Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 2683 |
|---|---|
| ensemblid | ENSG00000086062.13 |
| hgncid | 924 |
| symbol | B4GALT1 |
| name | beta-1,4-galactosyltransferase 1 |
| refseq_nuc | NM_001497.4 |
| refseq_prot | NP_001488.2 |
| ensembl_nuc | ENST00000379731.5 |
| ensembl_prot | ENSP00000369055.4 |
| mane_status | MANE Select |
| chr | chr9 |
| start | 33110642 |
| end | 33167336 |
| strand | - |
| ver | v1.2 |
| region | chr9:33110642-33167336 |
| region5000 | chr9:33105642-33172336 |
| regionname0 | B4GALT1_chr9_33110642_33167336 |
| regionname5000 | B4GALT1_chr9_33105642_33172336 |
| 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 | 398 | 360 | 88 | 68 | 147 | 13 | 42 | 117 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | copy fasta | chr9 | 33105642 | 33172336 |
| a0002 | 0/0 | 398 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | copy fasta | chr9 | 33105642 | 33172336 |
| a0003 | 0/0 | 398 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | copy fasta | chr9 | 33105642 | 33172336 |
| a0004 | 0/0 | 398 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | copy fasta | chr9 | 33105642 | 33172336 |
| a0005 | 0/0 | 398 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | copy fasta | chr9 | 33105642 | 33172336 |
| a0006 | 0/0 | 398 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | copy fasta | chr9 | 33105642 | 33172336 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/0 | 1197 | 339 | 84 | 67 | 133 | 12 | 42 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | copy fasta | chr9 | 33105642 | 33172336 |
| c0002 | 0/1 | 1197 | 21 | 4 | 1 | 14 | 1 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | copy fasta | chr9 | 33105642 | 33172336 |
| c0003 | 0/0 | 1197 | 2 | 2 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | copy fasta | chr9 | 33105642 | 33172336 |
| c0004 | 0/0 | 1197 | 1 | 0 | 0 | 0 | 1 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | copy fasta | chr9 | 33105642 | 33172336 |
| c0005 | 0/0 | 1197 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | copy fasta | chr9 | 33105642 | 33172336 |
| c0006 | 0/0 | 1197 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | copy fasta | chr9 | 33105642 | 33172336 |
| c0007 | 0/0 | 1197 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | copy fasta | chr9 | 33105642 | 33172336 |
| 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 | 2976 | 87 | 7 | 26 | 33 | 5 | 16 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | copy fasta | chr9 | 33105642 | 33172336 |
| t0002 | 0/0 | 2977 | 59 | 14 | 5 | 23 | 4 | 13 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | copy fasta | chr9 | 33105642 | 33172336 |
| t0003 | 0/0 | 2971 | 32 | 0 | 7 | 21 | 0 | 4 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | copy fasta | chr9 | 33105642 | 33172336 |
| t0004 | 0/0 | 2980 | 16 | 7 | 8 | 0 | 1 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | copy fasta | chr9 | 33105642 | 33172336 |
| t0005 | 0/0 | 2978 | 14 | 2 | 2 | 9 | 0 | 1 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | copy fasta | chr9 | 33105642 | 33172336 |
| t0006 | 0/0 | 2981 | 12 | 5 | 1 | 6 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | copy fasta | chr9 | 33105642 | 33172336 |
| t0007 | 0/0 | 2980 | 11 | 8 | 1 | 1 | 0 | 1 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | copy fasta | chr9 | 33105642 | 33172336 |
| t0008 | 0/0 | 2978 | 7 | 7 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | copy fasta | chr9 | 33105642 | 33172336 |
| t0009 | 0/0 | 2980 | 7 | 6 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | copy fasta | chr9 | 33105642 | 33172336 |
| t0010 | 0/0 | 2980 | 6 | 1 | 0 | 5 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | copy fasta | chr9 | 33105642 | 33172336 |
| t0011 | 0/0 | 2978 | 6 | 0 | 0 | 5 | 0 | 1 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | copy fasta | chr9 | 33105642 | 33172336 |
| t0012 | 0/0 | 2980 | 6 | 4 | 0 | 1 | 0 | 1 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | copy fasta | chr9 | 33105642 | 33172336 |
| t0013 | 0/0 | 2977 | 6 | 0 | 0 | 5 | 1 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | copy fasta | chr9 | 33105642 | 33172336 |
| t0014 | 0/0 | 2981 | 4 | 0 | 0 | 4 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | copy fasta | chr9 | 33105642 | 33172336 |
| t0015 | 0/0 | 2977 | 4 | 0 | 0 | 4 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | copy fasta | chr9 | 33105642 | 33172336 |
| t0016 | 0/0 | 2980 | 4 | 4 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | copy fasta | chr9 | 33105642 | 33172336 |
| t0017 | 0/0 | 2965 | 4 | 0 | 0 | 4 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | copy fasta | chr9 | 33105642 | 33172336 |
| t0018 | 0/0 | 2977 | 4 | 0 | 1 | 2 | 0 | 1 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | copy fasta | chr9 | 33105642 | 33172336 |
| t0019 | 0/0 | 2980 | 4 | 4 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | copy fasta | chr9 | 33105642 | 33172336 |
| t0020 | 0/0 | 2975 | 3 | 0 | 0 | 3 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | copy fasta | chr9 | 33105642 | 33172336 |
| t0021 | 0/0 | 2980 | 3 | 2 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | copy fasta | chr9 | 33105642 | 33172336 |
| t0022 | 0/0 | 2982 | 3 | 0 | 0 | 2 | 1 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | copy fasta | chr9 | 33105642 | 33172336 |
| t0023 | 0/0 | 2980 | 3 | 2 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | copy fasta | chr9 | 33105642 | 33172336 |
| t0024 | 0/0 | 2976 | 3 | 0 | 3 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | copy fasta | chr9 | 33105642 | 33172336 |
| t0025 | 0/0 | 2976 | 3 | 0 | 3 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | copy fasta | chr9 | 33105642 | 33172336 |
| t0026 | 0/1 | 2981 | 2 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | copy fasta | chr9 | 33105642 | 33172336 |
| t0027 | 0/0 | 2978 | 2 | 0 | 0 | 0 | 0 | 2 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | copy fasta | chr9 | 33105642 | 33172336 |
| t0028 | 0/0 | 2980 | 2 | 0 | 0 | 2 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | copy fasta | chr9 | 33105642 | 33172336 |
| t0029 | 0/0 | 2980 | 2 | 2 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | copy fasta | chr9 | 33105642 | 33172336 |
| t0030 | 0/0 | 2978 | 2 | 2 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | copy fasta | chr9 | 33105642 | 33172336 |
| t0031 | 0/0 | 2979 | 2 | 2 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | copy fasta | chr9 | 33105642 | 33172336 |
| t0032 | 0/0 | 2978 | 2 | 0 | 1 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | copy fasta | chr9 | 33105642 | 33172336 |
| t0033 | 0/0 | 2979 | 2 | 2 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | copy fasta | chr9 | 33105642 | 33172336 |
| t0034 | 0/0 | 2977 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | copy fasta | chr9 | 33105642 | 33172336 |
| t0035 | 0/0 | 2971 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | copy fasta | chr9 | 33105642 | 33172336 |
| t0036 | 0/0 | 2980 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | copy fasta | chr9 | 33105642 | 33172336 |
| t0037 | 0/0 | 2982 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | copy fasta | chr9 | 33105642 | 33172336 |
| t0038 | 0/0 | 2977 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | copy fasta | chr9 | 33105642 | 33172336 |
| t0039 | 0/0 | 2977 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | copy fasta | chr9 | 33105642 | 33172336 |
| t0040 | 0/0 | 2978 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | copy fasta | chr9 | 33105642 | 33172336 |
| t0041 | 0/0 | 2980 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | copy fasta | chr9 | 33105642 | 33172336 |
| t0042 | 0/0 | 2977 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | copy fasta | chr9 | 33105642 | 33172336 |
| t0043 | 0/0 | 2980 | 1 | 0 | 0 | 0 | 1 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | copy fasta | chr9 | 33105642 | 33172336 |
| t0044 | 0/0 | 2976 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | copy fasta | chr9 | 33105642 | 33172336 |
| t0045 | 0/0 | 2977 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | copy fasta | chr9 | 33105642 | 33172336 |
| t0046 | 0/0 | 2978 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | copy fasta | chr9 | 33105642 | 33172336 |
| t0047 | 0/0 | 2976 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | copy fasta | chr9 | 33105642 | 33172336 |
| t0048 | 0/0 | 2977 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | copy fasta | chr9 | 33105642 | 33172336 |
| t0049 | 0/0 | 2977 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | copy fasta | chr9 | 33105642 | 33172336 |
| t0050 | 0/0 | 2978 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | copy fasta | chr9 | 33105642 | 33172336 |
| t0051 | 0/0 | 2981 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | copy fasta | chr9 | 33105642 | 33172336 |
| t0052 | 0/0 | 2977 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | copy fasta | chr9 | 33105642 | 33172336 |
| t0053 | 0/0 | 2971 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | copy fasta | chr9 | 33105642 | 33172336 |
| t0054 | 0/0 | 2976 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | copy fasta | chr9 | 33105642 | 33172336 |
| t0055 | 0/0 | 2980 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | copy fasta | chr9 | 33105642 | 33172336 |
| t0056 | 0/0 | 2971 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | copy fasta | chr9 | 33105642 | 33172336 |
| t0057 | 0/0 | 2971 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | copy fasta | chr9 | 33105642 | 33172336 |
| t0058 | 0/0 | 2978 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | copy fasta | chr9 | 33105642 | 33172336 |
| t0059 | 0/0 | 2981 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | copy fasta | chr9 | 33105642 | 33172336 |
| t0060 | 0/0 | 2981 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | copy fasta | chr9 | 33105642 | 33172336 |
| t0061 | 0/0 | 2980 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | copy fasta | chr9 | 33105642 | 33172336 |
| t0062 | 0/0 | 2977 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | copy fasta | chr9 | 33105642 | 33172336 |
| t0063 | 0/0 | 2970 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | copy fasta | chr9 | 33105642 | 33172336 |
| t0064 | 1/0 | 2980 | 1 | 0 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | copy fasta | chr9 | 33105642 | 33172336 |
| t0065 | 0/0 | 2979 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | copy fasta | chr9 | 33105642 | 33172336 |
| t0066 | 0/0 | 3012 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | copy fasta | chr9 | 33105642 | 33172336 |
| t0067 | 0/0 | 2978 | 1 | 0 | 0 | 0 | 1 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | copy fasta | chr9 | 33105642 | 33172336 |
| t0068 | 0/0 | 3020 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | copy fasta | chr9 | 33105642 | 33172336 |
| t0069 | 0/0 | 2980 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | copy fasta | chr9 | 33105642 | 33172336 |
| t0070 | 0/0 | 2976 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | copy fasta | chr9 | 33105642 | 33172336 |
| t0071 | 0/0 | 2976 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | copy fasta | chr9 | 33105642 | 33172336 |
| t0072 | 0/0 | 2977 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | copy fasta | chr9 | 33105642 | 33172336 |
| 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 | 3 | 0 | 0 | 3 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0002 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0004 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0005 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0031 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0037 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0177 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0216 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0221 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0249 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0292 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0335 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0351 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0352 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| g0353 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 1197 | 339 | 84 | 67 | 133 | 12 | 42 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | copy fasta | chr9 | 33105642 | 33172336 |
| a0001c0002 | 0/1 | 1197 | 21 | 4 | 1 | 14 | 1 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | copy fasta | chr9 | 33105642 | 33172336 |
| a0002c0003 | 0/0 | 1197 | 2 | 2 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | copy fasta | chr9 | 33105642 | 33172336 |
| a0003c0006 | 0/0 | 1197 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | copy fasta | chr9 | 33105642 | 33172336 |
| a0004c0004 | 0/0 | 1197 | 1 | 0 | 0 | 0 | 1 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | copy fasta | chr9 | 33105642 | 33172336 |
| a0005c0005 | 0/0 | 1197 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | copy fasta | chr9 | 33105642 | 33172336 |
| a0006c0007 | 0/0 | 1197 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | copy fasta | chr9 | 33105642 | 33172336 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 4172 | 86 | 7 | 26 | 32 | 5 | 16 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | copy fasta | chr9 | 33105642 | 33172336 |
| a0001c0001t0002 | 0/0 | 4173 | 57 | 13 | 5 | 23 | 3 | 13 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | copy fasta | chr9 | 33105642 | 33172336 |
| a0001c0001t0003 | 0/0 | 4167 | 32 | 0 | 7 | 21 | 0 | 4 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | copy fasta | chr9 | 33105642 | 33172336 |
| a0001c0001t0004 | 0/0 | 4176 | 16 | 7 | 8 | 0 | 1 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | copy fasta | chr9 | 33105642 | 33172336 |
| a0001c0001t0005 | 0/0 | 4174 | 14 | 2 | 2 | 9 | 0 | 1 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | copy fasta | chr9 | 33105642 | 33172336 |
| a0001c0001t0006 | 0/0 | 4177 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | copy fasta | chr9 | 33105642 | 33172336 |
| a0001c0001t0007 | 0/0 | 4176 | 11 | 8 | 1 | 1 | 0 | 1 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | copy fasta | chr9 | 33105642 | 33172336 |
| a0001c0001t0008 | 0/0 | 4174 | 7 | 7 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | copy fasta | chr9 | 33105642 | 33172336 |
| a0001c0001t0009 | 0/0 | 4176 | 7 | 6 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | copy fasta | chr9 | 33105642 | 33172336 |
| a0001c0001t0010 | 0/0 | 4176 | 6 | 1 | 0 | 5 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | copy fasta | chr9 | 33105642 | 33172336 |
| a0001c0001t0011 | 0/0 | 4174 | 6 | 0 | 0 | 5 | 0 | 1 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | copy fasta | chr9 | 33105642 | 33172336 |
| a0001c0001t0012 | 0/0 | 4176 | 6 | 4 | 0 | 1 | 0 | 1 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | copy fasta | chr9 | 33105642 | 33172336 |
| a0001c0001t0013 | 0/0 | 4173 | 6 | 0 | 0 | 5 | 1 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | copy fasta | chr9 | 33105642 | 33172336 |
| a0001c0001t0015 | 0/0 | 4173 | 4 | 0 | 0 | 4 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | copy fasta | chr9 | 33105642 | 33172336 |
| a0001c0001t0016 | 0/0 | 4176 | 4 | 4 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | copy fasta | chr9 | 33105642 | 33172336 |
| a0001c0001t0017 | 0/0 | 4161 | 4 | 0 | 0 | 4 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | copy fasta | chr9 | 33105642 | 33172336 |
| a0001c0001t0018 | 0/0 | 4173 | 4 | 0 | 1 | 2 | 0 | 1 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | copy fasta | chr9 | 33105642 | 33172336 |
| a0001c0001t0019 | 0/0 | 4176 | 4 | 4 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | copy fasta | chr9 | 33105642 | 33172336 |
| a0001c0001t0020 | 0/0 | 4171 | 3 | 0 | 0 | 3 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | copy fasta | chr9 | 33105642 | 33172336 |
| a0001c0001t0021 | 0/0 | 4176 | 3 | 2 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | copy fasta | chr9 | 33105642 | 33172336 |
| a0001c0001t0023 | 0/0 | 4176 | 3 | 2 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | copy fasta | chr9 | 33105642 | 33172336 |
| a0001c0001t0024 | 0/0 | 4172 | 3 | 0 | 3 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | copy fasta | chr9 | 33105642 | 33172336 |
| a0001c0001t0025 | 0/0 | 4172 | 3 | 0 | 3 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | copy fasta | chr9 | 33105642 | 33172336 |
| a0001c0001t0026 | 0/0 | 4177 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | copy fasta | chr9 | 33105642 | 33172336 |
| a0001c0001t0027 | 0/0 | 4174 | 2 | 0 | 0 | 0 | 0 | 2 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | copy fasta | chr9 | 33105642 | 33172336 |
| a0001c0001t0028 | 0/0 | 4176 | 2 | 0 | 0 | 2 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | copy fasta | chr9 | 33105642 | 33172336 |
| a0001c0001t0030 | 0/0 | 4174 | 2 | 2 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | copy fasta | chr9 | 33105642 | 33172336 |
| a0001c0001t0031 | 0/0 | 4175 | 2 | 2 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | copy fasta | chr9 | 33105642 | 33172336 |
| a0001c0001t0032 | 0/0 | 4174 | 2 | 0 | 1 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | copy fasta | chr9 | 33105642 | 33172336 |
| a0001c0001t0033 | 0/0 | 4175 | 2 | 2 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | copy fasta | chr9 | 33105642 | 33172336 |
| a0001c0001t0034 | 0/0 | 4173 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | copy fasta | chr9 | 33105642 | 33172336 |
| a0001c0001t0035 | 0/0 | 4167 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | copy fasta | chr9 | 33105642 | 33172336 |
| a0001c0001t0038 | 0/0 | 4173 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | copy fasta | chr9 | 33105642 | 33172336 |
| a0001c0001t0039 | 0/0 | 4173 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | copy fasta | chr9 | 33105642 | 33172336 |
| a0001c0001t0040 | 0/0 | 4174 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | copy fasta | chr9 | 33105642 | 33172336 |
| a0001c0001t0041 | 0/0 | 4176 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | copy fasta | chr9 | 33105642 | 33172336 |
| a0001c0001t0042 | 0/0 | 4173 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | copy fasta | chr9 | 33105642 | 33172336 |
| a0001c0001t0043 | 0/0 | 4176 | 1 | 0 | 0 | 0 | 1 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | copy fasta | chr9 | 33105642 | 33172336 |
| a0001c0001t0044 | 0/0 | 4172 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | copy fasta | chr9 | 33105642 | 33172336 |
| a0001c0001t0045 | 0/0 | 4173 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | copy fasta | chr9 | 33105642 | 33172336 |
| a0001c0001t0046 | 0/0 | 4174 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | copy fasta | chr9 | 33105642 | 33172336 |
| a0001c0001t0047 | 0/0 | 4172 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | copy fasta | chr9 | 33105642 | 33172336 |
| a0001c0001t0049 | 0/0 | 4173 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | copy fasta | chr9 | 33105642 | 33172336 |
| a0001c0001t0050 | 0/0 | 4174 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | copy fasta | chr9 | 33105642 | 33172336 |
| a0001c0001t0051 | 0/0 | 4177 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | copy fasta | chr9 | 33105642 | 33172336 |
| a0001c0001t0052 | 0/0 | 4173 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | copy fasta | chr9 | 33105642 | 33172336 |
| a0001c0001t0053 | 0/0 | 4167 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | copy fasta | chr9 | 33105642 | 33172336 |
| a0001c0001t0054 | 0/0 | 4172 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | copy fasta | chr9 | 33105642 | 33172336 |
| a0001c0001t0055 | 0/0 | 4176 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | copy fasta | chr9 | 33105642 | 33172336 |
| a0001c0001t0056 | 0/0 | 4167 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | copy fasta | chr9 | 33105642 | 33172336 |
| a0001c0001t0057 | 0/0 | 4167 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | copy fasta | chr9 | 33105642 | 33172336 |
| a0001c0001t0058 | 0/0 | 4174 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | copy fasta | chr9 | 33105642 | 33172336 |
| a0001c0001t0059 | 0/0 | 4177 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | copy fasta | chr9 | 33105642 | 33172336 |
| a0001c0001t0060 | 0/0 | 4177 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | copy fasta | chr9 | 33105642 | 33172336 |
| a0001c0001t0061 | 0/0 | 4176 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | copy fasta | chr9 | 33105642 | 33172336 |
| a0001c0001t0062 | 0/0 | 4173 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | copy fasta | chr9 | 33105642 | 33172336 |
| a0001c0001t0063 | 0/0 | 4166 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | copy fasta | chr9 | 33105642 | 33172336 |
| a0001c0001t0064 | 1/0 | 4176 | 1 | 0 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | copy fasta | chr9 | 33105642 | 33172336 |
| a0001c0001t0065 | 0/0 | 4175 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | copy fasta | chr9 | 33105642 | 33172336 |
| a0001c0001t0066 | 0/0 | 4208 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | copy fasta | chr9 | 33105642 | 33172336 |
| a0001c0001t0067 | 0/0 | 4174 | 1 | 0 | 0 | 0 | 1 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | copy fasta | chr9 | 33105642 | 33172336 |
| a0001c0001t0068 | 0/0 | 4216 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | copy fasta | chr9 | 33105642 | 33172336 |
| a0001c0001t0069 | 0/0 | 4176 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | copy fasta | chr9 | 33105642 | 33172336 |
| a0001c0001t0070 | 0/0 | 4172 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | copy fasta | chr9 | 33105642 | 33172336 |
| a0001c0001t0071 | 0/0 | 4172 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | copy fasta | chr9 | 33105642 | 33172336 |
| a0001c0001t0072 | 0/0 | 4173 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | copy fasta | chr9 | 33105642 | 33172336 |
| a0001c0002t0006 | 0/0 | 4177 | 11 | 4 | 1 | 6 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | copy fasta | chr9 | 33105642 | 33172336 |
| a0001c0002t0014 | 0/0 | 4177 | 4 | 0 | 0 | 4 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | copy fasta | chr9 | 33105642 | 33172336 |
| a0001c0002t0022 | 0/0 | 4178 | 3 | 0 | 0 | 2 | 1 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | copy fasta | chr9 | 33105642 | 33172336 |
| a0001c0002t0026 | 0/1 | 4177 | 1 | 0 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | copy fasta | chr9 | 33105642 | 33172336 |
| a0001c0002t0036 | 0/0 | 4176 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | copy fasta | chr9 | 33105642 | 33172336 |
| a0001c0002t0037 | 0/0 | 4178 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | copy fasta | chr9 | 33105642 | 33172336 |
| a0002c0003t0029 | 0/0 | 4176 | 2 | 2 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | copy fasta | chr9 | 33105642 | 33172336 |
| a0003c0006t0001 | 0/0 | 4172 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | copy fasta | chr9 | 33105642 | 33172336 |
| a0004c0004t0002 | 0/0 | 4173 | 1 | 0 | 0 | 0 | 1 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | copy fasta | chr9 | 33105642 | 33172336 |
| a0005c0005t0048 | 0/0 | 4173 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | copy fasta | chr9 | 33105642 | 33172336 |
| a0006c0007t0002 | 0/0 | 4173 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | copy fasta | chr9 | 33105642 | 33172336 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0002g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0002g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0002g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0002g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0002g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0002g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0002g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0002g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0002g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0002g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0002g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0002g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0002g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0002g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0002g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0002g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0002g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0002g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0003g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0003g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0003g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0003g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0003g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0003g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0003g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0003g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0003g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0003g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0003g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0003g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0003g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0003g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0003g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0003g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0003g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0003g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0003g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0003g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0003g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0003g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0003g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0003g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0003g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0003g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0003g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0003g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0003g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0003g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0004g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0004g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0004g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0004g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0004g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0004g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0004g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0004g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0004g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0004g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0004g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0004g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0004g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0004g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0005g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0005g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0005g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0005g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0005g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0005g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0005g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0005g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0005g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0005g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0005g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0005g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0005g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0005g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0006g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0007g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0007g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0007g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0007g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0007g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0007g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0007g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0007g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0007g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0007g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0007g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0008g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0008g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0008g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0008g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0008g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0008g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0008g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0009g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0009g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0009g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0009g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0009g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0009g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0009g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0010g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0010g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0010g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0010g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0010g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0010g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0011g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0011g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0011g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0011g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0011g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0012g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0012g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0012g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0012g0335 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0012g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0012g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0013g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0013g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0013g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0013g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0013g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0013g0031 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0015g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0015g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0015g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0015g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0016g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0016g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0016g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0016g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0017g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0017g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0017g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0018g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0018g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0018g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0018g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0019g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0019g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0019g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0019g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0020g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0020g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0020g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0021g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0021g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0021g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0023g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0023g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0023g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0024g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0024g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0024g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0025g0351 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0025g0352 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0025g0353 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0026g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0027g0002 