70895338
|
T | A | 1 | a0001c0002t0005g0211 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.592-1066A>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70895338 | ||||||
| chr6:70895495
|
A | AT | 22 | a0001c0001t0002g0070a0001c0001t0003g0133a0001c0001t0010g0051others(19): Show | 22 | HG01069.hp2 HG01167.hp2 HG01256.hp1 others(19): Show |
intron_variant | MODIFIER | c.592-1224dupA | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70895495 | ||||||
| chr6:70895495
|
A | ATT | 61 | a0001c0001t0001g0048a0001c0001t0001g0054a0001c0001t0001g0060others(58): Show | 62 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(59): Show |
intron_variant | MODIFIER | c.592-1225_592-1224d others(4): Show |
B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70895495 | ||||||
| chr6:70895495
|
A | ATTT | 46 | a0001c0001t0001g0044a0001c0001t0001g0046a0001c0001t0001g0055others(43): Show | 46 | HG00408.hp2 HG00621.hp1 HG00621.hp2 others(43): Show |
intron_variant | MODIFIER | c.592-1226_592-1224d others(5): Show |
B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70895495 | ||||||
| chr6:70895495
|
A | T | 1 | a0001c0001t0017g0007 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.592-1223T>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70895495 | ||||||
| chr6:70895495
|
AT | A | 35 | a0001c0001t0002g0001a0001c0001t0002g0065a0001c0001t0002g0072others(32): Show | 36 | HG00642.hp1 HG00673.hp2 HG01069.hp1 others(33): Show |
intron_variant | MODIFIER | c.592-1224delA | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70895495 | ||||||
| chr6:70895495
|
ATT | A | 83 | a0001c0001t0001g0057a0001c0001t0002g0034a0001c0001t0002g0037others(80): Show | 83 | HG00099.hp1 HG00423.hp2 HG00741.hp1 others(80): Show |
intron_variant | MODIFIER | c.592-1225_592-1224d others(4): Show |
B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70895495 | ||||||
| chr6:70895528
|
C | T | 1 | a0001c0001t0002g0037 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.592-1256G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70895528 | ||||||
| chr6:70895537
|
A | ACTC | 117 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0046others(114): Show | 118 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(115): Show |
intron_variant | MODIFIER | c.592-1268_592-1266d others(5): Show |
B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70895537 | ||||||
| chr6:70895688
|
T | G | 1 | a0001c0002t0089g0297 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.592-1416A>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70895688 | ||||||
| chr6:70895731
|
G | A | 1 | a0001c0001t0004g0136 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.592-1459C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70895731 | ||||||
| chr6:70895833
|
C | CT | 55 | a0001c0001t0001g0171a0001c0001t0002g0065a0001c0001t0002g0069others(52): Show | 55 | HG00423.hp2 HG00642.hp1 HG00673.hp2 others(52): Show |
intron_variant | MODIFIER | c.592-1562dupA | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70895833 | ||||||
| chr6:70895923
|
GGTCTGCT others(12): Show |
G | 1 | a0001c0001t0001g0068 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.592-1670_592-1652d others(21): Show |
B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70895923 | ||||||
| chr6:70895969
|
T | C | 2 | a0001c0001t0003g0135a0001c0001t0055g0128 | 2 | HG02895.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.592-1697A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70895969 | ||||||
| chr6:70895988
|
C | T | 3 | a0001c0001t0003g0102a0001c0001t0003g0125a0001c0001t0004g0124 | 3 | HG00741.hp1 HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.592-1716G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70895988 | ||||||
| chr6:70896109
|
G | A | 232 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0046others(229): Show | 234 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(231): Show |
intron_variant | MODIFIER | c.592-1837C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70896109 | ||||||
| chr6:70896196
|
CAGAG | C | 8 | a0001c0001t0023g0076a0001c0001t0023g0077a0001c0001t0025g0109others(5): Show | 8 | HG01069.hp1 HG03139.hp2 HG03209.hp2 others(5): Show |
intron_variant | MODIFIER | c.592-1928_592-1925d others(6): Show |
B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70896196 | ||||||
| chr6:70896324
|
G | A | 1 | a0001c0001t0001g0054 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.592-2052C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70896324 | ||||||
| chr6:70896360
|
C | T | 3 | a0001c0001t0003g0135a0001c0001t0055g0128a0001c0001t0069g0103 | 3 | HG02717.hp1 HG02895.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.592-2088G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70896360 | ||||||
| chr6:70896452
|
T | A | 1 | a0001c0002t0016g0237 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.592-2180A>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70896452 | ||||||
| chr6:70896506
|
A | C | 1 | a0001c0001t0003g0135 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.592-2234T>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70896506 | ||||||
| chr6:70896532
|
T | A | 3 | a0001c0001t0003g0102a0001c0001t0003g0125a0001c0001t0004g0124 | 3 | HG00741.hp1 HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.592-2260A>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70896532 | ||||||
| chr6:70896720
|
CT | C | 9 | a0001c0001t0001g0171a0001c0001t0037g0061a0001c0001t0045g0003others(6): Show | 9 | HG02559.hp1 HG02572.hp1 HG02970.hp2 others(6): Show |
intron_variant | MODIFIER | c.592-2449delA | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70896720 | ||||||
| chr6:70896731
|
C | T | 1 | a0001c0002t0008g0219 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.592-2459G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70896731 | ||||||
| chr6:70896847
|
C | T | 1 | a0001c0002t0030g0302 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.592-2575G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70896847 | ||||||
| chr6:70896910
|
T | C | 18 | a0001c0001t0002g0065a0001c0001t0002g0069a0001c0001t0002g0072others(15): Show | 18 | HG00423.hp2 HG00673.hp2 HG02015.hp1 others(15): Show |
intron_variant | MODIFIER | c.592-2638A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70896910 | ||||||
| chr6:70896978
|
A | C | 1 | a0001c0001t0003g0129 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.592-2706T>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70896978 | ||||||
| chr6:70897023
|
A | C | 1 | a0001c0001t0009g0095 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.592-2751T>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70897023 | ||||||
| chr6:70897229
|
A | C | 7 | a0001c0001t0019g0012a0001c0001t0019g0024a0001c0001t0036g0104others(4): Show | 7 | HG01074.hp1 HG02027.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.592-2957T>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70897229 | ||||||
| chr6:70897249
|
CT | C | 109 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0046others(106): Show | 110 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.592-2978delA | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70897249 | ||||||
| chr6:70897284
|
C | T | 97 | a0001c0001t0001g0057a0001c0001t0001g0171a0001c0001t0002g0001others(94): Show | 98 | HG00099.hp1 HG00423.hp2 HG00673.hp2 others(95): Show |
intron_variant | MODIFIER | c.592-3012G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70897284 | ||||||
| chr6:70897470
|
C | T | 58 | a0001c0001t0001g0057a0001c0001t0002g0001a0001c0001t0002g0034others(55): Show | 59 | HG00099.hp1 HG00741.hp1 HG01167.hp1 others(56): Show |
intron_variant | MODIFIER | c.592-3198G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70897470 | ||||||
| chr6:70897514
|
G | A | 7 | a0001c0002t0005g0201a0001c0002t0014g0289a0001c0002t0014g0291others(4): Show | 7 | HG00738.hp2 HG01167.hp2 HG01433.hp2 others(4): Show |
intron_variant | MODIFIER | c.592-3242C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70897514 | ||||||
| chr6:70897522
|
T | G | 7 | a0001c0001t0019g0012a0001c0001t0019g0024a0001c0001t0036g0104others(4): Show | 7 | HG01074.hp1 HG02027.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.592-3250A>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70897522 | ||||||
| chr6:70897607
|
G | T | 1 | a0001c0001t0068g0167 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.592-3335C>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70897607 | ||||||
| chr6:70897658
|
GAA | G | 7 | a0001c0001t0019g0012a0001c0001t0019g0024a0001c0001t0036g0104others(4): Show | 7 | HG01074.hp1 HG02027.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.592-3388_592-3387d others(4): Show |
B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70897658 | ||||||
| chr6:70897658
|
GAAA | G | 6 | a0001c0001t0001g0171a0001c0001t0003g0126a0001c0001t0037g0061others(3): Show | 6 | HG02451.hp2 HG02970.hp2 HG03239.hp1 others(3): Show |
intron_variant | MODIFIER | c.592-3389_592-3387d others(5): Show |
B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70897658 | ||||||
| chr6:70897658
|
GAAAA | G | 12 | a0001c0001t0003g0102a0001c0001t0003g0125a0001c0001t0003g0142others(9): Show | 12 | HG00741.hp1 HG01167.hp1 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.592-3390_592-3387d others(6): Show |
B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70897658 | ||||||
| chr6:70897667
|
AAAAAT | A | 18 | a0001c0001t0003g0129a0001c0001t0003g0135a0001c0001t0004g0074others(15): Show | 18 | HG01069.hp1 HG02559.hp1 HG02572.hp2 others(15): Show |
intron_variant | MODIFIER | c.592-3400_592-3396d others(7): Show |
B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70897667 | ||||||
| chr6:70897668
|
A | T | 4 | a0001c0001t0019g0012a0001c0001t0019g0024a0001c0002t0021g0238others(1): Show | 4 | HG01074.hp1 HG02027.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.592-3396T>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70897668 | ||||||
| chr6:70897668
|
AAAAT | A | 60 | a0001c0001t0001g0057a0001c0001t0001g0145a0001c0001t0002g0001others(57): Show | 61 | HG00099.hp1 HG01884.hp1 HG02015.hp2 others(58): Show |
intron_variant | MODIFIER | c.592-3400_592-3397d others(6): Show |
B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70897668 | ||||||
| chr6:70897669
|
AAAT | A | 9 | a0001c0001t0012g0009a0001c0001t0012g0010a0001c0001t0066g0139others(6): Show | 9 | HG00621.hp1 HG02630.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.592-3400_592-3398d others(5): Show |
B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70897669 | ||||||
| chr6:70897669
|
AAATAT | A | 25 | a0001c0001t0003g0099a0001c0001t0003g0100a0001c0001t0020g0053others(22): Show | 25 | HG00642.hp1 HG01074.hp2 HG01099.hp1 others(22): Show |
intron_variant | MODIFIER | c.592-3402_592-3398d others(7): Show |
B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70897669 | ||||||
| chr6:70897670
|
A | T | 10 | a0001c0001t0004g0052a0001c0001t0004g0056a0001c0001t0019g0012others(7): Show | 10 | HG01074.hp1 HG02027.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.592-3398T>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70897670 | ||||||
| chr6:70897670
|
AATAT | A | 91 | a0001c0001t0001g0042a0001c0001t0001g0046a0001c0001t0001g0048others(88): Show | 92 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(89): Show |
intron_variant | MODIFIER | c.592-3402_592-3399d others(6): Show |
B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70897670 | ||||||
| chr6:70897671
|
ATAT | A | 11 | a0001c0001t0001g0044a0001c0001t0001g0172a0001c0001t0002g0065others(8): Show | 11 | HG00423.hp2 HG00673.hp2 HG02698.hp1 others(8): Show |
intron_variant | MODIFIER | c.592-3402_592-3400d others(5): Show |
B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70897671 | ||||||
| chr6:70897671
|
ATATAT | A | 3 | a0001c0001t0019g0019a0001c0001t0055g0128a0001c0002t0042g0254 | 3 | HG03195.hp1 HG03453.hp1 NA18945.hp1 |
intron_variant | MODIFIER | c.592-3404_592-3400d others(7): Show |
B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70897671 | ||||||
| chr6:70897672
|
T | A | 3 | a0001c0002t0026g0181a0001c0002t0026g0209a0001c0002t0082g0239 | 3 | HG01099.hp2 HG02040.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.592-3400A>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70897672 | ||||||
| chr6:70897676
|
T | A | 14 | a0001c0001t0001g0044a0001c0001t0001g0117a0001c0001t0001g0160others(11): Show | 14 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(11): Show |
intron_variant | MODIFIER | c.592-3404A>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70897676 | ||||||
| chr6:70897875
|
G | C | 1 | a0001c0001t0068g0167 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.592-3603C>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70897875 | ||||||
| chr6:70897917
|
T | C | 1 | a0001c0002t0042g0295 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.592-3645A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70897917 | ||||||
| chr6:70898105
|
T | C | 1 | a0002c0004t0063g0176 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.592-3833A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70898105 | ||||||
| chr6:70898111
|
C | G | 1 | a0001c0002t0022g0283 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.592-3839G>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70898111 | ||||||
| chr6:70898146
|
A | T | 14 | a0001c0001t0002g0065a0001c0001t0002g0069a0001c0001t0002g0072others(11): Show | 14 | HG00423.hp2 HG00673.hp2 HG02015.hp1 others(11): Show |
intron_variant | MODIFIER | c.592-3874T>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70898146 | ||||||
| chr6:70898388
|
T | TC | 9 | a0001c0001t0001g0042a0001c0001t0002g0050a0001c0001t0002g0158others(6): Show | 9 | HG02145.hp1 HG02738.hp2 HG03688.hp2 others(6): Show |
intron_variant | MODIFIER | c.592-4117dupG | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70898388 | ||||||
| chr6:70898472
|
C | T | 1 | a0001c0001t0045g0003 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.592-4200G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70898472 | ||||||
| chr6:70898515
|
C | T | 7 | a0001c0001t0019g0012a0001c0001t0019g0024a0001c0001t0036g0104others(4): Show | 7 | HG01074.hp1 HG02027.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.592-4243G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70898515 | ||||||
| chr6:70898677
|
A | T | 3 | a0001c0001t0003g0135a0001c0001t0055g0128a0001c0001t0069g0103 | 3 | HG02717.hp1 HG02895.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.592-4405T>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70898677 | ||||||
| chr6:70898963
|
A | AAAAT | 24 | a0001c0001t0002g0151a0001c0001t0003g0126a0001c0001t0004g0164others(21): Show | 24 | HG00408.hp1 HG00741.hp2 HG01192.hp1 others(21): Show |
intron_variant | MODIFIER | c.592-4695_592-4692d others(6): Show |
B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70898963 | ||||||
| chr6:70898963
|
AAAAT | A | 40 | a0001c0001t0003g0135a0001c0001t0004g0074a0001c0001t0004g0136others(37): Show | 40 | HG01069.hp1 HG01074.hp1 HG01433.hp1 others(37): Show |
intron_variant | MODIFIER | c.592-4695_592-4692d others(6): Show |
B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70898963 | ||||||
| chr6:70898987
|
T | TAAATA | 5 | a0001c0001t0012g0009a0001c0001t0012g0010a0001c0001t0066g0139others(2): Show | 5 | HG02630.hp2 HG02647.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.592-4720_592-4716d others(7): Show |
B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70898987 | ||||||
| chr6:70899019
|
A | G | 7 | a0001c0001t0004g0164a0001c0002t0006g0187a0001c0002t0006g0188others(4): Show | 7 | HG02622.hp1 HG02630.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.592-4747T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70899019 | ||||||
| chr6:70899195
|
T | C | 1 | a0001c0002t0080g0194 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.592-4923A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70899195 | ||||||
| chr6:70899239
|
C | T | 1 | a0001c0001t0018g0025 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.592-4967G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70899239 | ||||||
| chr6:70899286
|
T | C | 1 | a0001c0001t0049g0011 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.592-5014A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70899286 | ||||||
| chr6:70899302
|
C | T | 4 | a0001c0001t0056g0115a0001c0002t0006g0193a0001c0002t0011g0256others(1): Show | 4 | HG02559.hp2 HG02572.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.592-5030G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70899302 | ||||||
| chr6:70899346
|
C | T | 28 | a0001c0001t0001g0063a0001c0001t0002g0059a0001c0001t0002g0144others(25): Show | 28 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(25): Show |
intron_variant | MODIFIER | c.592-5074G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70899346 | ||||||
| chr6:70899473
|
G | C | 1 | a0001c0002t0014g0290 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.592-5201C>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70899473 | ||||||
| chr6:70899488
|
A | G | 5 | a0001c0002t0006g0230a0001c0002t0006g0235a0001c0002t0006g0246others(2): Show | 5 | HG02165.hp1 HG02602.hp2 HG03831.hp2 others(2): Show |
intron_variant | MODIFIER | c.592-5216T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70899488 | ||||||
| chr6:70899520
|
C | T | 1 | a0001c0001t0001g0060 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.592-5248G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70899520 | ||||||
| chr6:70899580
|
T | TA | 7 | a0001c0001t0023g0076a0001c0001t0023g0077a0001c0001t0045g0003others(4): Show | 7 | HG02559.hp1 HG03098.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.592-5309dupT | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70899580 | ||||||
| chr6:70899681
|
A | G | 148 | a0001c0001t0001g0042a0001c0001t0001g0054a0001c0001t0001g0055others(145): Show | 148 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(145): Show |
intron_variant | MODIFIER | c.592-5409T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70899681 | ||||||
| chr6:70899728
|
A | C | 1 | a0001c0001t0001g0064 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.592-5456T>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70899728 | ||||||
| chr6:70899777
|
G | A | 1 | a0001c0002t0022g0266 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.592-5505C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70899777 | ||||||
| chr6:70899784
|
T | G | 5 | a0001c0001t0033g0114a0001c0001t0056g0115a0001c0002t0043g0274others(2): Show | 5 | HG02970.hp2 HG02976.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.592-5512A>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70899784 | ||||||
| chr6:70899788
|
T | C | 1 | a0001c0001t0003g0135 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.592-5516A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70899788 | ||||||
| chr6:70899807
|
G | C | 2 | a0001c0002t0006g0235a0001c0002t0028g0222 | 2 | HG02165.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.592-5535C>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70899807 | ||||||
| chr6:70899921
|
A | G | 10 | a0001c0001t0001g0064a0001c0001t0017g0007a0001c0001t0017g0013others(7): Show | 10 | HG01255.hp1 HG01981.hp2 HG02004.hp2 others(7): Show |
intron_variant | MODIFIER | c.592-5649T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70899921 | ||||||
| chr6:70899967
|
G | A | 1 | a0001c0002t0042g0295 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.592-5695C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70899967 | ||||||
| chr6:70900004
|
