| geneid | 6820 |
|---|---|
| ensemblid | ENSG00000088002.12 |
| hgncid | 11459 |
| symbol | SULT2B1 |
| name | sulfotransferase family 2B member 1 |
| refseq_nuc | NM_177973.2 |
| refseq_prot | NP_814444.1 |
| ensembl_nuc | ENST00000201586.7 |
| ensembl_prot | ENSP00000201586.2 |
| mane_status | MANE Select |
| chr | chr19 |
| start | 48552172 |
| end | 48599423 |
| strand | + |
| ver | v1.2 |
| region | chr19:48552172-48599423 |
| region5000 | chr19:48547172-48604423 |
| regionname0 | SULT2B1_chr19_48552172_48599423 |
| regionname5000 | SULT2B1_chr19_48547172_48604423 |
| 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 | 365 | 356 | 92 | 81 | 131 | 11 | 39 | 91 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | copy fasta | chr19 | 48547172 | 48604423 |
| a0002 | 0/0 | 365 | 9 | 0 | 0 | 9 | 0 | 0 | 4 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | copy fasta | chr19 | 48547172 | 48604423 |
| a0003 | 0/0 | 365 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | copy fasta | chr19 | 48547172 | 48604423 |
| a0004 | 0/0 | 365 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | copy fasta | chr19 | 48547172 | 48604423 |
| a0005 | 0/0 | 365 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | copy fasta | chr19 | 48547172 | 48604423 |
| a0006 | 0/0 | 365 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | copy fasta | chr19 | 48547172 | 48604423 |
| a0007 | 0/0 | 365 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | copy fasta | chr19 | 48547172 | 48604423 |
| a0008 | 0/0 | 359 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | copy fasta | chr19 | 48547172 | 48604423 |
| a0009 | 0/0 | 365 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | copy fasta | chr19 | 48547172 | 48604423 |
| 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 | 1098 | 138 | 48 | 12 | 66 | 1 | 10 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | copy fasta | chr19 | 48547172 | 48604423 |
| c0002 | 0/0 | 1098 | 78 | 8 | 26 | 26 | 4 | 14 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | copy fasta | chr19 | 48547172 | 48604423 |
| c0003 | 0/0 | 1098 | 51 | 3 | 20 | 26 | 0 | 2 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | copy fasta | chr19 | 48547172 | 48604423 |
| c0004 | 0/1 | 1098 | 41 | 13 | 8 | 13 | 3 | 3 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | copy fasta | chr19 | 48547172 | 48604423 |
| c0005 | 0/0 | 1098 | 19 | 4 | 7 | 0 | 2 | 6 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | copy fasta | chr19 | 48547172 | 48604423 |
| c0006 | 0/0 | 1098 | 9 | 7 | 1 | 0 | 0 | 1 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | copy fasta | chr19 | 48547172 | 48604423 |
| c0007 | 0/0 | 1098 | 9 | 5 | 4 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | copy fasta | chr19 | 48547172 | 48604423 |
| c0008 | 0/0 | 1098 | 8 | 0 | 0 | 8 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | copy fasta | chr19 | 48547172 | 48604423 |
| c0009 | 0/0 | 1098 | 6 | 0 | 2 | 0 | 1 | 3 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | copy fasta | chr19 | 48547172 | 48604423 |
| c0010 | 0/0 | 1098 | 4 | 3 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | copy fasta | chr19 | 48547172 | 48604423 |
| c0011 | 0/0 | 1098 | 2 | 2 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | copy fasta | chr19 | 48547172 | 48604423 |
| c0012 | 0/0 | 1098 | 2 | 2 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | copy fasta | chr19 | 48547172 | 48604423 |
| c0013 | 0/0 | 1098 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | copy fasta | chr19 | 48547172 | 48604423 |
| c0014 | 0/0 | 1098 | 1 | 0 | 0 | 0 | 1 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | copy fasta | chr19 | 48547172 | 48604423 |
| c0015 | 0/0 | 1080 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | copy fasta | chr19 | 48547172 | 48604423 |
| c0016 | 0/0 | 1098 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | copy fasta | chr19 | 48547172 | 48604423 |
| c0017 | 0/0 | 1098 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | copy fasta | chr19 | 48547172 | 48604423 |
| c0018 | 0/0 | 1098 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | copy fasta | chr19 | 48547172 | 48604423 |
| c0019 | 0/0 | 1098 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | copy fasta | chr19 | 48547172 | 48604423 |
| c0020 | 0/0 | 1098 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | copy fasta | chr19 | 48547172 | 48604423 |
| c0021 | 0/0 | 1098 | 1 | 0 | 0 | 0 | 0 | 1 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | copy fasta | chr19 | 48547172 | 48604423 |
| 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 | 1/1 | 99 | 376 | 98 | 82 | 142 | 12 | 40 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | copy fasta | chr19 | 48547172 | 48604423 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0299 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0303 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0305 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0316 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0320 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0323 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0338 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0339 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0343 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0348 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0349 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0358 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0359 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0368 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0369 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0370 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0371 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0372 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0373 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0374 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| g0375 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| 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 | 1098 | 138 | 48 | 12 | 66 | 1 | 10 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | copy fasta | chr19 | 48547172 | 48604423 |
| a0001c0002 | 0/0 | 1098 | 78 | 8 | 26 | 26 | 4 | 14 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | copy fasta | chr19 | 48547172 | 48604423 |
| a0001c0003 | 0/0 | 1098 | 51 | 3 | 20 | 26 | 0 | 2 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | copy fasta | chr19 | 48547172 | 48604423 |
| a0001c0004 | 0/1 | 1098 | 41 | 13 | 8 | 13 | 3 | 3 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | copy fasta | chr19 | 48547172 | 48604423 |
| a0001c0005 | 0/0 | 1098 | 19 | 4 | 7 | 0 | 2 | 6 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | copy fasta | chr19 | 48547172 | 48604423 |
| a0001c0006 | 0/0 | 1098 | 9 | 7 | 1 | 0 | 0 | 1 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | copy fasta | chr19 | 48547172 | 48604423 |
| a0001c0007 | 0/0 | 1098 | 9 | 5 | 4 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | copy fasta | chr19 | 48547172 | 48604423 |
| a0001c0009 | 0/0 | 1098 | 6 | 0 | 2 | 0 | 1 | 3 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | copy fasta | chr19 | 48547172 | 48604423 |
| a0001c0010 | 0/0 | 1098 | 4 | 3 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | copy fasta | chr19 | 48547172 | 48604423 |
| a0001c0019 | 0/0 | 1098 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | copy fasta | chr19 | 48547172 | 48604423 |
| a0002c0008 | 0/0 | 1098 | 8 | 0 | 0 | 8 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | copy fasta | chr19 | 48547172 | 48604423 |
| a0002c0013 | 0/0 | 1098 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | copy fasta | chr19 | 48547172 | 48604423 |
| a0003c0011 | 0/0 | 1098 | 2 | 2 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | copy fasta | chr19 | 48547172 | 48604423 |
| a0003c0012 | 0/0 | 1098 | 2 | 2 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | copy fasta | chr19 | 48547172 | 48604423 |
| a0004c0016 | 0/0 | 1098 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | copy fasta | chr19 | 48547172 | 48604423 |
| a0004c0020 | 0/0 | 1098 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | copy fasta | chr19 | 48547172 | 48604423 |
| a0005c0021 | 0/0 | 1098 | 1 | 0 | 0 | 0 | 0 | 1 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | copy fasta | chr19 | 48547172 | 48604423 |
| a0006c0018 | 0/0 | 1098 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | copy fasta | chr19 | 48547172 | 48604423 |
| a0007c0017 | 0/0 | 1098 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | copy fasta | chr19 | 48547172 | 48604423 |
| a0008c0015 | 0/0 | 1080 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | copy fasta | chr19 | 48547172 | 48604423 |
| a0009c0014 | 0/0 | 1098 | 1 | 0 | 0 | 0 | 1 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | copy fasta | chr19 | 48547172 | 48604423 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 1196 | 138 | 48 | 12 | 66 | 1 | 10 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | copy fasta | chr19 | 48547172 | 48604423 |
| a0001c0002t0001 | 0/0 | 1196 | 78 | 8 | 26 | 26 | 4 | 14 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | copy fasta | chr19 | 48547172 | 48604423 |
| a0001c0003t0001 | 0/0 | 1196 | 51 | 3 | 20 | 26 | 0 | 2 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | copy fasta | chr19 | 48547172 | 48604423 |
| a0001c0004t0001 | 0/1 | 1196 | 41 | 13 | 8 | 13 | 3 | 3 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | copy fasta | chr19 | 48547172 | 48604423 |
| a0001c0005t0001 | 0/0 | 1196 | 19 | 4 | 7 | 0 | 2 | 6 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | copy fasta | chr19 | 48547172 | 48604423 |
| a0001c0006t0001 | 0/0 | 1196 | 9 | 7 | 1 | 0 | 0 | 1 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | copy fasta | chr19 | 48547172 | 48604423 |
| a0001c0007t0001 | 0/0 | 1196 | 9 | 5 | 4 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | copy fasta | chr19 | 48547172 | 48604423 |
| a0001c0009t0001 | 0/0 | 1196 | 6 | 0 | 2 | 0 | 1 | 3 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | copy fasta | chr19 | 48547172 | 48604423 |
| a0001c0010t0001 | 0/0 | 1196 | 4 | 3 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | copy fasta | chr19 | 48547172 | 48604423 |
| a0001c0019t0001 | 0/0 | 1196 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | copy fasta | chr19 | 48547172 | 48604423 |
| a0002c0008t0001 | 0/0 | 1196 | 8 | 0 | 0 | 8 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | copy fasta | chr19 | 48547172 | 48604423 |
| a0002c0013t0001 | 0/0 | 1196 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | copy fasta | chr19 | 48547172 | 48604423 |
| a0003c0011t0001 | 0/0 | 1196 | 2 | 2 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | copy fasta | chr19 | 48547172 | 48604423 |
| a0003c0012t0001 | 0/0 | 1196 | 2 | 2 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | copy fasta | chr19 | 48547172 | 48604423 |
| a0004c0016t0001 | 0/0 | 1196 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | copy fasta | chr19 | 48547172 | 48604423 |
| a0004c0020t0001 | 0/0 | 1196 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | copy fasta | chr19 | 48547172 | 48604423 |
| a0005c0021t0001 | 0/0 | 1196 | 1 | 0 | 0 | 0 | 0 | 1 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | copy fasta | chr19 | 48547172 | 48604423 |
| a0006c0018t0001 | 0/0 | 1196 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | copy fasta | chr19 | 48547172 | 48604423 |
| a0007c0017t0001 | 0/0 | 1196 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | copy fasta | chr19 | 48547172 | 48604423 |
| a0008c0015t0001 | 0/0 | 1178 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | copy fasta | chr19 | 48547172 | 48604423 |
| a0009c0014t0001 | 0/0 | 1196 | 1 | 0 | 0 | 0 | 1 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | copy fasta | chr19 | 48547172 | 48604423 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0299 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0368 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0373 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0001t0001g0374 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0002t0001g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0002t0001g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0002t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0002t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0002t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0002t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0002t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0002t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0002t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0002t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0002t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0002t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0002t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0002t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0002t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0002t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0002t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0002t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0002t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0002t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0002t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0002t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0002t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0002t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0002t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0002t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0002t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0002t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0002t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0002t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0002t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0002t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0002t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0002t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0002t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0002t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0002t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0002t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0002t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0002t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0002t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0002t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0002t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0002t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0002t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0002t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0002t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0002t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0002t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0002t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0002t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0002t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0002t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0002t0001g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0002t0001g0303 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0002t0001g0305 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0002t0001g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0002t0001g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0002t0001g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0002t0001g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0002t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0002t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0002t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0002t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0002t0001g0338 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0002t0001g0348 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0002t0001g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0002t0001g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0002t0001g0358 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0002t0001g0359 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0003t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0003t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0003t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0003t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0003t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0003t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0003t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0003t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0003t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0003t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0003t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0003t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0003t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0003t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0003t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0003t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0003t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0003t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0003t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0003t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0003t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0003t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0003t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0003t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0003t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0003t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0003t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0003t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0003t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0003t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0003t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0003t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0003t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0003t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0003t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0003t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0003t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0003t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0003t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0003t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0003t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0003t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0003t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0003t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0003t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0003t0001g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0003t0001g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0003t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0003t0001g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0003t0001g0370 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0003t0001g0375 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0004t0001g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0004t0001g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0004t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0004t0001g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0004t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0004t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0004t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0004t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0004t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0004t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0004t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0004t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0004t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0004t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0004t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0004t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0004t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0004t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0004t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0004t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0004t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0004t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0004t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0004t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0004t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0004t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0004t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0004t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0004t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0004t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0004t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0004t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0004t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0004t0001g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0004t0001g0316 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0004t0001g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0004t0001g0323 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0004t0001g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0004t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0004t0001g0343 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0004t0001g0371 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0005t0001g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0005t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0005t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0005t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0005t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0005t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0005t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0005t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0005t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0005t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0005t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0005t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0005t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0005t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0005t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0005t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0005t0001g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0005t0001g0349 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0006t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0006t0001g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0006t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0006t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0006t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0006t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0006t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0006t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0006t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0007t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0007t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0007t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0007t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0007t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0007t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0007t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0007t0001g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0007t0001g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0009t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0009t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0009t0001g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0009t0001g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0009t0001g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0009t0001g0339 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0010t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0010t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0010t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0010t0001g0369 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0001c0019t0001g0372 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0002c0008t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0002c0008t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0002c0008t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0002c0008t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0002c0008t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0002c0008t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0002c0008t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0002c0008t0001g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0002c0013t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0003c0011t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0003c0011t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0003c0012t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0003c0012t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0004c0016t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0004c0020t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0005c0021t0001g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0006c0018t0001g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0007c0017t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0008c0015t0001g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| a0009c0014t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0320 | EUR | GBR | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG00099 | hp2 | a0001 | c0005 | t0001 | g0113 | EUR | GBR | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG00140 | hp1 | a0001 | c0002 | t0001 | g0303 | EUR | GBR | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG00140 | hp2 | a0001 | c0005 | t0001 | g0071 | EUR | GBR | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG00280 | hp1 | a0001 | c0004 | t0001 | g0095 | EUR | FIN | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG00280 | hp2 | a0001 | c0002 | t0001 | g0305 | EUR | FIN | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | CHS | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG00408 | hp2 | a0002 | c0008 | t0001 | g0155 | EAS | CHS | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG00423 | hp1 | a0001 | c0003 | t0001 | g0142 | EAS | CHS | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG00423 | hp2 | a0001 | c0002 | t0001 | g0291 | EAS | CHS | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG00438 | hp1 | a0002 | c0008 | t0001 | g0154 | EAS | CHS | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG00438 | hp2 | a0001 | c0003 | t0001 | g0139 | EAS | CHS | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG00558 | hp1 | a0001 | c0004 | t0001 | g0223 | EAS | CHS | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0295 | EAS | CHS | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG00597 | hp1 | a0001 | c0003 | t0001 | g0272 | EAS | CHS | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG00597 | hp2 | a0001 | c0004 | t0001 | g0132 | EAS | CHS | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0331 | EAS | CHS | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG00609 | hp2 | a0001 | c0002 | t0001 | g0079 | EAS | CHS | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG00621 | hp1 | a0001 | c0002 | t0001 | g0208 | EAS | CHS | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG00621 | hp2 | a0001 | c0002 | t0001 | g0165 | EAS | CHS | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG00639 | hp1 | a0001 | c0009 | t0001 | g0188 | AMR | PUR | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG00639 | hp2 | a0001 | c0002 | t0001 | g0083 | AMR | PUR | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG00642 | hp1 | a0001 | c0002 | t0001 | g0206 | AMR | PUR | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG00642 | hp2 | a0001 | c0003 | t0001 | g0375 | AMR | PUR | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0289 | EAS | CHS | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0326 | EAS | CHS | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG00733 | hp1 | a0001 | c0002 | t0001 | g0034 | AMR | PUR | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG00733 | hp2 | a0001 | c0003 | t0001 | g0102 | AMR | PUR | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG00735 | hp1 | a0001 | c0002 | t0001 | g0308 | AMR | PUR | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG00735 | hp2 | a0001 | c0002 | t0001 | g0067 | AMR | PUR | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG00738 | hp1 | a0001 | c0004 | t0001 | g0062 | AMR | PUR | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG00738 | hp2 | a0001 | c0002 | t0001 | g0063 | AMR | PUR | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG00741 | hp1 | a0001 | c0004 | t0001 | g0242 | AMR | PUR | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG00741 | hp2 | a0001 | c0005 | t0001 | g0108 | AMR | PUR | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG01069 | hp1 | a0001 | c0003 | t0001 | g0222 | AMR | PUR | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG01069 | hp2 | a0001 | c0002 | t0001 | g0212 | AMR | PUR | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG01070 | hp1 | a0001 | c0002 | t0001 | g0185 | AMR | PUR | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG01070 | hp2 | a0001 | c0002 | t0001 | g0049 | AMR | PUR | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG01071 | hp1 | a0001 | c0002 | t0001 | g0211 | AMR | PUR | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG01071 | hp2 | a0001 | c0002 | t0001 | g0050 | AMR | PUR | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0178 | AMR | PUR | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0186 | AMR | PUR | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG01081 | hp1 | a0001 | c0005 | t0001 | g0173 | AMR | PUR | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG01081 | hp2 | a0001 | c0003 | t0001 | g0180 | AMR | PUR | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG01099 | hp1 | a0001 | c0005 | t0001 | g0236 | AMR | PUR | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG01099 | hp2 | a0001 | c0002 | t0001 | g0314 | AMR | PUR | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG01106 | hp1 | a0001 | c0006 | t0001 | g0250 | AMR | PUR | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0306 | AMR | PUR | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG01109 | hp1 | a0001 | c0003 | t0001 | g0261 | AMR | PUR | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG01109 | hp2 | a0001 | c0004 | t0001 | g0015 | AMR | PUR | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0175 | AMR | PUR | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG01167 | hp2 | a0004 | c0016 | t0001 | g0158 | AMR | PUR | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG01168 | hp1 | a0001 | c0004 | t0001 | g0324 | AMR | PUR | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG01168 | hp2 | a0001 | c0002 | t0001 | g0358 | AMR | PUR | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0101 | AMR | PUR | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG01169 | hp2 | a0001 | c0002 | t0001 | g0359 | AMR | PUR | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0215 | AMR | PUR | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG01175 | hp2 | a0001 | c0005 | t0001 | g0235 | AMR | PUR | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG01192 | hp1 | a0001 | c0005 | t0001 | g0255 | AMR | PUR | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG01192 | hp2 | a0001 | c0009 | t0001 | g0304 | AMR | PUR | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0092 | AMR | PUR | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0337 | AMR | PUR | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG01255 | hp1 | a0001 | c0004 | t0001 | g0315 | AMR | CLM | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG01255 | hp2 | a0001 | c0002 | t0001 | g0122 | AMR | CLM | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG01256 | hp1 | a0001 | c0007 | t0001 | g0110 | AMR | CLM | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG01256 | hp2 | a0001 | c0010 | t0001 | g0112 | AMR | CLM | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG01257 | hp1 | a0001 | c0003 | t0001 | g0266 | AMR | CLM | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG01257 | hp2 | a0001 | c0005 | t0001 | g0001 | AMR | CLM | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG01258 | hp1 | a0001 | c0007 | t0001 | g0111 | AMR | CLM | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG01258 | hp2 | a0001 | c0005 | t0001 | g0001 | AMR | CLM | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG01261 | hp1 | a0001 | c0002 | t0001 | g0217 | AMR | CLM | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG01261 | hp2 | a0001 | c0007 | t0001 | g0166 | AMR | CLM | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG01346 | hp1 | a0001 | c0002 | t0001 | g0252 | AMR | CLM | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG01346 | hp2 | a0001 | c0007 | t0001 | g0033 | AMR | CLM | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0251 | AMR | CLM | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG01358 | hp2 | a0001 | c0002 | t0001 | g0301 | AMR | CLM | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG01361 | hp1 | a0001 | c0002 | t0001 | g0163 | AMR | CLM | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG01361 | hp2 | a0001 | c0002 | t0001 | g0328 | AMR | CLM | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG01433 | hp2 | a0001 | c0004 | t0001 | g0145 | AMR | CLM | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0080 | AMR | CLM | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG01496 | hp2 | a0001 | c0002 | t0001 | g0085 | AMR | CLM | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG01515 | hp1 | a0001 | c0004 | t0001 | g0316 | EUR | IBS | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG01515 | hp2 | a0001 | c0009 | t0001 | g0339 | EUR | IBS | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG01884 | hp1 | a0003 | c0012 | t0001 | g0012 | AFR | ACB | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0366 | AFR | ACB | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG01891 | hp1 | a0001 | c0004 | t0001 | g0016 | AFR | ACB | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | ACB | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG01928 | hp1 | a0001 | c0003 | t0001 | g0170 | AMR | PEL | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG01928 | hp2 | a0001 | c0003 | t0001 | g0224 | AMR | PEL | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG01934 | hp1 | a0001 | c0002 | t0001 | g0131 | AMR | PEL | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG01934 | hp2 | a0001 | c0003 | t0001 | g0129 | AMR | PEL | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG01943 | hp1 | a0001 | c0003 | t0001 | g0169 | AMR | PEL | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG01943 | hp2 | a0001 | c0004 | t0001 | g0245 | AMR | PEL | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG01952 | hp1 | a0001 | c0002 | t0001 | g0048 | AMR | PEL | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG01952 | hp2 | a0001 | c0002 | t0001 | g0260 | AMR | PEL | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG01975 | hp1 | a0001 | c0003 | t0001 | g0256 | AMR | PEL | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG01975 | hp2 | a0001 | c0003 | t0001 | g0105 | AMR | PEL | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG01978 | hp1 | a0001 | c0003 | t0001 | g0318 | AMR | PEL | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0237 | AMR | PEL | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG01981 | hp1 | a0001 | c0003 | t0001 | g0225 | AMR | PEL | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG01981 | hp2 | a0001 | c0003 | t0001 | g0216 | AMR | PEL | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG01993 | hp1 | a0001 | c0003 | t0001 | g0148 | AMR | PEL | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG01993 | hp2 | a0001 | c0004 | t0001 | g0319 | AMR | PEL | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG02015 | hp1 | a0001 | c0003 | t0001 | g0286 | EAS | KHV | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | KHV | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | KHV | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | KHV | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG02040 | hp1 | a0001 | c0002 | t0001 | g0336 | EAS | KHV | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0342 | EAS | KHV | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0300 | AFR | ACB | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0290 | EAS | KHV | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0341 | EAS | KHV | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG02071 | hp1 | a0006 | c0018 | t0001 | g0350 | EAS | KHV | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0346 | EAS | KHV | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0344 | EAS | KHV | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | KHV | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0329 | EAS | KHV | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG02080 | hp2 | a0002 | c0008 | t0001 | g0244 | EAS | KHV | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | KHV | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0335 | EAS | KHV | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG02129 | hp1 | a0001 | c0002 | t0001 | g0077 | EAS | KHV | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | KHV | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0281 | EAS | KHV | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG02135 | hp2 | a0001 | c0004 | t0001 | g0138 | EAS | KHV | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0257 | AFR | ACB | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG02145 | hp2 | a0001 | c0006 | t0001 | g0061 | AFR | ACB | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG02148 | hp1 | a0001 | c0003 | t0001 | g0119 | AMR | PEL | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG02148 | hp2 | a0001 | c0003 | t0001 | g0120 | AMR | PEL | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0279 | EAS | CDX | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG02155 | hp2 | a0002 | c0008 | t0001 | g0157 | EAS | CDX | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0310 | EAS | CDX | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | CDX | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0051 | AFR | ACB | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | ACB | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG02258 | hp1 | a0001 | c0004 | t0001 | g0030 | AFR | ACB | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG02258 | hp2 | a0001 | c0004 | t0001 | g0089 | AFR | ACB | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG02273 | hp1 | a0001 | c0002 | t0001 | g0164 | AMR | PEL | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG02273 | hp2 | a0001 | c0003 | t0001 | g0309 | AMR | PEL | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG02280 | hp1 | a0001 | c0002 | t0001 | g0202 | AFR | ACB | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG02280 | hp2 | a0001 | c0007 | t0001 | g0356 | AFR | ACB | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0066 | AFR | ACB | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | ACB | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG02523 | hp1 | a0001 | c0004 | t0001 | g0230 | EAS | KHV | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG02523 | hp2 | a0001 | c0003 | t0001 | g0287 | EAS | KHV | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0360 | AFR | GWD | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG02572 | hp2 | a0001 | c0004 | t0001 | g0198 | AFR | GWD | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | GWD | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | GWD | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | GWD | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG02622 | hp2 | a0001 | c0002 | t0001 | g0035 | AFR | GWD | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0246 | AFR | GWD | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG02630 | hp2 | a0001 | c0002 | t0001 | g0093 | AFR | GWD | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | GWD | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG02647 | hp2 | a0001 | c0007 | t0001 | g0161 | AFR | GWD | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG02698 | hp1 | a0001 | c0002 | t0001 | g0103 | SAS | PJL | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG02698 | hp2 | a0001 | c0004 | t0001 | g0278 | SAS | PJL | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0053 | AFR | GWD | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG02717 | hp2 | a0003 | c0011 | t0001 | g0059 | AFR | GWD | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG02723 | hp1 | a0001 | c0004 | t0001 | g0371 | AFR | GWD | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG02723 | hp2 | a0001 | c0006 | t0001 | g0044 | AFR | GWD | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG02735 | hp1 | a0001 | c0006 | t0001 | g0020 | SAS | PJL | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG02735 | hp2 | a0001 | c0005 | t0001 | g0213 | SAS | PJL | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0259 | SAS | PJL | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG02738 | hp2 | a0001 | c0002 | t0001 | g0022 | SAS | PJL | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0363 | AFR | GWD | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0060 | AFR | GWD | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG02818 | hp1 | a0001 | c0003 | t0001 | g0011 | AFR | GWD | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0258 | AFR | GWD | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0362 | AFR | GWD | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG02886 | hp2 | a0001 | c0004 | t0001 | g0058 | AFR | GWD | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0199 | AFR | GWD | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | GWD | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG02896 | hp1 | a0001 | c0004 | t0001 | g0045 | AFR | GWD | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG02896 | hp2 | a0001 | c0005 | t0001 | g0009 | AFR | GWD | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG02897 | hp1 | a0001 | c0005 | t0001 | g0008 | AFR | GWD | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0204 | AFR | GWD | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | ESN | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | ESN | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG02965 | hp1 | a0001 | c0002 | t0001 | g0118 | AFR | ESN | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | ESN | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG02970 | hp1 | a0001 | c0002 | t0001 | g0003 | AFR | ESN | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG02970 | hp2 | a0001 | c0004 | t0001 | g0068 | AFR | ESN | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG02976 | hp1 | a0001 | c0010 | t0001 | g0037 | AFR | ESN | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG02976 | hp2 | a0003 | c0011 | t0001 | g0043 | AFR | ESN | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG03017 | hp1 | a0001 | c0003 | t0001 | g0254 | SAS | PJL | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG03017 | hp2 | a0001 | c0002 | t0001 | g0253 | SAS | PJL | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG03041 | hp1 | a0001 | c0010 | t0001 | g0369 | AFR | GWD | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG03041 | hp2 | a0001 | c0006 | t0001 | g0094 | AFR | GWD | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0075 | AFR | MSL | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG03098 | hp2 | a0001 | c0007 | t0001 | g0357 | AFR | MSL | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG03130 | hp1 | a0001 | c0007 | t0001 | g0057 | AFR | ESN | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0073 | AFR | ESN | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | ESN | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG03139 | hp2 | a0001 | c0004 | t0001 | g0052 | AFR | ESN | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG03195 | hp1 | a0001 | c0003 | t0001 | g0046 | AFR | ESN | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0055 | AFR | ESN | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0361 | AFR | MSL | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG03209 | hp2 | a0007 | c0017 | t0001 | g0029 | AFR | MSL | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG03225 | hp1 | a0001 | c0006 | t0001 | g0028 | AFR | MSL | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0368 | AFR | MSL | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG03453 | hp1 | a0001 | c0007 | t0001 | g0200 | AFR | MSL | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0364 | AFR | MSL | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG03491 | hp1 | a0001 | c0002 | t0001 | g0084 | SAS | PJL | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG03491 | hp2 | a0001 | c0009 | t0001 | g0321 | SAS | PJL | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG03492 | hp1 | a0001 | c0005 | t0001 | g0109 | SAS | PJL | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG03492 | hp2 | a0001 | c0009 | t0001 | g0322 | SAS | PJL | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG03516 | hp1 | a0001 | c0004 | t0001 | g0064 | AFR | ESN | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0365 | AFR | ESN | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG03540 | hp1 | a0001 | c0005 | t0001 | g0010 | AFR | GWD | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | GWD | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG03579 | hp1 | a0001 | c0006 | t0001 | g0038 | AFR | MSL | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG03579 | hp2 | a0001 | c0006 | t0001 | g0006 | AFR | MSL | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG03654 | hp1 | a0001 | c0002 | t0001 | g0248 | SAS | PJL | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG03654 | hp2 | a0001 | c0002 | t0001 | g0249 | SAS | PJL | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG03669 | hp1 | a0001 | c0005 | t0001 | g0349 | SAS | PJL | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG03669 | hp2 | a0001 | c0002 | t0001 | g0176 | SAS | PJL | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0205 | SAS | STU | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0087 | SAS | STU | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG03704 | hp1 | a0001 | c0002 | t0001 | g0317 | SAS | PJL | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG03704 | hp2 | a0001 | c0005 | t0001 | g0313 | SAS | PJL | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG03710 | hp1 | a0001 | c0002 | t0001 | g0156 | SAS | PJL | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG03710 | hp2 | a0001 | c0002 | t0001 | g0149 | SAS | PJL | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG03831 | hp1 | a0001 | c0004 | t0001 | g0018 | SAS | BEB | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0311 | SAS | BEB | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG03834 | hp1 | a0001 | c0004 | t0001 | g0343 | SAS | BEB | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG03834 | hp2 | a0001 | c0003 | t0001 | g0193 | SAS | BEB | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG03942 | hp1 | a0001 | c0002 | t0001 | g0348 | SAS | BEB | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG03942 | hp2 | a0001 | c0002 | t0001 | g0182 | SAS | BEB | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG04115 | hp1 | a0001 | c0009 | t0001 | g0121 | SAS | STU | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0268 | SAS | STU | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0312 | SAS | BEB | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG04184 | hp2 | a0001 | c0002 | t0001 | g0338 | SAS | BEB | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0238 | SAS | STU | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0288 | SAS | STU | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG04204 | hp1 | a0001 | c0002 | t0001 | g0081 | SAS | STU | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG04204 | hp2 | a0005 | c0021 | t0001 | g0307 | SAS | STU | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0187 | SAS | STU | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0196 | SAS | STU | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0074 | AFR | YRI | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | YRI | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | CHB | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA18612 | hp2 | a0002 | c0008 | t0001 | g0231 | EAS | CHB | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | CHB | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0347 | EAS | CHB | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0302 | AFR | YRI | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA18906 | hp2 | a0001 | c0004 | t0001 | g0072 | AFR | YRI | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA18942 | hp2 | a0001 | c0002 | t0001 | g0220 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA18943 | hp2 | a0001 | c0004 | t0001 | g0133 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA18944 | hp1 | a0001 | c0003 | t0001 | g0239 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA18944 | hp2 | a0001 | c0003 | t0001 | g0125 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA18947 | hp2 | a0001 | c0002 | t0001 | g0277 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA18948 | hp2 | a0001 | c0004 | t0001 | g0264 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA18949 | hp1 | a0001 | c0003 | t0001 | g0262 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA18950 | hp1 | a0001 | c0003 | t0001 | g0137 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA18950 | hp2 | a0001 | c0002 | t0001 | g0333 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA18951 | hp1 | a0001 | c0003 | t0001 | g0150 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA18952 | hp1 | a0002 | c0013 | t0001 | g0285 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA18952 | hp2 | a0002 | c0008 | t0001 | g0162 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA18954 | hp1 | a0001 | c0002 | t0001 | g0297 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA18957 | hp1 | a0001 | c0002 | t0001 | g0271 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA18959 | hp1 | a0001 | c0003 | t0001 | g0370 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA18961 | hp2 | a0002 | c0008 | t0001 | g0345 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA18964 | hp1 | a0001 | c0004 | t0001 | g0330 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA18964 | hp2 | a0001 | c0003 | t0001 | g0195 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA18966 | hp1 | a0001 | c0003 | t0001 | g0280 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0355 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA18970 | hp1 | a0001 | c0003 | t0001 | g0221 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA18970 | hp2 | a0001 | c0002 | t0001 | g0275 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA18971 | hp1 | a0001 | c0004 | t0001 | g0127 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA18971 | hp2 | a0001 | c0003 | t0001 | g0078 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA18974 | hp2 | a0001 | c0003 | t0001 | g0233 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA18980 | hp1 | a0001 | c0003 | t0001 | g0128 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA18982 | hp1 | a0001 | c0003 | t0001 | g0228 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA18983 | hp1 | a0001 | c0002 | t0001 | g0263 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA18983 | hp2 | a0001 | c0003 | t0001 | g0135 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA18986 | hp1 | a0001 | c0003 | t0001 | g0114 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA18986 | hp2 | a0001 | c0002 | t0001 | g0274 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA18990 | hp1 | a0001 | c0002 | t0001 | g0351 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA18990 | hp2 | a0001 | c0002 | t0001 | g0354 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA18998 | hp1 | a0001 | c0002 | t0001 | g0098 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA18998 | hp2 | a0001 | c0004 | t0001 | g0069 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA18999 | hp1 | a0001 | c0002 | t0001 | g0174 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA18999 | hp2 | a0001 | c0003 | t0001 | g0292 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0340 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA19000 | hp2 | a0001 | c0003 | t0001 | g0325 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA19003 | hp2 | a0001 | c0003 | t0001 | g0219 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA19005 | hp1 | a0001 | c0003 | t0001 | g0294 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA19009 | hp1 | a0001 | c0002 | t0001 | g0293 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA19009 | hp2 | a0001 | c0002 | t0001 | g0243 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA19011 | hp1 | a0001 | c0003 | t0001 | g0143 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA19012 | hp1 | a0001 | c0002 | t0001 | g0134 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA19012 | hp2 | a0001 | c0002 | t0001 | g0124 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA19030 | hp1 | a0003 | c0012 | t0001 | g0013 | AFR | LWK | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA19030 | hp2 | a0001 | c0004 | t0001 | g0005 | AFR | LWK | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | LWK | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA19043 | hp2 | a0001 | c0010 | t0001 | g0091 | AFR | LWK | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA19056 | hp1 | a0001 | c0004 | t0001 | g0099 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA19058 | hp1 | a0008 | c0015 | t0001 | g0352 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA19058 | hp2 | a0001 | c0004 | t0001 | g0184 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA19070 | hp1 | a0001 | c0003 | t0001 | g0203 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA19070 | hp2 | a0001 | c0002 | t0001 | g0332 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA19074 | hp1 | a0002 | c0008 | t0001 | g0269 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA19079 | hp1 | a0001 | c0004 | t0001 | g0194 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA19079 | hp2 | a0001 | c0004 | t0001 | g0141 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA19080 | hp2 | a0001 | c0002 | t0001 | g0276 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0353 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA19083 | hp2 | a0001 | c0002 | t0001 | g0100 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA19085 | hp2 | a0001 | c0002 | t0001 | g0334 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0374 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | YRI | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0056 | AFR | YRI | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | ASW | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | ASW | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA20752 | hp1 | a0009 | c0014 | t0001 | g0177 | EUR | TSI | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA20752 | hp2 | a0001 | c0002 | t0001 | g0096 | EUR | TSI | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA20805 | hp1 | a0001 | c0004 | t0001 | g0086 | EUR | TSI | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA20805 | hp2 | a0001 | c0002 | t0001 | g0076 | EUR | TSI | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA20905 | hp1 | a0001 | c0005 | t0001 | g0209 | SAS | GIH | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA20905 | hp2 | a0001 | c0005 | t0001 | g0197 | SAS | GIH | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG01123 | hp1 | a0001 | c0003 | t0001 | g0214 | AMR | CLM | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG01123 | hp2 | a0001 | c0002 | t0001 | g0147 | AMR | CLM | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG02109 | hp1 | a0001 | c0006 | t0001 | g0090 | AFR | ACB | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | ACB | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG02486 | hp1 | a0001 | c0002 | t0001 | g0047 | AFR | ACB | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG02486 | hp2 | a0001 | c0019 | t0001 | g0372 | AFR | ACB | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG02559 | hp1 | a0001 | c0003 | t0001 | g0327 | AFR | ACB | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0373 | AFR | ACB | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG03471 | hp1 | a0001 | c0005 | t0001 | g0019 | AFR | MSL | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG03471 | hp2 | a0001 | c0004 | t0001 | g0065 | AFR | MSL | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG06807 | hp1 | a0004 | c0020 | t0001 | g0181 | AFR | USA | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0367 | AFR | USA | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0171 | AFR | USA | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA20300 | hp2 | a0001 | c0002 | t0001 | g0160 | AFR | USA | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0088 | AFR | LWK | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| NA21309 | hp2 | a0001 | c0002 | t0001 | g0082 | AFR | LWK | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0004 | t0001 | g0323 | REF | REF | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0299 | REF | REF | SULT2B1_chr19_48547172_48604423 | SULT2B1 | chr19 | 48547172 | 48604423 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:48552281
|
C | T | 1 | a0005 | 1 | HG04204.hp2 | missense_variant | MODERATE | c.29C>T | p.Pro10Leu | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/7 | 110/1196 | 29/1098 | 10/365 | chr19 | 48552281 | ||
| chr19:48575967
|
G | A | 1 | a0002 | 9 | HG00408.hp2 HG00438.hp1 HG02080.hp2 others(6): Show |
missense_variant | MODERATE | c.98G>A | p.Arg33Gln | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/7 | 179/1196 | 98/1098 | 33/365 | chr19 | 48575967 | ||
| chr19:48576021
|
T | C | 1 | a0009 | 1 | NA20752.hp1 | missense_variant | MODERATE | c.152T>C | p.Leu51Ser | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/7 | 233/1196 | 152/1098 | 51/365 | chr19 | 48576021 | ||
| chr19:48596811
|
G | A | 1 | a0006 | 1 | HG02071.hp1 | missense_variant | MODERATE | c.718G>A | p.Val240Ile | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 6/7 | 799/1196 | 718/1098 | 240/365 | chr19 | 48596811 | ||
| chr19:48596827
|
C | T | 1 | a0007 | 1 | HG03209.hp2 | missense_variant | MODERATE | c.734C>T | p.Thr245Ile | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 6/7 | 815/1196 | 734/1098 | 245/365 | chr19 | 48596827 | ||
| chr19:48596853
|
ATGTCCAA others(11): Show |
A | 1 | a0008 | 1 | NA19058.hp1 | conservative_inframe_deletion | MODERATE | c.763_780delTCCAACTA others(10): Show |
p.Ser255_Leu260del | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 6/7 | 844/1196 | 763/1098 | 255/365 | INFO_REALIGN_3_PRIME | chr19 | 48596853 | |
| chr19:48599212
|
C | G | 1 | a0003 | 4 | HG01884.hp1 HG02717.hp2 HG02976.hp2 others(1): Show |
missense_variant | MODERATE | c.904C>G | p.Arg302Gly | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 7/7 | 985/1196 | 904/1098 | 302/365 | chr19 | 48599212 | ||
| chr19:48599342
|
C | T | 1 | a0004 | 2 | HG01167.hp2 HG06807.hp1 |
missense_variant | MODERATE | c.1034C>T | p.Pro345Leu | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 7/7 | 1115/1196 | 1034/1098 | 345/365 | chr19 | 48599342 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:48575989
|
C | T | 6 | a0001c0005a0001c0006a0001c0007others(3): Show | 44 | HG00099.hp2 HG00140.hp2 HG00741.hp2 others(41): Show |
synonymous_variant | LOW | c.120C>T | p.Pro40Pro | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/7 | 201/1196 | 120/1098 | 40/365 | chr19 | 48575989 | ||
| chr19:48592741
|
C | T | 1 | a0001c0019 | 1 | HG02486.hp2 | synonymous_variant | LOW | c.570C>T | p.Phe190Phe | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 5/7 | 651/1196 | 570/1098 | 190/365 | chr19 | 48592741 | ||
| chr19:48592808
|
C | T | 5 | a0001c0004a0001c0007a0001c0009others(2): Show | 58 | HG00280.hp1 HG00558.hp1 HG00597.hp2 others(55): Show |
synonymous_variant | LOW | c.637C>T | p.Leu213Leu | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 5/7 | 718/1196 | 637/1098 | 213/365 | chr19 | 48592808 | ||
| chr19:48599142
|
C | T | 5 | a0001c0002a0001c0005a0004c0016others(2): Show | 100 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(97): Show |
synonymous_variant | LOW | c.834C>T | p.Cys278Cys | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 7/7 | 915/1196 | 834/1098 | 278/365 | chr19 | 48599142 | ||
| chr19:48599256
|
C | T | 7 | a0001c0003a0001c0009a0001c0010others(4): Show | 67 | HG00423.hp1 HG00438.hp2 HG00597.hp1 others(64): Show |
synonymous_variant | LOW | c.948C>T | p.Asp316Asp | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 7/7 | 1029/1196 | 948/1098 | 316/365 | chr19 | 48599256 |
| 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 |
|---|
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:48552421
|
G | A | 6 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(3): Show | 6 | HG01433.hp1 HG02055.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.71+98G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48552421 | ||||||
| chr19:48552523
|
C | T | 1 | a0001c0003t0001g0375 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.71+200C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48552523 | ||||||
| chr19:48552539
|
T | C | 46 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(43): Show | 46 | HG00733.hp1 HG01109.hp2 HG01346.hp2 others(43): Show |
intron_variant | MODIFIER | c.71+216T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48552539 | ||||||
| chr19:48552564
|
G | C | 6 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(3): Show | 6 | HG01433.hp1 HG02055.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.71+241G>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48552564 | ||||||
| chr19:48552657
|
C | A | 1 | a0001c0002t0001g0048 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.71+334C>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48552657 | ||||||
| chr19:48552745
|
A | G | 1 | a0001c0001t0001g0374 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.71+422A>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48552745 | ||||||
| chr19:48552913
|
G | C | 6 | a0001c0003t0001g0011a0001c0005t0001g0008a0001c0005t0001g0009others(3): Show | 6 | HG01884.hp1 HG02818.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.71+590G>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48552913 | ||||||
| chr19:48553032
|
G | A | 2 | a0001c0002t0001g0049a0001c0002t0001g0050 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.71+709G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48553032 | ||||||
| chr19:48553456
|
C | T | 1 | a0001c0001t0001g0373 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.71+1133C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48553456 | ||||||
| chr19:48553517
|
C | T | 13 | a0001c0001t0001g0007a0001c0001t0001g0039a0001c0001t0001g0040others(10): Show | 13 | HG01433.hp1 HG02486.hp1 HG02723.hp2 others(10): Show |
intron_variant | MODIFIER | c.71+1194C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48553517 | ||||||
| chr19:48553569
|
T | C | 66 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(63): Show | 66 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(63): Show |
intron_variant | MODIFIER | c.71+1246T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48553569 | ||||||
| chr19:48553598
|
C | G | 7 | a0001c0001t0001g0032a0001c0001t0001g0036a0001c0002t0001g0034others(4): Show | 7 | HG00733.hp1 HG01346.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.71+1275C>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48553598 | ||||||
| chr19:48553638
|
G | C | 1 | a0001c0002t0001g0096 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.71+1315G>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48553638 | ||||||
| chr19:48553650
|
C | T | 1 | a0001c0003t0001g0370 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.71+1327C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48553650 | ||||||
| chr19:48553655
|
C | T | 9 | a0001c0001t0001g0361a0001c0001t0001g0362a0001c0001t0001g0363others(6): Show | 9 | HG01884.hp2 HG02809.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.71+1332C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48553655 | ||||||
| chr19:48553657
|
C | G | 1 | a0001c0001t0001g0360 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.71+1334C>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48553657 | ||||||
| chr19:48553675
|
T | A | 21 | a0001c0001t0001g0014a0001c0001t0001g0051a0001c0001t0001g0053others(18): Show | 21 | HG00735.hp2 HG00738.hp1 HG00738.hp2 others(18): Show |
intron_variant | MODIFIER | c.71+1352T>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48553675 | ||||||
| chr19:48553884
|
C | T | 2 | a0001c0002t0001g0358a0001c0002t0001g0359 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.71+1561C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48553884 | ||||||
| chr19:48553891
|
T | G | 1 | a0001c0001t0001g0097 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.71+1568T>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48553891 | ||||||
| chr19:48553910
|
G | T | 2 | a0001c0004t0001g0015a0001c0004t0001g0095 | 2 | HG00280.hp1 HG01109.hp2 |
intron_variant | MODIFIER | c.71+1587G>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48553910 | ||||||
| chr19:48553962
|
C | G | 1 | a0001c0019t0001g0372 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.71+1639C>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48553962 | ||||||
| chr19:48553971
|
C | CT | 46 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(43): Show | 46 | HG00735.hp2 HG00738.hp1 HG00738.hp2 others(43): Show |
intron_variant | MODIFIER | c.71+1656dupT | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48553971 | |||||
| chr19:48554066
|
T | C | 8 | a0001c0001t0001g0031a0001c0001t0001g0036a0001c0001t0001g0039others(5): Show | 8 | HG01891.hp2 HG02109.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.71+1743T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48554066 | ||||||
| chr19:48554173
|
T | C | 2 | a0001c0006t0001g0044a0003c0011t0001g0043 | 2 | HG02723.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.71+1850T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48554173 | ||||||
| chr19:48554411
|
C | T | 2 | a0001c0007t0001g0356a0001c0007t0001g0357 | 2 | HG02280.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.71+2088C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48554411 | ||||||
| chr19:48554461
|
G | A | 2 | a0001c0001t0001g0070a0001c0004t0001g0069 | 2 | HG00408.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.71+2138G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48554461 | ||||||
| chr19:48554532
|
C | A | 7 | a0001c0001t0001g0007a0001c0002t0001g0047a0001c0003t0001g0046others(4): Show | 7 | HG01433.hp1 HG02486.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.71+2209C>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48554532 | ||||||
| chr19:48554613
|
G | GC | 22 | a0001c0001t0001g0007a0001c0001t0001g0031a0001c0001t0001g0036others(19): Show | 22 | HG00642.hp2 HG01433.hp1 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.71+2297dupC | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48554613 | |||||
| chr19:48554620
|
C | A | 1 | a0001c0005t0001g0071 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.71+2297C>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48554620 | ||||||
| chr19:48554654
|
CT | C | 93 | a0001c0001t0001g0002a0001c0001t0001g0021a0001c0001t0001g0031others(90): Show | 93 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.71+2358delT | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48554654 | |||||
| chr19:48554654
|
CTT | C | 158 | a0001c0001t0001g0017a0001c0001t0001g0066a0001c0001t0001g0087others(155): Show | 159 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.71+2357_71+2358del others(2): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48554654 | |||||
| chr19:48554654
|
CTTT | C | 36 | a0001c0001t0001g0007a0001c0001t0001g0032a0001c0001t0001g0060others(33): Show | 36 | HG00280.hp1 HG00408.hp1 HG00609.hp2 others(33): Show |
intron_variant | MODIFIER | c.71+2356_71+2358del others(3): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48554654 | |||||
| chr19:48554654
|
CTTTT | C | 14 | a0001c0001t0001g0014a0001c0001t0001g0051a0001c0001t0001g0053others(11): Show | 14 | HG02257.hp1 HG02258.hp2 HG02717.hp1 others(11): Show |
intron_variant | MODIFIER | c.71+2355_71+2358del others(4): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48554654 | |||||
| chr19:48554681
|
T | C | 9 | a0001c0002t0001g0348a0001c0005t0001g0108a0001c0005t0001g0109others(6): Show | 9 | HG00099.hp2 HG00741.hp2 HG01175.hp2 others(6): Show |
intron_variant | MODIFIER | c.71+2358T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48554681 | ||||||
| chr19:48554717
|
A | G | 374 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(371): Show | 375 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(372): Show |
intron_variant | MODIFIER | c.71+2394A>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48554717 | ||||||
| chr19:48554749
|
C | T | 1 | a0001c0006t0001g0020 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.71+2426C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48554749 | ||||||
| chr19:48554920
|
C | T | 7 | a0001c0001t0001g0036a0001c0001t0001g0039a0001c0001t0001g0040others(4): Show | 7 | HG02109.hp2 HG02895.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.71+2597C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48554920 | ||||||
| chr19:48555069
|
G | A | 5 | a0001c0002t0001g0047a0001c0003t0001g0046a0001c0004t0001g0045others(2): Show | 5 | HG02486.hp1 HG02723.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.71+2746G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48555069 | ||||||
| chr19:48555115
|
G | A | 1 | a0001c0001t0001g0031 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.71+2792G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48555115 | ||||||
| chr19:48555136
|
C | T | 1 | a0001c0001t0001g0234 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.71+2813C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48555136 | ||||||
| chr19:48555212
|
C | T | 3 | a0001c0002t0001g0047a0001c0003t0001g0046a0001c0004t0001g0045 | 3 | HG02486.hp1 HG02896.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.71+2889C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48555212 | ||||||
| chr19:48555238
|
C | T | 7 | a0001c0001t0001g0036a0001c0001t0001g0039a0001c0001t0001g0040others(4): Show | 7 | HG02109.hp2 HG02895.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.71+2915C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48555238 | ||||||
| chr19:48555307
|
T | G | 43 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(40): Show | 43 | HG00735.hp2 HG00738.hp1 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.71+2984T>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48555307 | ||||||
| chr19:48555488
|
T | TTC | 6 | a0001c0001t0001g0036a0001c0001t0001g0039a0001c0001t0001g0040others(3): Show | 6 | HG02109.hp2 HG02895.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.71+3185_71+3186dup others(2): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48555488 | |||||
| chr19:48555544
|
G | A | 4 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0002t0001g0003others(1): Show | 4 | HG02055.hp1 HG02970.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.71+3221G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48555544 | ||||||
| chr19:48555549
|
C | CCT | 37 | a0001c0001t0001g0021a0001c0001t0001g0042a0001c0001t0001g0053others(34): Show | 37 | HG00733.hp2 HG00735.hp1 HG01074.hp1 others(34): Show |
intron_variant | MODIFIER | c.71+3265_71+3266dup others(2): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48555549 | |||||
| chr19:48555549
|
C | CCTCT | 38 | a0001c0001t0001g0092a0001c0001t0001g0151a0001c0001t0001g0152others(35): Show | 39 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(36): Show |
intron_variant | MODIFIER | c.71+3263_71+3266dup others(4): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48555549 | |||||
| chr19:48555549
|
C | CCTCTCT | 32 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(29): Show | 32 | HG00423.hp1 HG00438.hp2 HG00597.hp2 others(29): Show |
intron_variant | MODIFIER | c.71+3261_71+3266dup others(6): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48555549 | |||||
| chr19:48555549
|
C | CCTCTCTC others(1): Show |
19 | a0001c0001t0001g0036a0001c0001t0001g0123a0001c0001t0001g0126others(16): Show | 19 | HG01255.hp2 HG01884.hp2 HG01952.hp1 others(16): Show |
intron_variant | MODIFIER | c.71+3259_71+3266dup others(8): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48555549 | |||||
| chr19:48555549
|
C | CCTCTCTC others(3): Show |
5 | a0001c0001t0001g0024a0001c0001t0001g0041a0001c0001t0001g0117others(2): Show | 5 | HG02622.hp1 HG02886.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.71+3257_71+3266dup others(10): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48555549 | |||||
| chr19:48555549
|
C | CCTCTCTC others(5): Show |
2 | a0001c0001t0001g0040a0001c0001t0001g0116 | 2 | HG03540.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.71+3255_71+3266dup others(12): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48555549 | |||||
| chr19:48555549
|
C | CCTCTCTC others(7): Show |
6 | a0001c0001t0001g0023a0001c0001t0001g0039a0001c0004t0001g0016others(3): Show | 6 | HG01099.hp1 HG01891.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.71+3253_71+3266dup others(14): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48555549 | |||||
| chr19:48555549
|
C | CCTCTCTC others(9): Show |
1 | a0001c0001t0001g0017 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.71+3251_71+3266dup others(16): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48555549 | |||||
| chr19:48555549
|
C | CCTCTCTC others(11): Show |
1 | a0001c0001t0001g0115 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.71+3249_71+3266dup others(18): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48555549 | |||||
| chr19:48555549
|
C | CCTCTCTC others(15): Show |
1 | a0001c0001t0001g0031 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.71+3245_71+3266dup others(22): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48555549 | |||||
| chr19:48555549
|
CCT | C | 9 | a0001c0001t0001g0002a0001c0001t0001g0215a0001c0001t0001g0259others(6): Show | 9 | HG01123.hp1 HG01175.hp1 HG01981.hp2 others(6): Show |
intron_variant | MODIFIER | c.71+3265_71+3266del others(2): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48555549 | |||||
| chr19:48555549
|
CCTCT | C | 29 | a0001c0001t0001g0032a0001c0001t0001g0107a0001c0001t0001g0218others(26): Show | 29 | HG00558.hp1 HG00642.hp2 HG00733.hp1 others(26): Show |
intron_variant | MODIFIER | c.71+3263_71+3266del others(4): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48555549 | |||||
| chr19:48555549
|
CCTCTCT | C | 10 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0002t0001g0047others(7): Show | 10 | HG01433.hp1 HG02486.hp1 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.71+3261_71+3266del others(6): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48555549 | |||||
| chr19:48555549
|
CCTCTCTC others(1): Show |
C | 9 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0075others(6): Show | 9 | HG00673.hp2 HG01257.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.71+3259_71+3266del others(8): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48555549 | |||||
| chr19:48555549
|
CCTCTCTC others(3): Show |
C | 90 | a0001c0001t0001g0070a0001c0001t0001g0080a0001c0001t0001g0087others(87): Show | 90 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.71+3257_71+3266del others(10): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48555549 | |||||
| chr19:48555549
|
CCTCTCTC others(5): Show |
C | 1 | a0001c0003t0001g0233 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.71+3255_71+3266del others(12): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48555549 | |||||
| chr19:48555549
|
CCTCTCTC others(9): Show |
C | 1 | a0001c0004t0001g0086 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.71+3251_71+3266del others(16): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48555549 | |||||
| chr19:48555589
|
T | TC | 3 | a0001c0001t0001g0060a0001c0001t0001g0171a0001c0001t0001g0306 | 3 | HG01106.hp2 HG02809.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.71+3266_71+3267ins others(1): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48555589 | ||||||
| chr19:48555589
|
T | TCTC | 4 | a0001c0001t0001g0051a0001c0002t0001g0149a0001c0002t0001g0303others(1): Show | 4 | HG00140.hp1 HG01192.hp2 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.71+3266_71+3267ins others(3): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48555589 | ||||||
| chr19:48555589
|
T | TCTCTC | 5 | a0001c0001t0001g0130a0001c0002t0001g0098a0001c0002t0001g0131others(2): Show | 5 | HG01934.hp1 HG01934.hp2 HG02148.hp1 others(2): Show |
intron_variant | MODIFIER | c.71+3266_71+3267ins others(5): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48555589 | ||||||
| chr19:48555589
|
T | TCTCTCTC others(4): Show |
1 | a0001c0001t0001g0361 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.71+3266_71+3267ins others(11): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48555589 | ||||||
| chr19:48555589
|
T | TCTCTCTC others(14): Show |
1 | a0001c0006t0001g0020 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.71+3266_71+3267ins others(21): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48555589 | ||||||
| chr19:48555590
|
T | C | 5 | a0001c0001t0001g0092a0001c0002t0001g0093a0001c0003t0001g0120others(2): Show | 5 | HG01243.hp1 HG02109.hp1 HG02148.hp2 others(2): Show |
intron_variant | MODIFIER | c.71+3267T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48555590 | ||||||
| chr19:48555591
|
T | C | 1 | a0001c0003t0001g0119 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.71+3268T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48555591 | ||||||
| chr19:48555592
|
T | C | 5 | a0001c0001t0001g0092a0001c0002t0001g0093a0001c0006t0001g0090others(2): Show | 5 | HG01243.hp1 HG02109.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.71+3269T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48555592 | ||||||
| chr19:48555733
|
C | T | 4 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0002t0001g0003others(1): Show | 4 | HG02055.hp1 HG02970.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.71+3410C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48555733 | ||||||
| chr19:48555747
|
G | GT | 24 | a0001c0001t0001g0014a0001c0001t0001g0051a0001c0001t0001g0053others(21): Show | 24 | HG00735.hp2 HG00738.hp1 HG00738.hp2 others(21): Show |
intron_variant | MODIFIER | c.71+3433dupT | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48555747 | |||||
| chr19:48555825
|
C | T | 17 | a0001c0001t0001g0036a0001c0001t0001g0039a0001c0001t0001g0040others(14): Show | 17 | HG01243.hp1 HG01928.hp1 HG01943.hp1 others(14): Show |
intron_variant | MODIFIER | c.71+3502C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48555825 | ||||||
| chr19:48555906
|
A | AT | 5 | a0001c0001t0001g0092a0001c0002t0001g0093a0001c0006t0001g0090others(2): Show | 5 | HG01243.hp1 HG02109.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.71+3589dupT | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48555906 | |||||
| chr19:48555941
|
T | C | 20 | a0001c0001t0001g0014a0001c0001t0001g0051a0001c0001t0001g0053others(17): Show | 20 | HG00735.hp2 HG00738.hp1 HG00738.hp2 others(17): Show |
intron_variant | MODIFIER | c.71+3618T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48555941 | ||||||
| chr19:48556181
|
G | C | 4 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0075others(1): Show | 4 | HG03098.hp1 HG03130.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.71+3858G>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48556181 | ||||||
| chr19:48556228
|
C | T | 4 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0002t0001g0003others(1): Show | 4 | HG02055.hp1 HG02970.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.71+3905C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48556228 | ||||||
| chr19:48556268
|
T | G | 140 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(137): Show | 140 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(137): Show |
intron_variant | MODIFIER | c.71+3945T>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48556268 | ||||||
| chr19:48556272
|
A | G | 2 | a0001c0002t0001g0211a0001c0002t0001g0212 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.71+3949A>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48556272 | ||||||
| chr19:48556339
|
A | AAAGGACG others(5): Show |
1 | a0001c0001t0001g0267 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.71+4019_71+4030dup others(12): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48556339 | |||||
| chr19:48556351
|
G | C | 1 | a0001c0001t0001g0172 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.71+4028G>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48556351 | ||||||
| chr19:48556377
|
T | C | 1 | a0001c0001t0001g0116 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.71+4054T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48556377 | ||||||
| chr19:48556462
|
G | A | 1 | a0001c0001t0001g0268 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.71+4139G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48556462 | ||||||
| chr19:48556480
|
C | G | 30 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0021others(27): Show | 30 | HG00733.hp1 HG01070.hp2 HG01071.hp2 others(27): Show |
intron_variant | MODIFIER | c.71+4157C>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48556480 | ||||||
| chr19:48556614
|
G | A | 1 | a0001c0002t0001g0182 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.71+4291G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48556614 | ||||||
| chr19:48556652
|
T | TA | 21 | a0001c0001t0001g0014a0001c0001t0001g0032a0001c0001t0001g0051others(18): Show | 21 | HG00735.hp2 HG00738.hp1 HG00738.hp2 others(18): Show |
intron_variant | MODIFIER | c.71+4344dupA | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48556652 | |||||
| chr19:48556652
|
TA | T | 6 | a0001c0001t0001g0167a0001c0001t0001g0210a0001c0001t0001g0226others(3): Show | 6 | HG01884.hp1 NA18747.hp1 NA18747.hp2 others(3): Show |
intron_variant | MODIFIER | c.71+4344delA | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48556652 | |||||
| chr19:48556794
|
T | TA | 7 | a0001c0001t0001g0036a0001c0001t0001g0039a0001c0001t0001g0040others(4): Show | 7 | HG02109.hp2 HG02895.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.71+4478dupA | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48556794 | |||||
| chr19:48556863
|
T | A | 1 | a0001c0004t0001g0132 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.71+4540T>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48556863 | ||||||
| chr19:48556935
|
A | G | 168 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(165): Show | 168 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.71+4612A>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48556935 | ||||||
| chr19:48556936
|
C | T | 1 | a0001c0005t0001g0209 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.71+4613C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48556936 | ||||||
| chr19:48556949
|
C | CA | 103 | a0001c0001t0001g0070a0001c0001t0001g0073a0001c0001t0001g0074others(100): Show | 103 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(100): Show |
intron_variant | MODIFIER | c.71+4638dupA | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48556949 | |||||
| chr19:48557019
|
G | T | 21 | a0001c0001t0001g0070a0001c0001t0001g0073a0001c0001t0001g0074others(18): Show | 21 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(18): Show |
intron_variant | MODIFIER | c.71+4696G>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48557019 | ||||||
