| geneid | 9956 |
|---|---|
| ensemblid | ENSG00000122254.7 |
| hgncid | 5195 |
| symbol | HS3ST2 |
| name | heparan sulfate-glucosamine 3-sulfotransferase 2 |
| refseq_nuc | NM_006043.2 |
| refseq_prot | NP_006034.1 |
| ensembl_nuc | ENST00000261374.4 |
| ensembl_prot | ENSP00000261374.3 |
| mane_status | MANE Select |
| chr | chr16 |
| start | 22814162 |
| end | 22916338 |
| strand | + |
| ver | v1.2 |
| region | chr16:22814162-22916338 |
| region5000 | chr16:22809162-22921338 |
| regionname0 | HS3ST2_chr16_22814162_22916338 |
| regionname5000 | HS3ST2_chr16_22809162_22921338 |
| 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 | 367 | 341 | 91 | 73 | 123 | 12 | 40 | 90 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | copy fasta | chr16 | 22809162 | 22921338 |
| a0002 | 0/0 | 367 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | copy fasta | chr16 | 22809162 | 22921338 |
| a0003 | 0/0 | 367 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | copy fasta | chr16 | 22809162 | 22921338 |
| a0004 | 0/0 | 367 | 2 | 0 | 1 | 0 | 0 | 1 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | copy fasta | chr16 | 22809162 | 22921338 |
| a0005 | 0/0 | 367 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | copy fasta | chr16 | 22809162 | 22921338 |
| a0006 | 0/0 | 367 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | copy fasta | chr16 | 22809162 | 22921338 |
| a0007 | 0/0 | 367 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | copy fasta | chr16 | 22809162 | 22921338 |
| 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 | 1104 | 180 | 40 | 26 | 78 | 5 | 30 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | copy fasta | chr16 | 22809162 | 22921338 |
| c0002 | 0/1 | 1104 | 107 | 15 | 35 | 45 | 5 | 6 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | copy fasta | chr16 | 22809162 | 22921338 |
| c0003 | 0/0 | 1104 | 17 | 15 | 2 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | copy fasta | chr16 | 22809162 | 22921338 |
| c0004 | 0/0 | 1104 | 17 | 9 | 4 | 0 | 1 | 3 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | copy fasta | chr16 | 22809162 | 22921338 |
| c0005 | 0/0 | 1104 | 13 | 5 | 6 | 0 | 1 | 1 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | copy fasta | chr16 | 22809162 | 22921338 |
| c0006 | 0/0 | 1104 | 6 | 6 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | copy fasta | chr16 | 22809162 | 22921338 |
| c0007 | 0/0 | 1104 | 2 | 0 | 1 | 0 | 0 | 1 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | copy fasta | chr16 | 22809162 | 22921338 |
| c0008 | 0/0 | 1104 | 2 | 0 | 2 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | copy fasta | chr16 | 22809162 | 22921338 |
| c0009 | 0/0 | 1104 | 2 | 0 | 0 | 2 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | copy fasta | chr16 | 22809162 | 22921338 |
| c0010 | 0/0 | 1104 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | copy fasta | chr16 | 22809162 | 22921338 |
| c0011 | 0/0 | 1104 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | copy fasta | chr16 | 22809162 | 22921338 |
| c0012 | 0/0 | 1104 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | copy fasta | chr16 | 22809162 | 22921338 |
| c0013 | 0/0 | 1104 | 1 | 0 | 0 | 0 | 0 | 1 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | copy fasta | chr16 | 22809162 | 22921338 |
| 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 | 1226 | 251 | 51 | 41 | 116 | 10 | 31 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | copy fasta | chr16 | 22809162 | 22921338 |
| t0002 | 0/0 | 1226 | 30 | 12 | 11 | 0 | 2 | 5 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | copy fasta | chr16 | 22809162 | 22921338 |
| t0003 | 0/0 | 1226 | 18 | 16 | 2 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | copy fasta | chr16 | 22809162 | 22921338 |
| t0004 | 0/0 | 1226 | 15 | 0 | 8 | 3 | 0 | 4 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | copy fasta | chr16 | 22809162 | 22921338 |
| t0005 | 0/0 | 1226 | 9 | 1 | 8 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | copy fasta | chr16 | 22809162 | 22921338 |
| t0006 | 0/0 | 1226 | 8 | 7 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | copy fasta | chr16 | 22809162 | 22921338 |
| t0007 | 0/0 | 1227 | 6 | 1 | 0 | 4 | 0 | 1 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | copy fasta | chr16 | 22809162 | 22921338 |
| t0008 | 0/0 | 1226 | 5 | 0 | 5 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | copy fasta | chr16 | 22809162 | 22921338 |
| t0009 | 0/0 | 1226 | 2 | 0 | 0 | 2 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | copy fasta | chr16 | 22809162 | 22921338 |
| t0010 | 0/0 | 1226 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | copy fasta | chr16 | 22809162 | 22921338 |
| t0011 | 0/0 | 1226 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | copy fasta | chr16 | 22809162 | 22921338 |
| t0012 | 0/0 | 1226 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | copy fasta | chr16 | 22809162 | 22921338 |
| t0013 | 0/0 | 1226 | 1 | 0 | 0 | 0 | 0 | 1 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | copy fasta | chr16 | 22809162 | 22921338 |
| t0014 | 0/0 | 1226 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | copy fasta | chr16 | 22809162 | 22921338 |
| t0015 | 0/0 | 1226 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | copy fasta | chr16 | 22809162 | 22921338 |
| 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 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0068 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0234 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0282 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0308 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0309 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0320 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0334 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0338 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0340 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0345 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0349 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| 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 | 1104 | 180 | 40 | 26 | 78 | 5 | 30 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | copy fasta | chr16 | 22809162 | 22921338 |
| a0001c0002 | 0/1 | 1104 | 107 | 15 | 35 | 45 | 5 | 6 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | copy fasta | chr16 | 22809162 | 22921338 |
| a0001c0003 | 0/0 | 1104 | 17 | 15 | 2 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | copy fasta | chr16 | 22809162 | 22921338 |
| a0001c0004 | 0/0 | 1104 | 17 | 9 | 4 | 0 | 1 | 3 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | copy fasta | chr16 | 22809162 | 22921338 |
| a0001c0005 | 0/0 | 1104 | 13 | 5 | 6 | 0 | 1 | 1 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | copy fasta | chr16 | 22809162 | 22921338 |
| a0001c0006 | 0/0 | 1104 | 6 | 6 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | copy fasta | chr16 | 22809162 | 22921338 |
| a0001c0011 | 0/0 | 1104 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | copy fasta | chr16 | 22809162 | 22921338 |
| a0002c0009 | 0/0 | 1104 | 2 | 0 | 0 | 2 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | copy fasta | chr16 | 22809162 | 22921338 |
| a0003c0008 | 0/0 | 1104 | 2 | 0 | 2 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | copy fasta | chr16 | 22809162 | 22921338 |
| a0004c0007 | 0/0 | 1104 | 2 | 0 | 1 | 0 | 0 | 1 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | copy fasta | chr16 | 22809162 | 22921338 |
| a0005c0013 | 0/0 | 1104 | 1 | 0 | 0 | 0 | 0 | 1 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | copy fasta | chr16 | 22809162 | 22921338 |
| a0006c0012 | 0/0 | 1104 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | copy fasta | chr16 | 22809162 | 22921338 |
| a0007c0010 | 0/0 | 1104 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | copy fasta | chr16 | 22809162 | 22921338 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 2329 | 168 | 39 | 24 | 74 | 5 | 25 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | copy fasta | chr16 | 22809162 | 22921338 |
| a0001c0001t0004 | 0/0 | 2329 | 6 | 0 | 2 | 1 | 0 | 3 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | copy fasta | chr16 | 22809162 | 22921338 |
| a0001c0001t0007 | 0/0 | 2330 | 3 | 1 | 0 | 1 | 0 | 1 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | copy fasta | chr16 | 22809162 | 22921338 |
| a0001c0001t0009 | 0/0 | 2329 | 2 | 0 | 0 | 2 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | copy fasta | chr16 | 22809162 | 22921338 |
| a0001c0001t0013 | 0/0 | 2329 | 1 | 0 | 0 | 0 | 0 | 1 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | copy fasta | chr16 | 22809162 | 22921338 |
| a0001c0002t0001 | 0/1 | 2329 | 77 | 11 | 16 | 39 | 5 | 5 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | copy fasta | chr16 | 22809162 | 22921338 |
| a0001c0002t0003 | 0/0 | 2329 | 2 | 2 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | copy fasta | chr16 | 22809162 | 22921338 |
| a0001c0002t0004 | 0/0 | 2329 | 9 | 0 | 6 | 2 | 0 | 1 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | copy fasta | chr16 | 22809162 | 22921338 |
| a0001c0002t0005 | 0/0 | 2329 | 9 | 1 | 8 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | copy fasta | chr16 | 22809162 | 22921338 |
| a0001c0002t0007 | 0/0 | 2330 | 3 | 0 | 0 | 3 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | copy fasta | chr16 | 22809162 | 22921338 |
| a0001c0002t0008 | 0/0 | 2329 | 5 | 0 | 5 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | copy fasta | chr16 | 22809162 | 22921338 |
| a0001c0002t0010 | 0/0 | 2329 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | copy fasta | chr16 | 22809162 | 22921338 |
| a0001c0002t0012 | 0/0 | 2329 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | copy fasta | chr16 | 22809162 | 22921338 |
| a0001c0003t0003 | 0/0 | 2329 | 16 | 14 | 2 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | copy fasta | chr16 | 22809162 | 22921338 |
| a0001c0003t0015 | 0/0 | 2329 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | copy fasta | chr16 | 22809162 | 22921338 |
| a0001c0004t0002 | 0/0 | 2329 | 16 | 8 | 4 | 0 | 1 | 3 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | copy fasta | chr16 | 22809162 | 22921338 |
| a0001c0004t0014 | 0/0 | 2329 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | copy fasta | chr16 | 22809162 | 22921338 |
| a0001c0005t0002 | 0/0 | 2329 | 11 | 4 | 5 | 0 | 1 | 1 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | copy fasta | chr16 | 22809162 | 22921338 |
| a0001c0005t0006 | 0/0 | 2329 | 2 | 1 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | copy fasta | chr16 | 22809162 | 22921338 |
| a0001c0006t0006 | 0/0 | 2329 | 6 | 6 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | copy fasta | chr16 | 22809162 | 22921338 |
| a0001c0011t0011 | 0/0 | 2329 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | copy fasta | chr16 | 22809162 | 22921338 |
| a0002c0009t0001 | 0/0 | 2329 | 2 | 0 | 0 | 2 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | copy fasta | chr16 | 22809162 | 22921338 |
| a0003c0008t0002 | 0/0 | 2329 | 2 | 0 | 2 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | copy fasta | chr16 | 22809162 | 22921338 |
| a0004c0007t0001 | 0/0 | 2329 | 2 | 0 | 1 | 0 | 0 | 1 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | copy fasta | chr16 | 22809162 | 22921338 |
| a0005c0013t0002 | 0/0 | 2329 | 1 | 0 | 0 | 0 | 0 | 1 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | copy fasta | chr16 | 22809162 | 22921338 |
| a0006c0012t0001 | 0/0 | 2329 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | copy fasta | chr16 | 22809162 | 22921338 |
| a0007c0010t0001 | 0/0 | 2329 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | copy fasta | chr16 | 22809162 | 22921338 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0282 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0345 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0349 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0004g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0004g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0004g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0004g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0004g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0004g0340 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0007g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0007g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0007g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0009g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0009g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0013g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0001g0068 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0001g0308 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0001g0309 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0001g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0003g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0003g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0004g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0004g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0004g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0004g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0004g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0004g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0004g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0004g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0004g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0005g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0005g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0005g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0005g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0005g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0005g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0005g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0005g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0005g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0007g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0007g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0007g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0008g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0008g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0008g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0008g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0008g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0010g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0012g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0003t0003g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0003t0003g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0003t0003g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0003t0003g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0003t0003g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0003t0003g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0003t0003g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0003t0003g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0003t0003g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0003t0003g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0003t0003g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0003t0003g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0003t0003g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0003t0003g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0003t0003g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0003t0003g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0003t0015g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0004t0002g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0004t0002g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0004t0002g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0004t0002g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0004t0002g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0004t0002g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0004t0002g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0004t0002g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0004t0002g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0004t0002g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0004t0002g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0004t0002g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0004t0002g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0004t0002g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0004t0002g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0004t0002g0338 