A | C | 27 | a0001c0001t0002g0034a0001c0001t0003g0168a0001c0001t0013g0096others(24): Show | 27 | HG00099.hp1 HG00597.hp2 HG00621.hp2 others(24): Show |
intron_variant | MODIFIER | c.592-5732T>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70900004 | ||||||
| chr6:70900124
|
T | C | 8 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171others(5): Show | 8 | HG01074.hp1 HG01256.hp2 HG01257.hp1 others(5): Show |
intron_variant | MODIFIER | c.592-5852A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70900124 | ||||||
| chr6:70900311
|
G | C | 49 | a0001c0001t0001g0046a0001c0001t0001g0048a0001c0001t0004g0112others(46): Show | 49 | HG00099.hp1 HG00642.hp1 HG00738.hp2 others(46): Show |
intron_variant | MODIFIER | c.592-6039C>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70900311 | ||||||
| chr6:70900409
|
CT | C | 154 | a0001c0001t0001g0044a0001c0001t0001g0046a0001c0001t0001g0048others(151): Show | 154 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.592-6138delA | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70900409 | ||||||
| chr6:70900715
|
C | T | 1 | a0001c0001t0068g0167 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.592-6443G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70900715 | ||||||
| chr6:70900753
|
C | T | 4 | a0001c0001t0012g0009a0001c0001t0012g0010a0001c0001t0048g0008others(1): Show | 4 | HG02630.hp2 HG02723.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.592-6481G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70900753 | ||||||
| chr6:70900793
|
C | T | 2 | a0001c0001t0045g0003a0001c0002t0042g0295 | 2 | HG02559.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.592-6521G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70900793 | ||||||
| chr6:70900926
|
T | G | 1 | a0001c0001t0046g0029 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.592-6654A>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70900926 | ||||||
| chr6:70900958
|
T | C | 1 | a0001c0002t0041g0190 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.592-6686A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70900958 | ||||||
| chr6:70901075
|
A | T | 41 | a0001c0001t0004g0074a0001c0001t0053g0032a0001c0001t0054g0031others(38): Show | 41 | HG00099.hp1 HG00323.hp1 HG00642.hp1 others(38): Show |
intron_variant | MODIFIER | c.592-6803T>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70901075 | ||||||
| chr6:70901093
|
G | A | 61 | a0001c0001t0001g0117a0001c0001t0001g0145a0001c0001t0001g0156others(58): Show | 61 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(58): Show |
intron_variant | MODIFIER | c.592-6821C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70901093 | ||||||
| chr6:70901139
|
T | C | 1 | a0001c0002t0006g0230 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.592-6867A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70901139 | ||||||
| chr6:70901205
|
C | T | 1 | a0001c0001t0109g0310 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.592-6933G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70901205 | ||||||
| chr6:70901403
|
G | A | 4 | a0001c0001t0012g0009a0001c0001t0012g0010a0001c0001t0048g0008others(1): Show | 4 | HG02630.hp2 HG02723.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.592-7131C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70901403 | ||||||
| chr6:70901469
|
C | T | 1 | a0001c0002t0007g0251 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.592-7197G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70901469 | ||||||
| chr6:70901802
|
C | T | 1 | a0001c0001t0013g0096 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.592-7530G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70901802 | ||||||
| chr6:70901803
|
G | A | 7 | a0001c0001t0004g0052a0001c0001t0004g0056a0001c0001t0023g0076others(4): Show | 7 | HG02145.hp2 HG02258.hp2 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.592-7531C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70901803 | ||||||
| chr6:70901844
|
A | C | 1 | a0001c0002t0015g0288 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.592-7572T>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70901844 | ||||||
| chr6:70901893
|
G | C | 1 | a0001c0001t0073g0107 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.592-7621C>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70901893 | ||||||
| chr6:70902186
|
C | T | 249 | a0001c0001t0001g0044a0001c0001t0001g0046a0001c0001t0001g0048others(246): Show | 249 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(246): Show |
intron_variant | MODIFIER | c.592-7914G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70902186 | ||||||
| chr6:70902334
|
T | TA | 29 | a0001c0001t0001g0068a0001c0001t0012g0020a0001c0001t0012g0030others(26): Show | 29 | HG00673.hp2 HG01074.hp1 HG01255.hp1 others(26): Show |
intron_variant | MODIFIER | c.592-8063dupT | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70902334 | ||||||
| chr6:70902363
|
G | A | 12 | a0001c0002t0011g0270a0001c0002t0022g0266a0001c0002t0022g0269others(9): Show | 12 | HG02132.hp1 HG02135.hp1 NA18951.hp1 others(9): Show |
intron_variant | MODIFIER | c.592-8091C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70902363 | ||||||
| chr6:70902412
|
A | G | 1 | a0001c0001t0067g0113 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.592-8140T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70902412 | ||||||
| chr6:70902617
|
G | GAT | 39 | a0001c0001t0001g0068a0001c0001t0003g0102a0001c0001t0003g0125others(36): Show | 39 | HG00735.hp1 HG00741.hp1 HG01069.hp1 others(36): Show |
intron_variant | MODIFIER | c.592-8347_592-8346d others(4): Show |
B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70902617 | ||||||
| chr6:70902617
|
G | GATAT | 60 | a0001c0001t0001g0117a0001c0001t0001g0145a0001c0001t0001g0156others(57): Show | 60 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(57): Show |
intron_variant | MODIFIER | c.592-8349_592-8346d others(6): Show |
B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70902617 | ||||||
| chr6:70902617
|
G | GATATAT | 7 | a0001c0001t0003g0126a0001c0001t0019g0019a0001c0001t0032g0004others(4): Show | 7 | HG00323.hp1 HG01074.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.592-8351_592-8346d others(8): Show |
B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70902617 | ||||||
| chr6:70902617
|
G | GATATATA others(1): Show |
14 | a0001c0001t0003g0168a0001c0001t0012g0030a0001c0001t0017g0007others(11): Show | 14 | HG00673.hp2 HG01074.hp1 HG01168.hp1 others(11): Show |
intron_variant | MODIFIER | c.592-8353_592-8346d others(10): Show |
B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70902617 | ||||||
| chr6:70902617
|
G | GATATATA others(3): Show |
2 | a0001c0001t0050g0016a0001c0001t0066g0139 | 2 | NA18964.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.592-8355_592-8346d others(12): Show |
B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70902617 | ||||||
| chr6:70902617
|
G | GATATATA others(7): Show |
1 | a0001c0001t0012g0020 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.592-8359_592-8346d others(16): Show |
B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70902617 | ||||||
| chr6:70902617
|
G | GATATATA others(9): Show |
2 | a0001c0002t0011g0270a0001c0002t0093g0268 | 2 | NA18965.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.592-8361_592-8346d others(18): Show |
B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70902617 | ||||||
| chr6:70902617
|
G | GATATATA others(11): Show |
5 | a0001c0002t0030g0263a0001c0002t0030g0264a0001c0002t0030g0302others(2): Show | 5 | HG02132.hp1 NA18951.hp1 NA18962.hp2 others(2): Show |
intron_variant | MODIFIER | c.592-8363_592-8346d others(20): Show |
B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70902617 | ||||||
| chr6:70902617
|
G | GATATATA others(13): Show |
4 | a0001c0002t0022g0266a0001c0002t0022g0269a0001c0002t0029g0300others(1): Show | 4 | HG02135.hp1 NA18981.hp2 NA19012.hp1 others(1): Show |
intron_variant | MODIFIER | c.592-8365_592-8346d others(22): Show |
B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70902617 | ||||||
| chr6:70902617
|
GAT | G | 69 | a0001c0001t0001g0101a0001c0001t0001g0121a0001c0001t0002g0001others(66): Show | 71 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(68): Show |
intron_variant | MODIFIER | c.592-8347_592-8346d others(4): Show |
B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70902617 | ||||||
| chr6:70902617
|
GATAT | G | 4 | a0001c0001t0012g0009a0001c0001t0012g0010a0001c0001t0048g0008others(1): Show | 4 | HG02630.hp2 HG02723.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.592-8349_592-8346d others(6): Show |
B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70902617 | ||||||
| chr6:70902627
|
TATATATA others(9): Show |
T | 64 | a0001c0001t0001g0044a0001c0001t0001g0046a0001c0001t0001g0048others(61): Show | 64 | HG00099.hp2 HG00408.hp2 HG00597.hp1 others(61): Show |
intron_variant | MODIFIER | c.592-8371_592-8356d others(18): Show |
B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70902627 | ||||||
| chr6:70902631
|
T | TACACACA others(1): Show |
3 | a0001c0001t0036g0104a0001c0001t0036g0138a0001c0001t0045g0003 | 3 | HG02109.hp2 HG02559.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.592-8360_592-8359i others(10): Show |
B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70902631 | ||||||
| chr6:70902633
|
T | C | 4 | a0001c0001t0036g0104a0001c0001t0036g0138a0001c0001t0045g0003others(1): Show | 4 | HG02109.hp2 HG02559.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.592-8361A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70902633 | ||||||
| chr6:70902633
|
T | TAC | 7 | a0001c0002t0006g0187a0001c0002t0006g0188a0001c0002t0006g0189others(4): Show | 7 | HG02559.hp2 HG02572.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.592-8362_592-8361i others(4): Show |
B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70902633 | ||||||
| chr6:70902633
|
T | TACACACA others(5): Show |
1 | a0001c0001t0003g0081 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.592-8362_592-8361i others(14): Show |
B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70902633 | ||||||
| chr6:70902635
|
T | C | 14 | a0001c0001t0003g0081a0001c0001t0036g0104a0001c0001t0036g0138others(11): Show | 14 | HG02109.hp2 HG02559.hp1 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.592-8363A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70902635 | ||||||
| chr6:70902637
|
T | C | 30 | a0001c0001t0003g0081a0001c0001t0003g0089a0001c0001t0003g0090others(27): Show | 30 | HG00597.hp2 HG01256.hp1 HG01496.hp1 others(27): Show |
intron_variant | MODIFIER | c.592-8365A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70902637 | ||||||
| chr6:70902637
|
T | TATATATA others(17): Show |
1 | a0001c0002t0022g0299 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.592-8366_592-8365i others(26): Show |
B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70902637 | ||||||
| chr6:70902637
|
TAC | T | 8 | a0001c0001t0001g0042a0001c0001t0003g0099a0001c0001t0003g0100others(5): Show | 8 | HG01884.hp2 HG02258.hp1 HG02300.hp1 others(5): Show |
intron_variant | MODIFIER | c.592-8367_592-8366d others(4): Show |
B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70902637 | ||||||
| chr6:70902639
|
C | T | 111 | a0001c0001t0001g0068a0001c0001t0001g0117a0001c0001t0001g0145others(108): Show | 111 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(108): Show |
intron_variant | MODIFIER | c.592-8367G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70902639 | ||||||
| chr6:70902641
|
C | T | 64 | a0001c0001t0001g0068a0001c0001t0001g0156a0001c0001t0001g0160others(61): Show | 64 | HG00408.hp1 HG00544.hp1 HG00735.hp1 others(61): Show |
intron_variant | MODIFIER | c.592-8369G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70902641 | ||||||
| chr6:70902643
|
C | T | 12 | a0001c0001t0003g0102a0001c0001t0003g0125a0001c0001t0004g0124others(9): Show | 12 | HG00741.hp1 HG00741.hp2 HG01167.hp1 others(9): Show |
intron_variant | MODIFIER | c.592-8371G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70902643 | ||||||
| chr6:70902667
|
T | C | 80 | a0001c0001t0001g0044a0001c0001t0001g0046a0001c0001t0001g0048others(77): Show | 80 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.592-8395A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70902667 | ||||||
| chr6:70902669
|
T | C | 1 | a0001c0002t0006g0197 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.592-8397A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70902669 | ||||||
| chr6:70902687
|
C | G | 1 | a0001c0002t0042g0295 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.592-8415G>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70902687 | ||||||
| chr6:70902767
|
T | C | 133 | a0001c0001t0001g0042a0001c0001t0001g0117a0001c0001t0001g0145others(130): Show | 133 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(130): Show |
intron_variant | MODIFIER | c.592-8495A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70902767 | ||||||
| chr6:70902788
|
C | T | 1 | a0001c0001t0002g0152 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.592-8516G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70902788 | ||||||
| chr6:70903193
|
A | G | 8 | a0001c0001t0003g0099a0001c0001t0003g0100a0001c0001t0003g0132others(5): Show | 8 | HG00323.hp2 HG01884.hp1 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.592-8921T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70903193 | ||||||
| chr6:70903535
|
T | C | 11 | a0001c0001t0012g0009a0001c0001t0012g0010a0001c0001t0048g0008others(8): Show | 11 | HG02630.hp2 HG02647.hp2 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.592-9263A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70903535 | ||||||
| chr6:70903552
|
T | C | 4 | a0001c0001t0003g0132a0001c0001t0003g0133a0001c0001t0025g0134others(1): Show | 4 | HG01884.hp2 HG03225.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.592-9280A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70903552 | ||||||
| chr6:70903746
|
G | C | 2 | a0001c0001t0003g0081a0001c0002t0042g0254 | 2 | HG03453.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.592-9474C>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70903746 | ||||||
| chr6:70903749
|
C | T | 104 | a0001c0001t0001g0117a0001c0001t0001g0145a0001c0001t0001g0156others(101): Show | 104 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.592-9477G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70903749 | ||||||
| chr6:70903811
|
C | T | 1 | a0001c0002t0029g0300 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.592-9539G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70903811 | ||||||
| chr6:70903913
|
T | C | 20 | a0001c0001t0003g0081a0001c0001t0003g0129a0001c0001t0003g0132others(17): Show | 20 | HG01884.hp2 HG02132.hp1 HG02135.hp1 others(17): Show |
intron_variant | MODIFIER | c.592-9641A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70903913 | ||||||
| chr6:70903948
|
T | C | 255 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0046others(252): Show | 255 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(252): Show |
intron_variant | MODIFIER | c.592-9676A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70903948 | ||||||
| chr6:70904044
|
C | T | 186 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0046others(183): Show | 186 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(183): Show |
intron_variant | MODIFIER | c.592-9772G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70904044 | ||||||
| chr6:70904152
|
G | C | 184 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0046others(181): Show | 184 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(181): Show |
intron_variant | MODIFIER | c.592-9880C>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70904152 | ||||||
| chr6:70904198
|
C | T | 1 | a0001c0002t0087g0236 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.592-9926G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70904198 | ||||||
| chr6:70904406
|
G | A | 75 | a0001c0001t0001g0044a0001c0001t0001g0046a0001c0001t0001g0048others(72): Show | 75 | HG00099.hp2 HG00597.hp1 HG00673.hp1 others(72): Show |
intron_variant | MODIFIER | c.592-10134C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70904406 | ||||||
| chr6:70904593
|
C | T | 1 | a0001c0001t0033g0075 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.592-10321G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70904593 | ||||||
| chr6:70904773
|
A | C | 12 | a0001c0001t0012g0009a0001c0001t0012g0010a0001c0001t0018g0006others(9): Show | 12 | HG01256.hp2 HG01257.hp1 HG01346.hp2 others(9): Show |
intron_variant | MODIFIER | c.592-10501T>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70904773 | ||||||
| chr6:70904808
|
C | G | 1 | a0001c0001t0009g0095 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.592-10536G>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70904808 | ||||||
| chr6:70904959
|
T | C | 182 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0046others(179): Show | 182 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(179): Show |
intron_variant | MODIFIER | c.592-10687A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70904959 | ||||||
| chr6:70904982
|
C | A | 1 | a0001c0001t0003g0035 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.592-10710G>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70904982 | ||||||
| chr6:70905885
|
CTG | C | 218 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0046others(215): Show | 218 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(215): Show |
intron_variant | MODIFIER | c.592-11615_592-1161 others(6): Show |
B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70905885 | ||||||
| chr6:70906149
|
G | A | 2 | a0001c0002t0005g0233a0001c0002t0005g0234 | 2 | NA18960.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.592-11877C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70906149 | ||||||
| chr6:70906361
|
G | C | 1 | a0001c0001t0004g0161 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.592-12089C>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70906361 | ||||||
| chr6:70906442
|
C | A | 15 | a0001c0001t0001g0101a0001c0001t0003g0089a0001c0001t0003g0090others(12): Show | 15 | HG00323.hp2 HG01256.hp1 HG01975.hp2 others(12): Show |
intron_variant | MODIFIER | c.592-12170G>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70906442 | ||||||
| chr6:70906565
|
C | T | 3 | a0001c0002t0088g0298a0001c0002t0089g0297a0001c0002t0099g0292 | 3 | HG01074.hp2 HG02738.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.592-12293G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70906565 | ||||||
| chr6:70906596
|
A | T | 6 | a0001c0001t0018g0006a0001c0001t0018g0025a0001c0001t0018g0026others(3): Show | 6 | HG01256.hp2 HG01257.hp1 HG01346.hp2 others(3): Show |
intron_variant | MODIFIER | c.592-12324T>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70906596 | ||||||
| chr6:70906750
|
A | C | 182 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0046others(179): Show | 182 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(179): Show |
intron_variant | MODIFIER | c.592-12478T>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70906750 | ||||||
| chr6:70907327
|
G | A | 1 | a0001c0002t0021g0231 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.592-13055C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70907327 | ||||||
| chr6:70907569
|
T | C | 2 | a0001c0001t0001g0169a0001c0001t0001g0170 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.592-13297A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70907569 | ||||||
| chr6:70907720
|
G | C | 5 | a0001c0001t0002g0069a0001c0001t0010g0051a0001c0001t0010g0071others(2): Show | 5 | HG01261.hp1 HG01891.hp2 HG01952.hp2 others(2): Show |