| chr19:48557052
|
C | A | 1 | a0001c0001t0001g0363 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.71+4729C>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48557052 | ||||||
| chr19:48557068
|
A | G | 1 | a0001c0002t0001g0118 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.71+4745A>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48557068 | ||||||
| chr19:48557228
|
A | G | 20 | a0001c0001t0001g0014a0001c0001t0001g0051a0001c0001t0001g0053others(17): Show | 20 | HG00735.hp2 HG00738.hp1 HG00738.hp2 others(17): Show |
intron_variant | MODIFIER | c.71+4905A>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48557228 | ||||||
| chr19:48557240
|
G | GCTTT | 20 | a0001c0001t0001g0014a0001c0001t0001g0051a0001c0001t0001g0053others(17): Show | 20 | HG00735.hp2 HG00738.hp1 HG00738.hp2 others(17): Show |
intron_variant | MODIFIER | c.71+4917_71+4918ins others(4): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48557240 | ||||||
| chr19:48557278
|
G | A | 7 | a0001c0001t0001g0014a0001c0001t0001g0051a0001c0001t0001g0053others(4): Show | 7 | HG02257.hp1 HG02717.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.71+4955G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48557278 | ||||||
| chr19:48557539
|
C | CA | 6 | a0001c0002t0001g0328a0001c0004t0001g0058a0001c0004t0001g0089others(3): Show | 6 | HG01175.hp2 HG01361.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.71+5223dupA | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48557539 | |||||
| chr19:48557547
|
G | A | 124 | a0001c0001t0001g0014a0001c0001t0001g0051a0001c0001t0001g0053others(121): Show | 124 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.71+5224G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48557547 | ||||||
| chr19:48557643
|
A | C | 120 | a0001c0001t0001g0014a0001c0001t0001g0051a0001c0001t0001g0053others(117): Show | 120 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(117): Show |
intron_variant | MODIFIER | c.71+5320A>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48557643 | ||||||
| chr19:48557645
|
G | A | 2 | a0001c0007t0001g0356a0001c0007t0001g0357 | 2 | HG02280.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.71+5322G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48557645 | ||||||
| chr19:48557787
|
T | C | 120 | a0001c0001t0001g0014a0001c0001t0001g0051a0001c0001t0001g0053others(117): Show | 120 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(117): Show |
intron_variant | MODIFIER | c.71+5464T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48557787 | ||||||
| chr19:48558050
|
C | G | 2 | a0001c0001t0001g0346a0001c0001t0001g0355 | 2 | HG02071.hp2 NA18967.hp2 |
intron_variant | MODIFIER | c.71+5727C>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48558050 | ||||||
| chr19:48558058
|
C | A | 122 | a0001c0001t0001g0014a0001c0001t0001g0051a0001c0001t0001g0053others(119): Show | 122 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.71+5735C>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48558058 | ||||||
| chr19:48558322
|
C | T | 7 | a0001c0001t0001g0007a0001c0002t0001g0047a0001c0003t0001g0046others(4): Show | 7 | HG01433.hp1 HG02486.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.71+5999C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48558322 | ||||||
| chr19:48558335
|
GT | G | 121 | a0001c0001t0001g0014a0001c0001t0001g0051a0001c0001t0001g0053others(118): Show | 121 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(118): Show |
intron_variant | MODIFIER | c.71+6014delT | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48558335 | |||||
| chr19:48558337
|
T | G | 1 | a0002c0008t0001g0345 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.71+6014T>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48558337 | ||||||
| chr19:48558338
|
A | C | 1 | a0002c0008t0001g0345 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.71+6015A>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48558338 | ||||||
| chr19:48558351
|
C | T | 39 | a0001c0001t0001g0014a0001c0001t0001g0051a0001c0001t0001g0053others(36): Show | 39 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(36): Show |
intron_variant | MODIFIER | c.71+6028C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48558351 | ||||||
| chr19:48558393
|
G | A | 122 | a0001c0001t0001g0014a0001c0001t0001g0051a0001c0001t0001g0053others(119): Show | 122 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.71+6070G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48558393 | ||||||
| chr19:48558467
|
G | A | 161 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(158): Show | 161 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(158): Show |
intron_variant | MODIFIER | c.71+6144G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48558467 | ||||||
| chr19:48558498
|
G | T | 1 | a0001c0001t0001g0344 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.71+6175G>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48558498 | ||||||
| chr19:48558679
|
C | CT | 25 | a0001c0001t0001g0117a0001c0001t0001g0146a0001c0001t0001g0207others(22): Show | 25 | HG00621.hp1 HG00621.hp2 HG00642.hp1 others(22): Show |
intron_variant | MODIFIER | c.71+6378dupT | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48558679 | |||||
| chr19:48558679
|
C | CTTT | 28 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(25): Show | 28 | HG00733.hp1 HG01243.hp1 HG01346.hp2 others(25): Show |
intron_variant | MODIFIER | c.71+6376_71+6378dup others(3): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48558679 | |||||
| chr19:48558679
|
C | CTTTT | 16 | a0001c0001t0001g0021a0001c0001t0001g0039a0001c0001t0001g0040others(13): Show | 16 | HG01884.hp1 HG02257.hp2 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.71+6375_71+6378dup others(4): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48558679 | |||||
| chr19:48558679
|
CT | C | 12 | a0001c0001t0001g0017a0001c0001t0001g0361a0001c0001t0001g0362others(9): Show | 12 | HG01255.hp2 HG01884.hp2 HG02809.hp1 others(9): Show |
intron_variant | MODIFIER | c.71+6378delT | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48558679 | |||||
| chr19:48558679
|
CTT | C | 20 | a0001c0001t0001g0060a0001c0001t0001g0066a0001c0001t0001g0267others(17): Show | 20 | HG00423.hp2 HG00558.hp2 HG00735.hp2 others(17): Show |
intron_variant | MODIFIER | c.71+6377_71+6378del others(2): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48558679 | |||||
| chr19:48558679
|
CTTT | C | 93 | a0001c0001t0001g0070a0001c0001t0001g0073a0001c0001t0001g0074others(90): Show | 93 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(90): Show |
intron_variant | MODIFIER | c.71+6376_71+6378del others(3): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48558679 | |||||
| chr19:48558683
|
T | C | 1 | a0001c0002t0001g0098 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.71+6360T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48558683 | ||||||
| chr19:48558684
|
T | C | 6 | a0001c0001t0001g0310a0001c0001t0001g0311a0001c0001t0001g0312others(3): Show | 6 | HG00140.hp1 HG02165.hp1 HG03831.hp2 others(3): Show |
intron_variant | MODIFIER | c.71+6361T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48558684 | ||||||
| chr19:48558685
|
T | C | 1 | a0001c0001t0001g0183 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.71+6362T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48558685 | ||||||
| chr19:48558771
|
G | A | 1 | a0001c0002t0001g0077 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.71+6448G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48558771 | ||||||
| chr19:48558825
|
C | T | 11 | a0001c0001t0001g0007a0001c0002t0001g0047a0001c0003t0001g0046others(8): Show | 11 | HG01433.hp1 HG02145.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.71+6502C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48558825 | ||||||
| chr19:48558900
|
T | G | 157 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(154): Show | 157 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.71+6577T>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48558900 | ||||||
| chr19:48558906
|
A | G | 157 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(154): Show | 157 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.71+6583A>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48558906 | ||||||
| chr19:48558991
|
C | T | 1 | a0001c0004t0001g0127 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.71+6668C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48558991 | ||||||
| chr19:48559007
|
G | C | 7 | a0001c0001t0001g0036a0001c0001t0001g0039a0001c0001t0001g0040others(4): Show | 7 | HG02109.hp2 HG02895.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.71+6684G>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48559007 | ||||||
| chr19:48559065
|
G | C | 1 | a0001c0001t0001g0238 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.71+6742G>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48559065 | ||||||
| chr19:48559238
|
C | T | 29 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0021others(26): Show | 29 | HG00733.hp1 HG01243.hp1 HG01346.hp2 others(26): Show |
intron_variant | MODIFIER | c.71+6915C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48559238 | ||||||
| chr19:48559251
|
G | C | 2 | a0001c0002t0001g0122a0001c0009t0001g0121 | 2 | HG01255.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.71+6928G>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48559251 | ||||||
| chr19:48559282
|
G | C | 4 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0002t0001g0003others(1): Show | 4 | HG02055.hp1 HG02970.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.71+6959G>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48559282 | ||||||
| chr19:48559306
|
G | A | 29 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0021others(26): Show | 29 | HG00733.hp1 HG01243.hp1 HG01346.hp2 others(26): Show |
intron_variant | MODIFIER | c.71+6983G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48559306 | ||||||
| chr19:48559311
|
T | A | 5 | a0001c0001t0001g0168a0001c0002t0001g0100a0001c0003t0001g0128others(2): Show | 5 | HG01928.hp1 HG01943.hp1 HG02027.hp2 others(2): Show |
intron_variant | MODIFIER | c.71+6988T>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48559311 | ||||||
| chr19:48559322
|
A | G | 4 | a0001c0001t0001g0060a0001c0002t0001g0049a0001c0002t0001g0050others(1): Show | 4 | HG01070.hp2 HG01071.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.71+6999A>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48559322 | ||||||
| chr19:48559348
|
T | TTTTTG | 12 | a0001c0001t0001g0115a0001c0001t0001g0117a0001c0001t0001g0144others(9): Show | 12 | HG00423.hp1 HG01069.hp2 HG01071.hp1 others(9): Show |
intron_variant | MODIFIER | c.71+7061_71+7065dup others(5): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48559348 | |||||
| chr19:48559348
|
TTTTTG | T | 140 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0021others(137): Show | 140 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(137): Show |
intron_variant | MODIFIER | c.71+7061_71+7065del others(5): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48559348 | |||||
| chr19:48559348
|
TTTTTGTT others(3): Show |
T | 11 | a0001c0001t0001g0007a0001c0002t0001g0047a0001c0003t0001g0046others(8): Show | 11 | HG01433.hp1 HG02145.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.71+7056_71+7065del others(10): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48559348 | |||||
| chr19:48559348
|
TTTTTGTT others(8): Show |
T | 1 | a0001c0002t0001g0118 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.71+7051_71+7065del others(15): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48559348 | |||||
| chr19:48559388
|
G | T | 1 | a0001c0002t0001g0328 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.71+7065G>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48559388 | ||||||
| chr19:48559551
|
G | T | 2 | a0001c0001t0001g0130a0001c0007t0001g0166 | 2 | HG01261.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.71+7228G>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48559551 | ||||||
| chr19:48559579
|
C | A | 4 | a0001c0001t0001g0060a0001c0002t0001g0049a0001c0002t0001g0050others(1): Show | 4 | HG01070.hp2 HG01071.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.71+7256C>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48559579 | ||||||
| chr19:48559722
|
C | T | 77 | a0001c0001t0001g0227a0001c0001t0001g0229a0001c0001t0001g0232others(74): Show | 77 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(74): Show |
intron_variant | MODIFIER | c.71+7399C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48559722 | ||||||
| chr19:48559750
|
AG | A | 18 | a0001c0001t0001g0007a0001c0001t0001g0036a0001c0001t0001g0039others(15): Show | 18 | HG01433.hp1 HG02109.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.71+7429delG | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48559750 | |||||
| chr19:48559849
|
CA | C | 4 | a0001c0004t0001g0058a0001c0004t0001g0089a0001c0006t0001g0061others(1): Show | 4 | HG02145.hp2 HG02258.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.71+7527delA | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48559849 | ||||||
| chr19:48559959
|
T | TA | 6 | a0001c0001t0001g0107a0001c0001t0001g0117a0001c0001t0001g0306others(3): Show | 6 | HG01070.hp1 HG01106.hp2 HG01358.hp2 others(3): Show |
intron_variant | MODIFIER | c.71+7654dupA | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48559959 | |||||
| chr19:48559959
|
TA | T | 14 | a0001c0001t0001g0014a0001c0001t0001g0056a0001c0001t0001g0066others(11): Show | 14 | HG01081.hp2 HG01168.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.71+7654delA | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48559959 | |||||
| chr19:48559959
|
TAA | T | 22 | a0001c0001t0001g0007a0001c0001t0001g0036a0001c0001t0001g0039others(19): Show | 22 | HG01243.hp1 HG01433.hp1 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.71+7653_71+7654del others(2): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48559959 | |||||
| chr19:48559971
|
A | C | 1 | a0001c0003t0001g0216 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.71+7648A>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48559971 | ||||||
| chr19:48560072
|
C | G | 1 | a0001c0005t0001g0019 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.71+7749C>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48560072 | ||||||
| chr19:48560089
|
C | T | 1 | a0001c0004t0001g0095 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.71+7766C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48560089 | ||||||
| chr19:48560135
|
G | A | 7 | a0001c0001t0001g0036a0001c0001t0001g0039a0001c0001t0001g0040others(4): Show | 7 | HG02109.hp2 HG02895.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.71+7812G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48560135 | ||||||
| chr19:48560361
|
T | C | 1 | a0002c0008t0001g0162 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.71+8038T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48560361 | ||||||
| chr19:48560371
|
A | G | 5 | a0001c0001t0001g0092a0001c0002t0001g0093a0001c0006t0001g0090others(2): Show | 5 | HG01243.hp1 HG02109.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.71+8048A>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48560371 | ||||||
| chr19:48560434
|
C | A | 1 | a0001c0001t0001g0023 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.71+8111C>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48560434 | ||||||
| chr19:48560535
|
A | G | 1 | a0001c0004t0001g0095 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.71+8212A>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48560535 | ||||||
| chr19:48560579
|
T | A | 1 | a0001c0005t0001g0008 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.71+8256T>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48560579 | ||||||
| chr19:48560579
|
T | TA | 20 | a0001c0001t0001g0021a0001c0001t0001g0023a0001c0001t0001g0031others(17): Show | 20 | HG00733.hp1 HG01346.hp2 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.71+8263dupA | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48560579 | |||||
| chr19:48560651
|
T | C | 5 | a0001c0001t0001g0092a0001c0002t0001g0093a0001c0006t0001g0090others(2): Show | 5 | HG01243.hp1 HG02109.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.71+8328T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48560651 | ||||||
| chr19:48560657
|
C | A | 2 | a0002c0008t0001g0269a0002c0008t0001g0345 | 2 | NA18961.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.71+8334C>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48560657 | ||||||
| chr19:48560666
|
A | AAATTGTC others(9): Show |
1 | a0001c0001t0001g0270 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.71+8345_71+8346ins others(16): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48560666 | |||||
| chr19:48560669
|
C | T | 155 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(152): Show | 155 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.71+8346C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48560669 | ||||||
| chr19:48560703
|
ATAATCCC others(462): Show |
A | 2 | a0001c0006t0001g0044a0003c0011t0001g0043 | 2 | HG02723.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.71+8392_71+8860del | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48560703 | |||||
| chr19:48560863
|
G | A | 4 | a0001c0004t0001g0058a0001c0004t0001g0089a0001c0006t0001g0061others(1): Show | 4 | HG02145.hp2 HG02258.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.71+8540G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48560863 | ||||||
| chr19:48560899
|
C | T | 5 | a0001c0001t0001g0092a0001c0002t0001g0093a0001c0006t0001g0090others(2): Show | 5 | HG01243.hp1 HG02109.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.71+8576C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48560899 | ||||||
| chr19:48561004
|
C | T | 3 | a0001c0002t0001g0049a0001c0002t0001g0050a0001c0006t0001g0090 | 3 | HG01070.hp2 HG01071.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.71+8681C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48561004 | ||||||
| chr19:48561063
|
C | T | 1 | a0001c0005t0001g0019 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.71+8740C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48561063 | ||||||
| chr19:48561112
|
G | A | 1 | a0001c0001t0001g0186 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.71+8789G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48561112 | ||||||
| chr19:48561146
|
C | T | 3 | a0001c0001t0001g0007a0001c0001t0001g0055a0001c0006t0001g0006 | 3 | HG01433.hp1 HG03195.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.71+8823C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48561146 | ||||||
| chr19:48561152
|
C | T | 2 | a0001c0002t0001g0049a0001c0002t0001g0050 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.71+8829C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48561152 | ||||||
| chr19:48561195
|
C | T | 10 | a0001c0001t0001g0014a0001c0001t0001g0039a0001c0001t0001g0040others(7): Show | 10 | HG02257.hp1 HG02717.hp1 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.71+8872C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48561195 | ||||||
| chr19:48561227
|
C | T | 1 | a0001c0006t0001g0090 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.71+8904C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48561227 | ||||||
| chr19:48561258
|
C | T | 2 | a0001c0006t0001g0038a0001c0010t0001g0037 | 2 | HG02976.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.71+8935C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48561258 | ||||||
| chr19:48561287
|
T | G | 7 | a0001c0001t0001g0146a0001c0001t0001g0151a0001c0002t0001g0147others(4): Show | 7 | HG01123.hp2 HG01361.hp1 HG01433.hp2 others(4): Show |
intron_variant | MODIFIER | c.71+8964T>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48561287 | ||||||
| chr19:48561288
|
C | T | 7 | a0001c0001t0001g0146a0001c0001t0001g0151a0001c0002t0001g0147others(4): Show | 7 | HG01123.hp2 HG01361.hp1 HG01433.hp2 others(4): Show |
intron_variant | MODIFIER | c.71+8965C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48561288 | ||||||
| chr19:48561296
|
C | T | 7 | a0001c0001t0001g0146a0001c0001t0001g0151a0001c0002t0001g0147others(4): Show | 7 | HG01123.hp2 HG01361.hp1 HG01433.hp2 others(4): Show |
intron_variant | MODIFIER | c.71+8973C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48561296 | ||||||
| chr19:48561353
|
C | T | 1 | a0001c0001t0001g0172 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.71+9030C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48561353 | ||||||
| chr19:48561384
|
G | A | 3 | a0001c0002t0001g0122a0001c0002t0001g0252a0001c0009t0001g0121 | 3 | HG01255.hp2 HG01346.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.71+9061G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48561384 | ||||||
| chr19:48561390
|
T | C | 1 | a0001c0002t0001g0079 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.71+9067T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48561390 | ||||||
| chr19:48561416
|
T | C | 99 | a0001c0001t0001g0123a0001c0001t0001g0187a0001c0001t0001g0227others(96): Show | 99 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(96): Show |
intron_variant | MODIFIER | c.71+9093T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48561416 | ||||||
| chr19:48561422
|
A | T | 99 | a0001c0001t0001g0123a0001c0001t0001g0187a0001c0001t0001g0227others(96): Show | 99 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(96): Show |
intron_variant | MODIFIER | c.71+9099A>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48561422 | ||||||
| chr19:48561430
|
A | AAAAT | 96 | a0001c0001t0001g0123a0001c0001t0001g0187a0001c0001t0001g0227others(93): Show | 96 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.71+9121_71+9124dup others(4): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48561430 | |||||
| chr19:48561448
|
G | A | 3 | a0001c0002t0001g0049a0001c0002t0001g0050a0001c0006t0001g0090 | 3 | HG01070.hp2 HG01071.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.71+9125G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48561448 | ||||||
| chr19:48561456
|
A | G | 3 | a0001c0002t0001g0049a0001c0002t0001g0050a0001c0006t0001g0090 | 3 | HG01070.hp2 HG01071.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.71+9133A>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48561456 | ||||||
| chr19:48561458
|
A | T | 3 | a0001c0002t0001g0049a0001c0002t0001g0050a0001c0006t0001g0090 | 3 | HG01070.hp2 HG01071.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.71+9135A>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48561458 | ||||||
| chr19:48561459
|
T | A | 3 | a0001c0002t0001g0049a0001c0002t0001g0050a0001c0006t0001g0090 | 3 | HG01070.hp2 HG01071.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.71+9136T>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48561459 | ||||||
| chr19:48561462
|
ATAAAT | A | 96 | a0001c0001t0001g0123a0001c0001t0001g0187a0001c0001t0001g0227others(93): Show | 96 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.71+9143_71+9147del others(5): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48561462 | |||||
| chr19:48561466
|
AT | A | 3 | a0001c0002t0001g0049a0001c0002t0001g0050a0001c0006t0001g0090 | 3 | HG01070.hp2 HG01071.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.71+9145delT | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48561466 | |||||
| chr19:48561547
|
GA | G | 103 | a0001c0001t0001g0036a0001c0001t0001g0123a0001c0001t0001g0187others(100): Show | 103 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.71+9231delA | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48561547 | |||||
| chr19:48561597
|
C | T | 100 | a0001c0001t0001g0116a0001c0001t0001g0187a0001c0001t0001g0227others(97): Show | 100 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(97): Show |
intron_variant | MODIFIER | c.71+9274C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48561597 | ||||||
| chr19:48561598
|
A | G | 102 | a0001c0001t0001g0116a0001c0001t0001g0187a0001c0001t0001g0227others(99): Show | 102 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.71+9275A>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48561598 | ||||||
| chr19:48561702
|
C | T | 105 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(102): Show | 105 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.71+9379C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48561702 | ||||||
| chr19:48561724
|
G | A | 1 | a0001c0002t0001g0103 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.71+9401G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48561724 | ||||||
| chr19:48561752
|
C | T | 36 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(33): Show | 36 | HG00733.hp1 HG01069.hp2 HG01071.hp1 others(33): Show |
intron_variant | MODIFIER | c.71+9429C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48561752 | ||||||
| chr19:48561795
|
C | T | 2 | a0001c0002t0001g0047a0007c0017t0001g0029 | 2 | HG02486.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.71+9472C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48561795 | ||||||
| chr19:48561802
|
C | A | 84 | a0001c0001t0001g0123a0001c0001t0001g0187a0001c0001t0001g0227others(81): Show | 84 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(81): Show |
intron_variant | MODIFIER | c.71+9479C>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48561802 | ||||||
| chr19:48561905
|
G | A | 80 | a0001c0001t0001g0123a0001c0001t0001g0187a0001c0001t0001g0227others(77): Show | 80 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.71+9582G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48561905 | ||||||
| chr19:48561931
|
A | G | 1 | a0001c0004t0001g0069 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.71+9608A>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48561931 | ||||||
| chr19:48561988
|
G | A | 84 | a0001c0001t0001g0097a0001c0001t0001g0104a0001c0001t0001g0123others(81): Show | 84 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(81): Show |
intron_variant | MODIFIER | c.71+9665G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48561988 | ||||||
| chr19:48562037
|
A | G | 89 | a0001c0001t0001g0097a0001c0001t0001g0104a0001c0001t0001g0123others(86): Show | 89 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(86): Show |
intron_variant | MODIFIER | c.71+9714A>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48562037 | ||||||
| chr19:48562157
|
C | T | 2 | a0001c0002t0001g0049a0001c0002t0001g0050 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.71+9834C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48562157 | ||||||
| chr19:48562218
|
T | C | 25 | a0001c0001t0001g0017a0001c0001t0001g0024a0001c0001t0001g0025others(22): Show | 25 | HG01243.hp1 HG02055.hp2 HG02145.hp2 others(22): Show |
intron_variant | MODIFIER | c.71+9895T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48562218 | ||||||
| chr19:48562249
|
G | A | 2 | a0001c0001t0001g0199a0001c0001t0001g0204 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.71+9926G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48562249 | ||||||
| chr19:48562269
|
T | C | 2 | a0001c0001t0001g0101a0001c0001t0001g0175 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.71+9946T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48562269 | ||||||
| chr19:48562335
|
C | T | 1 | a0001c0001t0001g0116 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.71+10012C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48562335 | ||||||
| chr19:48562375
|
A | G | 41 | a0001c0001t0001g0007a0001c0001t0001g0017a0001c0001t0001g0021others(38): Show | 42 | HG00099.hp2 HG00140.hp2 HG00733.hp2 others(39): Show |
intron_variant | MODIFIER | c.71+10052A>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48562375 | ||||||
| chr19:48562386
|
C | CA | 14 | a0001c0001t0001g0115a0001c0001t0001g0257a0001c0001t0001g0364others(11): Show | 14 | HG00423.hp1 HG01109.hp1 HG01515.hp1 others(11): Show |
intron_variant | MODIFIER | c.71+10078dupA | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48562386 | |||||
| chr19:48562500
|
C | T | 1 | a0001c0001t0001g0300 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.71+10177C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48562500 | ||||||
| chr19:48562534
|
G | A | 110 | a0001c0001t0001g0031a0001c0001t0001g0039a0001c0001t0001g0040others(107): Show | 110 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.71+10211G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48562534 | ||||||
| chr19:48562590
|
T | C | 2 | a0001c0001t0001g0101a0001c0001t0001g0175 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.71+10267T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48562590 | ||||||
| chr19:48562604
|
T | A | 1 | a0001c0002t0001g0182 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.71+10281T>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48562604 | ||||||
| chr19:48562605
|
T | A | 1 | a0001c0003t0001g0125 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.71+10282T>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48562605 | ||||||
| chr19:48562633
|
T | C | 171 | a0001c0001t0001g0007a0001c0001t0001g0017a0001c0001t0001g0021others(168): Show | 172 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(169): Show |
intron_variant | MODIFIER | c.71+10310T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48562633 | ||||||
| chr19:48562666
|
T | G | 39 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0024others(36): Show | 39 | HG01070.hp2 HG01071.hp2 HG01243.hp1 others(36): Show |
intron_variant | MODIFIER | c.71+10343T>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48562666 | ||||||
| chr19:48562724
|
A | G | 110 | a0001c0001t0001g0017a0001c0001t0001g0031a0001c0001t0001g0039others(107): Show | 110 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.71+10401A>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48562724 | ||||||
| chr19:48562741
|
G | A | 6 | a0001c0005t0001g0008a0001c0005t0001g0009a0001c0005t0001g0010others(3): Show | 6 | HG01884.hp1 HG02896.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.71+10418G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48562741 | ||||||
| chr19:48562743
|
G | A | 5 | a0001c0005t0001g0008a0001c0005t0001g0009a0001c0005t0001g0010others(2): Show | 5 | HG01884.hp1 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.71+10420G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48562743 | ||||||
| chr19:48562780
|
G | A | 204 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(201): Show | 205 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(202): Show |
intron_variant | MODIFIER | c.71+10457G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48562780 | ||||||
| chr19:48563035
|
C | G | 124 | a0001c0001t0001g0007a0001c0001t0001g0017a0001c0001t0001g0031others(121): Show | 124 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(121): Show |
intron_variant | MODIFIER | c.71+10712C>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48563035 | ||||||
| chr19:48563055
|
T | A | 1 | a0001c0002t0001g0317 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.71+10732T>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48563055 | ||||||
| chr19:48563223
|
CG | C | 25 | a0001c0001t0001g0017a0001c0001t0001g0039a0001c0001t0001g0040others(22): Show | 25 | HG00642.hp1 HG00738.hp1 HG01168.hp2 others(22): Show |
intron_variant | MODIFIER | c.71+10902delG | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48563223 | |||||
| chr19:48563415
|
G | T | 1 | a0001c0001t0001g0373 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.71+11092G>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48563415 | ||||||
| chr19:48563461
|
C | T | 5 | a0001c0001t0001g0007a0001c0001t0001g0031a0001c0001t0001g0055others(2): Show | 5 | HG01433.hp1 HG01891.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.71+11138C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48563461 | ||||||
| chr19:48563473
|
T | A | 20 | a0001c0002t0001g0348a0001c0005t0001g0001a0001c0005t0001g0071others(17): Show | 21 | HG00099.hp2 HG00140.hp2 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.71+11150T>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48563473 | ||||||
| chr19:48563586
|
T | C | 1 | a0001c0005t0001g0313 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.71+11263T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48563586 | ||||||
| chr19:48563613
|
C | T | 1 | a0001c0007t0001g0357 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.71+11290C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48563613 | ||||||
| chr19:48563623
|
C | T | 1 | a0001c0006t0001g0090 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.71+11300C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48563623 | ||||||
| chr19:48563679
|
T | C | 139 | a0001c0001t0001g0007a0001c0001t0001g0017a0001c0001t0001g0031others(136): Show | 140 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(137): Show |
intron_variant | MODIFIER | c.71+11356T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48563679 | ||||||
| chr19:48563680
|
G | A | 20 | a0001c0002t0001g0348a0001c0005t0001g0001a0001c0005t0001g0071others(17): Show | 21 | HG00099.hp2 HG00140.hp2 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.71+11357G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48563680 | ||||||
| chr19:48563682
|
G | A | 3 | a0001c0004t0001g0052a0001c0004t0001g0089a0001c0004t0001g0198 | 3 | HG02258.hp2 HG02572.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.71+11359G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48563682 | ||||||
| chr19:48563694
|
G | A | 1 | a0002c0008t0001g0162 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.71+11371G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48563694 | ||||||
| chr19:48563792
|
G | A | 9 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0032others(6): Show | 9 | HG02055.hp1 HG02486.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.71+11469G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48563792 | ||||||
| chr19:48563797
|
T | C | 1 | a0001c0006t0001g0094 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.71+11474T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48563797 | ||||||
| chr19:48563951
|
C | T | 1 | a0001c0002t0001g0134 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.71+11628C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48563951 | ||||||
| chr19:48563959
|
C | CA | 15 | a0001c0001t0001g0306a0001c0001t0001g0340a0001c0001t0001g0364others(12): Show | 15 | HG01106.hp2 HG02015.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.71+11651dupA | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48563959 | |||||
| chr19:48563959
|
C | CAA | 14 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0026others(11): Show | 14 | HG01243.hp1 HG02055.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.71+11650_71+11651d others(4): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48563959 | |||||
| chr19:48563959
|
CA | C | 126 | a0001c0001t0001g0017a0001c0001t0001g0039a0001c0001t0001g0040others(123): Show | 127 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(124): Show |
intron_variant | MODIFIER | c.71+11651delA | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48563959 | |||||
| chr19:48563959
|
CAA | C | 7 | a0001c0001t0001g0007a0001c0001t0001g0031a0001c0001t0001g0055others(4): Show | 7 | HG01433.hp1 HG01891.hp2 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.71+11650_71+11651d others(4): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48563959 | |||||
| chr19:48563969
|
A | C | 4 | a0001c0001t0001g0054a0001c0001t0001g0101a0001c0001t0001g0175others(1): Show | 4 | HG00733.hp1 HG01167.hp1 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.71+11646A>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48563969 | ||||||
| chr19:48564107
|
G | A | 20 | a0001c0002t0001g0348a0001c0005t0001g0001a0001c0005t0001g0071others(17): Show | 21 | HG00099.hp2 HG00140.hp2 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.71+11784G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48564107 | ||||||
| chr19:48564282
|
A | G | 4 | a0001c0002t0001g0047a0001c0002t0001g0118a0001c0003t0001g0046others(1): Show | 4 | HG02486.hp1 HG02965.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.72-11659A>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48564282 | ||||||
| chr19:48564447
|
G | A | 14 | a0001c0001t0001g0136a0001c0001t0001g0152a0001c0001t0001g0167others(11): Show | 14 | HG00642.hp1 HG01168.hp2 HG01169.hp2 others(11): Show |
intron_variant | MODIFIER | c.72-11494G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48564447 | ||||||
| chr19:48564551
|
C | CA | 54 | a0001c0001t0001g0007a0001c0001t0001g0017a0001c0001t0001g0039others(51): Show | 54 | HG00642.hp1 HG00733.hp1 HG00733.hp2 others(51): Show |
intron_variant | MODIFIER | c.72-11366dupA | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48564551 | |||||
| chr19:48564551
|
C | CAA | 7 | a0001c0001t0001g0031a0001c0001t0001g0040a0001c0001t0001g0190others(4): Show | 7 | HG01891.hp2 HG02738.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.72-11367_72-11366d others(4): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48564551 | |||||
| chr19:48564551
|
CA | C | 168 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0021others(165): Show | 168 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(165): Show |
intron_variant | MODIFIER | c.72-11366delA | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48564551 | |||||
| chr19:48564551
|
CAA | C | 8 | a0001c0001t0001g0036a0001c0001t0001g0144a0001c0001t0001g0171others(5): Show | 8 | HG02109.hp2 HG02818.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.72-11367_72-11366d others(4): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48564551 | |||||
| chr19:48564572
|
A | AG | 4 | a0001c0001t0001g0080a0001c0005t0001g0209a0001c0005t0001g0213others(1): Show | 4 | HG01192.hp1 HG01496.hp1 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.72-11369_72-11368i others(3): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48564572 | ||||||
| chr19:48564572
|
A | G | 8 | a0001c0002t0001g0047a0001c0002t0001g0118a0001c0003t0001g0046others(5): Show | 8 | HG01261.hp2 HG02109.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.72-11369A>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48564572 | ||||||
| chr19:48564674
|
A | T | 10 | a0001c0001t0001g0088a0001c0001t0001g0215a0001c0001t0001g0257others(7): Show | 10 | HG00735.hp2 HG00738.hp2 HG01070.hp1 others(7): Show |
intron_variant | MODIFIER | c.72-11267A>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48564674 | ||||||
| chr19:48564677
|
A | T | 4 | a0001c0001t0001g0364a0001c0004t0001g0052a0001c0004t0001g0089others(1): Show | 4 | HG02258.hp2 HG02572.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.72-11264A>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48564677 | ||||||
| chr19:48564947
|
C | T | 114 | a0001c0001t0001g0014a0001c0001t0001g0036a0001c0001t0001g0054others(111): Show | 114 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(111): Show |
intron_variant | MODIFIER | c.72-10994C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48564947 | ||||||
| chr19:48564951
|
C | T | 3 | a0001c0001t0001g0123a0001c0001t0001g0191a0001c0001t0001g0353 | 3 | NA18973.hp2 NA18982.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.72-10990C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48564951 | ||||||
| chr19:48565050
|
A | T | 4 | a0001c0002t0001g0047a0001c0002t0001g0118a0001c0003t0001g0046others(1): Show | 4 | HG02486.hp1 HG02965.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.72-10891A>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48565050 | ||||||
| chr19:48565097
|
G | GT | 5 | a0001c0001t0001g0192a0001c0001t0001g0267a0001c0001t0001g0296others(2): Show | 5 | HG02145.hp2 NA19011.hp2 NA19058.hp1 others(2): Show |
intron_variant | MODIFIER | c.72-10836dupT | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48565097 | |||||
| chr19:48565333
|
G | T | 5 | a0001c0001t0001g0007a0001c0001t0001g0031a0001c0001t0001g0055others(2): Show | 5 | HG01433.hp1 HG01891.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.72-10608G>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48565333 | ||||||
| chr19:48565335
|
G | T | 186 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(183): Show | 186 | HG00280.hp1 HG00558.hp1 HG00597.hp2 others(183): Show |
intron_variant | MODIFIER | c.72-10606G>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48565335 | ||||||
| chr19:48565355
|
T | C | 172 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(169): Show | 172 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(169): Show |
intron_variant | MODIFIER | c.72-10586T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48565355 | ||||||
| chr19:48565357
|
T | G | 1 | a0001c0001t0001g0210 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.72-10584T>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48565357 | ||||||
| chr19:48565481
|
G | A | 1 | a0001c0004t0001g0138 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.72-10460G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48565481 | ||||||
| chr19:48565531
|
C | T | 2 | a0001c0001t0001g0196a0001c0002t0001g0103 | 2 | HG02698.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.72-10410C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48565531 | ||||||
| chr19:48565618
|
G | A | 5 | a0001c0001t0001g0060a0001c0002t0001g0047a0001c0002t0001g0118others(2): Show | 5 | HG02486.hp1 HG02809.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.72-10323G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48565618 | ||||||
| chr19:48565633
|
G | A | 1 | a0001c0003t0001g0011 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.72-10308G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48565633 | ||||||
| chr19:48565736
|
A | G | 1 | a0001c0002t0001g0160 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.72-10205A>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48565736 | ||||||
| chr19:48565755
|
TTTTG | T | 78 | a0001c0001t0001g0097a0001c0001t0001g0117a0001c0001t0001g0123others(75): Show | 78 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(75): Show |
intron_variant | MODIFIER | c.72-10166_72-10163d others(6): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48565755 | |||||
| chr19:48565904
|
A | G | 7 | a0001c0001t0001g0080a0001c0005t0001g0019a0001c0005t0001g0209others(4): Show | 7 | HG01192.hp1 HG01261.hp2 HG01496.hp1 others(4): Show |