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0028g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0028g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0030g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0030g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0031g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0031g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0032g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0032g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0033g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0033g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0034g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0035g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0038g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0039g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0040g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0041g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0042g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0043g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0044g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0045g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0046g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0047g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0049g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0050g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0051g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0052g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0053g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0054g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0055g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0056g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0057g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0058g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0059g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0060g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0061g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0062g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0063g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0064g0037 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0065g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0066g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0067g0292 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0068g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0069g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0070g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0071g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0001t0072g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0002t0006g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0002t0006g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0002t0006g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0002t0006g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0002t0006g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0002t0006g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0002t0006g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0002t0006g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0002t0006g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0002t0006g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0002t0006g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0002t0014g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0002t0014g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0002t0014g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0002t0014g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0002t0022g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0002t0022g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0002t0022g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0002t0026g0177 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0002t0036g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0001c0002t0037g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0002c0003t0029g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0003c0006t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0004c0004t0002g0216 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0005c0005t0048g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| a0006c0007t0002g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0065 | EUR | GBR | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0108 | EUR | GBR | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG00280 | hp1 | a0001 | c0001 | t0043 | g0168 | EUR | FIN | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG00280 | hp2 | a0001 | c0001 | t0013 | g0031 | EUR | FIN | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0074 | EUR | FIN | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG00323 | hp2 | a0001 | c0001 | t0002 | g0249 | EUR | FIN | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG00544 | hp1 | a0001 | c0002 | t0006 | g0183 | EAS | CHS | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG00544 | hp2 | a0001 | c0001 | t0010 | g0203 | EAS | CHS | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | CHS | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0265 | EAS | CHS | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG00597 | hp1 | a0001 | c0001 | t0020 | g0285 | EAS | CHS | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG00597 | hp2 | a0001 | c0001 | t0003 | g0349 | EAS | CHS | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG00609 | hp1 | a0001 | c0001 | t0005 | g0206 | EAS | CHS | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0056 | EAS | CHS | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0145 | AMR | PUR | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0055 | AMR | PUR | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG00673 | hp1 | a0001 | c0001 | t0039 | g0252 | EAS | CHS | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0243 | EAS | CHS | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG00733 | hp1 | a0001 | c0001 | t0032 | g0022 | AMR | PUR | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG00733 | hp2 | a0001 | c0001 | t0004 | g0077 | AMR | PUR | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0054 | AMR | PUR | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG00735 | hp2 | a0001 | c0001 | t0025 | g0352 | AMR | PUR | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG00738 | hp2 | a0001 | c0001 | t0004 | g0159 | AMR | PUR | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0214 | AMR | PUR | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG00741 | hp2 | a0001 | c0001 | t0018 | g0144 | AMR | PUR | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0069 | AMR | PUR | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0012 | AMR | PUR | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG01070 | hp1 | a0001 | c0001 | t0003 | g0319 | AMR | PUR | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG01070 | hp2 | a0001 | c0001 | t0004 | g0010 | AMR | PUR | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG01071 | hp1 | a0001 | c0001 | t0004 | g0010 | AMR | PUR | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0012 | AMR | PUR | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG01074 | hp1 | a0001 | c0001 | t0023 | g0174 | AMR | PUR | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0134 | AMR | PUR | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG01081 | hp1 | a0001 | c0001 | t0054 | g0114 | AMR | PUR | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG01081 | hp2 | a0001 | c0001 | t0069 | g0294 | AMR | PUR | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG01099 | hp1 | a0001 | c0001 | t0003 | g0127 | AMR | PUR | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0135 | AMR | PUR | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0245 | AMR | PUR | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG01106 | hp2 | a0001 | c0001 | t0062 | g0339 | AMR | PUR | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG01167 | hp2 | a0001 | c0001 | t0061 | g0162 | AMR | PUR | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0078 | AMR | PUR | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG01168 | hp2 | a0001 | c0001 | t0004 | g0157 | AMR | PUR | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG01169 | hp2 | a0001 | c0001 | t0004 | g0158 | AMR | PUR | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG01175 | hp1 | a0001 | c0001 | t0007 | g0344 | AMR | PUR | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0058 | AMR | PUR | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0083 | AMR | PUR | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG01192 | hp2 | a0001 | c0001 | t0021 | g0166 | AMR | PUR | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0053 | AMR | CLM | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0116 | AMR | CLM | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG01257 | hp1 | a0001 | c0002 | t0006 | g0178 | AMR | CLM | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0073 | AMR | CLM | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0215 | AMR | CLM | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG01261 | hp2 | a0001 | c0001 | t0003 | g0128 | AMR | CLM | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0118 | AMR | CLM | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0115 | AMR | CLM | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG01358 | hp1 | a0001 | c0001 | t0003 | g0129 | AMR | CLM | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG01358 | hp2 | a0001 | c0001 | t0024 | g0021 | AMR | CLM | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG01361 | hp1 | a0001 | c0001 | t0005 | g0217 | AMR | CLM | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG01361 | hp2 | a0001 | c0001 | t0004 | g0160 | AMR | CLM | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0198 | AMR | CLM | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | CLM | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG01496 | hp1 | a0001 | c0001 | t0009 | g0035 | AMR | CLM | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG01496 | hp2 | a0001 | c0001 | t0055 | g0283 | AMR | CLM | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG01515 | hp1 | a0001 | c0001 | t0067 | g0292 | EUR | IBS | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0221 | EUR | IBS | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0220 | EUR | IBS | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0005 | EUR | IBS | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG01884 | hp1 | a0001 | c0001 | t0004 | g0272 | AFR | ACB | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG01884 | hp2 | a0001 | c0001 | t0008 | g0347 | AFR | ACB | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | ACB | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG01891 | hp2 | a0001 | c0001 | t0019 | g0153 | AFR | ACB | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG01928 | hp1 | a0001 | c0001 | t0003 | g0138 | AMR | PEL | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0152 | AMR | PEL | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | PEL | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG01934 | hp2 | a0001 | c0001 | t0024 | g0019 | AMR | PEL | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0081 | AMR | PEL | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0097 | AMR | PEL | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG01975 | hp1 | a0001 | c0001 | t0005 | g0218 | AMR | PEL | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG01975 | hp2 | a0001 | c0001 | t0003 | g0133 | AMR | PEL | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG01978 | hp1 | a0001 | c0001 | t0066 | g0293 | AMR | PEL | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG01978 | hp2 | a0001 | c0001 | t0024 | g0020 | AMR | PEL | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0082 | AMR | PEL | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0143 | AMR | PEL | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG01993 | hp1 | a0001 | c0001 | t0025 | g0353 | AMR | PEL | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG01993 | hp2 | a0001 | c0001 | t0003 | g0126 | AMR | PEL | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | KHV | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | KHV | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0200 | EAS | KHV | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG02027 | hp2 | a0001 | c0001 | t0005 | g0264 | EAS | KHV | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG02055 | hp1 | a0001 | c0001 | t0051 | g0329 | AFR | ACB | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG02055 | hp2 | a0006 | c0007 | t0002 | g0350 | AFR | ACB | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG02071 | hp1 | a0001 | c0001 | t0007 | g0062 | EAS | KHV | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG02071 | hp2 | a0001 | c0001 | t0038 | g0258 | EAS | KHV | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG02080 | hp1 | a0001 | c0001 | t0018 | g0139 | EAS | KHV | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0239 | EAS | KHV | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | KHV | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0225 | EAS | KHV | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0238 | EAS | KHV | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | KHV | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG02145 | hp1 | a0001 | c0001 | t0068 | g0291 | AFR | ACB | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0099 | AFR | ACB | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG02165 | hp1 | a0001 | c0002 | t0006 | g0185 | EAS | CDX | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG02165 | hp2 | a0001 | c0001 | t0005 | g0207 | EAS | CDX | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG02257 | hp1 | a0001 | c0001 | t0063 | g0296 | AFR | ACB | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG02257 | hp2 | a0001 | c0001 | t0005 | g0278 | AFR | ACB | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG02258 | hp1 | a0001 | c0001 | t0021 | g0165 | AFR | ACB | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG02258 | hp2 | a0001 | c0002 | t0006 | g0290 | AFR | ACB | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG02280 | hp1 | a0001 | c0001 | t0008 | g0331 | AFR | ACB | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG02280 | hp2 | a0001 | c0001 | t0019 | g0051 | AFR | ACB | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG02293 | hp1 | a0001 | c0001 | t0025 | g0351 | AMR | PEL | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG02293 | hp2 | a0001 | c0001 | t0060 | g0334 | AMR | PEL | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG02451 | hp1 | a0001 | c0001 | t0010 | g0222 | AFR | ACB | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG02451 | hp2 | a0001 | c0001 | t0007 | g0298 | AFR | ACB | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG02523 | hp1 | a0001 | c0001 | t0047 | g0131 | EAS | KHV | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0192 | EAS | KHV | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG02572 | hp1 | a0001 | c0001 | t0046 | g0340 | AFR | GWD | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG02572 | hp2 | a0001 | c0001 | t0012 | g0346 | AFR | GWD | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0076 | SAS | PJL | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG02602 | hp2 | a0001 | c0001 | t0003 | g0311 | SAS | PJL | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG02615 | hp1 | a0001 | c0001 | t0007 | g0325 | AFR | GWD | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG02615 | hp2 | a0001 | c0001 | t0030 | g0015 | AFR | GWD | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG02622 | hp1 | a0001 | c0001 | t0008 | g0304 | AFR | GWD | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG02622 | hp2 | a0001 | c0001 | t0009 | g0039 | AFR | GWD | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG02630 | hp1 | a0001 | c0001 | t0002 | g0230 | AFR | GWD | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG02630 | hp2 | a0001 | c0001 | t0004 | g0170 | AFR | GWD | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG02647 | hp1 | a0001 | c0001 | t0002 | g0281 | AFR | GWD | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG02647 | hp2 | a0001 | c0001 | t0023 | g0173 | AFR | GWD | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG02683 | hp1 | a0001 | c0001 | t0012 | g0335 | SAS | PJL | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG02683 | hp2 | a0001 | c0001 | t0003 | g0300 | SAS | PJL | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG02698 | hp1 | a0001 | c0001 | t0011 | g0066 | SAS | PJL | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0087 | SAS | PJL | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG02717 | hp1 | a0001 | c0001 | t0019 | g0154 | AFR | GWD | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG02717 | hp2 | a0001 | c0001 | t0033 | g0303 | AFR | GWD | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0111 | SAS | PJL | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0288 | SAS | PJL | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG02738 | hp1 | a0001 | c0001 | t0044 | g0059 | SAS | PJL | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0211 | SAS | PJL | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG02809 | hp1 | a0001 | c0001 | t0033 | g0301 | AFR | GWD | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG02809 | hp2 | a0001 | c0001 | t0009 | g0040 | AFR | GWD | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG02818 | hp1 | a0001 | c0001 | t0009 | g0042 | AFR | GWD | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0093 | AFR | GWD | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG02895 | hp1 | a0001 | c0001 | t0008 | g0327 | AFR | GWD | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG02895 | hp2 | a0001 | c0001 | t0045 | g0156 | AFR | GWD | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG02896 | hp1 | a0001 | c0001 | t0007 | g0338 | AFR | GWD | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG02896 | hp2 | a0002 | c0003 | t0029 | g0011 | AFR | GWD | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG02897 | hp1 | a0002 | c0003 | t0029 | g0011 | AFR | GWD | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG02897 | hp2 | a0001 | c0001 | t0008 | g0328 | AFR | GWD | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | ESN | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG02922 | hp2 | a0001 | c0001 | t0004 | g0263 | AFR | ESN | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG02965 | hp1 | a0001 | c0001 | t0007 | g0345 | AFR | ESN | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG02965 | hp2 | a0001 | c0002 | t0006 | g0189 | AFR | ESN | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG02970 | hp1 | a0001 | c0001 | t0071 | g0171 | AFR | ESN | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG02970 | hp2 | a0001 | c0001 | t0002 | g0268 | AFR | ESN | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG02976 | hp1 | a0001 | c0001 | t0007 | g0036 | AFR | ESN | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG02976 | hp2 | a0001 | c0001 | t0050 | g0033 | AFR | ESN | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG03041 | hp1 | a0001 | c0001 | t0023 | g0172 | AFR | GWD | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG03041 | hp2 | a0001 | c0001 | t0008 | g0337 | AFR | GWD | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0169 | AFR | ESN | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG03130 | hp2 | a0001 | c0001 | t0002 | g0275 | AFR | ESN | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG03195 | hp1 | a0001 | c0002 | t0006 | g0188 | AFR | ESN | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG03195 | hp2 | a0001 | c0001 | t0007 | g0336 | AFR | ESN | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG03209 | hp1 | a0001 | c0001 | t0006 | g0106 | AFR | MSL | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG03209 | hp2 | a0001 | c0001 | t0002 | g0266 | AFR | MSL | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG03225 | hp1 | a0001 | c0001 | t0002 | g0212 | AFR | MSL | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG03225 | hp2 | a0001 | c0001 | t0002 | g0236 | AFR | MSL | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0045 | SAS | PJL | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG03239 | hp2 | a0001 | c0001 | t0003 | g0322 | SAS | PJL | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG03453 | hp1 | a0001 | c0001 | t0009 | g0034 | AFR | MSL | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG03453 | hp2 | a0001 | c0001 | t0007 | g0330 | AFR | MSL | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG03486 | hp1 | a0001 | c0001 | t0002 | g0210 | AFR | MSL | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG03486 | hp2 | a0001 | c0001 | t0008 | g0348 | AFR | MSL | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG03490 | hp1 | a0001 | c0001 | t0005 | g0233 | SAS | PJL | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0085 | SAS | PJL | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG03491 | hp1 | a0001 | c0001 | t0027 | g0002 | SAS | PJL | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG03491 | hp2 | a0001 | c0001 | t0007 | g0048 | SAS | PJL | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0235 | SAS | PJL | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG03492 | hp2 | a0001 | c0001 | t0027 | g0002 | SAS | PJL | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG03516 | hp1 | a0001 | c0001 | t0002 | g0279 | AFR | ESN | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG03516 | hp2 | a0001 | c0001 | t0005 | g0277 | AFR | ESN | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG03540 | hp1 | a0001 | c0001 | t0057 | g0052 | AFR | GWD | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG03540 | hp2 | a0001 | c0001 | t0012 | g0333 | AFR | GWD | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0213 | AFR | MSL | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG03579 | hp2 | a0001 | c0001 | t0004 | g0009 | AFR | MSL | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0227 | SAS | PJL | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0150 | SAS | PJL | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0297 | SAS | PJL | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0049 | SAS | PJL | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0067 | SAS | PJL | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0151 | SAS | PJL | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG03710 | hp2 | a0001 | c0001 | t0003 | g0305 | SAS | PJL | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0234 | SAS | BEB | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0070 | SAS | BEB | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0090 | SAS | BEB | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0237 | SAS | BEB | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0109 | SAS | BEB | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0244 | SAS | BEB | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG03942 | hp1 | a0001 | c0001 | t0072 | g0079 | SAS | BEB | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0270 | SAS | BEB | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0226 | SAS | STU | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0142 | SAS | STU | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0117 | SAS | STU | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0284 | SAS | STU | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0110 | SAS | STU | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0253 | SAS | STU | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| NA18522 | hp1 | a0001 | c0001 | t0016 | g0125 | AFR | YRI | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| NA18522 | hp2 | a0001 | c0001 | t0012 | g0332 | AFR | YRI | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| NA18612 | hp1 | a0001 | c0001 | t0049 | g0130 | EAS | CHB | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| NA18612 | hp2 | a0001 | c0002 | t0006 | g0184 | EAS | CHB | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| NA18747 | hp1 | a0001 | c0001 | t0056 | g0320 | EAS | CHB | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0251 | EAS | CHB | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| NA18906 | hp1 | a0001 | c0001 | t0002 | g0280 | AFR | YRI | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| NA18906 | hp2 | a0001 | c0001 | t0004 | g0302 | AFR | YRI | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| NA18940 | hp2 | a0001 | c0002 | t0022 | g0241 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| NA18945 | hp1 | a0001 | c0001 | t0005 | g0204 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| NA18945 | hp2 | a0001 | c0001 | t0015 | g0255 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| NA18946 | hp1 | a0001 | c0001 | t0012 | g0209 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| NA18946 | hp2 | a0001 | c0001 | t0053 | g0105 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| NA18947 | hp1 | a0001 | c0001 | t0003 | g0309 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| NA18948 | hp1 | a0001 | c0001 | t0003 | g0312 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| NA18950 | hp1 | a0001 | c0001 | t0013 | g0030 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| NA18951 | hp1 | a0001 | c0001 | t0003 | g0132 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| NA18951 | hp2 | a0001 | c0001 | t0003 | g0317 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| NA18952 | hp1 | a0001 | c0001 | t0011 | g0018 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| NA18952 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| NA18954 | hp1 | a0001 | c0001 | t0040 | g0242 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| NA18954 | hp2 | a0001 | c0001 | t0002 | g0260 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| NA18959 | hp1 | a0001 | c0001 | t0011 | g0025 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| NA18959 | hp2 | a0001 | c0001 | t0003 | g0310 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| NA18961 | hp1 | a0001 | c0001 | t0011 | g0003 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| NA18961 | hp2 | a0001 | c0001 | t0003 | g0061 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| NA18962 | hp1 | a0001 | c0002 | t0006 | g0182 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| NA18964 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| NA18964 | hp2 | a0001 | c0001 | t0070 | g0123 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| NA18966 | hp2 | a0001 | c0001 | t0010 | g0202 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| NA18970 | hp1 | a0001 | c0001 | t0003 | g0321 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| NA18971 | hp2 | a0001 | c0001 | t0003 | g0223 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| NA18972 | hp1 | a0001 | c0001 | t0059 | g0194 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| NA18974 | hp2 | a0001 | c0001 | t0013 | g0028 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| NA18975 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| NA18978 | hp1 | a0001 | c0001 | t0002 | g0274 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| NA18978 | hp2 | a0001 | c0002 | t0037 | g0191 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| NA18979 | hp1 | a0001 | c0001 | t0003 | g0318 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| NA18979 | hp2 | a0001 | c0001 | t0005 | g0250 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| NA18980 | hp1 | a0001 | c0001 | t0034 | g0197 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| NA18984 | hp1 | a0001 | c0001 | t0005 | g0205 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0316 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| NA18985 | hp1 | a0001 | c0001 | t0003 | g0013 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| NA18985 | hp2 | a0001 | c0001 | t0010 | g0232 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| NA18988 | hp1 | a0001 | c0001 | t0015 | g0262 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| NA18990 | hp1 | a0001 | c0001 | t0003 | g0307 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| NA18990 | hp2 | a0003 | c0006 | t0001 | g0089 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| NA18991 | hp1 | a0001 | c0001 | t0032 | g0024 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| NA18991 | hp2 | a0001 | c0001 | t0005 | g0193 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| NA18992 | hp1 | a0001 | c0001 | t0017 | g0007 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| NA18992 | hp2 | a0001 | c0001 | t0002 | g0259 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| NA18994 | hp1 | a0001 | c0001 | t0003 | g0308 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| NA18994 | hp2 | a0001 | c0001 | t0002 | g0195 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| NA18995 | hp1 | a0001 | c0001 | t0058 | g0016 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| NA18995 | hp2 | a0001 | c0001 | t0003 | g0306 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| NA18998 | hp1 | a0001 | c0002 | t0006 | g0187 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0240 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| NA18999 | hp1 | a0001 | c0001 | t0013 | g0023 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0208 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| NA19000 | hp1 | a0001 | c0001 | t0017 | g0047 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| NA19000 | hp2 | a0001 | c0001 | t0003 | g0044 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| NA19002 | hp1 | a0001 | c0001 | t0011 | g0003 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| NA19006 | hp1 | a0001 | c0002 | t0014 | g0287 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| NA19006 | hp2 | a0001 | c0001 | t0017 | g0007 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0257 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| NA19009 | hp2 | a0001 | c0001 | t0003 | g0315 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0273 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| NA19010 | hp2 | a0001 | c0001 | t0013 | g0027 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0219 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| NA19030 | hp1 | a0001 | c0001 | t0016 | g0137 | AFR | LWK | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| NA19030 | hp2 | a0001 | c0001 | t0016 | g0326 | AFR | LWK | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0282 | AFR | LWK | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| NA19043 | hp2 | a0001 | c0001 | t0007 | g0324 | AFR | LWK | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| NA19054 | hp1 | a0001 | c0001 | t0017 | g0102 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| NA19054 | hp2 | a0001 | c0001 | t0002 | g0247 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| NA19057 | hp1 | a0001 | c0001 | t0010 | g0231 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| NA19057 | hp2 | a0001 | c0001 | t0020 | g0075 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| NA19060 | hp1 | a0001 | c0001 | t0013 | g0029 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| NA19060 | hp2 | a0001 | c0001 | t0052 | g0267 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| NA19063 | hp1 | a0001 | c0002 | t0006 | g0229 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| NA19063 | hp2 | a0001 | c0001 | t0005 | g0246 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| NA19066 | hp2 | a0001 | c0002 | t0014 | g0175 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| NA19068 | hp1 | a0001 | c0001 | t0028 | g0323 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| NA19068 | hp2 | a0001 | c0001 | t0005 | g0199 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| NA19070 | hp2 | a0001 | c0001 | t0003 | g0314 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| NA19072 | hp1 | a0001 | c0002 | t0014 | g0176 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| NA19072 | hp2 | a0001 | c0001 | t0042 | g0224 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| NA19074 | hp1 | a0001 | c0001 | t0011 | g0026 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| NA19074 | hp2 | a0001 | c0002 | t0036 | g0181 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| NA19078 | hp1 | a0001 | c0001 | t0028 | g0100 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| NA19078 | hp2 | a0001 | c0001 | t0015 | g0261 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| NA19079 | hp2 | a0001 | c0001 | t0003 | g0299 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| NA19080 | hp2 | a0001 | c0001 | t0002 | g0269 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| NA19081 | hp1 | a0001 | c0001 | t0010 | g0256 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| NA19081 | hp2 | a0001 | c0002 | t0014 | g0180 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| NA19082 | hp2 | a0001 | c0002 | t0022 | g0186 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| NA19084 | hp1 | a0001 | c0001 | t0018 | g0101 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| NA19084 | hp2 | a0001 | c0001 | t0002 | g0228 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| NA19085 | hp1 | a0001 | c0001 | t0035 | g0313 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0248 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| NA19086 | hp1 | a0001 | c0001 | t0015 | g0254 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| NA19086 | hp2 | a0001 | c0001 | t0041 | g0201 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0271 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| NA19091 | hp1 | a0001 | c0001 | t0020 | g0286 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| NA19240 | hp1 | a0001 | c0001 | t0012 | g0341 | AFR | YRI | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| NA19240 | hp2 | a0001 | c0001 | t0030 | g0014 | AFR | YRI | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| NA20129 | hp1 | a0001 | c0001 | t0065 | g0041 | AFR | ASW | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| NA20129 | hp2 | a0001 | c0001 | t0026 | g0107 | AFR | ASW | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| NA20752 | hp1 | a0004 | c0004 | t0002 | g0216 | EUR | TSI | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| NA20752 | hp2 | a0001 | c0001 | t0004 | g0164 | EUR | TSI | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| NA20805 | hp1 | a0001 | c0002 | t0022 | g0190 | EUR | TSI | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0141 | EUR | TSI | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0196 | SAS | GIH | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| NA20905 | hp2 | a0001 | c0001 | t0018 | g0050 | SAS | GIH | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0112 | AMR | CLM | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG01123 | hp2 | a0001 | c0001 | t0004 | g0163 | AMR | CLM | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0276 | AFR | ACB | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG02109 | hp2 | a0001 | c0001 | t0004 | g0009 | AFR | ACB | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG02486 | hp1 | a0001 | c0001 | t0009 | g0038 | AFR | ACB | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG02486 | hp2 | a0001 | c0002 | t0006 | g0179 | AFR | ACB | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG02559 | hp1 | a0001 | c0001 | t0031 | g0342 | AFR | ACB | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG02559 | hp2 | a0005 | c0005 | t0048 | g0289 | AFR | ACB | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG03471 | hp1 | a0001 | c0001 | t0009 | g0043 | AFR | MSL | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG03471 | hp2 | a0001 | c0001 | t0019 | g0155 | AFR | MSL | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG06807 | hp1 | a0001 | c0001 | t0021 | g0167 | AFR | USA | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0295 | AFR | USA | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0080 | AFR | USA | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| NA20300 | hp2 | a0001 | c0001 | t0031 | g0343 | AFR | USA | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| NA21309 | hp1 | a0001 | c0001 | t0004 | g0161 | AFR | LWK | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| NA21309 | hp2 | a0001 | c0001 | t0016 | g0136 | AFR | LWK | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0002 | t0026 | g0177 | REF | REF | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0064 | g0037 | REF | REF | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:33113461