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0004t0014g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0005t0002g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0005t0002g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0005t0002g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0005t0002g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0005t0002g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0005t0002g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0005t0002g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0005t0002g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0005t0002g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0005t0002g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0005t0002g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0005t0006g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0005t0006g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0006t0006g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0006t0006g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0006t0006g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0006t0006g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0006t0006g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0006t0006g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0011t0011g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0002c0009t0001g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0002c0009t0001g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0003c0008t0002g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0003c0008t0002g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0004c0007t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0004c0007t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0005c0013t0002g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0006c0012t0001g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0007c0010t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0334 | EUR | GBR | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG00140 | hp2 | a0001 | c0002 | t0001 | g0142 | EUR | GBR | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG00280 | hp1 | a0001 | c0002 | t0001 | g0122 | EUR | FIN | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0159 | EUR | FIN | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG00323 | hp1 | a0001 | c0002 | t0001 | g0106 | EUR | FIN | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0320 | EUR | FIN | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG00423 | hp1 | a0001 | c0002 | t0001 | g0071 | EAS | CHS | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0315 | EAS | CHS | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | CHS | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG00438 | hp2 | a0001 | c0001 | t0009 | g0239 | EAS | CHS | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG00544 | hp1 | a0001 | c0002 | t0007 | g0044 | EAS | CHS | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG00544 | hp2 | a0001 | c0002 | t0001 | g0089 | EAS | CHS | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG00558 | hp1 | a0001 | c0002 | t0001 | g0086 | EAS | CHS | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0274 | EAS | CHS | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG00609 | hp1 | a0001 | c0002 | t0001 | g0048 | EAS | CHS | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | CHS | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | CHS | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG00621 | hp2 | a0001 | c0002 | t0001 | g0073 | EAS | CHS | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG00639 | hp1 | a0001 | c0005 | t0002 | g0014 | AMR | PUR | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG00639 | hp2 | a0004 | c0007 | t0001 | g0221 | AMR | PUR | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0278 | AMR | PUR | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG00735 | hp2 | a0001 | c0005 | t0002 | g0082 | AMR | PUR | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0318 | AMR | PUR | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG00738 | hp2 | a0001 | c0005 | t0002 | g0090 | AMR | PUR | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG00741 | hp1 | a0001 | c0002 | t0001 | g0052 | AMR | PUR | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0147 | AMR | PUR | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0160 | AMR | PUR | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG01070 | hp2 | a0003 | c0008 | t0002 | g0231 | AMR | PUR | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG01071 | hp1 | a0003 | c0008 | t0002 | g0232 | AMR | PUR | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG01071 | hp2 | a0001 | c0002 | t0004 | g0097 | AMR | PUR | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG01081 | hp1 | a0001 | c0004 | t0002 | g0261 | AMR | PUR | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG01081 | hp2 | a0001 | c0002 | t0001 | g0069 | AMR | PUR | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0257 | AMR | PUR | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0332 | AMR | PUR | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG01106 | hp1 | a0001 | c0004 | t0002 | g0241 | AMR | PUR | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG01106 | hp2 | a0001 | c0002 | t0001 | g0110 | AMR | PUR | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0331 | AMR | PUR | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG01109 | hp2 | a0001 | c0004 | t0002 | g0304 | AMR | PUR | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG01167 | hp1 | a0001 | c0002 | t0001 | g0100 | AMR | PUR | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG01167 | hp2 | a0001 | c0005 | t0006 | g0040 | AMR | PUR | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG01168 | hp1 | a0001 | c0002 | t0001 | g0127 | AMR | PUR | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0321 | AMR | PUR | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG01169 | hp1 | a0001 | c0002 | t0001 | g0126 | AMR | PUR | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG01169 | hp2 | a0001 | c0002 | t0001 | g0101 | AMR | PUR | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0223 | AMR | PUR | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0217 | AMR | PUR | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG01192 | hp1 | a0001 | c0002 | t0004 | g0096 | AMR | PUR | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG01192 | hp2 | a0001 | c0002 | t0001 | g0099 | AMR | PUR | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG01243 | hp1 | a0001 | c0002 | t0001 | g0105 | AMR | PUR | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0292 | AMR | PUR | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG01255 | hp1 | a0001 | c0002 | t0005 | g0131 | AMR | CLM | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG01255 | hp2 | a0001 | c0002 | t0001 | g0093 | AMR | CLM | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG01256 | hp1 | a0001 | c0005 | t0002 | g0005 | AMR | CLM | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0177 | AMR | CLM | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0153 | AMR | CLM | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG01257 | hp2 | a0001 | c0002 | t0001 | g0050 | AMR | CLM | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0176 | AMR | CLM | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0158 | AMR | CLM | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG01261 | hp1 | a0001 | c0002 | t0005 | g0129 | AMR | CLM | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG01261 | hp2 | a0001 | c0002 | t0001 | g0138 | AMR | CLM | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG01346 | hp1 | a0001 | c0005 | t0002 | g0004 | AMR | CLM | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0154 | AMR | CLM | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG01361 | hp1 | a0001 | c0001 | t0004 | g0193 | AMR | CLM | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG01361 | hp2 | a0001 | c0004 | t0002 | g0184 | AMR | CLM | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG01433 | hp1 | a0001 | c0002 | t0004 | g0088 | AMR | CLM | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0336 | AMR | CLM | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG01496 | hp1 | a0001 | c0002 | t0001 | g0094 | AMR | CLM | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG01496 | hp2 | a0001 | c0003 | t0003 | g0030 | AMR | CLM | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0234 | EUR | IBS | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG01516 | hp2 | a0001 | c0002 | t0001 | g0309 | EUR | IBS | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0164 | EUR | IBS | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG01517 | hp2 | a0001 | c0002 | t0001 | g0308 | EUR | IBS | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG01884 | hp1 | a0001 | c0005 | t0006 | g0038 | AFR | ACB | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG01884 | hp2 | a0001 | c0002 | t0001 | g0061 | AFR | ACB | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG01891 | hp1 | a0001 | c0003 | t0003 | g0021 | AFR | ACB | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0286 | AFR | ACB | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG01928 | hp1 | a0001 | c0002 | t0008 | g0134 | AMR | PEL | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG01928 | hp2 | a0001 | c0002 | t0005 | g0125 | AMR | PEL | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG01934 | hp1 | a0001 | c0003 | t0003 | g0033 | AMR | PEL | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0275 | AMR | PEL | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0157 | AMR | PEL | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG01943 | hp2 | a0001 | c0002 | t0005 | g0130 | AMR | PEL | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG01952 | hp1 | a0001 | c0002 | t0005 | g0123 | AMR | PEL | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG01952 | hp2 | a0001 | c0002 | t0008 | g0133 | AMR | PEL | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG01975 | hp1 | a0001 | c0001 | t0004 | g0152 | AMR | PEL | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG01975 | hp2 | a0001 | c0002 | t0005 | g0128 | AMR | PEL | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG01978 | hp1 | a0001 | c0002 | t0005 | g0132 | AMR | PEL | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG01978 | hp2 | a0001 | c0002 | t0004 | g0137 | AMR | PEL | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0276 | AMR | PEL | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG01981 | hp2 | a0001 | c0002 | t0008 | g0139 | AMR | PEL | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0185 | AMR | PEL | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG01993 | hp2 | a0001 | c0002 | t0001 | g0046 | AMR | PEL | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG02004 | hp1 | a0001 | c0002 | t0004 | g0049 | AMR | PEL | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0155 | AMR | PEL | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | KHV | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG02040 | hp2 | a0001 | c0001 | t0009 | g0209 | EAS | KHV | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG02055 | hp1 | a0001 | c0002 | t0001 | g0010 | AFR | ACB | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG02055 | hp2 | a0001 | c0001 | t0007 | g0285 | AFR | ACB | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG02071 | hp1 | a0001 | c0002 | t0004 | g0059 | EAS | KHV | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG02071 | hp2 | a0001 | c0002 | t0007 | g0056 | EAS | KHV | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG02074 | hp1 | a0001 | c0002 | t0001 | g0348 | EAS | KHV | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | KHV | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0269 | EAS | KHV | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG02080 | hp2 | a0001 | c0001 | t0004 | g0200 | EAS | KHV | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG02129 | hp1 | a0001 | c0002 | t0001 | g0081 | EAS | KHV | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | KHV | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0323 | EAS | KHV | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | KHV | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0216 | AFR | ACB | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG02145 | hp2 | a0001 | c0002 | t0001 | g0007 | AFR | ACB | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG02148 | hp1 | a0001 | c0002 | t0008 | g0143 | AMR | PEL | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG02148 | hp2 | a0001 | c0002 | t0001 | g0051 | AMR | PEL | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0273 | EAS | CDX | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | CDX | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | CDX | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0317 | EAS | CDX | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG02258 | hp1 | a0001 | c0002 | t0010 | g0043 | AFR | ACB | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0310 | AFR | ACB | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0151 | AMR | PEL | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG02273 | hp2 | a0001 | c0002 | t0005 | g0135 | AMR | PEL | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0294 | AFR | ACB | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0170 | AFR | ACB | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG02293 | hp1 | a0001 | c0002 | t0004 | g0095 | AMR | PEL | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG02293 | hp2 | a0001 | c0002 | t0008 | g0136 | AMR | PEL | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0299 | AFR | ACB | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG02451 | hp2 | a0001 | c0004 | t0002 | g0266 | AFR | ACB | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | KHV | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0281 | EAS | KHV | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0306 | AFR | GWD | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0168 | AFR | GWD | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0243 | SAS | PJL | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0180 | SAS | PJL | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG02615 | hp1 | a0001 | c0003 | t0003 | g0027 | AFR | GWD | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG02615 | hp2 | a0001 | c0002 | t0003 | g0002 | AFR | GWD | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG02622 | hp1 | a0001 | c0003 | t0015 | g0032 | AFR | GWD | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG02622 | hp2 | a0001 | c0003 | t0003 | g0028 | AFR | GWD | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG02647 | hp1 | a0007 | c0010 | t0001 | g0042 | AFR | GWD | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0172 | AFR | GWD | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0237 | SAS | PJL | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0316 | SAS | PJL | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG02698 | hp1 | a0001 | c0001 | t0007 | g0165 | SAS | PJL | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG02698 | hp2 | a0001 | c0002 | t0004 | g0140 | SAS | PJL | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0218 | AFR | GWD | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG02717 | hp2 | a0001 | c0003 | t0003 | g0024 | AFR | GWD | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0175 | AFR | GWD | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG02723 | hp2 | a0001 | c0004 | t0002 | g0291 | AFR | GWD | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0345 | SAS | PJL | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0197 | SAS | PJL | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0162 | SAS | PJL | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0198 | SAS | PJL | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG02809 | hp1 | a0001 | c0004 | t0002 | g0267 | AFR | GWD | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | GWD | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0169 | AFR | GWD | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG02818 | hp2 | a0001 | c0003 | t0003 | g0035 | AFR | GWD | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG02886 | hp1 | a0001 | c0002 | t0003 | g0039 | AFR | GWD | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG02886 | hp2 | a0001 | c0003 | t0003 | g0034 | AFR | GWD | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG02895 | hp1 | a0001 | c0002 | t0001 | g0065 | AFR | GWD | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0301 | AFR | GWD | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG02897 | hp1 | a0001 | c0003 | t0003 | g0015 | AFR | GWD | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG02897 | hp2 | a0001 | c0002 | t0001 | g0066 | AFR | GWD | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0305 | AFR | ESN | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0213 | AFR | ESN | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG02965 | hp1 | a0001 | c0003 | t0003 | g0020 | AFR | ESN | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0300 | AFR | ESN | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG02970 | hp1 | a0001 | c0006 | t0006 | g0022 | AFR | ESN | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG02970 | hp2 | a0001 | c0004 | t0002 | g0307 | AFR | ESN | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG02976 | hp1 | a0001 | c0003 | t0003 | g0019 | AFR | ESN | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG02976 | hp2 | a0001 | c0006 | t0006 | g0016 | AFR | ESN | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG03017 | hp1 | a0001 | c0002 | t0001 | g0063 | SAS | PJL | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0248 | SAS | PJL | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0290 | AFR | GWD | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG03041 | hp2 | a0001 | c0003 | t0003 | g0017 | AFR | GWD | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG03098 | hp1 | a0001 | c0002 | t0001 | g0011 | AFR | MSL | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0298 | AFR | MSL | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0214 | AFR | ESN | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0297 | AFR | ESN | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0296 | AFR | ESN | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG03139 | hp2 | a0001 | c0004 | t0002 | g0171 | AFR | ESN | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0215 | AFR | ESN | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG03195 | hp2 | a0001 | c0006 | t0006 | g0023 | AFR | ESN | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG03209 | hp1 | a0001 | c0005 | t0002 | g0041 | AFR | MSL | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG03209 | hp2 | a0001 | c0003 | t0003 | g0029 | AFR | MSL | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG03225 | hp1 | a0001 | c0006 | t0006 | g0031 | AFR | MSL | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG03225 | hp2 | a0001 | c0002 | t0001 | g0013 | AFR | MSL | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG03239 | hp1 | a0004 | c0007 | t0001 | g0222 | SAS | PJL | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0259 | SAS | PJL | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0186 | AFR | MSL | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0302 | AFR | MSL | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG03486 | hp1 | a0001 | c0006 | t0006 | g0026 | AFR | MSL | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0174 | AFR | MSL | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0319 | SAS | PJL | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG03492 | hp2 | a0001 | c0001 | t0004 | g0236 | SAS | PJL | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG03516 | hp1 | a0001 | c0005 | t0002 | g0012 | AFR | ESN | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0295 | AFR | ESN | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG03579 | hp1 | a0001 | c0003 | t0003 | g0037 | AFR | MSL | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG03579 | hp2 | a0001 | c0003 | t0003 | g0018 | AFR | MSL | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG03669 | hp1 | a0001 | c0004 | t0002 | g0338 | SAS | PJL | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG03669 | hp2 | a0001 | c0002 | t0001 | g0079 | SAS | PJL | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0156 | SAS | PJL | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG03704 | hp2 | a0001 | c0005 | t0002 | g0102 | SAS | PJL | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG03710 | hp1 | a0001 | c0002 | t0001 | g0067 | SAS | PJL | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0227 | SAS | PJL | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0327 | SAS | BEB | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG03831 | hp2 | a0001 | c0004 | t0002 | g0272 | SAS | BEB | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0253 | SAS | BEB | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0349 | SAS | BEB | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0280 | SAS | BEB | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG03927 | hp2 | a0001 | c0001 | t0004 | g0340 | SAS | BEB | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG03942 | hp1 | a0001 | c0004 | t0002 | g0202 | SAS | BEB | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG03942 | hp2 | a0001 | c0001 | t0004 | g0235 | SAS | BEB | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0220 | SAS | STU | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0260 | SAS | STU | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0265 | SAS | BEB | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0199 | SAS | BEB | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0233 | SAS | STU | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG04199 | hp2 | a0001 | c0001 | t0013 | g0264 | SAS | STU | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG04204 | hp1 | a0005 | c0013 | t0002 | g0263 | SAS | STU | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0283 | SAS | STU | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG04228 | hp1 | a0001 | c0002 | t0001 | g0085 | SAS | STU | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0262 | SAS | STU | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0167 | AFR | YRI | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0289 | AFR | YRI | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0330 | EAS | CHB | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA18612 | hp2 | a0001 | c0002 | t0001 | g0084 | EAS | CHB | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA18747 | hp1 | a0006 | c0012 | t0001 | g0347 | EAS | CHB | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0339 | EAS | CHB | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0271 | AFR | YRI | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0173 | AFR | YRI | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0322 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA18946 | hp2 | a0001 | c0002 | t0001 | g0103 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA18947 | hp2 | a0001 | c0002 | t0001 | g0075 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA18953 | hp1 | a0001 | c0002 | t0012 | g0080 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA18957 | hp1 | a0001 | c0002 | t0001 | g0055 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA18959 | hp2 | a0001 | c0002 | t0004 | g0072 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA18960 | hp1 | a0001 | c0002 | t0001 | g0074 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA18962 | hp1 | a0001 | c0002 | t0001 | g0087 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA18962 | hp2 | a0002 | c0009 | t0001 | g0344 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA18966 | hp1 | a0001 | c0002 | t0001 | g0117 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA18967 | hp1 | a0001 | c0002 | t0001 | g0108 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0311 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0314 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0313 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0312 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA18973 | hp1 | a0001 | c0002 | t0001 | g0054 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0329 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA18979 | hp1 | a0001 | c0002 | t0001 | g0115 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0328 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA18980 | hp2 | a0001 | c0002 | t0001 | g0077 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0337 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA18990 | hp2 | a0001 | c0002 | t0001 | g0076 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA18991 | hp1 | a0001 | c0002 | t0001 | g0109 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA18993 | hp1 | a0001 | c0002 | t0001 | g0064 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA18994 | hp1 | a0001 | c0002 | t0001 | g0070 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA18994 | hp2 | a0001 | c0002 | t0001 | g0091 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0346 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA18995 | hp2 | a0001 | c0002 | t0001 | g0114 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0326 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA19005 | hp1 | a0001 | c0002 | t0001 | g0078 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA19005 | hp2 | a0001 | c0002 | t0001 | g0113 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0343 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0350 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA19009 | hp1 | a0001 | c0002 | t0001 | g0119 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA19009 | hp2 | a0001 | c0002 | t0001 | g0111 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA19011 | hp1 | a0001 | c0002 | t0001 | g0053 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA19030 | hp1 | a0001 | c0004 | t0014 | g0242 | AFR | LWK | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA19030 | hp2 | a0001 | c0005 | t0002 | g0009 | AFR | LWK | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA19043 | hp1 | a0001 | c0004 | t0002 | g0144 | AFR | LWK | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA19043 | hp2 | a0001 | c0004 | t0002 | g0179 | AFR | LWK | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA19054 | hp1 | a0001 | c0002 | t0007 | g0047 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA19056 | hp1 | a0001 | c0002 | t0001 | g0045 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA19056 | hp2 | a0001 | c0002 | t0001 | g0107 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA19060 | hp1 | a0001 | c0002 | t0001 | g0112 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA19060 | hp2 | a0001 | c0002 | t0001 | g0057 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0335 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0341 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA19065 | hp2 | a0002 | c0009 | t0001 | g0342 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA19068 | hp2 | a0001 | c0002 | t0001 | g0062 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA19070 | hp2 | a0001 | c0002 | t0001 | g0116 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA19074 | hp1 | a0001 | c0002 | t0001 | g0120 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA19077 | hp2 | a0001 | c0001 | t0007 | g0208 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA19079 | hp2 | a0001 | c0002 | t0001 | g0058 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA19083 | hp1 | a0001 | c0002 | t0001 | g0092 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA19083 | hp2 | a0001 | c0002 | t0001 | g0118 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0333 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0325 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0324 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0181 | AFR | YRI | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA19240 | hp2 | a0001 | c0002 | t0001 | g0008 | AFR | YRI | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA20129 | hp1 | a0001 | c0002 | t0005 | g0141 | AFR | ASW | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA20129 | hp2 | a0001 | c0006 | t0006 | g0025 | AFR | ASW | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA20752 | hp1 | a0001 | c0004 | t0002 | g0183 | EUR | TSI | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA20752 | hp2 | a0001 | c0005 | t0002 | g0098 | EUR | TSI | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA20905 | hp1 | a0001 | c0002 | t0001 | g0121 | SAS | GIH | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0178 | SAS | GIH | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG01123 | hp1 | a0001 | c0002 | t0001 | g0104 | AMR | CLM | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0163 | AMR | CLM | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG02109 | hp1 | a0001 | c0002 | t0001 | g0124 | AFR | ACB | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | ACB | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0166 | AFR | ACB | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG02486 | hp2 | a0001 | c0005 | t0002 | g0060 | AFR | ACB | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0182 | AFR | ACB | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG02559 | hp2 | a0001 | c0003 | t0003 | g0036 | AFR | ACB | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG03471 | hp1 | a0001 | c0011 | t0011 | g0003 | AFR | MSL | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0293 | AFR | MSL | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0288 | AFR | USA | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG06807 | hp2 | a0001 | c0002 | t0001 | g0083 | AFR | USA | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0303 | AFR | USA | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0287 | AFR | USA | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA21309 | hp1 | a0001 | c0004 | t0002 | g0149 | AFR | LWK | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA21309 | hp2 | a0001 | c0002 | t0001 | g0006 | AFR | LWK | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0002 | t0001 | g0068 | REF | REF | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0282 | REF | REF | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:22814725