intron_variant | MODIFIER | c.72-10037A>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48565904 | ||||||
| chr19:48565917
|
A | AT | 188 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(185): Show | 189 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(186): Show |
intron_variant | MODIFIER | c.72-10010dupT | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48565917 | |||||
| chr19:48565934
|
A | G | 177 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(174): Show | 177 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(174): Show |
intron_variant | MODIFIER | c.72-10007A>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48565934 | ||||||
| chr19:48565935
|
C | T | 1 | a0001c0001t0001g0017 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.72-10006C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48565935 | ||||||
| chr19:48566017
|
A | G | 86 | a0001c0001t0001g0080a0001c0001t0001g0097a0001c0001t0001g0117others(83): Show | 86 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(83): Show |
intron_variant | MODIFIER | c.72-9924A>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48566017 | ||||||
| chr19:48566019
|
T | G | 1 | a0001c0002t0001g0317 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.72-9922T>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48566019 | ||||||
| chr19:48566061
|
C | T | 30 | a0001c0001t0001g0007a0001c0001t0001g0031a0001c0001t0001g0055others(27): Show | 31 | HG00099.hp2 HG00140.hp2 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.72-9880C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48566061 | ||||||
| chr19:48566075
|
G | A | 30 | a0001c0001t0001g0007a0001c0001t0001g0031a0001c0001t0001g0055others(27): Show | 31 | HG00099.hp2 HG00140.hp2 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.72-9866G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48566075 | ||||||
| chr19:48566100
|
C | G | 1 | a0001c0002t0001g0248 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.72-9841C>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48566100 | ||||||
| chr19:48566100
|
C | T | 171 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(168): Show | 171 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(168): Show |
intron_variant | MODIFIER | c.72-9841C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48566100 | ||||||
| chr19:48566102
|
G | A | 30 | a0001c0001t0001g0007a0001c0001t0001g0031a0001c0001t0001g0055others(27): Show | 31 | HG00099.hp2 HG00140.hp2 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.72-9839G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48566102 | ||||||
| chr19:48566127
|
G | C | 1 | a0001c0003t0001g0102 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.72-9814G>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48566127 | ||||||
| chr19:48566146
|
G | A | 5 | a0001c0001t0001g0060a0001c0002t0001g0047a0001c0002t0001g0118others(2): Show | 5 | HG02486.hp1 HG02809.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.72-9795G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48566146 | ||||||
| chr19:48566151
|
C | T | 5 | a0001c0001t0001g0060a0001c0002t0001g0047a0001c0002t0001g0118others(2): Show | 5 | HG02486.hp1 HG02809.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.72-9790C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48566151 | ||||||
| chr19:48566159
|
G | C | 30 | a0001c0001t0001g0007a0001c0001t0001g0031a0001c0001t0001g0055others(27): Show | 31 | HG00099.hp2 HG00140.hp2 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.72-9782G>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48566159 | ||||||
| chr19:48566228
|
A | T | 30 | a0001c0001t0001g0007a0001c0001t0001g0031a0001c0001t0001g0055others(27): Show | 31 | HG00099.hp2 HG00140.hp2 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.72-9713A>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48566228 | ||||||
| chr19:48566277
|
G | A | 8 | a0001c0006t0001g0038a0001c0006t0001g0061a0001c0007t0001g0057others(5): Show | 8 | HG02145.hp2 HG02280.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.72-9664G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48566277 | ||||||
| chr19:48566333
|
T | C | 1 | a0001c0002t0001g0165 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.72-9608T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48566333 | ||||||
| chr19:48566366
|
G | A | 25 | a0001c0001t0001g0007a0001c0001t0001g0031a0001c0001t0001g0055others(22): Show | 26 | HG00099.hp2 HG00140.hp2 HG00741.hp2 others(23): Show |
intron_variant | MODIFIER | c.72-9575G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48566366 | ||||||
| chr19:48566382
|
G | C | 30 | a0001c0001t0001g0007a0001c0001t0001g0031a0001c0001t0001g0055others(27): Show | 31 | HG00099.hp2 HG00140.hp2 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.72-9559G>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48566382 | ||||||
| chr19:48566420
|
G | A | 3 | a0001c0001t0001g0190a0001c0001t0001g0201a0001c0002t0001g0124 | 3 | NA19002.hp2 NA19012.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.72-9521G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48566420 | ||||||
| chr19:48566631
|
C | T | 11 | a0001c0001t0001g0021a0001c0001t0001g0023a0001c0001t0001g0051others(8): Show | 11 | HG01884.hp2 HG02257.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.72-9310C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48566631 | ||||||
| chr19:48566659
|
T | C | 2 | a0001c0001t0001g0007a0001c0001t0001g0055 | 2 | HG01433.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.72-9282T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48566659 | ||||||
| chr19:48566670
|
C | T | 1 | a0001c0003t0001g0375 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.72-9271C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48566670 | ||||||
| chr19:48566708
|
A | G | 30 | a0001c0001t0001g0007a0001c0001t0001g0031a0001c0001t0001g0055others(27): Show | 31 | HG00099.hp2 HG00140.hp2 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.72-9233A>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48566708 | ||||||
| chr19:48566791
|
A | G | 30 | a0001c0001t0001g0007a0001c0001t0001g0031a0001c0001t0001g0055others(27): Show | 31 | HG00099.hp2 HG00140.hp2 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.72-9150A>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48566791 | ||||||
| chr19:48566813
|
G | T | 1 | a0001c0003t0001g0180 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.72-9128G>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48566813 | ||||||
| chr19:48566839
|
CA | C | 29 | a0001c0001t0001g0007a0001c0001t0001g0031a0001c0001t0001g0055others(26): Show | 30 | HG00099.hp2 HG00140.hp2 HG00741.hp2 others(27): Show |
intron_variant | MODIFIER | c.72-9088delA | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48566839 | |||||
| chr19:48566864
|
G | A | 1 | a0002c0008t0001g0231 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.72-9077G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48566864 | ||||||
| chr19:48566877
|
C | T | 30 | a0001c0001t0001g0007a0001c0001t0001g0031a0001c0001t0001g0055others(27): Show | 31 | HG00099.hp2 HG00140.hp2 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.72-9064C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48566877 | ||||||
| chr19:48566892
|
T | A | 30 | a0001c0001t0001g0007a0001c0001t0001g0031a0001c0001t0001g0055others(27): Show | 31 | HG00099.hp2 HG00140.hp2 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.72-9049T>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48566892 | ||||||
| chr19:48566918
|
A | G | 30 | a0001c0001t0001g0007a0001c0001t0001g0031a0001c0001t0001g0055others(27): Show | 31 | HG00099.hp2 HG00140.hp2 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.72-9023A>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48566918 | ||||||
| chr19:48566981
|
C | T | 1 | a0001c0005t0001g0313 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.72-8960C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48566981 | ||||||
| chr19:48566989
|
C | G | 5 | a0001c0001t0001g0060a0001c0002t0001g0047a0001c0002t0001g0118others(2): Show | 5 | HG02486.hp1 HG02809.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.72-8952C>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48566989 | ||||||
| chr19:48567002
|
T | A | 2 | a0001c0001t0001g0295a0001c0003t0001g0309 | 2 | HG00558.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.72-8939T>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48567002 | ||||||
| chr19:48567002
|
T | C | 30 | a0001c0001t0001g0007a0001c0001t0001g0031a0001c0001t0001g0055others(27): Show | 31 | HG00099.hp2 HG00140.hp2 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.72-8939T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48567002 | ||||||
| chr19:48567002
|
T | TA | 12 | a0001c0001t0001g0021a0001c0001t0001g0023a0001c0001t0001g0051others(9): Show | 12 | HG01884.hp2 HG02257.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.72-8930dupA | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48567002 | |||||
| chr19:48567003
|
A | T | 1 | a0001c0001t0001g0295 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.72-8938A>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48567003 | ||||||
| chr19:48567128
|
G | A | 2 | a0001c0001t0001g0025a0001c0004t0001g0145 | 2 | HG01433.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.72-8813G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48567128 | ||||||
| chr19:48567135
|
G | A | 30 | a0001c0001t0001g0007a0001c0001t0001g0031a0001c0001t0001g0055others(27): Show | 31 | HG00099.hp2 HG00140.hp2 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.72-8806G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48567135 | ||||||
| chr19:48567148
|
T | C | 30 | a0001c0001t0001g0007a0001c0001t0001g0031a0001c0001t0001g0055others(27): Show | 31 | HG00099.hp2 HG00140.hp2 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.72-8793T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48567148 | ||||||
| chr19:48567195
|
C | T | 1 | a0001c0002t0001g0084 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.72-8746C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48567195 | ||||||
| chr19:48567269
|
G | GAA | 5 | a0001c0001t0001g0007a0001c0001t0001g0031a0001c0001t0001g0055others(2): Show | 5 | HG01433.hp1 HG01891.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.72-8671_72-8670dup others(2): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48567269 | |||||
| chr19:48567335
|
G | A | 171 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(168): Show | 171 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(168): Show |
intron_variant | MODIFIER | c.72-8606G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48567335 | ||||||
| chr19:48567391
|
G | C | 31 | a0001c0001t0001g0007a0001c0001t0001g0031a0001c0001t0001g0055others(28): Show | 32 | HG00099.hp2 HG00140.hp2 HG00741.hp2 others(29): Show |
intron_variant | MODIFIER | c.72-8550G>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48567391 | ||||||
| chr19:48567423
|
G | A | 4 | a0001c0001t0001g0054a0001c0001t0001g0101a0001c0001t0001g0175others(1): Show | 4 | HG00733.hp1 HG01167.hp1 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.72-8518G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48567423 | ||||||
| chr19:48567425
|
G | A | 31 | a0001c0001t0001g0007a0001c0001t0001g0031a0001c0001t0001g0055others(28): Show | 32 | HG00099.hp2 HG00140.hp2 HG00741.hp2 others(29): Show |
intron_variant | MODIFIER | c.72-8516G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48567425 | ||||||
| chr19:48567434
|
C | T | 20 | a0001c0002t0001g0348a0001c0005t0001g0001a0001c0005t0001g0071others(17): Show | 21 | HG00099.hp2 HG00140.hp2 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.72-8507C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48567434 | ||||||
| chr19:48567526
|
C | T | 1 | a0001c0001t0001g0331 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.72-8415C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48567526 | ||||||
| chr19:48567542
|
T | C | 31 | a0001c0001t0001g0007a0001c0001t0001g0031a0001c0001t0001g0055others(28): Show | 32 | HG00099.hp2 HG00140.hp2 HG00741.hp2 others(29): Show |
intron_variant | MODIFIER | c.72-8399T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48567542 | ||||||
| chr19:48567557
|
A | C | 111 | a0001c0001t0001g0014a0001c0001t0001g0036a0001c0001t0001g0088others(108): Show | 111 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(108): Show |
intron_variant | MODIFIER | c.72-8384A>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48567557 | ||||||
| chr19:48567611
|
G | A | 5 | a0001c0001t0001g0007a0001c0001t0001g0031a0001c0001t0001g0055others(2): Show | 5 | HG01433.hp1 HG01891.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.72-8330G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48567611 | ||||||
| chr19:48567617
|
A | G | 31 | a0001c0001t0001g0007a0001c0001t0001g0031a0001c0001t0001g0055others(28): Show | 32 | HG00099.hp2 HG00140.hp2 HG00741.hp2 others(29): Show |
intron_variant | MODIFIER | c.72-8324A>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48567617 | ||||||
| chr19:48567707
|
C | T | 19 | a0001c0001t0001g0246a0001c0002t0001g0081a0001c0002t0001g0082others(16): Show | 19 | HG00639.hp2 HG00735.hp1 HG01069.hp2 others(16): Show |
intron_variant | MODIFIER | c.72-8234C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48567707 | ||||||
| chr19:48567788
|
G | A | 172 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(169): Show | 172 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(169): Show |
intron_variant | MODIFIER | c.72-8153G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48567788 | ||||||
| chr19:48567861
|
T | C | 172 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(169): Show | 172 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(169): Show |
intron_variant | MODIFIER | c.72-8080T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48567861 | ||||||
| chr19:48567918
|
T | G | 5 | a0001c0001t0001g0080a0001c0005t0001g0209a0001c0005t0001g0213others(2): Show | 5 | HG01192.hp1 HG01261.hp2 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.72-8023T>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48567918 | ||||||
| chr19:48567956
|
C | T | 111 | a0001c0001t0001g0014a0001c0001t0001g0036a0001c0001t0001g0088others(108): Show | 111 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(108): Show |
intron_variant | MODIFIER | c.72-7985C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48567956 | ||||||
| chr19:48568132
|
G | T | 1 | a0001c0004t0001g0132 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.72-7809G>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48568132 | ||||||
| chr19:48568145
|
CA | C | 6 | a0001c0001t0001g0144a0001c0001t0001g0183a0001c0001t0001g0241others(3): Show | 6 | HG00423.hp1 NA18945.hp1 NA18954.hp2 others(3): Show |
intron_variant | MODIFIER | c.72-7795delA | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48568145 | ||||||
| chr19:48568213
|
G | A | 1 | a0001c0005t0001g0197 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.72-7728G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48568213 | ||||||
| chr19:48568281
|
A | G | 172 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(169): Show | 172 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(169): Show |
intron_variant | MODIFIER | c.72-7660A>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48568281 | ||||||
| chr19:48568285
|
C | CA | 62 | a0001c0001t0001g0021a0001c0001t0001g0023a0001c0001t0001g0024others(59): Show | 62 | HG00438.hp2 HG00597.hp1 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.72-7639dupA | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48568285 | |||||
| chr19:48568285
|
C | CAA | 9 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0032others(6): Show | 9 | HG02055.hp1 HG02486.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.72-7640_72-7639dup others(2): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48568285 | |||||
| chr19:48568311
|
A | T | 172 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(169): Show | 172 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(169): Show |
intron_variant | MODIFIER | c.72-7630A>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48568311 | ||||||
| chr19:48568499
|
A | G | 177 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(174): Show | 177 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(174): Show |
intron_variant | MODIFIER | c.72-7442A>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48568499 | ||||||
| chr19:48568514
|
C | T | 5 | a0001c0001t0001g0153a0001c0003t0001g0214a0001c0003t0001g0256others(2): Show | 5 | HG01123.hp1 HG01975.hp1 HG01978.hp1 others(2): Show |
intron_variant | MODIFIER | c.72-7427C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48568514 | ||||||
| chr19:48568520
|
G | A | 18 | a0001c0001t0001g0151a0001c0001t0001g0159a0001c0001t0001g0178others(15): Show | 18 | HG01074.hp1 HG01167.hp2 HG01358.hp1 others(15): Show |
intron_variant | MODIFIER | c.72-7421G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48568520 | ||||||
| chr19:48568559
|
G | A | 1 | a0001c0006t0001g0090 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.72-7382G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48568559 | ||||||
| chr19:48568617
|
C | G | 5 | a0001c0001t0001g0060a0001c0002t0001g0047a0001c0002t0001g0118others(2): Show | 5 | HG02486.hp1 HG02809.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.72-7324C>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48568617 | ||||||
| chr19:48568628
|
C | G | 2 | a0001c0006t0001g0061a0001c0007t0001g0057 | 2 | HG02145.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.72-7313C>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48568628 | ||||||
| chr19:48568758
|
T | C | 9 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0032others(6): Show | 9 | HG02055.hp1 HG02486.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.72-7183T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48568758 | ||||||
| chr19:48568768
|
C | T | 9 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0032others(6): Show | 9 | HG02055.hp1 HG02486.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.72-7173C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48568768 | ||||||
| chr19:48568849
|
T | C | 4 | a0001c0001t0001g0054a0001c0001t0001g0101a0001c0001t0001g0175others(1): Show | 4 | HG00733.hp1 HG01167.hp1 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.72-7092T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48568849 | ||||||
| chr19:48568852
|
C | A | 21 | a0001c0002t0001g0348a0001c0005t0001g0001a0001c0005t0001g0071others(18): Show | 22 | HG00099.hp2 HG00140.hp2 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.72-7089C>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48568852 | ||||||
| chr19:48568854
|
C | A | 1 | a0001c0001t0001g0159 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.72-7087C>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48568854 | ||||||
| chr19:48568859
|
G | A | 373 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(370): Show | 374 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(371): Show |
intron_variant | MODIFIER | c.72-7082G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48568859 | ||||||
| chr19:48568890
|
T | TC | 120 | a0001c0001t0001g0014a0001c0001t0001g0036a0001c0001t0001g0054others(117): Show | 120 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(117): Show |
intron_variant | MODIFIER | c.72-7050dupC | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48568890 | |||||
| chr19:48568899
|
T | G | 115 | a0001c0001t0001g0014a0001c0001t0001g0036a0001c0001t0001g0054others(112): Show | 115 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(112): Show |
intron_variant | MODIFIER | c.72-7042T>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48568899 | ||||||
| chr19:48568982
|
C | A | 8 | a0001c0001t0001g0237a0001c0002t0001g0217a0001c0003t0001g0129others(5): Show | 8 | HG01168.hp1 HG01261.hp1 HG01928.hp2 others(5): Show |
intron_variant | MODIFIER | c.72-6959C>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48568982 | ||||||
| chr19:48569008
|
A | G | 115 | a0001c0001t0001g0014a0001c0001t0001g0036a0001c0001t0001g0054others(112): Show | 115 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(112): Show |
intron_variant | MODIFIER | c.72-6933A>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48569008 | ||||||
| chr19:48569020
|
G | A | 115 | a0001c0001t0001g0014a0001c0001t0001g0036a0001c0001t0001g0054others(112): Show | 115 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(112): Show |
intron_variant | MODIFIER | c.72-6921G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48569020 | ||||||
| chr19:48569101
|
A | G | 115 | a0001c0001t0001g0014a0001c0001t0001g0036a0001c0001t0001g0054others(112): Show | 115 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(112): Show |
intron_variant | MODIFIER | c.72-6840A>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48569101 | ||||||
| chr19:48569135
|
G | A | 1 | a0001c0003t0001g0219 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.72-6806G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48569135 | ||||||
| chr19:48569148
|
C | T | 2 | a0001c0002t0001g0049a0001c0002t0001g0050 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.72-6793C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48569148 | ||||||
| chr19:48569192
|
A | C | 1 | a0001c0001t0001g0364 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.72-6749A>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48569192 | ||||||
| chr19:48569203
|
G | A | 115 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0031others(112): Show | 115 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(112): Show |
intron_variant | MODIFIER | c.72-6738G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48569203 | ||||||
| chr19:48569210
|
C | T | 115 | a0001c0001t0001g0014a0001c0001t0001g0036a0001c0001t0001g0054others(112): Show | 115 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(112): Show |
intron_variant | MODIFIER | c.72-6731C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48569210 | ||||||
| chr19:48569264
|
T | C | 21 | a0001c0002t0001g0348a0001c0005t0001g0001a0001c0005t0001g0071others(18): Show | 22 | HG00099.hp2 HG00140.hp2 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.72-6677T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48569264 | ||||||
| chr19:48569298
|
C | T | 11 | a0001c0001t0001g0232a0001c0001t0001g0265a0001c0001t0001g0279others(8): Show | 11 | HG00673.hp2 HG01257.hp1 HG01952.hp2 others(8): Show |
intron_variant | MODIFIER | c.72-6643C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48569298 | ||||||
| chr19:48569299
|
G | C | 141 | a0001c0001t0001g0014a0001c0001t0001g0036a0001c0001t0001g0054others(138): Show | 142 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(139): Show |
intron_variant | MODIFIER | c.72-6642G>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48569299 | ||||||
| chr19:48569300
|
C | A | 141 | a0001c0001t0001g0014a0001c0001t0001g0036a0001c0001t0001g0054others(138): Show | 142 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(139): Show |
intron_variant | MODIFIER | c.72-6641C>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48569300 | ||||||
| chr19:48569328
|
A | C | 193 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(190): Show | 194 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.72-6613A>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48569328 | ||||||
| chr19:48569329
|
G | A | 1 | a0001c0001t0001g0258 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.72-6612G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48569329 | ||||||
| chr19:48569341
|
CA | C | 6 | a0001c0001t0001g0031a0001c0001t0001g0367a0001c0005t0001g0008others(3): Show | 6 | HG01884.hp1 HG01891.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.72-6579delA | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48569341 | |||||
| chr19:48569347
|
A | G | 193 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(190): Show | 194 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.72-6594A>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48569347 | ||||||
| chr19:48569352
|
A | G | 193 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(190): Show | 194 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.72-6589A>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48569352 | ||||||
| chr19:48569357
|
A | G | 193 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(190): Show | 194 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.72-6584A>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48569357 | ||||||
| chr19:48569361
|
A | AAAACATA others(3): Show |
3 | a0001c0001t0001g0237a0001c0003t0001g0129a0001c0003t0001g0224 | 3 | HG01928.hp2 HG01934.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.72-6579_72-6578ins others(10): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48569361 | |||||
| chr19:48569361
|
A | AAAC | 8 | a0001c0001t0001g0289a0001c0001t0001g0344a0001c0002t0001g0022others(5): Show | 8 | HG00423.hp2 HG00673.hp1 HG02074.hp1 others(5): Show |
intron_variant | MODIFIER | c.72-6579_72-6578ins others(3): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48569361 | |||||
| chr19:48569361
|
A | AAACAT | 10 | a0001c0001t0001g0117a0001c0001t0001g0168a0001c0001t0001g0290others(7): Show | 10 | HG00140.hp1 HG00738.hp1 HG01943.hp2 others(7): Show |
intron_variant | MODIFIER | c.72-6579_72-6578ins others(5): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48569361 | |||||
| chr19:48569361
|
A | AAACATAT | 10 | a0001c0001t0001g0167a0001c0001t0001g0240a0001c0001t0001g0267others(7): Show | 10 | HG02896.hp1 HG02970.hp2 HG03516.hp1 others(7): Show |
intron_variant | MODIFIER | c.72-6579_72-6578ins others(7): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48569361 | |||||
| chr19:48569361
|
A | T | 2 | a0001c0005t0001g0019a0001c0006t0001g0028 | 2 | HG03225.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.72-6580A>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48569361 | ||||||
| chr19:48569361
|
AACATATA others(11): Show |
A | 14 | a0001c0001t0001g0042a0001c0001t0001g0073a0001c0001t0001g0074others(11): Show | 14 | HG02145.hp2 HG02280.hp2 HG02647.hp2 others(11): Show |
intron_variant | MODIFIER | c.72-6578_72-6561del others(18): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48569361 | |||||
| chr19:48569361
|
AACATATA others(13): Show |
A | 178 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(175): Show | 179 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(176): Show |
intron_variant | MODIFIER | c.72-6578_72-6559del others(20): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48569361 | |||||
| chr19:48569361
|
AACATATA others(15): Show |
A | 1 | a0001c0003t0001g0046 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.72-6578_72-6557del others(22): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48569361 | |||||
| chr19:48569362
|
AC | A | 10 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0140others(7): Show | 10 | HG00280.hp2 HG00597.hp2 HG00639.hp1 others(7): Show |
intron_variant | MODIFIER | c.72-6578delC | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48569362 | ||||||
| chr19:48569363
|
C | A | 2 | a0001c0001t0001g0130a0001c0003t0001g0292 | 2 | HG02647.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.72-6578C>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48569363 | ||||||
| chr19:48569363
|
C | CAT | 16 | a0001c0001t0001g0080a0001c0001t0001g0172a0001c0001t0001g0232others(13): Show | 16 | HG00558.hp2 HG01243.hp2 HG01496.hp1 others(13): Show |
intron_variant | MODIFIER | c.72-6543_72-6542dup others(2): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48569363 | |||||
| chr19:48569363
|
C | CATAT | 18 | a0001c0001t0001g0007a0001c0001t0001g0055a0001c0001t0001g0097others(15): Show | 18 | HG00733.hp2 HG01361.hp1 HG01361.hp2 others(15): Show |
intron_variant | MODIFIER | c.72-6545_72-6542dup others(4): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48569363 | |||||
| chr19:48569363
|
C | CATATAT | 18 | a0001c0001t0001g0017a0001c0001t0001g0066a0001c0001t0001g0116others(15): Show | 18 | HG00423.hp1 HG00609.hp1 HG00642.hp1 others(15): Show |
intron_variant | MODIFIER | c.72-6547_72-6542dup others(6): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48569363 | |||||
| chr19:48569363
|
C | CATATATA others(1): Show |
32 | a0001c0001t0001g0031a0001c0001t0001g0070a0001c0001t0001g0087others(29): Show | 32 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(29): Show |
intron_variant | MODIFIER | c.72-6549_72-6542dup others(8): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48569363 | |||||
| chr19:48569363
|
C | CATATATA others(3): Show |
1 | a0001c0001t0001g0367 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.72-6551_72-6542dup others(10): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48569363 | |||||
| chr19:48569363
|
C | T | 39 | a0001c0001t0001g0117a0001c0001t0001g0167a0001c0001t0001g0168others(36): Show | 39 | HG00140.hp1 HG00423.hp2 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.72-6578C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48569363 | ||||||
| chr19:48569363
|
CAT | C | 15 | a0001c0001t0001g0123a0001c0001t0001g0329a0001c0001t0001g0353others(12): Show | 15 | HG00621.hp2 HG01123.hp2 HG01257.hp1 others(12): Show |
intron_variant | MODIFIER | c.72-6543_72-6542del others(2): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48569363 | |||||
| chr19:48569363
|
CATATATA others(3): Show |
C | 4 | a0001c0002t0001g0271a0001c0003t0001g0228a0001c0003t0001g0294others(1): Show | 4 | NA18957.hp1 NA18982.hp1 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.72-6551_72-6542del others(10): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48569363 | |||||
| chr19:48569365
|
T | A | 1 | a0001c0005t0001g0255 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.72-6576T>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48569365 | ||||||
| chr19:48569365
|
T | C | 11 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0130others(8): Show | 11 | HG00280.hp2 HG00597.hp2 HG00639.hp1 others(8): Show |
intron_variant | MODIFIER | c.72-6576T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48569365 | ||||||
| chr19:48569365
|
T | TATATATA others(5335): Show |
1 | a0003c0012t0001g0013 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.72-6544_72-6543ins others(5342): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48569365 | |||||
| chr19:48569365
|
T | TATATATA others(5334): Show |
1 | a0003c0012t0001g0012 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.72-6544_72-6543ins others(5341): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48569365 | |||||
| chr19:48569365
|
T | TATATATA others(5333): Show |
3 | a0001c0005t0001g0008a0001c0005t0001g0009a0001c0005t0001g0010 | 3 | HG02896.hp2 HG02897.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.72-6544_72-6543ins others(5340): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48569365 | |||||
| chr19:48569367
|
T | A | 1 | a0001c0005t0001g0255 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.72-6574T>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48569367 | ||||||
| chr19:48569367
|
T | C | 1 | a0001c0003t0001g0375 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.72-6574T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48569367 | ||||||
| chr19:48569369
|
T | A | 4 | a0001c0005t0001g0209a0001c0005t0001g0213a0001c0005t0001g0255others(1): Show | 4 | HG01192.hp1 HG01261.hp2 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.72-6572T>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48569369 | ||||||
| chr19:48569371
|
T | A | 3 | a0001c0005t0001g0209a0001c0005t0001g0213a0001c0007t0001g0166 | 3 | HG01261.hp2 HG02735.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.72-6570T>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48569371 | ||||||
| chr19:48569373
|
T | A | 4 | a0001c0005t0001g0209a0001c0005t0001g0213a0001c0006t0001g0090others(1): Show | 4 | HG01261.hp2 HG02109.hp1 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.72-6568T>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48569373 | ||||||
| chr19:48569373
|
T | C | 1 | a0001c0002t0001g0293 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.72-6568T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48569373 | ||||||
| chr19:48569375
|
T | A | 1 | a0001c0005t0001g0213 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.72-6566T>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48569375 | ||||||
| chr19:48569381
|
T | A | 14 | a0001c0001t0001g0042a0001c0001t0001g0073a0001c0001t0001g0074others(11): Show | 14 | HG02145.hp2 HG02280.hp2 HG02647.hp2 others(11): Show |
intron_variant | MODIFIER | c.72-6560T>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48569381 | ||||||
| chr19:48569383
|
T | A | 182 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(179): Show | 183 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.72-6558T>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48569383 | ||||||
| chr19:48569385
|
T | A | 94 | a0001c0001t0001g0021a0001c0001t0001g0024a0001c0001t0001g0025others(91): Show | 95 | HG00140.hp2 HG00280.hp1 HG00621.hp1 others(92): Show |
intron_variant | MODIFIER | c.72-6556T>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48569385 | ||||||
| chr19:48569387
|
T | A | 1 | a0001c0003t0001g0370 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.72-6554T>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48569387 | ||||||
| chr19:48569398
|
A | G | 193 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(190): Show | 194 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.72-6543A>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48569398 | ||||||
| chr19:48569399
|
T | A | 193 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(190): Show | 194 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.72-6542T>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48569399 | ||||||
| chr19:48569433
|
T | C | 193 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(190): Show | 194 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.72-6508T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48569433 | ||||||
| chr19:48569453
|
CATCT | C | 193 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(190): Show | 194 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.72-6483_72-6480del others(4): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48569453 | |||||
| chr19:48569459
|
T | C | 193 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(190): Show | 194 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.72-6482T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48569459 | ||||||
| chr19:48569535
|
A | T | 2 | a0001c0001t0001g0031a0001c0001t0001g0367 | 2 | HG01891.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.72-6406A>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48569535 | ||||||
| chr19:48569537
|
T | C | 193 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(190): Show | 194 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.72-6404T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48569537 | ||||||
| chr19:48569554
|
T | G | 193 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(190): Show | 194 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.72-6387T>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48569554 | ||||||
| chr19:48569559
|
A | G | 193 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(190): Show | 194 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.72-6382A>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48569559 | ||||||
| chr19:48569569
|
G | C | 193 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(190): Show | 194 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.72-6372G>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48569569 | ||||||
| chr19:48569645
|
T | C | 193 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(190): Show | 194 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.72-6296T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48569645 | ||||||
| chr19:48569654
|
A | G | 193 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(190): Show | 194 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.72-6287A>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48569654 | ||||||
| chr19:48569656
|
G | A | 193 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(190): Show | 194 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.72-6285G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48569656 | ||||||
| chr19:48569672
|
G | T | 193 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(190): Show | 194 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.72-6269G>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48569672 | ||||||
| chr19:48569673
|
G | T | 193 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(190): Show | 194 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.72-6268G>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48569673 | ||||||
| chr19:48569680
|
G | T | 193 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(190): Show | 194 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.72-6261G>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48569680 | ||||||
| chr19:48569744
|
A | G | 193 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(190): Show | 194 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.72-6197A>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48569744 | ||||||
| chr19:48569753
|
G | A | 193 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(190): Show | 194 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.72-6188G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48569753 | ||||||
| chr19:48569769
|
T | G | 5 | a0001c0001t0001g0060a0001c0002t0001g0047a0001c0002t0001g0118others(2): Show | 5 | HG02486.hp1 HG02809.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.72-6172T>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48569769 | ||||||
| chr19:48569792
|
G | C | 11 | a0001c0001t0001g0021a0001c0001t0001g0023a0001c0001t0001g0051others(8): Show | 11 | HG01884.hp2 HG02257.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.72-6149G>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48569792 | ||||||
| chr19:48569816
|
G | A | 4 | a0001c0001t0001g0007a0001c0001t0001g0031a0001c0001t0001g0055others(1): Show | 4 | HG01433.hp1 HG01891.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.72-6125G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48569816 | ||||||
| chr19:48569912
|
T | C | 193 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(190): Show | 194 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.72-6029T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48569912 | ||||||
| chr19:48569948
|
G | A | 21 | a0001c0002t0001g0348a0001c0005t0001g0001a0001c0005t0001g0071others(18): Show | 22 | HG00099.hp2 HG00140.hp2 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.72-5993G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48569948 | ||||||
| chr19:48569958
|
G | A | 1 | a0001c0001t0001g0055 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.72-5983G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48569958 | ||||||
| chr19:48570027
|
A | G | 1 | a0001c0002t0001g0103 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.72-5914A>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48570027 | ||||||
| chr19:48570179
|
CTTT | C | 193 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(190): Show | 194 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.72-5749_72-5747del others(3): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48570179 | |||||
| chr19:48570380
|
T | C | 53 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0021others(50): Show | 53 | HG01070.hp2 HG01071.hp2 HG01243.hp1 others(50): Show |
intron_variant | MODIFIER | c.72-5561T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48570380 | ||||||
| chr19:48570422
|
G | C | 193 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(190): Show | 194 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.72-5519G>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48570422 | ||||||
| chr19:48570537
|
T | C | 1 | a0001c0005t0001g0108 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.72-5404T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48570537 | ||||||
| chr19:48570542
|
A | G | 193 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(190): Show | 194 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.72-5399A>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48570542 | ||||||
| chr19:48570717
|
C | T | 193 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(190): Show | 194 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.72-5224C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48570717 | ||||||
| chr19:48570718
|
G | GTTTC | 193 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(190): Show | 194 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.72-5220_72-5219ins others(4): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48570718 | |||||
| chr19:48570727
|
T | G | 193 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(190): Show | 194 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.72-5214T>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48570727 | ||||||
| chr19:48570730
|
GT | G | 193 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(190): Show | 194 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.72-5201delT | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48570730 | |||||
| chr19:48570734
|
T | G | 2 | a0001c0007t0001g0110a0001c0007t0001g0111 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.72-5207T>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48570734 | ||||||
| chr19:48570788
|
G | A | 1 | a0001c0001t0001g0172 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.72-5153G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48570788 | ||||||
| chr19:48570798
|
C | T | 1 | a0001c0006t0001g0090 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.72-5143C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48570798 | ||||||
| chr19:48570839
|
G | C | 193 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(190): Show | 194 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.72-5102G>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48570839 | ||||||