|
G | A | 1 | a0004 | 1 | NA20752.hp1 | missense_variant | MODERATE | c.1190C>T | p.Pro397Leu | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 6/6 | 1357/4176 | 1190/1197 | 397/398 | chr9 | 33113461 | ||
| chr9:33116058
|
G | C | 1 | a0002 | 2 | HG02896.hp2 HG02897.hp1 |
missense_variant | MODERATE | c.892C>G | p.Leu298Val | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 4/6 | 1059/4176 | 892/1197 | 298/398 | chr9 | 33116058 | ||
| chr9:33120479
|
G | C | 1 | a0005 | 1 | HG02559.hp2 | missense_variant | MODERATE | c.776C>G | p.Ala259Gly | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 3/6 | 943/4176 | 776/1197 | 259/398 | chr9 | 33120479 | ||
| chr9:33135266
|
G | A | 1 | a0003 | 1 | NA18990.hp2 | missense_variant | MODERATE | c.571C>T | p.Leu191Phe | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/6 | 738/4176 | 571/1197 | 191/398 | chr9 | 33135266 | ||
| chr9:33166911
|
G | A | 1 | a0006 | 1 | HG02055.hp2 | missense_variant | MODERATE | c.259C>T | p.Pro87Ser | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/6 | 426/4176 | 259/1197 | 87/398 | chr9 | 33166911 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:33135240
|
G | A | 1 | a0001c0002 | 21 | HG00544.hp1 HG01257.hp1 HG02165.hp1 others(18): Show |
synonymous_variant | LOW | c.597C>T | p.His199His | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/6 | 764/4176 | 597/1197 | 199/398 | chr9 | 33135240 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:33110695
|
A | C | 4 | a0001c0001t0011a0001c0001t0027a0001c0001t0030others(1): Show | 11 | HG02615.hp2 HG02698.hp1 HG03491.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*2759T>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 6/6 | 2759 | chr9 | 33110695 | |||||
| chr9:33110725
|
G | A | 2 | a0001c0001t0047a0001c0001t0049 | 2 | HG02523.hp1 NA18612.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2729C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 6/6 | 2729 | chr9 | 33110725 | |||||
| chr9:33110841
|
C | T | 12 | a0001c0001t0006a0001c0001t0009a0001c0001t0021others(9): Show | 35 | HG00544.hp1 HG01192.hp2 HG01257.hp1 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*2613G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 6/6 | 2613 | chr9 | 33110841 | |||||
| chr9:33110948
|
TCA | T | 1 | a0001c0001t0020 | 3 | HG00597.hp1 NA19057.hp2 NA19091.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2504_*2505delTG | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 6/6 | 2504 | chr9 | 33110948 | |||||
| chr9:33110996
|
G | A | 1 | a0001c0001t0039 | 1 | HG00673.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2458C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 6/6 | 2458 | chr9 | 33110996 | |||||
| chr9:33111013
|
C | T | 2 | a0001c0001t0015a0001c0001t0040 | 5 | NA18945.hp2 NA18954.hp1 NA18988.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2441G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 6/6 | 2441 | chr9 | 33111013 | |||||
| chr9:33111049
|
A | AC | 9 | a0001c0001t0006a0001c0001t0026a0001c0001t0059others(6): Show | 24 | HG00544.hp1 HG01257.hp1 HG02165.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*2404dupG | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 6/6 | 2404 | chr9 | 33111049 | |||||
| chr9:33111052
|
C | T | 1 | a0001c0001t0038 | 1 | HG02071.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2402G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 6/6 | 2402 | chr9 | 33111052 | |||||
| chr9:33111173
|
C | T | 1 | a0001c0001t0008 | 7 | HG01884.hp2 HG02280.hp1 HG02622.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2281G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 6/6 | 2281 | chr9 | 33111173 | |||||
| chr9:33111185
|
G | C | 1 | a0001c0001t0057 | 1 | HG03540.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2269C>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 6/6 | 2269 | chr9 | 33111185 | |||||
| chr9:33111201
|
C | T | 4 | a0001c0001t0066a0001c0001t0067a0001c0001t0068others(1): Show | 4 | HG01081.hp2 HG01515.hp1 HG01978.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2253G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 6/6 | 2253 | chr9 | 33111201 | |||||
| chr9:33111250
|
C | CA | 4 | a0001c0001t0051a0001c0001t0060a0001c0002t0022others(1): Show | 6 | HG02055.hp1 HG02293.hp2 NA18940.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2203dupT | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 6/6 | 2203 | chr9 | 33111250 | |||||
| chr9:33111250
|
CA | C | 4 | a0001c0001t0031a0001c0001t0033a0001c0001t0065others(1): Show | 6 | HG02559.hp1 HG02717.hp2 HG02809.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2203delT | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 6/6 | 2203 | chr9 | 33111250 | |||||
| chr9:33111250
|
CAA | C | 8 | a0001c0001t0008a0001c0001t0011a0001c0001t0027others(5): Show | 21 | HG01515.hp1 HG01884.hp2 HG02280.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*2202_*2203delTT | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 6/6 | 2202 | chr9 | 33111250 | |||||
| chr9:33111250
|
CAAA | C | 5 | a0001c0001t0018a0001c0001t0045a0001c0001t0049others(2): Show | 8 | HG00741.hp2 HG02080.hp1 HG02559.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2201_*2203delTTT | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 6/6 | 2201 | chr9 | 33111250 | |||||
| chr9:33111250
|
CAAAA | C | 8 | a0001c0001t0001a0001c0001t0025a0001c0001t0044others(5): Show | 95 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(92): Show |
3_prime_UTR_variant | MODIFIER | c.*2200_*2203delTTTT | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 6/6 | 2200 | chr9 | 33111250 | |||||
| chr9:33111250
|
CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0063 | 1 | HG02257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2194_*2203delTTTT others(6): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 6/6 | 2194 | chr9 | 33111250 | |||||
| chr9:33111250
|
CAAAAAAA others(8): Show |
C | 1 | a0001c0001t0017 | 4 | NA18992.hp1 NA19000.hp1 NA19006.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2189_*2203delTTTT others(11): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 6/6 | 2189 | chr9 | 33111250 | |||||
| chr9:33111269
|
A | C | 5 | a0001c0001t0004a0001c0001t0016a0001c0001t0019others(2): Show | 26 | HG00280.hp1 HG00733.hp2 HG00738.hp2 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*2185T>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 6/6 | 2185 | chr9 | 33111269 | |||||
| chr9:33111270
|
AAAAAAAA others(2): Show |
A | 5 | a0001c0001t0003a0001c0001t0035a0001c0001t0053others(2): Show | 36 | HG00597.hp2 HG01070.hp1 HG01099.hp1 others(33): Show |
3_prime_UTR_variant | MODIFIER | c.*2175_*2183delGTTT others(5): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 6/6 | 2175 | chr9 | 33111270 | |||||
| chr9:33111276
|
A | AAAAAAAA others(33): Show |
1 | a0001c0001t0068 | 1 | HG02145.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2177_*2178insGTTT others(36): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 6/6 | 2177 | chr9 | 33111276 | |||||
| chr9:33111276
|
A | AAAAAAAA others(25): Show |
1 | a0001c0001t0066 | 1 | HG01978.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2177_*2178insGTTG others(28): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 6/6 | 2177 | chr9 | 33111276 | |||||
| chr9:33111276
|
A | C | 1 | a0001c0001t0067 | 1 | HG01515.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2178T>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 6/6 | 2178 | chr9 | 33111276 | |||||
| chr9:33111276
|
AAAC | A | 13 | a0001c0001t0002a0001c0001t0013a0001c0001t0015others(10): Show | 81 | HG00280.hp2 HG00323.hp2 HG00558.hp2 others(78): Show |
3_prime_UTR_variant | MODIFIER | c.*2175_*2177delGTT | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 6/6 | 2175 | chr9 | 33111276 | |||||
| chr9:33111277
|
AAC | A | 3 | a0001c0001t0005a0001c0001t0032a0001c0001t0040 | 17 | HG00609.hp1 HG00733.hp1 HG01361.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*2175_*2176delGT | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 6/6 | 2175 | chr9 | 33111277 | |||||
| chr9:33111279
|
C | A | 1 | a0001c0001t0041 | 1 | NA19086.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2175G>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 6/6 | 2175 | chr9 | 33111279 | |||||
| chr9:33111350
|
A | G | 6 | a0001c0001t0003a0001c0001t0028a0001c0001t0035others(3): Show | 38 | HG00597.hp2 HG01070.hp1 HG01099.hp1 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*2104T>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 6/6 | 2104 | chr9 | 33111350 | |||||
| chr9:33111413
|
C | T | 11 | a0001c0001t0003a0001c0001t0023a0001c0001t0028others(8): Show | 45 | HG00597.hp2 HG01070.hp1 HG01074.hp1 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*2041G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 6/6 | 2041 | chr9 | 33111413 | |||||
| chr9:33111563
|
GA | G | 8 | a0001c0001t0003a0001c0001t0019a0001c0001t0028others(5): Show | 44 | HG00597.hp2 HG01070.hp1 HG01099.hp1 others(41): Show |
3_prime_UTR_variant | MODIFIER | c.*1890delT | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 6/6 | 1890 | chr9 | 33111563 | |||||
| chr9:33111593
|
G | A | 1 | a0001c0001t0058 | 1 | NA18995.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1861C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 6/6 | 1861 | chr9 | 33111593 | |||||
| chr9:33111688
|
G | A | 5 | a0001c0001t0023a0001c0001t0066a0001c0001t0067others(2): Show | 7 | HG01074.hp1 HG01081.hp2 HG01515.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1766C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 6/6 | 1766 | chr9 | 33111688 | |||||
| chr9:33111716
|
T | G | 4 | a0001c0001t0066a0001c0001t0067a0001c0001t0068others(1): Show | 4 | HG01081.hp2 HG01515.hp1 HG01978.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1738A>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 6/6 | 1738 | chr9 | 33111716 | |||||
| chr9:33111766
|
G | A | 4 | a0001c0001t0066a0001c0001t0067a0001c0001t0068others(1): Show | 4 | HG01081.hp2 HG01515.hp1 HG01978.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1688C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 6/6 | 1688 | chr9 | 33111766 | |||||
| chr9:33111778
|
G | GA | 8 | a0001c0001t0003a0001c0001t0019a0001c0001t0028others(5): Show | 44 | HG00597.hp2 HG01070.hp1 HG01099.hp1 others(41): Show |
3_prime_UTR_variant | MODIFIER | c.*1675dupT | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 6/6 | 1675 | chr9 | 33111778 | |||||
| chr9:33111790
|
T | C | 13 | a0001c0001t0003a0001c0001t0019a0001c0001t0023others(10): Show | 51 | HG00597.hp2 HG01070.hp1 HG01074.hp1 others(48): Show |
3_prime_UTR_variant | MODIFIER | c.*1664A>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 6/6 | 1664 | chr9 | 33111790 | |||||
| chr9:33111826
|
A | T | 1 | a0001c0001t0056 | 1 | NA18747.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1628T>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 6/6 | 1628 | chr9 | 33111826 | |||||
| chr9:33111909
|
G | A | 1 | a0001c0001t0054 | 1 | HG01081.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1545C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 6/6 | 1545 | chr9 | 33111909 | |||||
| chr9:33111954
|
C | T | 1 | a0001c0001t0030 | 2 | HG02615.hp2 NA19240.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1500G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 6/6 | 1500 | chr9 | 33111954 | |||||
| chr9:33111955
|
G | A | 5 | a0001c0001t0023a0001c0001t0066a0001c0001t0067others(2): Show | 7 | HG01074.hp1 HG01081.hp2 HG01515.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1499C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 6/6 | 1499 | chr9 | 33111955 | |||||
| chr9:33112084
|
C | T | 1 | a0001c0001t0055 | 1 | HG01496.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1370G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 6/6 | 1370 | chr9 | 33112084 | |||||
| chr9:33112440
|
T | C | 4 | a0001c0001t0066a0001c0001t0067a0001c0001t0068others(1): Show | 4 | HG01081.hp2 HG01515.hp1 HG01978.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1014A>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 6/6 | 1014 | chr9 | 33112440 | |||||
| chr9:33112575
|
A | G | 4 | a0001c0001t0011a0001c0001t0027a0001c0001t0030others(1): Show | 11 | HG02615.hp2 HG02698.hp1 HG03491.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*879T>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 6/6 | 879 | chr9 | 33112575 | |||||
| chr9:33112625
|
A | C | 10 | a0001c0001t0003a0001c0001t0019a0001c0001t0021others(7): Show | 49 | HG00597.hp2 HG01070.hp1 HG01099.hp1 others(46): Show |
3_prime_UTR_variant | MODIFIER | c.*829T>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 6/6 | 829 | chr9 | 33112625 | |||||
| chr9:33112634
|
A | C | 1 | a0001c0001t0034 | 1 | NA18980.hp1 | 3_prime_UTR_variant | MODIFIER | c.*820T>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 6/6 | 820 | chr9 | 33112634 | |||||
| chr9:33112977
|
G | A | 1 | a0001c0001t0042 | 1 | NA19072.hp2 | 3_prime_UTR_variant | MODIFIER | c.*477C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 6/6 | 477 | chr9 | 33112977 | |||||
| chr9:33113000
|
T | A | 1 | a0001c0001t0061 | 1 | HG01167.hp2 | 3_prime_UTR_variant | MODIFIER | c.*454A>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 6/6 | 454 | chr9 | 33113000 | |||||
| chr9:33113068
|
G | A | 6 | a0001c0001t0023a0001c0001t0065a0001c0001t0066others(3): Show | 8 | HG01074.hp1 HG01081.hp2 HG01515.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*386C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 6/6 | 386 | chr9 | 33113068 | |||||
| chr9:33113071
|
T | C | 1 | a0001c0001t0062 | 1 | HG01106.hp2 | 3_prime_UTR_variant | MODIFIER | c.*383A>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 6/6 | 383 | chr9 | 33113071 | |||||
| chr9:33113123
|
G | A | 53 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(50): Show | 230 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(227): Show |
3_prime_UTR_variant | MODIFIER | c.*331C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 6/6 | 331 | chr9 | 33113123 | |||||
| chr9:33113186
|
A | G | 2 | a0001c0001t0045a0001c0001t0046 | 2 | HG02572.hp1 HG02895.hp2 |
3_prime_UTR_variant | MODIFIER | c.*268T>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 6/6 | 268 | chr9 | 33113186 | |||||
| chr9:33113198
|
G | T | 67 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(64): Show | 347 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(344): Show |
3_prime_UTR_variant | MODIFIER | c.*256C>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 6/6 | 256 | chr9 | 33113198 | |||||
| chr9:33113207
|
CT | C | 1 | a0001c0001t0024 | 3 | HG01358.hp2 HG01934.hp2 HG01978.hp2 |
3_prime_UTR_variant | MODIFIER | c.*246delA | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 6/6 | 246 | chr9 | 33113207 | |||||
| chr9:33113235
|
G | T | 1 | a0001c0001t0044 | 1 | HG02738.hp1 | 3_prime_UTR_variant | MODIFIER | c.*219C>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 6/6 | 219 | chr9 | 33113235 | |||||
| chr9:33113285
|
G | A | 1 | a0001c0001t0070 | 1 | NA18964.hp2 | 3_prime_UTR_variant | MODIFIER | c.*169C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 6/6 | 169 | chr9 | 33113285 | |||||
| chr9:33113300
|
C | T | 1 | a0001c0001t0043 | 1 | HG00280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*154G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 6/6 | 154 | chr9 | 33113300 | |||||
| chr9:33113301
|
G | A | 2 | a0001c0001t0071a0001c0001t0072 | 2 | HG02970.hp1 HG03942.hp1 |
3_prime_UTR_variant | MODIFIER | c.*153C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 6/6 | 153 | chr9 | 33113301 | |||||
| chr9:33113324
|
C | T | 17 | a0001c0001t0002a0001c0001t0005a0001c0001t0010others(14): Show | 99 | HG00323.hp2 HG00544.hp2 HG00558.hp2 others(96): Show |
3_prime_UTR_variant | MODIFIER | c.*130G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 6/6 | 130 | chr9 | 33113324 | |||||
| chr9:33167229
|
G | A | 1 | a0001c0001t0025 | 3 | HG00735.hp2 HG01993.hp1 HG02293.hp1 |
5_prime_UTR_variant | MODIFIER | c.-60C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/6 | 60 | chr9 | 33167229 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:33113714
|
C | G | 3 | a0001c0001t0004g0302a0001c0001t0023g0172a0001c0001t0023g0174 | 3 | HG01074.hp1 HG03041.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1064+60G>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 5/5 | chr9 | 33113714 | ||||||
| chr9:33113742
|
G | C | 8 | a0001c0001t0007g0345a0001c0001t0008g0304a0001c0001t0008g0327others(5): Show | 8 | HG01884.hp2 HG02280.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1064+32C>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 5/5 | chr9 | 33113742 | ||||||
| chr9:33113769
|
T | A | 1 | a0001c0001t0003g0319 | 1 | HG01070.hp1 | splice_region_variant&intron_variant | LOW | c.1064+5A>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 5/5 | chr9 | 33113769 | ||||||
| chr9:33113890
|
A | G | 1 | a0001c0001t0001g0143 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.960-12T>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 4/5 | chr9 | 33113890 | ||||||
| chr9:33113906
|
T | C | 1 | a0001c0001t0065g0041 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.960-28A>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 4/5 | chr9 | 33113906 | ||||||
| chr9:33113972
|
C | T | 11 | a0001c0001t0019g0051a0001c0001t0019g0153a0001c0001t0019g0154others(8): Show | 12 | HG01081.hp2 HG01515.hp1 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.960-94G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 4/5 | chr9 | 33113972 | ||||||
| chr9:33114029
|
T | A | 1 | a0001c0001t0001g0085 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.960-151A>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 4/5 | chr9 | 33114029 | ||||||
| chr9:33114084
|
G | A | 29 | a0001c0001t0003g0044a0001c0001t0003g0061a0001c0001t0003g0126others(26): Show | 29 | HG01070.hp1 HG01074.hp1 HG01081.hp2 others(26): Show |
intron_variant | MODIFIER | c.960-206C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 4/5 | chr9 | 33114084 | ||||||
| chr9:33114121
|
G | A | 1 | a0001c0001t0065g0041 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.960-243C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 4/5 | chr9 | 33114121 | ||||||
| chr9:33114283
|
G | T | 2 | a0001c0001t0002g0226a0001c0001t0002g0297 | 2 | HG03669.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.960-405C>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 4/5 | chr9 | 33114283 | ||||||
| chr9:33114547
|
G | GTC | 306 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(303): Show | 316 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(313): Show |
intron_variant | MODIFIER | c.960-671_960-670dup others(2): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 4/5 | chr9 | 33114547 | ||||||
| chr9:33114846
|
C | T | 1 | a0001c0001t0001g0032 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.960-968G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 4/5 | chr9 | 33114846 | ||||||
| chr9:33114921
|
T | C | 1 | a0001c0001t0007g0345 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.960-1043A>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 4/5 | chr9 | 33114921 | ||||||
| chr9:33114934
|
C | CA | 4 | a0001c0001t0066g0293a0001c0001t0067g0292a0001c0001t0068g0291others(1): Show | 4 | HG01081.hp2 HG01515.hp1 HG01978.hp1 others(1): Show |
intron_variant | MODIFIER | c.959+1056dupT | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 4/5 | chr9 | 33114934 | ||||||
| chr9:33115109
|
A | C | 1 | a0001c0001t0063g0296 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.959+882T>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 4/5 | chr9 | 33115109 | ||||||
| chr9:33115168
|
G | T | 306 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(303): Show | 316 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(313): Show |
intron_variant | MODIFIER | c.959+823C>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 4/5 | chr9 | 33115168 | ||||||
| chr9:33115170
|
G | C | 1 | a0001c0002t0036g0181 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.959+821C>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 4/5 | chr9 | 33115170 | ||||||
| chr9:33115503
|
G | T | 306 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(303): Show | 316 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(313): Show |
intron_variant | MODIFIER | c.959+488C>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 4/5 | chr9 | 33115503 | ||||||
| chr9:33115522
|
G | A | 1 | a0001c0001t0003g0299 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.959+469C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 4/5 | chr9 | 33115522 | ||||||
| chr9:33115558
|
A | G | 297 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(294): Show | 307 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.959+433T>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 4/5 | chr9 | 33115558 | ||||||
| chr9:33115582
|
C | T | 5 | a0001c0001t0002g0195a0001c0001t0002g0219a0001c0001t0002g0269others(2): Show | 5 | NA18994.hp2 NA19012.hp1 NA19063.hp2 others(2): Show |
intron_variant | MODIFIER | c.959+409G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 4/5 | chr9 | 33115582 | ||||||
| chr9:33115856
|
C | T | 1 | a0001c0001t0057g0052 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.959+135G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 4/5 | chr9 | 33115856 | ||||||
| chr9:33115962
|
G | T | 1 | a0001c0001t0004g0170 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.959+29C>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 4/5 | chr9 | 33115962 | ||||||
| chr9:33115969
|
A | G | 2 | a0001c0001t0001g0053a0001c0001t0055g0283 | 2 | HG01255.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.959+22T>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 4/5 | chr9 | 33115969 | ||||||
| chr9:33115972
|
T | C | 1 | a0001c0001t0027g0002 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.959+19A>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 4/5 | chr9 | 33115972 | ||||||
| chr9:33116146
|
T | A | 1 | a0001c0002t0022g0241 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.837-33A>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 3/5 | chr9 | 33116146 | ||||||
| chr9:33116240
|
AT | A | 305 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(302): Show | 315 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(312): Show |
intron_variant | MODIFIER | c.837-128delA | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 3/5 | chr9 | 33116240 | ||||||
| chr9:33116256
|
G | A | 1 | a0001c0001t0056g0320 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.837-143C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 3/5 | chr9 | 33116256 | ||||||
| chr9:33116388
|
C | T | 1 | a0001c0001t0001g0110 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.837-275G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 3/5 | chr9 | 33116388 | ||||||
| chr9:33116458
|
G | A | 1 | a0001c0001t0010g0231 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.837-345C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 3/5 | chr9 | 33116458 | ||||||
| chr9:33116468
|
G | A | 1 | a0001c0001t0007g0325 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.837-355C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 3/5 | chr9 | 33116468 | ||||||
| chr9:33116500
|
T | C | 297 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(294): Show | 307 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.837-387A>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 3/5 | chr9 | 33116500 | ||||||
| chr9:33116504
|
A | G | 305 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(302): Show | 315 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(312): Show |
intron_variant | MODIFIER | c.837-391T>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 3/5 | chr9 | 33116504 | ||||||
| chr9:33116516
|
C | A | 5 | a0001c0001t0019g0051a0001c0001t0019g0153a0001c0001t0019g0154others(2): Show | 6 | HG01891.hp2 HG02280.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.837-403G>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 3/5 | chr9 | 33116516 | ||||||
| chr9:33116516
|
C | T | 4 | a0001c0001t0023g0172a0001c0001t0023g0173a0001c0001t0023g0174others(1): Show | 4 | HG01074.hp1 HG02647.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.837-403G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 3/5 | chr9 | 33116516 | ||||||
| chr9:33116519
|
A | C | 4 | a0001c0001t0066g0293a0001c0001t0067g0292a0001c0001t0068g0291others(1): Show | 4 | HG01081.hp2 HG01515.hp1 HG01978.hp1 others(1): Show |
intron_variant | MODIFIER | c.837-406T>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 3/5 | chr9 | 33116519 | ||||||
| chr9:33116521
|
C | CT | 66 | a0001c0001t0001g0053a0001c0001t0002g0249a0001c0001t0002g0274others(63): Show | 70 | HG00280.hp1 HG00323.hp2 HG00733.hp2 others(67): Show |
intron_variant | MODIFIER | c.837-409dupA | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 3/5 | chr9 | 33116521 | ||||||
| chr9:33116521
|
C | CTT | 129 | a0001c0001t0001g0074a0001c0001t0001g0078a0001c0001t0001g0086others(126): Show | 130 | HG00280.hp2 HG00323.hp1 HG00544.hp1 others(127): Show |
intron_variant | MODIFIER | c.837-410_837-409dup others(2): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 3/5 | chr9 | 33116521 | ||||||
| chr9:33116521
|
C | CTTT | 101 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(98): Show | 106 | HG00140.hp1 HG00558.hp1 HG00642.hp1 others(103): Show |
intron_variant | MODIFIER | c.837-411_837-409dup others(3): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 3/5 | chr9 | 33116521 | ||||||
| chr9:33116709
|
G | C | 1 | a0001c0001t0028g0323 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.837-596C>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 3/5 | chr9 | 33116709 | ||||||
| chr9:33116789
|
C | A | 2 | a0001c0001t0006g0106a0001c0001t0026g0107 | 2 | HG03209.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.837-676G>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 3/5 | chr9 | 33116789 | ||||||
| chr9:33116943
|
G | C | 107 | a0001c0001t0002g0012a0001c0001t0002g0056a0001c0001t0002g0192others(104): Show | 108 | HG00280.hp2 HG00323.hp2 HG00544.hp2 others(105): Show |
intron_variant | MODIFIER | c.837-830C>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 3/5 | chr9 | 33116943 | ||||||
| chr9:33117496
|
A | G | 1 | a0001c0001t0057g0052 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.837-1383T>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 3/5 | chr9 | 33117496 | ||||||
| chr9:33117526
|
C | T | 117 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(114): Show | 124 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.837-1413G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 3/5 | chr9 | 33117526 | ||||||
| chr9:33117573
|
C | T | 1 | a0001c0001t0057g0052 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.837-1460G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 3/5 | chr9 | 33117573 | ||||||
| chr9:33117702
|
A | C | 2 | a0001c0001t0001g0068a0001c0001t0007g0062 | 2 | HG02071.hp1 NA18977.hp1 |
intron_variant | MODIFIER | c.837-1589T>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 3/5 | chr9 | 33117702 | ||||||
| chr9:33117775
|
T | C | 343 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(340): Show | 356 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(353): Show |
intron_variant | MODIFIER | c.837-1662A>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 3/5 | chr9 | 33117775 | ||||||
| chr9:33117784
|
C | T | 1 | a0001c0001t0004g0170 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.837-1671G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 3/5 | chr9 | 33117784 | ||||||
| chr9:33117800
|
C | G | 9 | a0001c0001t0011g0003a0001c0001t0011g0018a0001c0001t0011g0025others(6): Show | 11 | HG02615.hp2 HG02698.hp1 HG03491.hp1 others(8): Show |
intron_variant | MODIFIER | c.837-1687G>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 3/5 | chr9 | 33117800 | ||||||
| chr9:33117920
|
A | G | 1 | a0001c0001t0002g0208 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.837-1807T>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 3/5 | chr9 | 33117920 | ||||||
| chr9:33117956
|
C | T | 64 | a0001c0001t0002g0012a0001c0001t0002g0195a0001c0001t0002g0196others(61): Show | 65 | HG00323.hp2 HG00544.hp2 HG00609.hp1 others(62): Show |
intron_variant | MODIFIER | c.837-1843G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 3/5 | chr9 | 33117956 | ||||||
| chr9:33117967
|
C | T | 224 | a0001c0001t0001g0053a0001c0001t0002g0012a0001c0001t0002g0192others(221): Show | 231 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(228): Show |
intron_variant | MODIFIER | c.837-1854G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 3/5 | chr9 | 33117967 | ||||||
| chr9:33118112
|
G | C | 29 | a0001c0001t0001g0053a0001c0001t0004g0009a0001c0001t0004g0010others(26): Show | 31 | HG00280.hp1 HG00733.hp2 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.837-1999C>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 3/5 | chr9 | 33118112 | ||||||
| chr9:33118113
|
T | C | 113 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(110): Show | 119 | HG00140.hp1 HG00323.hp1 HG00597.hp2 others(116): Show |
intron_variant | MODIFIER | c.837-2000A>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 3/5 | chr9 | 33118113 | ||||||
| chr9:33118260
|
T | A | 3 | a0001c0001t0003g0300a0001c0001t0003g0305a0001c0001t0003g0322 | 3 | HG02683.hp2 HG03239.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.837-2147A>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 3/5 | chr9 | 33118260 | ||||||
| chr9:33118271
|
G | T | 1 | a0005c0005t0048g0289 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.836+2148C>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 3/5 | chr9 | 33118271 | ||||||
| chr9:33118301
|
G | A | 2 | a0001c0001t0001g0090a0001c0001t0001g0117 | 2 | HG03834.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.836+2118C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 3/5 | chr9 | 33118301 | ||||||
| chr9:33118319
|
A | G | 56 | a0001c0001t0001g0005a0001c0001t0001g0169a0001c0001t0001g0316others(53): Show | 60 | HG00597.hp2 HG01070.hp1 HG01099.hp1 others(57): Show |
intron_variant | MODIFIER | c.836+2100T>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 3/5 | chr9 | 33118319 | ||||||
| chr9:33118325
|
G | A | 2 | a0001c0001t0007g0324a0001c0001t0007g0325 | 2 | HG02615.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.836+2094C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 3/5 | chr9 | 33118325 | ||||||
| chr9:33118389
|
G | C | 111 | a0001c0001t0001g0008a0001c0001t0001g0055a0001c0001t0001g0057others(108): Show | 116 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(113): Show |
intron_variant | MODIFIER | c.836+2030C>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 3/5 | chr9 | 33118389 | ||||||
| chr9:33118412
|
C | T | 343 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(340): Show | 356 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(353): Show |
intron_variant | MODIFIER | c.836+2007G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 3/5 | chr9 | 33118412 | ||||||
| chr9:33118504
|
A | AT | 21 | a0001c0001t0011g0003a0001c0001t0011g0018a0001c0001t0011g0025others(18): Show | 23 | HG00280.hp2 HG00733.hp1 HG01358.hp2 others(20): Show |
intron_variant | MODIFIER | c.836+1914dupA | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 3/5 | chr9 | 33118504 | ||||||