|
T | G | 1 | a0004 | 2 | HG00639.hp2 HG03239.hp1 |
missense_variant | MODERATE | c.115T>G | p.Cys39Gly | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/2 | 564/2329 | 115/1104 | 39/367 | chr16 | 22814725 | ||
| chr16:22814741
|
T | C | 1 | a0003 | 2 | HG01070.hp2 HG01071.hp1 |
missense_variant | MODERATE | c.131T>C | p.Leu44Pro | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/2 | 580/2329 | 131/1104 | 44/367 | chr16 | 22814741 | ||
| chr16:22814756
|
T | C | 1 | a0002 | 2 | NA18962.hp2 NA19065.hp2 |
missense_variant | MODERATE | c.146T>C | p.Leu49Pro | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/2 | 595/2329 | 146/1104 | 49/367 | chr16 | 22814756 | ||
| chr16:22814794
|
G | A | 1 | a0007 | 1 | HG02647.hp1 | missense_variant | MODERATE | c.184G>A | p.Gly62Ser | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/2 | 633/2329 | 184/1104 | 62/367 | chr16 | 22814794 | ||
| chr16:22814853
|
C | G | 1 | a0005 | 1 | HG04204.hp1 | missense_variant | MODERATE | c.243C>G | p.Ser81Arg | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/2 | 692/2329 | 243/1104 | 81/367 | chr16 | 22814853 | ||
| chr16:22814900
|
G | T | 1 | a0006 | 1 | NA18747.hp1 | missense_variant | MODERATE | c.290G>T | p.Arg97Leu | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/2 | 739/2329 | 290/1104 | 97/367 | chr16 | 22814900 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:22815000
|
G | A | 2 | a0001c0003a0001c0006 | 23 | HG01496.hp2 HG01891.hp1 HG01934.hp1 others(20): Show |
synonymous_variant | LOW | c.390G>A | p.Val130Val | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/2 | 839/2329 | 390/1104 | 130/367 | chr16 | 22815000 | ||
| chr16:22815018
|
A | G | 6 | a0001c0002a0001c0003a0001c0005others(3): Show | 145 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(142): Show |
synonymous_variant | LOW | c.408A>G | p.Val136Val | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/2 | 857/2329 | 408/1104 | 136/367 | chr16 | 22815018 | ||
| chr16:22915190
|
A | G | 6 | a0001c0004a0001c0005a0001c0006others(3): Show | 40 | HG00639.hp1 HG00735.hp2 HG00738.hp2 others(37): Show |
synonymous_variant | LOW | c.732A>G | p.Ser244Ser | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 2/2 | 1181/2329 | 732/1104 | 244/367 | chr16 | 22915190 | ||
| chr16:22915361
|
G | A | 1 | a0001c0011 | 1 | HG03471.hp1 | synonymous_variant | LOW | c.903G>A | p.Lys301Lys | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 2/2 | 1352/2329 | 903/1104 | 301/367 | chr16 | 22915361 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:22814223
|
G | T | 1 | a0001c0003t0015 | 1 | HG02622.hp1 | 5_prime_UTR_variant | MODIFIER | c.-388G>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/2 | 388 | chr16 | 22814223 | |||||
| chr16:22814254
|
C | A | 1 | a0001c0002t0010 | 1 | HG02258.hp1 | 5_prime_UTR_variant | MODIFIER | c.-357C>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/2 | 357 | chr16 | 22814254 | |||||
| chr16:22814317
|
G | A | 6 | a0001c0002t0003a0001c0003t0003a0001c0003t0015others(3): Show | 28 | HG01167.hp2 HG01496.hp2 HG01884.hp1 others(25): Show |
5_prime_UTR_variant | MODIFIER | c.-294G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/2 | 294 | chr16 | 22814317 | |||||
| chr16:22814428
|
C | G | 2 | a0001c0002t0005a0001c0002t0008 | 14 | HG01255.hp1 HG01261.hp1 HG01928.hp1 others(11): Show |
5_prime_UTR_variant | MODIFIER | c.-183C>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/2 | 183 | chr16 | 22814428 | |||||
| chr16:22814507
|
C | G | 6 | a0001c0002t0003a0001c0003t0003a0001c0003t0015others(3): Show | 28 | HG01167.hp2 HG01496.hp2 HG01884.hp1 others(25): Show |
5_prime_UTR_variant | MODIFIER | c.-104C>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/2 | 104 | chr16 | 22814507 | |||||
| chr16:22814539
|
C | T | 1 | a0001c0004t0014 | 1 | NA19030.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-72C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/2 | chr16 | 22814539 | ||||||
| chr16:22814568
|
G | GC | 2 | a0001c0001t0007a0001c0002t0007 | 6 | HG00544.hp1 HG02055.hp2 HG02071.hp2 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-38dupC | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/2 | 37 | INFO_REALIGN_3_PRIME | chr16 | 22814568 | ||||
| chr16:22915635
|
G | T | 7 | a0001c0004t0002a0001c0004t0014a0001c0005t0002others(4): Show | 39 | HG00639.hp1 HG00735.hp2 HG00738.hp2 others(36): Show |
3_prime_UTR_variant | MODIFIER | c.*73G>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 2/2 | 73 | chr16 | 22915635 | |||||
| chr16:22915736
|
C | T | 7 | a0001c0004t0002a0001c0004t0014a0001c0005t0002others(4): Show | 39 | HG00639.hp1 HG00735.hp2 HG00738.hp2 others(36): Show |
3_prime_UTR_variant | MODIFIER | c.*174C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 2/2 | 174 | chr16 | 22915736 | |||||
| chr16:22915801
|
T | C | 1 | a0001c0002t0012 | 1 | NA18953.hp1 | 3_prime_UTR_variant | MODIFIER | c.*239T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 2/2 | 239 | chr16 | 22915801 | |||||
| chr16:22915891
|
G | T | 1 | a0001c0001t0009 | 2 | HG00438.hp2 HG02040.hp2 |
3_prime_UTR_variant | MODIFIER | c.*329G>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 2/2 | 329 | chr16 | 22915891 | |||||
| chr16:22915893
|
T | C | 10 | a0001c0001t0004a0001c0002t0004a0001c0002t0008others(7): Show | 59 | HG00639.hp1 HG00735.hp2 HG00738.hp2 others(56): Show |
3_prime_UTR_variant | MODIFIER | c.*331T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 2/2 | 331 | chr16 | 22915893 | |||||
| chr16:22915934
|
A | G | 1 | a0001c0001t0013 | 1 | HG04199.hp2 | 3_prime_UTR_variant | MODIFIER | c.*372A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 2/2 | 372 | chr16 | 22915934 | |||||
| chr16:22915968
|
G | A | 1 | a0001c0011t0011 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*406G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 2/2 | 406 | chr16 | 22915968 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:22815145
|
T | C | 1 | a0001c0001t0001g0001 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.485+50T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22815145 | ||||||
| chr16:22815277
|
G | A | 2 | a0001c0002t0003g0002a0001c0011t0011g0003 | 2 | HG02615.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.485+182G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22815277 | ||||||
| chr16:22815442
|
G | A | 11 | a0001c0002t0001g0006a0001c0002t0001g0007a0001c0002t0001g0008others(8): Show | 11 | HG00639.hp1 HG01256.hp1 HG01346.hp1 others(8): Show |
intron_variant | MODIFIER | c.485+347G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22815442 | ||||||
| chr16:22815612
|
C | G | 41 | a0001c0001t0001g0001a0001c0001t0001g0311a0001c0001t0001g0312others(38): Show | 41 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(38): Show |
intron_variant | MODIFIER | c.485+517C>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22815612 | ||||||
| chr16:22815732
|
G | A | 31 | a0001c0002t0003g0002a0001c0002t0003g0039a0001c0002t0010g0043others(28): Show | 31 | HG01167.hp2 HG01496.hp2 HG01884.hp1 others(28): Show |
intron_variant | MODIFIER | c.485+637G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22815732 | ||||||
| chr16:22815840
|
C | A | 26 | a0001c0002t0003g0039a0001c0003t0003g0015a0001c0003t0003g0017others(23): Show | 26 | HG01167.hp2 HG01496.hp2 HG01884.hp1 others(23): Show |
intron_variant | MODIFIER | c.485+745C>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22815840 | ||||||
| chr16:22815847
|
G | A | 142 | a0001c0002t0001g0006a0001c0002t0001g0007a0001c0002t0001g0008others(139): Show | 142 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(139): Show |
intron_variant | MODIFIER | c.485+752G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22815847 | ||||||
| chr16:22816051
|
A | C | 1 | a0001c0001t0001g0350 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.485+956A>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22816051 | ||||||
| chr16:22816140
|
T | A | 2 | a0001c0002t0003g0002a0001c0011t0011g0003 | 2 | HG02615.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.485+1045T>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22816140 | ||||||
| chr16:22816196
|
A | C | 151 | a0001c0001t0001g0286a0001c0001t0001g0287a0001c0001t0001g0288others(148): Show | 151 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(148): Show |
intron_variant | MODIFIER | c.485+1101A>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22816196 | ||||||
| chr16:22816256
|
G | A | 2 | a0001c0002t0003g0002a0001c0011t0011g0003 | 2 | HG02615.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.485+1161G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22816256 | ||||||
| chr16:22816315
|
T | G | 25 | a0001c0002t0001g0006a0001c0003t0003g0017a0001c0003t0003g0018others(22): Show | 25 | HG01256.hp1 HG01346.hp1 HG01496.hp2 others(22): Show |
intron_variant | MODIFIER | c.485+1220T>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22816315 | ||||||
| chr16:22816392
|
A | G | 26 | a0001c0002t0001g0121a0001c0002t0001g0122a0001c0002t0001g0124others(23): Show | 26 | HG00140.hp2 HG00280.hp1 HG01168.hp1 others(23): Show |
intron_variant | MODIFIER | c.485+1297A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22816392 | ||||||
| chr16:22816415
|
A | G | 22 | a0001c0003t0003g0017a0001c0003t0003g0018a0001c0003t0003g0019others(19): Show | 22 | HG01496.hp2 HG01891.hp1 HG01934.hp1 others(19): Show |
intron_variant | MODIFIER | c.485+1320A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22816415 | ||||||
| chr16:22816423
|
C | T | 11 | a0001c0002t0001g0110a0001c0002t0001g0111a0001c0002t0001g0112others(8): Show | 11 | HG01106.hp2 NA18966.hp1 NA18979.hp1 others(8): Show |
intron_variant | MODIFIER | c.485+1328C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22816423 | ||||||
| chr16:22816464
|
G | A | 2 | a0001c0001t0001g0145a0001c0004t0002g0144 | 2 | HG02809.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.485+1369G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22816464 | ||||||
| chr16:22816585
|
A | G | 1 | a0001c0001t0001g0349 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.485+1490A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22816585 | ||||||
| chr16:22817015
|
A | T | 1 | a0001c0002t0004g0059 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.485+1920A>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22817015 | ||||||
| chr16:22817031
|
T | C | 2 | a0001c0002t0003g0002a0001c0011t0011g0003 | 2 | HG02615.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.485+1936T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22817031 | ||||||
| chr16:22817125
|
T | A | 27 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0148others(24): Show | 27 | HG00741.hp2 HG01243.hp2 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.485+2030T>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22817125 | ||||||
| chr16:22817281
|
C | T | 1 | a0001c0001t0001g0284 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.485+2186C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22817281 | ||||||
| chr16:22817290
|
C | G | 3 | a0001c0002t0001g0107a0001c0002t0001g0108a0001c0002t0001g0109 | 3 | NA18967.hp1 NA18991.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.485+2195C>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22817290 | ||||||
| chr16:22817299
|
A | G | 1 | a0001c0002t0008g0143 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.485+2204A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22817299 | ||||||
| chr16:22817476
|
T | G | 1 | a0001c0003t0003g0020 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.485+2381T>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22817476 | ||||||
| chr16:22817550
|
T | C | 19 | a0001c0001t0001g0286a0001c0001t0001g0287a0001c0001t0001g0288others(16): Show | 19 | HG01243.hp2 HG01884.hp2 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.485+2455T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22817550 | ||||||
| chr16:22817689
|
T | C | 120 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0153others(117): Show | 120 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(117): Show |
intron_variant | MODIFIER | c.485+2594T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22817689 | ||||||
| chr16:22817892
|
GC | G | 98 | a0001c0001t0001g0166a0001c0001t0001g0167a0001c0001t0001g0168others(95): Show | 98 | HG00323.hp2 HG00544.hp1 HG00738.hp1 others(95): Show |
intron_variant | MODIFIER | c.485+2798delC | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22817892 | ||||||
| chr16:22817917
|
T | A | 1 | a0001c0001t0001g0350 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.485+2822T>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22817917 | ||||||
| chr16:22817918
|
A | T | 1 | a0001c0001t0001g0350 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.485+2823A>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22817918 | ||||||
| chr16:22817968
|
A | C | 1 | a0001c0001t0001g0350 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.485+2873A>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22817968 | ||||||
| chr16:22818137
|
G | A | 88 | a0001c0001t0001g0150a0001c0001t0001g0166a0001c0001t0001g0167others(85): Show | 88 | HG00323.hp2 HG00544.hp1 HG00738.hp1 others(85): Show |
intron_variant | MODIFIER | c.485+3042G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818137 | ||||||
| chr16:22818147
|
C | G | 1 | a0001c0001t0001g0283 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.485+3052C>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818147 | ||||||
| chr16:22818164
|
C | T | 3 | a0001c0001t0001g0298a0001c0003t0003g0036a0001c0003t0003g0037 | 3 | HG02559.hp2 HG03098.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.485+3069C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818164 | ||||||
| chr16:22818316
|
C | T | 1 | a0001c0001t0001g0297 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.485+3221C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818316 | ||||||
| chr16:22818555
|
G | A | 4 | a0001c0001t0001g0217a0001c0001t0001g0218a0001c0001t0001g0299others(1): Show | 4 | HG01175.hp2 HG01952.hp1 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.485+3460G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818555 | ||||||
| chr16:22818649
|
T | G | 3 | a0001c0002t0001g0107a0001c0002t0001g0108a0001c0002t0001g0109 | 3 | NA18967.hp1 NA18991.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.485+3554T>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818649 | ||||||
| chr16:22818665
|
T | TTCCTTCC others(9): Show |
9 | a0001c0001t0001g0216a0001c0001t0001g0292a0001c0001t0001g0293others(6): Show | 9 | HG01243.hp2 HG01884.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.485+3582_485+3583i others(18): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22818665 | |||||
| chr16:22818666
|
TCCTTCCT others(21): Show |
T | 3 | a0001c0001t0001g0217a0001c0001t0001g0218a0001c0001t0001g0299 | 3 | HG01175.hp2 HG02451.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.485+3583_485+3610d others(30): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22818666 | |||||
| chr16:22818669
|
T | TTCCTTCC others(5): Show |
7 | a0001c0001t0001g0286a0001c0001t0001g0287a0001c0001t0001g0288others(4): Show | 7 | HG01891.hp2 HG02145.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.485+3582_485+3583i others(14): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22818669 | |||||
| chr16:22818674