| chr19:48570847
|
C | T | 193 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(190): Show | 194 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.72-5094C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48570847 | ||||||
| chr19:48570914
|
G | C | 1 | a0001c0003t0001g0142 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.72-5027G>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48570914 | ||||||
| chr19:48570916
|
G | T | 4 | a0001c0001t0001g0007a0001c0001t0001g0031a0001c0001t0001g0055others(1): Show | 4 | HG01433.hp1 HG01891.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.72-5025G>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48570916 | ||||||
| chr19:48570943
|
C | T | 1 | a0001c0002t0001g0217 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.72-4998C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48570943 | ||||||
| chr19:48570966
|
C | T | 1 | a0001c0004t0001g0133 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.72-4975C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48570966 | ||||||
| chr19:48570999
|
T | C | 2 | a0001c0009t0001g0321a0001c0009t0001g0322 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.72-4942T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48570999 | ||||||
| chr19:48571004
|
A | G | 2 | a0001c0009t0001g0321a0001c0009t0001g0322 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.72-4937A>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48571004 | ||||||
| chr19:48571207
|
A | TTTTTTTT others(3139): Show |
2 | a0001c0001t0001g0007a0001c0001t0001g0055 | 2 | HG01433.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.72-4735_72-4734ins others(3146): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48571207 | ||||||
| chr19:48571207
|
A | TTTTTTTT others(3139): Show |
2 | a0001c0001t0001g0031a0001c0001t0001g0367 | 2 | HG01891.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.72-4735_72-4734ins others(3146): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48571207 | ||||||
| chr19:48571211
|
A | ATTTATTT others(2): Show |
157 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(154): Show | 157 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(154): Show |
intron_variant | MODIFIER | c.72-4727_72-4726ins others(9): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48571211 | |||||
| chr19:48571211
|
A | ATTTATTT others(6): Show |
31 | a0001c0001t0001g0042a0001c0001t0001g0073a0001c0001t0001g0074others(28): Show | 32 | HG00099.hp2 HG00140.hp2 HG00741.hp2 others(29): Show |
intron_variant | MODIFIER | c.72-4727_72-4726ins others(13): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48571211 | |||||
| chr19:48571211
|
A | ATTTATTT others(10): Show |
5 | a0001c0002t0001g0047a0001c0002t0001g0118a0001c0003t0001g0046others(2): Show | 5 | HG02486.hp1 HG02723.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.72-4727_72-4726ins others(17): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48571211 | |||||
| chr19:48571211
|
A | T | 4 | a0001c0001t0001g0007a0001c0001t0001g0031a0001c0001t0001g0055others(1): Show | 4 | HG01433.hp1 HG01891.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.72-4730A>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48571211 | ||||||
| chr19:48571321
|
C | T | 4 | a0001c0002t0001g0047a0001c0002t0001g0118a0001c0003t0001g0046others(1): Show | 4 | HG02486.hp1 HG02965.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.72-4620C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48571321 | ||||||
| chr19:48571357
|
C | T | 193 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(190): Show | 194 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.72-4584C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48571357 | ||||||
| chr19:48571378
|
G | C | 5 | a0001c0001t0001g0066a0001c0004t0001g0062a0001c0004t0001g0064others(2): Show | 5 | HG00738.hp1 HG02451.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.72-4563G>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48571378 | ||||||
| chr19:48571439
|
C | T | 1 | a0001c0004t0001g0324 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.72-4502C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48571439 | ||||||
| chr19:48571507
|
G | A | 193 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(190): Show | 194 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.72-4434G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48571507 | ||||||
| chr19:48571636
|
C | CA | 99 | a0001c0001t0001g0053a0001c0001t0001g0088a0001c0001t0001g0104others(96): Show | 100 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(97): Show |
intron_variant | MODIFIER | c.72-4301dupA | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48571636 | |||||
| chr19:48571636
|
C | CAA | 5 | a0001c0001t0001g0126a0001c0001t0001g0159a0001c0001t0001g0270others(2): Show | 5 | HG02071.hp2 HG02074.hp2 NA18612.hp1 others(2): Show |
intron_variant | MODIFIER | c.72-4302_72-4301dup others(2): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48571636 | |||||
| chr19:48571640
|
AG | A | 5 | a0001c0002t0001g0047a0001c0002t0001g0118a0001c0003t0001g0046others(2): Show | 5 | HG02486.hp1 HG02965.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.72-4300delG | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48571640 | ||||||
| chr19:48571641
|
G | A | 188 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(185): Show | 189 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(186): Show |
intron_variant | MODIFIER | c.72-4300G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48571641 | ||||||
| chr19:48571648
|
A | C | 1 | a0001c0004t0001g0030 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.72-4293A>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48571648 | ||||||
| chr19:48571649
|
C | A | 193 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(190): Show | 194 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.72-4292C>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48571649 | ||||||
| chr19:48571655
|
AT | A | 193 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(190): Show | 194 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.72-4279delT | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48571655 | |||||
| chr19:48571697
|
GAGA | G | 193 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(190): Show | 194 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.72-4240_72-4238del others(3): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48571697 | |||||
| chr19:48571706
|
G | T | 193 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(190): Show | 194 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.72-4235G>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48571706 | ||||||
| chr19:48571825
|
G | C | 193 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(190): Show | 194 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.72-4116G>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48571825 | ||||||
| chr19:48571904
|
T | C | 193 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(190): Show | 194 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.72-4037T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48571904 | ||||||
| chr19:48572020
|
T | C | 193 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(190): Show | 194 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.72-3921T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48572020 | ||||||
| chr19:48572080
|
G | C | 39 | a0001c0001t0001g0021a0001c0001t0001g0023a0001c0001t0001g0024others(36): Show | 39 | HG01070.hp2 HG01071.hp2 HG01243.hp1 others(36): Show |
intron_variant | MODIFIER | c.72-3861G>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48572080 | ||||||
| chr19:48572084
|
G | A | 193 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(190): Show | 194 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.72-3857G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48572084 | ||||||
| chr19:48572099
|
T | G | 4 | a0001c0001t0001g0054a0001c0001t0001g0101a0001c0001t0001g0175others(1): Show | 4 | HG00733.hp1 HG01167.hp1 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.72-3842T>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48572099 | ||||||
| chr19:48572123
|
T | C | 2 | a0001c0004t0001g0089a0001c0004t0001g0198 | 2 | HG02258.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.72-3818T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48572123 | ||||||
| chr19:48572197
|
T | G | 193 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(190): Show | 194 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.72-3744T>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48572197 | ||||||
| chr19:48572208
|
G | A | 11 | a0001c0001t0001g0021a0001c0001t0001g0023a0001c0001t0001g0051others(8): Show | 11 | HG01884.hp2 HG02257.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.72-3733G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48572208 | ||||||
| chr19:48572255
|
C | T | 2 | a0001c0001t0001g0041a0001c0001t0001g0300 | 2 | HG02055.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.72-3686C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48572255 | ||||||
| chr19:48572281
|
G | A | 193 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(190): Show | 194 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.72-3660G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48572281 | ||||||
| chr19:48572289
|
C | T | 193 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(190): Show | 194 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.72-3652C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48572289 | ||||||
| chr19:48572299
|
G | A | 193 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(190): Show | 194 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.72-3642G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48572299 | ||||||
| chr19:48572317
|
A | T | 1 | a0001c0001t0001g0355 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.72-3624A>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48572317 | ||||||
| chr19:48572374
|
A | G | 193 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(190): Show | 194 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.72-3567A>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48572374 | ||||||
| chr19:48572388
|
C | A | 140 | a0001c0001t0001g0014a0001c0001t0001g0036a0001c0001t0001g0054others(137): Show | 141 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(138): Show |
intron_variant | MODIFIER | c.72-3553C>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48572388 | ||||||
| chr19:48572396
|
C | T | 1 | a0001c0004t0001g0058 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.72-3545C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48572396 | ||||||
| chr19:48572414
|
G | A | 1 | a0001c0001t0001g0136 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.72-3527G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48572414 | ||||||
| chr19:48572437
|
C | G | 140 | a0001c0001t0001g0014a0001c0001t0001g0036a0001c0001t0001g0054others(137): Show | 141 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(138): Show |
intron_variant | MODIFIER | c.72-3504C>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48572437 | ||||||
| chr19:48572446
|
G | A | 1 | a0001c0002t0001g0149 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.72-3495G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48572446 | ||||||
| chr19:48572455
|
A | T | 140 | a0001c0001t0001g0014a0001c0001t0001g0036a0001c0001t0001g0054others(137): Show | 141 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(138): Show |
intron_variant | MODIFIER | c.72-3486A>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48572455 | ||||||
| chr19:48572485
|
G | A | 2 | a0001c0001t0001g0126a0001c0001t0001g0341 | 2 | HG02056.hp2 HG02074.hp2 |
intron_variant | MODIFIER | c.72-3456G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48572485 | ||||||
| chr19:48572509
|
A | G | 144 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0031others(141): Show | 145 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.72-3432A>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48572509 | ||||||
| chr19:48572513
|
C | CA | 143 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0031others(140): Show | 144 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.72-3420dupA | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48572513 | |||||
| chr19:48572524
|
A | G | 184 | a0001c0001t0001g0014a0001c0001t0001g0021a0001c0001t0001g0023others(181): Show | 185 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.72-3417A>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48572524 | ||||||
| chr19:48572554
|
C | G | 188 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0021others(185): Show | 189 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(186): Show |
intron_variant | MODIFIER | c.72-3387C>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48572554 | ||||||
| chr19:48572579
|
G | A | 1 | a0001c0002t0001g0305 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.72-3362G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48572579 | ||||||
| chr19:48572617
|
G | T | 1 | a0001c0001t0001g0151 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.72-3324G>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48572617 | ||||||
| chr19:48572827
|
G | C | 1 | a0001c0004t0001g0052 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.72-3114G>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48572827 | ||||||
| chr19:48573018
|
G | A | 4 | a0001c0001t0001g0054a0001c0001t0001g0101a0001c0001t0001g0175others(1): Show | 4 | HG00733.hp1 HG01167.hp1 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.72-2923G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48573018 | ||||||
| chr19:48573080
|
T | C | 4 | a0001c0001t0001g0007a0001c0001t0001g0031a0001c0001t0001g0055others(1): Show | 4 | HG01433.hp1 HG01891.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.72-2861T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48573080 | ||||||
| chr19:48573112
|
G | A | 4 | a0001c0001t0001g0007a0001c0001t0001g0031a0001c0001t0001g0055others(1): Show | 4 | HG01433.hp1 HG01891.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.72-2829G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48573112 | ||||||
| chr19:48573123
|
C | T | 10 | a0001c0001t0001g0104a0001c0001t0001g0189a0001c0001t0001g0229others(7): Show | 10 | HG02071.hp2 NA18948.hp1 NA18959.hp2 others(7): Show |
intron_variant | MODIFIER | c.72-2818C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48573123 | ||||||
| chr19:48573128
|
G | C | 4 | a0001c0001t0001g0007a0001c0001t0001g0031a0001c0001t0001g0055others(1): Show | 4 | HG01433.hp1 HG01891.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.72-2813G>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48573128 | ||||||
| chr19:48573155
|
C | CA | 10 | a0001c0001t0001g0031a0001c0001t0001g0087a0001c0001t0001g0374others(7): Show | 10 | HG00438.hp1 HG00738.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.72-2767dupA | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48573155 | |||||
| chr19:48573155
|
CA | C | 171 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(168): Show | 171 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(168): Show |
intron_variant | MODIFIER | c.72-2767delA | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48573155 | |||||
| chr19:48573155
|
CAA | C | 21 | a0001c0001t0001g0196a0001c0002t0001g0348a0001c0005t0001g0001others(18): Show | 22 | HG00099.hp2 HG00140.hp2 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.72-2768_72-2767del others(2): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48573155 | |||||
| chr19:48573177
|
T | C | 4 | a0001c0001t0001g0007a0001c0001t0001g0031a0001c0001t0001g0055others(1): Show | 4 | HG01433.hp1 HG01891.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.72-2764T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48573177 | ||||||
| chr19:48573181
|
T | C | 5 | a0001c0001t0001g0060a0001c0002t0001g0047a0001c0002t0001g0118others(2): Show | 5 | HG02486.hp1 HG02809.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.72-2760T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48573181 | ||||||
| chr19:48573204
|
A | G | 291 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(288): Show | 292 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(289): Show |
intron_variant | MODIFIER | c.72-2737A>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48573204 | ||||||
| chr19:48573345
|
G | A | 119 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0031others(116): Show | 119 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(116): Show |
intron_variant | MODIFIER | c.72-2596G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48573345 | ||||||
| chr19:48573374
|
G | A | 4 | a0001c0001t0001g0007a0001c0001t0001g0031a0001c0001t0001g0055others(1): Show | 4 | HG01433.hp1 HG01891.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.72-2567G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48573374 | ||||||
| chr19:48573430
|
G | A | 127 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(124): Show | 127 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(124): Show |
intron_variant | MODIFIER | c.72-2511G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48573430 | ||||||
| chr19:48573493
|
C | T | 1 | a0001c0002t0001g0354 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.72-2448C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48573493 | ||||||
| chr19:48573498
|
A | G | 3 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0002t0001g0003 | 3 | HG02055.hp1 HG02970.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.72-2443A>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48573498 | ||||||
| chr19:48573528
|
C | T | 118 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0031others(115): Show | 118 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(115): Show |
intron_variant | MODIFIER | c.72-2413C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48573528 | ||||||
| chr19:48573565
|
G | A | 43 | a0001c0001t0001g0021a0001c0001t0001g0023a0001c0001t0001g0024others(40): Show | 43 | HG01070.hp2 HG01071.hp2 HG01243.hp1 others(40): Show |
intron_variant | MODIFIER | c.72-2376G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48573565 | ||||||
| chr19:48573574
|
G | A | 1 | a0001c0007t0001g0166 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.72-2367G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48573574 | ||||||
| chr19:48573653
|
G | C | 1 | a0001c0001t0001g0355 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.72-2288G>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48573653 | ||||||
| chr19:48573654
|
G | A | 1 | a0001c0001t0001g0355 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.72-2287G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48573654 | ||||||
| chr19:48573657
|
G | A | 1 | a0001c0001t0001g0355 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.72-2284G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48573657 | ||||||
| chr19:48573664
|
G | C | 1 | a0001c0001t0001g0355 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.72-2277G>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48573664 | ||||||
| chr19:48573666
|
C | G | 117 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0031others(114): Show | 117 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(114): Show |
intron_variant | MODIFIER | c.72-2275C>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48573666 | ||||||
| chr19:48573671
|
A | G | 1 | a0001c0001t0001g0355 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.72-2270A>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48573671 | ||||||
| chr19:48573672
|
T | G | 117 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0031others(114): Show | 117 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(114): Show |
intron_variant | MODIFIER | c.72-2269T>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48573672 | ||||||
| chr19:48573673
|
G | T | 1 | a0001c0001t0001g0355 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.72-2268G>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48573673 | ||||||
| chr19:48573769
|
G | C | 118 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0031others(115): Show | 118 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(115): Show |
intron_variant | MODIFIER | c.72-2172G>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48573769 | ||||||
| chr19:48573800
|
G | A | 236 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0031others(233): Show | 237 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(234): Show |
intron_variant | MODIFIER | c.72-2141G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48573800 | ||||||
| chr19:48573807
|
T | C | 120 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0031others(117): Show | 120 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(117): Show |
intron_variant | MODIFIER | c.72-2134T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48573807 | ||||||
| chr19:48573848
|
C | T | 3 | a0001c0005t0001g0209a0001c0005t0001g0213a0001c0005t0001g0255 | 3 | HG01192.hp1 HG02735.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.72-2093C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48573848 | ||||||
| chr19:48573856
|
G | A | 1 | a0001c0004t0001g0052 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.72-2085G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48573856 | ||||||
| chr19:48573865
|
C | G | 236 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0031others(233): Show | 237 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(234): Show |
intron_variant | MODIFIER | c.72-2076C>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48573865 | ||||||
| chr19:48573921
|
G | A | 9 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0032others(6): Show | 9 | HG02055.hp1 HG02486.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.72-2020G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48573921 | ||||||
| chr19:48573922
|
C | T | 1 | a0001c0002t0001g0174 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.72-2019C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48573922 | ||||||
| chr19:48573974
|
C | T | 94 | a0001c0001t0001g0080a0001c0001t0001g0097a0001c0001t0001g0117others(91): Show | 94 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.72-1967C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48573974 | ||||||
| chr19:48573991
|
G | A | 1 | a0001c0001t0001g0040 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.72-1950G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48573991 | ||||||
| chr19:48574019
|
G | C | 125 | a0001c0001t0001g0007a0001c0001t0001g0031a0001c0001t0001g0054others(122): Show | 126 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(123): Show |
intron_variant | MODIFIER | c.72-1922G>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48574019 | ||||||
| chr19:48574139
|
G | A | 1 | a0001c0002t0001g0305 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.72-1802G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48574139 | ||||||
| chr19:48574195
|
A | G | 290 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(287): Show | 291 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(288): Show |
intron_variant | MODIFIER | c.72-1746A>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48574195 | ||||||
| chr19:48574264
|
CTTCA | C | 4 | a0001c0001t0001g0007a0001c0001t0001g0031a0001c0001t0001g0055others(1): Show | 4 | HG01433.hp1 HG01891.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.72-1673_72-1670del others(4): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48574264 | |||||
| chr19:48574268
|
A | C | 6 | a0001c0001t0001g0054a0001c0001t0001g0101a0001c0001t0001g0175others(3): Show | 6 | HG00733.hp1 HG01070.hp2 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.72-1673A>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48574268 | ||||||
| chr19:48574374
|
G | A | 1 | a0001c0001t0001g0031 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.72-1567G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48574374 | ||||||
| chr19:48574410
|
C | T | 124 | a0001c0001t0001g0007a0001c0001t0001g0031a0001c0001t0001g0054others(121): Show | 125 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(122): Show |
intron_variant | MODIFIER | c.72-1531C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48574410 | ||||||
| chr19:48574781
|
C | A | 1 | a0001c0007t0001g0033 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.72-1160C>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48574781 | ||||||
| chr19:48574876
|
C | A | 1 | a0001c0006t0001g0006 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.72-1065C>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48574876 | ||||||
| chr19:48574884
|
G | A | 137 | a0001c0001t0001g0007a0001c0001t0001g0031a0001c0001t0001g0042others(134): Show | 138 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(135): Show |
intron_variant | MODIFIER | c.72-1057G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48574884 | ||||||
| chr19:48574950
|
T | C | 10 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0032others(7): Show | 10 | HG01243.hp1 HG02055.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.72-991T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48574950 | ||||||
| chr19:48575054
|
A | G | 10 | a0001c0001t0001g0007a0001c0001t0001g0031a0001c0001t0001g0054others(7): Show | 10 | HG00733.hp1 HG01070.hp2 HG01071.hp2 others(7): Show |
intron_variant | MODIFIER | c.72-887A>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48575054 | ||||||
| chr19:48575100
|
C | CT | 63 | a0001c0001t0001g0017a0001c0001t0001g0040a0001c0001t0001g0066others(60): Show | 63 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.72-815dupT | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48575100 | |||||
| chr19:48575100
|
C | CTT | 10 | a0001c0001t0001g0240a0001c0001t0001g0329a0001c0001t0001g0337others(7): Show | 10 | HG00423.hp2 HG01243.hp2 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.72-816_72-815dupTT | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48575100 | |||||
| chr19:48575100
|
CT | C | 7 | a0001c0001t0001g0042a0001c0001t0001g0073a0001c0001t0001g0302others(4): Show | 7 | HG02280.hp2 HG02572.hp1 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.72-815delT | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48575100 | |||||
| chr19:48575100
|
CTT | C | 24 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0026others(21): Show | 24 | HG00735.hp2 HG00738.hp2 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.72-816_72-815delTT | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48575100 | |||||
| chr19:48575100
|
CTTT | C | 128 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(125): Show | 128 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(125): Show |
intron_variant | MODIFIER | c.72-817_72-815delTT others(1): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48575100 | |||||
| chr19:48575100
|
CTTTT | C | 8 | a0001c0001t0001g0036a0001c0001t0001g0171a0001c0001t0001g0199others(5): Show | 8 | HG02109.hp2 HG02818.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.72-818_72-815delTT others(2): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48575100 | |||||
| chr19:48575170
|
A | G | 172 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(169): Show | 172 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(169): Show |
intron_variant | MODIFIER | c.72-771A>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48575170 | ||||||
| chr19:48575436
|
G | T | 299 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(296): Show | 300 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(297): Show |
intron_variant | MODIFIER | c.72-505G>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48575436 | ||||||
| chr19:48575447
|
A | G | 1 | a0001c0004t0001g0016 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.72-494A>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48575447 | ||||||
| chr19:48575461
|
AAAAT | A | 13 | a0001c0005t0001g0008a0001c0005t0001g0009a0001c0005t0001g0010others(10): Show | 13 | HG01192.hp1 HG01261.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.72-478_72-475delAA others(2): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48575461 | |||||
| chr19:48575463
|
A | T | 33 | a0001c0001t0001g0042a0001c0001t0001g0073a0001c0001t0001g0074others(30): Show | 34 | HG00099.hp2 HG00140.hp2 HG00741.hp2 others(31): Show |
intron_variant | MODIFIER | c.72-478A>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48575463 | ||||||
| chr19:48575463
|
AAT | A | 5 | a0001c0001t0001g0041a0001c0001t0001g0295a0001c0001t0001g0300others(2): Show | 5 | HG00558.hp2 HG02055.hp2 HG02129.hp1 others(2): Show |
intron_variant | MODIFIER | c.72-461_72-460delAT | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48575463 | |||||
| chr19:48575463
|
AATAT | A | 238 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(235): Show | 238 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(235): Show |
intron_variant | MODIFIER | c.72-463_72-460delAT others(2): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 48575463 | |||||
| chr19:48575465
|
T | A | 1 | a0001c0004t0001g0230 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.72-476T>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48575465 | ||||||
| chr19:48575469
|
T | A | 11 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0032others(8): Show | 11 | HG01243.hp1 HG02055.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.72-472T>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48575469 | ||||||
| chr19:48575513
|
T | C | 10 | a0001c0001t0001g0007a0001c0001t0001g0031a0001c0001t0001g0054others(7): Show | 10 | HG00733.hp1 HG01070.hp2 HG01071.hp2 others(7): Show |
intron_variant | MODIFIER | c.72-428T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48575513 | ||||||
| chr19:48575516
|
C | T | 10 | a0001c0001t0001g0007a0001c0001t0001g0031a0001c0001t0001g0054others(7): Show | 10 | HG00733.hp1 HG01070.hp2 HG01071.hp2 others(7): Show |
intron_variant | MODIFIER | c.72-425C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48575516 | ||||||
| chr19:48575582
|
A | G | 253 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(250): Show | 253 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(250): Show |
intron_variant | MODIFIER | c.72-359A>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48575582 | ||||||
| chr19:48575640
|
C | T | 101 | a0001c0001t0001g0007a0001c0001t0001g0024a0001c0001t0001g0025others(98): Show | 101 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(98): Show |
intron_variant | MODIFIER | c.72-301C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48575640 | ||||||
| chr19:48575652
|
T | C | 1 | a0001c0004t0001g0052 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.72-289T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | 48575652 | ||||||
| chr19:48576107
|
G | A | 6 | a0001c0003t0001g0119a0001c0003t0001g0170a0001c0003t0001g0222others(3): Show | 6 | HG01069.hp1 HG01109.hp1 HG01928.hp1 others(3): Show |
intron_variant | MODIFIER | c.214+24G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48576107 | ||||||
| chr19:48576162
|
G | A | 1 | a0001c0001t0001g0326 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.214+79G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48576162 | ||||||
| chr19:48576205
|
G | A | 48 | a0001c0001t0001g0042a0001c0001t0001g0073a0001c0001t0001g0074others(45): Show | 49 | HG00099.hp2 HG00140.hp2 HG00741.hp2 others(46): Show |
intron_variant | MODIFIER | c.214+122G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48576205 | ||||||
| chr19:48576344
|
T | C | 1 | a0001c0006t0001g0028 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.214+261T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48576344 | ||||||
| chr19:48576346
|
A | C | 49 | a0001c0001t0001g0042a0001c0001t0001g0073a0001c0001t0001g0074others(46): Show | 50 | HG00099.hp2 HG00140.hp2 HG00741.hp2 others(47): Show |
intron_variant | MODIFIER | c.214+263A>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48576346 | ||||||
| chr19:48576347
|
C | CTTTTCTT others(5): Show |
1 | a0001c0006t0001g0028 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.214+264_214+265ins others(12): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48576347 | ||||||
| chr19:48576348
|
C | T | 1 | a0001c0006t0001g0028 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.214+265C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48576348 | ||||||
| chr19:48576351
|
C | T | 1 | a0001c0006t0001g0028 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.214+268C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48576351 | ||||||
| chr19:48576353
|
A | ACTTTT | 4 | a0001c0001t0001g0337a0001c0002t0001g0303a0001c0004t0001g0278others(1): Show | 4 | HG00140.hp1 HG01243.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.214+273_214+274ins others(5): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48576353 | |||||
| chr19:48576353
|
A | T | 1 | a0001c0006t0001g0028 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.214+270A>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48576353 | ||||||
| chr19:48576354
|
C | CTTTTCTT others(6): Show |
1 | a0001c0002t0001g0076 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.214+273_214+274ins others(13): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48576354 | |||||
| chr19:48576354
|
C | CTTTTTTT | 26 | a0001c0001t0001g0036a0001c0001t0001g0171a0001c0001t0001g0199others(23): Show | 26 | HG00639.hp2 HG00735.hp1 HG01071.hp1 others(23): Show |
intron_variant | MODIFIER | c.214+273_214+274ins others(7): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48576354 | |||||
| chr19:48576354
|
C | CTTTTTTT others(1): Show |
24 | a0001c0001t0001g0014a0001c0001t0001g0088a0001c0001t0001g0106others(21): Show | 24 | HG00280.hp1 HG00735.hp2 HG00738.hp2 others(21): Show |
intron_variant | MODIFIER | c.214+273_214+274ins others(8): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48576354 | |||||
| chr19:48576354
|
C | CTTTTTTT others(2): Show |
44 | a0001c0001t0001g0021a0001c0001t0001g0087a0001c0001t0001g0104others(41): Show | 44 | HG00558.hp1 HG00621.hp1 HG01074.hp1 others(41): Show |
intron_variant | MODIFIER | c.214+273_214+274ins others(9): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48576354 | |||||
| chr19:48576354
|
C | CTTTTTTT others(3): Show |
14 | a0001c0001t0001g0189a0001c0001t0001g0192a0001c0001t0001g0259others(11): Show | 14 | HG00438.hp1 HG00558.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.214+273_214+274ins others(10): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48576354 | |||||
| chr19:48576354
|
C | CTTTTTTT others(4): Show |
17 | a0001c0001t0001g0023a0001c0001t0001g0051a0001c0001t0001g0053others(14): Show | 17 | HG00408.hp2 HG01070.hp1 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.214+273_214+274ins others(11): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48576354 | |||||
| chr19:48576354
|
C | CTTTTTTT others(5): Show |
2 | a0001c0001t0001g0346a0001c0001t0001g0364 | 2 | HG02071.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.214+273_214+274ins others(12): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48576354 | |||||
| chr19:48576354
|
C | CTTTTTTT others(6): Show |
1 | a0001c0001t0001g0196 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.214+273_214+274ins others(13): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48576354 | |||||
| chr19:48576354
|
C | CTTTTTTT others(7): Show |
1 | a0001c0002t0001g0249 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.214+273_214+274ins others(14): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48576354 | |||||
| chr19:48576354
|
C | T | 1 | a0001c0006t0001g0028 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.214+271C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48576354 | ||||||
| chr19:48576356
|
TCTC | T | 4 | a0001c0003t0001g0170a0001c0003t0001g0222a0001c0003t0001g0225others(1): Show | 4 | HG01069.hp1 HG01109.hp1 HG01928.hp1 others(1): Show |
intron_variant | MODIFIER | c.214+274_214+276del others(3): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48576356 | ||||||
| chr19:48576357
|
C | T | 293 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(290): Show | 294 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(291): Show |
intron_variant | MODIFIER | c.214+274C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48576357 | ||||||
| chr19:48576359
|
C | CT | 15 | a0001c0001t0001g0153a0001c0001t0001g0207a0001c0001t0001g0237others(12): Show | 15 | HG01123.hp1 HG01975.hp1 HG01975.hp2 others(12): Show |
intron_variant | MODIFIER | c.214+294dupT | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48576359 | |||||
| chr19:48576359
|
C | CTTTTCTT others(10): Show |
1 | a0001c0005t0001g0213 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.214+280_214+281ins others(17): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48576359 | |||||
| chr19:48576359
|
C | CTTTTCTT others(11): Show |
3 | a0001c0005t0001g0209a0001c0005t0001g0255a0001c0007t0001g0166 | 3 | HG01192.hp1 HG01261.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.214+280_214+281ins others(18): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48576359 | |||||
| chr19:48576359
|
C | CTTTTCTT others(12): Show |
5 | a0001c0001t0001g0042a0001c0001t0001g0073a0001c0001t0001g0074others(2): Show | 5 | HG03041.hp2 HG03130.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.214+280_214+281ins others(19): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48576359 | |||||
| chr19:48576359
|
C | CTTTTCTT others(13): Show |
2 | a0001c0001t0001g0075a0001c0004t0001g0072 | 2 | HG03098.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.214+280_214+281ins others(20): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48576359 | |||||
| chr19:48576359
|
C | CTTTTCTT others(14): Show |
3 | a0001c0006t0001g0090a0001c0007t0001g0200a0001c0010t0001g0037 | 3 | HG02109.hp1 HG02976.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.214+280_214+281ins others(21): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48576359 | |||||
| chr19:48576359
|
C | CTTTTCTT others(15): Show |
4 | a0001c0006t0001g0038a0001c0007t0001g0161a0001c0007t0001g0356others(1): Show | 4 | HG02280.hp2 HG02647.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.214+280_214+281ins others(22): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48576359 | |||||
| chr19:48576359
|
C | CTTTTCTT others(16): Show |
5 | a0001c0005t0001g0008a0001c0005t0001g0009a0001c0005t0001g0010others(2): Show | 5 | HG01884.hp1 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.214+280_214+281ins others(23): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48576359 | |||||
| chr19:48576359
|
C | CTTTTCTT others(17): Show |
6 | a0001c0006t0001g0044a0001c0006t0001g0061a0001c0007t0001g0057others(3): Show | 6 | HG01256.hp2 HG02145.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.214+280_214+281ins others(24): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48576359 | |||||
| chr19:48576359
|
C | CTTTTCTT others(18): Show |
7 | a0001c0005t0001g0108a0001c0005t0001g0173a0001c0005t0001g0197others(4): Show | 7 | HG00741.hp2 HG01081.hp1 HG01099.hp1 others(4): Show |
intron_variant | MODIFIER | c.214+280_214+281ins others(25): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48576359 | |||||
| chr19:48576359
|
C | CTTTTCTT others(19): Show |
7 | a0001c0005t0001g0001a0001c0005t0001g0071a0001c0005t0001g0109others(4): Show | 8 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.214+280_214+281ins others(26): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48576359 | |||||
| chr19:48576359
|
C | CTTTTCTT others(20): Show |
2 | a0001c0006t0001g0020a0004c0020t0001g0181 | 2 | HG02735.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.214+280_214+281ins others(27): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48576359 | |||||
| chr19:48576359
|
C | CTTTTCTT others(23): Show |
2 | a0001c0006t0001g0006a0001c0007t0001g0033 | 2 | HG01346.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.214+280_214+281ins others(30): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48576359 | |||||
| chr19:48576359
|
C | CTTTTCTT others(19): Show |
1 | a0001c0001t0001g0031 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.214+280_214+281ins others(26): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48576359 | |||||
| chr19:48576359
|
C | CTTTTCTT others(4): Show |
8 | a0001c0001t0001g0140a0001c0001t0001g0344a0001c0002t0001g0049others(5): Show | 8 | HG01070.hp2 HG01071.hp2 HG01361.hp1 others(5): Show |
intron_variant | MODIFIER | c.214+280_214+281ins others(11): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48576359 | |||||
| chr19:48576359
|
C | CTTTTCTT others(5): Show |
65 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0026others(62): Show | 65 | HG00280.hp2 HG00423.hp2 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.214+280_214+281ins others(12): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48576359 | |||||
| chr19:48576359
|
C | CTTTTCTT others(6): Show |
12 | a0001c0001t0001g0168a0001c0001t0001g0227a0001c0001t0001g0281others(9): Show | 12 | HG00597.hp1 HG00597.hp2 HG02027.hp2 others(9): Show |
intron_variant | MODIFIER | c.214+280_214+281ins others(13): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48576359 | |||||
| chr19:48576359
|
C | CTTTTCTT others(7): Show |
2 | a0001c0002t0001g0354a0001c0003t0001g0292 | 2 | NA18990.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.214+280_214+281ins others(14): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48576359 | |||||
| chr19:48576359
|
C | CTTTTCTT others(11): Show |
1 | a0001c0002t0001g0034 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.214+280_214+281ins others(18): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48576359 | |||||
| chr19:48576359
|
C | CTTTTCTT others(12): Show |
1 | a0001c0001t0001g0054 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.214+280_214+281ins others(19): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48576359 | |||||
| chr19:48576359
|
C | CTTTTCTT others(20): Show |
1 | a0001c0001t0001g0367 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.214+280_214+281ins others(27): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48576359 | |||||