intron_variant | MODIFIER | c.592-13448C>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70907720 | ||||||
| chr6:70908127
|
A | T | 6 | a0001c0001t0018g0006a0001c0001t0018g0025a0001c0001t0018g0026others(3): Show | 6 | HG01256.hp2 HG01257.hp1 HG01346.hp2 others(3): Show |
intron_variant | MODIFIER | c.592-13855T>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70908127 | ||||||
| chr6:70908296
|
C | T | 12 | a0001c0001t0012g0009a0001c0001t0012g0010a0001c0001t0018g0006others(9): Show | 12 | HG01256.hp2 HG01257.hp1 HG01346.hp2 others(9): Show |
intron_variant | MODIFIER | c.592-14024G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70908296 | ||||||
| chr6:70908331
|
G | C | 4 | a0001c0001t0036g0104a0001c0001t0045g0003a0001c0001t0069g0103others(1): Show | 4 | HG02559.hp1 HG02717.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.592-14059C>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70908331 | ||||||
| chr6:70908465
|
G | A | 199 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0046others(196): Show | 199 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(196): Show |
intron_variant | MODIFIER | c.592-14193C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70908465 | ||||||
| chr6:70908704
|
G | A | 12 | a0001c0002t0011g0270a0001c0002t0022g0266a0001c0002t0022g0269others(9): Show | 12 | HG02132.hp1 HG02135.hp1 NA18951.hp1 others(9): Show |
intron_variant | MODIFIER | c.592-14432C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70908704 | ||||||
| chr6:70908929
|
T | C | 200 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0046others(197): Show | 200 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(197): Show |
intron_variant | MODIFIER | c.592-14657A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70908929 | ||||||
| chr6:70909023
|
A | C | 1 | a0001c0001t0001g0079 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.592-14751T>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70909023 | ||||||
| chr6:70909027
|
T | C | 199 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0046others(196): Show | 199 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(196): Show |
intron_variant | MODIFIER | c.592-14755A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70909027 | ||||||
| chr6:70909147
|
C | T | 1 | a0001c0001t0109g0310 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.592-14875G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70909147 | ||||||
| chr6:70909152
|
T | A | 54 | a0001c0002t0006g0187a0001c0002t0006g0188a0001c0002t0006g0189others(51): Show | 54 | HG00099.hp1 HG00323.hp1 HG00642.hp1 others(51): Show |
intron_variant | MODIFIER | c.592-14880A>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70909152 | ||||||
| chr6:70909154
|
A | T | 199 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0046others(196): Show | 199 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(196): Show |
intron_variant | MODIFIER | c.592-14882T>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70909154 | ||||||
| chr6:70909380
|
G | A | 1 | a0001c0001t0073g0107 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.592-15108C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70909380 | ||||||
| chr6:70909383
|
T | C | 3 | a0001c0002t0088g0298a0001c0002t0089g0297a0001c0002t0099g0292 | 3 | HG01074.hp2 HG02738.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.592-15111A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70909383 | ||||||
| chr6:70909575
|
G | A | 1 | a0001c0001t0003g0129 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.592-15303C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70909575 | ||||||
| chr6:70909576
|
C | T | 1 | a0001c0002t0082g0239 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.592-15304G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70909576 | ||||||
| chr6:70909893
|
A | G | 1 | a0001c0001t0012g0020 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.592-15621T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70909893 | ||||||
| chr6:70910026
|
A | G | 1 | a0001c0001t0073g0107 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.592-15754T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70910026 | ||||||
| chr6:70910040
|
ATTTTTTG others(3): Show |
A | 40 | a0001c0002t0008g0250a0001c0002t0011g0255a0001c0002t0011g0256others(37): Show | 40 | HG00099.hp1 HG00323.hp1 HG00642.hp1 others(37): Show |
intron_variant | MODIFIER | c.592-15778_592-1576 others(14): Show |
B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70910040 | ||||||
| chr6:70910080
|
G | A | 198 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0046others(195): Show | 198 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(195): Show |
intron_variant | MODIFIER | c.592-15808C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70910080 | ||||||
| chr6:70910207
|
G | A | 3 | a0001c0001t0003g0102a0001c0001t0003g0125a0001c0001t0004g0124 | 3 | HG00741.hp1 HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.592-15935C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70910207 | ||||||
| chr6:70910364
|
C | G | 1 | a0001c0001t0013g0140 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.592-16092G>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70910364 | ||||||
| chr6:70910378
|
T | C | 4 | a0001c0001t0036g0104a0001c0001t0045g0003a0001c0001t0069g0103others(1): Show | 4 | HG02559.hp1 HG02717.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.592-16106A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70910378 | ||||||
| chr6:70910420
|
C | T | 1 | a0001c0001t0020g0078 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.592-16148G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70910420 | ||||||
| chr6:70910525
|
G | A | 6 | a0001c0001t0012g0009a0001c0001t0012g0010a0001c0001t0048g0008others(3): Show | 6 | HG02630.hp2 HG02723.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.592-16253C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70910525 | ||||||
| chr6:70910682
|
C | T | 2 | a0001c0001t0004g0112a0001c0001t0025g0110 | 2 | HG02965.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.592-16410G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70910682 | ||||||
| chr6:70910920
|
T | C | 5 | a0001c0002t0005g0215a0001c0002t0005g0232a0001c0002t0005g0233others(2): Show | 5 | NA18949.hp1 NA18960.hp2 NA19057.hp2 others(2): Show |
intron_variant | MODIFIER | c.592-16648A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70910920 | ||||||
| chr6:70911011
|
T | A | 6 | a0001c0001t0012g0009a0001c0001t0012g0010a0001c0001t0048g0008others(3): Show | 6 | HG02630.hp2 HG02723.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.592-16739A>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70911011 | ||||||
| chr6:70911375
|
C | T | 1 | a0001c0002t0005g0217 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.592-17103G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70911375 | ||||||
| chr6:70911888
|
T | C | 4 | a0001c0001t0036g0104a0001c0001t0045g0003a0001c0001t0069g0103others(1): Show | 4 | HG02559.hp1 HG02717.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.592-17616A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70911888 | ||||||
| chr6:70911930
|
T | C | 16 | a0001c0001t0001g0042a0001c0001t0001g0101a0001c0001t0003g0089others(13): Show | 16 | HG00323.hp2 HG01256.hp1 HG01975.hp2 others(13): Show |
intron_variant | MODIFIER | c.592-17658A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70911930 | ||||||
| chr6:70912411
|
T | C | 1 | a0001c0001t0046g0029 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.592-18139A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70912411 | ||||||
| chr6:70912448
|
T | C | 1 | a0001c0001t0010g0094 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.592-18176A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70912448 | ||||||
| chr6:70912497
|
T | C | 1 | a0001c0001t0071g0038 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.592-18225A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70912497 | ||||||
| chr6:70912541
|
T | C | 4 | a0001c0001t0036g0104a0001c0001t0045g0003a0001c0001t0069g0103others(1): Show | 4 | HG02559.hp1 HG02717.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.592-18269A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70912541 | ||||||
| chr6:70912607
|
C | T | 1 | a0001c0002t0011g0272 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.592-18335G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70912607 | ||||||
| chr6:70912630
|
AGCTGGCC others(15): Show |
A | 193 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0046others(190): Show | 193 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(190): Show |
intron_variant | MODIFIER | c.592-18380_592-1835 others(26): Show |
B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70912630 | ||||||
| chr6:70912660
|
TTATATCA others(14): Show |
T | 1 | a0001c0001t0019g0024 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.592-18409_592-1838 others(25): Show |
B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70912660 | ||||||
| chr6:70912683
|
T | C | 1 | a0001c0001t0047g0028 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.592-18411A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70912683 | ||||||
| chr6:70912763
|
T | C | 4 | a0001c0001t0036g0104a0001c0001t0045g0003a0001c0001t0069g0103others(1): Show | 4 | HG02559.hp1 HG02717.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.592-18491A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70912763 | ||||||
| chr6:70912783
|
T | C | 252 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0046others(249): Show | 252 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(249): Show |
intron_variant | MODIFIER | c.592-18511A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70912783 | ||||||
| chr6:70912829
|
C | T | 1 | a0001c0001t0056g0115 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.592-18557G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70912829 | ||||||
| chr6:70912934
|
T | G | 1 | a0001c0002t0078g0207 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.592-18662A>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70912934 | ||||||
| chr6:70913032
|
T | A | 1 | a0001c0001t0068g0167 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.592-18760A>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70913032 | ||||||
| chr6:70913268
|
G | T | 1 | a0001c0003t0062g0105 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.592-18996C>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70913268 | ||||||
| chr6:70913290
|
G | GGGTGTTT others(3): Show |
1 | a0001c0001t0052g0015 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.592-19028_592-1901 others(14): Show |
B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70913290 | ||||||
| chr6:70913550
|
G | A | 169 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0046others(166): Show | 169 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(166): Show |
intron_variant | MODIFIER | c.592-19278C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70913550 | ||||||
| chr6:70913594
|
T | A | 1 | a0001c0002t0014g0290 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.592-19322A>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70913594 | ||||||
| chr6:70913834
|
T | C | 2 | a0001c0001t0001g0145a0001c0001t0034g0148 | 2 | NA18951.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.592-19562A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70913834 | ||||||
| chr6:70913952
|
G | C | 238 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0046others(235): Show | 238 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(235): Show |
intron_variant | MODIFIER | c.592-19680C>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70913952 | ||||||
| chr6:70914007
|
A | G | 40 | a0001c0002t0008g0250a0001c0002t0011g0255a0001c0002t0011g0256others(37): Show | 40 | HG00099.hp1 HG00323.hp1 HG00642.hp1 others(37): Show |
intron_variant | MODIFIER | c.592-19735T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70914007 | ||||||
| chr6:70914057
|
C | T | 2 | a0001c0001t0001g0169a0001c0001t0001g0170 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.592-19785G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70914057 | ||||||
| chr6:70914366
|
A | T | 4 | a0001c0001t0036g0104a0001c0001t0045g0003a0001c0001t0069g0103others(1): Show | 4 | HG02559.hp1 HG02717.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.592-20094T>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70914366 | ||||||
| chr6:70914753
|
T | A | 1 | a0001c0002t0026g0181 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.592-20481A>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70914753 | ||||||
| chr6:70914760
|
C | CT | 198 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0046others(195): Show | 198 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(195): Show |
intron_variant | MODIFIER | c.592-20489dupA | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70914760 | ||||||
| chr6:70914810
|
G | A | 4 | a0001c0001t0004g0112a0001c0001t0025g0110a0001c0001t0067g0113others(1): Show | 4 | HG02886.hp2 HG02965.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.592-20538C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70914810 | ||||||
| chr6:70914922
|
C | T | 12 | a0001c0001t0012g0009a0001c0001t0012g0010a0001c0001t0018g0006others(9): Show | 12 | HG01256.hp2 HG01257.hp1 HG01346.hp2 others(9): Show |
intron_variant | MODIFIER | c.592-20650G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70914922 | ||||||
| chr6:70914938
|
G | C | 16 | a0001c0001t0001g0117a0001c0001t0001g0121a0001c0001t0001g0173others(13): Show | 16 | HG00408.hp2 HG00735.hp1 HG01257.hp2 others(13): Show |
intron_variant | MODIFIER | c.592-20666C>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70914938 | ||||||
| chr6:70915089
|
A | G | 1 | a0001c0001t0002g0151 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.592-20817T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70915089 | ||||||
| chr6:70915090
|
T | C | 1 | a0001c0001t0050g0016 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.592-20818A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70915090 | ||||||
| chr6:70915354
|
T | C | 3 | a0001c0001t0009g0095a0001c0001t0013g0096a0001c0001t0037g0088 | 3 | HG01256.hp1 HG02055.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.592-21082A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70915354 | ||||||
| chr6:70915360
|
A | G | 1 | a0001c0001t0001g0062 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.592-21088T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70915360 | ||||||
| chr6:70915582
|
A | G | 1 | a0001c0002t0007g0214 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.592-21310T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70915582 | ||||||
| chr6:70915896
|
G | A | 13 | a0001c0001t0068g0167a0001c0002t0011g0270a0001c0002t0022g0266others(10): Show | 13 | HG02132.hp1 HG02135.hp1 HG06807.hp2 others(10): Show |
intron_variant | MODIFIER | c.592-21624C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70915896 | ||||||
| chr6:70916044
|
C | A | 1 | a0001c0001t0002g0072 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.592-21772G>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70916044 | ||||||
| chr6:70916297
|
G | A | 2 | a0001c0001t0019g0018a0001c0001t0019g0019 | 2 | NA18945.hp1 NA18963.hp2 |
intron_variant | MODIFIER | c.592-22025C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70916297 | ||||||
| chr6:70916312
|
A | G | 198 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0046others(195): Show | 198 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(195): Show |
intron_variant | MODIFIER | c.592-22040T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70916312 | ||||||
| chr6:70916441
|
T | C | 1 | a0001c0001t0076g0177 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.592-22169A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70916441 | ||||||
| chr6:70916500
|
G | C | 12 | a0001c0001t0012g0009a0001c0001t0012g0010a0001c0001t0018g0006others(9): Show | 12 | HG01256.hp2 HG01257.hp1 HG01346.hp2 others(9): Show |
intron_variant | MODIFIER | c.592-22228C>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70916500 | ||||||
| chr6:70916508
|
C | T | 1 | a0001c0001t0003g0126 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.592-22236G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70916508 | ||||||
| chr6:70916586
|
T | C | 1 | a0001c0003t0062g0105 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.592-22314A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70916586 | ||||||
| chr6:70916636
|
T | A | 1 | a0001c0001t0004g0112 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.592-22364A>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70916636 | ||||||
| chr6:70917064
|
C | T | 2 | a0001c0002t0005g0217a0001c0002t0005g0218 | 2 | NA18963.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.592-22792G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70917064 | ||||||
| chr6:70917234
|
C | T | 12 | a0001c0002t0011g0270a0001c0002t0022g0266a0001c0002t0022g0269others(9): Show | 12 | HG02132.hp1 HG02135.hp1 NA18951.hp1 others(9): Show |
intron_variant | MODIFIER | c.592-22962G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70917234 | ||||||
| chr6:70917497
|
G | A | 5 | a0001c0001t0003g0102a0001c0001t0003g0125a0001c0001t0004g0124others(2): Show | 5 | HG00741.hp1 HG01167.hp1 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.592-23225C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70917497 | ||||||
| chr6:70917502
|
T | C | 13 | a0001c0001t0068g0167a0001c0002t0011g0270a0001c0002t0022g0266others(10): Show | 13 | HG02132.hp1 HG02135.hp1 HG06807.hp2 others(10): Show |
intron_variant | MODIFIER | c.592-23230A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70917502 | ||||||
| chr6:70917765
|
T | A | 1 | a0001c0001t0033g0114 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.592-23493A>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70917765 | ||||||
| chr6:70917905
|
T | C | 40 | a0001c0002t0008g0250a0001c0002t0011g0255a0001c0002t0011g0256others(37): Show | 40 | HG00099.hp1 HG00323.hp1 HG00642.hp1 others(37): Show |
intron_variant | MODIFIER | c.592-23633A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70917905 | ||||||
| chr6:70918113
|
T | C | 1 | a0001c0002t0011g0272 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.592-23841A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70918113 | ||||||
| chr6:70918337
|
A | T | 40 | a0001c0002t0008g0250a0001c0002t0011g0255a0001c0002t0011g0256others(37): Show | 40 | HG00099.hp1 HG00323.hp1 HG00642.hp1 others(37): Show |
intron_variant | MODIFIER | c.592-24065T>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70918337 | ||||||
| chr6:70918679
|
T | A | 1 | a0001c0001t0002g0175 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.592-24407A>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70918679 | ||||||
| chr6:70918763
|
T | C | 1 | a0001c0002t0006g0235 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.592-24491A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70918763 | ||||||
| chr6:70918825
|
A | C | 5 | a0001c0001t0001g0054a0001c0001t0001g0055a0001c0001t0001g0079others(2): Show | 5 | HG00099.hp2 HG02486.hp1 HG02683.hp2 others(2): Show |
intron_variant | MODIFIER | c.592-24553T>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70918825 | ||||||
| chr6:70919068
|
G | A | 198 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0046others(195): Show | 198 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(195): Show |
intron_variant | MODIFIER | c.592-24796C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70919068 | ||||||
| chr6:70919174