| chr9:33118603
|
A | G | 32 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0093others(29): Show | 32 | HG01106.hp2 HG01175.hp1 HG01884.hp2 others(29): Show |
intron_variant | MODIFIER | c.836+1816T>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 3/5 | chr9 | 33118603 | ||||||
| chr9:33118741
|
A | G | 1 | a0001c0001t0063g0296 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.836+1678T>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 3/5 | chr9 | 33118741 | ||||||
| chr9:33118760
|
A | G | 1 | a0001c0001t0011g0018 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.836+1659T>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 3/5 | chr9 | 33118760 | ||||||
| chr9:33118857
|
T | C | 23 | a0001c0001t0042g0224a0001c0001t0059g0194a0001c0002t0006g0178others(20): Show | 23 | HG00544.hp1 HG01257.hp1 HG02165.hp1 others(20): Show |
intron_variant | MODIFIER | c.836+1562A>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 3/5 | chr9 | 33118857 | ||||||
| chr9:33118860
|
GT | G | 22 | a0001c0001t0001g0017a0001c0001t0011g0003a0001c0001t0011g0018others(19): Show | 24 | HG00280.hp2 HG00733.hp1 HG01358.hp2 others(21): Show |
intron_variant | MODIFIER | c.836+1558delA | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 3/5 | chr9 | 33118860 | ||||||
| chr9:33118898
|
G | GT | 198 | a0001c0001t0001g0017a0001c0001t0001g0053a0001c0001t0001g0169others(195): Show | 203 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(200): Show |
intron_variant | MODIFIER | c.836+1520dupA | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 3/5 | chr9 | 33118898 | ||||||
| chr9:33118906
|
A | G | 198 | a0001c0001t0001g0017a0001c0001t0001g0053a0001c0001t0001g0169others(195): Show | 203 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(200): Show |
intron_variant | MODIFIER | c.836+1513T>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 3/5 | chr9 | 33118906 | ||||||
| chr9:33118958
|
T | C | 1 | a0005c0005t0048g0289 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.836+1461A>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 3/5 | chr9 | 33118958 | ||||||
| chr9:33119082
|
G | A | 3 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0093 | 3 | HG01891.hp1 HG02818.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.836+1337C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 3/5 | chr9 | 33119082 | ||||||
| chr9:33119122
|
A | G | 1 | a0001c0001t0003g0223 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.836+1297T>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 3/5 | chr9 | 33119122 | ||||||
| chr9:33119243
|
C | T | 168 | a0001c0001t0001g0017a0001c0001t0001g0198a0001c0001t0002g0012others(165): Show | 171 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(168): Show |
intron_variant | MODIFIER | c.836+1176G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 3/5 | chr9 | 33119243 | ||||||
| chr9:33119256
|
AC | A | 23 | a0001c0001t0042g0224a0001c0001t0059g0194a0001c0002t0006g0178others(20): Show | 23 | HG00544.hp1 HG01257.hp1 HG02165.hp1 others(20): Show |
intron_variant | MODIFIER | c.836+1162delG | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 3/5 | chr9 | 33119256 | ||||||
| chr9:33119315
|
C | T | 1 | a0002c0003t0029g0011 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.836+1104G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 3/5 | chr9 | 33119315 | ||||||
| chr9:33119585
|
T | A | 95 | a0001c0001t0001g0198a0001c0001t0002g0012a0001c0001t0002g0192others(92): Show | 96 | HG00323.hp2 HG00544.hp2 HG00558.hp2 others(93): Show |
intron_variant | MODIFIER | c.836+834A>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 3/5 | chr9 | 33119585 | ||||||
| chr9:33119702
|
C | T | 1 | a0001c0001t0001g0116 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.836+717G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 3/5 | chr9 | 33119702 | ||||||
| chr9:33119820
|
A | G | 168 | a0001c0001t0001g0017a0001c0001t0001g0198a0001c0001t0002g0012others(165): Show | 171 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(168): Show |
intron_variant | MODIFIER | c.836+599T>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 3/5 | chr9 | 33119820 | ||||||
| chr9:33119964
|
G | T | 4 | a0001c0001t0066g0293a0001c0001t0067g0292a0001c0001t0068g0291others(1): Show | 4 | HG01081.hp2 HG01515.hp1 HG01978.hp1 others(1): Show |
intron_variant | MODIFIER | c.836+455C>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 3/5 | chr9 | 33119964 | ||||||
| chr9:33120108
|
C | T | 1 | a0001c0001t0003g0306 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.836+311G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 3/5 | chr9 | 33120108 | ||||||
| chr9:33120115
|
C | G | 2 | a0001c0001t0005g0193a0001c0001t0010g0202 | 2 | NA18966.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.836+304G>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 3/5 | chr9 | 33120115 | ||||||
| chr9:33120125
|
G | A | 1 | a0001c0001t0001g0045 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.836+294C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 3/5 | chr9 | 33120125 | ||||||
| chr9:33120204
|
A | G | 1 | a0001c0001t0002g0260 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.836+215T>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 3/5 | chr9 | 33120204 | ||||||
| chr9:33120205
|
A | G | 118 | a0001c0001t0001g0198a0001c0001t0002g0012a0001c0001t0002g0192others(115): Show | 119 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(116): Show |
intron_variant | MODIFIER | c.836+214T>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 3/5 | chr9 | 33120205 | ||||||
| chr9:33120206
|
A | G | 170 | a0001c0001t0001g0017a0001c0001t0001g0103a0001c0001t0001g0198others(167): Show | 173 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(170): Show |
intron_variant | MODIFIER | c.836+213T>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 3/5 | chr9 | 33120206 | ||||||
| chr9:33120213
|
A | G | 37 | a0001c0001t0001g0316a0001c0001t0003g0001a0001c0001t0003g0299others(34): Show | 41 | HG00280.hp1 HG00597.hp2 HG00738.hp2 others(38): Show |
intron_variant | MODIFIER | c.836+206T>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 3/5 | chr9 | 33120213 | ||||||
| chr9:33120263
|
T | C | 26 | a0001c0001t0001g0053a0001c0001t0001g0169a0001c0001t0004g0009others(23): Show | 28 | HG00280.hp1 HG00738.hp2 HG01070.hp2 others(25): Show |
intron_variant | MODIFIER | c.836+156A>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 3/5 | chr9 | 33120263 | ||||||
| chr9:33120645
|
A | G | 1 | a0001c0001t0002g0275 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.649-39T>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33120645 | ||||||
| chr9:33120708
|
A | G | 95 | a0001c0001t0001g0198a0001c0001t0002g0012a0001c0001t0002g0192others(92): Show | 96 | HG00323.hp2 HG00544.hp2 HG00558.hp2 others(93): Show |
intron_variant | MODIFIER | c.649-102T>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33120708 | ||||||
| chr9:33120752
|
G | C | 1 | a0001c0001t0003g0319 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.649-146C>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33120752 | ||||||
| chr9:33120767
|
T | C | 21 | a0001c0001t0042g0224a0001c0001t0059g0194a0001c0002t0006g0178others(18): Show | 21 | HG00544.hp1 HG01257.hp1 HG02165.hp1 others(18): Show |
intron_variant | MODIFIER | c.649-161A>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33120767 | ||||||
| chr9:33120768
|
G | C | 1 | a0001c0001t0002g0210 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.649-162C>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33120768 | ||||||
| chr9:33121035
|
G | A | 2 | a0001c0002t0014g0180a0001c0002t0036g0181 | 2 | NA19074.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.649-429C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33121035 | ||||||
| chr9:33121174
|
T | A | 2 | a0001c0001t0031g0342a0001c0001t0031g0343 | 2 | HG02559.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.649-568A>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33121174 | ||||||
| chr9:33121183
|
C | G | 1 | a0001c0001t0057g0052 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.649-577G>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33121183 | ||||||
| chr9:33121482
|
C | T | 118 | a0001c0001t0001g0198a0001c0001t0002g0012a0001c0001t0002g0192others(115): Show | 119 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(116): Show |
intron_variant | MODIFIER | c.649-876G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33121482 | ||||||
| chr9:33121487
|
C | T | 1 | a0001c0001t0003g0128 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.649-881G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33121487 | ||||||
| chr9:33121526
|
C | CT | 7 | a0001c0001t0001g0076a0001c0001t0001g0145a0001c0001t0009g0034others(4): Show | 7 | HG00642.hp1 HG01081.hp2 HG01978.hp1 others(4): Show |
intron_variant | MODIFIER | c.649-921dupA | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33121526 | ||||||
| chr9:33121526
|
CT | C | 29 | a0001c0001t0001g0053a0001c0001t0001g0169a0001c0001t0001g0316others(26): Show | 32 | HG00280.hp1 HG00738.hp2 HG01070.hp2 others(29): Show |
intron_variant | MODIFIER | c.649-921delA | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33121526 | ||||||
| chr9:33121526
|
CTTT | C | 25 | a0001c0001t0002g0259a0001c0001t0002g0273a0001c0001t0042g0224others(22): Show | 25 | HG00544.hp1 HG01257.hp1 HG02165.hp1 others(22): Show |
intron_variant | MODIFIER | c.649-923_649-921del others(3): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33121526 | ||||||
| chr9:33121526
|
CTTTT | C | 141 | a0001c0001t0001g0017a0001c0001t0001g0198a0001c0001t0002g0012others(138): Show | 144 | HG00280.hp2 HG00323.hp2 HG00544.hp2 others(141): Show |
intron_variant | MODIFIER | c.649-924_649-921del others(4): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33121526 | ||||||
| chr9:33121537
|
T | G | 1 | a0001c0001t0007g0062 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.649-931A>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33121537 | ||||||
| chr9:33121546
|
T | A | 2 | a0001c0001t0001g0072a0001c0001t0001g0150 | 2 | HG03654.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.649-940A>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33121546 | ||||||
| chr9:33121572
|
G | A | 168 | a0001c0001t0001g0017a0001c0001t0001g0198a0001c0001t0002g0012others(165): Show | 171 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(168): Show |
intron_variant | MODIFIER | c.649-966C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33121572 | ||||||
| chr9:33121978
|
A | G | 1 | a0001c0001t0002g0260 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.649-1372T>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33121978 | ||||||
| chr9:33122026
|
C | A | 95 | a0001c0001t0001g0198a0001c0001t0002g0012a0001c0001t0002g0192others(92): Show | 96 | HG00323.hp2 HG00544.hp2 HG00558.hp2 others(93): Show |
intron_variant | MODIFIER | c.649-1420G>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33122026 | ||||||
| chr9:33122128
|
G | C | 3 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0093 | 3 | HG01891.hp1 HG02818.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.649-1522C>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33122128 | ||||||
| chr9:33122135
|
C | T | 3 | a0001c0001t0008g0304a0001c0001t0033g0301a0001c0001t0033g0303 | 3 | HG02622.hp1 HG02717.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.649-1529G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33122135 | ||||||
| chr9:33122159
|
T | C | 27 | a0001c0001t0001g0053a0001c0001t0001g0169a0001c0001t0004g0009others(24): Show | 30 | HG00280.hp1 HG00738.hp2 HG01070.hp2 others(27): Show |
intron_variant | MODIFIER | c.649-1553A>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33122159 | ||||||
| chr9:33122214
|
C | A | 23 | a0001c0001t0001g0053a0001c0001t0001g0169a0001c0001t0004g0009others(20): Show | 25 | HG00280.hp1 HG00738.hp2 HG01070.hp2 others(22): Show |
intron_variant | MODIFIER | c.649-1608G>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33122214 | ||||||
| chr9:33122259
|
T | C | 344 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(341): Show | 357 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(354): Show |
intron_variant | MODIFIER | c.649-1653A>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33122259 | ||||||
| chr9:33122307
|
T | C | 1 | a0005c0005t0048g0289 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.649-1701A>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33122307 | ||||||
| chr9:33122372
|
T | A | 168 | a0001c0001t0001g0017a0001c0001t0001g0198a0001c0001t0002g0012others(165): Show | 171 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(168): Show |
intron_variant | MODIFIER | c.649-1766A>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33122372 | ||||||
| chr9:33122462
|
G | A | 29 | a0001c0001t0001g0017a0001c0001t0001g0053a0001c0001t0001g0169others(26): Show | 31 | HG00280.hp1 HG00280.hp2 HG00733.hp1 others(28): Show |
intron_variant | MODIFIER | c.649-1856C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33122462 | ||||||
| chr9:33122511
|
AAAAT | A | 162 | a0001c0001t0001g0017a0001c0001t0001g0096a0001c0001t0001g0198others(159): Show | 167 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(164): Show |
intron_variant | MODIFIER | c.649-1909_649-1906d others(6): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33122511 | ||||||
| chr9:33122628
|
T | C | 194 | a0001c0001t0001g0017a0001c0001t0001g0053a0001c0001t0001g0169others(191): Show | 200 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(197): Show |
intron_variant | MODIFIER | c.649-2022A>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33122628 | ||||||
| chr9:33122647
|
G | C | 171 | a0001c0001t0001g0017a0001c0001t0001g0198a0001c0001t0002g0012others(168): Show | 174 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(171): Show |
intron_variant | MODIFIER | c.649-2041C>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33122647 | ||||||
| chr9:33122696
|
G | A | 1 | a0001c0001t0001g0096 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.649-2090C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33122696 | ||||||
| chr9:33122776
|
T | C | 3 | a0001c0001t0023g0172a0001c0001t0023g0173a0001c0001t0023g0174 | 3 | HG01074.hp1 HG02647.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.649-2170A>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33122776 | ||||||
| chr9:33123000
|
C | T | 1 | a0001c0001t0050g0033 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.649-2394G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33123000 | ||||||
| chr9:33123015
|
A | G | 168 | a0001c0001t0001g0017a0001c0001t0001g0198a0001c0001t0002g0012others(165): Show | 171 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(168): Show |
intron_variant | MODIFIER | c.649-2409T>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33123015 | ||||||
| chr9:33123106
|
C | T | 1 | a0001c0001t0001g0008 | 2 | NA18971.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.649-2500G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33123106 | ||||||
| chr9:33123108
|
T | A | 168 | a0001c0001t0001g0017a0001c0001t0001g0198a0001c0001t0002g0012others(165): Show | 171 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(168): Show |
intron_variant | MODIFIER | c.649-2502A>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33123108 | ||||||
| chr9:33123132
|
G | T | 1 | a0005c0005t0048g0289 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.649-2526C>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33123132 | ||||||
| chr9:33123135
|
G | C | 25 | a0001c0001t0001g0169a0001c0001t0004g0009a0001c0001t0004g0010others(22): Show | 28 | HG00280.hp1 HG00738.hp2 HG01070.hp2 others(25): Show |
intron_variant | MODIFIER | c.649-2529C>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33123135 | ||||||
| chr9:33123276
|
T | A | 1 | a0002c0003t0029g0011 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.649-2670A>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33123276 | ||||||
| chr9:33123277
|
C | CA | 133 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(130): Show | 140 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(137): Show |
intron_variant | MODIFIER | c.649-2672dupT | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33123277 | ||||||
| chr9:33123277
|
C | CAA | 29 | a0001c0001t0001g0060a0001c0001t0001g0063a0001c0001t0001g0064others(26): Show | 31 | HG00280.hp1 HG00738.hp2 HG01070.hp2 others(28): Show |
intron_variant | MODIFIER | c.649-2673_649-2672d others(4): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33123277 | ||||||
| chr9:33123277
|
CA | C | 42 | a0001c0001t0002g0213a0001c0001t0002g0215a0001c0001t0002g0236others(39): Show | 42 | HG01074.hp1 HG01106.hp2 HG01175.hp1 others(39): Show |
intron_variant | MODIFIER | c.649-2672delT | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33123277 | ||||||
| chr9:33123277
|
CAA | C | 121 | a0001c0001t0001g0017a0001c0001t0001g0198a0001c0001t0002g0012others(118): Show | 124 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(121): Show |
intron_variant | MODIFIER | c.649-2673_649-2672d others(4): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33123277 | ||||||
| chr9:33123277
|
CAAAAAAA others(7): Show |
C | 4 | a0001c0001t0066g0293a0001c0001t0067g0292a0001c0001t0068g0291others(1): Show | 4 | HG01081.hp2 HG01515.hp1 HG01978.hp1 others(1): Show |
intron_variant | MODIFIER | c.649-2685_649-2672d others(16): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33123277 | ||||||
| chr9:33123388
|
A | G | 193 | a0001c0001t0001g0017a0001c0001t0001g0169a0001c0001t0001g0198others(190): Show | 199 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(196): Show |
intron_variant | MODIFIER | c.649-2782T>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33123388 | ||||||
| chr9:33123466
|
G | A | 169 | a0001c0001t0001g0017a0001c0001t0001g0198a0001c0001t0002g0012others(166): Show | 172 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(169): Show |
intron_variant | MODIFIER | c.649-2860C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33123466 | ||||||
| chr9:33123629
|
A | G | 172 | a0001c0001t0001g0017a0001c0001t0001g0198a0001c0001t0002g0012others(169): Show | 175 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(172): Show |
intron_variant | MODIFIER | c.649-3023T>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33123629 | ||||||
| chr9:33123853
|
C | T | 4 | a0001c0001t0066g0293a0001c0001t0067g0292a0001c0001t0068g0291others(1): Show | 4 | HG01081.hp2 HG01515.hp1 HG01978.hp1 others(1): Show |
intron_variant | MODIFIER | c.649-3247G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33123853 | ||||||
| chr9:33124044
|
T | C | 194 | a0001c0001t0001g0017a0001c0001t0001g0169a0001c0001t0001g0198others(191): Show | 200 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(197): Show |
intron_variant | MODIFIER | c.649-3438A>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33124044 | ||||||
| chr9:33124163
|
T | C | 168 | a0001c0001t0001g0017a0001c0001t0001g0198a0001c0001t0002g0012others(165): Show | 171 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(168): Show |
intron_variant | MODIFIER | c.649-3557A>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33124163 | ||||||
| chr9:33124319
|
T | C | 22 | a0001c0001t0042g0224a0001c0002t0006g0178a0001c0002t0006g0179others(19): Show | 22 | HG00544.hp1 HG01257.hp1 HG02165.hp1 others(19): Show |
intron_variant | MODIFIER | c.649-3713A>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33124319 | ||||||
| chr9:33124567
|
C | T | 1 | a0001c0001t0050g0033 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.649-3961G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33124567 | ||||||
| chr9:33124636
|
A | G | 117 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(114): Show | 122 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.649-4030T>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33124636 | ||||||
| chr9:33124686
|
G | A | 1 | a0001c0001t0052g0267 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.649-4080C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33124686 | ||||||
| chr9:33124874
|
T | C | 118 | a0001c0001t0001g0198a0001c0001t0002g0012a0001c0001t0002g0192others(115): Show | 119 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(116): Show |
intron_variant | MODIFIER | c.649-4268A>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33124874 | ||||||
| chr9:33125002
|
T | C | 168 | a0001c0001t0001g0017a0001c0001t0001g0198a0001c0001t0002g0012others(165): Show | 171 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(168): Show |
intron_variant | MODIFIER | c.649-4396A>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33125002 | ||||||
| chr9:33125029
|
G | C | 1 | a0002c0003t0029g0011 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.649-4423C>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33125029 | ||||||
| chr9:33125281
|
G | A | 118 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(115): Show | 123 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(120): Show |
intron_variant | MODIFIER | c.649-4675C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33125281 | ||||||
| chr9:33125361
|
C | T | 20 | a0001c0001t0001g0017a0001c0001t0011g0003a0001c0001t0011g0018others(17): Show | 22 | HG00280.hp2 HG00733.hp1 HG01358.hp2 others(19): Show |
intron_variant | MODIFIER | c.649-4755G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33125361 | ||||||
| chr9:33125487
|
C | A | 1 | a0001c0002t0006g0179 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.649-4881G>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33125487 | ||||||
| chr9:33125659
|
C | A | 1 | a0001c0001t0002g0269 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.649-5053G>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33125659 | ||||||
| chr9:33125659
|
CGA | C | 70 | a0001c0001t0001g0008a0001c0001t0001g0032a0001c0001t0001g0045others(67): Show | 72 | HG00140.hp2 HG00558.hp1 HG00609.hp2 others(69): Show |
intron_variant | MODIFIER | c.649-5055_649-5054d others(4): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33125659 | ||||||
| chr9:33125806
|
T | C | 168 | a0001c0001t0001g0017a0001c0001t0001g0198a0001c0001t0002g0012others(165): Show | 171 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(168): Show |
intron_variant | MODIFIER | c.649-5200A>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33125806 | ||||||
| chr9:33125944
|
A | C | 168 | a0001c0001t0001g0017a0001c0001t0001g0198a0001c0001t0002g0012others(165): Show | 171 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(168): Show |
intron_variant | MODIFIER | c.649-5338T>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33125944 | ||||||
| chr9:33126012
|
T | C | 1 | a0001c0001t0050g0033 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.649-5406A>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33126012 | ||||||
| chr9:33126095
|
G | A | 2 | a0001c0001t0012g0335a0002c0003t0029g0011 | 3 | HG02683.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.649-5489C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33126095 | ||||||
| chr9:33126186
|
C | A | 21 | a0001c0002t0006g0178a0001c0002t0006g0179a0001c0002t0006g0182others(18): Show | 21 | HG00544.hp1 HG01257.hp1 HG02165.hp1 others(18): Show |
intron_variant | MODIFIER | c.649-5580G>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33126186 | ||||||
| chr9:33126226
|
T | C | 20 | a0001c0001t0001g0017a0001c0001t0011g0003a0001c0001t0011g0018others(17): Show | 22 | HG00280.hp2 HG00733.hp1 HG01358.hp2 others(19): Show |
intron_variant | MODIFIER | c.649-5620A>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33126226 | ||||||
| chr9:33126348
|
C | G | 344 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(341): Show | 357 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(354): Show |
intron_variant | MODIFIER | c.649-5742G>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33126348 | ||||||
| chr9:33126365
|
A | T | 30 | a0001c0001t0004g0302a0001c0001t0007g0298a0001c0001t0007g0324others(27): Show | 30 | HG01106.hp2 HG01175.hp1 HG01884.hp2 others(27): Show |
intron_variant | MODIFIER | c.649-5759T>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33126365 | ||||||
| chr9:33126394
|
T | C | 3 | a0001c0001t0023g0172a0001c0001t0023g0173a0001c0001t0023g0174 | 3 | HG01074.hp1 HG02647.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.649-5788A>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33126394 | ||||||
| chr9:33126396
|
T | C | 1 | a0001c0001t0004g0077 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.649-5790A>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33126396 | ||||||
| chr9:33126439
|
T | A | 24 | a0001c0001t0001g0169a0001c0001t0004g0009a0001c0001t0004g0010others(21): Show | 26 | HG00280.hp1 HG00738.hp2 HG01070.hp2 others(23): Show |
intron_variant | MODIFIER | c.649-5833A>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33126439 | ||||||
| chr9:33126572
|
A | G | 168 | a0001c0001t0001g0017a0001c0001t0001g0198a0001c0001t0002g0012others(165): Show | 171 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(168): Show |
intron_variant | MODIFIER | c.649-5966T>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33126572 | ||||||
| chr9:33126594
|
A | AAACATTG others(32): Show |
1 | a0005c0005t0048g0289 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.649-5989_649-5988i others(41): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33126594 | ||||||
| chr9:33126594
|
A | AAACATTG others(110): Show |
1 | a0001c0001t0001g0115 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.649-5989_649-5988i others(119): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33126594 | ||||||
| chr9:33126594
|
A | AAACATTG others(149): Show |
1 | a0001c0001t0001g0112 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.649-5989_649-5988i others(158): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33126594 | ||||||
| chr9:33126594
|
A | AAACATTG others(188): Show |
1 | a0001c0001t0001g0116 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.649-5989_649-5988i others(197): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33126594 | ||||||
| chr9:33126594
|
A | AAACATTG others(188): Show |
1 | a0001c0001t0001g0049 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.649-5989_649-5988i others(197): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33126594 | ||||||
| chr9:33126594
|
A | AAACATTG others(149): Show |
2 | a0001c0001t0002g0056a0001c0001t0071g0171 | 2 | HG00609.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.649-5989_649-5988i others(158): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33126594 | ||||||
| chr9:33126594
|
A | AAACATTG others(149): Show |
4 | a0001c0001t0001g0045a0001c0001t0001g0122a0001c0001t0007g0048others(1): Show | 4 | HG03239.hp1 HG03491.hp2 NA18980.hp2 others(1): Show |
intron_variant | MODIFIER | c.649-5989_649-5988i others(158): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33126594 | ||||||
| chr9:33126594
|
A | AAACATTG others(149): Show |
4 | a0001c0001t0001g0169a0001c0001t0021g0165a0001c0001t0021g0166others(1): Show | 4 | HG01192.hp2 HG02258.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.649-5989_649-5988i others(158): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33126594 | ||||||
| chr9:33126594
|
A | AAACATTG others(32): Show |
69 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(66): Show | 74 | HG00323.hp1 HG00597.hp2 HG00642.hp1 others(71): Show |
intron_variant | MODIFIER | c.649-6027_649-5989d others(41): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33126594 | ||||||
| chr9:33126594
|
A | AAACATTG others(71): Show |
8 | a0001c0001t0001g0053a0001c0001t0057g0052a0001c0001t0063g0296others(5): Show | 8 | HG01081.hp2 HG01255.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.649-5989_649-5988i others(80): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33126594 | ||||||
| chr9:33126594
|
A | AAACATTG others(344): Show |
1 | a0002c0003t0029g0011 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.649-5989_649-5988i others(353): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33126594 | ||||||
| chr9:33126594
|
A | AAACATTG others(305): Show |
1 | a0001c0001t0023g0174 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.649-5989_649-5988i others(314): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33126594 | ||||||
| chr9:33126594
|
A | AAACATTG others(149): Show |
3 | a0001c0001t0019g0154a0001c0001t0019g0155a0001c0001t0045g0156 | 3 | HG02717.hp1 HG02895.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.649-5989_649-5988i others(158): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33126594 | ||||||
| chr9:33126594
|
A | AAACATTG others(188): Show |
1 | a0001c0001t0019g0153 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.649-5989_649-5988i others(197): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33126594 | ||||||
| chr9:33126594
|
A | AAACATTG others(266): Show |
1 | a0001c0001t0023g0173 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.649-5989_649-5988i others(275): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33126594 | ||||||
| chr9:33126594
|
A | AAACATTG others(305): Show |
1 | a0001c0001t0023g0172 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.649-5989_649-5988i others(314): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33126594 | ||||||
| chr9:33126610
|
T | G | 11 | a0001c0001t0001g0045a0001c0001t0001g0049a0001c0001t0001g0112others(8): Show | 11 | HG00609.hp2 HG01123.hp1 HG01255.hp2 others(8): Show |
intron_variant | MODIFIER | c.649-6004A>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33126610 | ||||||
| chr9:33126610
|
T | TGTTAACC others(149): Show |
3 | a0001c0001t0001g0087a0001c0001t0001g0140a0001c0001t0047g0131 | 3 | HG02523.hp1 HG02698.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.649-6005_649-6004i others(158): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33126610 | ||||||
| chr9:33126610
|
T | TGTTAACC others(188): Show |
1 | a0001c0001t0001g0110 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.649-6005_649-6004i others(197): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33126610 | ||||||
| chr9:33126610
|
T | TGTTAACC others(149): Show |
2 | a0001c0001t0001g0124a0001c0001t0003g0013 | 2 | HG00558.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.649-6005_649-6004i others(158): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33126610 | ||||||
| chr9:33126610
|
T | TGTTAACC others(168): Show |
1 | a0001c0001t0001g0141 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.649-6005_649-6004i others(177): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33126610 | ||||||
| chr9:33126610
|
T | TGTTAACC others(110): Show |
3 | a0001c0001t0025g0351a0001c0001t0025g0352a0001c0001t0025g0353 | 3 | HG00735.hp2 HG01993.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.649-6005_649-6004i others(119): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33126610 | ||||||
| chr9:33126610
|
T | TGTTAACC others(149): Show |
7 | a0001c0001t0001g0054a0001c0001t0001g0117a0001c0001t0001g0147others(4): Show | 7 | HG00735.hp1 HG00741.hp2 HG01358.hp1 others(4): Show |
intron_variant | MODIFIER | c.649-6005_649-6004i others(158): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33126610 | ||||||
| chr9:33126610
|
T | TGTTAACC others(149): Show |
41 | a0001c0001t0001g0032a0001c0001t0001g0046a0001c0001t0001g0055others(38): Show | 42 | HG00642.hp2 HG01074.hp2 HG01081.hp1 others(39): Show |
intron_variant | MODIFIER | c.649-6005_649-6004i others(158): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33126610 | ||||||
| chr9:33126610
|
T | TGTTAACC others(188): Show |
5 | a0001c0001t0001g0008a0001c0001t0001g0104a0001c0001t0001g0142others(2): Show | 6 | HG01981.hp2 HG02135.hp2 HG04199.hp2 others(3): Show |
intron_variant | MODIFIER | c.649-6005_649-6004i others(197): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33126610 | ||||||
| chr9:33126610
|
T | TGTTAACC others(149): Show |
10 | a0001c0001t0004g0009a0001c0001t0004g0010a0001c0001t0004g0157others(7): Show | 12 | HG00280.hp1 HG00738.hp2 HG01070.hp2 others(9): Show |
intron_variant | MODIFIER | c.649-6005_649-6004i others(158): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33126610 | ||||||
| chr9:33126649
|
T | TGTTAACC others(149): Show |
1 | a0001c0001t0001g0108 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.649-6044_649-6043i others(158): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33126649 | ||||||
| chr9:33126955
|
T | G | 1 | a0001c0001t0001g0109 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.649-6349A>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33126955 | ||||||
| chr9:33126960
|
TTTTG | T | 24 | a0001c0001t0001g0169a0001c0001t0004g0009a0001c0001t0004g0010others(21): Show | 26 | HG00280.hp1 HG00738.hp2 HG01070.hp2 others(23): Show |
intron_variant | MODIFIER | c.649-6358_649-6355d others(6): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33126960 | ||||||
| chr9:33127000
|
C | T | 1 | a0001c0001t0009g0038 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.649-6394G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33127000 | ||||||
| chr9:33127001
|
G | A | 5 | a0001c0001t0001g0108a0001c0001t0019g0153a0001c0001t0019g0154others(2): Show | 5 | HG00140.hp2 HG01891.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.649-6395C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33127001 | ||||||
| chr9:33127023
|
G | A | 24 | a0001c0001t0001g0169a0001c0001t0004g0009a0001c0001t0004g0010others(21): Show | 26 | HG00280.hp1 HG00738.hp2 HG01070.hp2 others(23): Show |
intron_variant | MODIFIER | c.649-6417C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33127023 | ||||||