| chr19:48576359
|
C | CTTTTCTT others(24): Show |
2 | a0001c0001t0001g0101a0001c0001t0001g0175 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.214+280_214+281ins others(31): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48576359 | |||||
| chr19:48576359
|
C | CTTTTCTT others(27): Show |
1 | a0001c0001t0001g0007 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.214+280_214+281ins others(34): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48576359 | |||||
| chr19:48576359
|
C | CTTTTCTT others(31): Show |
1 | a0001c0001t0001g0055 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.214+280_214+281ins others(38): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48576359 | |||||
| chr19:48576359
|
C | T | 136 | a0001c0001t0001g0014a0001c0001t0001g0021a0001c0001t0001g0023others(133): Show | 136 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(133): Show |
intron_variant | MODIFIER | c.214+276C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48576359 | ||||||
| chr19:48576360
|
T | TTTTCTTT others(5): Show |
1 | a0001c0002t0001g0328 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.214+280_214+281ins others(12): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48576360 | |||||
| chr19:48576364
|
T | C | 1 | a0001c0001t0001g0187 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.214+281T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48576364 | ||||||
| chr19:48576394
|
G | A | 140 | a0001c0001t0001g0014a0001c0001t0001g0021a0001c0001t0001g0023others(137): Show | 140 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(137): Show |
intron_variant | MODIFIER | c.214+311G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48576394 | ||||||
| chr19:48576453
|
T | TC | 140 | a0001c0001t0001g0014a0001c0001t0001g0021a0001c0001t0001g0023others(137): Show | 140 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(137): Show |
intron_variant | MODIFIER | c.214+373dupC | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48576453 | |||||
| chr19:48576460
|
G | A | 19 | a0001c0005t0001g0001a0001c0005t0001g0071a0001c0005t0001g0108others(16): Show | 20 | HG00099.hp2 HG00140.hp2 HG00741.hp2 others(17): Show |
intron_variant | MODIFIER | c.214+377G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48576460 | ||||||
| chr19:48576533
|
T | C | 1 | a0001c0006t0001g0044 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.214+450T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48576533 | ||||||
| chr19:48576640
|
C | CT | 24 | a0001c0001t0001g0042a0001c0001t0001g0073a0001c0001t0001g0074others(21): Show | 24 | HG00140.hp2 HG00741.hp2 HG01192.hp1 others(21): Show |
intron_variant | MODIFIER | c.214+578dupT | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48576640 | |||||
| chr19:48576640
|
CT | C | 6 | a0001c0002t0001g0079a0001c0003t0001g0078a0001c0004t0001g0127others(3): Show | 6 | HG00609.hp2 HG03041.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.214+578delT | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48576640 | |||||
| chr19:48576640
|
CTTT | C | 18 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0032others(15): Show | 18 | HG00438.hp2 HG01175.hp1 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.214+576_214+578del others(3): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48576640 | |||||
| chr19:48576640
|
CTTTT | C | 139 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0021others(136): Show | 139 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(136): Show |
intron_variant | MODIFIER | c.214+575_214+578del others(4): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48576640 | |||||
| chr19:48576640
|
CTTTTT | C | 89 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0026others(86): Show | 89 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.214+574_214+578del others(5): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48576640 | |||||
| chr19:48576665
|
G | A | 4 | a0001c0001t0001g0364a0001c0004t0001g0052a0001c0004t0001g0089others(1): Show | 4 | HG02258.hp2 HG02572.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.214+582G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48576665 | ||||||
| chr19:48576686
|
C | T | 1 | a0001c0003t0001g0375 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.214+603C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48576686 | ||||||
| chr19:48576797
|
T | C | 5 | a0001c0001t0001g0042a0001c0001t0001g0073a0001c0001t0001g0074others(2): Show | 5 | HG03098.hp1 HG03130.hp2 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.214+714T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48576797 | ||||||
| chr19:48576841
|
A | G | 1 | a0001c0004t0001g0045 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.214+758A>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48576841 | ||||||
| chr19:48576919
|
G | A | 139 | a0001c0001t0001g0014a0001c0001t0001g0021a0001c0001t0001g0023others(136): Show | 139 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(136): Show |
intron_variant | MODIFIER | c.214+836G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48576919 | ||||||
| chr19:48577028
|
A | AT | 27 | a0001c0001t0001g0017a0001c0001t0001g0039a0001c0001t0001g0040others(24): Show | 27 | HG01168.hp2 HG01169.hp2 HG01978.hp1 others(24): Show |
intron_variant | MODIFIER | c.214+970dupT | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48577028 | |||||
| chr19:48577028
|
A | ATT | 8 | a0001c0001t0001g0042a0001c0001t0001g0073a0001c0001t0001g0074others(5): Show | 8 | HG03130.hp2 HG03942.hp1 NA18522.hp1 others(5): Show |
intron_variant | MODIFIER | c.214+969_214+970dup others(2): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48577028 | |||||
| chr19:48577028
|
AT | A | 17 | a0001c0001t0001g0238a0001c0002t0001g0217a0001c0003t0001g0105others(14): Show | 17 | HG01168.hp1 HG01261.hp1 HG01928.hp2 others(14): Show |
intron_variant | MODIFIER | c.214+970delT | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48577028 | |||||
| chr19:48577028
|
ATTT | A | 34 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0021others(31): Show | 34 | HG01243.hp1 HG01358.hp1 HG01358.hp2 others(31): Show |
intron_variant | MODIFIER | c.214+968_214+970del others(3): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48577028 | |||||
| chr19:48577028
|
ATTTT | A | 110 | a0001c0001t0001g0014a0001c0001t0001g0036a0001c0001t0001g0060others(107): Show | 110 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.214+967_214+970del others(4): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48577028 | |||||
| chr19:48577028
|
ATTTTT | A | 12 | a0001c0001t0001g0101a0001c0001t0001g0107a0001c0001t0001g0175others(9): Show | 12 | HG00673.hp2 HG01167.hp1 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.214+966_214+970del others(5): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48577028 | |||||
| chr19:48577028
|
ATTTTTT | A | 99 | a0001c0001t0001g0007a0001c0001t0001g0024a0001c0001t0001g0025others(96): Show | 99 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.214+965_214+970del others(6): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48577028 | |||||
| chr19:48577028
|
ATTTTTTT others(3): Show |
A | 18 | a0001c0005t0001g0001a0001c0005t0001g0071a0001c0005t0001g0108others(15): Show | 19 | HG00099.hp2 HG00140.hp2 HG00741.hp2 others(16): Show |
intron_variant | MODIFIER | c.214+961_214+970del others(10): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48577028 | |||||
| chr19:48577128
|
G | A | 3 | a0001c0001t0001g0289a0001c0001t0001g0290a0001c0004t0001g0230 | 3 | HG00673.hp1 HG02056.hp1 HG02523.hp1 |
intron_variant | MODIFIER | c.214+1045G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48577128 | ||||||
| chr19:48577149
|
C | A | 23 | a0001c0001t0001g0017a0001c0001t0001g0039a0001c0001t0001g0040others(20): Show | 23 | HG00738.hp1 HG01168.hp2 HG01169.hp2 others(20): Show |
intron_variant | MODIFIER | c.214+1066C>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48577149 | ||||||
| chr19:48577176
|
G | A | 3 | a0001c0001t0001g0289a0001c0001t0001g0290a0001c0004t0001g0230 | 3 | HG00673.hp1 HG02056.hp1 HG02523.hp1 |
intron_variant | MODIFIER | c.214+1093G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48577176 | ||||||
| chr19:48577352
|
C | CT | 76 | a0001c0001t0001g0017a0001c0001t0001g0024a0001c0001t0001g0025others(73): Show | 76 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(73): Show |
intron_variant | MODIFIER | c.214+1299dupT | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48577352 | |||||
| chr19:48577352
|
C | CTT | 44 | a0001c0001t0001g0080a0001c0001t0001g0097a0001c0001t0001g0123others(41): Show | 44 | HG00140.hp1 HG00280.hp2 HG00609.hp1 others(41): Show |
intron_variant | MODIFIER | c.214+1298_214+1299d others(4): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48577352 | |||||
| chr19:48577352
|
C | CTTT | 8 | a0001c0001t0001g0326a0001c0002t0001g0206a0001c0002t0001g0263others(5): Show | 8 | HG00438.hp2 HG00642.hp1 HG00673.hp2 others(5): Show |
intron_variant | MODIFIER | c.214+1297_214+1299d others(5): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48577352 | |||||
| chr19:48577352
|
C | CTTTT | 7 | a0001c0001t0001g0107a0001c0001t0001g0240a0001c0001t0001g0246others(4): Show | 7 | HG02109.hp1 HG02630.hp1 HG04204.hp2 others(4): Show |
intron_variant | MODIFIER | c.214+1296_214+1299d others(6): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48577352 | |||||
| chr19:48577352
|
C | CTTTTT | 18 | a0001c0001t0001g0159a0001c0001t0001g0205a0001c0001t0001g0229others(15): Show | 18 | HG00558.hp1 HG02965.hp1 HG03017.hp1 others(15): Show |
intron_variant | MODIFIER | c.214+1295_214+1299d others(7): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48577352 | |||||
| chr19:48577352
|
C | CTTTTTT | 49 | a0001c0001t0001g0023a0001c0001t0001g0031a0001c0001t0001g0036others(46): Show | 49 | HG00408.hp2 HG00438.hp1 HG01069.hp1 others(46): Show |
intron_variant | MODIFIER | c.214+1294_214+1299d others(8): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48577352 | |||||
| chr19:48577352
|
C | CTTTTTTT | 42 | a0001c0001t0001g0021a0001c0001t0001g0051a0001c0001t0001g0055others(39): Show | 42 | HG00280.hp1 HG00558.hp2 HG01069.hp2 others(39): Show |
intron_variant | MODIFIER | c.214+1293_214+1299d others(9): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48577352 | |||||
| chr19:48577352
|
C | CTTTTTTT others(1): Show |
28 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0088others(25): Show | 28 | HG00735.hp1 HG00735.hp2 HG00738.hp2 others(25): Show |
intron_variant | MODIFIER | c.214+1292_214+1299d others(10): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48577352 | |||||
| chr19:48577352
|
C | CTTTTTTT others(2): Show |
9 | a0001c0001t0001g0032a0001c0001t0001g0311a0001c0002t0001g0083others(6): Show | 9 | HG00621.hp1 HG00639.hp2 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.214+1291_214+1299d others(11): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48577352 | |||||
| chr19:48577352
|
C | CTTTTTTT others(3): Show |
8 | a0001c0002t0001g0093a0001c0002t0001g0176a0001c0004t0001g0089others(5): Show | 8 | HG01167.hp2 HG01192.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.214+1290_214+1299d others(12): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48577352 | |||||
| chr19:48577352
|
C | CTTTTTTT others(4): Show |
2 | a0001c0002t0001g0035a0001c0019t0001g0372 | 2 | HG02486.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.214+1289_214+1299d others(13): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48577352 | |||||
| chr19:48577352
|
CT | C | 10 | a0001c0001t0001g0241a0001c0003t0001g0233a0001c0006t0001g0038others(7): Show | 10 | HG02280.hp2 HG02647.hp2 HG02976.hp1 others(7): Show |
intron_variant | MODIFIER | c.214+1299delT | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48577352 | |||||
| chr19:48577352
|
CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0001g0191 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.214+1290_214+1299d others(12): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48577352 | |||||
| chr19:48577352
|
CTTTTTTT others(5): Show |
C | 1 | a0001c0007t0001g0033 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.214+1288_214+1299d others(14): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48577352 | |||||
| chr19:48577390
|
G | T | 4 | a0001c0002t0001g0217a0001c0003t0001g0256a0001c0004t0001g0319others(1): Show | 4 | HG01168.hp1 HG01261.hp1 HG01975.hp1 others(1): Show |
intron_variant | MODIFIER | c.214+1307G>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48577390 | ||||||
| chr19:48577475
|
C | T | 152 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(149): Show | 152 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(149): Show |
intron_variant | MODIFIER | c.214+1392C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48577475 | ||||||
| chr19:48577511
|
G | T | 105 | a0001c0001t0001g0007a0001c0001t0001g0024a0001c0001t0001g0025others(102): Show | 105 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.214+1428G>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48577511 | ||||||
| chr19:48577569
|
C | T | 105 | a0001c0001t0001g0007a0001c0001t0001g0024a0001c0001t0001g0025others(102): Show | 105 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.214+1486C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48577569 | ||||||
| chr19:48577629
|
G | C | 1 | a0001c0002t0001g0118 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.214+1546G>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48577629 | ||||||
| chr19:48577674
|
G | A | 1 | a0001c0001t0001g0191 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.214+1591G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48577674 | ||||||
| chr19:48577971
|
C | T | 1 | a0001c0003t0001g0203 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.214+1888C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48577971 | ||||||
| chr19:48578051
|
TA | T | 229 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0024others(226): Show | 229 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(226): Show |
intron_variant | MODIFIER | c.214+1980delA | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48578051 | |||||
| chr19:48578071
|
G | A | 19 | a0001c0005t0001g0001a0001c0005t0001g0071a0001c0005t0001g0108others(16): Show | 20 | HG00099.hp2 HG00140.hp2 HG00741.hp2 others(17): Show |
intron_variant | MODIFIER | c.214+1988G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48578071 | ||||||
| chr19:48578138
|
G | T | 105 | a0001c0001t0001g0007a0001c0001t0001g0024a0001c0001t0001g0025others(102): Show | 105 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.214+2055G>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48578138 | ||||||
| chr19:48578227
|
G | C | 141 | a0001c0001t0001g0014a0001c0001t0001g0021a0001c0001t0001g0023others(138): Show | 141 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(138): Show |
intron_variant | MODIFIER | c.214+2144G>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48578227 | ||||||
| chr19:48578255
|
G | A | 10 | a0001c0006t0001g0038a0001c0006t0001g0061a0001c0007t0001g0057others(7): Show | 10 | HG02145.hp2 HG02280.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.214+2172G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48578255 | ||||||
| chr19:48578379
|
C | T | 2 | a0001c0002t0001g0081a0001c0003t0001g0180 | 2 | HG01081.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.214+2296C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48578379 | ||||||
| chr19:48578490
|
G | A | 5 | a0001c0001t0001g0042a0001c0001t0001g0073a0001c0001t0001g0074others(2): Show | 5 | HG03098.hp1 HG03130.hp2 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.214+2407G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48578490 | ||||||
| chr19:48578494
|
A | T | 8 | a0001c0005t0001g0019a0001c0005t0001g0209a0001c0005t0001g0213others(5): Show | 8 | HG01192.hp1 HG01261.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.214+2411A>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48578494 | ||||||
| chr19:48578513
|
T | C | 1 | a0001c0001t0001g0290 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.214+2430T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48578513 | ||||||
| chr19:48578530
|
C | T | 96 | a0001c0001t0001g0007a0001c0001t0001g0024a0001c0001t0001g0025others(93): Show | 96 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.214+2447C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48578530 | ||||||
| chr19:48578531
|
G | A | 2 | a0001c0005t0001g0008a0001c0005t0001g0009 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.214+2448G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48578531 | ||||||
| chr19:48578647
|
C | T | 1 | a0001c0001t0001g0192 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.214+2564C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48578647 | ||||||
| chr19:48578705
|
C | T | 1 | a0001c0004t0001g0316 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.214+2622C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48578705 | ||||||
| chr19:48578732
|
C | A | 1 | a0001c0002t0001g0332 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.214+2649C>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48578732 | ||||||
| chr19:48578769
|
G | A | 99 | a0001c0001t0001g0007a0001c0001t0001g0024a0001c0001t0001g0025others(96): Show | 99 | HG00280.hp2 HG00423.hp2 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.214+2686G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48578769 | ||||||
| chr19:48578801
|
G | C | 2 | a0001c0005t0001g0019a0001c0006t0001g0028 | 2 | HG03225.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.214+2718G>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48578801 | ||||||
| chr19:48578834
|
C | T | 1 | a0001c0001t0001g0295 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.214+2751C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48578834 | ||||||
| chr19:48579008
|
G | A | 105 | a0001c0001t0001g0007a0001c0001t0001g0024a0001c0001t0001g0025others(102): Show | 105 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.214+2925G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48579008 | ||||||
| chr19:48579010
|
T | C | 1 | a0001c0006t0001g0090 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.214+2927T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48579010 | ||||||
| chr19:48579149
|
A | T | 105 | a0001c0001t0001g0007a0001c0001t0001g0024a0001c0001t0001g0025others(102): Show | 105 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.214+3066A>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48579149 | ||||||
| chr19:48579172
|
T | C | 10 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0032others(7): Show | 10 | HG01243.hp1 HG02055.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.214+3089T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48579172 | ||||||
| chr19:48579283
|
C | CT | 7 | a0001c0001t0001g0115a0001c0001t0001g0205a0001c0001t0001g0240others(4): Show | 7 | HG00408.hp2 HG00738.hp1 HG02027.hp1 others(4): Show |
intron_variant | MODIFIER | c.214+3217dupT | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48579283 | |||||
| chr19:48579283
|
CT | C | 108 | a0001c0001t0001g0007a0001c0001t0001g0024a0001c0001t0001g0025others(105): Show | 108 | HG00280.hp2 HG00423.hp2 HG00438.hp2 others(105): Show |
intron_variant | MODIFIER | c.214+3217delT | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48579283 | |||||
| chr19:48579314
|
G | A | 1 | a0001c0001t0001g0014 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.214+3231G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48579314 | ||||||
| chr19:48579343
|
C | A | 141 | a0001c0001t0001g0014a0001c0001t0001g0021a0001c0001t0001g0023others(138): Show | 141 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(138): Show |
intron_variant | MODIFIER | c.214+3260C>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48579343 | ||||||
| chr19:48579393
|
T | C | 105 | a0001c0001t0001g0007a0001c0001t0001g0024a0001c0001t0001g0025others(102): Show | 105 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.214+3310T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48579393 | ||||||
| chr19:48579430
|
C | T | 1 | a0001c0001t0001g0268 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.214+3347C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48579430 | ||||||
| chr19:48579432
|
A | G | 3 | a0001c0005t0001g0209a0001c0005t0001g0213a0001c0005t0001g0255 | 3 | HG01192.hp1 HG02735.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.214+3349A>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48579432 | ||||||
| chr19:48579442
|
C | T | 10 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0032others(7): Show | 10 | HG01243.hp1 HG02055.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.214+3359C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48579442 | ||||||
| chr19:48579455
|
TG | T | 10 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0032others(7): Show | 10 | HG01243.hp1 HG02055.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.214+3373delG | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48579455 | ||||||
| chr19:48579529
|
G | A | 1 | a0001c0005t0001g0019 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.214+3446G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48579529 | ||||||
| chr19:48579563
|
C | G | 4 | a0001c0001t0001g0054a0001c0002t0001g0034a0001c0002t0001g0049others(1): Show | 4 | HG00733.hp1 HG01070.hp2 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.214+3480C>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48579563 | ||||||
| chr19:48579593
|
T | TTTC | 10 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0026others(7): Show | 10 | HG02055.hp2 HG02258.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.214+3512_214+3513i others(5): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48579593 | |||||
| chr19:48579593
|
T | TTTTCTTT others(2): Show |
6 | a0001c0001t0001g0036a0001c0001t0001g0171a0001c0001t0001g0199others(3): Show | 6 | HG01891.hp1 HG02109.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.214+3517_214+3518i others(11): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48579593 | |||||
| chr19:48579605
|
C | CT | 44 | a0001c0001t0001g0042a0001c0001t0001g0073a0001c0001t0001g0074others(41): Show | 45 | HG00099.hp2 HG00140.hp2 HG01081.hp1 others(42): Show |
intron_variant | MODIFIER | c.214+3540dupT | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48579605 | |||||
| chr19:48579605
|
C | CTTT | 7 | a0001c0001t0001g0036a0001c0001t0001g0171a0001c0001t0001g0199others(4): Show | 7 | HG01346.hp2 HG01891.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.214+3538_214+3540d others(5): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48579605 | |||||
| chr19:48579605
|
C | CTTTCTTT others(3): Show |
4 | a0001c0001t0001g0226a0001c0002t0001g0085a0001c0002t0001g0317others(1): Show | 4 | HG01496.hp2 HG03195.hp1 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.214+3525_214+3526i others(12): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48579605 | |||||
| chr19:48579605
|
C | CTTTCTTT others(4): Show |
84 | a0001c0001t0001g0014a0001c0001t0001g0021a0001c0001t0001g0023others(81): Show | 84 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(81): Show |
intron_variant | MODIFIER | c.214+3525_214+3526i others(13): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48579605 | |||||
| chr19:48579605
|
C | CTTTCTTT others(5): Show |
39 | a0001c0001t0001g0087a0001c0001t0001g0104a0001c0001t0001g0159others(36): Show | 39 | HG00408.hp2 HG00438.hp1 HG00558.hp2 others(36): Show |
intron_variant | MODIFIER | c.214+3525_214+3526i others(14): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48579605 | |||||
| chr19:48579605
|
C | CTTTCTTT others(6): Show |
5 | a0001c0001t0001g0283a0001c0001t0001g0284a0001c0001t0001g0312others(2): Show | 5 | HG02056.hp2 HG02080.hp2 HG04184.hp1 others(2): Show |
intron_variant | MODIFIER | c.214+3525_214+3526i others(15): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48579605 | |||||
| chr19:48579605
|
C | CTTTCTTT others(1): Show |
65 | a0001c0001t0001g0080a0001c0001t0001g0123a0001c0001t0001g0140others(62): Show | 65 | HG00280.hp2 HG00423.hp2 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.214+3525_214+3526i others(10): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48579605 | |||||
| chr19:48579605
|
C | CTTTCTTT others(2): Show |
18 | a0001c0001t0001g0054a0001c0001t0001g0097a0001c0001t0001g0175others(15): Show | 18 | HG00140.hp1 HG00609.hp1 HG00642.hp2 others(15): Show |
intron_variant | MODIFIER | c.214+3525_214+3526i others(11): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48579605 | |||||
| chr19:48579605
|
C | CTTTCTTT others(3): Show |
7 | a0001c0001t0001g0007a0001c0001t0001g0031a0001c0001t0001g0055others(4): Show | 7 | HG01169.hp1 HG01433.hp1 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.214+3525_214+3526i others(12): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48579605 | |||||
| chr19:48579605
|
C | T | 10 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0026others(7): Show | 10 | HG02055.hp2 HG02258.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.214+3522C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48579605 | ||||||
| chr19:48579607
|
T | TTC | 10 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0032others(7): Show | 10 | HG01243.hp1 HG02055.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.214+3525_214+3526i others(4): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48579607 | |||||
| chr19:48579611
|
T | C | 10 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0032others(7): Show | 10 | HG01243.hp1 HG02055.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.214+3528T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48579611 | ||||||
| chr19:48579726
|
C | T | 4 | a0001c0001t0001g0054a0001c0002t0001g0034a0001c0002t0001g0049others(1): Show | 4 | HG00733.hp1 HG01070.hp2 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.214+3643C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48579726 | ||||||
| chr19:48579738
|
T | C | 4 | a0001c0001t0001g0054a0001c0002t0001g0034a0001c0002t0001g0049others(1): Show | 4 | HG00733.hp1 HG01070.hp2 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.214+3655T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48579738 | ||||||
| chr19:48579740
|
G | A | 1 | a0001c0002t0001g0248 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.214+3657G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48579740 | ||||||
| chr19:48579742
|
A | G | 4 | a0001c0001t0001g0054a0001c0002t0001g0034a0001c0002t0001g0049others(1): Show | 4 | HG00733.hp1 HG01070.hp2 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.214+3659A>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48579742 | ||||||
| chr19:48579745
|
T | C | 4 | a0001c0001t0001g0054a0001c0002t0001g0034a0001c0002t0001g0049others(1): Show | 4 | HG00733.hp1 HG01070.hp2 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.214+3662T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48579745 | ||||||
| chr19:48579760
|
C | T | 5 | a0001c0005t0001g0008a0001c0005t0001g0009a0001c0005t0001g0010others(2): Show | 5 | HG01884.hp1 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.214+3677C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48579760 | ||||||
| chr19:48579795
|
C | T | 1 | a0001c0002t0001g0093 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.214+3712C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48579795 | ||||||
| chr19:48580066
|
A | G | 291 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(288): Show | 292 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(289): Show |
intron_variant | MODIFIER | c.214+3983A>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48580066 | ||||||
| chr19:48580081
|
G | T | 1 | a0002c0008t0001g0154 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.214+3998G>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48580081 | ||||||
| chr19:48580100
|
C | CT | 151 | a0001c0001t0001g0014a0001c0001t0001g0021a0001c0001t0001g0023others(148): Show | 151 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(148): Show |
intron_variant | MODIFIER | c.214+4030dupT | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48580100 | |||||
| chr19:48580236
|
A | G | 142 | a0001c0001t0001g0014a0001c0001t0001g0021a0001c0001t0001g0036others(139): Show | 142 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(139): Show |
intron_variant | MODIFIER | c.214+4153A>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48580236 | ||||||
| chr19:48580249
|
C | T | 4 | a0001c0001t0001g0023a0001c0001t0001g0051a0001c0001t0001g0053others(1): Show | 4 | HG02257.hp1 HG02717.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.214+4166C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48580249 | ||||||
| chr19:48580372
|
GC | G | 121 | a0001c0001t0001g0007a0001c0001t0001g0024a0001c0001t0001g0025others(118): Show | 121 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(118): Show |
intron_variant | MODIFIER | c.214+4291delC | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48580372 | |||||
| chr19:48580799
|
G | A | 163 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0021others(160): Show | 163 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(160): Show |
intron_variant | MODIFIER | c.214+4716G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48580799 | ||||||
| chr19:48580831
|
G | A | 2 | a0001c0004t0001g0089a0001c0004t0001g0198 | 2 | HG02258.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.214+4748G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48580831 | ||||||
| chr19:48580857
|
C | T | 105 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0026others(102): Show | 105 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.214+4774C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48580857 | ||||||
| chr19:48580992
|
C | T | 4 | a0001c0001t0001g0140a0001c0001t0001g0342a0001c0001t0001g0344others(1): Show | 4 | HG02040.hp2 HG02074.hp1 HG02129.hp2 others(1): Show |
intron_variant | MODIFIER | c.214+4909C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48580992 | ||||||
| chr19:48581029
|
C | CT | 114 | a0001c0001t0001g0014a0001c0001t0001g0036a0001c0001t0001g0051others(111): Show | 114 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.214+4970dupT | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48581029 | |||||
| chr19:48581029
|
C | CTT | 98 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0026others(95): Show | 98 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.214+4969_214+4970d others(4): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48581029 | |||||
| chr19:48581029
|
C | CTTT | 15 | a0001c0001t0001g0151a0001c0001t0001g0331a0001c0001t0001g0337others(12): Show | 15 | HG00438.hp2 HG00609.hp1 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.214+4968_214+4970d others(5): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48581029 | |||||
| chr19:48581029
|
CTT | C | 12 | a0001c0001t0001g0021a0001c0001t0001g0042a0001c0001t0001g0073others(9): Show | 12 | HG01884.hp2 HG02257.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.214+4969_214+4970d others(4): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48581029 | |||||
| chr19:48581029
|
CTTTT | C | 35 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(32): Show | 35 | HG00733.hp1 HG00738.hp1 HG01167.hp1 others(32): Show |
intron_variant | MODIFIER | c.214+4967_214+4970d others(6): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48581029 | |||||
| chr19:48581029
|
CTTTTTTT | C | 21 | a0001c0005t0001g0001a0001c0005t0001g0071a0001c0005t0001g0108others(18): Show | 22 | HG00099.hp2 HG00140.hp2 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.214+4964_214+4970d others(9): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48581029 | |||||
| chr19:48581099
|
C | T | 50 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(47): Show | 50 | HG00733.hp1 HG00738.hp1 HG01167.hp1 others(47): Show |
intron_variant | MODIFIER | c.214+5016C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48581099 | ||||||
| chr19:48581207
|
AT | A | 153 | a0001c0001t0001g0014a0001c0001t0001g0036a0001c0001t0001g0087others(150): Show | 154 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.214+5140delT | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48581207 | |||||
| chr19:48581207
|
ATT | A | 108 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0026others(105): Show | 108 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.214+5139_214+5140d others(4): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48581207 | |||||
| chr19:48581207
|
ATTT | A | 49 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(46): Show | 49 | HG00733.hp1 HG00738.hp1 HG01167.hp1 others(46): Show |
intron_variant | MODIFIER | c.214+5138_214+5140d others(5): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48581207 | |||||
| chr19:48581223
|
T | C | 1 | a0001c0001t0001g0259 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.214+5140T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48581223 | ||||||
| chr19:48581264
|
G | A | 3 | a0001c0001t0001g0237a0001c0003t0001g0129a0001c0003t0001g0224 | 3 | HG01928.hp2 HG01934.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.214+5181G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48581264 | ||||||
| chr19:48581274
|
T | C | 50 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(47): Show | 50 | HG00733.hp1 HG00738.hp1 HG01167.hp1 others(47): Show |
intron_variant | MODIFIER | c.214+5191T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48581274 | ||||||
| chr19:48581296
|
G | A | 1 | a0002c0008t0001g0244 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.214+5213G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48581296 | ||||||
| chr19:48581299
|
C | T | 105 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0026others(102): Show | 105 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.214+5216C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48581299 | ||||||
| chr19:48581334
|
G | A | 4 | a0001c0001t0001g0023a0001c0001t0001g0051a0001c0001t0001g0053others(1): Show | 4 | HG02257.hp1 HG02717.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.214+5251G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48581334 | ||||||
| chr19:48581339
|
T | C | 310 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(307): Show | 311 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(308): Show |
intron_variant | MODIFIER | c.214+5256T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48581339 | ||||||
| chr19:48581346
|
A | G | 1 | a0001c0001t0001g0241 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.214+5263A>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48581346 | ||||||
| chr19:48581398
|
G | A | 312 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(309): Show | 313 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(310): Show |
intron_variant | MODIFIER | c.214+5315G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48581398 | ||||||
| chr19:48581418
|
G | A | 86 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(83): Show | 87 | HG00099.hp2 HG00140.hp2 HG00733.hp1 others(84): Show |
intron_variant | MODIFIER | c.214+5335G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48581418 | ||||||
| chr19:48581455
|
A | G | 86 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(83): Show | 87 | HG00099.hp2 HG00140.hp2 HG00733.hp1 others(84): Show |
intron_variant | MODIFIER | c.214+5372A>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48581455 | ||||||
| chr19:48581470
|
G | GTTT | 6 | a0001c0001t0001g0021a0001c0001t0001g0361a0001c0001t0001g0362others(3): Show | 6 | HG01884.hp2 HG02257.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.214+5387_214+5388i others(5): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48581470 | ||||||
| chr19:48581471
|
A | T | 7 | a0001c0001t0001g0021a0001c0001t0001g0361a0001c0001t0001g0362others(4): Show | 7 | HG01884.hp2 HG02257.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.214+5388A>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48581471 | ||||||
| chr19:48581472
|
G | GT | 7 | a0001c0001t0001g0270a0001c0001t0001g0283a0001c0001t0001g0284others(4): Show | 7 | HG03139.hp2 NA18973.hp1 NA18974.hp1 others(4): Show |
intron_variant | MODIFIER | c.214+5405dupT | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48581472 | |||||
| chr19:48581472
|
G | GTT | 87 | a0001c0001t0001g0036a0001c0001t0001g0087a0001c0001t0001g0088others(84): Show | 87 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.214+5404_214+5405d others(4): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48581472 | |||||
| chr19:48581472
|
G | GTTT | 152 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(149): Show | 152 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(149): Show |
intron_variant | MODIFIER | c.214+5403_214+5405d others(5): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48581472 | |||||
| chr19:48581472
|
G | GTTTT | 25 | a0001c0001t0001g0032a0001c0001t0001g0073a0001c0001t0001g0075others(22): Show | 25 | HG00423.hp1 HG01243.hp1 HG01261.hp1 others(22): Show |
intron_variant | MODIFIER | c.214+5402_214+5405d others(6): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48581472 | |||||
| chr19:48581472
|
G | GTTTTT | 32 | a0001c0001t0001g0042a0001c0001t0001g0074a0001c0002t0001g0354others(29): Show | 33 | HG00099.hp2 HG00140.hp2 HG00741.hp2 others(30): Show |
intron_variant | MODIFIER | c.214+5401_214+5405d others(7): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48581472 | |||||
| chr19:48581472
|
G | GTTTTTT | 7 | a0001c0001t0001g0014a0001c0001t0001g0258a0001c0005t0001g0019others(4): Show | 7 | HG02818.hp2 HG03041.hp1 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.214+5400_214+5405d others(8): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48581472 | |||||
| chr19:48581472
|
G | T | 7 | a0001c0001t0001g0021a0001c0001t0001g0361a0001c0001t0001g0362others(4): Show | 7 | HG01884.hp2 HG02257.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.214+5389G>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48581472 | ||||||
| chr19:48581582
|
C | T | 86 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(83): Show | 87 | HG00099.hp2 HG00140.hp2 HG00733.hp1 others(84): Show |
intron_variant | MODIFIER | c.214+5499C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48581582 | ||||||
| chr19:48581875
|
TTTA | T | 33 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0017others(30): Show | 33 | HG00733.hp1 HG01081.hp2 HG01346.hp2 others(30): Show |
intron_variant | MODIFIER | c.215-5340_215-5338d others(5): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48581875 | |||||
| chr19:48581882
|
T | TTATTA | 6 | a0001c0001t0001g0361a0001c0001t0001g0362a0001c0001t0001g0365others(3): Show | 6 | HG01884.hp2 HG02559.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.215-5345_215-5341d others(7): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48581882 | |||||
| chr19:48581885
|
T | TTA | 3 | a0001c0005t0001g0071a0001c0006t0001g0020a0001c0006t0001g0044 | 3 | HG00140.hp2 HG02723.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.215-5342_215-5341d others(4): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48581885 | |||||
| chr19:48581887
|
A | T | 13 | a0001c0001t0001g0007a0001c0001t0001g0031a0001c0001t0001g0055others(10): Show | 13 | HG00738.hp1 HG01167.hp1 HG01169.hp1 others(10): Show |
intron_variant | MODIFIER | c.215-5342A>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48581887 | ||||||
| chr19:48581887
|
ATTATATT others(2): Show |
A | 5 | a0001c0005t0001g0209a0001c0005t0001g0213a0001c0005t0001g0255others(2): Show | 5 | HG01192.hp1 HG01261.hp2 HG02735.hp2 others(2): Show |
intron_variant | MODIFIER | c.215-5340_215-5332d others(11): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48581887 | |||||
| chr19:48581889
|
T | A | 38 | a0001c0001t0001g0007a0001c0001t0001g0031a0001c0001t0001g0042others(35): Show | 39 | HG00099.hp2 HG00738.hp1 HG00741.hp2 others(36): Show |
intron_variant | MODIFIER | c.215-5340T>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48581889 | ||||||
| chr19:48581890
|
A | AT | 10 | a0001c0001t0001g0021a0001c0001t0001g0361a0001c0001t0001g0362others(7): Show | 10 | HG00140.hp2 HG01884.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.215-5338dupT | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48581890 | |||||
| chr19:48581890
|
A | T | 63 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(60): Show | 64 | HG00099.hp2 HG00733.hp1 HG00738.hp1 others(61): Show |
intron_variant | MODIFIER | c.215-5339A>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48581890 | ||||||
| chr19:48581890
|
ATAT | A | 217 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(214): Show | 217 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.215-5309_215-5307d others(5): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48581890 | |||||
| chr19:48581924
|
A | G | 6 | a0001c0001t0001g0021a0001c0001t0001g0361a0001c0001t0001g0362others(3): Show | 6 | HG01884.hp2 HG02257.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.215-5305A>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48581924 | ||||||
| chr19:48581943
|
C | T | 86 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(83): Show | 87 | HG00099.hp2 HG00140.hp2 HG00733.hp1 others(84): Show |
intron_variant | MODIFIER | c.215-5286C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48581943 | ||||||
| chr19:48581944
|
G | A | 1 | a0001c0003t0001g0046 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.215-5285G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48581944 | ||||||
| chr19:48581951
|
C | G | 1 | a0001c0001t0001g0283 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.215-5278C>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48581951 | ||||||
| chr19:48581952
|
T | C | 1 | a0001c0001t0001g0283 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.215-5277T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48581952 | ||||||
| chr19:48581990
|
C | T | 2 | a0001c0001t0001g0267a0001c0003t0001g0325 | 2 | NA19000.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.215-5239C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48581990 | ||||||
| chr19:48582145
|
T | A | 1 | a0001c0002t0001g0160 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.215-5084T>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48582145 | ||||||