|
C | T | 1 | a0001c0001t0002g0072 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.592-24902G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70919174 | ||||||
| chr6:70919791
|
G | A | 194 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0046others(191): Show | 194 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(191): Show |
intron_variant | MODIFIER | c.592-25519C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70919791 | ||||||
| chr6:70919900
|
C | T | 2 | a0001c0001t0067g0113a0001c0002t0005g0199 | 2 | HG01496.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.592-25628G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70919900 | ||||||
| chr6:70919976
|
C | T | 3 | a0001c0001t0002g0120a0001c0001t0050g0016a0001c0001t0052g0015 | 3 | NA18948.hp2 NA18964.hp1 NA18997.hp1 |
intron_variant | MODIFIER | c.592-25704G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70919976 | ||||||
| chr6:70920038
|
T | C | 1 | a0001c0002t0007g0214 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.592-25766A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70920038 | ||||||
| chr6:70920056
|
G | A | 181 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0046others(178): Show | 181 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(178): Show |
intron_variant | MODIFIER | c.592-25784C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70920056 | ||||||
| chr6:70920089
|
G | A | 199 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0046others(196): Show | 199 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(196): Show |
intron_variant | MODIFIER | c.592-25817C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70920089 | ||||||
| chr6:70920091
|
T | C | 40 | a0001c0002t0008g0250a0001c0002t0011g0255a0001c0002t0011g0256others(37): Show | 40 | HG00099.hp1 HG00323.hp1 HG00642.hp1 others(37): Show |
intron_variant | MODIFIER | c.592-25819A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70920091 | ||||||
| chr6:70920248
|
T | C | 198 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0046others(195): Show | 198 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(195): Show |
intron_variant | MODIFIER | c.592-25976A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70920248 | ||||||
| chr6:70920272
|
G | A | 2 | a0001c0001t0002g0119a0001c0001t0103g0308 | 2 | HG01261.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.592-26000C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70920272 | ||||||
| chr6:70920381
|
G | A | 4 | a0001c0001t0036g0104a0001c0001t0045g0003a0001c0001t0069g0103others(1): Show | 4 | HG02559.hp1 HG02717.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.592-26109C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70920381 | ||||||
| chr6:70920574
|
A | G | 1 | a0001c0002t0022g0299 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.592-26302T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70920574 | ||||||
| chr6:70921291
|
T | C | 26 | a0001c0002t0008g0250a0001c0002t0014g0279a0001c0002t0014g0285others(23): Show | 26 | HG00099.hp1 HG00323.hp1 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.592-27019A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70921291 | ||||||
| chr6:70921425
|
C | T | 1 | a0001c0001t0012g0030 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.592-27153G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70921425 | ||||||
| chr6:70921531
|
A | G | 169 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0046others(166): Show | 169 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(166): Show |
intron_variant | MODIFIER | c.592-27259T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70921531 | ||||||
| chr6:70921819
|
G | A | 4 | a0001c0001t0036g0104a0001c0001t0045g0003a0001c0001t0069g0103others(1): Show | 4 | HG02559.hp1 HG02717.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.592-27547C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70921819 | ||||||
| chr6:70921844
|
A | G | 299 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0046others(296): Show | 301 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(298): Show |
intron_variant | MODIFIER | c.592-27572T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70921844 | ||||||
| chr6:70922120
|
G | A | 40 | a0001c0002t0008g0250a0001c0002t0011g0255a0001c0002t0011g0256others(37): Show | 40 | HG00099.hp1 HG00323.hp1 HG00642.hp1 others(37): Show |
intron_variant | MODIFIER | c.592-27848C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70922120 | ||||||
| chr6:70922195
|
A | T | 2 | a0001c0002t0014g0293a0001c0002t0029g0280 | 2 | HG00738.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.592-27923T>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70922195 | ||||||
| chr6:70922325
|
T | C | 169 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0046others(166): Show | 169 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(166): Show |
intron_variant | MODIFIER | c.592-28053A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70922325 | ||||||
| chr6:70922353
|
T | C | 78 | a0001c0001t0001g0044a0001c0001t0001g0046a0001c0001t0001g0048others(75): Show | 78 | HG00099.hp2 HG00597.hp1 HG00673.hp1 others(75): Show |
intron_variant | MODIFIER | c.592-28081A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70922353 | ||||||
| chr6:70922588
|
A | T | 1 | a0001c0001t0010g0071 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.592-28316T>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70922588 | ||||||
| chr6:70922679
|
G | T | 71 | a0001c0001t0001g0117a0001c0001t0001g0121a0001c0001t0001g0145others(68): Show | 71 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(68): Show |
intron_variant | MODIFIER | c.592-28407C>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70922679 | ||||||
| chr6:70922726
|
T | C | 1 | a0001c0001t0056g0115 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.592-28454A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70922726 | ||||||
| chr6:70923300
|
C | T | 2 | a0001c0001t0003g0089a0001c0001t0003g0090 | 2 | NA18962.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.592-29028G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70923300 | ||||||
| chr6:70923584
|
A | G | 1 | a0001c0002t0031g0277 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.592-29312T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70923584 | ||||||
| chr6:70923637
|
C | T | 1 | a0001c0002t0006g0187 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.592-29365G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70923637 | ||||||
| chr6:70923647
|
G | C | 1 | a0001c0002t0043g0273 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.592-29375C>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70923647 | ||||||
| chr6:70923687
|
C | A | 4 | a0001c0001t0036g0104a0001c0001t0045g0003a0001c0001t0069g0103others(1): Show | 4 | HG02559.hp1 HG02717.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.592-29415G>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70923687 | ||||||
| chr6:70923786
|
T | C | 1 | a0001c0001t0002g0175 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.592-29514A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70923786 | ||||||
| chr6:70923818
|
G | A | 1 | a0001c0001t0002g0119 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.592-29546C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70923818 | ||||||
| chr6:70923836
|
T | C | 1 | a0001c0002t0014g0291 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.592-29564A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70923836 | ||||||
| chr6:70923904
|
A | C | 1 | a0001c0001t0012g0030 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.592-29632T>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70923904 | ||||||
| chr6:70924658
|
C | T | 1 | a0001c0002t0011g0255 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.592-30386G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70924658 | ||||||
| chr6:70924859
|
T | C | 1 | a0001c0001t0004g0098 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.592-30587A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70924859 | ||||||
| chr6:70924905
|
G | A | 4 | a0001c0001t0036g0104a0001c0001t0045g0003a0001c0001t0069g0103others(1): Show | 4 | HG02559.hp1 HG02717.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.592-30633C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70924905 | ||||||
| chr6:70924918
|
T | C | 1 | a0001c0002t0042g0295 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.592-30646A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70924918 | ||||||
| chr6:70925022
|
G | A | 1 | a0001c0001t0061g0093 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.592-30750C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70925022 | ||||||
| chr6:70925023
|
C | A | 1 | a0001c0001t0061g0093 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.592-30751G>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70925023 | ||||||
| chr6:70925029
|
A | T | 194 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0046others(191): Show | 194 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(191): Show |
intron_variant | MODIFIER | c.592-30757T>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70925029 | ||||||
| chr6:70925037
|
G | A | 3 | a0001c0002t0016g0237a0001c0002t0079g0202a0001c0002t0087g0236 | 3 | HG00597.hp2 HG00621.hp1 HG02132.hp2 |
intron_variant | MODIFIER | c.592-30765C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70925037 | ||||||
| chr6:70925122
|
C | G | 1 | a0001c0002t0021g0249 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.591+30717G>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70925122 | ||||||
| chr6:70925123
|
C | T | 60 | a0001c0001t0001g0044a0001c0001t0001g0046a0001c0001t0001g0048others(57): Show | 60 | HG00099.hp2 HG00597.hp1 HG00673.hp1 others(57): Show |
intron_variant | MODIFIER | c.591+30716G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70925123 | ||||||
| chr6:70925143
|
C | A | 1 | a0001c0001t0013g0033 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.591+30696G>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70925143 | ||||||
| chr6:70925180
|
C | T | 1 | a0001c0001t0004g0164 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.591+30659G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70925180 | ||||||
| chr6:70925226
|
G | A | 13 | a0001c0001t0068g0167a0001c0002t0011g0270a0001c0002t0022g0266others(10): Show | 13 | HG02132.hp1 HG02135.hp1 HG06807.hp2 others(10): Show |
intron_variant | MODIFIER | c.591+30613C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70925226 | ||||||
| chr6:70925245
|
C | G | 1 | a0001c0001t0067g0113 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.591+30594G>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70925245 | ||||||
| chr6:70925378
|
G | C | 1 | a0001c0001t0013g0049 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.591+30461C>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70925378 | ||||||
| chr6:70925407
|
C | T | 1 | a0001c0003t0062g0105 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.591+30432G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70925407 | ||||||
| chr6:70925408
|
G | A | 2 | a0001c0001t0012g0020a0001c0001t0046g0029 | 2 | HG02523.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.591+30431C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70925408 | ||||||
| chr6:70925455
|
C | T | 1 | a0001c0003t0062g0105 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.591+30384G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70925455 | ||||||
| chr6:70925513
|
C | T | 1 | a0001c0001t0004g0098 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.591+30326G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70925513 | ||||||
| chr6:70925610
|
C | T | 13 | a0001c0001t0068g0167a0001c0002t0011g0270a0001c0002t0022g0266others(10): Show | 13 | HG02132.hp1 HG02135.hp1 HG06807.hp2 others(10): Show |
intron_variant | MODIFIER | c.591+30229G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70925610 | ||||||
| chr6:70926026
|
A | C | 1 | a0001c0002t0006g0191 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.591+29813T>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70926026 | ||||||
| chr6:70926033
|
G | A | 3 | a0001c0002t0038g0178a0001c0002t0038g0180a0001c0002t0077g0179 | 3 | NA18975.hp2 NA19056.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.591+29806C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70926033 | ||||||
| chr6:70926106
|
A | T | 2 | a0001c0001t0003g0089a0001c0001t0003g0090 | 2 | NA18962.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.591+29733T>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70926106 | ||||||
| chr6:70926131
|
C | G | 1 | a0001c0001t0003g0081 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.591+29708G>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70926131 | ||||||
| chr6:70926210
|
A | G | 4 | a0001c0002t0022g0266a0001c0002t0030g0263a0001c0002t0030g0264others(1): Show | 4 | HG02135.hp1 NA18951.hp1 NA18962.hp2 others(1): Show |
intron_variant | MODIFIER | c.591+29629T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70926210 | ||||||
| chr6:70926217
|
G | A | 1 | a0002c0004t0063g0176 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.591+29622C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70926217 | ||||||
| chr6:70926260
|
C | T | 1 | a0001c0001t0009g0159 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.591+29579G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70926260 | ||||||
| chr6:70926261
|
G | T | 13 | a0001c0001t0068g0167a0001c0002t0011g0270a0001c0002t0022g0266others(10): Show | 13 | HG02132.hp1 HG02135.hp1 HG06807.hp2 others(10): Show |
intron_variant | MODIFIER | c.591+29578C>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70926261 | ||||||
| chr6:70926279
|
C | T | 1 | a0001c0001t0034g0106 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.591+29560G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70926279 | ||||||
| chr6:70926280
|
G | A | 1 | a0001c0001t0002g0120 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.591+29559C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70926280 | ||||||
| chr6:70926377
|
C | T | 194 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0046others(191): Show | 194 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(191): Show |
intron_variant | MODIFIER | c.591+29462G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70926377 | ||||||
| chr6:70926397
|
G | A | 3 | a0001c0001t0012g0030a0001c0001t0032g0004a0001c0001t0032g0021 | 3 | HG00673.hp2 NA18981.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.591+29442C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70926397 | ||||||
| chr6:70926578
|
G | C | 1 | a0001c0002t0022g0269 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.591+29261C>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70926578 | ||||||
| chr6:70926580
|
T | C | 1 | a0001c0002t0043g0273 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.591+29259A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70926580 | ||||||
| chr6:70926590
|
A | G | 4 | a0001c0001t0018g0025a0001c0001t0018g0026a0001c0001t0018g0027others(1): Show | 4 | HG01256.hp2 HG01257.hp1 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.591+29249T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70926590 | ||||||
| chr6:70926607
|
G | T | 15 | a0001c0001t0001g0101a0001c0001t0003g0089a0001c0001t0003g0090others(12): Show | 15 | HG00323.hp2 HG01256.hp1 HG01975.hp2 others(12): Show |
intron_variant | MODIFIER | c.591+29232C>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70926607 | ||||||
| chr6:70926652
|
G | A | 1 | a0001c0001t0001g0174 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.591+29187C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70926652 | ||||||
| chr6:70926682
|
G | C | 4 | a0001c0001t0036g0104a0001c0001t0045g0003a0001c0001t0069g0103others(1): Show | 4 | HG02559.hp1 HG02717.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.591+29157C>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70926682 | ||||||
| chr6:70926684
|
C | T | 1 | a0001c0002t0007g0212 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.591+29155G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70926684 | ||||||
| chr6:70926727
|
A | G | 3 | a0001c0002t0014g0279a0001c0002t0015g0253a0001c0002t0097g0296 | 3 | HG00741.hp2 HG02300.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.591+29112T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70926727 | ||||||
| chr6:70926821
|
C | G | 12 | a0001c0002t0011g0270a0001c0002t0022g0266a0001c0002t0022g0269others(9): Show | 12 | HG02132.hp1 HG02135.hp1 NA18951.hp1 others(9): Show |
intron_variant | MODIFIER | c.591+29018G>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70926821 | ||||||
| chr6:70926825
|
A | T | 1 | a0001c0002t0015g0278 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.591+29014T>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70926825 | ||||||
| chr6:70926909
|
G | T | 2 | a0001c0001t0010g0084a0001c0002t0031g0277 | 2 | HG01261.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.591+28930C>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70926909 | ||||||
| chr6:70927201
|
A | G | 198 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0046others(195): Show | 198 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(195): Show |
intron_variant | MODIFIER | c.591+28638T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70927201 | ||||||
| chr6:70927296
|
A | T | 4 | a0001c0001t0036g0104a0001c0001t0045g0003a0001c0001t0069g0103others(1): Show | 4 | HG02559.hp1 HG02717.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.591+28543T>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70927296 | ||||||
| chr6:70927385
|
T | C | 4 | a0001c0002t0042g0254a0001c0002t0042g0295a0001c0002t0043g0273others(1): Show | 4 | HG03098.hp1 HG03225.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.591+28454A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70927385 | ||||||
| chr6:70927454
|
T | C | 2 | a0001c0001t0002g0050a0001c0001t0002g0070 | 2 | NA18940.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.591+28385A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70927454 | ||||||
| chr6:70927516
|
G | A | 4 | a0001c0001t0036g0104a0001c0001t0045g0003a0001c0001t0069g0103others(1): Show | 4 | HG02559.hp1 HG02717.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.591+28323C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70927516 | ||||||
| chr6:70927765
|
A | G | 1 | a0001c0003t0062g0105 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.591+28074T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70927765 | ||||||
| chr6:70927826
|
C | A | 3 | a0001c0001t0004g0136a0001c0001t0004g0137a0001c0001t0036g0138 | 3 | HG02109.hp2 HG03130.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.591+28013G>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70927826 | ||||||
| chr6:70928019
|
A | C | 1 | a0001c0001t0019g0012 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.591+27820T>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70928019 | ||||||
| chr6:70928137
|
G | A | 181 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0046others(178): Show | 181 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(178): Show |
intron_variant | MODIFIER | c.591+27702C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70928137 | ||||||
| chr6:70928177
|
T | A | 2 | a0001c0002t0006g0246a0001c0002t0016g0245 | 2 | HG03831.hp2 NA18955.hp2 |
intron_variant | MODIFIER | c.591+27662A>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70928177 | ||||||
| chr6:70928177
|