| chr9:33127048
|
G | A | 1 | a0005c0005t0048g0289 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.649-6442C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33127048 | ||||||
| chr9:33127061
|
A | C | 1 | a0002c0003t0029g0011 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.649-6455T>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33127061 | ||||||
| chr9:33127122
|
C | A | 1 | a0001c0001t0049g0130 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.649-6516G>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33127122 | ||||||
| chr9:33127154
|
G | A | 23 | a0001c0001t0001g0316a0001c0001t0003g0001a0001c0001t0003g0299others(20): Show | 25 | HG00597.hp2 HG01070.hp1 HG02602.hp2 others(22): Show |
intron_variant | MODIFIER | c.649-6548C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33127154 | ||||||
| chr9:33127157
|
G | A | 2 | a0001c0001t0001g0053a0001c0001t0057g0052 | 2 | HG01255.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.649-6551C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33127157 | ||||||
| chr9:33127180
|
G | C | 3 | a0001c0001t0001g0053a0001c0001t0019g0051a0001c0001t0057g0052 | 3 | HG01255.hp1 HG02280.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.649-6574C>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33127180 | ||||||
| chr9:33127185
|
G | A | 1 | a0001c0001t0001g0104 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.649-6579C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33127185 | ||||||
| chr9:33127185
|
G | C | 3 | a0001c0001t0001g0053a0001c0001t0019g0051a0001c0001t0057g0052 | 3 | HG01255.hp1 HG02280.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.649-6579C>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33127185 | ||||||
| chr9:33127198
|
A | C | 3 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0093 | 3 | HG01891.hp1 HG02818.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.649-6592T>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33127198 | ||||||
| chr9:33127206
|
G | C | 3 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0093 | 3 | HG01891.hp1 HG02818.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.649-6600C>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33127206 | ||||||
| chr9:33127215
|
G | A | 3 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0093 | 3 | HG01891.hp1 HG02818.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.649-6609C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33127215 | ||||||
| chr9:33127226
|
G | A | 1 | a0002c0003t0029g0011 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.649-6620C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33127226 | ||||||
| chr9:33127228
|
A | C | 3 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0093 | 3 | HG01891.hp1 HG02818.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.649-6622T>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33127228 | ||||||
| chr9:33127253
|
A | G | 344 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(341): Show | 357 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(354): Show |
intron_variant | MODIFIER | c.649-6647T>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33127253 | ||||||
| chr9:33127349
|
G | A | 2 | a0001c0001t0030g0014a0001c0001t0030g0015 | 2 | HG02615.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.649-6743C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33127349 | ||||||
| chr9:33127642
|
G | A | 168 | a0001c0001t0001g0017a0001c0001t0001g0198a0001c0001t0002g0012others(165): Show | 171 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(168): Show |
intron_variant | MODIFIER | c.649-7036C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33127642 | ||||||
| chr9:33127685
|
C | A | 1 | a0001c0001t0002g0208 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.649-7079G>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33127685 | ||||||
| chr9:33127688
|
C | T | 4 | a0001c0001t0066g0293a0001c0001t0067g0292a0001c0001t0068g0291others(1): Show | 4 | HG01081.hp2 HG01515.hp1 HG01978.hp1 others(1): Show |
intron_variant | MODIFIER | c.649-7082G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33127688 | ||||||
| chr9:33127744
|
T | A | 1 | a0001c0001t0070g0123 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.649-7138A>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33127744 | ||||||
| chr9:33127788
|
C | T | 19 | a0001c0002t0006g0178a0001c0002t0006g0179a0001c0002t0006g0182others(16): Show | 19 | HG00544.hp1 HG01257.hp1 HG02165.hp1 others(16): Show |
intron_variant | MODIFIER | c.649-7182G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33127788 | ||||||
| chr9:33127866
|
G | A | 2 | a0001c0001t0001g0006a0001c0001t0002g0265 | 3 | HG00558.hp2 HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.649-7260C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33127866 | ||||||
| chr9:33128023
|
A | G | 118 | a0001c0001t0001g0198a0001c0001t0002g0012a0001c0001t0002g0192others(115): Show | 119 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(116): Show |
intron_variant | MODIFIER | c.648+7166T>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33128023 | ||||||
| chr9:33128053
|
C | T | 11 | a0001c0001t0002g0208a0001c0001t0002g0240a0001c0001t0002g0243others(8): Show | 11 | HG00673.hp2 HG02071.hp2 NA18945.hp2 others(8): Show |
intron_variant | MODIFIER | c.648+7136G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33128053 | ||||||
| chr9:33128078
|
G | A | 117 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(114): Show | 122 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.648+7111C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33128078 | ||||||
| chr9:33128181
|
T | A | 3 | a0001c0001t0001g0118a0001c0001t0001g0135a0001c0001t0054g0114 | 3 | HG01081.hp1 HG01099.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.648+7008A>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33128181 | ||||||
| chr9:33128431
|
A | G | 198 | a0001c0001t0001g0017a0001c0001t0001g0169a0001c0001t0001g0198others(195): Show | 204 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(201): Show |
intron_variant | MODIFIER | c.648+6758T>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33128431 | ||||||
| chr9:33128619
|
G | A | 30 | a0001c0001t0001g0169a0001c0001t0004g0009a0001c0001t0004g0010others(27): Show | 33 | HG00280.hp1 HG00738.hp2 HG01070.hp2 others(30): Show |
intron_variant | MODIFIER | c.648+6570C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33128619 | ||||||
| chr9:33128660
|
C | A | 30 | a0001c0001t0004g0302a0001c0001t0007g0298a0001c0001t0007g0324others(27): Show | 30 | HG01106.hp2 HG01175.hp1 HG01884.hp2 others(27): Show |
intron_variant | MODIFIER | c.648+6529G>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33128660 | ||||||
| chr9:33128765
|
C | T | 1 | a0001c0001t0008g0348 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.648+6424G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33128765 | ||||||
| chr9:33129126
|
C | A | 1 | a0001c0001t0057g0052 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.648+6063G>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33129126 | ||||||
| chr9:33129144
|
T | C | 344 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(341): Show | 357 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(354): Show |
intron_variant | MODIFIER | c.648+6045A>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33129144 | ||||||
| chr9:33129433
|
C | T | 1 | a0001c0002t0006g0187 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.648+5756G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33129433 | ||||||
| chr9:33129583
|
T | C | 2 | a0001c0001t0012g0209a0001c0001t0042g0224 | 2 | NA18946.hp1 NA19072.hp2 |
intron_variant | MODIFIER | c.648+5606A>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33129583 | ||||||
| chr9:33129609
|
A | G | 198 | a0001c0001t0001g0017a0001c0001t0001g0169a0001c0001t0001g0198others(195): Show | 204 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(201): Show |
intron_variant | MODIFIER | c.648+5580T>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33129609 | ||||||
| chr9:33129627
|
G | A | 1 | a0001c0001t0002g0266 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.648+5562C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33129627 | ||||||
| chr9:33129841
|
A | G | 168 | a0001c0001t0001g0017a0001c0001t0001g0198a0001c0001t0002g0012others(165): Show | 171 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(168): Show |
intron_variant | MODIFIER | c.648+5348T>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33129841 | ||||||
| chr9:33129846
|
G | T | 168 | a0001c0001t0001g0017a0001c0001t0001g0198a0001c0001t0002g0012others(165): Show | 171 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(168): Show |
intron_variant | MODIFIER | c.648+5343C>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33129846 | ||||||
| chr9:33129898
|
G | A | 1 | a0001c0001t0002g0266 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.648+5291C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33129898 | ||||||
| chr9:33130166
|
C | G | 1 | a0001c0001t0001g0316 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.648+5023G>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33130166 | ||||||
| chr9:33130220
|
C | T | 1 | a0001c0001t0004g0077 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.648+4969G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33130220 | ||||||
| chr9:33130291
|
G | C | 2 | a0001c0001t0001g0090a0001c0001t0001g0117 | 2 | HG03834.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.648+4898C>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33130291 | ||||||
| chr9:33130297
|
G | A | 2 | a0001c0001t0016g0136a0001c0001t0016g0137 | 2 | NA19030.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.648+4892C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33130297 | ||||||
| chr9:33130327
|
T | C | 3 | a0001c0001t0001g0058a0001c0001t0001g0085a0001c0001t0004g0077 | 3 | HG00733.hp2 HG01175.hp2 HG03490.hp2 |
intron_variant | MODIFIER | c.648+4862A>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33130327 | ||||||
| chr9:33130411
|
G | A | 8 | a0001c0001t0007g0298a0001c0001t0007g0324a0001c0001t0007g0325others(5): Show | 8 | HG02055.hp1 HG02451.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.648+4778C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33130411 | ||||||
| chr9:33130434
|
T | C | 1 | a0001c0001t0009g0040 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.648+4755A>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33130434 | ||||||
| chr9:33130487
|
A | C | 22 | a0001c0001t0001g0169a0001c0001t0004g0009a0001c0001t0004g0010others(19): Show | 25 | HG00280.hp1 HG00738.hp2 HG01070.hp2 others(22): Show |
intron_variant | MODIFIER | c.648+4702T>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33130487 | ||||||
| chr9:33130488
|
G | A | 10 | a0001c0001t0004g0010a0001c0001t0004g0157a0001c0001t0004g0158others(7): Show | 11 | HG00280.hp1 HG00738.hp2 HG01070.hp2 others(8): Show |
intron_variant | MODIFIER | c.648+4701C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33130488 | ||||||
| chr9:33130550
|
T | TTCAATAT others(2045): Show |
1 | a0001c0002t0014g0180 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.648+4638_648+4639i others(2054): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33130550 | ||||||
| chr9:33130550
|
T | TTCAATAT others(1715): Show |
1 | a0001c0001t0012g0332 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.648+4638_648+4639i others(1724): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33130550 | ||||||
| chr9:33130550
|
T | TTCAATAT others(2041): Show |
2 | a0001c0001t0012g0341a0001c0001t0060g0334 | 2 | HG02293.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.648+4638_648+4639i others(2050): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33130550 | ||||||
| chr9:33130550
|
T | TTCAATAT others(2041): Show |
2 | a0001c0001t0007g0324a0001c0001t0007g0325 | 2 | HG02615.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.648+4638_648+4639i others(2050): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33130550 | ||||||
| chr9:33130550
|
T | TTCAATAT others(2041): Show |
17 | a0001c0001t0007g0298a0001c0001t0007g0330a0001c0001t0007g0336others(14): Show | 17 | HG01106.hp2 HG01884.hp2 HG02280.hp1 others(14): Show |
intron_variant | MODIFIER | c.648+4638_648+4639i others(2050): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33130550 | ||||||
| chr9:33130550
|
T | TTCAATAT others(2044): Show |
1 | a0001c0001t0016g0326 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.648+4638_648+4639i others(2053): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33130550 | ||||||
| chr9:33130550
|
T | TTCAATAT others(2042): Show |
1 | a0001c0001t0051g0329 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.648+4638_648+4639i others(2051): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33130550 | ||||||
| chr9:33130550
|
T | TTCAATAT others(1993): Show |
4 | a0001c0001t0004g0302a0001c0001t0008g0304a0001c0001t0033g0301others(1): Show | 4 | HG02622.hp1 HG02717.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.648+4638_648+4639i others(2002): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33130550 | ||||||
| chr9:33130550
|
T | TTCAATAT others(2042): Show |
2 | a0001c0001t0007g0344a0001c0001t0008g0348 | 2 | HG01175.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.648+4638_648+4639i others(2051): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33130550 | ||||||
| chr9:33130550
|
T | TTCAATAT others(2044): Show |
1 | a0001c0001t0002g0260 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.648+4638_648+4639i others(2053): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33130550 | ||||||
| chr9:33130550
|
T | TTCAATAT others(2027): Show |
1 | a0001c0001t0013g0031 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.648+4638_648+4639i others(2036): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33130550 | ||||||
| chr9:33130550
|
T | TTCAATAT others(2044): Show |
2 | a0001c0002t0006g0189a0001c0002t0006g0229 | 2 | HG02965.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.648+4638_648+4639i others(2053): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33130550 | ||||||
| chr9:33130550
|
T | TTCAATAT others(2045): Show |
12 | a0001c0001t0002g0192a0001c0001t0002g0221a0001c0001t0002g0225others(9): Show | 12 | HG00558.hp2 HG00673.hp1 HG01515.hp2 others(9): Show |
intron_variant | MODIFIER | c.648+4638_648+4639i others(2054): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33130550 | ||||||
| chr9:33130550
|
T | TTCAATAT others(2046): Show |
2 | a0001c0001t0002g0244a0001c0001t0002g0297 | 2 | HG03669.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.648+4638_648+4639i others(2055): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33130550 | ||||||
| chr9:33130550
|
T | TTCAATAT others(2046): Show |
1 | a0001c0001t0020g0286 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.648+4638_648+4639i others(2055): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33130550 | ||||||
| chr9:33130550
|
T | TTCAATAT others(2047): Show |
1 | a0001c0001t0020g0285 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.648+4638_648+4639i others(2056): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33130550 | ||||||
| chr9:33130550
|
T | TTCAATAT others(2029): Show |
2 | a0001c0001t0001g0017a0001c0001t0032g0022 | 2 | HG00733.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.648+4638_648+4639i others(2038): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33130550 | ||||||
| chr9:33130550
|
T | TTCAATAT others(2028): Show |
3 | a0001c0001t0011g0025a0001c0001t0013g0023a0001c0001t0024g0021 | 3 | HG01358.hp2 NA18959.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.648+4638_648+4639i others(2037): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33130550 | ||||||
| chr9:33130550
|
T | TTCAATAT others(2028): Show |
2 | a0001c0001t0013g0027a0001c0001t0013g0028 | 2 | NA18974.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.648+4638_648+4639i others(2037): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33130550 | ||||||
| chr9:33130550
|
T | TTCAATAT others(2029): Show |
1 | a0001c0001t0024g0019 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.648+4638_648+4639i others(2038): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33130550 | ||||||
| chr9:33130550
|
T | TTCAATAT others(2029): Show |
1 | a0001c0001t0024g0020 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.648+4638_648+4639i others(2038): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33130550 | ||||||
| chr9:33130550
|
T | TTCAATAT others(1975): Show |
2 | a0001c0001t0013g0029a0001c0001t0013g0030 | 2 | NA18950.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.648+4638_648+4639i others(1984): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33130550 | ||||||
| chr9:33130550
|
T | TTCAATAT others(2045): Show |
1 | a0001c0002t0006g0188 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.648+4638_648+4639i others(2054): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33130550 | ||||||
| chr9:33130550
|
T | TTCAATAT others(2059): Show |
5 | a0001c0001t0002g0195a0001c0001t0002g0219a0001c0001t0002g0269others(2): Show | 5 | NA18994.hp2 NA19012.hp1 NA19063.hp2 others(2): Show |
intron_variant | MODIFIER | c.648+4638_648+4639i others(2068): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33130550 | ||||||
| chr9:33130550
|
T | TTCAATAT others(2046): Show |
1 | a0001c0001t0002g0214 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.648+4638_648+4639i others(2055): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33130550 | ||||||
| chr9:33130550
|
T | TTCAATAT others(2045): Show |
17 | a0001c0001t0002g0230a0001c0002t0006g0178a0001c0002t0006g0179others(14): Show | 17 | HG00544.hp1 HG01257.hp1 HG02165.hp1 others(14): Show |
intron_variant | MODIFIER | c.648+4638_648+4639i others(2054): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33130550 | ||||||
| chr9:33130550
|
T | TTCAATAT others(2046): Show |
1 | a0001c0001t0002g0271 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.648+4638_648+4639i others(2055): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33130550 | ||||||
| chr9:33130550
|
T | TTCAATAT others(2047): Show |
1 | a0001c0001t0010g0232 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.648+4638_648+4639i others(2056): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33130550 | ||||||
| chr9:33130550
|
T | TTCAATAT others(2046): Show |
2 | a0001c0001t0002g0276a0001c0001t0005g0277 | 2 | HG02109.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.648+4638_648+4639i others(2055): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33130550 | ||||||
| chr9:33130550
|
T | TTCAATAT others(2046): Show |
1 | a0001c0001t0040g0242 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.648+4638_648+4639i others(2055): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33130550 | ||||||
| chr9:33130550
|
T | TTCAATAT others(2046): Show |
52 | a0001c0001t0001g0198a0001c0001t0002g0012a0001c0001t0002g0196others(49): Show | 53 | HG00323.hp2 HG00544.hp2 HG00609.hp1 others(50): Show |
intron_variant | MODIFIER | c.648+4638_648+4639i others(2055): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33130550 | ||||||
| chr9:33130550
|
T | TTCAATAT others(2049): Show |
1 | a0001c0001t0002g0215 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.648+4638_648+4639i others(2058): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33130550 | ||||||
| chr9:33130550
|
T | TTCAATAT others(2048): Show |
1 | a0001c0001t0002g0234 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.648+4638_648+4639i others(2057): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33130550 | ||||||
| chr9:33130550
|
T | TTCAATAT others(2048): Show |
1 | a0001c0001t0002g0211 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.648+4638_648+4639i others(2057): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33130550 | ||||||
| chr9:33130550
|
T | TTCAATAT others(2048): Show |
1 | a0001c0001t0002g0275 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.648+4638_648+4639i others(2057): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33130550 | ||||||
| chr9:33130550
|
T | TTCAATAT others(2047): Show |
1 | a0001c0001t0010g0202 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.648+4638_648+4639i others(2056): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33130550 | ||||||
| chr9:33130550
|
T | TTCAATAT others(2047): Show |
2 | a0001c0001t0002g0240a0001c0001t0002g0281 | 2 | HG02647.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.648+4638_648+4639i others(2056): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33130550 | ||||||
| chr9:33130550
|
T | TTCAATAT others(1997): Show |
2 | a0001c0001t0002g0212a0001c0001t0010g0222 | 2 | HG02451.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.648+4638_648+4639i others(2006): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33130550 | ||||||
| chr9:33130550
|
T | TTCAATAT others(2046): Show |
1 | a0001c0002t0022g0186 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.648+4638_648+4639i others(2055): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33130550 | ||||||
| chr9:33130550
|
T | TTCAATAT others(2029): Show |
3 | a0001c0001t0027g0002a0001c0001t0030g0014a0001c0001t0030g0015 | 4 | HG02615.hp2 HG03491.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.648+4638_648+4639i others(2038): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33130550 | ||||||
| chr9:33130550
|
T | TTCAATAT others(2029): Show |
1 | a0001c0001t0011g0026 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.648+4638_648+4639i others(2038): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33130550 | ||||||
| chr9:33130550
|
T | TTCAATAT others(2030): Show |
1 | a0001c0001t0032g0024 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.648+4638_648+4639i others(2039): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33130550 | ||||||
| chr9:33130550
|
T | TTCAATAT others(2048): Show |
1 | a0001c0001t0015g0254 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.648+4638_648+4639i others(2057): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33130550 | ||||||
| chr9:33130550
|
T | TTCAATAT others(2047): Show |
2 | a0001c0001t0015g0255a0001c0001t0015g0262 | 2 | NA18945.hp2 NA18988.hp1 |
intron_variant | MODIFIER | c.648+4638_648+4639i others(2056): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33130550 | ||||||
| chr9:33130550
|
T | TTCAATAT others(2047): Show |
2 | a0001c0001t0002g0248a0001c0001t0052g0267 | 2 | NA19060.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.648+4638_648+4639i others(2056): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33130550 | ||||||
| chr9:33130550
|
T | TTCAATAT others(2048): Show |
1 | a0001c0001t0002g0274 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.648+4638_648+4639i others(2057): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33130550 | ||||||
| chr9:33130550
|
T | TTCAATAT others(2053): Show |
1 | a0001c0001t0015g0261 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.648+4638_648+4639i others(2062): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33130550 | ||||||
| chr9:33130550
|
T | TTCAATAT others(2029): Show |
3 | a0001c0001t0011g0003a0001c0001t0011g0018a0001c0001t0058g0016 | 4 | NA18952.hp1 NA18961.hp1 NA18995.hp1 others(1): Show |
intron_variant | MODIFIER | c.648+4638_648+4639i others(2038): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33130550 | ||||||
| chr9:33130603
|
G | A | 1 | a0001c0001t0003g0307 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.648+4586C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33130603 | ||||||
| chr9:33130639
|
A | G | 1 | a0001c0001t0018g0101 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.648+4550T>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33130639 | ||||||
| chr9:33130642
|
A | G | 25 | a0001c0001t0001g0169a0001c0001t0004g0009a0001c0001t0004g0010others(22): Show | 28 | HG00280.hp1 HG00738.hp2 HG01070.hp2 others(25): Show |
intron_variant | MODIFIER | c.648+4547T>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33130642 | ||||||
| chr9:33130683
|
A | G | 1 | a0006c0007t0002g0350 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.648+4506T>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33130683 | ||||||
| chr9:33130723
|
C | T | 3 | a0001c0001t0001g0045a0001c0001t0001g0049a0001c0001t0007g0048 | 3 | HG03239.hp1 HG03491.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.648+4466G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33130723 | ||||||
| chr9:33130765
|
T | C | 25 | a0001c0001t0001g0169a0001c0001t0004g0009a0001c0001t0004g0010others(22): Show | 28 | HG00280.hp1 HG00738.hp2 HG01070.hp2 others(25): Show |
intron_variant | MODIFIER | c.648+4424A>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33130765 | ||||||
| chr9:33130879
|
A | G | 143 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(140): Show | 150 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(147): Show |
intron_variant | MODIFIER | c.648+4310T>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33130879 | ||||||
| chr9:33130879
|
AGAAGCAG others(6): Show |
A | 20 | a0001c0001t0001g0017a0001c0001t0011g0003a0001c0001t0011g0018others(17): Show | 22 | HG00280.hp2 HG00733.hp1 HG01358.hp2 others(19): Show |
intron_variant | MODIFIER | c.648+4297_648+4309d others(15): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33130879 | ||||||
| chr9:33130981
|
T | C | 1 | a0001c0001t0001g0295 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.648+4208A>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33130981 | ||||||
| chr9:33131025
|
A | T | 1 | a0001c0001t0032g0022 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.648+4164T>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33131025 | ||||||
| chr9:33131306
|
A | G | 1 | a0005c0005t0048g0289 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.648+3883T>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33131306 | ||||||
| chr9:33131421
|
G | A | 23 | a0001c0001t0001g0316a0001c0001t0003g0001a0001c0001t0003g0299others(20): Show | 25 | HG00597.hp2 HG01070.hp1 HG02602.hp2 others(22): Show |
intron_variant | MODIFIER | c.648+3768C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33131421 | ||||||
| chr9:33131473
|
C | A | 1 | a0001c0001t0002g0226 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.648+3716G>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33131473 | ||||||
| chr9:33131593
|
T | A | 13 | a0001c0001t0004g0009a0001c0001t0004g0010a0001c0001t0004g0157others(10): Show | 15 | HG00280.hp1 HG00738.hp2 HG01070.hp2 others(12): Show |
intron_variant | MODIFIER | c.648+3596A>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33131593 | ||||||
| chr9:33131653
|
G | A | 168 | a0001c0001t0001g0017a0001c0001t0001g0198a0001c0001t0002g0012others(165): Show | 171 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(168): Show |
intron_variant | MODIFIER | c.648+3536C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33131653 | ||||||
| chr9:33131961
|
T | C | 1 | a0001c0001t0063g0296 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.648+3228A>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33131961 | ||||||
| chr9:33132046
|
A | G | 168 | a0001c0001t0001g0017a0001c0001t0001g0198a0001c0001t0002g0012others(165): Show | 171 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(168): Show |
intron_variant | MODIFIER | c.648+3143T>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33132046 | ||||||
| chr9:33132136
|
A | G | 168 | a0001c0001t0001g0017a0001c0001t0001g0198a0001c0001t0002g0012others(165): Show | 171 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(168): Show |
intron_variant | MODIFIER | c.648+3053T>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33132136 | ||||||
| chr9:33132217
|
T | TG | 97 | a0001c0001t0001g0198a0001c0001t0002g0012a0001c0001t0002g0192others(94): Show | 98 | HG00323.hp2 HG00544.hp2 HG00558.hp2 others(95): Show |
intron_variant | MODIFIER | c.648+2971dupC | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33132217 | ||||||
| chr9:33132356
|
C | T | 97 | a0001c0001t0001g0198a0001c0001t0002g0012a0001c0001t0002g0192others(94): Show | 98 | HG00323.hp2 HG00544.hp2 HG00558.hp2 others(95): Show |
intron_variant | MODIFIER | c.648+2833G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33132356 | ||||||
| chr9:33132494
|
G | A | 168 | a0001c0001t0001g0017a0001c0001t0001g0198a0001c0001t0002g0012others(165): Show | 171 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(168): Show |
intron_variant | MODIFIER | c.648+2695C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33132494 | ||||||
| chr9:33132520
|
G | C | 25 | a0001c0001t0001g0169a0001c0001t0004g0009a0001c0001t0004g0010others(22): Show | 28 | HG00280.hp1 HG00738.hp2 HG01070.hp2 others(25): Show |
intron_variant | MODIFIER | c.648+2669C>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33132520 | ||||||
| chr9:33132572
|
C | T | 2 | a0001c0001t0011g0066a0001c0001t0025g0353 | 2 | HG01993.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.648+2617G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33132572 | ||||||
| chr9:33132644
|
G | C | 1 | a0001c0001t0002g0282 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.648+2545C>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33132644 | ||||||
| chr9:33132661
|
T | C | 15 | a0001c0001t0001g0060a0001c0001t0001g0063a0001c0001t0001g0064others(12): Show | 15 | HG01192.hp1 HG01952.hp1 HG01981.hp1 others(12): Show |
intron_variant | MODIFIER | c.648+2528A>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33132661 | ||||||
| chr9:33132790
|
G | A | 17 | a0001c0001t0001g0169a0001c0001t0004g0009a0001c0001t0004g0010others(14): Show | 19 | HG00280.hp1 HG00738.hp2 HG01070.hp2 others(16): Show |
intron_variant | MODIFIER | c.648+2399C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33132790 | ||||||
| chr9:33132841
|
A | C | 1 | a0001c0001t0009g0043 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.648+2348T>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33132841 | ||||||
| chr9:33132876
|
C | T | 2 | a0001c0001t0001g0067a0001c0001t0001g0070 | 2 | HG03704.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.648+2313G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33132876 | ||||||
| chr9:33132966
|
G | C | 2 | a0001c0001t0001g0111a0001c0001t0001g0151 | 2 | HG02735.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.648+2223C>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33132966 | ||||||
| chr9:33133043
|
C | T | 1 | a0001c0001t0065g0041 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.648+2146G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33133043 | ||||||
| chr9:33133132
|
A | T | 1 | a0001c0001t0001g0054 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.648+2057T>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33133132 | ||||||
| chr9:33133193
|
G | A | 20 | a0001c0001t0001g0017a0001c0001t0011g0003a0001c0001t0011g0018others(17): Show | 22 | HG00280.hp2 HG00733.hp1 HG01358.hp2 others(19): Show |
intron_variant | MODIFIER | c.648+1996C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33133193 | ||||||
| chr9:33133296
|
G | A | 1 | a0001c0001t0063g0296 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.648+1893C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33133296 | ||||||
| chr9:33133415
|
T | C | 4 | a0001c0001t0001g0169a0001c0001t0021g0165a0001c0001t0021g0166others(1): Show | 4 | HG01192.hp2 HG02258.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.648+1774A>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33133415 | ||||||
| chr9:33133429
|
G | A | 2 | a0001c0002t0006g0182a0001c0002t0006g0185 | 2 | HG02165.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.648+1760C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33133429 | ||||||
| chr9:33133807
|
CA | C | 72 | a0001c0001t0001g0008a0001c0001t0001g0032a0001c0001t0001g0045others(69): Show | 74 | HG00140.hp2 HG00558.hp1 HG00609.hp2 others(71): Show |
intron_variant | MODIFIER | c.648+1381delT | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33133807 | ||||||
| chr9:33133814
|
T | C | 168 | a0001c0001t0001g0017a0001c0001t0001g0198a0001c0001t0002g0012others(165): Show | 171 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(168): Show |
intron_variant | MODIFIER | c.648+1375A>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33133814 | ||||||
| chr9:33133835
|
C | T | 3 | a0001c0001t0008g0304a0001c0001t0033g0301a0001c0001t0033g0303 | 3 | HG02622.hp1 HG02717.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.648+1354G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33133835 | ||||||
| chr9:33133991
|
C | G | 1 | a0001c0001t0063g0296 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.648+1198G>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33133991 | ||||||
| chr9:33134030
|
C | T | 2 | a0001c0001t0003g0132a0001c0001t0028g0100 | 2 | NA18951.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.648+1159G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33134030 | ||||||
| chr9:33134149
|
G | A | 4 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0122others(1): Show | 4 | NA18946.hp2 NA18948.hp2 NA18980.hp2 others(1): Show |
intron_variant | MODIFIER | c.648+1040C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33134149 | ||||||
| chr9:33134200
|
G | C | 1 | a0005c0005t0048g0289 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.648+989C>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33134200 | ||||||
| chr9:33134245
|
C | T | 1 | a0001c0001t0002g0196 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.648+944G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33134245 | ||||||