| chr19:48582168
|
G | C | 86 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(83): Show | 87 | HG00099.hp2 HG00140.hp2 HG00733.hp1 others(84): Show |
intron_variant | MODIFIER | c.215-5061G>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48582168 | ||||||
| chr19:48582184
|
C | T | 1 | a0001c0001t0001g0373 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.215-5045C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48582184 | ||||||
| chr19:48582387
|
GTA | G | 86 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(83): Show | 87 | HG00099.hp2 HG00140.hp2 HG00733.hp1 others(84): Show |
intron_variant | MODIFIER | c.215-4837_215-4836d others(4): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48582387 | |||||
| chr19:48582453
|
C | T | 86 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(83): Show | 87 | HG00099.hp2 HG00140.hp2 HG00733.hp1 others(84): Show |
intron_variant | MODIFIER | c.215-4776C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48582453 | ||||||
| chr19:48582476
|
A | T | 86 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(83): Show | 87 | HG00099.hp2 HG00140.hp2 HG00733.hp1 others(84): Show |
intron_variant | MODIFIER | c.215-4753A>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48582476 | ||||||
| chr19:48582583
|
A | C | 86 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(83): Show | 87 | HG00099.hp2 HG00140.hp2 HG00733.hp1 others(84): Show |
intron_variant | MODIFIER | c.215-4646A>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48582583 | ||||||
| chr19:48582642
|
A | G | 86 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(83): Show | 87 | HG00099.hp2 HG00140.hp2 HG00733.hp1 others(84): Show |
intron_variant | MODIFIER | c.215-4587A>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48582642 | ||||||
| chr19:48582654
|
A | C | 86 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(83): Show | 87 | HG00099.hp2 HG00140.hp2 HG00733.hp1 others(84): Show |
intron_variant | MODIFIER | c.215-4575A>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48582654 | ||||||
| chr19:48582677
|
T | C | 86 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(83): Show | 87 | HG00099.hp2 HG00140.hp2 HG00733.hp1 others(84): Show |
intron_variant | MODIFIER | c.215-4552T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48582677 | ||||||
| chr19:48582711
|
T | C | 86 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(83): Show | 87 | HG00099.hp2 HG00140.hp2 HG00733.hp1 others(84): Show |
intron_variant | MODIFIER | c.215-4518T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48582711 | ||||||
| chr19:48582712
|
G | A | 86 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(83): Show | 87 | HG00099.hp2 HG00140.hp2 HG00733.hp1 others(84): Show |
intron_variant | MODIFIER | c.215-4517G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48582712 | ||||||
| chr19:48582736
|
G | A | 106 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0026others(103): Show | 106 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(103): Show |
intron_variant | MODIFIER | c.215-4493G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48582736 | ||||||
| chr19:48582779
|
G | A | 1 | a0001c0004t0001g0223 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.215-4450G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48582779 | ||||||
| chr19:48582797
|
C | T | 1 | a0001c0004t0001g0133 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.215-4432C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48582797 | ||||||
| chr19:48582798
|
G | A | 85 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(82): Show | 86 | HG00099.hp2 HG00140.hp2 HG00733.hp1 others(83): Show |
intron_variant | MODIFIER | c.215-4431G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48582798 | ||||||
| chr19:48582869
|
G | T | 2 | a0001c0001t0001g0186a0001c0001t0001g0306 | 2 | HG01074.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.215-4360G>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48582869 | ||||||
| chr19:48582881
|
G | A | 1 | a0001c0001t0001g0116 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.215-4348G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48582881 | ||||||
| chr19:48582961
|
T | A | 86 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(83): Show | 87 | HG00099.hp2 HG00140.hp2 HG00733.hp1 others(84): Show |
intron_variant | MODIFIER | c.215-4268T>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48582961 | ||||||
| chr19:48582979
|
C | T | 3 | a0001c0002t0001g0076a0001c0002t0001g0328a0001c0004t0001g0133 | 3 | HG01361.hp2 NA18943.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.215-4250C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48582979 | ||||||
| chr19:48582989
|
C | CA | 108 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0026others(105): Show | 108 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(105): Show |
intron_variant | MODIFIER | c.215-4228dupA | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48582989 | |||||
| chr19:48582989
|
C | CAAA | 48 | a0001c0001t0001g0014a0001c0001t0001g0021a0001c0001t0001g0042others(45): Show | 49 | HG00099.hp2 HG00140.hp2 HG00741.hp2 others(46): Show |
intron_variant | MODIFIER | c.215-4230_215-4228d others(5): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48582989 | |||||
| chr19:48582989
|
C | CAAAA | 38 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(35): Show | 38 | HG00733.hp1 HG00738.hp1 HG01167.hp1 others(35): Show |
intron_variant | MODIFIER | c.215-4231_215-4228d others(6): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48582989 | |||||
| chr19:48583017
|
C | CGTGCGTG others(700): Show |
3 | a0001c0001t0001g0031a0001c0001t0001g0066a0001c0001t0001g0367 | 3 | HG01891.hp2 HG02451.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.215-4208_215-4207i others(709): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48583017 | |||||
| chr19:48583017
|
C | CGTGCGTG others(681): Show |
3 | a0001c0001t0001g0014a0001c0010t0001g0091a0001c0010t0001g0369 | 3 | HG03041.hp1 NA19043.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.215-4208_215-4207i others(690): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48583017 | |||||
| chr19:48583017
|
C | CGTGCGTG others(695): Show |
79 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(76): Show | 80 | HG00099.hp2 HG00140.hp2 HG00733.hp1 others(77): Show |
intron_variant | MODIFIER | c.215-4208_215-4207i others(704): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48583017 | |||||
| chr19:48583031
|
G | A | 85 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(82): Show | 86 | HG00099.hp2 HG00140.hp2 HG00733.hp1 others(83): Show |
intron_variant | MODIFIER | c.215-4198G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48583031 | ||||||
| chr19:48583031
|
G | GTCCCAGC others(695): Show |
1 | a0001c0006t0001g0090 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.215-4174_215-4173i others(704): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48583031 | |||||
| chr19:48583046
|
G | A | 7 | a0001c0001t0001g0237a0001c0003t0001g0129a0001c0003t0001g0224others(4): Show | 7 | HG01168.hp1 HG01928.hp2 HG01934.hp2 others(4): Show |
intron_variant | MODIFIER | c.215-4183G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48583046 | ||||||
| chr19:48583108
|
T | G | 86 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(83): Show | 87 | HG00099.hp2 HG00140.hp2 HG00733.hp1 others(84): Show |
intron_variant | MODIFIER | c.215-4121T>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48583108 | ||||||
| chr19:48583176
|
C | CAGAAT | 86 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(83): Show | 87 | HG00099.hp2 HG00140.hp2 HG00733.hp1 others(84): Show |
intron_variant | MODIFIER | c.215-4049_215-4048i others(7): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48583176 | |||||
| chr19:48583540
|
G | A | 85 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(82): Show | 86 | HG00099.hp2 HG00140.hp2 HG00733.hp1 others(83): Show |
intron_variant | MODIFIER | c.215-3689G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48583540 | ||||||
| chr19:48583588
|
C | G | 1 | a0008c0015t0001g0352 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.215-3641C>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48583588 | ||||||
| chr19:48583589
|
G | C | 1 | a0008c0015t0001g0352 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.215-3640G>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48583589 | ||||||
| chr19:48583670
|
T | A | 1 | a0001c0004t0001g0184 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.215-3559T>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48583670 | ||||||
| chr19:48583689
|
G | A | 6 | a0001c0005t0001g0019a0001c0005t0001g0209a0001c0005t0001g0213others(3): Show | 6 | HG01192.hp1 HG01261.hp2 HG02735.hp2 others(3): Show |
intron_variant | MODIFIER | c.215-3540G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48583689 | ||||||
| chr19:48583690
|
C | G | 1 | a0001c0001t0001g0117 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.215-3539C>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48583690 | ||||||
| chr19:48583691
|
G | C | 1 | a0001c0001t0001g0117 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.215-3538G>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48583691 | ||||||
| chr19:48583737
|
G | C | 1 | a0001c0001t0001g0066 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.215-3492G>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48583737 | ||||||
| chr19:48583738
|
A | G | 1 | a0001c0004t0001g0184 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.215-3491A>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48583738 | ||||||
| chr19:48583740
|
C | A | 1 | a0001c0004t0001g0184 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.215-3489C>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48583740 | ||||||
| chr19:48583807
|
G | C | 3 | a0001c0001t0001g0210a0001c0001t0001g0346a0001c0001t0001g0355 | 3 | HG02071.hp2 NA18966.hp2 NA18967.hp2 |
intron_variant | MODIFIER | c.215-3422G>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48583807 | ||||||
| chr19:48583814
|
TCAAA | T | 82 | a0001c0001t0001g0080a0001c0001t0001g0097a0001c0001t0001g0117others(79): Show | 82 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.215-3402_215-3399d others(6): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48583814 | |||||
| chr19:48583830
|
A | G | 1 | a0001c0007t0001g0033 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.215-3399A>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48583830 | ||||||
| chr19:48583844
|
T | A | 1 | a0008c0015t0001g0352 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.215-3385T>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48583844 | ||||||
| chr19:48583940
|
T | C | 85 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(82): Show | 86 | HG00099.hp2 HG00140.hp2 HG00733.hp1 others(83): Show |
intron_variant | MODIFIER | c.215-3289T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48583940 | ||||||
| chr19:48584035
|
C | T | 85 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(82): Show | 86 | HG00099.hp2 HG00140.hp2 HG00733.hp1 others(83): Show |
intron_variant | MODIFIER | c.215-3194C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48584035 | ||||||
| chr19:48584277
|
G | A | 8 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0026others(5): Show | 8 | HG02055.hp2 HG02572.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.215-2952G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48584277 | ||||||
| chr19:48584313
|
A | T | 3 | a0001c0001t0001g0365a0001c0001t0001g0366a0001c0001t0001g0368 | 3 | HG01884.hp2 HG03225.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.215-2916A>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48584313 | ||||||
| chr19:48584314
|
C | A | 1 | a0001c0001t0001g0117 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.215-2915C>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48584314 | ||||||
| chr19:48584315
|
A | C | 1 | a0001c0001t0001g0117 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.215-2914A>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48584315 | ||||||
| chr19:48584316
|
G | A | 1 | a0001c0001t0001g0117 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.215-2913G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48584316 | ||||||
| chr19:48584373
|
T | A | 1 | a0001c0001t0001g0282 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.215-2856T>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48584373 | ||||||
| chr19:48584410
|
T | C | 316 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(313): Show | 317 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(314): Show |
intron_variant | MODIFIER | c.215-2819T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48584410 | ||||||
| chr19:48584499
|
G | A | 5 | a0001c0001t0001g0042a0001c0001t0001g0073a0001c0001t0001g0074others(2): Show | 5 | HG03098.hp1 HG03130.hp2 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.215-2730G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48584499 | ||||||
| chr19:48584527
|
T | C | 1 | a0001c0005t0001g0197 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.215-2702T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48584527 | ||||||
| chr19:48584532
|
CA | C | 88 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(85): Show | 89 | HG00099.hp2 HG00140.hp2 HG00733.hp1 others(86): Show |
intron_variant | MODIFIER | c.215-2692delA | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48584532 | |||||
| chr19:48584541
|
C | G | 88 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(85): Show | 89 | HG00099.hp2 HG00140.hp2 HG00733.hp1 others(86): Show |
intron_variant | MODIFIER | c.215-2688C>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48584541 | ||||||
| chr19:48584638
|
C | T | 3 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0130 | 3 | HG02647.hp1 HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.215-2591C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48584638 | ||||||
| chr19:48584685
|
G | T | 1 | a0005c0021t0001g0307 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.215-2544G>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48584685 | ||||||
| chr19:48584789
|
G | A | 2 | a0001c0006t0001g0061a0001c0007t0001g0057 | 2 | HG02145.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.215-2440G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48584789 | ||||||
| chr19:48584808
|
T | C | 110 | a0001c0001t0001g0036a0001c0001t0001g0087a0001c0001t0001g0088others(107): Show | 110 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(107): Show |
intron_variant | MODIFIER | c.215-2421T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48584808 | ||||||
| chr19:48584827
|
G | T | 2 | a0001c0002t0001g0049a0001c0002t0001g0050 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.215-2402G>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48584827 | ||||||
| chr19:48584911
|
C | T | 107 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0026others(104): Show | 107 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(104): Show |
intron_variant | MODIFIER | c.215-2318C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48584911 | ||||||
| chr19:48584912
|
G | A | 6 | a0001c0001t0001g0310a0001c0001t0001g0311a0001c0002t0001g0149others(3): Show | 6 | HG00621.hp1 HG02165.hp1 HG03017.hp2 others(3): Show |
intron_variant | MODIFIER | c.215-2317G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48584912 | ||||||
| chr19:48584959
|
G | A | 1 | a0001c0001t0001g0326 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.215-2270G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48584959 | ||||||
| chr19:48585048
|
C | CA | 146 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(143): Show | 146 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(143): Show |
intron_variant | MODIFIER | c.215-2157dupA | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48585048 | |||||
| chr19:48585048
|
C | CAA | 39 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0026others(36): Show | 40 | HG00140.hp2 HG00597.hp1 HG01081.hp1 others(37): Show |
intron_variant | MODIFIER | c.215-2158_215-2157d others(4): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48585048 | |||||
| chr19:48585048
|
C | CAAA | 17 | a0001c0001t0001g0042a0001c0001t0001g0073a0001c0001t0001g0074others(14): Show | 17 | HG00741.hp2 HG01106.hp1 HG01175.hp2 others(14): Show |
intron_variant | MODIFIER | c.215-2159_215-2157d others(5): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48585048 | |||||
| chr19:48585048
|
CA | C | 70 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0106others(67): Show | 70 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(67): Show |
intron_variant | MODIFIER | c.215-2157delA | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48585048 | |||||
| chr19:48585048
|
CAA | C | 36 | a0001c0001t0001g0036a0001c0001t0001g0171a0001c0001t0001g0199others(33): Show | 36 | HG00621.hp1 HG00639.hp2 HG00642.hp1 others(33): Show |
intron_variant | MODIFIER | c.215-2158_215-2157d others(4): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48585048 | |||||
| chr19:48585073
|
G | A | 1 | a0001c0001t0001g0117 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.215-2156G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48585073 | ||||||
| chr19:48585074
|
C | G | 1 | a0001c0001t0001g0117 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.215-2155C>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48585074 | ||||||
| chr19:48585096
|
C | T | 1 | a0001c0003t0001g0046 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.215-2133C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48585096 | ||||||
| chr19:48585142
|
G | C | 4 | a0001c0001t0001g0007a0001c0001t0001g0055a0001c0001t0001g0101others(1): Show | 4 | HG01167.hp1 HG01169.hp1 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.215-2087G>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48585142 | ||||||
| chr19:48585142
|
G | T | 14 | a0001c0001t0001g0117a0001c0001t0001g0151a0001c0001t0001g0273others(11): Show | 14 | HG00423.hp2 HG02040.hp1 NA18949.hp1 others(11): Show |
intron_variant | MODIFIER | c.215-2087G>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48585142 | ||||||
| chr19:48585389
|
C | T | 3 | a0001c0002t0001g0022a0001c0002t0001g0358a0001c0002t0001g0359 | 3 | HG01168.hp2 HG01169.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.215-1840C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48585389 | ||||||
| chr19:48585433
|
T | C | 46 | a0001c0001t0001g0014a0001c0001t0001g0021a0001c0001t0001g0032others(43): Show | 47 | HG00099.hp2 HG00140.hp2 HG00741.hp2 others(44): Show |
intron_variant | MODIFIER | c.215-1796T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48585433 | ||||||
| chr19:48585624
|
G | C | 1 | a0001c0001t0001g0117 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.215-1605G>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48585624 | ||||||
| chr19:48585665
|
G | A | 38 | a0001c0001t0001g0014a0001c0001t0001g0021a0001c0001t0001g0032others(35): Show | 39 | HG00099.hp2 HG00140.hp2 HG00741.hp2 others(36): Show |
intron_variant | MODIFIER | c.215-1564G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48585665 | ||||||
| chr19:48585684
|
T | G | 45 | a0001c0001t0001g0014a0001c0001t0001g0021a0001c0001t0001g0032others(42): Show | 46 | HG00099.hp2 HG00140.hp2 HG00741.hp2 others(43): Show |
intron_variant | MODIFIER | c.215-1545T>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48585684 | ||||||
| chr19:48585691
|
A | AG | 22 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0017others(19): Show | 22 | HG02055.hp1 HG02071.hp2 HG02165.hp2 others(19): Show |
intron_variant | MODIFIER | c.215-1532dupG | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48585691 | |||||
| chr19:48585735
|
T | C | 128 | a0001c0001t0001g0014a0001c0001t0001g0021a0001c0001t0001g0032others(125): Show | 129 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(126): Show |
intron_variant | MODIFIER | c.215-1494T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48585735 | ||||||
| chr19:48585817
|
C | T | 1 | a0001c0004t0001g0278 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.215-1412C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48585817 | ||||||
| chr19:48585829
|
TA | T | 5 | a0001c0001t0001g0042a0001c0001t0001g0073a0001c0001t0001g0074others(2): Show | 5 | HG03098.hp1 HG03130.hp2 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.215-1393delA | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48585829 | |||||
| chr19:48585947
|
G | A | 2 | a0001c0005t0001g0071a0001c0006t0001g0020 | 2 | HG00140.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.215-1282G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48585947 | ||||||
| chr19:48585948
|
G | A | 100 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0026others(97): Show | 100 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(97): Show |
intron_variant | MODIFIER | c.215-1281G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48585948 | ||||||
| chr19:48585975
|
G | A | 1 | a0001c0006t0001g0044 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.215-1254G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48585975 | ||||||
| chr19:48586052
|
T | A | 305 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(302): Show | 306 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(303): Show |
intron_variant | MODIFIER | c.215-1177T>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48586052 | ||||||
| chr19:48586061
|
A | G | 1 | a0001c0006t0001g0028 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.215-1168A>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48586061 | ||||||
| chr19:48586120
|
G | T | 2 | a0001c0001t0001g0027a0001c0002t0001g0160 | 2 | NA19043.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.215-1109G>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48586120 | ||||||
| chr19:48586229
|
A | G | 5 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0367others(2): Show | 5 | HG01891.hp2 HG02486.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.215-1000A>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48586229 | ||||||
| chr19:48586269
|
C | G | 1 | a0001c0001t0001g0027 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.215-960C>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48586269 | ||||||
| chr19:48586307
|
T | G | 56 | a0001c0001t0001g0014a0001c0001t0001g0021a0001c0001t0001g0031others(53): Show | 57 | HG00099.hp2 HG00140.hp2 HG00738.hp1 others(54): Show |
intron_variant | MODIFIER | c.215-922T>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48586307 | ||||||
| chr19:48586330
|
C | A | 1 | a0001c0007t0001g0166 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.215-899C>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48586330 | ||||||
| chr19:48586348
|
G | T | 5 | a0001c0005t0001g0008a0001c0005t0001g0009a0001c0005t0001g0010others(2): Show | 5 | HG01884.hp1 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.215-881G>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48586348 | ||||||
| chr19:48586364
|
C | T | 1 | a0001c0006t0001g0094 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.215-865C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48586364 | ||||||
| chr19:48586454
|
A | G | 56 | a0001c0001t0001g0014a0001c0001t0001g0021a0001c0001t0001g0031others(53): Show | 57 | HG00099.hp2 HG00140.hp2 HG00738.hp1 others(54): Show |
intron_variant | MODIFIER | c.215-775A>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48586454 | ||||||
| chr19:48586538
|
T | C | 311 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(308): Show | 312 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(309): Show |
intron_variant | MODIFIER | c.215-691T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48586538 | ||||||
| chr19:48586640
|
T | G | 1 | a0001c0004t0001g0133 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.215-589T>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48586640 | ||||||
| chr19:48586672
|
C | T | 1 | a0001c0004t0001g0089 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.215-557C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48586672 | ||||||
| chr19:48586675
|
C | G | 56 | a0001c0001t0001g0014a0001c0001t0001g0021a0001c0001t0001g0031others(53): Show | 57 | HG00099.hp2 HG00140.hp2 HG00738.hp1 others(54): Show |
intron_variant | MODIFIER | c.215-554C>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48586675 | ||||||
| chr19:48586908
|
C | T | 56 | a0001c0001t0001g0014a0001c0001t0001g0021a0001c0001t0001g0031others(53): Show | 57 | HG00099.hp2 HG00140.hp2 HG00738.hp1 others(54): Show |
intron_variant | MODIFIER | c.215-321C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48586908 | ||||||
| chr19:48586967
|
A | G | 50 | a0001c0001t0001g0014a0001c0001t0001g0021a0001c0001t0001g0031others(47): Show | 51 | HG00099.hp2 HG00140.hp2 HG00741.hp2 others(48): Show |
intron_variant | MODIFIER | c.215-262A>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48586967 | ||||||
| chr19:48586996
|
G | C | 50 | a0001c0001t0001g0014a0001c0001t0001g0021a0001c0001t0001g0031others(47): Show | 51 | HG00099.hp2 HG00140.hp2 HG00741.hp2 others(48): Show |
intron_variant | MODIFIER | c.215-233G>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48586996 | ||||||
| chr19:48587041
|
G | A | 4 | a0001c0001t0001g0007a0001c0001t0001g0055a0001c0001t0001g0101others(1): Show | 4 | HG01167.hp1 HG01169.hp1 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.215-188G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48587041 | ||||||
| chr19:48587049
|
T | C | 50 | a0001c0001t0001g0014a0001c0001t0001g0021a0001c0001t0001g0031others(47): Show | 51 | HG00099.hp2 HG00140.hp2 HG00741.hp2 others(48): Show |
intron_variant | MODIFIER | c.215-180T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48587049 | ||||||
| chr19:48587085
|
G | C | 50 | a0001c0001t0001g0014a0001c0001t0001g0021a0001c0001t0001g0031others(47): Show | 51 | HG00099.hp2 HG00140.hp2 HG00741.hp2 others(48): Show |
intron_variant | MODIFIER | c.215-144G>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48587085 | ||||||
| chr19:48587091
|
A | G | 50 | a0001c0001t0001g0014a0001c0001t0001g0021a0001c0001t0001g0031others(47): Show | 51 | HG00099.hp2 HG00140.hp2 HG00741.hp2 others(48): Show |
intron_variant | MODIFIER | c.215-138A>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48587091 | ||||||
| chr19:48587111
|
T | TA | 206 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0026others(203): Show | 206 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(203): Show |
intron_variant | MODIFIER | c.215-109dupA | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48587111 | |||||
| chr19:48587111
|
T | TAA | 33 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(30): Show | 33 | HG00733.hp1 HG01167.hp1 HG01169.hp1 others(30): Show |
intron_variant | MODIFIER | c.215-110_215-109dup others(2): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48587111 | |||||
| chr19:48587111
|
TA | T | 50 | a0001c0001t0001g0014a0001c0001t0001g0021a0001c0001t0001g0031others(47): Show | 51 | HG00099.hp2 HG00140.hp2 HG00741.hp2 others(48): Show |
intron_variant | MODIFIER | c.215-109delA | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48587111 | |||||
| chr19:48587118
|
A | AAT | 12 | a0001c0001t0001g0039a0001c0001t0001g0042a0001c0001t0001g0066others(9): Show | 12 | HG00738.hp1 HG02451.hp1 HG02895.hp2 others(9): Show |
intron_variant | MODIFIER | c.215-110_215-109ins others(2): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 48587118 | |||||
| chr19:48587118
|
A | AT | 4 | a0001c0002t0001g0049a0001c0002t0001g0050a0001c0002t0001g0305others(1): Show | 4 | HG00280.hp2 HG01070.hp2 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.215-111_215-110ins others(1): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48587118 | ||||||
| chr19:48587190
|
C | T | 1 | a0001c0001t0001g0241 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.215-39C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48587190 | ||||||
| chr19:48587191
|
T | C | 1 | a0001c0001t0001g0241 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.215-38T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 2/6 | chr19 | 48587191 | ||||||
| chr19:48587474
|
G | A | 1 | a0001c0004t0001g0184 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.423+37G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 3/6 | chr19 | 48587474 | ||||||
| chr19:48587552
|
T | A | 52 | a0001c0001t0001g0014a0001c0001t0001g0021a0001c0001t0001g0031others(49): Show | 53 | HG00099.hp2 HG00140.hp2 HG00741.hp2 others(50): Show |
intron_variant | MODIFIER | c.423+115T>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 3/6 | chr19 | 48587552 | ||||||
| chr19:48587725
|
T | C | 150 | a0001c0001t0001g0014a0001c0001t0001g0021a0001c0001t0001g0024others(147): Show | 151 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(148): Show |
intron_variant | MODIFIER | c.423+288T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 3/6 | chr19 | 48587725 | ||||||
| chr19:48587754
|
G | A | 41 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(38): Show | 41 | HG00733.hp1 HG00738.hp1 HG01167.hp1 others(38): Show |
intron_variant | MODIFIER | c.423+317G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 3/6 | chr19 | 48587754 | ||||||
| chr19:48587890
|
CA | C | 31 | a0001c0001t0001g0060a0001c0001t0001g0104a0001c0001t0001g0126others(28): Show | 31 | HG00733.hp2 HG01168.hp1 HG01928.hp2 others(28): Show |
intron_variant | MODIFIER | c.423+486delA | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 48587890 | |||||
| chr19:48587890
|
CAA | C | 17 | a0001c0001t0001g0070a0001c0001t0001g0116a0001c0001t0001g0153others(14): Show | 17 | HG00408.hp1 HG00609.hp2 HG01123.hp1 others(14): Show |
intron_variant | MODIFIER | c.423+485_423+486del others(2): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 48587890 | |||||
| chr19:48587890
|
CAAA | C | 11 | a0001c0001t0001g0039a0001c0001t0001g0054a0001c0001t0001g0075others(8): Show | 11 | HG00733.hp1 HG00738.hp1 HG02015.hp2 others(8): Show |
intron_variant | MODIFIER | c.423+484_423+486del others(3): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 48587890 | |||||
| chr19:48587890
|
CAAAA | C | 29 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(26): Show | 29 | HG01167.hp1 HG01169.hp1 HG01433.hp1 others(26): Show |
intron_variant | MODIFIER | c.423+483_423+486del others(4): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 48587890 | |||||
| chr19:48587890
|
CAAAAA | C | 23 | a0001c0001t0001g0087a0001c0001t0001g0092a0001c0001t0001g0140others(20): Show | 23 | HG00558.hp2 HG00621.hp2 HG00735.hp1 others(20): Show |
intron_variant | MODIFIER | c.423+482_423+486del others(5): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 48587890 | |||||
| chr19:48587890
|
CAAAAAA | C | 109 | a0001c0001t0001g0088a0001c0001t0001g0106a0001c0001t0001g0107others(106): Show | 109 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.423+481_423+486del others(6): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 48587890 | |||||
| chr19:48587890
|
CAAAAAAA | C | 88 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0026others(85): Show | 88 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.423+480_423+486del others(7): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 48587890 | |||||
| chr19:48587890
|
CAAAAAAA others(1): Show |
C | 32 | a0001c0001t0001g0014a0001c0001t0001g0021a0001c0001t0001g0032others(29): Show | 32 | HG00741.hp2 HG01081.hp1 HG01175.hp2 others(29): Show |
intron_variant | MODIFIER | c.423+479_423+486del others(8): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 48587890 | |||||
| chr19:48587890
|
CAAAAAAA others(2): Show |
C | 15 | a0001c0005t0001g0001a0001c0005t0001g0071a0001c0005t0001g0113others(12): Show | 16 | HG00099.hp2 HG00140.hp2 HG01099.hp1 others(13): Show |
intron_variant | MODIFIER | c.423+478_423+486del others(9): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 48587890 | |||||
| chr19:48587890
|
CAAAAAAA others(4): Show |
C | 4 | a0001c0001t0001g0023a0001c0001t0001g0051a0001c0001t0001g0053others(1): Show | 4 | HG02257.hp1 HG02717.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.423+476_423+486del others(11): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 48587890 | |||||
| chr19:48587890
|
CAAAAAAA others(7): Show |
C | 1 | a0001c0003t0001g0078 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.423+473_423+486del others(14): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 48587890 | |||||
| chr19:48587890
|
CAAAAAAA others(12): Show |
C | 1 | a0001c0004t0001g0052 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.423+468_423+486del others(19): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 48587890 | |||||
| chr19:48588017
|
T | C | 307 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(304): Show | 308 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(305): Show |
intron_variant | MODIFIER | c.423+580T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 3/6 | chr19 | 48588017 | ||||||
| chr19:48588096
|
G | C | 1 | a0001c0004t0001g0184 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.423+659G>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 3/6 | chr19 | 48588096 | ||||||
| chr19:48588209
|
C | CA | 48 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0025others(45): Show | 49 | HG00099.hp2 HG00140.hp2 HG00733.hp2 others(46): Show |
intron_variant | MODIFIER | c.423+789dupA | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 48588209 | |||||
| chr19:48588209
|
C | CAA | 13 | a0001c0001t0001g0021a0001c0001t0001g0258a0001c0001t0001g0361others(10): Show | 13 | HG01884.hp2 HG02257.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.423+788_423+789dup others(2): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 48588209 | |||||
| chr19:48588209
|
C | CAAAAA | 6 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0367others(3): Show | 6 | HG01891.hp2 HG02258.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.423+785_423+789dup others(5): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 48588209 | |||||
| chr19:48588209
|
CA | C | 132 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(129): Show | 132 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(129): Show |
intron_variant | MODIFIER | c.423+789delA | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 48588209 | |||||
| chr19:48588238
|
C | T | 3 | a0001c0001t0001g0092a0001c0001t0001g0363a0001c0002t0001g0093 | 3 | HG01243.hp1 HG02630.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.423+801C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 3/6 | chr19 | 48588238 | ||||||
| chr19:48588250
|
C | G | 1 | a0001c0001t0001g0361 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.423+813C>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 3/6 | chr19 | 48588250 | ||||||
| chr19:48588258
|
C | A | 14 | a0001c0001t0001g0023a0001c0001t0001g0031a0001c0001t0001g0032others(11): Show | 14 | HG01891.hp2 HG02257.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.423+821C>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 3/6 | chr19 | 48588258 | ||||||
| chr19:48588487
|
G | A | 20 | a0001c0001t0001g0023a0001c0001t0001g0031a0001c0001t0001g0032others(17): Show | 20 | HG01346.hp2 HG01891.hp2 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.423+1050G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 3/6 | chr19 | 48588487 | ||||||
| chr19:48588490
|
CA | C | 20 | a0001c0001t0001g0023a0001c0001t0001g0031a0001c0001t0001g0032others(17): Show | 20 | HG01346.hp2 HG01891.hp2 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.423+1055delA | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 48588490 | |||||
| chr19:48588496
|
A | G | 36 | a0001c0001t0001g0014a0001c0001t0001g0023a0001c0001t0001g0024others(33): Show | 36 | HG01243.hp1 HG01346.hp2 HG01891.hp2 others(33): Show |
intron_variant | MODIFIER | c.423+1059A>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 3/6 | chr19 | 48588496 | ||||||
| chr19:48588500
|
A | G | 36 | a0001c0001t0001g0014a0001c0001t0001g0023a0001c0001t0001g0024others(33): Show | 36 | HG01243.hp1 HG01346.hp2 HG01891.hp2 others(33): Show |
intron_variant | MODIFIER | c.423+1063A>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 3/6 | chr19 | 48588500 | ||||||
| chr19:48588507
|
C | T | 4 | a0001c0001t0001g0101a0001c0001t0001g0175a0001c0001t0001g0364others(1): Show | 4 | HG01167.hp1 HG01169.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.423+1070C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 3/6 | chr19 | 48588507 | ||||||
| chr19:48588512
|
C | CA | 9 | a0001c0001t0001g0153a0001c0001t0001g0167a0001c0002t0001g0301others(6): Show | 9 | HG00438.hp2 HG01192.hp1 HG01358.hp2 others(6): Show |
intron_variant | MODIFIER | c.423+1085dupA | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 48588512 | |||||
| chr19:48588512
|
CA | C | 17 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0025others(14): Show | 17 | HG01243.hp1 HG02055.hp2 HG02572.hp1 others(14): Show |
intron_variant | MODIFIER | c.423+1085delA | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 48588512 | |||||
| chr19:48588523
|
C | A | 20 | a0001c0001t0001g0021a0001c0001t0001g0258a0001c0001t0001g0361others(17): Show | 20 | HG00642.hp1 HG01070.hp2 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.423+1086C>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 3/6 | chr19 | 48588523 | ||||||
| chr19:48588526
|
CCATAT | C | 20 | a0001c0001t0001g0023a0001c0001t0001g0031a0001c0001t0001g0032others(17): Show | 20 | HG01346.hp2 HG01891.hp2 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.423+1090_423+1094d others(7): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 3/6 | chr19 | 48588526 | ||||||
| chr19:48588595
|
A | G | 4 | a0001c0001t0001g0310a0001c0001t0001g0311a0001c0002t0001g0208others(1): Show | 4 | HG00621.hp1 HG02165.hp1 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.423+1158A>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 3/6 | chr19 | 48588595 | ||||||
| chr19:48588605
|
C | T | 35 | a0001c0001t0001g0014a0001c0001t0001g0023a0001c0001t0001g0024others(32): Show | 35 | HG01243.hp1 HG01346.hp2 HG01891.hp2 others(32): Show |
intron_variant | MODIFIER | c.423+1168C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 3/6 | chr19 | 48588605 | ||||||
| chr19:48588607
|
TATA | T | 4 | a0001c0001t0001g0364a0001c0002t0001g0160a0001c0003t0001g0046others(1): Show | 4 | HG03139.hp2 HG03195.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.423+1175_423+1177d others(5): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 48588607 | |||||
| chr19:48588621
|
G | A | 373 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(370): Show | 374 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(371): Show |
intron_variant | MODIFIER | c.423+1184G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 3/6 | chr19 | 48588621 | ||||||
| chr19:48588637
|
C | T | 19 | a0001c0001t0001g0023a0001c0001t0001g0031a0001c0001t0001g0042others(16): Show | 19 | HG01346.hp2 HG01891.hp2 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.423+1200C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 3/6 | chr19 | 48588637 | ||||||
| chr19:48588672
|
G | A | 2 | a0001c0001t0001g0362a0001c0007t0001g0033 | 2 | HG01346.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.423+1235G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 3/6 | chr19 | 48588672 | ||||||
| chr19:48588683
|
G | A | 3 | a0001c0001t0001g0364a0001c0003t0001g0046a0001c0004t0001g0052 | 3 | HG03139.hp2 HG03195.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.423+1246G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 3/6 | chr19 | 48588683 | ||||||
| chr19:48588855
|
G | A | 91 | a0001c0001t0001g0070a0001c0001t0001g0080a0001c0001t0001g0097others(88): Show | 91 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(88): Show |
intron_variant | MODIFIER | c.423+1418G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 3/6 | chr19 | 48588855 | ||||||
| chr19:48588885
|
A | G | 6 | a0001c0001t0001g0042a0001c0001t0001g0073a0001c0001t0001g0074others(3): Show | 6 | HG02486.hp2 HG03098.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.423+1448A>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 3/6 | chr19 | 48588885 | ||||||
| chr19:48588977
|
C | A | 128 | a0001c0001t0001g0032a0001c0001t0001g0036a0001c0001t0001g0042others(125): Show | 128 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(125): Show |
intron_variant | MODIFIER | c.423+1540C>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 3/6 | chr19 | 48588977 | ||||||
| chr19:48589173
|
A | G | 241 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(238): Show | 242 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(239): Show |
intron_variant | MODIFIER | c.423+1736A>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 3/6 | chr19 | 48589173 | ||||||
| chr19:48589234
|
T | C | 39 | a0001c0001t0001g0051a0001c0001t0001g0054a0001c0001t0001g0066others(36): Show | 39 | HG00438.hp1 HG00735.hp2 HG00738.hp1 others(36): Show |
intron_variant | MODIFIER | c.423+1797T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 3/6 | chr19 | 48589234 | ||||||
| chr19:48589268
|
A | C | 3 | a0001c0001t0001g0060a0001c0001t0001g0092a0001c0004t0001g0058 | 3 | HG01243.hp1 HG02809.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.423+1831A>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 3/6 | chr19 | 48589268 | ||||||
| chr19:48589280
|
A | C | 1 | a0001c0001t0001g0032 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.423+1843A>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 3/6 | chr19 | 48589280 | ||||||
| chr19:48589294
|
G | A | 224 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(221): Show | 225 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(222): Show |
intron_variant | MODIFIER | c.423+1857G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 3/6 | chr19 | 48589294 | ||||||
| chr19:48589319
|
G | A | 1 | a0001c0010t0001g0037 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.423+1882G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 3/6 | chr19 | 48589319 | ||||||
| chr19:48589322
|
G | A | 1 | a0001c0002t0001g0275 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.423+1885G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 3/6 | chr19 | 48589322 | ||||||