|
T | TCCTTCCC others(294): Show |
1 | a0001c0001t0007g0285 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.485+3582_485+3583i others(303): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22818674 | |||||
| chr16:22818674
|
T | TCCTTCCC others(293): Show |
2 | a0001c0001t0001g0289a0001c0001t0001g0290 | 2 | HG03041.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.485+3582_485+3583i others(302): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22818674 | |||||
| chr16:22818678
|
C | T | 7 | a0001c0001t0001g0286a0001c0001t0001g0287a0001c0001t0001g0288others(4): Show | 7 | HG01891.hp2 HG02145.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.485+3583C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818678 | ||||||
| chr16:22818686
|
CCTTGCCT others(413): Show |
C | 1 | a0001c0001t0001g0310 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.485+3593_485+4012d others(2): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22818686 | |||||
| chr16:22818688
|
T | C | 19 | a0001c0001t0001g0216a0001c0001t0001g0286a0001c0001t0001g0287others(16): Show | 19 | HG01243.hp2 HG01884.hp2 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.485+3593T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818688 | ||||||
| chr16:22818690
|
G | C | 10 | a0001c0001t0001g0286a0001c0001t0001g0287a0001c0001t0001g0288others(7): Show | 10 | HG01891.hp2 HG02055.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.485+3595G>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818690 | ||||||
| chr16:22818690
|
G | T | 9 | a0001c0001t0001g0216a0001c0001t0001g0292a0001c0001t0001g0293others(6): Show | 9 | HG01243.hp2 HG01884.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.485+3595G>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818690 | ||||||
| chr16:22818694
|
G | T | 19 | a0001c0001t0001g0216a0001c0001t0001g0286a0001c0001t0001g0287others(16): Show | 19 | HG01243.hp2 HG01884.hp2 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.485+3599G>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818694 | ||||||
| chr16:22818705
|
T | C | 1 | a0001c0005t0002g0004 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.485+3610T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818705 | ||||||
| chr16:22818709
|
C | T | 17 | a0001c0001t0001g0216a0001c0001t0001g0286a0001c0001t0001g0287others(14): Show | 17 | HG01243.hp2 HG01346.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.485+3614C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818709 | ||||||
| chr16:22818715
|
C | A | 1 | a0001c0001t0001g0219 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.485+3620C>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818715 | ||||||
| chr16:22818720
|
CT | C | 12 | a0001c0001t0001g0217a0001c0001t0001g0218a0001c0001t0001g0299others(9): Show | 12 | HG01109.hp2 HG01175.hp2 HG01256.hp1 others(9): Show |
intron_variant | MODIFIER | c.485+3627delT | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22818720 | |||||
| chr16:22818721
|
T | C | 1 | a0001c0005t0002g0004 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.485+3626T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818721 | ||||||
| chr16:22818724
|
C | T | 1 | a0001c0001t0001g0219 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.485+3629C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818724 | ||||||
| chr16:22818725
|
C | T | 19 | a0001c0001t0001g0216a0001c0001t0001g0286a0001c0001t0001g0287others(16): Show | 19 | HG01243.hp2 HG01884.hp2 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.485+3630C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818725 | ||||||
| chr16:22818729
|
C | T | 20 | a0001c0001t0001g0216a0001c0001t0001g0219a0001c0001t0001g0286others(17): Show | 20 | HG01243.hp2 HG01884.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.485+3634C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818729 | ||||||
| chr16:22818732
|
C | A | 16 | a0001c0001t0001g0216a0001c0001t0001g0286a0001c0001t0001g0287others(13): Show | 16 | HG01243.hp2 HG01884.hp2 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.485+3637C>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818732 | ||||||
| chr16:22818733
|
C | T | 17 | a0001c0001t0001g0216a0001c0001t0001g0219a0001c0001t0001g0286others(14): Show | 17 | HG01243.hp2 HG01884.hp2 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.485+3638C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818733 | ||||||
| chr16:22818733
|
CTCCT | C | 17 | a0001c0001t0001g0151a0001c0001t0001g0153a0001c0001t0001g0154others(14): Show | 17 | HG00280.hp2 HG01070.hp1 HG01257.hp1 others(14): Show |
intron_variant | MODIFIER | c.485+3642_485+3645d others(6): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22818733 | |||||
| chr16:22818734
|
T | TC | 6 | a0001c0002t0001g0045a0001c0002t0001g0074a0001c0002t0001g0075others(3): Show | 6 | HG01978.hp2 HG03239.hp1 NA18947.hp2 others(3): Show |
intron_variant | MODIFIER | c.485+3641dupC | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22818734 | |||||
| chr16:22818737
|
T | C | 303 | a0001c0001t0001g0001a0001c0001t0001g0145a0001c0001t0001g0146others(300): Show | 303 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(300): Show |
intron_variant | MODIFIER | c.485+3642T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818737 | ||||||
| chr16:22818738
|
TC | T | 3 | a0001c0001t0001g0289a0001c0001t0001g0290a0001c0001t0007g0285 | 3 | HG02055.hp2 HG03041.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.485+3646delC | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22818738 | |||||
| chr16:22818739
|
C | CCTTCCTT others(76): Show |
6 | a0001c0002t0001g0045a0001c0002t0001g0074a0001c0002t0001g0075others(3): Show | 6 | HG01978.hp2 HG03239.hp1 NA18947.hp2 others(3): Show |
intron_variant | MODIFIER | c.485+3645_485+3646i others(85): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22818739 | |||||
| chr16:22818739
|
C | T | 303 | a0001c0001t0001g0001a0001c0001t0001g0145a0001c0001t0001g0146others(300): Show | 303 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(300): Show |
intron_variant | MODIFIER | c.485+3644C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818739 | ||||||
| chr16:22818741
|
CT | C | 16 | a0001c0001t0001g0216a0001c0001t0001g0286a0001c0001t0001g0287others(13): Show | 16 | HG01243.hp2 HG01884.hp2 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.485+3648delT | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22818741 | |||||
| chr16:22818749
|
C | A | 1 | a0001c0001t0001g0219 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.485+3654C>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818749 | ||||||
| chr16:22818753
|
C | A | 3 | a0001c0002t0001g0124a0001c0005t0002g0004a0001c0005t0002g0041 | 3 | HG01346.hp1 HG02109.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.485+3658C>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818753 | ||||||
| chr16:22818754
|
T | TTCCC | 45 | a0001c0001t0001g0001a0001c0001t0001g0161a0001c0001t0001g0223others(42): Show | 45 | HG00423.hp1 HG00438.hp1 HG00609.hp2 others(42): Show |
intron_variant | MODIFIER | c.485+3662_485+3663i others(6): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22818754 | |||||
| chr16:22818758
|
T | C | 19 | a0001c0001t0001g0216a0001c0001t0001g0286a0001c0001t0001g0287others(16): Show | 19 | HG01243.hp2 HG01884.hp2 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.485+3663T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818758 | ||||||
| chr16:22818761
|
A | ATTCCTTC others(17): Show |
1 | a0001c0002t0007g0044 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.485+3678_485+3679i others(26): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22818761 | |||||
| chr16:22818761
|
A | ATTCCTTC others(309): Show |
1 | a0001c0004t0002g0179 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.485+3678_485+3679i others(318): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22818761 | |||||
| chr16:22818761
|
A | C | 75 | a0001c0001t0001g0001a0001c0001t0001g0161a0001c0001t0001g0213others(72): Show | 75 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(72): Show |
intron_variant | MODIFIER | c.485+3666A>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818761 | ||||||
| chr16:22818766
|
TTCCTTCC others(32): Show |
T | 1 | a0001c0001t0001g0219 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.485+3672_485+3710d others(41): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818766 | ||||||
| chr16:22818769
|
C | A | 2 | a0001c0001t0001g0217a0001c0001t0001g0218 | 2 | HG01175.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.485+3674C>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818769 | ||||||
| chr16:22818770
|
TTCCC | T | 6 | a0001c0002t0001g0045a0001c0002t0001g0074a0001c0002t0001g0075others(3): Show | 6 | HG01978.hp2 HG03239.hp1 NA18947.hp2 others(3): Show |
intron_variant | MODIFIER | c.485+3679_485+3682d others(6): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22818770 | |||||
| chr16:22818773
|
C | A | 5 | a0001c0001t0001g0213a0001c0001t0001g0214a0001c0001t0001g0215others(2): Show | 5 | HG02258.hp1 HG02451.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.485+3678C>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818773 | ||||||
| chr16:22818774
|
C | G | 9 | a0001c0001t0001g0302a0001c0001t0001g0303a0001c0001t0001g0305others(6): Show | 9 | HG01109.hp2 HG01256.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.485+3679C>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818774 | ||||||
| chr16:22818774
|
C | T | 88 | a0001c0001t0001g0166a0001c0001t0001g0167a0001c0001t0001g0168others(85): Show | 88 | HG00323.hp1 HG00323.hp2 HG00738.hp1 others(85): Show |
intron_variant | MODIFIER | c.485+3679C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818774 | ||||||
| chr16:22818775
|
T | C | 6 | a0001c0002t0001g0045a0001c0002t0001g0074a0001c0002t0001g0075others(3): Show | 6 | HG01978.hp2 HG03239.hp1 NA18947.hp2 others(3): Show |
intron_variant | MODIFIER | c.485+3680T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818775 | ||||||
| chr16:22818778
|
T | C | 2 | a0001c0001t0001g0217a0001c0001t0001g0218 | 2 | HG01175.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.485+3683T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818778 | ||||||
| chr16:22818782
|
T | C | 91 | a0001c0001t0001g0166a0001c0001t0001g0167a0001c0001t0001g0168others(88): Show | 91 | HG00323.hp1 HG00323.hp2 HG00738.hp1 others(88): Show |
intron_variant | MODIFIER | c.485+3687T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818782 | ||||||
| chr16:22818785
|
CT | C | 13 | a0001c0001t0001g0216a0001c0001t0001g0289a0001c0001t0001g0290others(10): Show | 13 | HG01884.hp2 HG02055.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.485+3692delT | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22818785 | |||||
| chr16:22818786
|
T | TCCC | 7 | a0001c0001t0001g0286a0001c0001t0001g0287a0001c0001t0001g0288others(4): Show | 7 | HG00544.hp1 HG01243.hp2 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.485+3691_485+3692i others(5): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818786 | ||||||
| chr16:22818786
|
T | TTCCCTCC others(8): Show |
4 | a0001c0001t0001g0150a0001c0002t0001g0064a0001c0002t0001g0067others(1): Show | 4 | HG02109.hp1 HG03710.hp1 NA18993.hp1 others(1): Show |
intron_variant | MODIFIER | c.485+3698_485+3699i others(17): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22818786 | |||||
| chr16:22818790
|
C | T | 98 | a0001c0001t0001g0166a0001c0001t0001g0167a0001c0001t0001g0168others(95): Show | 98 | HG00323.hp1 HG00323.hp2 HG00738.hp1 others(95): Show |
intron_variant | MODIFIER | c.485+3695C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818790 | ||||||
| chr16:22818791
|
TCCCTC | T | 6 | a0001c0002t0001g0045a0001c0002t0001g0074a0001c0002t0001g0075others(3): Show | 6 | HG01978.hp2 HG03239.hp1 NA18947.hp2 others(3): Show |
intron_variant | MODIFIER | c.485+3699_485+3703d others(7): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22818791 | |||||
| chr16:22818792
|
C | CCTTCCTT others(48): Show |
2 | a0001c0002t0001g0065a0001c0002t0001g0066 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.485+3698_485+3699i others(57): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22818792 | |||||
| chr16:22818794
|
C | T | 132 | a0001c0001t0001g0001a0001c0001t0001g0161a0001c0001t0001g0166others(129): Show | 132 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(129): Show |
intron_variant | MODIFIER | c.485+3699C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818794 | ||||||
| chr16:22818796
|
C | CCTTCCTC others(64): Show |
35 | a0001c0001t0001g0001a0001c0001t0001g0161a0001c0001t0001g0223others(32): Show | 35 | HG00423.hp1 HG00438.hp1 HG00609.hp2 others(32): Show |
intron_variant | MODIFIER | c.485+3702_485+3703i others(73): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22818796 | |||||
| chr16:22818796
|
C | CCTTCCTT others(260): Show |
4 | a0001c0001t0001g0213a0001c0001t0001g0214a0001c0001t0001g0215others(1): Show | 4 | HG02258.hp1 HG02922.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.485+3702_485+3703i others(269): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22818796 | |||||
| chr16:22818798
|
C | T | 6 | a0001c0002t0001g0068a0001c0002t0001g0069a0001c0002t0001g0110others(3): Show | 6 | HG00639.hp2 HG01081.hp2 HG01106.hp2 others(3): Show |
intron_variant | MODIFIER | c.485+3703C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818798 | ||||||
| chr16:22818799
|
TC | T | 10 | a0001c0001t0001g0299a0001c0001t0001g0302a0001c0001t0001g0303others(7): Show | 10 | HG01109.hp2 HG01256.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.485+3707delC | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22818799 | |||||
| chr16:22818800
|
C | CCCTT | 115 | a0001c0001t0001g0145a0001c0001t0001g0147a0001c0001t0001g0148others(112): Show | 115 | HG00140.hp1 HG00438.hp2 HG00544.hp2 others(112): Show |
intron_variant | MODIFIER | c.485+3736_485+3739d others(6): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22818800 | |||||
| chr16:22818800
|
C | CCCTTCCT others(1): Show |
4 | a0001c0001t0001g0279a0001c0001t0001g0280a0001c0001t0001g0317others(1): Show | 4 | HG01123.hp1 HG02165.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.485+3732_485+3739d others(10): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22818800 | |||||
| chr16:22818800
|
C | CCTCCCTC others(60): Show |
6 | a0001c0002t0001g0068a0001c0002t0001g0069a0001c0002t0001g0110others(3): Show | 6 | HG00639.hp2 HG01081.hp2 HG01106.hp2 others(3): Show |
intron_variant | MODIFIER | c.485+3706_485+3707i others(69): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22818800 | |||||
| chr16:22818800
|
C | CCTTCCTT others(316): Show |
11 | a0001c0001t0001g0166a0001c0001t0001g0167a0001c0001t0001g0168others(8): Show | 11 | HG02280.hp2 HG02486.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.485+3706_485+3707i others(325): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22818800 | |||||
| chr16:22818800
|
C | CCTTCCTT others(318): Show |
1 | a0001c0001t0001g0350 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.485+3706_485+3707i others(327): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22818800 | |||||
| chr16:22818800
|
C | CCTTCCTT others(320): Show |
1 | a0001c0002t0005g0125 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.485+3706_485+3707i others(329): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22818800 | |||||
| chr16:22818800
|
C | CCTTCCTT others(296): Show |
2 | a0001c0002t0001g0126a0001c0002t0001g0127 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.485+3706_485+3707i others(305): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22818800 | |||||