| chr9:33134325
|
G | T | 30 | a0001c0001t0004g0302a0001c0001t0007g0298a0001c0001t0007g0324others(27): Show | 30 | HG01106.hp2 HG01175.hp1 HG01884.hp2 others(27): Show |
intron_variant | MODIFIER | c.648+864C>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33134325 | ||||||
| chr9:33134619
|
C | T | 20 | a0001c0001t0001g0017a0001c0001t0011g0003a0001c0001t0011g0018others(17): Show | 22 | HG00280.hp2 HG00733.hp1 HG01358.hp2 others(19): Show |
intron_variant | MODIFIER | c.648+570G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33134619 | ||||||
| chr9:33134772
|
G | A | 344 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(341): Show | 357 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(354): Show |
intron_variant | MODIFIER | c.648+417C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33134772 | ||||||
| chr9:33134794
|
T | C | 1 | a0001c0001t0002g0248 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.648+395A>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33134794 | ||||||
| chr9:33134864
|
A | T | 1 | a0001c0001t0001g0054 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.648+325T>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33134864 | ||||||
| chr9:33135037
|
T | C | 1 | a0001c0001t0001g0295 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.648+152A>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33135037 | ||||||
| chr9:33135087
|
G | A | 166 | a0001c0001t0001g0017a0001c0001t0001g0198a0001c0001t0002g0012others(163): Show | 169 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(166): Show |
intron_variant | MODIFIER | c.648+102C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33135087 | ||||||
| chr9:33135156
|
CA | C | 4 | a0001c0001t0019g0153a0001c0001t0019g0154a0001c0001t0019g0155others(1): Show | 4 | HG01891.hp2 HG02717.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.648+32delT | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33135156 | ||||||
| chr9:33135439
|
G | A | 1 | a0001c0002t0014g0180 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.413-15C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33135439 | ||||||
| chr9:33135466
|
C | G | 1 | a0001c0001t0004g0302 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.413-42G>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33135466 | ||||||
| chr9:33135539
|
G | A | 20 | a0001c0001t0001g0017a0001c0001t0011g0003a0001c0001t0011g0018others(17): Show | 22 | HG00280.hp2 HG00733.hp1 HG01358.hp2 others(19): Show |
intron_variant | MODIFIER | c.413-115C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33135539 | ||||||
| chr9:33135636
|
T | C | 168 | a0001c0001t0001g0017a0001c0001t0001g0198a0001c0001t0002g0012others(165): Show | 171 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(168): Show |
intron_variant | MODIFIER | c.413-212A>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33135636 | ||||||
| chr9:33135661
|
C | G | 1 | a0001c0001t0011g0066 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.413-237G>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33135661 | ||||||
| chr9:33135809
|
G | C | 1 | a0001c0001t0003g0305 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.413-385C>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33135809 | ||||||
| chr9:33135835
|
C | T | 1 | a0001c0001t0012g0346 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.413-411G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33135835 | ||||||
| chr9:33135889
|
A | AAG | 33 | a0001c0001t0001g0198a0001c0001t0002g0195a0001c0001t0002g0208others(30): Show | 33 | HG00673.hp2 HG00733.hp1 HG01175.hp1 others(30): Show |
intron_variant | MODIFIER | c.413-467_413-466dup others(2): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33135889 | ||||||
| chr9:33135890
|
A | AGAGT | 9 | a0001c0001t0002g0269a0001c0001t0002g0288a0001c0001t0012g0332others(6): Show | 9 | HG01106.hp2 HG02572.hp2 HG02735.hp2 others(6): Show |
intron_variant | MODIFIER | c.413-467_413-466ins others(4): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33135890 | ||||||
| chr9:33135890
|
A | AGAGTGT | 3 | a0001c0001t0002g0225a0001c0001t0002g0234a0001c0001t0031g0342 | 3 | HG02132.hp2 HG02559.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.413-467_413-466ins others(6): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33135890 | ||||||
| chr9:33135890
|
A | AGTGTGT | 5 | a0001c0001t0001g0169a0001c0001t0004g0164a0001c0001t0043g0168others(2): Show | 5 | HG00280.hp1 HG01167.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.413-472_413-467dup others(6): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33135890 | ||||||
| chr9:33135890
|
A | AGTGTGTG others(1): Show |
7 | a0001c0001t0004g0159a0001c0001t0004g0160a0001c0001t0004g0161others(4): Show | 7 | HG00738.hp2 HG01123.hp2 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.413-474_413-467dup others(8): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33135890 | ||||||
| chr9:33135890
|
A | AGTGTGTG others(3): Show |
1 | a0001c0001t0019g0153 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.413-476_413-467dup others(10): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33135890 | ||||||
| chr9:33135890
|
A | AGTGTGTG others(5): Show |
1 | a0001c0001t0019g0155 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.413-478_413-467dup others(12): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33135890 | ||||||
| chr9:33135890
|
A | AGTGTGTG others(7): Show |
2 | a0001c0001t0004g0158a0001c0001t0021g0165 | 2 | HG01169.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.413-480_413-467dup others(14): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33135890 | ||||||
| chr9:33135890
|
A | AGTGTGTG others(9): Show |
2 | a0001c0001t0004g0157a0001c0001t0021g0167 | 2 | HG01168.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.413-482_413-467dup others(16): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33135890 | ||||||
| chr9:33135892
|
T | A | 123 | a0001c0001t0001g0017a0001c0001t0002g0012a0001c0001t0002g0192others(120): Show | 126 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(123): Show |
intron_variant | MODIFIER | c.413-468A>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33135892 | ||||||
| chr9:33135897
|
GTGTGTGT others(7): Show |
G | 1 | a0001c0001t0002g0196 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.413-487_413-474del others(14): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33135897 | ||||||
| chr9:33135901
|
GTGTGTGT others(3): Show |
G | 1 | a0001c0001t0031g0343 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.413-487_413-478del others(10): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33135901 | ||||||
| chr9:33135905
|
G | GTGTGTGT others(1): Show |
17 | a0001c0001t0001g0008a0001c0001t0001g0046a0001c0001t0001g0057others(14): Show | 19 | HG00140.hp2 HG00609.hp2 HG01934.hp1 others(16): Show |
intron_variant | MODIFIER | c.413-482_413-481ins others(8): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33135905 | ||||||
| chr9:33135905
|
G | GTGTGTGT others(5): Show |
1 | a0001c0001t0001g0119 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.413-482_413-481ins others(12): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33135905 | ||||||
| chr9:33135907
|
G | GTGTGTA | 4 | a0001c0001t0001g0055a0001c0001t0001g0141a0001c0001t0001g0143others(1): Show | 4 | HG00642.hp2 HG00741.hp2 HG01981.hp2 others(1): Show |
intron_variant | MODIFIER | c.413-484_413-483ins others(6): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33135907 | ||||||
| chr9:33135907
|
GTGTA | G | 9 | a0001c0001t0002g0270a0001c0001t0008g0348a0001c0001t0066g0293others(6): Show | 9 | HG01081.hp2 HG01515.hp1 HG01978.hp1 others(6): Show |
intron_variant | MODIFIER | c.413-487_413-484del others(4): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33135907 | ||||||
| chr9:33135909
|
GTA | G | 49 | a0001c0001t0002g0012a0001c0001t0002g0200a0001c0001t0002g0214others(46): Show | 50 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(47): Show |
intron_variant | MODIFIER | c.413-487_413-486del others(2): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33135909 | ||||||
| chr9:33135911
|
A | ATG | 3 | a0001c0001t0001g0094a0001c0001t0001g0115a0001c0001t0018g0139 | 3 | HG01346.hp2 HG02080.hp1 NA18974.hp1 |
intron_variant | MODIFIER | c.413-489_413-488dup others(2): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33135911 | ||||||
| chr9:33135911
|
A | ATGTG | 4 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0093others(1): Show | 4 | HG01891.hp1 HG02818.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.413-491_413-488dup others(4): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33135911 | ||||||
| chr9:33135911
|
A | ATGTGTG | 69 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(66): Show | 72 | HG00558.hp1 HG00642.hp1 HG00733.hp2 others(69): Show |
intron_variant | MODIFIER | c.413-493_413-488dup others(6): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33135911 | ||||||
| chr9:33135911
|
A | ATGTGTGT others(1): Show |
19 | a0001c0001t0001g0058a0001c0001t0001g0060a0001c0001t0001g0063others(16): Show | 19 | HG00140.hp1 HG00323.hp1 HG01123.hp1 others(16): Show |
intron_variant | MODIFIER | c.413-495_413-488dup others(8): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33135911 | ||||||
| chr9:33135911
|
A | G | 159 | a0001c0001t0001g0008a0001c0001t0001g0017a0001c0001t0001g0046others(156): Show | 166 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(163): Show |
intron_variant | MODIFIER | c.413-487T>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33135911 | ||||||
| chr9:33136235
|
T | G | 168 | a0001c0001t0001g0017a0001c0001t0001g0198a0001c0001t0002g0012others(165): Show | 171 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(168): Show |
intron_variant | MODIFIER | c.413-811A>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33136235 | ||||||
| chr9:33136419
|
G | A | 198 | a0001c0001t0001g0017a0001c0001t0001g0169a0001c0001t0001g0198others(195): Show | 204 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(201): Show |
intron_variant | MODIFIER | c.413-995C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33136419 | ||||||
| chr9:33136430
|
G | C | 2 | a0001c0001t0004g0263a0001c0001t0004g0272 | 2 | HG01884.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.413-1006C>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33136430 | ||||||
| chr9:33136518
|
T | A | 25 | a0001c0001t0001g0169a0001c0001t0004g0009a0001c0001t0004g0010others(22): Show | 28 | HG00280.hp1 HG00738.hp2 HG01070.hp2 others(25): Show |
intron_variant | MODIFIER | c.413-1094A>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33136518 | ||||||
| chr9:33136538
|
G | A | 21 | a0001c0001t0001g0017a0001c0001t0002g0213a0001c0001t0011g0003others(18): Show | 23 | HG00280.hp2 HG00733.hp1 HG01358.hp2 others(20): Show |
intron_variant | MODIFIER | c.413-1114C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33136538 | ||||||
| chr9:33136548
|
C | T | 1 | a0001c0001t0001g0017 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.413-1124G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33136548 | ||||||
| chr9:33136830
|
C | T | 1 | a0001c0001t0002g0244 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.413-1406G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33136830 | ||||||
| chr9:33136908
|
G | C | 26 | a0001c0001t0007g0298a0001c0001t0007g0324a0001c0001t0007g0325others(23): Show | 26 | HG01106.hp2 HG01175.hp1 HG01884.hp2 others(23): Show |
intron_variant | MODIFIER | c.413-1484C>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33136908 | ||||||
| chr9:33136917
|
G | A | 1 | a0005c0005t0048g0289 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.413-1493C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33136917 | ||||||
| chr9:33136990
|
ACC | A | 168 | a0001c0001t0001g0017a0001c0001t0001g0198a0001c0001t0002g0012others(165): Show | 171 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(168): Show |
intron_variant | MODIFIER | c.413-1568_413-1567d others(4): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33136990 | ||||||
| chr9:33137006
|
C | T | 2 | a0001c0001t0030g0014a0001c0001t0030g0015 | 2 | HG02615.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.413-1582G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33137006 | ||||||
| chr9:33137305
|
C | T | 193 | a0001c0001t0001g0017a0001c0001t0001g0169a0001c0001t0001g0198others(190): Show | 199 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(196): Show |
intron_variant | MODIFIER | c.413-1881G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33137305 | ||||||
| chr9:33137423
|
A | C | 1 | a0001c0001t0046g0340 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.413-1999T>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33137423 | ||||||
| chr9:33137461
|
C | T | 30 | a0001c0001t0004g0302a0001c0001t0007g0298a0001c0001t0007g0324others(27): Show | 30 | HG01106.hp2 HG01175.hp1 HG01884.hp2 others(27): Show |
intron_variant | MODIFIER | c.413-2037G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33137461 | ||||||
| chr9:33137598
|
A | C | 168 | a0001c0001t0001g0017a0001c0001t0001g0198a0001c0001t0002g0012others(165): Show | 171 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(168): Show |
intron_variant | MODIFIER | c.413-2174T>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33137598 | ||||||
| chr9:33137647
|
CTTAGA | C | 145 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(142): Show | 152 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(149): Show |
intron_variant | MODIFIER | c.413-2228_413-2224d others(7): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33137647 | ||||||
| chr9:33137794
|
A | G | 1 | a0001c0001t0050g0033 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.413-2370T>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33137794 | ||||||
| chr9:33137851
|
G | A | 1 | a0001c0001t0001g0117 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.413-2427C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33137851 | ||||||
| chr9:33138029
|
G | A | 1 | a0001c0001t0004g0077 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.413-2605C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33138029 | ||||||
| chr9:33138117
|
T | C | 344 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(341): Show | 357 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(354): Show |
intron_variant | MODIFIER | c.413-2693A>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33138117 | ||||||
| chr9:33138156
|
C | A | 2 | a0001c0001t0016g0136a0001c0001t0016g0137 | 2 | NA19030.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.413-2732G>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33138156 | ||||||
| chr9:33138221
|
C | T | 4 | a0001c0001t0066g0293a0001c0001t0067g0292a0001c0001t0068g0291others(1): Show | 4 | HG01081.hp2 HG01515.hp1 HG01978.hp1 others(1): Show |
intron_variant | MODIFIER | c.413-2797G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33138221 | ||||||
| chr9:33138249
|
G | A | 168 | a0001c0001t0001g0017a0001c0001t0001g0198a0001c0001t0002g0012others(165): Show | 171 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(168): Show |
intron_variant | MODIFIER | c.413-2825C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33138249 | ||||||
| chr9:33138354
|
A | T | 168 | a0001c0001t0001g0017a0001c0001t0001g0198a0001c0001t0002g0012others(165): Show | 171 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(168): Show |
intron_variant | MODIFIER | c.413-2930T>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33138354 | ||||||
| chr9:33138777
|
T | C | 168 | a0001c0001t0001g0017a0001c0001t0001g0198a0001c0001t0002g0012others(165): Show | 171 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(168): Show |
intron_variant | MODIFIER | c.413-3353A>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33138777 | ||||||
| chr9:33138807
|
A | T | 1 | a0001c0001t0001g0065 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.413-3383T>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33138807 | ||||||
| chr9:33138927
|
C | T | 25 | a0001c0001t0001g0169a0001c0001t0004g0009a0001c0001t0004g0010others(22): Show | 28 | HG00280.hp1 HG00738.hp2 HG01070.hp2 others(25): Show |
intron_variant | MODIFIER | c.413-3503G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33138927 | ||||||
| chr9:33138935
|
C | T | 2 | a0001c0001t0067g0292a0001c0001t0068g0291 | 2 | HG01515.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.413-3511G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33138935 | ||||||
| chr9:33138975
|
T | TAC | 4 | a0001c0001t0001g0118a0001c0001t0001g0135a0001c0001t0003g0127others(1): Show | 4 | HG01081.hp1 HG01099.hp1 HG01099.hp2 others(1): Show |
intron_variant | MODIFIER | c.413-3553_413-3552d others(4): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33138975 | ||||||
| chr9:33139049
|
C | T | 1 | a0001c0001t0010g0256 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.413-3625G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33139049 | ||||||
| chr9:33139239
|
T | C | 168 | a0001c0001t0001g0017a0001c0001t0001g0198a0001c0001t0002g0012others(165): Show | 171 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(168): Show |
intron_variant | MODIFIER | c.413-3815A>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33139239 | ||||||
| chr9:33139455
|
C | T | 118 | a0001c0001t0001g0198a0001c0001t0002g0012a0001c0001t0002g0192others(115): Show | 119 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(116): Show |
intron_variant | MODIFIER | c.413-4031G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33139455 | ||||||
| chr9:33139620
|
T | C | 20 | a0001c0001t0001g0017a0001c0001t0011g0003a0001c0001t0011g0018others(17): Show | 22 | HG00280.hp2 HG00733.hp1 HG01358.hp2 others(19): Show |
intron_variant | MODIFIER | c.413-4196A>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33139620 | ||||||
| chr9:33139793
|
T | G | 1 | a0005c0005t0048g0289 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.413-4369A>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33139793 | ||||||
| chr9:33140218
|
C | G | 1 | a0001c0001t0003g0322 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.413-4794G>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33140218 | ||||||
| chr9:33140246
|
T | C | 1 | a0001c0001t0001g0083 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.413-4822A>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33140246 | ||||||
| chr9:33140249
|
T | C | 3 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0093 | 3 | HG01891.hp1 HG02818.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.413-4825A>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33140249 | ||||||
| chr9:33140354
|
A | C | 168 | a0001c0001t0001g0017a0001c0001t0001g0198a0001c0001t0002g0012others(165): Show | 171 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(168): Show |
intron_variant | MODIFIER | c.413-4930T>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33140354 | ||||||
| chr9:33140366
|
G | C | 1 | a0001c0001t0001g0169 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.413-4942C>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33140366 | ||||||
| chr9:33140478
|
AT | A | 142 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(139): Show | 149 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.413-5055delA | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33140478 | ||||||
| chr9:33140495
|
TA | T | 166 | a0001c0001t0001g0017a0001c0001t0001g0198a0001c0001t0002g0012others(163): Show | 169 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(166): Show |
intron_variant | MODIFIER | c.413-5072delT | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33140495 | ||||||
| chr9:33140599
|
G | A | 1 | a0005c0005t0048g0289 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.413-5175C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33140599 | ||||||
| chr9:33140664
|
G | A | 1 | a0001c0001t0002g0200 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.413-5240C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33140664 | ||||||
| chr9:33140753
|
C | T | 3 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0093 | 3 | HG01891.hp1 HG02818.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.413-5329G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33140753 | ||||||
| chr9:33140767
|
A | C | 1 | a0001c0001t0002g0237 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.413-5343T>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33140767 | ||||||
| chr9:33140791
|
C | G | 117 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(114): Show | 122 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.413-5367G>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33140791 | ||||||
| chr9:33140945
|
G | A | 1 | a0001c0001t0003g0317 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.413-5521C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33140945 | ||||||
| chr9:33140978
|
G | A | 168 | a0001c0001t0001g0017a0001c0001t0001g0198a0001c0001t0002g0012others(165): Show | 171 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(168): Show |
intron_variant | MODIFIER | c.413-5554C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33140978 | ||||||
| chr9:33141231
|
A | G | 193 | a0001c0001t0001g0017a0001c0001t0001g0169a0001c0001t0001g0198others(190): Show | 199 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(196): Show |
intron_variant | MODIFIER | c.413-5807T>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33141231 | ||||||
| chr9:33141252
|
C | T | 20 | a0001c0001t0001g0017a0001c0001t0011g0003a0001c0001t0011g0018others(17): Show | 22 | HG00280.hp2 HG00733.hp1 HG01358.hp2 others(19): Show |
intron_variant | MODIFIER | c.413-5828G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33141252 | ||||||
| chr9:33141322
|
A | G | 168 | a0001c0001t0001g0017a0001c0001t0001g0198a0001c0001t0002g0012others(165): Show | 171 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(168): Show |
intron_variant | MODIFIER | c.413-5898T>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33141322 | ||||||
| chr9:33141379
|
G | A | 1 | a0001c0001t0001g0099 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.413-5955C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33141379 | ||||||
| chr9:33141473
|
C | T | 2 | a0001c0001t0002g0213a0001c0001t0002g0236 | 2 | HG03225.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.413-6049G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33141473 | ||||||
| chr9:33141574
|
A | G | 1 | a0001c0001t0011g0026 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.413-6150T>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33141574 | ||||||
| chr9:33141605
|
T | C | 233 | a0001c0001t0001g0017a0001c0001t0001g0053a0001c0001t0001g0169others(230): Show | 241 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(238): Show |
intron_variant | MODIFIER | c.413-6181A>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33141605 | ||||||
| chr9:33141754
|
G | A | 233 | a0001c0001t0001g0017a0001c0001t0001g0053a0001c0001t0001g0169others(230): Show | 241 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(238): Show |
intron_variant | MODIFIER | c.413-6330C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33141754 | ||||||
| chr9:33141793
|
C | T | 168 | a0001c0001t0001g0017a0001c0001t0001g0198a0001c0001t0002g0012others(165): Show | 171 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(168): Show |
intron_variant | MODIFIER | c.413-6369G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33141793 | ||||||
| chr9:33141907
|
G | A | 1 | a0001c0001t0001g0053 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.413-6483C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33141907 | ||||||
| chr9:33141916
|
G | A | 1 | a0001c0001t0003g0312 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.413-6492C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33141916 | ||||||
| chr9:33142007
|
G | A | 27 | a0001c0001t0001g0316a0001c0001t0003g0001a0001c0001t0003g0299others(24): Show | 29 | HG00597.hp2 HG01070.hp1 HG02602.hp2 others(26): Show |
intron_variant | MODIFIER | c.413-6583C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33142007 | ||||||
| chr9:33142172
|
G | A | 168 | a0001c0001t0001g0017a0001c0001t0001g0198a0001c0001t0002g0012others(165): Show | 171 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(168): Show |
intron_variant | MODIFIER | c.413-6748C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33142172 | ||||||
| chr9:33142260
|
C | A | 168 | a0001c0001t0001g0017a0001c0001t0001g0198a0001c0001t0002g0012others(165): Show | 171 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(168): Show |
intron_variant | MODIFIER | c.413-6836G>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33142260 | ||||||
| chr9:33142414
|
G | A | 233 | a0001c0001t0001g0017a0001c0001t0001g0053a0001c0001t0001g0169others(230): Show | 241 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(238): Show |
intron_variant | MODIFIER | c.413-6990C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33142414 | ||||||
| chr9:33142648
|
G | A | 1 | a0001c0001t0001g0104 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.413-7224C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33142648 | ||||||
| chr9:33142730
|
G | A | 168 | a0001c0001t0001g0017a0001c0001t0001g0198a0001c0001t0002g0012others(165): Show | 171 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(168): Show |
intron_variant | MODIFIER | c.413-7306C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33142730 | ||||||
| chr9:33143006
|
G | A | 21 | a0001c0001t0001g0169a0001c0001t0004g0009a0001c0001t0004g0010others(18): Show | 23 | HG00280.hp1 HG00738.hp2 HG01070.hp2 others(20): Show |
intron_variant | MODIFIER | c.413-7582C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33143006 | ||||||
| chr9:33143027
|
C | G | 1 | a0001c0001t0020g0286 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.413-7603G>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33143027 | ||||||
| chr9:33143059
|
C | T | 1 | a0001c0001t0021g0166 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.413-7635G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33143059 | ||||||
| chr9:33143265
|
T | G | 1 | a0001c0001t0057g0052 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.413-7841A>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33143265 | ||||||
| chr9:33143579
|
T | C | 1 | a0001c0002t0006g0189 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.413-8155A>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33143579 | ||||||
| chr9:33143735
|
G | C | 20 | a0001c0001t0001g0017a0001c0001t0011g0003a0001c0001t0011g0018others(17): Show | 22 | HG00280.hp2 HG00733.hp1 HG01358.hp2 others(19): Show |
intron_variant | MODIFIER | c.413-8311C>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33143735 | ||||||
| chr9:33143824
|
T | C | 168 | a0001c0001t0001g0017a0001c0001t0001g0198a0001c0001t0002g0012others(165): Show | 171 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(168): Show |
intron_variant | MODIFIER | c.413-8400A>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33143824 | ||||||
| chr9:33143881
|
C | CT | 190 | a0001c0001t0001g0017a0001c0001t0001g0169a0001c0001t0001g0198others(187): Show | 196 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(193): Show |
intron_variant | MODIFIER | c.413-8458dupA | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33143881 | ||||||
| chr9:33143936
|
G | C | 3 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0093 | 3 | HG01891.hp1 HG02818.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.413-8512C>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33143936 | ||||||
| chr9:33144142
|
C | T | 1 | a0005c0005t0048g0289 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.413-8718G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33144142 | ||||||
| chr9:33144170
|
C | A | 1 | a0001c0001t0053g0105 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.413-8746G>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33144170 | ||||||
| chr9:33144338
|
G | A | 2 | a0001c0001t0006g0106a0001c0001t0026g0107 | 2 | HG03209.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.413-8914C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33144338 | ||||||
| chr9:33144425
|
G | A | 1 | a0002c0003t0029g0011 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.413-9001C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33144425 | ||||||
| chr9:33144605
|
C | G | 2 | a0001c0001t0001g0074a0001c0001t0001g0076 | 2 | HG00323.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.413-9181G>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33144605 | ||||||
| chr9:33144659
|
T | C | 1 | a0001c0001t0065g0041 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.413-9235A>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33144659 | ||||||
| chr9:33144697
|
G | A | 1 | a0001c0001t0003g0322 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.413-9273C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33144697 | ||||||
| chr9:33144780
|
G | A | 1 | a0001c0001t0002g0211 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.413-9356C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33144780 | ||||||
| chr9:33144811
|
C | T | 168 | a0001c0001t0001g0017a0001c0001t0001g0198a0001c0001t0002g0012others(165): Show | 171 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(168): Show |
intron_variant | MODIFIER | c.413-9387G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33144811 | ||||||
| chr9:33144877
|
G | A | 1 | a0001c0001t0019g0155 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.413-9453C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33144877 | ||||||
| chr9:33144935
|
G | A | 4 | a0001c0001t0066g0293a0001c0001t0067g0292a0001c0001t0068g0291others(1): Show | 4 | HG01081.hp2 HG01515.hp1 HG01978.hp1 others(1): Show |
intron_variant | MODIFIER | c.413-9511C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33144935 | ||||||
| chr9:33144937
|
G | C | 3 | a0001c0001t0001g0053a0001c0001t0019g0051a0001c0001t0057g0052 | 3 | HG01255.hp1 HG02280.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.413-9513C>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33144937 | ||||||
| chr9:33145083
|
G | A | 13 | a0001c0001t0001g0094a0001c0001t0001g0147a0001c0001t0001g0149others(10): Show | 13 | HG01099.hp1 HG01261.hp2 HG01358.hp1 others(10): Show |
intron_variant | MODIFIER | c.413-9659C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33145083 | ||||||
| chr9:33145545
|
T | C | 221 | a0001c0001t0001g0017a0001c0001t0001g0169a0001c0001t0001g0198others(218): Show | 229 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(226): Show |
intron_variant | MODIFIER | c.413-10121A>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33145545 | ||||||
| chr9:33145550
|
C | T | 1 | a0001c0001t0049g0130 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.413-10126G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33145550 | ||||||
| chr9:33145574
|
G | T | 1 | a0001c0001t0001g0135 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.413-10150C>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33145574 | ||||||
| chr9:33145649
|
C | CA | 191 | a0001c0001t0001g0017a0001c0001t0001g0198a0001c0001t0001g0316others(188): Show | 197 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(194): Show |
intron_variant | MODIFIER | c.413-10226dupT | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33145649 | ||||||
| chr9:33145805
|
G | T | 1 | a0001c0001t0003g0305 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.413-10381C>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33145805 | ||||||
| chr9:33146177
|
T | C | 3 | a0001c0001t0001g0053a0001c0001t0019g0051a0001c0001t0057g0052 | 3 | HG01255.hp1 HG02280.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.413-10753A>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33146177 | ||||||
| chr9:33146245
|
T | A | 1 | a0005c0005t0048g0289 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.413-10821A>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33146245 | ||||||
| chr9:33146305
|
T | C | 1 | a0002c0003t0029g0011 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.413-10881A>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33146305 | ||||||
| chr9:33146395
|
C | A | 213 | a0001c0001t0001g0017a0001c0001t0001g0198a0001c0001t0001g0316others(210): Show | 221 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(218): Show |
intron_variant | MODIFIER | c.413-10971G>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33146395 | ||||||
| chr9:33146403
|
T | A | 213 | a0001c0001t0001g0017a0001c0001t0001g0198a0001c0001t0001g0316others(210): Show | 221 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(218): Show |
intron_variant | MODIFIER | c.413-10979A>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33146403 | ||||||
| chr9:33146530
|
T | C | 216 | a0001c0001t0001g0017a0001c0001t0001g0169a0001c0001t0001g0198others(213): Show | 224 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(221): Show |
intron_variant | MODIFIER | c.413-11106A>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33146530 | ||||||
| chr9:33146697
|
CT | C | 310 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(307): Show | 320 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(317): Show |
intron_variant | MODIFIER | c.413-11274delA | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33146697 | ||||||
| chr9:33146697
|
CTT | C | 26 | a0001c0001t0001g0169a0001c0001t0004g0009a0001c0001t0004g0010others(23): Show | 29 | HG00280.hp1 HG00733.hp2 HG00738.hp2 others(26): Show |
intron_variant | MODIFIER | c.413-11275_413-1127 others(6): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33146697 | ||||||