| chr19:48589370
|
A | T | 46 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(43): Show | 47 | HG00597.hp2 HG00639.hp1 HG01074.hp2 others(44): Show |
intron_variant | MODIFIER | c.423+1933A>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 3/6 | chr19 | 48589370 | ||||||
| chr19:48589644
|
A | G | 8 | a0001c0001t0001g0024a0001c0001t0001g0042a0001c0001t0001g0074others(5): Show | 8 | HG01346.hp2 HG02486.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.424-1965A>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 3/6 | chr19 | 48589644 | ||||||
| chr19:48589855
|
G | A | 1 | a0002c0013t0001g0285 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.424-1754G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 3/6 | chr19 | 48589855 | ||||||
| chr19:48589868
|
G | A | 1 | a0001c0004t0001g0184 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.424-1741G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 3/6 | chr19 | 48589868 | ||||||
| chr19:48589978
|
C | CTTTATTT | 4 | a0001c0001t0001g0032a0001c0001t0001g0039a0001c0001t0001g0040others(1): Show | 4 | HG02615.hp2 HG02647.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.424-1628_424-1627i others(9): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 48589978 | |||||
| chr19:48590136
|
C | T | 211 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0021others(208): Show | 211 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(208): Show |
intron_variant | MODIFIER | c.424-1473C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 3/6 | chr19 | 48590136 | ||||||
| chr19:48590367
|
C | T | 48 | a0001c0001t0001g0070a0001c0001t0001g0087a0001c0001t0001g0104others(45): Show | 48 | HG00408.hp1 HG00597.hp1 HG00642.hp2 others(45): Show |
intron_variant | MODIFIER | c.424-1242C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 3/6 | chr19 | 48590367 | ||||||
| chr19:48590368
|
G | A | 3 | a0001c0001t0001g0246a0001c0001t0001g0258a0001c0001t0001g0364 | 3 | HG02630.hp1 HG02818.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.424-1241G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 3/6 | chr19 | 48590368 | ||||||
| chr19:48590394
|
G | T | 57 | a0001c0001t0001g0041a0001c0004t0001g0005a0001c0004t0001g0015others(54): Show | 57 | HG00280.hp1 HG00558.hp1 HG00597.hp2 others(54): Show |
intron_variant | MODIFIER | c.424-1215G>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 3/6 | chr19 | 48590394 | ||||||
| chr19:48590590
|
A | G | 7 | a0001c0001t0001g0023a0001c0001t0001g0051a0001c0001t0001g0053others(4): Show | 7 | HG02145.hp1 HG02257.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.424-1019A>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 3/6 | chr19 | 48590590 | ||||||
| chr19:48590838
|
GTTTA | G | 27 | a0001c0001t0001g0024a0001c0001t0001g0031a0001c0001t0001g0032others(24): Show | 27 | HG00558.hp2 HG01074.hp1 HG01257.hp1 others(24): Show |
intron_variant | MODIFIER | c.424-767_424-764del others(4): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 48590838 | |||||
| chr19:48590887
|
G | A | 1 | a0001c0001t0001g0066 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.424-722G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 3/6 | chr19 | 48590887 | ||||||
| chr19:48590918
|
C | T | 1 | a0001c0006t0001g0006 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.424-691C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 3/6 | chr19 | 48590918 | ||||||
| chr19:48591025
|
G | C | 1 | a0001c0003t0001g0120 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.424-584G>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 3/6 | chr19 | 48591025 | ||||||
| chr19:48591213
|
T | C | 23 | a0001c0001t0001g0024a0001c0001t0001g0031a0001c0001t0001g0032others(20): Show | 23 | HG00558.hp2 HG01074.hp1 HG01358.hp1 others(20): Show |
intron_variant | MODIFIER | c.424-396T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 3/6 | chr19 | 48591213 | ||||||
| chr19:48591513
|
G | A | 3 | a0001c0001t0001g0246a0001c0001t0001g0258a0001c0001t0001g0364 | 3 | HG02630.hp1 HG02818.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.424-96G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 3/6 | chr19 | 48591513 | ||||||
| chr19:48591599
|
C | T | 49 | a0001c0001t0001g0070a0001c0001t0001g0087a0001c0001t0001g0104others(46): Show | 49 | HG00408.hp1 HG00597.hp1 HG00642.hp2 others(46): Show |
intron_variant | MODIFIER | c.424-10C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 3/6 | chr19 | 48591599 | ||||||
| chr19:48591754
|
G | A | 1 | a0001c0001t0001g0066 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.550+19G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 4/6 | chr19 | 48591754 | ||||||
| chr19:48591843
|
G | A | 1 | a0002c0008t0001g0154 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.550+108G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 4/6 | chr19 | 48591843 | ||||||
| chr19:48591885
|
G | GAGA | 331 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(328): Show | 331 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(328): Show |
intron_variant | MODIFIER | c.550+154_550+156dup others(3): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 48591885 | |||||
| chr19:48591918
|
G | A | 2 | a0001c0001t0001g0199a0001c0001t0001g0204 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.550+183G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 4/6 | chr19 | 48591918 | ||||||
| chr19:48592017
|
G | A | 2 | a0001c0002t0001g0156a0001c0005t0001g0255 | 2 | HG01192.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.550+282G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 4/6 | chr19 | 48592017 | ||||||
| chr19:48592021
|
T | C | 316 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0017others(313): Show | 316 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(313): Show |
intron_variant | MODIFIER | c.550+286T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 4/6 | chr19 | 48592021 | ||||||
| chr19:48592109
|
T | C | 1 | a0001c0001t0001g0041 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.550+374T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 4/6 | chr19 | 48592109 | ||||||
| chr19:48592117
|
CCCCGTCT others(8): Show |
C | 1 | a0001c0001t0001g0270 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.550+383_550+397del others(15): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 4/6 | chr19 | 48592117 | ||||||
| chr19:48592162
|
G | A | 1 | a0001c0002t0001g0093 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.550+427G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 4/6 | chr19 | 48592162 | ||||||
| chr19:48592206
|
G | C | 58 | a0001c0004t0001g0005a0001c0004t0001g0015a0001c0004t0001g0016others(55): Show | 58 | HG00280.hp1 HG00558.hp1 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.550+471G>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 4/6 | chr19 | 48592206 | ||||||
| chr19:48592257
|
A | C | 3 | a0001c0001t0001g0246a0001c0001t0001g0258a0001c0001t0001g0364 | 3 | HG02630.hp1 HG02818.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.551-465A>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 4/6 | chr19 | 48592257 | ||||||
| chr19:48592307
|
TAA | T | 16 | a0001c0001t0001g0032a0001c0001t0001g0039a0001c0001t0001g0040others(13): Show | 16 | HG00558.hp2 HG01074.hp1 HG01358.hp1 others(13): Show |
intron_variant | MODIFIER | c.551-411_551-410del others(2): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 48592307 | |||||
| chr19:48592354
|
A | G | 1 | a0001c0001t0001g0041 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.551-368A>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 4/6 | chr19 | 48592354 | ||||||
| chr19:48592383
|
G | A | 8 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0054others(5): Show | 8 | HG01884.hp2 HG02055.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.551-339G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 4/6 | chr19 | 48592383 | ||||||
| chr19:48592388
|
AGGCCCCT | A | 6 | a0001c0001t0001g0146a0001c0001t0001g0190a0001c0001t0001g0191others(3): Show | 6 | NA18945.hp2 NA18957.hp2 NA18967.hp1 others(3): Show |
intron_variant | MODIFIER | c.551-331_551-325del others(7): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 48592388 | |||||
| chr19:48592389
|
GGCCCCTG others(3): Show |
G | 1 | a0001c0002t0001g0048 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.551-332_551-323del others(10): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 4/6 | chr19 | 48592389 | ||||||
| chr19:48592506
|
A | C | 1 | a0001c0002t0001g0131 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.551-216A>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 4/6 | chr19 | 48592506 | ||||||
| chr19:48592507
|
T | A | 1 | a0001c0002t0001g0131 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.551-215T>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 4/6 | chr19 | 48592507 | ||||||
| chr19:48592508
|
A | C | 1 | a0001c0002t0001g0131 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.551-214A>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 4/6 | chr19 | 48592508 | ||||||
| chr19:48592513
|
A | C | 1 | a0001c0002t0001g0131 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.551-209A>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 4/6 | chr19 | 48592513 | ||||||
| chr19:48592514
|
A | G | 1 | a0001c0002t0001g0131 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.551-208A>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 4/6 | chr19 | 48592514 | ||||||
| chr19:48592515
|
G | A | 1 | a0001c0002t0001g0131 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.551-207G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 4/6 | chr19 | 48592515 | ||||||
| chr19:48592516
|
G | C | 1 | a0001c0002t0001g0131 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.551-206G>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 4/6 | chr19 | 48592516 | ||||||
| chr19:48592517
|
C | G | 1 | a0001c0002t0001g0131 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.551-205C>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 4/6 | chr19 | 48592517 | ||||||
| chr19:48592517
|
C | T | 1 | a0001c0001t0001g0167 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.551-205C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 4/6 | chr19 | 48592517 | ||||||
| chr19:48592518
|
C | A | 49 | a0001c0001t0001g0115a0001c0001t0001g0144a0001c0001t0001g0168others(46): Show | 49 | HG00423.hp1 HG00438.hp2 HG00733.hp2 others(46): Show |
intron_variant | MODIFIER | c.551-204C>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 4/6 | chr19 | 48592518 | ||||||
| chr19:48592519
|
C | T | 1 | a0001c0002t0001g0131 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.551-203C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 4/6 | chr19 | 48592519 | ||||||
| chr19:48592520
|
C | G | 1 | a0001c0002t0001g0131 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.551-202C>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 4/6 | chr19 | 48592520 | ||||||
| chr19:48592521
|
C | T | 1 | a0001c0002t0001g0131 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.551-201C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 4/6 | chr19 | 48592521 | ||||||
| chr19:48592522
|
C | T | 1 | a0001c0002t0001g0131 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.551-200C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 4/6 | chr19 | 48592522 | ||||||
| chr19:48592548
|
G | C | 24 | a0001c0001t0001g0024a0001c0001t0001g0031a0001c0001t0001g0032others(21): Show | 24 | HG00558.hp2 HG01074.hp1 HG01358.hp1 others(21): Show |
intron_variant | MODIFIER | c.551-174G>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 4/6 | chr19 | 48592548 | ||||||
| chr19:48592614
|
G | A | 48 | a0001c0001t0001g0115a0001c0001t0001g0144a0001c0001t0001g0168others(45): Show | 48 | HG00423.hp1 HG00438.hp2 HG00733.hp2 others(45): Show |
intron_variant | MODIFIER | c.551-108G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 4/6 | chr19 | 48592614 | ||||||
| chr19:48592641
|
G | A | 15 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0036others(12): Show | 15 | HG01243.hp1 HG01884.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.551-81G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 4/6 | chr19 | 48592641 | ||||||
| chr19:48592651
|
C | T | 5 | a0003c0011t0001g0043a0003c0011t0001g0059a0003c0012t0001g0012others(2): Show | 5 | HG01884.hp1 HG02717.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.551-71C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 4/6 | chr19 | 48592651 | ||||||
| chr19:48592682
|
C | T | 1 | a0001c0006t0001g0090 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.551-40C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 4/6 | chr19 | 48592682 | ||||||
| chr19:48592701
|
C | T | 1 | a0001c0006t0001g0090 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.551-21C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 4/6 | chr19 | 48592701 | ||||||
| chr19:48592904
|
C | A | 23 | a0001c0001t0001g0024a0001c0001t0001g0031a0001c0001t0001g0032others(20): Show | 23 | HG00558.hp2 HG01074.hp1 HG01358.hp1 others(20): Show |
intron_variant | MODIFIER | c.645+88C>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 5/6 | chr19 | 48592904 | ||||||
| chr19:48592910
|
G | A | 50 | a0001c0001t0001g0070a0001c0001t0001g0087a0001c0001t0001g0104others(47): Show | 50 | HG00408.hp1 HG00597.hp1 HG00642.hp2 others(47): Show |
intron_variant | MODIFIER | c.645+94G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 5/6 | chr19 | 48592910 | ||||||
| chr19:48592957
|
A | G | 1 | a0001c0001t0001g0066 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.645+141A>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 5/6 | chr19 | 48592957 | ||||||
| chr19:48593020
|
C | T | 2 | a0001c0001t0001g0199a0001c0001t0001g0204 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.645+204C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 5/6 | chr19 | 48593020 | ||||||
| chr19:48593035
|
G | A | 245 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0017others(242): Show | 245 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(242): Show |
intron_variant | MODIFIER | c.645+219G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 5/6 | chr19 | 48593035 | ||||||
| chr19:48593054
|
G | A | 50 | a0001c0001t0001g0070a0001c0001t0001g0087a0001c0001t0001g0104others(47): Show | 50 | HG00408.hp1 HG00597.hp1 HG00642.hp2 others(47): Show |
intron_variant | MODIFIER | c.645+238G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 5/6 | chr19 | 48593054 | ||||||
| chr19:48593279
|
T | C | 1 | a0001c0003t0001g0325 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.645+463T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 5/6 | chr19 | 48593279 | ||||||
| chr19:48593569
|
A | T | 1 | a0001c0001t0001g0066 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.645+753A>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 5/6 | chr19 | 48593569 | ||||||
| chr19:48593594
|
C | T | 298 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0017others(295): Show | 298 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(295): Show |
intron_variant | MODIFIER | c.645+778C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 5/6 | chr19 | 48593594 | ||||||
| chr19:48593641
|
T | A | 186 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0017others(183): Show | 187 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(184): Show |
intron_variant | MODIFIER | c.645+825T>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 5/6 | chr19 | 48593641 | ||||||
| chr19:48593869
|
G | A | 51 | a0001c0001t0001g0017a0001c0001t0001g0186a0001c0001t0001g0306others(48): Show | 51 | HG00558.hp1 HG00597.hp2 HG00738.hp1 others(48): Show |
intron_variant | MODIFIER | c.645+1053G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 5/6 | chr19 | 48593869 | ||||||
| chr19:48593943
|
C | T | 1 | a0001c0003t0001g0143 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.645+1127C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 5/6 | chr19 | 48593943 | ||||||
| chr19:48593963
|
A | C | 1 | a0001c0001t0001g0302 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.645+1147A>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 5/6 | chr19 | 48593963 | ||||||
| chr19:48593964
|
A | G | 1 | a0001c0001t0001g0302 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.645+1148A>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 5/6 | chr19 | 48593964 | ||||||
| chr19:48593972
|
A | G | 2 | a0001c0001t0001g0031a0001c0001t0001g0367 | 2 | HG01891.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.645+1156A>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 5/6 | chr19 | 48593972 | ||||||
| chr19:48593980
|
T | C | 1 | a0001c0001t0001g0302 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.645+1164T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 5/6 | chr19 | 48593980 | ||||||
| chr19:48593982
|
G | A | 1 | a0001c0001t0001g0302 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.645+1166G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 5/6 | chr19 | 48593982 | ||||||
| chr19:48593983
|
G | C | 1 | a0001c0001t0001g0302 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.645+1167G>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 5/6 | chr19 | 48593983 | ||||||
| chr19:48593983
|
G | T | 3 | a0001c0003t0001g0102a0001c0003t0001g0180a0001c0010t0001g0112 | 3 | HG00733.hp2 HG01081.hp2 HG01256.hp2 |
intron_variant | MODIFIER | c.645+1167G>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 5/6 | chr19 | 48593983 | ||||||
| chr19:48593990
|
G | T | 1 | a0001c0001t0001g0302 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.645+1174G>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 5/6 | chr19 | 48593990 | ||||||
| chr19:48593991
|
G | A | 1 | a0001c0001t0001g0302 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.645+1175G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 5/6 | chr19 | 48593991 | ||||||
| chr19:48593992
|
C | T | 1 | a0001c0001t0001g0302 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.645+1176C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 5/6 | chr19 | 48593992 | ||||||
| chr19:48593993
|
T | A | 1 | a0001c0001t0001g0302 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.645+1177T>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 5/6 | chr19 | 48593993 | ||||||
| chr19:48593994
|
C | T | 1 | a0001c0001t0001g0302 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.645+1178C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 5/6 | chr19 | 48593994 | ||||||
| chr19:48593996
|
C | A | 1 | a0001c0001t0001g0302 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.645+1180C>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 5/6 | chr19 | 48593996 | ||||||
| chr19:48593997
|
G | A | 63 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0036others(60): Show | 64 | HG00408.hp2 HG00438.hp1 HG00609.hp1 others(61): Show |
intron_variant | MODIFIER | c.645+1181G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 5/6 | chr19 | 48593997 | ||||||
| chr19:48593998
|
C | T | 1 | a0001c0001t0001g0302 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.645+1182C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 5/6 | chr19 | 48593998 | ||||||
| chr19:48593999
|
C | A | 1 | a0001c0001t0001g0302 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.645+1183C>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 5/6 | chr19 | 48593999 | ||||||
| chr19:48594001
|
G | A | 1 | a0001c0001t0001g0302 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.645+1185G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 5/6 | chr19 | 48594001 | ||||||
| chr19:48594008
|
C | T | 1 | a0001c0001t0001g0302 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.645+1192C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 5/6 | chr19 | 48594008 | ||||||
| chr19:48594011
|
C | A | 1 | a0001c0001t0001g0302 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.645+1195C>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 5/6 | chr19 | 48594011 | ||||||
| chr19:48594033
|
C | T | 1 | a0001c0001t0001g0302 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.645+1217C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 5/6 | chr19 | 48594033 | ||||||
| chr19:48594034
|
A | G | 1 | a0001c0001t0001g0302 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.645+1218A>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 5/6 | chr19 | 48594034 | ||||||
| chr19:48594178
|
T | C | 1 | a0001c0002t0001g0260 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.645+1362T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 5/6 | chr19 | 48594178 | ||||||
| chr19:48594406
|
C | T | 62 | a0001c0003t0001g0011a0001c0003t0001g0046a0001c0003t0001g0078others(59): Show | 62 | HG00423.hp1 HG00438.hp2 HG00597.hp1 others(59): Show |
intron_variant | MODIFIER | c.645+1590C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 5/6 | chr19 | 48594406 | ||||||
| chr19:48594490
|
C | T | 3 | a0001c0001t0001g0055a0001c0001t0001g0300a0001c0001t0001g0362 | 3 | HG02055.hp2 HG02886.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.645+1674C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 5/6 | chr19 | 48594490 | ||||||
| chr19:48594538
|
G | A | 1 | a0001c0003t0001g0292 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.645+1722G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 5/6 | chr19 | 48594538 | ||||||
| chr19:48594630
|
A | T | 348 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(345): Show | 349 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(346): Show |
intron_variant | MODIFIER | c.645+1814A>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 5/6 | chr19 | 48594630 | ||||||
| chr19:48594692
|
C | T | 63 | a0001c0003t0001g0011a0001c0003t0001g0046a0001c0003t0001g0078others(60): Show | 63 | HG00423.hp1 HG00438.hp2 HG00597.hp1 others(60): Show |
intron_variant | MODIFIER | c.645+1876C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 5/6 | chr19 | 48594692 | ||||||
| chr19:48594902
|
CCAG | C | 274 | a0001c0001t0001g0017a0001c0001t0001g0023a0001c0001t0001g0041others(271): Show | 275 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(272): Show |
intron_variant | MODIFIER | c.646-1832_646-1830d others(5): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr19 | 48594902 | |||||
| chr19:48594997
|
G | C | 1 | a0001c0003t0001g0327 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.646-1742G>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 5/6 | chr19 | 48594997 | ||||||
| chr19:48595079
|
T | C | 1 | a0005c0021t0001g0307 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.646-1660T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 5/6 | chr19 | 48595079 | ||||||
| chr19:48595099
|
A | G | 97 | a0001c0001t0001g0017a0001c0001t0001g0041a0001c0001t0001g0097others(94): Show | 98 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.646-1640A>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 5/6 | chr19 | 48595099 | ||||||
| chr19:48595151
|
A | G | 1 | a0001c0006t0001g0044 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.646-1588A>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 5/6 | chr19 | 48595151 | ||||||
| chr19:48595154
|
T | C | 4 | a0003c0011t0001g0043a0003c0011t0001g0059a0003c0012t0001g0012others(1): Show | 4 | HG01884.hp1 HG02717.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.646-1585T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 5/6 | chr19 | 48595154 | ||||||
| chr19:48595222
|
C | T | 1 | a0001c0003t0001g0216 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.646-1517C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 5/6 | chr19 | 48595222 | ||||||
| chr19:48595269
|
C | T | 63 | a0001c0003t0001g0011a0001c0003t0001g0046a0001c0003t0001g0078others(60): Show | 63 | HG00423.hp1 HG00438.hp2 HG00597.hp1 others(60): Show |
intron_variant | MODIFIER | c.646-1470C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 5/6 | chr19 | 48595269 | ||||||
| chr19:48595278
|
G | A | 4 | a0003c0011t0001g0043a0003c0011t0001g0059a0003c0012t0001g0012others(1): Show | 4 | HG01884.hp1 HG02717.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.646-1461G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 5/6 | chr19 | 48595278 | ||||||
| chr19:48595281
|
TA | T | 346 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(343): Show | 347 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(344): Show |
intron_variant | MODIFIER | c.646-1447delA | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr19 | 48595281 | |||||
| chr19:48595305
|
CA | C | 274 | a0001c0001t0001g0017a0001c0001t0001g0023a0001c0001t0001g0041others(271): Show | 275 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(272): Show |
intron_variant | MODIFIER | c.646-1433delA | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 5/6 | chr19 | 48595305 | ||||||
| chr19:48595359
|
T | C | 1 | a0001c0001t0001g0268 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.646-1380T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 5/6 | chr19 | 48595359 | ||||||
| chr19:48595450
|
G | A | 1 | a0007c0017t0001g0029 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.646-1289G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 5/6 | chr19 | 48595450 | ||||||
| chr19:48595493
|
A | G | 173 | a0001c0001t0001g0023a0001c0001t0001g0051a0001c0001t0001g0053others(170): Show | 173 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(170): Show |
intron_variant | MODIFIER | c.646-1246A>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 5/6 | chr19 | 48595493 | ||||||
| chr19:48595518
|
C | T | 274 | a0001c0001t0001g0017a0001c0001t0001g0023a0001c0001t0001g0041others(271): Show | 275 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(272): Show |
intron_variant | MODIFIER | c.646-1221C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 5/6 | chr19 | 48595518 | ||||||
| chr19:48595522
|
C | T | 97 | a0001c0001t0001g0017a0001c0001t0001g0041a0001c0001t0001g0097others(94): Show | 98 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.646-1217C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 5/6 | chr19 | 48595522 | ||||||
| chr19:48595654
|
GGTTTTTT others(8): Show |
G | 15 | a0001c0001t0001g0117a0001c0001t0001g0300a0001c0001t0001g0355others(12): Show | 15 | HG01106.hp1 HG01192.hp1 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.646-1084_646-1070d others(17): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 5/6 | chr19 | 48595654 | ||||||
| chr19:48595654
|
GGTTTTTT others(9): Show |
G | 248 | a0001c0001t0001g0017a0001c0001t0001g0041a0001c0001t0001g0055others(245): Show | 249 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(246): Show |
intron_variant | MODIFIER | c.646-1084_646-1069d others(18): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 5/6 | chr19 | 48595654 | ||||||
| chr19:48595654
|
GGTTTTTT others(10): Show |
G | 2 | a0001c0003t0001g0114a0008c0015t0001g0352 | 2 | NA18986.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.646-1084_646-1068d others(19): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 5/6 | chr19 | 48595654 | ||||||
| chr19:48595655
|
GTTTTTTT others(9): Show |
G | 9 | a0001c0001t0001g0023a0001c0001t0001g0051a0001c0001t0001g0053others(6): Show | 9 | HG02145.hp1 HG02257.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.646-1074_646-1059d others(18): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr19 | 48595655 | |||||
| chr19:48595668
|
G | GTT | 66 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(63): Show | 66 | HG00408.hp1 HG01167.hp1 HG01169.hp1 others(63): Show |
intron_variant | MODIFIER | c.646-1055_646-1054d others(4): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr19 | 48595668 | |||||
| chr19:48595668
|
G | GTTT | 8 | a0001c0001t0001g0060a0001c0001t0001g0092a0001c0001t0001g0215others(5): Show | 8 | HG01175.hp1 HG01243.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.646-1056_646-1054d others(5): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr19 | 48595668 | |||||
| chr19:48595668
|
G | T | 1 | a0001c0001t0001g0039 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.646-1071G>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 5/6 | chr19 | 48595668 | ||||||
| chr19:48595675
|
T | G | 1 | a0001c0004t0001g0141 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.646-1064T>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 5/6 | chr19 | 48595675 | ||||||
| chr19:48595677
|
T | A | 1 | a0001c0001t0001g0117 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.646-1062T>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 5/6 | chr19 | 48595677 | ||||||
| chr19:48595749
|
A | C | 265 | a0001c0001t0001g0017a0001c0001t0001g0041a0001c0001t0001g0055others(262): Show | 266 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(263): Show |
intron_variant | MODIFIER | c.646-990A>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 5/6 | chr19 | 48595749 | ||||||
| chr19:48595895
|
G | A | 1 | a0001c0002t0001g0317 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.646-844G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 5/6 | chr19 | 48595895 | ||||||
| chr19:48595933
|
A | G | 283 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0017others(280): Show | 284 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(281): Show |
intron_variant | MODIFIER | c.646-806A>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 5/6 | chr19 | 48595933 | ||||||
| chr19:48596055
|
G | C | 4 | a0003c0011t0001g0043a0003c0011t0001g0059a0003c0012t0001g0012others(1): Show | 4 | HG01884.hp1 HG02717.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.646-684G>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 5/6 | chr19 | 48596055 | ||||||
| chr19:48596093
|
G | T | 1 | a0001c0001t0001g0039 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.646-646G>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 5/6 | chr19 | 48596093 | ||||||
| chr19:48596124
|
A | G | 347 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(344): Show | 348 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(345): Show |
intron_variant | MODIFIER | c.646-615A>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 5/6 | chr19 | 48596124 | ||||||
| chr19:48596190
|
G | A | 18 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0054others(15): Show | 18 | HG01243.hp1 HG01884.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.646-549G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 5/6 | chr19 | 48596190 | ||||||
| chr19:48596234
|
T | C | 282 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0017others(279): Show | 283 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(280): Show |
intron_variant | MODIFIER | c.646-505T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 5/6 | chr19 | 48596234 | ||||||
| chr19:48596249
|
G | A | 1 | a0001c0002t0001g0301 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.646-490G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 5/6 | chr19 | 48596249 | ||||||
| chr19:48596325
|
G | A | 1 | a0008c0015t0001g0352 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.646-414G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 5/6 | chr19 | 48596325 | ||||||
| chr19:48596376
|
G | A | 1 | a0001c0002t0001g0248 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.646-363G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 5/6 | chr19 | 48596376 | ||||||
| chr19:48596408
|
C | G | 98 | a0001c0001t0001g0373a0001c0002t0001g0003a0001c0002t0001g0022others(95): Show | 98 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(95): Show |
intron_variant | MODIFIER | c.646-331C>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 5/6 | chr19 | 48596408 | ||||||
| chr19:48596436
|
A | ACTGTGAC others(12): Show |
19 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0054others(16): Show | 19 | HG01243.hp1 HG01884.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.646-285_646-267dup others(19): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr19 | 48596436 | |||||
| chr19:48596454
|
GGCTGTGA others(12): Show |
G | 6 | a0001c0001t0001g0117a0001c0001t0001g0144a0001c0001t0001g0210others(3): Show | 6 | HG02071.hp2 HG02738.hp1 NA18945.hp1 others(3): Show |
intron_variant | MODIFIER | c.646-248_646-230del others(19): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr19 | 48596454 | |||||
| chr19:48596470
|
C | G | 98 | a0001c0001t0001g0373a0001c0002t0001g0003a0001c0002t0001g0022others(95): Show | 98 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(95): Show |
intron_variant | MODIFIER | c.646-269C>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 5/6 | chr19 | 48596470 | ||||||
| chr19:48596473
|
T | G | 258 | a0001c0001t0001g0017a0001c0001t0001g0041a0001c0001t0001g0055others(255): Show | 259 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(256): Show |
intron_variant | MODIFIER | c.646-266T>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 5/6 | chr19 | 48596473 | ||||||
| chr19:48596492
|
T | G | 5 | a0001c0001t0001g0136a0001c0001t0001g0207a0001c0001t0001g0259others(2): Show | 5 | HG02738.hp1 HG03041.hp1 NA19007.hp2 others(2): Show |
intron_variant | MODIFIER | c.646-247T>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 5/6 | chr19 | 48596492 | ||||||
| chr19:48596569
|
T | C | 1 | a0001c0006t0001g0250 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.646-170T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 5/6 | chr19 | 48596569 | ||||||
| chr19:48596577
|
G | A | 1 | a0001c0002t0001g0134 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.646-162G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 5/6 | chr19 | 48596577 | ||||||
| chr19:48596698
|
C | T | 66 | a0001c0003t0001g0011a0001c0003t0001g0046a0001c0003t0001g0078others(63): Show | 66 | HG00423.hp1 HG00438.hp2 HG00597.hp1 others(63): Show |
intron_variant | MODIFIER | c.646-41C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 5/6 | chr19 | 48596698 | ||||||
| chr19:48596922
|
G | A | 2 | a0001c0001t0001g0302a0001c0006t0001g0061 | 2 | HG02145.hp2 NA18906.hp1 |
splice_region_variant&intron_variant | LOW | c.826+3G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 6/6 | chr19 | 48596922 | ||||||
| chr19:48597135
|
C | T | 1 | a0001c0001t0001g0329 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.826+216C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 6/6 | chr19 | 48597135 | ||||||
| chr19:48597139
|
A | G | 1 | a0001c0010t0001g0037 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.826+220A>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 6/6 | chr19 | 48597139 | ||||||
| chr19:48597166
|
G | A | 1 | a0001c0001t0001g0186 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.826+247G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 6/6 | chr19 | 48597166 | ||||||
| chr19:48597337
|
CT | C | 100 | a0001c0001t0001g0017a0001c0001t0001g0031a0001c0001t0001g0039others(97): Show | 101 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.826+438delT | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr19 | 48597337 | |||||
| chr19:48597337
|
CTT | C | 221 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(218): Show | 221 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(218): Show |
intron_variant | MODIFIER | c.826+437_826+438del others(2): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr19 | 48597337 | |||||
| chr19:48597337
|
CTTT | C | 26 | a0001c0001t0001g0023a0001c0001t0001g0051a0001c0001t0001g0053others(23): Show | 26 | HG00140.hp1 HG00140.hp2 HG00423.hp2 others(23): Show |
intron_variant | MODIFIER | c.826+436_826+438del others(3): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr19 | 48597337 | |||||
| chr19:48597338
|
T | G | 1 | a0001c0006t0001g0250 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.826+419T>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 6/6 | chr19 | 48597338 | ||||||
| chr19:48597339
|
T | C | 1 | a0001c0003t0001g0262 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.826+420T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 6/6 | chr19 | 48597339 | ||||||
| chr19:48597369
|
G | A | 1 | a0003c0011t0001g0059 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.826+450G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 6/6 | chr19 | 48597369 | ||||||
| chr19:48597395
|
T | TTGCAG | 56 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0021others(53): Show | 56 | HG00408.hp1 HG01167.hp1 HG01169.hp1 others(53): Show |
intron_variant | MODIFIER | c.826+479_826+483dup others(5): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr19 | 48597395 | |||||
| chr19:48597406
|
C | T | 291 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0017others(288): Show | 292 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(289): Show |
intron_variant | MODIFIER | c.826+487C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 6/6 | chr19 | 48597406 | ||||||
| chr19:48597446
|
T | C | 335 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0017others(332): Show | 336 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(333): Show |
intron_variant | MODIFIER | c.826+527T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 6/6 | chr19 | 48597446 | ||||||
| chr19:48597512
|
T | C | 1 | a0007c0017t0001g0029 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.826+593T>C | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 6/6 | chr19 | 48597512 | ||||||
| chr19:48597595
|
G | A | 1 | a0001c0001t0001g0115 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.826+676G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 6/6 | chr19 | 48597595 | ||||||
| chr19:48597647
|
C | CTTTTTTT others(3): Show |
1 | a0001c0001t0001g0270 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.826+734_826+735ins others(10): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr19 | 48597647 | |||||
| chr19:48597654
|
C | CTTTTTTT others(2): Show |
55 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0021others(52): Show | 55 | HG00408.hp1 HG01167.hp1 HG01169.hp1 others(52): Show |
intron_variant | MODIFIER | c.826+741_826+742ins others(9): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr19 | 48597654 | |||||
| chr19:48597654
|
C | CTTTTTTT others(3): Show |
195 | a0001c0001t0001g0017a0001c0001t0001g0023a0001c0001t0001g0041others(192): Show | 195 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(192): Show |
intron_variant | MODIFIER | c.826+741_826+742ins others(10): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr19 | 48597654 | |||||
| chr19:48597654
|
C | CTTTTTTT others(4): Show |
97 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0054others(94): Show | 98 | HG00423.hp1 HG00438.hp2 HG00597.hp1 others(95): Show |
intron_variant | MODIFIER | c.826+741_826+742ins others(11): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr19 | 48597654 | |||||
| chr19:48597654
|
C | T | 1 | a0001c0001t0001g0270 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.826+735C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 6/6 | chr19 | 48597654 | ||||||
| chr19:48597919
|
C | T | 2 | a0001c0002t0001g0134a0001c0002t0001g0275 | 2 | NA18970.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.826+1000C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 6/6 | chr19 | 48597919 | ||||||
| chr19:48597964
|
C | T | 1 | a0001c0002t0001g0165 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.826+1045C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 6/6 | chr19 | 48597964 | ||||||
| chr19:48598079
|
A | G | 9 | a0001c0001t0001g0002a0001c0001t0001g0023a0001c0001t0001g0051others(6): Show | 9 | HG02145.hp1 HG02257.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.827-1056A>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 6/6 | chr19 | 48598079 | ||||||
| chr19:48598145
|
C | T | 4 | a0003c0011t0001g0043a0003c0011t0001g0059a0003c0012t0001g0012others(1): Show | 4 | HG01884.hp1 HG02717.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.827-990C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 6/6 | chr19 | 48598145 | ||||||
| chr19:48598291
|
A | G | 62 | a0001c0003t0001g0011a0001c0003t0001g0046a0001c0003t0001g0078others(59): Show | 62 | HG00423.hp1 HG00438.hp2 HG00597.hp1 others(59): Show |
intron_variant | MODIFIER | c.827-844A>G | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 6/6 | chr19 | 48598291 | ||||||
| chr19:48598320
|
C | T | 41 | a0001c0001t0001g0041a0001c0001t0001g0097a0001c0001t0001g0116others(38): Show | 41 | HG00408.hp2 HG00438.hp1 HG00609.hp1 others(38): Show |
intron_variant | MODIFIER | c.827-815C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 6/6 | chr19 | 48598320 | ||||||
| chr19:48598417
|
C | T | 1 | a0001c0001t0001g0178 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.827-718C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 6/6 | chr19 | 48598417 | ||||||
| chr19:48598570
|
C | T | 7 | a0001c0009t0001g0121a0001c0009t0001g0188a0001c0009t0001g0304others(4): Show | 7 | HG00639.hp1 HG01192.hp2 HG01515.hp2 others(4): Show |
intron_variant | MODIFIER | c.827-565C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 6/6 | chr19 | 48598570 | ||||||
| chr19:48598571
|
G | A | 4 | a0001c0002t0001g0077a0001c0002t0001g0149a0001c0002t0001g0253others(1): Show | 4 | HG02129.hp1 HG03017.hp2 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.827-564G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 6/6 | chr19 | 48598571 | ||||||
| chr19:48598699
|
C | T | 187 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0017others(184): Show | 187 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(184): Show |
intron_variant | MODIFIER | c.827-436C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 6/6 | chr19 | 48598699 | ||||||
| chr19:48598733
|
G | A | 94 | a0001c0001t0001g0017a0001c0001t0001g0041a0001c0001t0001g0097others(91): Show | 94 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(91): Show |
intron_variant | MODIFIER | c.827-402G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 6/6 | chr19 | 48598733 | ||||||
| chr19:48598777
|
G | A | 1 | a0001c0001t0001g0104 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.827-358G>A | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 6/6 | chr19 | 48598777 | ||||||
| chr19:48598937
|
C | T | 1 | a0001c0001t0001g0196 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.827-198C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 6/6 | chr19 | 48598937 | ||||||
| chr19:48598940
|
C | T | 1 | a0007c0017t0001g0029 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.827-195C>T | SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 6/6 | chr19 | 48598940 |