T | G | 1 | a0001c0001t0003g0126 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.591+27662A>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70928177 | ||||||
| chr6:70928385
|
C | A | 4 | a0001c0001t0010g0051a0001c0001t0010g0071a0001c0001t0010g0084others(1): Show | 4 | HG01261.hp1 HG01891.hp2 HG01952.hp2 others(1): Show |
intron_variant | MODIFIER | c.591+27454G>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70928385 | ||||||
| chr6:70928422
|
A | G | 5 | a0001c0001t0003g0102a0001c0001t0003g0125a0001c0001t0004g0124others(2): Show | 5 | HG00741.hp1 HG01167.hp1 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.591+27417T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70928422 | ||||||
| chr6:70928592
|
T | C | 16 | a0001c0001t0001g0042a0001c0001t0001g0101a0001c0001t0003g0089others(13): Show | 16 | HG00323.hp2 HG01256.hp1 HG01975.hp2 others(13): Show |
intron_variant | MODIFIER | c.591+27247A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70928592 | ||||||
| chr6:70928702
|
C | T | 1 | a0001c0002t0007g0251 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.591+27137G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70928702 | ||||||
| chr6:70928759
|
C | A | 1 | a0001c0001t0013g0141 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.591+27080G>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70928759 | ||||||
| chr6:70928796
|
G | C | 75 | a0001c0001t0001g0117a0001c0001t0001g0121a0001c0001t0001g0145others(72): Show | 75 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(72): Show |
intron_variant | MODIFIER | c.591+27043C>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70928796 | ||||||
| chr6:70928923
|
A | C | 197 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0046others(194): Show | 197 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(194): Show |
intron_variant | MODIFIER | c.591+26916T>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70928923 | ||||||
| chr6:70928923
|
A | T | 1 | a0001c0001t0044g0306 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.591+26916T>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70928923 | ||||||
| chr6:70929236
|
A | G | 12 | a0001c0001t0012g0009a0001c0001t0012g0010a0001c0001t0018g0006others(9): Show | 12 | HG01256.hp2 HG01257.hp1 HG01346.hp2 others(9): Show |
intron_variant | MODIFIER | c.591+26603T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70929236 | ||||||
| chr6:70929301
|
A | AC | 198 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0046others(195): Show | 198 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(195): Show |
intron_variant | MODIFIER | c.591+26537_591+2653 others(5): Show |
B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70929301 | ||||||
| chr6:70929421
|
A | G | 1 | a0001c0002t0006g0191 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.591+26418T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70929421 | ||||||
| chr6:70929437
|
T | A | 60 | a0001c0001t0001g0044a0001c0001t0001g0046a0001c0001t0001g0048others(57): Show | 60 | HG00099.hp2 HG00597.hp1 HG00673.hp1 others(57): Show |
intron_variant | MODIFIER | c.591+26402A>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70929437 | ||||||
| chr6:70929455
|
G | A | 1 | a0001c0001t0037g0088 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.591+26384C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70929455 | ||||||
| chr6:70929523
|
G | C | 78 | a0001c0001t0001g0044a0001c0001t0001g0046a0001c0001t0001g0048others(75): Show | 78 | HG00099.hp2 HG00597.hp1 HG00673.hp1 others(75): Show |
intron_variant | MODIFIER | c.591+26316C>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70929523 | ||||||
| chr6:70929548
|
C | T | 6 | a0001c0001t0012g0009a0001c0001t0012g0010a0001c0001t0048g0008others(3): Show | 6 | HG02630.hp2 HG02723.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.591+26291G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70929548 | ||||||
| chr6:70929584
|
C | T | 60 | a0001c0001t0001g0044a0001c0001t0001g0046a0001c0001t0001g0048others(57): Show | 60 | HG00099.hp2 HG00597.hp1 HG00673.hp1 others(57): Show |
intron_variant | MODIFIER | c.591+26255G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70929584 | ||||||
| chr6:70929622
|
G | A | 1 | a0001c0002t0016g0237 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.591+26217C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70929622 | ||||||
| chr6:70929679
|
T | C | 12 | a0001c0001t0012g0009a0001c0001t0012g0010a0001c0001t0018g0006others(9): Show | 12 | HG01256.hp2 HG01257.hp1 HG01346.hp2 others(9): Show |
intron_variant | MODIFIER | c.591+26160A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70929679 | ||||||
| chr6:70930088
|
G | A | 40 | a0001c0002t0008g0250a0001c0002t0011g0255a0001c0002t0011g0256others(37): Show | 40 | HG00099.hp1 HG00323.hp1 HG00642.hp1 others(37): Show |
intron_variant | MODIFIER | c.591+25751C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70930088 | ||||||
| chr6:70930286
|
G | A | 78 | a0001c0001t0001g0044a0001c0001t0001g0046a0001c0001t0001g0048others(75): Show | 78 | HG00099.hp2 HG00597.hp1 HG00673.hp1 others(75): Show |
intron_variant | MODIFIER | c.591+25553C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70930286 | ||||||
| chr6:70930433
|
A | C | 1 | a0001c0001t0001g0060 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.591+25406T>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70930433 | ||||||
| chr6:70930559
|
C | T | 193 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0046others(190): Show | 193 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(190): Show |
intron_variant | MODIFIER | c.591+25280G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70930559 | ||||||
| chr6:70930578
|
C | T | 3 | a0001c0001t0017g0013a0001c0001t0017g0014a0001c0001t0017g0023 | 3 | HG01255.hp1 HG01981.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.591+25261G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70930578 | ||||||
| chr6:70930615
|
A | G | 198 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0046others(195): Show | 198 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(195): Show |
intron_variant | MODIFIER | c.591+25224T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70930615 | ||||||
| chr6:70930955
|
T | C | 1 | a0001c0001t0003g0089 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.591+24884A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70930955 | ||||||
| chr6:70930984
|
C | T | 1 | a0001c0002t0029g0276 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.591+24855G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70930984 | ||||||
| chr6:70930994
|
C | T | 2 | a0001c0001t0003g0099a0001c0001t0003g0100 | 2 | HG03669.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.591+24845G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70930994 | ||||||
| chr6:70931069
|
C | G | 1 | a0001c0002t0005g0241 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.591+24770G>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70931069 | ||||||
| chr6:70931075
|
A | G | 1 | a0001c0002t0021g0238 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.591+24764T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70931075 | ||||||
| chr6:70931189
|
T | TG | 24 | a0001c0001t0001g0101a0001c0001t0001g0121a0001c0001t0002g0151others(21): Show | 24 | HG00408.hp1 HG00408.hp2 HG01099.hp2 others(21): Show |
intron_variant | MODIFIER | c.591+24649dupC | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70931189 | ||||||
| chr6:70931264
|
G | A | 1 | a0001c0001t0034g0106 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.591+24575C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70931264 | ||||||
| chr6:70931680
|
G | T | 1 | a0001c0001t0001g0044 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.591+24159C>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70931680 | ||||||
| chr6:70931821
|
G | A | 3 | a0001c0002t0088g0298a0001c0002t0089g0297a0001c0002t0099g0292 | 3 | HG01074.hp2 HG02738.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.591+24018C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70931821 | ||||||
| chr6:70931821
|
G | T | 13 | a0001c0001t0068g0167a0001c0002t0011g0270a0001c0002t0022g0266others(10): Show | 13 | HG02132.hp1 HG02135.hp1 HG06807.hp2 others(10): Show |
intron_variant | MODIFIER | c.591+24018C>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70931821 | ||||||
| chr6:70932184
|
C | T | 13 | a0001c0001t0068g0167a0001c0002t0011g0270a0001c0002t0022g0266others(10): Show | 13 | HG02132.hp1 HG02135.hp1 HG06807.hp2 others(10): Show |
intron_variant | MODIFIER | c.591+23655G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70932184 | ||||||
| chr6:70933129
|
C | A | 1 | a0001c0002t0005g0241 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.591+22710G>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70933129 | ||||||
| chr6:70933570
|
T | C | 1 | a0001c0002t0084g0244 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.591+22269A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70933570 | ||||||
| chr6:70933687
|
T | C | 204 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0046others(201): Show | 205 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(202): Show |
intron_variant | MODIFIER | c.591+22152A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70933687 | ||||||
| chr6:70933701
|
G | A | 40 | a0001c0002t0008g0250a0001c0002t0011g0255a0001c0002t0011g0256others(37): Show | 40 | HG00099.hp1 HG00323.hp1 HG00642.hp1 others(37): Show |
intron_variant | MODIFIER | c.591+22138C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70933701 | ||||||
| chr6:70933731
|
C | T | 1 | a0001c0002t0008g0216 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.591+22108G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70933731 | ||||||
| chr6:70933858
|
T | A | 7 | a0001c0001t0001g0145a0001c0001t0003g0143a0001c0001t0003g0146others(4): Show | 7 | HG00423.hp1 HG00544.hp2 HG02129.hp1 others(4): Show |
intron_variant | MODIFIER | c.591+21981A>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70933858 | ||||||
| chr6:70934050
|
G | A | 4 | a0001c0001t0036g0104a0001c0001t0045g0003a0001c0001t0069g0103others(1): Show | 4 | HG02559.hp1 HG02717.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.591+21789C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70934050 | ||||||
| chr6:70934366
|
C | A | 1 | a0001c0001t0002g0058 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.591+21473G>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70934366 | ||||||
| chr6:70934461
|
T | C | 1 | a0001c0001t0004g0074 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.591+21378A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70934461 | ||||||
| chr6:70934480
|
C | A | 15 | a0001c0001t0001g0101a0001c0001t0003g0089a0001c0001t0003g0090others(12): Show | 15 | HG00323.hp2 HG01256.hp1 HG01975.hp2 others(12): Show |
intron_variant | MODIFIER | c.591+21359G>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70934480 | ||||||
| chr6:70934770
|
A | C | 1 | a0001c0001t0003g0035 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.591+21069T>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70934770 | ||||||
| chr6:70934800
|
G | A | 1 | a0001c0001t0004g0164 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.591+21039C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70934800 | ||||||
| chr6:70935217
|
G | A | 4 | a0001c0002t0042g0254a0001c0002t0042g0295a0001c0002t0043g0273others(1): Show | 4 | HG03098.hp1 HG03225.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.591+20622C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70935217 | ||||||
| chr6:70935408
|
C | T | 1 | a0001c0001t0009g0092 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.591+20431G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70935408 | ||||||
| chr6:70935456
|
T | G | 1 | a0001c0001t0073g0107 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.591+20383A>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70935456 | ||||||
| chr6:70935530
|
T | C | 1 | a0001c0002t0098g0294 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.591+20309A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70935530 | ||||||
| chr6:70935700
|
G | T | 5 | a0001c0001t0003g0099a0001c0001t0003g0100a0001c0001t0004g0098others(2): Show | 5 | HG00323.hp2 HG01975.hp2 HG02300.hp1 others(2): Show |
intron_variant | MODIFIER | c.591+20139C>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70935700 | ||||||
| chr6:70935737
|
G | A | 1 | a0001c0001t0001g0060 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.591+20102C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70935737 | ||||||
| chr6:70935767
|
A | G | 1 | a0001c0002t0084g0244 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.591+20072T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70935767 | ||||||
| chr6:70935777
|
G | A | 1 | a0001c0001t0001g0042 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.591+20062C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70935777 | ||||||
| chr6:70935841
|
C | T | 1 | a0001c0001t0056g0115 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.591+19998G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70935841 | ||||||
| chr6:70936015
|
G | A | 12 | a0001c0002t0011g0270a0001c0002t0022g0266a0001c0002t0022g0269others(9): Show | 12 | HG02132.hp1 HG02135.hp1 NA18951.hp1 others(9): Show |
intron_variant | MODIFIER | c.591+19824C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70936015 | ||||||
| chr6:70936053
|
G | A | 7 | a0001c0001t0036g0104a0001c0001t0045g0003a0001c0001t0069g0103others(4): Show | 7 | HG02559.hp1 HG02717.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.591+19786C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70936053 | ||||||
| chr6:70936069
|
A | C | 1 | a0001c0002t0005g0215 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.591+19770T>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70936069 | ||||||
| chr6:70936160
|
C | T | 1 | a0001c0001t0002g0144 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.591+19679G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70936160 | ||||||
| chr6:70936282
|
A | G | 4 | a0001c0001t0036g0104a0001c0001t0045g0003a0001c0001t0069g0103others(1): Show | 4 | HG02559.hp1 HG02717.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.591+19557T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70936282 | ||||||
| chr6:70936326
|
G | C | 5 | a0001c0001t0017g0023a0001c0001t0036g0104a0001c0001t0045g0003others(2): Show | 5 | HG02004.hp2 HG02559.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.591+19513C>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70936326 | ||||||
| chr6:70936352
|
A | G | 1 | a0001c0001t0001g0145 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.591+19487T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70936352 | ||||||
| chr6:70936402
|
C | T | 4 | a0001c0002t0006g0187a0001c0002t0006g0188a0001c0002t0006g0189others(1): Show | 4 | HG02622.hp1 HG02630.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.591+19437G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70936402 | ||||||
| chr6:70936408
|
A | G | 1 | a0001c0002t0007g0214 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.591+19431T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70936408 | ||||||
| chr6:70936432
|
C | A | 2 | a0001c0001t0053g0032a0001c0001t0054g0031 | 2 | HG02818.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.591+19407G>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70936432 | ||||||
| chr6:70936444
|
A | G | 1 | a0001c0001t0064g0165 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.591+19395T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70936444 | ||||||
| chr6:70936445
|
A | T | 8 | a0001c0001t0064g0165a0001c0002t0005g0203a0001c0002t0006g0208others(5): Show | 8 | HG00423.hp2 HG00621.hp2 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.591+19394T>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70936445 | ||||||
| chr6:70936610
|
C | T | 1 | a0001c0001t0037g0061 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.591+19229G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70936610 | ||||||
| chr6:70936737
|
G | A | 2 | a0001c0001t0017g0007a0001c0001t0019g0024 | 2 | NA19078.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.591+19102C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70936737 | ||||||
| chr6:70936741
|
T | C | 3 | a0001c0001t0017g0007a0001c0001t0019g0024a0001c0002t0028g0252 | 3 | HG02738.hp2 NA19078.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.591+19098A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70936741 | ||||||
| chr6:70936806
|
G | A | 15 | a0001c0001t0001g0101a0001c0001t0003g0089a0001c0001t0003g0090others(12): Show | 15 | HG00323.hp2 HG01256.hp1 HG01975.hp2 others(12): Show |
intron_variant | MODIFIER | c.591+19033C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70936806 | ||||||
| chr6:70936809
|
C | T | 1 | a0001c0002t0027g0213 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.591+19030G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70936809 | ||||||
| chr6:70937012
|
C | A | 1 | a0001c0001t0001g0101 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.591+18827G>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70937012 | ||||||
| chr6:70937117
|
T | C | 1 | a0001c0001t0001g0060 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.591+18722A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70937117 | ||||||
| chr6:70937251
|
C | G | 194 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0046others(191): Show | 194 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(191): Show |
intron_variant | MODIFIER | c.591+18588G>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70937251 | ||||||
| chr6:70937299
|
T | G | 13 | a0001c0001t0068g0167a0001c0002t0011g0270a0001c0002t0022g0266others(10): Show | 13 | HG02132.hp1 HG02135.hp1 HG06807.hp2 others(10): Show |
intron_variant | MODIFIER | c.591+18540A>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70937299 | ||||||
| chr6:70937306
|
C | T | 17 | a0001c0001t0012g0017a0001c0001t0012g0020a0001c0001t0012g0022others(14): Show | 17 | HG00673.hp2 HG01074.hp1 HG01255.hp1 others(14): Show |
intron_variant | MODIFIER | c.591+18533G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70937306 | ||||||
| chr6:70937327
|
G | A | 4 | a0001c0001t0036g0104a0001c0001t0045g0003a0001c0001t0069g0103others(1): Show | 4 | HG02559.hp1 HG02717.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.591+18512C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70937327 | ||||||
| chr6:70937571
|
A | G | 1 | a0001c0001t0002g0059 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.591+18268T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70937571 | ||||||
| chr6:70937601
|
T | C | 3 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171 | 3 | HG03490.hp2 HG03492.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.591+18238A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70937601 | ||||||
| chr6:70937704
|
G | A | 1 | a0001c0002t0084g0244 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.591+18135C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70937704 | ||||||
| chr6:70937761
|
T | C | 4 | a0001c0001t0004g0161a0001c0001t0004g0163a0001c0001t0004g0164others(1): Show | 4 | HG02109.hp1 HG02809.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.591+18078A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70937761 | ||||||
| chr6:70937905
|
C | T | 29 | a0001c0001t0001g0145a0001c0001t0001g0156a0001c0001t0001g0160others(26): Show | 29 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(26): Show |
intron_variant | MODIFIER | c.591+17934G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70937905 | ||||||