| chr9:33146819
|
G | C | 1 | a0001c0001t0003g0299 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.413-11395C>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33146819 | ||||||
| chr9:33146876
|
T | G | 1 | a0001c0001t0063g0296 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.413-11452A>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33146876 | ||||||
| chr9:33147007
|
T | C | 3 | a0001c0001t0023g0172a0001c0001t0023g0173a0001c0001t0023g0174 | 3 | HG01074.hp1 HG02647.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.413-11583A>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33147007 | ||||||
| chr9:33147105
|
A | G | 13 | a0001c0001t0004g0009a0001c0001t0004g0010a0001c0001t0004g0157others(10): Show | 15 | HG00280.hp1 HG00738.hp2 HG01070.hp2 others(12): Show |
intron_variant | MODIFIER | c.413-11681T>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33147105 | ||||||
| chr9:33147245
|
CT | C | 18 | a0001c0001t0001g0053a0001c0001t0001g0074a0001c0001t0001g0076others(15): Show | 18 | HG00323.hp1 HG01081.hp2 HG01255.hp1 others(15): Show |
intron_variant | MODIFIER | c.413-11822delA | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33147245 | ||||||
| chr9:33147245
|
CTT | C | 212 | a0001c0001t0001g0017a0001c0001t0001g0169a0001c0001t0001g0198others(209): Show | 220 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(217): Show |
intron_variant | MODIFIER | c.413-11823_413-1182 others(6): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33147245 | ||||||
| chr9:33147257
|
T | C | 1 | a0001c0001t0001g0060 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.413-11833A>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33147257 | ||||||
| chr9:33147388
|
C | T | 3 | a0001c0001t0016g0125a0001c0001t0016g0136a0001c0001t0016g0137 | 3 | NA18522.hp1 NA19030.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.413-11964G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33147388 | ||||||
| chr9:33147433
|
G | C | 3 | a0001c0001t0023g0172a0001c0001t0023g0173a0001c0001t0023g0174 | 3 | HG01074.hp1 HG02647.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.413-12009C>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33147433 | ||||||
| chr9:33147481
|
G | A | 191 | a0001c0001t0001g0017a0001c0001t0001g0198a0001c0001t0001g0316others(188): Show | 196 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(193): Show |
intron_variant | MODIFIER | c.413-12057C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33147481 | ||||||
| chr9:33147529
|
GAGCC | G | 99 | a0001c0001t0001g0198a0001c0001t0002g0012a0001c0001t0002g0192others(96): Show | 100 | HG00323.hp2 HG00544.hp2 HG00558.hp2 others(97): Show |
intron_variant | MODIFIER | c.413-12109_413-1210 others(8): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33147529 | ||||||
| chr9:33147534
|
C | G | 99 | a0001c0001t0001g0198a0001c0001t0002g0012a0001c0001t0002g0192others(96): Show | 100 | HG00323.hp2 HG00544.hp2 HG00558.hp2 others(97): Show |
intron_variant | MODIFIER | c.413-12110G>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33147534 | ||||||
| chr9:33147646
|
C | T | 1 | a0001c0002t0006g0183 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.413-12222G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33147646 | ||||||
| chr9:33147860
|
T | C | 216 | a0001c0001t0001g0017a0001c0001t0001g0169a0001c0001t0001g0198others(213): Show | 224 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(221): Show |
intron_variant | MODIFIER | c.413-12436A>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33147860 | ||||||
| chr9:33147864
|
T | C | 1 | a0001c0001t0065g0041 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.413-12440A>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33147864 | ||||||
| chr9:33147993
|
C | T | 1 | a0001c0001t0001g0115 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.413-12569G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33147993 | ||||||
| chr9:33148001
|
T | C | 3 | a0001c0001t0007g0344a0001c0001t0007g0345a0001c0001t0012g0346 | 3 | HG01175.hp1 HG02572.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.413-12577A>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33148001 | ||||||
| chr9:33148035
|
TA | T | 4 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0093others(1): Show | 5 | HG01891.hp1 HG02818.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.413-12612delT | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33148035 | ||||||
| chr9:33148139
|
G | A | 2 | a0001c0001t0002g0279a0001c0001t0002g0280 | 2 | HG03516.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.413-12715C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33148139 | ||||||
| chr9:33148148
|
C | G | 1 | a0001c0001t0019g0155 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.413-12724G>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33148148 | ||||||
| chr9:33148300
|
T | C | 25 | a0001c0001t0001g0169a0001c0001t0004g0009a0001c0001t0004g0010others(22): Show | 28 | HG00280.hp1 HG00738.hp2 HG01070.hp2 others(25): Show |
intron_variant | MODIFIER | c.413-12876A>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33148300 | ||||||
| chr9:33148554
|
G | A | 191 | a0001c0001t0001g0017a0001c0001t0001g0198a0001c0001t0001g0316others(188): Show | 196 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(193): Show |
intron_variant | MODIFIER | c.413-13130C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33148554 | ||||||
| chr9:33148633
|
G | A | 24 | a0001c0001t0001g0169a0001c0001t0004g0009a0001c0001t0004g0010others(21): Show | 26 | HG00280.hp1 HG00738.hp2 HG01070.hp2 others(23): Show |
intron_variant | MODIFIER | c.413-13209C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33148633 | ||||||
| chr9:33148804
|
T | TAA | 7 | a0001c0001t0005g0193a0001c0001t0005g0218a0001c0001t0005g0233others(4): Show | 7 | HG01975.hp1 HG02451.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.413-13382_413-1338 others(6): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33148804 | ||||||
| chr9:33148804
|
T | TAAA | 170 | a0001c0001t0001g0017a0001c0001t0001g0198a0001c0001t0001g0316others(167): Show | 175 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(172): Show |
intron_variant | MODIFIER | c.413-13383_413-1338 others(7): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33148804 | ||||||
| chr9:33148804
|
T | TAAAA | 11 | a0001c0001t0002g0257a0001c0001t0004g0302a0001c0001t0012g0335others(8): Show | 11 | HG01106.hp2 HG01496.hp2 HG02293.hp2 others(8): Show |
intron_variant | MODIFIER | c.413-13384_413-1338 others(8): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33148804 | ||||||
| chr9:33148804
|
T | TAAAAAA | 19 | a0001c0001t0001g0169a0001c0001t0004g0009a0001c0001t0004g0010others(16): Show | 21 | HG00280.hp1 HG00738.hp2 HG01070.hp2 others(18): Show |
intron_variant | MODIFIER | c.413-13386_413-1338 others(10): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33148804 | ||||||
| chr9:33148804
|
T | TAAAAAAA | 6 | a0001c0001t0004g0160a0001c0001t0019g0153a0001c0001t0019g0154others(3): Show | 7 | HG01361.hp2 HG01891.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.413-13387_413-1338 others(11): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33148804 | ||||||
| chr9:33148824
|
C | T | 4 | a0001c0001t0066g0293a0001c0001t0067g0292a0001c0001t0068g0291others(1): Show | 4 | HG01081.hp2 HG01515.hp1 HG01978.hp1 others(1): Show |
intron_variant | MODIFIER | c.413-13400G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33148824 | ||||||
| chr9:33148836
|
T | C | 216 | a0001c0001t0001g0017a0001c0001t0001g0169a0001c0001t0001g0198others(213): Show | 224 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(221): Show |
intron_variant | MODIFIER | c.413-13412A>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33148836 | ||||||
| chr9:33149061
|
C | T | 2 | a0001c0001t0021g0165a0001c0001t0021g0167 | 2 | HG02258.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.413-13637G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33149061 | ||||||
| chr9:33149186
|
T | C | 25 | a0001c0001t0001g0169a0001c0001t0004g0009a0001c0001t0004g0010others(22): Show | 28 | HG00280.hp1 HG00738.hp2 HG01070.hp2 others(25): Show |
intron_variant | MODIFIER | c.413-13762A>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33149186 | ||||||
| chr9:33149194
|
A | T | 1 | a0001c0001t0001g0120 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.413-13770T>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33149194 | ||||||
| chr9:33149200
|
TA | T | 197 | a0001c0001t0001g0017a0001c0001t0001g0073a0001c0001t0001g0198others(194): Show | 202 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(199): Show |
intron_variant | MODIFIER | c.413-13777delT | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33149200 | ||||||
| chr9:33149209
|
A | G | 118 | a0001c0001t0001g0198a0001c0001t0002g0012a0001c0001t0002g0192others(115): Show | 119 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(116): Show |
intron_variant | MODIFIER | c.413-13785T>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33149209 | ||||||
| chr9:33149269
|
A | T | 1 | a0001c0001t0001g0110 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.413-13845T>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33149269 | ||||||
| chr9:33149270
|
A | T | 334 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(331): Show | 347 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(344): Show |
intron_variant | MODIFIER | c.413-13846T>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33149270 | ||||||
| chr9:33149342
|
G | A | 20 | a0001c0001t0001g0017a0001c0001t0011g0003a0001c0001t0011g0018others(17): Show | 22 | HG00280.hp2 HG00733.hp1 HG01358.hp2 others(19): Show |
intron_variant | MODIFIER | c.413-13918C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33149342 | ||||||
| chr9:33149367
|
G | A | 30 | a0001c0001t0004g0302a0001c0001t0007g0298a0001c0001t0007g0324others(27): Show | 30 | HG01106.hp2 HG01175.hp1 HG01884.hp2 others(27): Show |
intron_variant | MODIFIER | c.413-13943C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33149367 | ||||||
| chr9:33150047
|
T | C | 23 | a0001c0001t0001g0316a0001c0001t0003g0001a0001c0001t0003g0299others(20): Show | 25 | HG00597.hp2 HG01070.hp1 HG02602.hp2 others(22): Show |
intron_variant | MODIFIER | c.413-14623A>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33150047 | ||||||
| chr9:33150049
|
C | T | 5 | a0001c0001t0001g0088a0001c0001t0001g0095a0001c0001t0001g0097others(2): Show | 5 | HG01952.hp2 NA18962.hp2 NA18977.hp2 others(2): Show |
intron_variant | MODIFIER | c.413-14625G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33150049 | ||||||
| chr9:33150126
|
TATATAG | T | 27 | a0001c0001t0001g0053a0001c0001t0001g0169a0001c0001t0004g0009others(24): Show | 29 | HG00280.hp1 HG00738.hp2 HG01070.hp2 others(26): Show |
intron_variant | MODIFIER | c.413-14708_413-1470 others(10): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33150126 | ||||||
| chr9:33150142
|
T | TATACACA others(15): Show |
21 | a0001c0001t0001g0017a0001c0001t0011g0003a0001c0001t0011g0018others(18): Show | 24 | HG00280.hp2 HG00733.hp1 HG01358.hp2 others(21): Show |
intron_variant | MODIFIER | c.413-14719_413-1471 others(26): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33150142 | ||||||
| chr9:33150144
|
G | GATATATA others(21): Show |
194 | a0001c0001t0001g0169a0001c0001t0001g0198a0001c0001t0001g0316others(191): Show | 199 | HG00280.hp1 HG00323.hp2 HG00544.hp1 others(196): Show |
intron_variant | MODIFIER | c.413-14721_413-1472 others(32): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33150144 | ||||||
| chr9:33150144
|
G | T | 21 | a0001c0001t0001g0017a0001c0001t0011g0003a0001c0001t0011g0018others(18): Show | 24 | HG00280.hp2 HG00733.hp1 HG01358.hp2 others(21): Show |
intron_variant | MODIFIER | c.413-14720C>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33150144 | ||||||
| chr9:33150152
|
C | CACACATA others(19): Show |
2 | a0001c0002t0006g0182a0001c0002t0006g0185 | 2 | HG02165.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.413-14729_413-1472 others(30): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33150152 | ||||||
| chr9:33150159
|
A | T | 3 | a0001c0001t0023g0172a0001c0001t0023g0173a0001c0001t0023g0174 | 3 | HG01074.hp1 HG02647.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.413-14735T>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33150159 | ||||||
| chr9:33150162
|
T | C | 2 | a0001c0002t0006g0182a0001c0002t0006g0185 | 2 | HG02165.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.413-14738A>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33150162 | ||||||
| chr9:33150168
|
T | TGA | 21 | a0001c0001t0001g0046a0001c0001t0002g0208a0001c0001t0002g0238others(18): Show | 21 | HG00323.hp2 HG00673.hp1 HG00673.hp2 others(18): Show |
intron_variant | MODIFIER | c.413-14746_413-1474 others(6): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33150168 | ||||||
| chr9:33150233
|
T | TAC | 122 | a0001c0001t0001g0017a0001c0001t0001g0078a0001c0001t0001g0096others(119): Show | 124 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(121): Show |
intron_variant | MODIFIER | c.413-14811_413-1481 others(6): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33150233 | ||||||
| chr9:33150233
|
T | TACAC | 84 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(81): Show | 87 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(84): Show |
intron_variant | MODIFIER | c.413-14813_413-1481 others(8): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33150233 | ||||||
| chr9:33150233
|
T | TACACAC | 81 | a0001c0001t0001g0032a0001c0001t0001g0045a0001c0001t0001g0046others(78): Show | 84 | HG00140.hp2 HG00558.hp1 HG00597.hp2 others(81): Show |
intron_variant | MODIFIER | c.413-14815_413-1481 others(10): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33150233 | ||||||
| chr9:33150233
|
T | TACACACA others(1): Show |
14 | a0001c0001t0001g0008a0001c0001t0001g0088a0001c0001t0001g0093others(11): Show | 15 | HG01099.hp1 HG01358.hp1 HG01928.hp1 others(12): Show |
intron_variant | MODIFIER | c.413-14817_413-1481 others(12): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33150233 | ||||||
| chr9:33150233
|
T | TACACACA others(3): Show |
4 | a0001c0001t0001g0119a0001c0001t0001g0134a0001c0001t0003g0128others(1): Show | 4 | HG01070.hp1 HG01074.hp2 HG01261.hp2 others(1): Show |
intron_variant | MODIFIER | c.413-14819_413-1481 others(14): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33150233 | ||||||
| chr9:33150233
|
TAC | T | 9 | a0001c0001t0002g0196a0001c0001t0010g0232a0001c0001t0019g0153others(6): Show | 11 | HG01891.hp2 HG02559.hp2 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.413-14811_413-1481 others(6): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33150233 | ||||||
| chr9:33150233
|
TACAC | T | 18 | a0001c0001t0004g0010a0001c0001t0004g0157a0001c0001t0004g0158others(15): Show | 19 | HG00280.hp1 HG00738.hp2 HG01070.hp2 others(16): Show |
intron_variant | MODIFIER | c.413-14813_413-1481 others(8): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33150233 | ||||||
| chr9:33150233
|
TACACAC | T | 4 | a0001c0001t0001g0169a0001c0001t0004g0009a0001c0001t0021g0165others(1): Show | 5 | HG01192.hp2 HG02109.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.413-14815_413-1481 others(10): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33150233 | ||||||
| chr9:33150267
|
G | C | 1 | a0001c0001t0001g0078 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.413-14843C>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33150267 | ||||||
| chr9:33150270
|
C | A | 2 | a0001c0001t0001g0055a0001c0001t0001g0078 | 2 | HG00642.hp2 HG01168.hp1 |
intron_variant | MODIFIER | c.413-14846G>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33150270 | ||||||
| chr9:33150271
|
G | A | 4 | a0001c0001t0004g0302a0001c0001t0008g0304a0001c0001t0033g0301others(1): Show | 4 | HG02622.hp1 HG02717.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.413-14847C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33150271 | ||||||
| chr9:33150272
|
A | C | 1 | a0001c0001t0001g0078 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.413-14848T>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33150272 | ||||||
| chr9:33150320
|
C | T | 3 | a0001c0001t0023g0172a0001c0001t0023g0173a0001c0001t0023g0174 | 3 | HG01074.hp1 HG02647.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.413-14896G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33150320 | ||||||
| chr9:33150411
|
T | TA | 216 | a0001c0001t0001g0017a0001c0001t0001g0169a0001c0001t0001g0198others(213): Show | 224 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(221): Show |
intron_variant | MODIFIER | c.413-14988dupT | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33150411 | ||||||
| chr9:33150552
|
G | A | 4 | a0001c0001t0001g0169a0001c0001t0021g0165a0001c0001t0021g0166others(1): Show | 4 | HG01192.hp2 HG02258.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.413-15128C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33150552 | ||||||
| chr9:33150606
|
A | G | 1 | a0001c0001t0001g0120 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.413-15182T>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33150606 | ||||||
| chr9:33150719
|
A | G | 1 | a0005c0005t0048g0289 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.413-15295T>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33150719 | ||||||
| chr9:33150764
|
T | C | 1 | a0001c0001t0003g0321 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.413-15340A>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33150764 | ||||||
| chr9:33150845
|
G | A | 344 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(341): Show | 357 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(354): Show |
intron_variant | MODIFIER | c.413-15421C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33150845 | ||||||
| chr9:33150973
|
AGAAG | A | 118 | a0001c0001t0001g0198a0001c0001t0002g0012a0001c0001t0002g0192others(115): Show | 119 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(116): Show |
intron_variant | MODIFIER | c.413-15553_413-1555 others(8): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33150973 | ||||||
| chr9:33151098
|
G | A | 4 | a0001c0001t0019g0153a0001c0001t0019g0154a0001c0001t0019g0155others(1): Show | 4 | HG01891.hp2 HG02717.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.412+15660C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33151098 | ||||||
| chr9:33151237
|
T | G | 1 | a0001c0001t0056g0320 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.412+15521A>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33151237 | ||||||
| chr9:33151417
|
C | T | 20 | a0001c0001t0001g0017a0001c0001t0011g0003a0001c0001t0011g0018others(17): Show | 22 | HG00280.hp2 HG00733.hp1 HG01358.hp2 others(19): Show |
intron_variant | MODIFIER | c.412+15341G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33151417 | ||||||
| chr9:33151492
|
C | T | 1 | a0001c0001t0001g0090 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.412+15266G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33151492 | ||||||
| chr9:33151858
|
A | G | 1 | a0001c0001t0001g0124 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.412+14900T>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33151858 | ||||||
| chr9:33152122
|
T | C | 1 | a0001c0001t0001g0060 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.412+14636A>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33152122 | ||||||
| chr9:33152134
|
G | A | 4 | a0001c0001t0019g0153a0001c0001t0019g0154a0001c0001t0019g0155others(1): Show | 4 | HG01891.hp2 HG02717.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.412+14624C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33152134 | ||||||
| chr9:33152241
|
T | G | 1 | a0001c0001t0070g0123 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.412+14517A>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33152241 | ||||||
| chr9:33152309
|
A | AATAAC | 39 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(36): Show | 43 | HG00140.hp1 HG00323.hp1 HG00609.hp2 others(40): Show |
intron_variant | MODIFIER | c.412+14444_412+1444 others(9): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33152309 | ||||||
| chr9:33152309
|
A | AATAACAT others(3): Show |
15 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0081others(12): Show | 15 | HG01099.hp1 HG01167.hp2 HG01261.hp2 others(12): Show |
intron_variant | MODIFIER | c.412+14439_412+1444 others(14): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33152309 | ||||||
| chr9:33152309
|
A | AATAACAT others(8): Show |
3 | a0001c0001t0001g0080a0001c0001t0003g0126a0001c0001t0007g0062 | 3 | HG01993.hp2 HG02071.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.412+14434_412+1444 others(19): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33152309 | ||||||
| chr9:33152309
|
AATAAC | A | 23 | a0001c0001t0001g0057a0001c0001t0001g0092a0001c0001t0001g0093others(20): Show | 23 | HG00140.hp2 HG00735.hp2 HG00741.hp2 others(20): Show |
intron_variant | MODIFIER | c.412+14444_412+1444 others(9): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33152309 | ||||||
| chr9:33152309
|
AATAACAT others(3): Show |
A | 8 | a0001c0001t0001g0142a0001c0001t0001g0145a0001c0001t0018g0139others(5): Show | 8 | HG00642.hp1 HG01993.hp1 HG02080.hp1 others(5): Show |
intron_variant | MODIFIER | c.412+14439_412+1444 others(14): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33152309 | ||||||
| chr9:33152309
|
AATAACAT others(8): Show |
A | 3 | a0001c0001t0023g0172a0001c0001t0023g0173a0001c0001t0023g0174 | 3 | HG01074.hp1 HG02647.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.412+14434_412+1444 others(19): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33152309 | ||||||
| chr9:33152339
|
CAT | C | 118 | a0001c0001t0001g0198a0001c0001t0002g0012a0001c0001t0002g0192others(115): Show | 119 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(116): Show |
intron_variant | MODIFIER | c.412+14417_412+1441 others(6): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33152339 | ||||||
| chr9:33152351
|
TAACATAA others(12): Show |
T | 3 | a0001c0001t0007g0338a0001c0001t0012g0332a0001c0001t0012g0333 | 3 | HG02896.hp1 HG03540.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.412+14388_412+1440 others(23): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33152351 | ||||||
| chr9:33152356
|
TAACATAA others(7): Show |
T | 4 | a0001c0001t0003g0299a0001c0001t0003g0309a0001c0001t0003g0314others(1): Show | 4 | NA18947.hp1 NA19070.hp2 NA19079.hp2 others(1): Show |
intron_variant | MODIFIER | c.412+14388_412+1440 others(18): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33152356 | ||||||
| chr9:33152356
|
TAACATAA others(8): Show |
T | 1 | a0001c0001t0001g0078 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.412+14387_412+1440 others(19): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33152356 | ||||||
| chr9:33152361
|
TAACATAA others(2): Show |
T | 40 | a0001c0001t0001g0316a0001c0001t0003g0001a0001c0001t0003g0300others(37): Show | 43 | HG00280.hp2 HG00597.hp2 HG00733.hp1 others(40): Show |
intron_variant | MODIFIER | c.412+14388_412+1439 others(13): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33152361 | ||||||
| chr9:33152361
|
TAACATAA others(3): Show |
T | 1 | a0001c0001t0001g0058 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.412+14387_412+1439 others(14): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33152361 | ||||||
| chr9:33152366
|
TAACA | T | 138 | a0001c0001t0001g0017a0001c0001t0001g0198a0001c0001t0002g0012others(135): Show | 140 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(137): Show |
intron_variant | MODIFIER | c.412+14388_412+1439 others(8): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33152366 | ||||||
| chr9:33152370
|
A | AT | 6 | a0001c0001t0003g0318a0001c0001t0010g0232a0001c0001t0011g0025others(3): Show | 6 | NA18747.hp1 NA18950.hp1 NA18959.hp1 others(3): Show |
intron_variant | MODIFIER | c.412+14387_412+1438 others(5): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33152370 | ||||||
| chr9:33152371
|
A | T | 36 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(33): Show | 39 | HG00140.hp1 HG00323.hp1 HG00642.hp2 others(36): Show |
intron_variant | MODIFIER | c.412+14387T>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33152371 | ||||||
| chr9:33152400
|
AAAG | A | 4 | a0001c0001t0004g0302a0001c0001t0008g0304a0001c0001t0033g0301others(1): Show | 4 | HG02622.hp1 HG02717.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.412+14355_412+1435 others(7): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33152400 | ||||||
| chr9:33152453
|
A | G | 2 | a0001c0001t0011g0003a0001c0001t0058g0016 | 3 | NA18961.hp1 NA18995.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.412+14305T>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33152453 | ||||||
| chr9:33152556
|
T | TA | 6 | a0001c0001t0001g0169a0001c0001t0002g0228a0001c0001t0003g0308others(3): Show | 6 | HG02258.hp1 HG02622.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.412+14201dupT | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33152556 | ||||||
| chr9:33152624
|
C | T | 68 | a0001c0001t0001g0198a0001c0001t0002g0012a0001c0001t0002g0195others(65): Show | 69 | HG00323.hp2 HG00544.hp2 HG00609.hp1 others(66): Show |
intron_variant | MODIFIER | c.412+14134G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33152624 | ||||||
| chr9:33153020
|
A | G | 5 | a0001c0001t0015g0254a0001c0001t0015g0255a0001c0001t0015g0261others(2): Show | 5 | NA18945.hp2 NA18954.hp1 NA18988.hp1 others(2): Show |
intron_variant | MODIFIER | c.412+13738T>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33153020 | ||||||
| chr9:33153088
|
G | A | 4 | a0001c0001t0001g0169a0001c0001t0021g0165a0001c0001t0021g0166others(1): Show | 4 | HG01192.hp2 HG02258.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.412+13670C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33153088 | ||||||
| chr9:33153275
|
G | A | 7 | a0001c0001t0001g0112a0001c0001t0001g0113a0001c0001t0001g0115others(4): Show | 7 | HG01081.hp1 HG01099.hp2 HG01123.hp1 others(4): Show |
intron_variant | MODIFIER | c.412+13483C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33153275 | ||||||
| chr9:33153529
|
G | T | 118 | a0001c0001t0001g0198a0001c0001t0002g0012a0001c0001t0002g0192others(115): Show | 119 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(116): Show |
intron_variant | MODIFIER | c.412+13229C>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33153529 | ||||||
| chr9:33153708
|
G | A | 53 | a0001c0001t0001g0316a0001c0001t0003g0001a0001c0001t0003g0299others(50): Show | 55 | HG00597.hp2 HG01070.hp1 HG01106.hp2 others(52): Show |
intron_variant | MODIFIER | c.412+13050C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33153708 | ||||||
| chr9:33153767
|
T | G | 1 | a0001c0001t0009g0042 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.412+12991A>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33153767 | ||||||
| chr9:33153871
|
C | A | 1 | a0001c0001t0003g0319 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.412+12887G>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33153871 | ||||||
| chr9:33153900
|
G | A | 1 | a0001c0001t0002g0282 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.412+12858C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33153900 | ||||||
| chr9:33153912
|
C | G | 1 | a0002c0003t0029g0011 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.412+12846G>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33153912 | ||||||
| chr9:33154002
|
G | GGA | 11 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0001t0001g0080others(8): Show | 11 | HG01192.hp1 HG01952.hp1 HG01981.hp1 others(8): Show |
intron_variant | MODIFIER | c.412+12754_412+1275 others(6): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33154002 | ||||||
| chr9:33154018
|
A | G | 1 | a0001c0001t0005g0264 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.412+12740T>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33154018 | ||||||
| chr9:33154019
|
G | A | 1 | a0001c0001t0005g0264 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.412+12739C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33154019 | ||||||
| chr9:33154019
|
GAGGA | G | 4 | a0001c0001t0004g0302a0001c0001t0008g0304a0001c0001t0033g0301others(1): Show | 4 | HG02622.hp1 HG02717.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.412+12735_412+1273 others(8): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33154019 | ||||||
| chr9:33154031
|
A | AAGGG | 28 | a0001c0001t0002g0192a0001c0001t0002g0210a0001c0001t0002g0212others(25): Show | 28 | HG00558.hp2 HG00597.hp1 HG00673.hp1 others(25): Show |
intron_variant | MODIFIER | c.412+12723_412+1272 others(8): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33154031 | ||||||
| chr9:33154031
|
A | G | 1 | a0001c0001t0005g0264 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.412+12727T>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33154031 | ||||||
| chr9:33154031
|
AAGGG | A | 111 | a0001c0001t0001g0017a0001c0001t0001g0117a0001c0001t0001g0169others(108): Show | 116 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(113): Show |
intron_variant | MODIFIER | c.412+12723_412+1272 others(8): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33154031 | ||||||
| chr9:33154031
|
AAGGGAGG others(5): Show |
A | 8 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0055others(5): Show | 10 | HG00642.hp2 HG01081.hp2 HG01167.hp1 others(7): Show |
intron_variant | MODIFIER | c.412+12715_412+1272 others(16): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33154031 | ||||||
| chr9:33154110
|
C | T | 4 | a0001c0001t0066g0293a0001c0001t0067g0292a0001c0001t0068g0291others(1): Show | 4 | HG01081.hp2 HG01515.hp1 HG01978.hp1 others(1): Show |
intron_variant | MODIFIER | c.412+12648G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33154110 | ||||||
| chr9:33154187
|
T | C | 1 | a0001c0002t0006g0184 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.412+12571A>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33154187 | ||||||
| chr9:33154410
|
T | C | 2 | a0001c0002t0006g0229a0001c0002t0022g0241 | 2 | NA18940.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.412+12348A>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33154410 | ||||||
| chr9:33154481
|
C | T | 1 | a0001c0001t0001g0032 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.412+12277G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33154481 | ||||||
| chr9:33154578
|
C | A | 1 | a0001c0001t0002g0284 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.412+12180G>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33154578 | ||||||
| chr9:33154592
|
C | T | 343 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(340): Show | 356 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(353): Show |
intron_variant | MODIFIER | c.412+12166G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33154592 | ||||||
| chr9:33154796
|
T | A | 1 | a0001c0001t0001g0169 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.412+11962A>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33154796 | ||||||
| chr9:33155427
|
T | C | 18 | a0001c0002t0006g0178a0001c0002t0006g0179a0001c0002t0006g0182others(15): Show | 18 | HG00544.hp1 HG01257.hp1 HG02165.hp1 others(15): Show |
intron_variant | MODIFIER | c.412+11331A>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33155427 | ||||||
| chr9:33155630
|
T | C | 1 | a0001c0001t0001g0118 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.412+11128A>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33155630 | ||||||
| chr9:33155678
|
C | G | 2 | a0001c0002t0014g0175a0001c0002t0014g0176 | 2 | NA19066.hp2 NA19072.hp1 |
intron_variant | MODIFIER | c.412+11080G>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33155678 | ||||||
| chr9:33155957
|
C | T | 27 | a0001c0001t0001g0316a0001c0001t0003g0001a0001c0001t0003g0299others(24): Show | 29 | HG00597.hp2 HG01070.hp1 HG02602.hp2 others(26): Show |
intron_variant | MODIFIER | c.412+10801G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33155957 | ||||||
| chr9:33156166
|
C | T | 1 | a0001c0001t0019g0051 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.412+10592G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33156166 | ||||||
| chr9:33156674
|
A | G | 1 | a0001c0001t0001g0054 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.412+10084T>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33156674 | ||||||
| chr9:33156723
|
G | A | 1 | a0001c0001t0001g0119 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.412+10035C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33156723 | ||||||
| chr9:33156741
|
G | A | 6 | a0001c0001t0002g0251a0001c0001t0002g0265a0001c0001t0005g0264others(3): Show | 6 | HG00558.hp2 HG00597.hp1 HG00673.hp1 others(3): Show |
intron_variant | MODIFIER | c.412+10017C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33156741 | ||||||
| chr9:33157063
|
T | TAC | 30 | a0001c0001t0001g0017a0001c0001t0001g0055a0001c0001t0001g0094others(27): Show | 32 | HG00280.hp2 HG00558.hp1 HG00642.hp2 others(29): Show |
intron_variant | MODIFIER | c.412+9693_412+9694d others(4): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33157063 | ||||||
| chr9:33157063
|
T | TACAC | 8 | a0001c0001t0004g0170a0001c0001t0008g0327a0001c0001t0008g0328others(5): Show | 8 | HG01891.hp2 HG02280.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.412+9691_412+9694d others(6): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33157063 | ||||||
| chr9:33157063
|
T | TACACAC | 10 | a0001c0001t0001g0006a0001c0001t0001g0053a0001c0001t0002g0211others(7): Show | 12 | HG01167.hp1 HG01169.hp1 HG01255.hp1 others(9): Show |