| chr16:22818800
|
C | CCTTCCTT others(296): Show |
2 | a0001c0001t0001g0176a0001c0001t0001g0177 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.485+3706_485+3707i others(305): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22818800 | |||||
| chr16:22818800
|
C | CCTTCCTT others(316): Show |
1 | a0001c0001t0001g0178 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.485+3706_485+3707i others(325): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22818800 | |||||
| chr16:22818800
|
C | CCTTCCTT others(288): Show |
3 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0002t0005g0128 | 3 | HG01975.hp2 HG02559.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.485+3706_485+3707i others(297): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22818800 | |||||
| chr16:22818800
|
C | CCTTCCTT others(300): Show |
2 | a0001c0004t0002g0183a0001c0004t0002g0184 | 2 | HG01361.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.485+3706_485+3707i others(309): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22818800 | |||||
| chr16:22818800
|
C | CCTTCCTT others(316): Show |
1 | a0001c0001t0001g0180 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.485+3706_485+3707i others(325): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22818800 | |||||
| chr16:22818800
|
C | CCTTCCTT others(304): Show |
4 | a0001c0001t0001g0186a0001c0003t0003g0018a0001c0003t0003g0021others(1): Show | 4 | HG01891.hp1 HG02647.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.485+3706_485+3707i others(313): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22818800 | |||||
| chr16:22818800
|
C | CCTTCCTT others(316): Show |
4 | a0001c0001t0001g0320a0001c0001t0001g0321a0001c0002t0001g0105others(1): Show | 4 | HG00323.hp1 HG00323.hp2 HG01168.hp2 others(1): Show |
intron_variant | MODIFIER | c.485+3706_485+3707i others(325): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22818800 | |||||
| chr16:22818800
|
C | CCTTCCTT others(320): Show |
39 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0189others(36): Show | 39 | HG01255.hp1 HG01261.hp1 HG01361.hp1 others(36): Show |
intron_variant | MODIFIER | c.485+3706_485+3707i others(329): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22818800 | |||||
| chr16:22818800
|
C | CCTTCCTT others(392): Show |
3 | a0001c0001t0001g0185a0001c0001t0001g0318a0001c0001t0001g0319 | 3 | HG00738.hp1 HG01993.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.485+3706_485+3707i others(401): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22818800 | |||||
| chr16:22818800
|
C | CCTTCCTT others(316): Show |
2 | a0001c0001t0001g0284a0001c0001t0007g0208 | 2 | NA18942.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.485+3706_485+3707i others(325): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22818800 | |||||
| chr16:22818800
|
C | CCTTCCTT others(320): Show |
1 | a0001c0001t0001g0210 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.485+3706_485+3707i others(329): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22818800 | |||||
| chr16:22818800
|
C | CCTTCCTT others(324): Show |
1 | a0001c0001t0009g0209 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.485+3706_485+3707i others(333): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22818800 | |||||
| chr16:22818800
|
C | CCTTCCTT others(316): Show |
1 | a0001c0001t0001g0211 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.485+3706_485+3707i others(325): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22818800 | |||||
| chr16:22818800
|
C | CCTTCCTT others(248): Show |
1 | a0001c0006t0006g0022 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.485+3706_485+3707i others(257): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22818800 | |||||
| chr16:22818800
|
C | CCTTCCTT others(320): Show |
1 | a0001c0001t0001g0212 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.485+3706_485+3707i others(329): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22818800 | |||||
| chr16:22818800
|
C | T | 60 | a0001c0001t0001g0001a0001c0001t0001g0161a0001c0001t0001g0213others(57): Show | 60 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(57): Show |
intron_variant | MODIFIER | c.485+3705C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818800 | ||||||
| chr16:22818803
|
T | C | 67 | a0001c0001t0001g0166a0001c0001t0001g0167a0001c0001t0001g0168others(64): Show | 67 | HG01255.hp1 HG01261.hp1 HG01361.hp1 others(64): Show |
intron_variant | MODIFIER | c.485+3708T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818803 | ||||||
| chr16:22818803
|
T | TCCCTCCC others(289): Show |
1 | a0001c0005t0002g0004 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.485+3708_485+3709i others(298): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818803 | ||||||
| chr16:22818803
|
T | TCCCTCCC others(305): Show |
1 | a0001c0002t0001g0142 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.485+3708_485+3709i others(314): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818803 | ||||||
| chr16:22818807
|
T | C | 12 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0210others(9): Show | 12 | HG00323.hp1 HG00323.hp2 HG01168.hp1 others(9): Show |
intron_variant | MODIFIER | c.485+3712T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818807 | ||||||
| chr16:22818810
|
C | A | 1 | a0001c0002t0001g0124 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.485+3715C>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818810 | ||||||
| chr16:22818811
|
T | C | 5 | a0001c0001t0001g0217a0001c0001t0001g0218a0001c0001t0001g0219others(2): Show | 5 | HG01175.hp2 HG02717.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.485+3716T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818811 | ||||||
| chr16:22818812
|
T | C | 10 | a0001c0001t0001g0302a0001c0001t0001g0303a0001c0001t0001g0305others(7): Show | 10 | HG01109.hp2 HG01256.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.485+3717T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818812 | ||||||
| chr16:22818815
|
T | C | 1 | a0001c0001t0001g0299 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.485+3720T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818815 | ||||||
| chr16:22818816
|
T | C | 10 | a0001c0001t0001g0302a0001c0001t0001g0303a0001c0001t0001g0305others(7): Show | 10 | HG01109.hp2 HG01256.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.485+3721T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818816 | ||||||
| chr16:22818819
|
T | C | 117 | a0001c0001t0001g0001a0001c0001t0001g0161a0001c0001t0001g0166others(114): Show | 117 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.485+3724T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818819 | ||||||
| chr16:22818819
|
T | TTCCTTCA others(529): Show |
3 | a0001c0001t0001g0289a0001c0001t0001g0290a0001c0001t0007g0285 | 3 | HG02055.hp2 HG03041.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.485+3730_485+3731i others(538): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22818819 | |||||
| chr16:22818819
|
T | TTCCTTCC others(33): Show |
4 | a0001c0001t0001g0286a0001c0001t0001g0292a0001c0001t0001g0297others(1): Show | 4 | HG01243.hp2 HG01891.hp2 HG02145.hp2 others(1): Show |
intron_variant | MODIFIER | c.485+3738_485+3739i others(42): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22818819 | |||||
| chr16:22818819
|
T | TTCCTTCC others(37): Show |
8 | a0001c0001t0001g0216a0001c0001t0001g0287a0001c0001t0001g0294others(5): Show | 8 | HG01884.hp2 HG02145.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.485+3739_485+3740i others(46): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22818819 | |||||
| chr16:22818819
|
T | TTCCTTCC others(41): Show |
4 | a0001c0001t0001g0288a0001c0001t0001g0293a0001c0001t0001g0300others(1): Show | 4 | HG02723.hp2 HG02965.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.485+3739_485+3740i others(50): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22818819 | |||||
| chr16:22818819
|
TTCCTTCC others(9): Show |
T | 1 | a0001c0005t0002g0012 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.485+3737_485+3752d others(18): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22818819 | |||||
| chr16:22818820
|
T | C | 11 | a0001c0001t0001g0219a0001c0001t0001g0302a0001c0001t0001g0303others(8): Show | 11 | HG01109.hp2 HG01256.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.485+3725T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818820 | ||||||
| chr16:22818820
|
TCCTTCCT others(29): Show |
T | 15 | a0001c0001t0001g0146a0001c0003t0003g0020a0001c0003t0003g0024others(12): Show | 15 | HG01496.hp2 HG01934.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.485+3729_485+3764d others(38): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22818820 | |||||
| chr16:22818821
|
C | CCTTCATT others(51): Show |
1 | a0001c0002t0001g0064 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.485+3730_485+3731i others(60): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22818821 | |||||
| chr16:22818823
|
T | C | 19 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0210others(16): Show | 19 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(16): Show |
intron_variant | MODIFIER | c.485+3728T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818823 | ||||||
| chr16:22818823
|
TTCCTTCC others(5): Show |
T | 1 | a0001c0002t0001g0121 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.485+3740_485+3751d others(14): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22818823 | |||||
| chr16:22818824
|
T | C | 4 | a0001c0001t0001g0217a0001c0001t0001g0218a0001c0005t0002g0041others(1): Show | 4 | HG01175.hp2 HG02717.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.485+3729T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818824 | ||||||
| chr16:22818824
|
T | TCATTCCT others(148): Show |
1 | a0001c0002t0001g0067 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.485+3730_485+3731i others(157): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22818824 | |||||
| chr16:22818825
|
C | CATTCCTT others(291): Show |
1 | a0001c0001t0001g0150 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.485+3730_485+3731i others(300): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818825 | ||||||
| chr16:22818827
|
TTCCTTCC others(1): Show |
T | 16 | a0001c0001t0001g0151a0001c0001t0001g0153a0001c0001t0001g0154others(13): Show | 16 | HG00280.hp1 HG00280.hp2 HG00423.hp2 others(13): Show |
intron_variant | MODIFIER | c.485+3740_485+3747d others(10): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22818827 | |||||
| chr16:22818828
|
T | C | 2 | a0001c0001t0001g0217a0001c0001t0001g0218 | 2 | HG01175.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.485+3733T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818828 | ||||||
| chr16:22818831
|
T | C | 1 | a0001c0001t0001g0299 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.485+3736T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818831 | ||||||
| chr16:22818832
|
T | C | 4 | a0001c0001t0001g0217a0001c0001t0001g0218a0001c0002t0001g0010others(1): Show | 4 | HG01175.hp2 HG02055.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.485+3737T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818832 | ||||||
| chr16:22818834
|
C | A | 1 | a0001c0005t0002g0041 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.485+3739C>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818834 | ||||||
| chr16:22818835
|
C | T | 38 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0210others(35): Show | 38 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(35): Show |
intron_variant | MODIFIER | c.485+3740C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818835 | ||||||
| chr16:22818836
|
T | C | 6 | a0001c0001t0001g0217a0001c0001t0001g0218a0001c0001t0001g0238others(3): Show | 6 | HG01175.hp2 HG02055.hp1 HG02523.hp1 others(3): Show |
intron_variant | MODIFIER | c.485+3741T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818836 | ||||||
| chr16:22818839
|
T | C | 22 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0210others(19): Show | 22 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(19): Show |
intron_variant | MODIFIER | c.485+3744T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818839 | ||||||
| chr16:22818840
|
T | C | 7 | a0001c0001t0001g0217a0001c0001t0001g0218a0001c0001t0001g0238others(4): Show | 7 | HG01175.hp2 HG02055.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.485+3745T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818840 | ||||||
| chr16:22818840
|
TCCTTCCT others(17): Show |
T | 1 | a0001c0006t0006g0023 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.485+3753_485+3776d others(26): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22818840 | |||||
| chr16:22818843
|
T | C | 9 | a0001c0001t0001g0302a0001c0001t0001g0303a0001c0001t0001g0305others(6): Show | 9 | HG01109.hp2 HG01256.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.485+3748T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818843 | ||||||
| chr16:22818844
|
T | C | 5 | a0001c0001t0001g0238a0001c0002t0001g0006a0001c0002t0001g0010others(2): Show | 5 | HG02055.hp1 HG02523.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.485+3749T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818844 | ||||||
| chr16:22818846
|
C | CTTCCCTC others(22): Show |
1 | a0001c0002t0001g0124 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.485+3752_485+3753i others(31): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22818846 | |||||
| chr16:22818848
|
C | T | 33 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0210others(30): Show | 33 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(30): Show |
intron_variant | MODIFIER | c.485+3753C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818848 | ||||||
| chr16:22818850
|
C | T | 1 | a0001c0002t0001g0124 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.485+3755C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818850 | ||||||
| chr16:22818852
|
C | T | 15 | a0001c0001t0001g0217a0001c0001t0001g0218a0001c0001t0001g0219others(12): Show | 15 | HG01109.hp2 HG01175.hp2 HG01256.hp1 others(12): Show |
intron_variant | MODIFIER | c.485+3757C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818852 | ||||||
| chr16:22818856
|
C | T | 8 | a0001c0001t0001g0217a0001c0001t0001g0218a0001c0001t0001g0238others(5): Show | 8 | HG01175.hp2 HG02055.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.485+3761C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818856 | ||||||
| chr16:22818858
|
C | T | 1 | a0001c0005t0002g0041 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.485+3763C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818858 | ||||||
| chr16:22818860
|
C | T | 8 | a0001c0001t0001g0217a0001c0001t0001g0218a0001c0001t0001g0238others(5): Show | 8 | HG01175.hp2 HG02055.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.485+3765C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818860 | ||||||
| chr16:22818862
|
C | T | 1 | a0001c0005t0002g0041 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.485+3767C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818862 | ||||||
| chr16:22818864
|
C | T | 97 | a0001c0001t0001g0001a0001c0001t0001g0146a0001c0001t0001g0161others(94): Show | 97 | HG00423.hp1 HG00438.hp1 HG00609.hp2 others(94): Show |
intron_variant | MODIFIER | c.485+3769C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818864 | ||||||
| chr16:22818868
|
T | C | 2 | a0001c0001t0001g0320a0001c0001t0001g0321 | 2 | HG00323.hp2 HG01168.hp2 |
intron_variant | MODIFIER | c.485+3773T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818868 | ||||||
| chr16:22818869
|