| chr6:70937913
|
C | T | 1 | a0001c0001t0003g0154 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.591+17926G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70937913 | ||||||
| chr6:70937951
|
G | A | 15 | a0001c0001t0001g0101a0001c0001t0003g0089a0001c0001t0003g0090others(12): Show | 15 | HG00323.hp2 HG01256.hp1 HG01975.hp2 others(12): Show |
intron_variant | MODIFIER | c.591+17888C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70937951 | ||||||
| chr6:70937953
|
G | A | 169 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0046others(166): Show | 169 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(166): Show |
intron_variant | MODIFIER | c.591+17886C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70937953 | ||||||
| chr6:70937978
|
C | T | 182 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0046others(179): Show | 182 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(179): Show |
intron_variant | MODIFIER | c.591+17861G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70937978 | ||||||
| chr6:70937997
|
C | G | 2 | a0001c0001t0004g0074a0001c0002t0005g0203 | 2 | NA19005.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.591+17842G>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70937997 | ||||||
| chr6:70938018
|
A | C | 1 | a0001c0001t0003g0129 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.591+17821T>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70938018 | ||||||
| chr6:70938145
|
CA | C | 3 | a0001c0002t0030g0263a0001c0002t0030g0264a0001c0002t0092g0265 | 3 | NA18951.hp1 NA18962.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.591+17693delT | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70938145 | ||||||
| chr6:70938146
|
AT | A | 9 | a0001c0002t0011g0270a0001c0002t0022g0266a0001c0002t0022g0269others(6): Show | 9 | HG02132.hp1 HG02135.hp1 NA18965.hp1 others(6): Show |
intron_variant | MODIFIER | c.591+17692delA | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70938146 | ||||||
| chr6:70938147
|
T | C | 3 | a0001c0002t0030g0263a0001c0002t0030g0264a0001c0002t0092g0265 | 3 | NA18951.hp1 NA18962.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.591+17692A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70938147 | ||||||
| chr6:70938193
|
C | A | 1 | a0001c0003t0062g0105 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.591+17646G>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70938193 | ||||||
| chr6:70938242
|
T | C | 194 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0046others(191): Show | 194 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(191): Show |
intron_variant | MODIFIER | c.591+17597A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70938242 | ||||||
| chr6:70938243
|
G | A | 194 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0046others(191): Show | 194 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(191): Show |
intron_variant | MODIFIER | c.591+17596C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70938243 | ||||||
| chr6:70938255
|
GATAC | G | 193 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0046others(190): Show | 193 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(190): Show |
intron_variant | MODIFIER | c.591+17580_591+1758 others(8): Show |
B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70938255 | ||||||
| chr6:70938257
|
T | C | 1 | a0001c0001t0001g0060 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.591+17582A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70938257 | ||||||
| chr6:70938261
|
A | AATGGAAG others(20664): Show |
1 | a0001c0001t0001g0060 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.591+17577_591+1757 others(20675): Show |
B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70938261 | ||||||
| chr6:70938261
|
A | C | 193 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0046others(190): Show | 193 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(190): Show |
intron_variant | MODIFIER | c.591+17578T>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70938261 | ||||||
| chr6:70938292
|
T | C | 4 | a0001c0001t0036g0104a0001c0001t0045g0003a0001c0001t0069g0103others(1): Show | 4 | HG02559.hp1 HG02717.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.591+17547A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70938292 | ||||||
| chr6:70938308
|
T | C | 194 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0046others(191): Show | 194 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(191): Show |
intron_variant | MODIFIER | c.591+17531A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70938308 | ||||||
| chr6:70938309
|
G | C | 194 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0046others(191): Show | 194 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(191): Show |
intron_variant | MODIFIER | c.591+17530C>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70938309 | ||||||
| chr6:70938335
|
A | G | 1 | a0001c0001t0066g0139 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.591+17504T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70938335 | ||||||
| chr6:70938413
|
T | C | 1 | a0001c0001t0013g0096 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.591+17426A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70938413 | ||||||
| chr6:70938425
|
T | A | 1 | a0001c0001t0013g0096 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.591+17414A>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70938425 | ||||||
| chr6:70938432
|
G | A | 2 | a0001c0001t0003g0129a0001c0001t0013g0096 | 2 | HG01256.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.591+17407C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70938432 | ||||||
| chr6:70938440
|
C | T | 6 | a0001c0001t0003g0102a0001c0001t0003g0125a0001c0001t0004g0124others(3): Show | 6 | HG00741.hp1 HG01167.hp1 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.591+17399G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70938440 | ||||||
| chr6:70938676
|
A | G | 5 | a0001c0001t0004g0052a0001c0001t0044g0304a0001c0001t0044g0306others(2): Show | 5 | HG00735.hp1 HG01257.hp2 HG01261.hp2 others(2): Show |
intron_variant | MODIFIER | c.591+17163T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70938676 | ||||||
| chr6:70938677
|
G | A | 4 | a0001c0001t0044g0304a0001c0001t0044g0306a0001c0001t0103g0308others(1): Show | 4 | HG00735.hp1 HG01257.hp2 HG01261.hp2 others(1): Show |
intron_variant | MODIFIER | c.591+17162C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70938677 | ||||||
| chr6:70938981
|
A | T | 1 | a0001c0002t0106g0309 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.591+16858T>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70938981 | ||||||
| chr6:70938984
|
A | T | 1 | a0001c0002t0106g0309 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.591+16855T>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70938984 | ||||||
| chr6:70939074
|
C | G | 4 | a0001c0001t0012g0009a0001c0001t0012g0010a0001c0001t0048g0008others(1): Show | 4 | HG02630.hp2 HG02723.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.591+16765G>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70939074 | ||||||
| chr6:70939086
|
G | A | 1 | a0001c0001t0002g0072 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.591+16753C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70939086 | ||||||
| chr6:70939109
|
C | A | 1 | a0001c0001t0067g0113 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.591+16730G>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70939109 | ||||||
| chr6:70939223
|
T | C | 313 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0046others(310): Show | 315 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(312): Show |
intron_variant | MODIFIER | c.591+16616A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70939223 | ||||||
| chr6:70939224
|
G | A | 313 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0046others(310): Show | 315 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(312): Show |
intron_variant | MODIFIER | c.591+16615C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70939224 | ||||||
| chr6:70939285
|
T | A | 8 | a0001c0002t0011g0255a0001c0002t0011g0256a0001c0002t0011g0259others(5): Show | 8 | HG02647.hp2 HG02717.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.591+16554A>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70939285 | ||||||
| chr6:70939314
|
A | T | 313 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0046others(310): Show | 315 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(312): Show |
intron_variant | MODIFIER | c.591+16525T>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70939314 | ||||||
| chr6:70939315
|
A | C | 313 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0046others(310): Show | 315 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(312): Show |
intron_variant | MODIFIER | c.591+16524T>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70939315 | ||||||
| chr6:70939336
|
C | T | 6 | a0001c0001t0033g0114a0001c0001t0036g0104a0001c0001t0044g0304others(3): Show | 6 | HG00735.hp1 HG02071.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.591+16503G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70939336 | ||||||
| chr6:70939369
|
C | T | 30 | a0001c0001t0001g0145a0001c0001t0001g0156a0001c0001t0001g0160others(27): Show | 30 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(27): Show |
intron_variant | MODIFIER | c.591+16470G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70939369 | ||||||
| chr6:70939426
|
T | C | 1 | a0001c0001t0058g0082 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.591+16413A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70939426 | ||||||
| chr6:70939441
|
T | C | 1 | a0001c0001t0019g0012 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.591+16398A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70939441 | ||||||
| chr6:70939461
|
A | G | 38 | a0001c0001t0001g0145a0001c0001t0001g0156a0001c0001t0001g0160others(35): Show | 38 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(35): Show |
intron_variant | MODIFIER | c.591+16378T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70939461 | ||||||
| chr6:70939597
|
G | A | 194 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0046others(191): Show | 194 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(191): Show |
intron_variant | MODIFIER | c.591+16242C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70939597 | ||||||
| chr6:70939612
|
T | C | 1 | a0001c0002t0014g0293 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.591+16227A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70939612 | ||||||
| chr6:70939619
|
T | G | 8 | a0001c0002t0011g0255a0001c0002t0011g0256a0001c0002t0011g0259others(5): Show | 8 | HG02647.hp2 HG02717.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.591+16220A>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70939619 | ||||||
| chr6:70939662
|
C | T | 13 | a0001c0001t0068g0167a0001c0002t0011g0270a0001c0002t0022g0266others(10): Show | 13 | HG02132.hp1 HG02135.hp1 HG06807.hp2 others(10): Show |
intron_variant | MODIFIER | c.591+16177G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70939662 | ||||||
| chr6:70939663
|
G | A | 2 | a0001c0002t0006g0246a0001c0002t0016g0245 | 2 | HG03831.hp2 NA18955.hp2 |
intron_variant | MODIFIER | c.591+16176C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70939663 | ||||||
| chr6:70939705
|
A | G | 197 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0046others(194): Show | 197 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(194): Show |
intron_variant | MODIFIER | c.591+16134T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70939705 | ||||||
| chr6:70939721
|
A | G | 1 | a0001c0001t0002g0058 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.591+16118T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70939721 | ||||||
| chr6:70939755
|
T | G | 12 | a0001c0001t0012g0009a0001c0001t0012g0010a0001c0001t0018g0006others(9): Show | 12 | HG01256.hp2 HG01257.hp1 HG01346.hp2 others(9): Show |
intron_variant | MODIFIER | c.591+16084A>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70939755 | ||||||
| chr6:70939756
|
T | A | 12 | a0001c0001t0012g0009a0001c0001t0012g0010a0001c0001t0018g0006others(9): Show | 12 | HG01256.hp2 HG01257.hp1 HG01346.hp2 others(9): Show |
intron_variant | MODIFIER | c.591+16083A>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70939756 | ||||||
| chr6:70939801
|
T | G | 1 | a0001c0002t0039g0247 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.591+16038A>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70939801 | ||||||
| chr6:70939936
|
A | T | 9 | a0001c0002t0005g0203a0001c0002t0005g0211a0001c0002t0006g0208others(6): Show | 9 | HG00423.hp2 HG00621.hp2 HG02040.hp1 others(6): Show |
intron_variant | MODIFIER | c.591+15903T>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70939936 | ||||||
| chr6:70940000
|
G | A | 1 | a0001c0001t0003g0135 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.591+15839C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70940000 | ||||||
| chr6:70940157
|
C | T | 1 | a0001c0001t0003g0081 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.591+15682G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70940157 | ||||||
| chr6:70940384
|
G | A | 5 | a0001c0001t0001g0054a0001c0001t0001g0055a0001c0001t0001g0079others(2): Show | 5 | HG00099.hp2 HG02486.hp1 HG02683.hp2 others(2): Show |
intron_variant | MODIFIER | c.591+15455C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70940384 | ||||||
| chr6:70940469
|
A | C | 198 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0046others(195): Show | 198 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(195): Show |
intron_variant | MODIFIER | c.591+15370T>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70940469 | ||||||
| chr6:70940509
|
C | G | 4 | a0001c0001t0001g0172a0001c0001t0003g0168a0001c0001t0035g0166others(1): Show | 4 | HG01168.hp1 HG01169.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.591+15330G>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70940509 | ||||||
| chr6:70940601
|
C | T | 1 | a0001c0001t0046g0029 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.591+15238G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70940601 | ||||||
| chr6:70940653
|
C | G | 1 | a0001c0002t0079g0202 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.591+15186G>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70940653 | ||||||
| chr6:70940699
|
G | A | 40 | a0001c0002t0008g0250a0001c0002t0011g0255a0001c0002t0011g0256others(37): Show | 40 | HG00099.hp1 HG00323.hp1 HG00642.hp1 others(37): Show |
intron_variant | MODIFIER | c.591+15140C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70940699 | ||||||
| chr6:70940814
|
G | T | 2 | a0001c0002t0008g0250a0001c0002t0094g0275 | 2 | HG00099.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.591+15025C>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70940814 | ||||||
| chr6:70940843
|
G | A | 9 | a0001c0001t0003g0102a0001c0001t0003g0125a0001c0001t0004g0124others(6): Show | 9 | HG00741.hp1 HG01167.hp1 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.591+14996C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70940843 | ||||||
| chr6:70941091
|
G | T | 2 | a0001c0001t0018g0006a0001c0001t0051g0005 | 2 | HG02280.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.591+14748C>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70941091 | ||||||
| chr6:70941333
|
T | G | 4 | a0001c0001t0003g0129a0001c0001t0003g0132a0001c0001t0003g0133others(1): Show | 4 | HG01884.hp2 HG02572.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.591+14506A>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70941333 | ||||||
| chr6:70941336
|
T | A | 194 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0046others(191): Show | 194 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(191): Show |
intron_variant | MODIFIER | c.591+14503A>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70941336 | ||||||
| chr6:70941562
|
A | T | 1 | a0001c0002t0011g0271 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.591+14277T>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70941562 | ||||||
| chr6:70941602
|
TA | T | 4 | a0001c0001t0036g0104a0001c0001t0045g0003a0001c0001t0069g0103others(1): Show | 4 | HG02559.hp1 HG02717.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.591+14236delT | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70941602 | ||||||
| chr6:70941682
|
C | G | 198 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0046others(195): Show | 198 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(195): Show |
intron_variant | MODIFIER | c.591+14157G>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70941682 | ||||||
| chr6:70941811
|
T | C | 4 | a0001c0001t0036g0104a0001c0001t0045g0003a0001c0001t0069g0103others(1): Show | 4 | HG02559.hp1 HG02717.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.591+14028A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70941811 | ||||||
| chr6:70941940
|
T | C | 17 | a0001c0001t0012g0017a0001c0001t0012g0020a0001c0001t0012g0022others(14): Show | 17 | HG00673.hp2 HG01074.hp1 HG01255.hp1 others(14): Show |
intron_variant | MODIFIER | c.591+13899A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70941940 | ||||||
| chr6:70942642
|
G | T | 198 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0046others(195): Show | 198 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(195): Show |
intron_variant | MODIFIER | c.591+13197C>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70942642 | ||||||
| chr6:70942845
|
G | A | 198 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0046others(195): Show | 198 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(195): Show |
intron_variant | MODIFIER | c.591+12994C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70942845 | ||||||
| chr6:70942924
|
T | G | 1 | a0001c0001t0037g0088 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.591+12915A>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70942924 | ||||||
| chr6:70943044
|
C | T | 3 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171 | 3 | HG03490.hp2 HG03492.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.591+12795G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70943044 | ||||||
| chr6:70943246
|
G | A | 1 | a0001c0002t0038g0180 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.591+12593C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70943246 | ||||||
| chr6:70943346
|
A | G | 1 | a0001c0001t0003g0126 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.591+12493T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70943346 | ||||||
| chr6:70943580
|
T | C | 4 | a0001c0001t0036g0104a0001c0001t0045g0003a0001c0001t0069g0103others(1): Show | 4 | HG02559.hp1 HG02717.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.591+12259A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70943580 | ||||||
| chr6:70943805
|
G | A | 4 | a0001c0001t0036g0104a0001c0001t0045g0003a0001c0001t0069g0103others(1): Show | 4 | HG02559.hp1 HG02717.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.591+12034C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70943805 | ||||||
| chr6:70943858
|
G | T | 15 | a0001c0001t0001g0101a0001c0001t0003g0089a0001c0001t0003g0090others(12): Show | 15 | HG00323.hp2 HG01256.hp1 HG01975.hp2 others(12): Show |
intron_variant | MODIFIER | c.591+11981C>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70943858 | ||||||
| chr6:70943975
|
T | C | 1 | a0001c0001t0068g0167 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.591+11864A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70943975 | ||||||