intron_variant | MODIFIER | c.412+9689_412+9694d others(8): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33157063 | ||||||
| chr9:33157063
|
T | TACACACA others(1): Show |
12 | a0001c0001t0003g0319a0001c0001t0007g0330a0001c0001t0008g0331others(9): Show | 13 | HG01070.hp1 HG01884.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.412+9687_412+9694d others(10): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33157063 | ||||||
| chr9:33157063
|
T | TACACACA others(3): Show |
17 | a0001c0001t0002g0210a0001c0001t0002g0266a0001c0001t0003g0310others(14): Show | 17 | HG01496.hp2 HG02293.hp2 HG02559.hp1 others(14): Show |
intron_variant | MODIFIER | c.412+9685_412+9694d others(12): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33157063 | ||||||
| chr9:33157063
|
T | TACACACA others(5): Show |
25 | a0001c0001t0001g0169a0001c0001t0002g0212a0001c0001t0002g0275others(22): Show | 25 | HG00544.hp1 HG01106.hp2 HG01175.hp1 others(22): Show |
intron_variant | MODIFIER | c.412+9683_412+9694d others(14): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33157063 | ||||||
| chr9:33157063
|
T | TACACACA others(7): Show |
22 | a0001c0001t0002g0192a0001c0001t0002g0200a0001c0001t0002g0208others(19): Show | 24 | HG00597.hp2 HG00741.hp1 HG02027.hp1 others(21): Show |
intron_variant | MODIFIER | c.412+9681_412+9694d others(16): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33157063 | ||||||
| chr9:33157063
|
T | TACACACA others(9): Show |
13 | a0001c0001t0001g0316a0001c0001t0002g0230a0001c0001t0002g0234others(10): Show | 13 | HG02257.hp2 HG02630.hp1 HG02683.hp2 others(10): Show |
intron_variant | MODIFIER | c.412+9679_412+9694d others(18): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33157063 | ||||||
| chr9:33157063
|
T | TACACACA others(11): Show |
18 | a0001c0001t0002g0215a0001c0001t0002g0236a0001c0001t0002g0237others(15): Show | 18 | HG01261.hp1 HG01361.hp1 HG02080.hp2 others(15): Show |
intron_variant | MODIFIER | c.412+9677_412+9694d others(20): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33157063 | ||||||
| chr9:33157063
|
T | TACACACA others(13): Show |
11 | a0001c0001t0002g0196a0001c0001t0002g0269a0001c0001t0002g0279others(8): Show | 11 | HG00544.hp2 HG01975.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.412+9675_412+9694d others(22): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33157063 | ||||||
| chr9:33157063
|
T | TACACACA others(15): Show |
20 | a0001c0001t0001g0198a0001c0001t0002g0195a0001c0001t0002g0219others(17): Show | 20 | HG00323.hp2 HG00609.hp1 HG00673.hp1 others(17): Show |
intron_variant | MODIFIER | c.412+9673_412+9694d others(24): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33157063 | ||||||
| chr9:33157063
|
T | TACACACA others(17): Show |
12 | a0001c0001t0002g0253a0001c0001t0002g0257a0001c0001t0002g0259others(9): Show | 12 | HG01884.hp1 HG02071.hp2 HG02165.hp2 others(9): Show |
intron_variant | MODIFIER | c.412+9671_412+9694d others(26): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33157063 | ||||||
| chr9:33157063
|
T | TACACACA others(19): Show |
8 | a0001c0001t0002g0012a0001c0001t0002g0273a0001c0001t0002g0274others(5): Show | 9 | HG01069.hp2 HG01071.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.412+9669_412+9694d others(28): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33157063 | ||||||
| chr9:33157063
|
T | TACACACA others(21): Show |
3 | a0001c0001t0005g0264a0001c0001t0020g0285a0001c0001t0023g0173 | 3 | HG00597.hp1 HG02027.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.412+9667_412+9694d others(30): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33157063 | ||||||
| chr9:33157063
|
T | TACACACA others(23): Show |
2 | a0001c0001t0020g0286a0006c0007t0002g0350 | 2 | HG02055.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.412+9665_412+9694d others(32): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33157063 | ||||||
| chr9:33157063
|
T | TACACACA others(25): Show |
1 | a0001c0001t0023g0174 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.412+9663_412+9694d others(34): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33157063 | ||||||
| chr9:33157063
|
T | TACACACA others(27): Show |
1 | a0001c0001t0002g0265 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.412+9661_412+9694d others(36): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33157063 | ||||||
| chr9:33157063
|
T | TCACACAC others(18): Show |
1 | a0001c0001t0002g0260 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.412+9694_412+9695i others(27): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33157063 | ||||||
| chr9:33157063
|
TAC | T | 95 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(92): Show | 99 | HG00140.hp1 HG00140.hp2 HG00609.hp2 others(96): Show |
intron_variant | MODIFIER | c.412+9693_412+9694d others(4): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33157063 | ||||||
| chr9:33157063
|
TACACACA others(5): Show |
T | 10 | a0001c0001t0004g0010a0001c0001t0004g0157a0001c0001t0004g0158others(7): Show | 11 | HG00280.hp1 HG00738.hp2 HG01070.hp2 others(8): Show |
intron_variant | MODIFIER | c.412+9683_412+9694d others(14): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33157063 | ||||||
| chr9:33157063
|
TACACACA others(9): Show |
T | 1 | a0005c0005t0048g0289 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.412+9679_412+9694d others(18): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33157063 | ||||||
| chr9:33157101
|
C | CACACACA others(16): Show |
1 | a0001c0001t0005g0199 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.412+9656_412+9657i others(25): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33157101 | ||||||
| chr9:33157121
|
T | TAC | 88 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0032others(85): Show | 92 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(89): Show |
intron_variant | MODIFIER | c.412+9635_412+9636d others(4): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33157121 | ||||||
| chr9:33157121
|
T | TACAC | 62 | a0001c0001t0001g0005a0001c0001t0001g0055a0001c0001t0001g0080others(59): Show | 63 | HG00642.hp2 HG00741.hp1 HG01074.hp2 others(60): Show |
intron_variant | MODIFIER | c.412+9633_412+9636d others(6): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33157121 | ||||||
| chr9:33157121
|
T | TACACAC | 84 | a0001c0001t0001g0006a0001c0001t0001g0084a0001c0001t0001g0085others(81): Show | 87 | HG00323.hp2 HG00558.hp2 HG00597.hp1 others(84): Show |
intron_variant | MODIFIER | c.412+9631_412+9636d others(8): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33157121 | ||||||
| chr9:33157121
|
T | TACACACA others(1): Show |
54 | a0001c0001t0001g0198a0001c0001t0002g0192a0001c0001t0002g0196others(51): Show | 55 | HG00280.hp2 HG00544.hp1 HG00544.hp2 others(52): Show |
intron_variant | MODIFIER | c.412+9629_412+9636d others(10): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33157121 | ||||||
| chr9:33157121
|
T | TACACACA others(3): Show |
20 | a0001c0001t0001g0017a0001c0001t0002g0275a0001c0001t0002g0276others(17): Show | 21 | HG00280.hp1 HG01358.hp2 HG01433.hp2 others(18): Show |
intron_variant | MODIFIER | c.412+9627_412+9636d others(12): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33157121 | ||||||
| chr9:33157121
|
T | TACACACA others(5): Show |
7 | a0001c0001t0001g0169a0001c0001t0002g0284a0001c0001t0003g0319others(4): Show | 8 | HG00733.hp1 HG01070.hp1 HG01070.hp2 others(5): Show |
intron_variant | MODIFIER | c.412+9625_412+9636d others(14): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33157121 | ||||||
| chr9:33157121
|
T | TACACACA others(7): Show |
2 | a0001c0001t0019g0155a0001c0001t0032g0024 | 2 | HG03471.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.412+9623_412+9636d others(16): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33157121 | ||||||
| chr9:33157121
|
T | TACACACA others(9): Show |
3 | a0001c0001t0004g0170a0001c0001t0011g0025a0001c0001t0019g0051 | 3 | HG02280.hp2 HG02630.hp2 NA18959.hp1 |
intron_variant | MODIFIER | c.412+9621_412+9636d others(18): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33157121 | ||||||
| chr9:33157121
|
T | TACACACA others(11): Show |
1 | a0001c0001t0057g0052 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.412+9619_412+9636d others(20): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33157121 | ||||||
| chr9:33157121
|
T | TACACACA others(13): Show |
2 | a0001c0001t0001g0053a0001c0001t0011g0026 | 2 | HG01255.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.412+9617_412+9636d others(22): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33157121 | ||||||
| chr9:33157121
|
T | TACACACA others(15): Show |
1 | a0001c0001t0045g0156 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.412+9615_412+9636d others(24): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33157121 | ||||||
| chr9:33157121
|
TAC | T | 5 | a0001c0001t0001g0058a0001c0001t0001g0088a0001c0001t0025g0351others(2): Show | 5 | HG01175.hp2 HG02293.hp1 HG02738.hp1 others(2): Show |
intron_variant | MODIFIER | c.412+9635_412+9636d others(4): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33157121 | ||||||
| chr9:33157303
|
T | C | 1 | a0001c0001t0002g0195 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.412+9455A>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33157303 | ||||||
| chr9:33157421
|
G | T | 217 | a0001c0001t0001g0017a0001c0001t0001g0169a0001c0001t0001g0198others(214): Show | 225 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(222): Show |
intron_variant | MODIFIER | c.412+9337C>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33157421 | ||||||
| chr9:33157594
|
A | C | 23 | a0001c0001t0001g0316a0001c0001t0003g0001a0001c0001t0003g0299others(20): Show | 25 | HG00597.hp2 HG01070.hp1 HG02602.hp2 others(22): Show |
intron_variant | MODIFIER | c.412+9164T>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33157594 | ||||||
| chr9:33157636
|
T | C | 4 | a0001c0001t0066g0293a0001c0001t0067g0292a0001c0001t0068g0291others(1): Show | 4 | HG01081.hp2 HG01515.hp1 HG01978.hp1 others(1): Show |
intron_variant | MODIFIER | c.412+9122A>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33157636 | ||||||
| chr9:33157654
|
T | C | 23 | a0001c0001t0001g0316a0001c0001t0003g0001a0001c0001t0003g0299others(20): Show | 25 | HG00597.hp2 HG01070.hp1 HG02602.hp2 others(22): Show |
intron_variant | MODIFIER | c.412+9104A>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33157654 | ||||||
| chr9:33157658
|
G | T | 2 | a0001c0001t0007g0324a0001c0001t0007g0325 | 2 | HG02615.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.412+9100C>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33157658 | ||||||
| chr9:33157717
|
TA | T | 154 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(151): Show | 161 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(158): Show |
intron_variant | MODIFIER | c.412+9040delT | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33157717 | ||||||
| chr9:33157853
|
G | T | 1 | a0002c0003t0029g0011 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.412+8905C>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33157853 | ||||||
| chr9:33158282
|
G | A | 344 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(341): Show | 357 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(354): Show |
intron_variant | MODIFIER | c.412+8476C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33158282 | ||||||
| chr9:33158342
|
A | G | 1 | a0001c0002t0014g0287 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.412+8416T>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33158342 | ||||||
| chr9:33158401
|
T | C | 18 | a0001c0002t0006g0178a0001c0002t0006g0179a0001c0002t0006g0182others(15): Show | 18 | HG00544.hp1 HG01257.hp1 HG02165.hp1 others(15): Show |
intron_variant | MODIFIER | c.412+8357A>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33158401 | ||||||
| chr9:33158559
|
G | A | 20 | a0001c0001t0001g0017a0001c0001t0011g0003a0001c0001t0011g0018others(17): Show | 22 | HG00280.hp2 HG00733.hp1 HG01358.hp2 others(19): Show |
intron_variant | MODIFIER | c.412+8199C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33158559 | ||||||
| chr9:33158579
|
G | A | 53 | a0001c0001t0001g0316a0001c0001t0003g0001a0001c0001t0003g0299others(50): Show | 55 | HG00597.hp2 HG01070.hp1 HG01106.hp2 others(52): Show |
intron_variant | MODIFIER | c.412+8179C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33158579 | ||||||
| chr9:33158673
|
G | A | 2 | a0001c0001t0001g0145a0001c0001t0018g0144 | 2 | HG00642.hp1 HG00741.hp2 |
intron_variant | MODIFIER | c.412+8085C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33158673 | ||||||
| chr9:33158678
|
G | T | 2 | a0001c0002t0014g0175a0001c0002t0014g0176 | 2 | NA19066.hp2 NA19072.hp1 |
intron_variant | MODIFIER | c.412+8080C>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33158678 | ||||||
| chr9:33158703
|
G | A | 1 | a0001c0001t0050g0033 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.412+8055C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33158703 | ||||||
| chr9:33159747
|
G | A | 5 | a0001c0001t0013g0027a0001c0001t0013g0028a0001c0001t0013g0029others(2): Show | 5 | HG00280.hp2 NA18950.hp1 NA18974.hp2 others(2): Show |
intron_variant | MODIFIER | c.412+7011C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33159747 | ||||||
| chr9:33160119
|
A | G | 10 | a0001c0001t0002g0200a0001c0001t0005g0193a0001c0001t0005g0199others(7): Show | 10 | HG00544.hp2 HG00609.hp1 HG02027.hp1 others(7): Show |
intron_variant | MODIFIER | c.412+6639T>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33160119 | ||||||
| chr9:33160248
|
CT | C | 24 | a0001c0001t0001g0169a0001c0001t0004g0009a0001c0001t0004g0010others(21): Show | 26 | HG00280.hp1 HG00738.hp2 HG01070.hp2 others(23): Show |
intron_variant | MODIFIER | c.412+6509delA | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33160248 | ||||||
| chr9:33160613
|
A | G | 39 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(36): Show | 42 | HG00140.hp1 HG00323.hp1 HG00642.hp2 others(39): Show |
intron_variant | MODIFIER | c.412+6145T>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33160613 | ||||||
| chr9:33160689
|
C | T | 1 | a0001c0001t0001g0198 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.412+6069G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33160689 | ||||||
| chr9:33160714
|
C | T | 1 | a0001c0001t0001g0032 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.412+6044G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33160714 | ||||||
| chr9:33160781
|
A | T | 4 | a0001c0001t0066g0293a0001c0001t0067g0292a0001c0001t0068g0291others(1): Show | 4 | HG01081.hp2 HG01515.hp1 HG01978.hp1 others(1): Show |
intron_variant | MODIFIER | c.412+5977T>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33160781 | ||||||
| chr9:33160976
|
C | A | 1 | a0001c0001t0050g0033 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.412+5782G>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33160976 | ||||||
| chr9:33161005
|
T | C | 1 | a0001c0001t0012g0346 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.412+5753A>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33161005 | ||||||
| chr9:33161021
|
T | TTC | 138 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(135): Show | 145 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.412+5735_412+5736d others(4): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33161021 | ||||||
| chr9:33161021
|
T | TTCTC | 11 | a0001c0001t0001g0140a0001c0001t0001g0141a0001c0001t0001g0142others(8): Show | 11 | HG00642.hp1 HG00741.hp2 HG01081.hp2 others(8): Show |
intron_variant | MODIFIER | c.412+5733_412+5736d others(6): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33161021 | ||||||
| chr9:33161080
|
C | A | 1 | a0001c0001t0009g0042 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.412+5678G>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33161080 | ||||||
| chr9:33161179
|
C | G | 5 | a0001c0001t0019g0153a0001c0001t0019g0154a0001c0001t0019g0155others(2): Show | 6 | HG01891.hp2 HG02717.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.412+5579G>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33161179 | ||||||
| chr9:33161223
|
G | A | 1 | a0001c0001t0008g0348 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.412+5535C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33161223 | ||||||
| chr9:33161443
|
T | G | 1 | a0001c0001t0001g0146 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.412+5315A>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33161443 | ||||||
| chr9:33161545
|
G | A | 1 | a0001c0002t0022g0190 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.412+5213C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33161545 | ||||||
| chr9:33161833
|
G | C | 4 | a0001c0001t0066g0293a0001c0001t0067g0292a0001c0001t0068g0291others(1): Show | 4 | HG01081.hp2 HG01515.hp1 HG01978.hp1 others(1): Show |
intron_variant | MODIFIER | c.412+4925C>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33161833 | ||||||
| chr9:33161840
|
A | G | 1 | a0001c0001t0034g0197 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.412+4918T>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33161840 | ||||||
| chr9:33161891
|
T | C | 1 | a0001c0001t0056g0320 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.412+4867A>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33161891 | ||||||
| chr9:33162258
|
AGTTTCTG others(15): Show |
A | 1 | a0001c0001t0001g0086 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.412+4478_412+4499d others(24): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33162258 | ||||||
| chr9:33162281
|
A | C | 1 | a0001c0001t0001g0086 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.412+4477T>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33162281 | ||||||
| chr9:33162283
|
A | G | 1 | a0001c0001t0001g0086 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.412+4475T>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33162283 | ||||||
| chr9:33162294
|
A | G | 1 | a0001c0001t0001g0086 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.412+4464T>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33162294 | ||||||
| chr9:33162390
|
C | T | 1 | a0001c0001t0001g0150 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.412+4368G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33162390 | ||||||
| chr9:33162437
|
G | A | 1 | a0001c0001t0001g0053 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.412+4321C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33162437 | ||||||
| chr9:33162463
|
T | A | 1 | a0001c0001t0001g0086 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.412+4295A>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33162463 | ||||||
| chr9:33162528
|
C | A | 1 | a0001c0001t0001g0086 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.412+4230G>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33162528 | ||||||
| chr9:33162574
|
C | G | 1 | a0001c0001t0001g0086 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.412+4184G>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33162574 | ||||||
| chr9:33162575
|
G | C | 1 | a0001c0001t0001g0086 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.412+4183C>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33162575 | ||||||
| chr9:33162716
|
T | A | 1 | a0001c0001t0001g0086 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.412+4042A>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33162716 | ||||||
| chr9:33162799
|
A | G | 1 | a0001c0001t0027g0002 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.412+3959T>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33162799 | ||||||
| chr9:33162902
|
G | T | 1 | a0001c0001t0001g0086 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.412+3856C>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33162902 | ||||||
| chr9:33162941
|
G | T | 1 | a0001c0001t0001g0086 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.412+3817C>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33162941 | ||||||
| chr9:33162961
|
A | T | 1 | a0001c0001t0001g0086 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.412+3797T>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33162961 | ||||||
| chr9:33162973
|
G | A | 1 | a0001c0001t0001g0053 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.412+3785C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33162973 | ||||||
| chr9:33163048
|
T | TCCAC | 3 | a0001c0001t0002g0282a0001c0001t0002g0284a0001c0001t0055g0283 | 3 | HG01496.hp2 HG04204.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.412+3706_412+3709d others(6): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33163048 | ||||||
| chr9:33163061
|
G | A | 39 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(36): Show | 42 | HG00140.hp1 HG00323.hp1 HG00642.hp2 others(39): Show |
intron_variant | MODIFIER | c.412+3697C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33163061 | ||||||
| chr9:33163067
|
T | A | 1 | a0001c0001t0001g0086 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.412+3691A>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33163067 | ||||||
| chr9:33163076
|
T | A | 1 | a0001c0001t0001g0086 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.412+3682A>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33163076 | ||||||
| chr9:33163083
|
C | G | 1 | a0001c0001t0001g0087 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.412+3675G>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33163083 | ||||||
| chr9:33163149
|
C | A | 1 | a0001c0001t0001g0086 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.412+3609G>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33163149 | ||||||
| chr9:33163150
|
T | G | 1 | a0001c0001t0001g0086 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.412+3608A>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33163150 | ||||||
| chr9:33163151
|
G | C | 1 | a0001c0001t0001g0086 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.412+3607C>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33163151 | ||||||
| chr9:33163152
|
C | A | 1 | a0001c0001t0001g0086 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.412+3606G>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33163152 | ||||||
| chr9:33163193
|
C | G | 1 | a0001c0001t0001g0086 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.412+3565G>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33163193 | ||||||
| chr9:33163194
|
T | C | 1 | a0001c0001t0001g0086 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.412+3564A>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33163194 | ||||||
| chr9:33163273
|
A | G | 216 | a0001c0001t0001g0017a0001c0001t0001g0169a0001c0001t0001g0198others(213): Show | 224 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(221): Show |
intron_variant | MODIFIER | c.412+3485T>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33163273 | ||||||
| chr9:33163300
|
C | T | 20 | a0001c0001t0001g0017a0001c0001t0011g0003a0001c0001t0011g0018others(17): Show | 22 | HG00280.hp2 HG00733.hp1 HG01358.hp2 others(19): Show |
intron_variant | MODIFIER | c.412+3458G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33163300 | ||||||
| chr9:33163388
|
C | T | 3 | a0001c0001t0023g0172a0001c0001t0023g0173a0001c0001t0023g0174 | 3 | HG01074.hp1 HG02647.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.412+3370G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33163388 | ||||||
| chr9:33163481
|
C | G | 5 | a0001c0001t0019g0153a0001c0001t0019g0154a0001c0001t0019g0155others(2): Show | 6 | HG01891.hp2 HG02717.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.412+3277G>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33163481 | ||||||
| chr9:33163488
|
G | T | 115 | a0001c0001t0001g0198a0001c0001t0002g0012a0001c0001t0002g0192others(112): Show | 116 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(113): Show |
intron_variant | MODIFIER | c.412+3270C>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33163488 | ||||||
| chr9:33163509
|
G | A | 1 | a0001c0001t0003g0321 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.412+3249C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33163509 | ||||||
| chr9:33163525
|
C | G | 39 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(36): Show | 42 | HG00140.hp1 HG00323.hp1 HG00642.hp2 others(39): Show |
intron_variant | MODIFIER | c.412+3233G>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33163525 | ||||||
| chr9:33163542
|
C | G | 1 | a0001c0001t0028g0323 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.412+3216G>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33163542 | ||||||
| chr9:33163558
|
C | G | 1 | a0001c0001t0028g0323 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.412+3200G>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33163558 | ||||||
| chr9:33163625
|
T | C | 2 | a0001c0001t0001g0147a0001c0001t0001g0149 | 2 | NA18988.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.412+3133A>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33163625 | ||||||
| chr9:33163667
|
C | T | 18 | a0001c0002t0006g0178a0001c0002t0006g0179a0001c0002t0006g0182others(15): Show | 18 | HG00544.hp1 HG01257.hp1 HG02165.hp1 others(15): Show |
intron_variant | MODIFIER | c.412+3091G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33163667 | ||||||
| chr9:33163668
|
G | T | 1 | a0001c0001t0002g0196 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.412+3090C>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33163668 | ||||||
| chr9:33163773
|
C | G | 2 | a0001c0001t0001g0057a0001c0001t0002g0056 | 2 | HG00609.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.412+2985G>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33163773 | ||||||
| chr9:33163811
|
T | C | 3 | a0001c0001t0023g0172a0001c0001t0023g0173a0001c0001t0023g0174 | 3 | HG01074.hp1 HG02647.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.412+2947A>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33163811 | ||||||
| chr9:33163886
|
C | A | 1 | a0001c0002t0037g0191 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.412+2872G>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33163886 | ||||||
| chr9:33163964
|
C | T | 1 | a0001c0001t0001g0055 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.412+2794G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33163964 | ||||||
| chr9:33164078
|
C | T | 4 | a0001c0001t0019g0153a0001c0001t0019g0154a0001c0001t0019g0155others(1): Show | 4 | HG01891.hp2 HG02717.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.412+2680G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33164078 | ||||||
| chr9:33164118
|
T | A | 20 | a0001c0001t0001g0017a0001c0001t0011g0003a0001c0001t0011g0018others(17): Show | 22 | HG00280.hp2 HG00733.hp1 HG01358.hp2 others(19): Show |
intron_variant | MODIFIER | c.412+2640A>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33164118 | ||||||
| chr9:33164157
|
T | C | 1 | a0001c0001t0009g0043 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.412+2601A>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33164157 | ||||||
| chr9:33164529
|
T | A | 20 | a0001c0001t0001g0017a0001c0001t0011g0003a0001c0001t0011g0018others(17): Show | 22 | HG00280.hp2 HG00733.hp1 HG01358.hp2 others(19): Show |
intron_variant | MODIFIER | c.412+2229A>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33164529 | ||||||
| chr9:33164669
|
T | A | 53 | a0001c0001t0001g0316a0001c0001t0003g0001a0001c0001t0003g0299others(50): Show | 55 | HG00597.hp2 HG01070.hp1 HG01106.hp2 others(52): Show |
intron_variant | MODIFIER | c.412+2089A>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33164669 | ||||||
| chr9:33164676
|
C | T | 1 | a0001c0001t0001g0054 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.412+2082G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33164676 | ||||||
| chr9:33164679
|
G | A | 118 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(115): Show | 123 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(120): Show |
intron_variant | MODIFIER | c.412+2079C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33164679 | ||||||
| chr9:33164736
|
C | T | 2 | a0001c0001t0003g0300a0001c0001t0003g0322 | 2 | HG02683.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.412+2022G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33164736 | ||||||
| chr9:33164960
|
G | A | 1 | a0001c0001t0003g0322 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.412+1798C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33164960 | ||||||
| chr9:33164970
|
AT | A | 117 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(114): Show | 123 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(120): Show |
intron_variant | MODIFIER | c.412+1787delA | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33164970 | ||||||
| chr9:33164970
|
ATT | A | 188 | a0001c0001t0001g0017a0001c0001t0001g0148a0001c0001t0001g0149others(185): Show | 195 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(192): Show |
intron_variant | MODIFIER | c.412+1786_412+1787d others(4): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33164970 | ||||||
| chr9:33164970
|
ATTT | A | 28 | a0001c0001t0002g0288a0001c0001t0007g0324a0001c0001t0007g0325others(25): Show | 28 | HG01106.hp2 HG01175.hp1 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.412+1785_412+1787d others(5): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33164970 | ||||||
| chr9:33165227
|
C | G | 1 | a0001c0001t0002g0297 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.412+1531G>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33165227 | ||||||
| chr9:33165239
|
A | AT | 18 | a0001c0002t0006g0178a0001c0002t0006g0179a0001c0002t0006g0182others(15): Show | 18 | HG00544.hp1 HG01257.hp1 HG02165.hp1 others(15): Show |
intron_variant | MODIFIER | c.412+1518dupA | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33165239 | ||||||
| chr9:33165285
|
T | C | 3 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0152 | 3 | HG01928.hp2 HG03654.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.412+1473A>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33165285 | ||||||
| chr9:33165307
|
T | TA | 139 | a0001c0001t0001g0017a0001c0001t0001g0198a0001c0001t0002g0012others(136): Show | 143 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(140): Show |
intron_variant | MODIFIER | c.412+1450dupT | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33165307 | ||||||
| chr9:33165374
|
C | T | 53 | a0001c0001t0001g0316a0001c0001t0003g0001a0001c0001t0003g0299others(50): Show | 55 | HG00597.hp2 HG01070.hp1 HG01106.hp2 others(52): Show |
intron_variant | MODIFIER | c.412+1384G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33165374 | ||||||
| chr9:33165454
|
A | T | 1 | a0001c0001t0003g0013 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.412+1304T>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33165454 | ||||||
| chr9:33165646
|
T | C | 1 | a0001c0001t0003g0349 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.412+1112A>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33165646 | ||||||
| chr9:33165691
|
A | G | 1 | a0001c0001t0050g0033 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.412+1067T>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33165691 | ||||||
| chr9:33165836
|
C | G | 1 | a0001c0001t0001g0032 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.412+922G>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33165836 | ||||||
| chr9:33165987
|
A | G | 217 | a0001c0001t0001g0017a0001c0001t0001g0169a0001c0001t0001g0198others(214): Show | 225 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(222): Show |
intron_variant | MODIFIER | c.412+771T>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33165987 | ||||||
| chr9:33166236
|
T | C | 216 | a0001c0001t0001g0017a0001c0001t0001g0169a0001c0001t0001g0198others(213): Show | 224 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(221): Show |
intron_variant | MODIFIER | c.412+522A>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33166236 | ||||||
| chr9:33166271
|
ATCAGGAG others(10): Show |
A | 1 | a0005c0005t0048g0289 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.412+470_412+486del others(17): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33166271 | ||||||
| chr9:33166350
|
G | A | 1 | a0001c0002t0006g0290 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.412+408C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33166350 | ||||||
| chr9:33166617
|
T | C | 4 | a0001c0001t0066g0293a0001c0001t0067g0292a0001c0001t0068g0291others(1): Show | 4 | HG01081.hp2 HG01515.hp1 HG01978.hp1 others(1): Show |
intron_variant | MODIFIER | c.412+141A>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33166617 | ||||||
| chr9:33166643
|
G | A | 1 | a0001c0001t0001g0295 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.412+115C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33166643 | ||||||
| chr9:33166649
|
G | A | 1 | a0001c0001t0063g0296 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.412+109C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33166649 | ||||||
| chr9:33166664
|
T | C | 1 | a0001c0001t0002g0297 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.412+94A>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33166664 | ||||||
| chr9:33166713
|
C | CG | 21 | a0001c0001t0001g0017a0001c0001t0003g0013a0001c0001t0011g0003others(18): Show | 23 | HG00280.hp2 HG00733.hp1 HG01358.hp2 others(20): Show |
intron_variant | MODIFIER | c.412+44dupC | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33166713 | ||||||
| chr9:33166747
|
C | A | 53 | a0001c0001t0001g0316a0001c0001t0003g0001a0001c0001t0003g0299others(50): Show | 55 | HG00597.hp2 HG01070.hp1 HG01106.hp2 others(52): Show |
intron_variant | MODIFIER | c.412+11G>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33166747 |