C | T | 1 | a0001c0001t0001g0219 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.485+3774C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818869 | ||||||
| chr16:22818870
|
C | A | 5 | a0001c0001t0001g0217a0001c0001t0001g0218a0001c0001t0001g0299others(2): Show | 5 | HG01175.hp2 HG02055.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.485+3775C>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818870 | ||||||
| chr16:22818872
|
T | C | 16 | a0001c0001t0001g0216a0001c0001t0001g0286a0001c0001t0001g0287others(13): Show | 16 | HG01243.hp2 HG01884.hp2 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.485+3777T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818872 | ||||||
| chr16:22818874
|
C | A | 1 | a0001c0002t0001g0006 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.485+3779C>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818874 | ||||||
| chr16:22818875
|
T | C | 15 | a0001c0001t0001g0146a0001c0003t0003g0020a0001c0003t0003g0024others(12): Show | 15 | HG01496.hp2 HG01934.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.485+3780T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818875 | ||||||
| chr16:22818876
|
T | C | 16 | a0001c0001t0001g0216a0001c0001t0001g0286a0001c0001t0001g0287others(13): Show | 16 | HG01243.hp2 HG01884.hp2 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.485+3781T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818876 | ||||||
| chr16:22818879
|
T | C | 1 | a0001c0006t0006g0023 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.485+3784T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818879 | ||||||
| chr16:22818880
|
T | C | 1 | a0001c0002t0001g0124 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.485+3785T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818880 | ||||||
| chr16:22818882
|
C | A | 1 | a0004c0007t0001g0222 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.485+3787C>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818882 | ||||||
| chr16:22818883
|
T | C | 2 | a0001c0002t0007g0044a0001c0005t0002g0041 | 2 | HG00544.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.485+3788T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818883 | ||||||
| chr16:22818886
|
A | C | 25 | a0001c0001t0001g0146a0001c0001t0001g0238a0001c0002t0001g0006others(22): Show | 25 | HG00544.hp1 HG01496.hp2 HG01934.hp1 others(22): Show |
intron_variant | MODIFIER | c.485+3791A>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818886 | ||||||
| chr16:22818891
|
T | C | 19 | a0001c0001t0001g0146a0001c0001t0001g0238a0001c0002t0001g0010others(16): Show | 19 | HG01496.hp2 HG01934.hp1 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.485+3796T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818891 | ||||||
| chr16:22818891
|
T | TTCCGTCC others(5): Show |
1 | a0004c0007t0001g0222 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.485+3799_485+3800i others(14): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22818891 | |||||
| chr16:22818895
|
T | C | 21 | a0001c0001t0001g0216a0001c0001t0001g0217a0001c0001t0001g0218others(18): Show | 21 | HG01175.hp2 HG01243.hp2 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.485+3800T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818895 | ||||||
| chr16:22818899
|
T | C | 1 | a0001c0005t0002g0041 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.485+3804T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818899 | ||||||
| chr16:22818899
|
T | G | 38 | a0001c0001t0001g0001a0001c0001t0001g0161a0001c0001t0001g0223others(35): Show | 38 | HG00423.hp1 HG00438.hp1 HG00609.hp2 others(35): Show |
intron_variant | MODIFIER | c.485+3804T>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818899 | ||||||
| chr16:22818907
|
C | T | 21 | a0001c0001t0001g0216a0001c0001t0001g0217a0001c0001t0001g0218others(18): Show | 21 | HG01175.hp2 HG01243.hp2 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.485+3812C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818907 | ||||||
| chr16:22818908
|
T | TCCTTCCT others(13): Show |
2 | a0001c0001t0001g0286a0001c0004t0002g0291 | 2 | HG01891.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.485+3820_485+3821i others(22): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22818908 | |||||
| chr16:22818911
|
T | C | 9 | a0001c0001t0001g0217a0001c0001t0001g0218a0001c0001t0001g0238others(6): Show | 9 | HG01175.hp2 HG02055.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.485+3816T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818911 | ||||||
| chr16:22818914
|
CT | C | 14 | a0001c0001t0001g0216a0001c0001t0001g0287a0001c0001t0001g0288others(11): Show | 14 | HG01243.hp2 HG01884.hp2 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.485+3821delT | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22818914 | |||||
| chr16:22818915
|
T | C | 7 | a0001c0001t0001g0238a0001c0002t0001g0006a0001c0002t0001g0010others(4): Show | 7 | HG02055.hp1 HG02523.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.485+3820T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818915 | ||||||
| chr16:22818919
|
T | C | 21 | a0001c0001t0001g0216a0001c0001t0001g0238a0001c0001t0001g0287others(18): Show | 21 | HG01243.hp2 HG01884.hp2 HG02055.hp1 others(18): Show |
intron_variant | MODIFIER | c.485+3824T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818919 | ||||||
| chr16:22818919
|
T | TCCC | 15 | a0001c0001t0001g0146a0001c0003t0003g0020a0001c0003t0003g0024others(12): Show | 15 | HG01496.hp2 HG01934.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.485+3824_485+3825i others(5): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818919 | ||||||
| chr16:22818919
|
T | TTCCC | 71 | a0001c0001t0001g0147a0001c0001t0001g0220a0001c0001t0001g0233others(68): Show | 71 | HG00140.hp1 HG00558.hp1 HG00621.hp1 others(68): Show |
intron_variant | MODIFIER | c.485+3842_485+3845d others(6): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22818919 | |||||
| chr16:22818919
|
T | TTCCCTCC others(5): Show |
1 | a0001c0001t0001g0315 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.485+3834_485+3845d others(14): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22818919 | |||||
| chr16:22818919
|
T | TTCCCTCC others(8): Show |
1 | a0001c0001t0001g0284 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.485+3831_485+3832i others(17): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22818919 | |||||
| chr16:22818919
|
T | TTCCCTCC others(12): Show |
1 | a0001c0001t0007g0208 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.485+3831_485+3832i others(21): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22818919 | |||||
| chr16:22818919
|
T | TTCCCTCC others(13): Show |
3 | a0001c0002t0001g0099a0001c0002t0001g0100a0001c0002t0001g0101 | 3 | HG01167.hp1 HG01169.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.485+3831_485+3832i others(22): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22818919 | |||||
| chr16:22818920
|
TC | T | 3 | a0001c0001t0001g0217a0001c0001t0001g0218a0001c0001t0001g0299 | 3 | HG01175.hp2 HG02451.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.485+3828delC | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22818920 | |||||
| chr16:22818921
|
C | CCCTCCTT others(4): Show |
136 | a0001c0001t0001g0001a0001c0001t0001g0150a0001c0001t0001g0161others(133): Show | 136 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(133): Show |
intron_variant | MODIFIER | c.485+3831_485+3832i others(13): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22818921 | |||||
| chr16:22818923
|
C | T | 4 | a0001c0001t0001g0286a0001c0002t0001g0067a0001c0002t0007g0044others(1): Show | 4 | HG00544.hp1 HG01891.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.485+3828C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818923 | ||||||
| chr16:22818925
|
C | CCTTCCTT | 11 | a0001c0002t0001g0065a0001c0002t0001g0066a0001c0002t0001g0111others(8): Show | 11 | HG01070.hp2 HG01071.hp1 HG02895.hp1 others(8): Show |
intron_variant | MODIFIER | c.485+3831_485+3832i others(9): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22818925 | |||||
| chr16:22818929
|
C | CCTTCCTT others(68): Show |
1 | a0001c0002t0001g0067 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.485+3835_485+3836i others(77): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22818929 | |||||
| chr16:22818929
|
C | CCTTCCTT others(20): Show |
1 | a0001c0002t0007g0044 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.485+3835_485+3836i others(29): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22818929 | |||||
| chr16:22818929
|
C | T | 3 | a0001c0001t0001g0223a0001c0005t0002g0041a0001c0006t0006g0023 | 3 | HG01175.hp1 HG03195.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.485+3834C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818929 | ||||||
| chr16:22818933
|
C | T | 6 | a0001c0001t0001g0286a0001c0002t0001g0067a0001c0002t0007g0044others(3): Show | 6 | HG00544.hp1 HG01891.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.485+3838C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818933 | ||||||
| chr16:22818937
|
C | CCCTCCCT others(9): Show |
1 | a0001c0001t0001g0278 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.485+3845_485+3846i others(18): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22818937 | |||||
| chr16:22818937
|
C | CCCTCCCT others(13): Show |
1 | a0001c0005t0002g0012 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.485+3845_485+3846i others(22): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22818937 | |||||
| chr16:22818937
|
C | CCCTCCCT others(5): Show |
14 | a0001c0001t0001g0151a0001c0001t0001g0153a0001c0001t0001g0154others(11): Show | 14 | HG00280.hp1 HG00280.hp2 HG00639.hp1 others(11): Show |
intron_variant | MODIFIER | c.485+3845_485+3846i others(14): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22818937 | |||||
| chr16:22818937
|
C | CCCTCCCT others(1): Show |
3 | a0001c0001t0001g0162a0001c0002t0003g0002a0001c0003t0003g0015 | 3 | HG02615.hp2 HG02738.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.485+3845_485+3846i others(10): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22818937 | |||||
| chr16:22818937
|
C | CCCTCCCT others(9): Show |
1 | a0001c0011t0011g0003 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.485+3845_485+3846i others(18): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22818937 | |||||
| chr16:22818937
|
C | T | 40 | a0001c0001t0001g0146a0001c0001t0001g0216a0001c0001t0001g0238others(37): Show | 40 | HG00544.hp1 HG01243.hp2 HG01496.hp2 others(37): Show |
intron_variant | MODIFIER | c.485+3842C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818937 | ||||||
| chr16:22818941
|
T | C | 28 | a0001c0001t0001g0145a0001c0001t0001g0219a0001c0001t0001g0223others(25): Show | 28 | HG00438.hp2 HG00609.hp1 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.485+3846T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818941 | ||||||
| chr16:22818945
|
T | C | 1 | a0001c0001t0001g0223 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.485+3850T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818945 | ||||||
| chr16:22818948
|
T | C | 2 | a0001c0001t0001g0286a0001c0004t0002g0291 | 2 | HG01891.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.485+3853T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818948 | ||||||
| chr16:22818948
|
T | TTCCCTCC others(21): Show |
14 | a0001c0001t0001g0216a0001c0001t0001g0287a0001c0001t0001g0288others(11): Show | 14 | HG01243.hp2 HG01884.hp2 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.485+3856_485+3857i others(30): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22818948 | |||||
| chr16:22818949
|
T | C | 3 | a0001c0001t0001g0217a0001c0001t0001g0218a0001c0001t0001g0299 | 3 | HG01175.hp2 HG02451.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.485+3854T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818949 | ||||||
| chr16:22818951
|
C | A | 2 | a0001c0001t0007g0208a0001c0002t0007g0044 | 2 | HG00544.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.485+3856C>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818951 | ||||||
| chr16:22818951
|
C | CTTCA | 6 | a0001c0001t0001g0146a0001c0003t0003g0020a0001c0003t0003g0033others(3): Show | 6 | HG01934.hp1 HG02109.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.485+3859_485+3860i others(6): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22818951 | |||||
| chr16:22818951
|
C | CTTCCCTC others(89): Show |
1 | a0001c0001t0001g0318 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.485+3860_485+3861i others(98): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22818951 | |||||
| chr16:22818951
|
C | CTTCCCTC others(93): Show |
2 | a0001c0001t0001g0185a0001c0001t0001g0319 | 2 | HG01993.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.485+3860_485+3861i others(102): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22818951 | |||||
| chr16:22818951
|
C | CTTCCTCA | 36 | a0001c0001t0001g0001a0001c0001t0001g0161a0001c0001t0001g0224others(33): Show | 36 | HG00423.hp1 HG00438.hp1 HG00609.hp2 others(33): Show |
intron_variant | MODIFIER | c.485+3861_485+3862i others(9): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22818951 | |||||
| chr16:22818951
|
C | CTTCCTTC others(1): Show |
4 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0284others(1): Show | 4 | HG01256.hp1 HG01256.hp2 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.485+3863_485+3864i others(10): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22818951 | |||||
| chr16:22818951
|
C | CTTCCTTC others(5): Show |
86 | a0001c0001t0001g0150a0001c0001t0001g0166a0001c0001t0001g0167others(83): Show | 86 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(83): Show |
intron_variant | MODIFIER | c.485+3867_485+3868i others(14): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22818951 | |||||
| chr16:22818952
|
T | TTCCTCAT others(124): Show |
1 | a0001c0002t0001g0069 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.485+3861_485+3862i others(133): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22818952 | |||||
| chr16:22818952
|
T | TTCCTTCC others(25): Show |
5 | a0001c0001t0001g0213a0001c0001t0001g0214a0001c0001t0001g0215others(2): Show | 5 | HG02258.hp1 HG02922.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.485+3867_485+3868i others(34): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22818952 | |||||
| chr16:22818953
|
T | C | 3 | a0001c0001t0001g0217a0001c0001t0001g0218a0001c0001t0001g0299 | 3 | HG01175.hp2 HG02451.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.485+3858T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818953 | ||||||
| chr16:22818955
|
C | A | 10 | a0001c0003t0003g0024a0001c0003t0003g0027a0001c0003t0003g0028others(7): Show | 10 | HG01496.hp2 HG02615.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.485+3860C>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818955 | ||||||
| chr16:22818956
|
T | TTCCTTCA others(145): Show |
1 | a0001c0001t0001g0178 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.485+3867_485+3868i others(154): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22818956 | |||||
| chr16:22818963
|
C | A | 4 | a0001c0001t0001g0217a0001c0001t0001g0218a0001c0001t0001g0299others(1): Show | 4 | HG01175.hp2 HG02451.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.485+3868C>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818963 | ||||||
| chr16:22818967
|
C | A | 13 | a0001c0001t0001g0223a0001c0002t0001g0065a0001c0002t0001g0066others(10): Show | 13 | HG01070.hp2 HG01071.hp1 HG01175.hp1 others(10): Show |
intron_variant | MODIFIER | c.485+3872C>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818967 | ||||||
| chr16:22818972
|