| chr6:70944004
|
A | G | 1 | a0001c0002t0005g0201 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.591+11835T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70944004 | ||||||
| chr6:70944122
|
G | T | 69 | a0001c0001t0001g0117a0001c0001t0001g0121a0001c0001t0001g0145others(66): Show | 69 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(66): Show |
intron_variant | MODIFIER | c.591+11717C>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70944122 | ||||||
| chr6:70944194
|
A | G | 235 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0046others(232): Show | 236 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(233): Show |
intron_variant | MODIFIER | c.591+11645T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70944194 | ||||||
| chr6:70944215
|
C | G | 1 | a0002c0004t0063g0176 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.591+11624G>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70944215 | ||||||
| chr6:70944346
|
C | T | 1 | a0001c0001t0068g0167 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.591+11493G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70944346 | ||||||
| chr6:70944357
|
G | A | 57 | a0001c0002t0005g0182a0001c0002t0005g0201a0001c0002t0005g0203others(54): Show | 58 | HG00423.hp2 HG00597.hp2 HG00621.hp1 others(55): Show |
intron_variant | MODIFIER | c.591+11482C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70944357 | ||||||
| chr6:70944390
|
A | G | 1 | a0001c0001t0001g0055 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.591+11449T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70944390 | ||||||
| chr6:70944435
|
G | GCTCGGAG others(7): Show |
226 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0046others(223): Show | 227 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(224): Show |
intron_variant | MODIFIER | c.591+11403_591+1140 others(18): Show |
B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70944435 | ||||||
| chr6:70944435
|
G | GCTTGGAG others(7): Show |
13 | a0001c0001t0068g0167a0001c0002t0011g0270a0001c0002t0022g0266others(10): Show | 13 | HG02132.hp1 HG02135.hp1 HG06807.hp2 others(10): Show |
intron_variant | MODIFIER | c.591+11403_591+1140 others(18): Show |
B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70944435 | ||||||
| chr6:70944501
|
G | A | 1 | a0001c0001t0066g0139 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.591+11338C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70944501 | ||||||
| chr6:70944501
|
G | T | 4 | a0001c0001t0004g0161a0001c0001t0004g0163a0001c0001t0004g0164others(1): Show | 4 | HG02109.hp1 HG02809.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.591+11338C>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70944501 | ||||||
| chr6:70944615
|
C | T | 29 | a0001c0001t0012g0009a0001c0001t0012g0010a0001c0001t0012g0017others(26): Show | 29 | HG00673.hp2 HG01074.hp1 HG01255.hp1 others(26): Show |
intron_variant | MODIFIER | c.591+11224G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70944615 | ||||||
| chr6:70944630
|
CCT | C | 239 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0046others(236): Show | 240 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(237): Show |
intron_variant | MODIFIER | c.591+11207_591+1120 others(6): Show |
B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70944630 | ||||||
| chr6:70944836
|
C | A | 1 | a0001c0001t0003g0126 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.591+11003G>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70944836 | ||||||
| chr6:70944849
|
C | T | 6 | a0001c0001t0001g0101a0001c0001t0003g0089a0001c0001t0003g0090others(3): Show | 6 | HG02015.hp1 NA18940.hp1 NA18962.hp1 others(3): Show |
intron_variant | MODIFIER | c.591+10990G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70944849 | ||||||
| chr6:70944865
|
T | C | 4 | a0001c0001t0036g0104a0001c0001t0045g0003a0001c0001t0069g0103others(1): Show | 4 | HG02559.hp1 HG02717.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.591+10974A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70944865 | ||||||
| chr6:70944901
|
C | G | 15 | a0001c0001t0001g0101a0001c0001t0003g0089a0001c0001t0003g0090others(12): Show | 15 | HG00323.hp2 HG01256.hp1 HG01975.hp2 others(12): Show |
intron_variant | MODIFIER | c.591+10938G>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70944901 | ||||||
| chr6:70945177
|
C | A | 1 | a0001c0001t0013g0096 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.591+10662G>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70945177 | ||||||
| chr6:70945204
|
C | T | 1 | a0001c0001t0001g0057 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.591+10635G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70945204 | ||||||
| chr6:70945219
|
C | T | 2 | a0001c0002t0008g0250a0001c0002t0094g0275 | 2 | HG00099.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.591+10620G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70945219 | ||||||
| chr6:70945220
|
A | G | 234 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0046others(231): Show | 235 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(232): Show |
intron_variant | MODIFIER | c.591+10619T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70945220 | ||||||
| chr6:70945232
|
T | C | 2 | a0001c0001t0002g0175a0001c0001t0013g0141 | 2 | NA18997.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.591+10607A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70945232 | ||||||
| chr6:70945337
|
C | T | 3 | a0001c0001t0002g0144a0001c0001t0002g0152a0001c0001t0002g0153 | 3 | HG00544.hp1 NA18965.hp2 NA18969.hp1 |
intron_variant | MODIFIER | c.591+10502G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70945337 | ||||||
| chr6:70945343
|
T | C | 1 | a0001c0001t0002g0037 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.591+10496A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70945343 | ||||||
| chr6:70945390
|
A | G | 239 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0046others(236): Show | 240 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(237): Show |
intron_variant | MODIFIER | c.591+10449T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70945390 | ||||||
| chr6:70945582
|
A | C | 2 | a0001c0001t0002g0150a0001c0001t0002g0151 | 2 | HG00408.hp1 NA18950.hp1 |
intron_variant | MODIFIER | c.591+10257T>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70945582 | ||||||
| chr6:70945587
|
C | A | 1 | a0001c0001t0024g0127 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.591+10252G>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70945587 | ||||||
| chr6:70945806
|
T | G | 1 | a0001c0001t0003g0129 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.591+10033A>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70945806 | ||||||
| chr6:70945829
|
C | T | 12 | a0001c0002t0011g0270a0001c0002t0022g0266a0001c0002t0022g0269others(9): Show | 12 | HG02132.hp1 HG02135.hp1 NA18951.hp1 others(9): Show |
intron_variant | MODIFIER | c.591+10010G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70945829 | ||||||
| chr6:70945876
|
G | A | 1 | a0001c0001t0055g0128 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.591+9963C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70945876 | ||||||
| chr6:70945967
|
A | T | 29 | a0001c0001t0012g0009a0001c0001t0012g0010a0001c0001t0012g0017others(26): Show | 29 | HG00673.hp2 HG01074.hp1 HG01255.hp1 others(26): Show |
intron_variant | MODIFIER | c.591+9872T>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70945967 | ||||||
| chr6:70946074
|
A | G | 113 | a0001c0001t0001g0117a0001c0001t0001g0121a0001c0001t0001g0145others(110): Show | 113 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(110): Show |
intron_variant | MODIFIER | c.591+9765T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70946074 | ||||||
| chr6:70946133
|
G | A | 1 | a0001c0001t0004g0098 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.591+9706C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70946133 | ||||||
| chr6:70946140
|
G | A | 40 | a0001c0002t0008g0250a0001c0002t0011g0255a0001c0002t0011g0256others(37): Show | 40 | HG00099.hp1 HG00323.hp1 HG00642.hp1 others(37): Show |
intron_variant | MODIFIER | c.591+9699C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70946140 | ||||||
| chr6:70946168
|
C | T | 1 | a0001c0002t0011g0271 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.591+9671G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70946168 | ||||||
| chr6:70946249
|
A | G | 1 | a0001c0001t0003g0129 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.591+9590T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70946249 | ||||||
| chr6:70946273
|
C | T | 4 | a0001c0001t0036g0104a0001c0001t0045g0003a0001c0001t0069g0103others(1): Show | 4 | HG02559.hp1 HG02717.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.591+9566G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70946273 | ||||||
| chr6:70946307
|
C | T | 1 | a0001c0001t0002g0037 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.591+9532G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70946307 | ||||||
| chr6:70946388
|
C | T | 4 | a0001c0001t0036g0104a0001c0001t0045g0003a0001c0001t0069g0103others(1): Show | 4 | HG02559.hp1 HG02717.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.591+9451G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70946388 | ||||||
| chr6:70946489
|
G | A | 1 | a0001c0001t0066g0139 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.591+9350C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70946489 | ||||||
| chr6:70946512
|
A | G | 1 | a0001c0001t0001g0101 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.591+9327T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70946512 | ||||||
| chr6:70946646
|
C | A | 2 | a0001c0002t0011g0262a0001c0002t0096g0261 | 2 | HG02965.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.591+9193G>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70946646 | ||||||
| chr6:70946697
|
A | C | 3 | a0001c0002t0030g0263a0001c0002t0030g0264a0001c0002t0092g0265 | 3 | NA18951.hp1 NA18962.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.591+9142T>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70946697 | ||||||
| chr6:70946726
|
C | T | 1 | a0001c0001t0058g0082 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.591+9113G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70946726 | ||||||
| chr6:70946727
|
G | A | 1 | a0001c0001t0003g0135 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.591+9112C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70946727 | ||||||
| chr6:70946748
|
A | G | 3 | a0001c0001t0003g0089a0001c0001t0003g0090a0001c0001t0061g0093 | 3 | NA18962.hp1 NA19006.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.591+9091T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70946748 | ||||||
| chr6:70946760
|
C | A | 238 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0046others(235): Show | 239 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(236): Show |
intron_variant | MODIFIER | c.591+9079G>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70946760 | ||||||
| chr6:70946772
|
A | G | 239 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0046others(236): Show | 240 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(237): Show |
intron_variant | MODIFIER | c.591+9067T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70946772 | ||||||
| chr6:70946853
|
C | T | 239 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0046others(236): Show | 240 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(237): Show |
intron_variant | MODIFIER | c.591+8986G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70946853 | ||||||
| chr6:70946870
|
T | C | 69 | a0001c0001t0001g0117a0001c0001t0001g0121a0001c0001t0001g0145others(66): Show | 69 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(66): Show |
intron_variant | MODIFIER | c.591+8969A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70946870 | ||||||
| chr6:70947137
|
T | C | 1 | a0001c0002t0007g0185 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.591+8702A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70947137 | ||||||
| chr6:70947287
|
C | T | 13 | a0001c0001t0068g0167a0001c0002t0011g0270a0001c0002t0022g0266others(10): Show | 13 | HG02132.hp1 HG02135.hp1 HG06807.hp2 others(10): Show |
intron_variant | MODIFIER | c.591+8552G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70947287 | ||||||
| chr6:70947324
|
T | C | 1 | a0001c0002t0098g0294 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.591+8515A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70947324 | ||||||
| chr6:70947336
|
A | G | 1 | a0001c0001t0020g0078 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.591+8503T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70947336 | ||||||
| chr6:70947344
|
T | C | 40 | a0001c0002t0008g0250a0001c0002t0011g0255a0001c0002t0011g0256others(37): Show | 40 | HG00099.hp1 HG00323.hp1 HG00642.hp1 others(37): Show |
intron_variant | MODIFIER | c.591+8495A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70947344 | ||||||
| chr6:70947423
|
G | C | 1 | a0001c0001t0057g0073 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.591+8416C>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70947423 | ||||||
| chr6:70947436
|
G | A | 2 | a0001c0002t0088g0298a0001c0002t0089g0297 | 2 | HG02738.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.591+8403C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70947436 | ||||||
| chr6:70947470
|
A | G | 1 | a0001c0002t0040g0186 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.591+8369T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70947470 | ||||||
| chr6:70947580
|
G | C | 26 | a0001c0002t0008g0250a0001c0002t0014g0279a0001c0002t0014g0285others(23): Show | 26 | HG00099.hp1 HG00323.hp1 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.591+8259C>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70947580 | ||||||
| chr6:70947585
|
A | G | 69 | a0001c0001t0001g0117a0001c0001t0001g0121a0001c0001t0001g0145others(66): Show | 69 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(66): Show |
intron_variant | MODIFIER | c.591+8254T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70947585 | ||||||
| chr6:70947635
|
C | T | 238 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0046others(235): Show | 239 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(236): Show |
intron_variant | MODIFIER | c.591+8204G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70947635 | ||||||
| chr6:70947654
|
A | G | 4 | a0001c0001t0036g0104a0001c0001t0045g0003a0001c0001t0069g0103others(1): Show | 4 | HG02559.hp1 HG02717.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.591+8185T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70947654 | ||||||
| chr6:70947694
|
C | G | 29 | a0001c0001t0012g0009a0001c0001t0012g0010a0001c0001t0012g0017others(26): Show | 29 | HG00673.hp2 HG01074.hp1 HG01255.hp1 others(26): Show |
intron_variant | MODIFIER | c.591+8145G>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70947694 | ||||||
| chr6:70947746
|
C | T | 15 | a0001c0001t0001g0101a0001c0001t0003g0089a0001c0001t0003g0090others(12): Show | 15 | HG00323.hp2 HG01256.hp1 HG01975.hp2 others(12): Show |
intron_variant | MODIFIER | c.591+8093G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70947746 | ||||||
| chr6:70947760
|
C | T | 1 | a0001c0001t0003g0081 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.591+8079G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70947760 | ||||||
| chr6:70947861
|
C | T | 1 | a0001c0001t0019g0012 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.591+7978G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70947861 | ||||||
| chr6:70947894
|
A | G | 239 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0046others(236): Show | 240 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(237): Show |
intron_variant | MODIFIER | c.591+7945T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70947894 | ||||||
| chr6:70947978
|
A | G | 239 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0046others(236): Show | 240 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(237): Show |
intron_variant | MODIFIER | c.591+7861T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70947978 | ||||||
| chr6:70948023
|
T | C | 1 | a0001c0002t0008g0248 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.591+7816A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70948023 | ||||||
| chr6:70948075
|
G | A | 1 | a0001c0001t0057g0073 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.591+7764C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70948075 | ||||||
| chr6:70948108
|
G | A | 239 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0046others(236): Show | 240 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(237): Show |
intron_variant | MODIFIER | c.591+7731C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70948108 | ||||||
| chr6:70948197
|
C | T | 239 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0046others(236): Show | 240 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(237): Show |
intron_variant | MODIFIER | c.591+7642G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70948197 | ||||||
| chr6:70948252
|
G | C | 239 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0046others(236): Show | 240 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(237): Show |
intron_variant | MODIFIER | c.591+7587C>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70948252 | ||||||
| chr6:70948313
|
G | A | 239 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0046others(236): Show | 240 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(237): Show |
intron_variant | MODIFIER | c.591+7526C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70948313 | ||||||
| chr6:70948325
|
G | C | 9 | a0001c0001t0003g0129a0001c0001t0003g0132a0001c0001t0003g0133others(6): Show | 9 | HG01884.hp2 HG02280.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.591+7514C>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70948325 | ||||||
| chr6:70948418
|
G | A | 26 | a0001c0002t0008g0250a0001c0002t0014g0279a0001c0002t0014g0285others(23): Show | 26 | HG00099.hp1 HG00323.hp1 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.591+7421C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70948418 | ||||||
| chr6:70948428
|
A | G | 3 | a0001c0001t0018g0025a0001c0001t0018g0026a0001c0001t0018g0027 | 3 | HG01256.hp2 HG01257.hp1 HG01346.hp2 |
intron_variant | MODIFIER | c.591+7411T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70948428 | ||||||
| chr6:70948434
|
A | G | 1 | a0001c0001t0001g0042 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.591+7405T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70948434 | ||||||
| chr6:70948545
|
A | G | 1 | a0001c0002t0007g0185 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.591+7294T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70948545 | ||||||
| chr6:70948574
|
A | G | 1 | a0001c0001t0073g0107 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.591+7265T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70948574 | ||||||
| chr6:70948591
|
C | G | 3 | a0001c0001t0003g0168a0001c0001t0035g0166a0001c0001t0064g0165 | 3 | HG01168.hp1 HG01169.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.591+7248G>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70948591 | ||||||
| chr6:70948637
|
G | C | 235 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0046others(232): Show | 236 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(233): Show |
intron_variant | MODIFIER | c.591+7202C>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70948637 | ||||||
| chr6:70948749
|
A | G | 1 | a0001c0002t0086g0184 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.591+7090T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70948749 | ||||||
| chr6:70948760
|
A | G | 1 | a0001c0001t0034g0106 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.591+7079T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70948760 | ||||||
| chr6:70949143
|
G | A | 2 | a0001c0001t0017g0007a0001c0001t0019g0024 | 2 | NA19078.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.591+6696C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70949143 | ||||||
| chr6:70949190
|
C | A | 2 | a0001c0001t0003g0099a0001c0001t0003g0100 | 2 | HG03669.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.591+6649G>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70949190 | ||||||
| chr6:70949203
|
A | G | 69 | a0001c0001t0001g0117a0001c0001t0001g0121a0001c0001t0001g0145others(66): Show | 69 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(66): Show |
intron_variant | MODIFIER | c.591+6636T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70949203 | ||||||
| chr6:70949258
|
G | A | 1 | a0001c0001t0102g0303 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.591+6581C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70949258 | ||||||
| chr6:70949266
|
G | A | 1 | a0001c0002t0011g0270 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.591+6573C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70949266 | ||||||
| chr6:70949287
|
T | A | 1 | a0001c0001t0068g0167 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.591+6552A>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70949287 | ||||||
| chr6:70949290
|
T | A | 1 | a0001c0001t0068g0167 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.591+6549A>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70949290 | ||||||
| chr6:70949460
|
G | T | 238 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0046others(235): Show | 239 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(236): Show |
intron_variant | MODIFIER | c.591+6379C>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70949460 | ||||||
| chr6:70949581
|
T | C | 238 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0046others(235): Show | 239 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(236): Show |
intron_variant | MODIFIER | c.591+6258A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70949581 | ||||||
| chr6:70949625
|
C | T | 239 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0046others(236): Show | 240 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(237): Show |
intron_variant | MODIFIER | c.591+6214G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70949625 | ||||||
| chr6:70949646
|
T | C | 239 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0046others(236): Show | 240 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(237): Show |
intron_variant | MODIFIER | c.591+6193A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70949646 | ||||||
| chr6:70949713
|
C | A | 4 | a0001c0001t0004g0136a0001c0001t0004g0137a0001c0001t0036g0138others(1): Show | 4 | HG02109.hp2 HG03130.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.591+6126G>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70949713 | ||||||
| chr6:70950014
|
T | C | 1 | a0001c0001t0013g0033 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.591+5825A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70950014 | ||||||
| chr6:70950039
|
C | G | 6 | a0001c0001t0001g0145a0001c0001t0003g0143a0001c0001t0003g0146others(3): Show | 6 | HG00423.hp1 HG02129.hp1 HG02135.hp2 others(3): Show |
intron_variant | MODIFIER | c.591+5800G>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70950039 | ||||||
| chr6:70950111
|
G | T | 69 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0046others(66): Show | 70 | HG00099.hp2 HG00597.hp1 HG00673.hp1 others(67): Show |
intron_variant | MODIFIER | c.591+5728C>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70950111 | ||||||
| chr6:70950134
|
G | C | 4 | a0001c0001t0036g0104a0001c0001t0045g0003a0001c0001t0069g0103others(1): Show | 4 | HG02559.hp1 HG02717.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.591+5705C>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70950134 | ||||||
| chr6:70950229
|
G | T | 1 | a0001c0001t0003g0081 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.591+5610C>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70950229 | ||||||
| chr6:70950299
|
AATT | A | 16 | a0001c0001t0012g0017a0001c0001t0012g0020a0001c0001t0012g0022others(13): Show | 16 | HG00673.hp2 HG01074.hp1 HG01255.hp1 others(13): Show |
intron_variant | MODIFIER | c.591+5537_591+5539d others(5): Show |
B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70950299 | ||||||
| chr6:70950300
|
AT | A | 176 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0046others(173): Show | 177 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(174): Show |
intron_variant | MODIFIER | c.591+5538delA | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70950300 | ||||||
| chr6:70950300
|
ATT | A | 29 | a0001c0001t0001g0101a0001c0001t0002g0037a0001c0001t0002g0041others(26): Show | 29 | HG00323.hp2 HG00423.hp1 HG01256.hp1 others(26): Show |
intron_variant | MODIFIER | c.591+5537_591+5538d others(4): Show |
B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70950300 | ||||||
| chr6:70950301
|
T | A | 5 | a0001c0001t0003g0080a0001c0001t0003g0142a0001c0001t0013g0140others(2): Show | 5 | HG02738.hp1 HG03041.hp1 HG04184.hp2 others(2): Show |
intron_variant | MODIFIER | c.591+5538A>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70950301 | ||||||
| chr6:70950302
|
T | A | 177 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0046others(174): Show | 178 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(175): Show |
intron_variant | MODIFIER | c.591+5537A>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70950302 | ||||||
| chr6:70950408
|
A | G | 226 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0046others(223): Show | 227 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(224): Show |
intron_variant | MODIFIER | c.591+5431T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70950408 | ||||||
| chr6:70950493
|
T | C | 8 | a0001c0001t0004g0052a0001c0001t0004g0056a0001c0001t0004g0074others(5): Show | 8 | HG02145.hp2 HG02258.hp2 HG03139.hp2 others(5): Show |
intron_variant | MODIFIER | c.591+5346A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70950493 | ||||||
| chr6:70950530
|
C | T | 113 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0046others(110): Show | 114 | HG00099.hp2 HG00323.hp2 HG00597.hp1 others(111): Show |
intron_variant | MODIFIER | c.591+5309G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70950530 | ||||||
| chr6:70950625
|
C | T | 239 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0046others(236): Show | 240 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(237): Show |
intron_variant | MODIFIER | c.591+5214G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70950625 | ||||||
| chr6:70950630
|
A | T | 53 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0046others(50): Show | 54 | HG00099.hp2 HG00597.hp1 HG00673.hp1 others(51): Show |
intron_variant | MODIFIER | c.591+5209T>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70950630 | ||||||
| chr6:70950660
|
C | G | 1 | a0001c0001t0102g0303 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.591+5179G>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70950660 | ||||||
| chr6:70950892
|
A | G | 6 | a0001c0001t0012g0009a0001c0001t0012g0010a0001c0001t0048g0008others(3): Show | 6 | HG02630.hp2 HG02723.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.591+4947T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70950892 | ||||||
| chr6:70951010
|
A | G | 2 | a0001c0001t0004g0056a0001c0001t0024g0040 | 2 | HG02145.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.591+4829T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70951010 | ||||||
| chr6:70951049
|
G | A | 112 | a0001c0001t0001g0117a0001c0001t0001g0121a0001c0001t0001g0145others(109): Show | 112 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.591+4790C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70951049 | ||||||
| chr6:70951147
|
C | T | 12 | a0001c0002t0011g0270a0001c0002t0022g0266a0001c0002t0022g0269others(9): Show | 12 | HG02132.hp1 HG02135.hp1 NA18951.hp1 others(9): Show |
intron_variant | MODIFIER | c.591+4692G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70951147 | ||||||
| chr6:70951264
|
T | C | 1 | a0001c0002t0021g0249 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.591+4575A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70951264 | ||||||
| chr6:70951307
|
A | G | 69 | a0001c0001t0001g0117a0001c0001t0001g0121a0001c0001t0001g0145others(66): Show | 69 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(66): Show |
intron_variant | MODIFIER | c.591+4532T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70951307 | ||||||
| chr6:70951383
|
G | A | 1 | a0001c0002t0042g0295 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.591+4456C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70951383 | ||||||
| chr6:70951383
|
G | C | 1 | a0001c0003t0062g0105 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.591+4456C>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70951383 | ||||||
| chr6:70951920
|
T | C | 5 | a0001c0001t0003g0099a0001c0001t0003g0100a0001c0001t0004g0098others(2): Show | 5 | HG00323.hp2 HG01975.hp2 HG02300.hp1 others(2): Show |
intron_variant | MODIFIER | c.591+3919A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70951920 | ||||||
| chr6:70951938
|
T | C | 61 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0046others(58): Show | 62 | HG00099.hp2 HG00597.hp1 HG00673.hp1 others(59): Show |
intron_variant | MODIFIER | c.591+3901A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70951938 | ||||||
| chr6:70951986
|
A | T | 226 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0046others(223): Show | 227 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(224): Show |
intron_variant | MODIFIER | c.591+3853T>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70951986 | ||||||
| chr6:70952032
|
G | T | 62 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0046others(59): Show | 63 | HG00099.hp2 HG00597.hp1 HG00673.hp1 others(60): Show |
intron_variant | MODIFIER | c.591+3807C>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70952032 | ||||||
| chr6:70952163
|
T | C | 69 | a0001c0001t0001g0117a0001c0001t0001g0121a0001c0001t0001g0145others(66): Show | 69 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(66): Show |
intron_variant | MODIFIER | c.591+3676A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70952163 | ||||||
| chr6:70952299
|
T | C | 40 | a0001c0002t0008g0250a0001c0002t0011g0255a0001c0002t0011g0256others(37): Show | 40 | HG00099.hp1 HG00323.hp1 HG00642.hp1 others(37): Show |
intron_variant | MODIFIER | c.591+3540A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70952299 | ||||||
| chr6:70952332
|
T | C | 13 | a0001c0001t0068g0167a0001c0002t0011g0270a0001c0002t0022g0266others(10): Show | 13 | HG02132.hp1 HG02135.hp1 HG06807.hp2 others(10): Show |
intron_variant | MODIFIER | c.591+3507A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70952332 | ||||||
| chr6:70952500
|
T | TA | 29 | a0001c0001t0012g0009a0001c0001t0012g0010a0001c0001t0012g0017others(26): Show | 29 | HG00673.hp2 HG01074.hp1 HG01255.hp1 others(26): Show |
intron_variant | MODIFIER | c.591+3338dupT | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70952500 | ||||||
| chr6:70952527
|
T | C | 1 | a0001c0001t0017g0007 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.591+3312A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70952527 | ||||||
| chr6:70952579
|
G | A | 5 | a0001c0001t0003g0099a0001c0001t0003g0100a0001c0001t0004g0098others(2): Show | 5 | HG00323.hp2 HG01975.hp2 HG02300.hp1 others(2): Show |
intron_variant | MODIFIER | c.591+3260C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70952579 | ||||||
| chr6:70952583
|
G | T | 226 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0046others(223): Show | 227 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(224): Show |
intron_variant | MODIFIER | c.591+3256C>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70952583 | ||||||
| chr6:70952618
|
T | C | 1 | a0001c0001t0001g0055 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.591+3221A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70952618 | ||||||
| chr6:70952626
|
A | G | 69 | a0001c0001t0001g0117a0001c0001t0001g0121a0001c0001t0001g0145others(66): Show | 69 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(66): Show |
intron_variant | MODIFIER | c.591+3213T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70952626 | ||||||
| chr6:70952986
|
C | T | 1 | a0001c0002t0022g0299 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.591+2853G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70952986 | ||||||
| chr6:70952990
|
C | T | 1 | a0001c0002t0021g0183 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.591+2849G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70952990 | ||||||
| chr6:70953006
|
G | C | 239 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0046others(236): Show | 240 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(237): Show |
intron_variant | MODIFIER | c.591+2833C>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70953006 | ||||||
| chr6:70953139
|
G | C | 18 | a0001c0001t0001g0145a0001c0001t0001g0156a0001c0001t0001g0160others(15): Show | 18 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(15): Show |
intron_variant | MODIFIER | c.591+2700C>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70953139 | ||||||
| chr6:70953200
|
A | G | 5 | a0001c0001t0001g0101a0001c0001t0003g0089a0001c0001t0003g0090others(2): Show | 5 | NA18940.hp1 NA18962.hp1 NA19005.hp1 others(2): Show |
intron_variant | MODIFIER | c.591+2639T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70953200 | ||||||
| chr6:70953495
|
A | G | 186 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0046others(183): Show | 187 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(184): Show |
intron_variant | MODIFIER | c.591+2344T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70953495 | ||||||
| chr6:70953659
|
T | G | 7 | a0001c0001t0001g0054a0001c0001t0001g0055a0001c0001t0001g0079others(4): Show | 7 | HG00099.hp2 HG01433.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.591+2180A>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70953659 | ||||||
| chr6:70954016
|
G | A | 1 | a0001c0001t0076g0177 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.591+1823C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70954016 | ||||||
| chr6:70954246
|
T | A | 186 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0046others(183): Show | 187 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(184): Show |
intron_variant | MODIFIER | c.591+1593A>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70954246 | ||||||
| chr6:70954749
|
C | T | 1 | a0001c0002t0015g0253 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.591+1090G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70954749 | ||||||
| chr6:70954854
|
A | ACC | 84 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0046others(81): Show | 85 | HG00099.hp2 HG00323.hp2 HG00597.hp1 others(82): Show |
intron_variant | MODIFIER | c.591+983_591+984dup others(2): Show |
B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70954854 | ||||||
| chr6:70954915
|
C | CG | 25 | a0001c0001t0017g0007a0001c0002t0005g0182a0001c0002t0011g0255others(22): Show | 25 | HG01978.hp2 HG02132.hp1 HG02135.hp1 others(22): Show |
intron_variant | MODIFIER | c.591+923dupC | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70954915 | ||||||
| chr6:70954915
|
C | CGGG | 37 | a0001c0001t0001g0057a0001c0001t0001g0060a0001c0001t0001g0062others(34): Show | 38 | HG00673.hp1 HG01975.hp1 HG01993.hp1 others(35): Show |
intron_variant | MODIFIER | c.591+921_591+923dup others(3): Show |
B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70954915 | ||||||
| chr6:70954915
|
C | CGGGG | 22 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0046others(19): Show | 22 | HG00099.hp2 HG00597.hp1 HG01168.hp1 others(19): Show |
intron_variant | MODIFIER | c.591+920_591+923dup others(4): Show |
B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70954915 | ||||||
| chr6:70954918
|
G | A | 4 | a0001c0001t0004g0161a0001c0001t0004g0163a0001c0001t0004g0164others(1): Show | 4 | HG02109.hp1 HG02809.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.591+921C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70954918 | ||||||
| chr6:70954923
|
G | C | 4 | a0001c0001t0036g0104a0001c0001t0045g0003a0001c0001t0069g0103others(1): Show | 4 | HG02559.hp1 HG02717.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.591+916C>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70954923 | ||||||
| chr6:70955175
|
C | CA | 18 | a0001c0001t0002g0037a0001c0001t0003g0035a0001c0001t0003g0102others(15): Show | 18 | HG01167.hp1 HG02280.hp1 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.591+663dupT | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70955175 | ||||||
| chr6:70955175
|
C | CAA | 161 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0046others(158): Show | 162 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(159): Show |
intron_variant | MODIFIER | c.591+662_591+663dup others(2): Show |
B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70955175 | ||||||
| chr6:70955175
|
C | CAAA | 12 | a0001c0001t0001g0101a0001c0001t0001g0169a0001c0001t0001g0170others(9): Show | 12 | HG01168.hp1 HG01169.hp2 HG02818.hp1 others(9): Show |
intron_variant | MODIFIER | c.591+661_591+663dup others(3): Show |
B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70955175 | ||||||
| chr6:70955208
|
A | T | 1 | a0001c0001t0002g0034 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.591+631T>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70955208 | ||||||
| chr6:70955223
|
G | C | 4 | a0001c0002t0022g0299a0001c0002t0029g0300a0001c0002t0030g0302others(1): Show | 4 | HG02132.hp1 NA18981.hp2 NA19009.hp2 others(1): Show |
intron_variant | MODIFIER | c.591+616C>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70955223 | ||||||
| chr6:70955269
|
C | T | 1 | a0001c0001t0013g0033 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.591+570G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70955269 | ||||||
| chr6:70955296
|
C | T | 77 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0046others(74): Show | 78 | HG00099.hp2 HG00323.hp2 HG00597.hp1 others(75): Show |
intron_variant | MODIFIER | c.591+543G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70955296 | ||||||
| chr6:70955639
|
C | A | 1 | a0001c0001t0012g0030 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.591+200G>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70955639 | ||||||
| chr6:70955769
|
G | A | 1 | a0001c0001t0002g0175 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.591+70C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70955769 | ||||||
| chr6:70955770
|
A | G | 187 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0046others(184): Show | 188 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(185): Show |
intron_variant | MODIFIER | c.591+69T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70955770 | ||||||
| chr6:70955776
|
G | A | 96 | a0001c0001t0001g0101a0001c0001t0001g0117a0001c0001t0001g0121others(93): Show | 96 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(93): Show |
intron_variant | MODIFIER | c.591+63C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70955776 |