C | T | 19 | a0001c0001t0001g0223a0001c0001t0001g0349a0001c0002t0001g0065others(16): Show | 19 | HG00639.hp1 HG01070.hp2 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.485+3877C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818972 | ||||||
| chr16:22818976
|
T | C | 4 | a0001c0001t0001g0349a0001c0002t0001g0104a0001c0004t0002g0338others(1): Show | 4 | HG01123.hp1 HG03669.hp1 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.485+3881T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818976 | ||||||
| chr16:22818977
|
T | TCCTCCCT others(9): Show |
36 | a0001c0001t0001g0001a0001c0001t0001g0161a0001c0001t0001g0224others(33): Show | 36 | HG00423.hp1 HG00438.hp1 HG00609.hp2 others(33): Show |
intron_variant | MODIFIER | c.485+3885_485+3886i others(18): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22818977 | |||||
| chr16:22818980
|
T | G | 11 | a0001c0002t0001g0065a0001c0002t0001g0066a0001c0002t0001g0111others(8): Show | 11 | HG01070.hp2 HG01071.hp1 HG02895.hp1 others(8): Show |
intron_variant | MODIFIER | c.485+3885T>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818980 | ||||||
| chr16:22818984
|
T | C | 1 | a0001c0001t0001g0330 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.485+3889T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818984 | ||||||
| chr16:22818988
|
C | T | 43 | a0001c0001t0001g0001a0001c0001t0001g0161a0001c0001t0001g0217others(40): Show | 43 | HG00423.hp1 HG00438.hp1 HG00609.hp2 others(40): Show |
intron_variant | MODIFIER | c.485+3893C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818988 | ||||||
| chr16:22818992
|
T | C | 40 | a0001c0001t0001g0001a0001c0001t0001g0161a0001c0001t0001g0224others(37): Show | 40 | HG00423.hp1 HG00438.hp1 HG00609.hp2 others(37): Show |
intron_variant | MODIFIER | c.485+3897T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818992 | ||||||
| chr16:22818992
|
T | TTCCTTCC others(108): Show |
11 | a0001c0002t0001g0065a0001c0002t0001g0066a0001c0002t0001g0111others(8): Show | 11 | HG01070.hp2 HG01071.hp1 HG02895.hp1 others(8): Show |
intron_variant | MODIFIER | c.485+3905_485+3906i others(117): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22818992 | |||||
| chr16:22818993
|
T | C | 3 | a0001c0001t0001g0217a0001c0001t0001g0218a0001c0001t0001g0299 | 3 | HG01175.hp2 HG02451.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.485+3898T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818993 | ||||||
| chr16:22818997
|
T | C | 3 | a0001c0001t0001g0217a0001c0001t0001g0218a0001c0001t0001g0299 | 3 | HG01175.hp2 HG02451.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.485+3902T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818997 | ||||||
| chr16:22818997
|
TCCTC | T | 7 | a0001c0001t0001g0163a0001c0001t0001g0164a0001c0002t0001g0099others(4): Show | 7 | HG00735.hp2 HG01123.hp2 HG01167.hp1 others(4): Show |
intron_variant | MODIFIER | c.485+3922_485+3925d others(6): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22818997 | |||||
| chr16:22818999
|
C | CT | 5 | a0001c0001t0001g0330a0001c0002t0001g0124a0001c0002t0003g0039others(2): Show | 5 | HG01167.hp2 HG01884.hp1 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.485+3905dupT | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22818999 | |||||
| chr16:22819001
|
C | CCCTCCCT others(92): Show |
1 | a0001c0001t0001g0223 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.485+3921_485+3922i others(101): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22819001 | |||||
| chr16:22819001
|
C | T | 52 | a0001c0001t0001g0001a0001c0001t0001g0161a0001c0001t0001g0219others(49): Show | 52 | HG00423.hp1 HG00438.hp1 HG00609.hp2 others(49): Show |
intron_variant | MODIFIER | c.485+3906C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22819001 | ||||||
| chr16:22819005
|
C | CCTT | 3 | a0001c0002t0003g0039a0001c0005t0006g0038a0001c0005t0006g0040 | 3 | HG01167.hp2 HG01884.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.485+3911_485+3912i others(5): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22819005 | |||||
| chr16:22819007
|
C | T | 1 | a0001c0002t0001g0124 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.485+3912C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22819007 | ||||||
| chr16:22819009
|
C | T | 3 | a0001c0002t0003g0039a0001c0005t0006g0038a0001c0005t0006g0040 | 3 | HG01167.hp2 HG01884.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.485+3914C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22819009 | ||||||
| chr16:22819011
|
C | T | 1 | a0001c0002t0001g0124 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.485+3916C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22819011 | ||||||
| chr16:22819013
|
C | T | 3 | a0001c0001t0001g0217a0001c0001t0001g0218a0001c0001t0001g0299 | 3 | HG01175.hp2 HG02451.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.485+3918C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22819013 | ||||||
| chr16:22819015
|
C | T | 1 | a0001c0002t0001g0124 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.485+3920C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22819015 | ||||||
| chr16:22819017
|
C | T | 123 | a0001c0001t0001g0150a0001c0001t0001g0166a0001c0001t0001g0167others(120): Show | 123 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(120): Show |
intron_variant | MODIFIER | c.485+3922C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22819017 | ||||||
| chr16:22819021
|
T | C | 4 | a0001c0002t0001g0124a0001c0002t0003g0039a0001c0005t0006g0038others(1): Show | 4 | HG01167.hp2 HG01884.hp1 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.485+3926T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22819021 | ||||||
| chr16:22819025
|
T | C | 4 | a0001c0002t0001g0124a0001c0002t0003g0039a0001c0005t0006g0038others(1): Show | 4 | HG01167.hp2 HG01884.hp1 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.485+3930T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22819025 | ||||||
| chr16:22819028
|
T | C | 3 | a0001c0001t0001g0217a0001c0001t0001g0218a0001c0001t0001g0299 | 3 | HG01175.hp2 HG02451.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.485+3933T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22819028 | ||||||
| chr16:22819029
|
T | C | 4 | a0001c0002t0001g0124a0001c0002t0003g0039a0001c0005t0006g0038others(1): Show | 4 | HG01167.hp2 HG01884.hp1 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.485+3934T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22819029 | ||||||
| chr16:22819032
|
T | C | 14 | a0001c0001t0001g0213a0001c0001t0001g0214a0001c0001t0001g0215others(11): Show | 14 | HG01109.hp2 HG01256.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.485+3937T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22819032 | ||||||
| chr16:22819039
|
A | C | 18 | a0001c0001t0001g0213a0001c0001t0001g0214a0001c0001t0001g0215others(15): Show | 18 | HG01109.hp2 HG01175.hp2 HG01256.hp1 others(15): Show |
intron_variant | MODIFIER | c.485+3944A>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22819039 | ||||||
| chr16:22819045
|
T | C | 1 | a0001c0002t0001g0124 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.485+3950T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22819045 | ||||||
| chr16:22819045
|
T | TCCTC | 15 | a0001c0001t0001g0216a0001c0001t0001g0286a0001c0001t0001g0287others(12): Show | 15 | HG01243.hp2 HG01884.hp2 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.485+3953_485+3954i others(6): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22819045 | |||||
| chr16:22819049
|
T | C | 1 | a0001c0002t0001g0008 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.485+3954T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22819049 | ||||||
| chr16:22819052
|
T | C | 3 | a0001c0001t0001g0217a0001c0001t0001g0218a0001c0001t0001g0299 | 3 | HG01175.hp2 HG02451.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.485+3957T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22819052 | ||||||
| chr16:22819056
|
T | C | 9 | a0001c0001t0001g0302a0001c0001t0001g0303a0001c0001t0001g0305others(6): Show | 9 | HG01109.hp2 HG01256.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.485+3961T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22819056 | ||||||
| chr16:22819060
|
C | T | 15 | a0001c0001t0001g0217a0001c0001t0001g0218a0001c0001t0001g0299others(12): Show | 15 | HG01081.hp2 HG01109.hp2 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.485+3965C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22819060 | ||||||
| chr16:22819064
|
T | C | 1 | a0001c0002t0001g0008 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.485+3969T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22819064 | ||||||
| chr16:22819076
|
C | T | 76 | a0001c0001t0001g0001a0001c0001t0001g0161a0001c0001t0001g0185others(73): Show | 76 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(73): Show |
intron_variant | MODIFIER | c.485+3981C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22819076 | ||||||
| chr16:22819078
|
C | CCTT | 83 | a0001c0001t0001g0166a0001c0001t0001g0167a0001c0001t0001g0168others(80): Show | 83 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(80): Show |
intron_variant | MODIFIER | c.485+3984_485+3985i others(5): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22819078 | |||||
| chr16:22819078
|
C | CCTTCCTT others(187): Show |
7 | a0001c0001t0001g0305a0001c0001t0001g0306a0001c0003t0003g0017others(4): Show | 7 | HG01109.hp2 HG01256.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.485+3984_485+3985i others(196): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22819078 | |||||
| chr16:22819080
|
C | T | 9 | a0001c0001t0001g0150a0001c0001t0001g0217a0001c0001t0001g0218others(6): Show | 9 | HG01081.hp2 HG01175.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.485+3985C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22819080 | ||||||
| chr16:22819081
|
TC | T | 6 | a0001c0001t0001g0213a0001c0001t0001g0214a0001c0001t0001g0215others(3): Show | 6 | HG02258.hp1 HG02922.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.485+3989delC | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22819081 | |||||
| chr16:22819082
|
C | CCTT | 19 | a0001c0001t0001g0185a0001c0001t0001g0216a0001c0001t0001g0286others(16): Show | 19 | HG00544.hp1 HG00738.hp1 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.485+3988_485+3989i others(5): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22819082 | |||||
| chr16:22819082
|
C | CCTTCCTC others(161): Show |
1 | a0001c0001t0001g0150 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.485+3988_485+3989i others(170): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22819082 | |||||
| chr16:22819082
|
C | CCTTCCTT others(8): Show |
49 | a0001c0001t0001g0001a0001c0001t0001g0161a0001c0001t0001g0223others(46): Show | 49 | HG00423.hp1 HG00438.hp1 HG00609.hp2 others(46): Show |
intron_variant | MODIFIER | c.485+3988_485+3989i others(17): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22819082 | |||||
| chr16:22819082
|
C | CCTTCCTT others(183): Show |
2 | a0001c0001t0001g0302a0001c0001t0001g0303 | 2 | HG03453.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.485+3988_485+3989i others(192): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22819082 | |||||
| chr16:22819082
|
C | T | 90 | a0001c0001t0001g0166a0001c0001t0001g0167a0001c0001t0001g0168others(87): Show | 90 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(87): Show |
intron_variant | MODIFIER | c.485+3987C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22819082 | ||||||
| chr16:22819084
|
C | T | 4 | a0001c0001t0001g0217a0001c0001t0001g0218a0001c0001t0001g0299others(1): Show | 4 | HG01175.hp2 HG02451.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.485+3989C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22819084 | ||||||
| chr16:22819086
|
C | CCTTCCCT | 3 | a0001c0001t0001g0217a0001c0001t0001g0218a0001c0001t0001g0299 | 3 | HG01175.hp2 HG02451.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.485+3992_485+3993i others(9): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22819086 | |||||
| chr16:22819086
|
C | T | 85 | a0001c0001t0001g0001a0001c0001t0001g0150a0001c0001t0001g0161others(82): Show | 85 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.485+3991C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22819086 | ||||||
| chr16:22819088
|
C | T | 1 | a0001c0005t0002g0041 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.485+3993C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22819088 | ||||||
| chr16:22819090
|
T | C | 91 | a0001c0001t0001g0166a0001c0001t0001g0167a0001c0001t0001g0168others(88): Show | 91 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(88): Show |
intron_variant | MODIFIER | c.485+3995T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22819090 | ||||||
| chr16:22819093
|
T | C | 19 | a0001c0001t0001g0185a0001c0001t0001g0216a0001c0001t0001g0286others(16): Show | 19 | HG00544.hp1 HG00738.hp1 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.485+3998T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22819093 | ||||||
| chr16:22819094
|
C | T | 29 | a0001c0001t0001g0185a0001c0001t0001g0213a0001c0001t0001g0214others(26): Show | 29 | HG00544.hp1 HG00738.hp1 HG01175.hp2 others(26): Show |
intron_variant | MODIFIER | c.485+3999C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22819094 | ||||||
| chr16:22819094
|
CCCTCCCT others(9): Show |
C | 4 | a0001c0003t0003g0020a0001c0003t0003g0033a0001c0003t0003g0034others(1): Show | 4 | HG01934.hp1 HG02818.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.485+4003_485+4018d others(18): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22819094 | |||||
| chr16:22819094
|
CCCTCCCT others(13): Show |
C | 12 | a0001c0001t0001g0146a0001c0003t0003g0024a0001c0003t0003g0027others(9): Show | 12 | HG01496.hp2 HG02109.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.485+4003_485+4022d others(22): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22819094 | |||||
| chr16:22819097
|
T | C | 1 | a0001c0002t0001g0067 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.485+4002T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22819097 | ||||||
| chr16:22819098
|
C | T | 26 | a0001c0001t0001g0185a0001c0001t0001g0213a0001c0001t0001g0214others(23): Show | 26 | HG00544.hp1 HG00738.hp1 HG01243.hp2 others(23): Show |
intron_variant | MODIFIER | c.485+4003C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22819098 | ||||||
| chr16:22819101
|
T | C | 1 | a0001c0002t0001g0008 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.485+4006T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22819101 | ||||||
| chr16:22819102
|
C | T | 109 | a0001c0001t0001g0166a0001c0001t0001g0167a0001c0001t0001g0168others(106): Show | 109 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.485+4007C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22819102 | ||||||
| chr16:22819102
|
CCCTT | C | 5 | a0001c0001t0001g0147a0001c0001t0001g0268a0001c0002t0003g0002others(2): Show | 5 | HG00741.hp2 HG02071.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.485+4033_485+4036d others(6): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22819102 | |||||
| chr16:22819104
|
C | A | 5 | a0001c0001t0001g0213a0001c0001t0001g0214a0001c0001t0001g0215others(2): Show | 5 | HG02258.hp1 HG02922.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.485+4009C>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22819104 | ||||||
| chr16:22819106
|
T | C | 57 | a0001c0001t0001g0001a0001c0001t0001g0150a0001c0001t0001g0161others(54): Show | 57 | HG00423.hp1 HG00438.hp1 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.485+4011T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22819106 | ||||||
| chr16:22819110
|
T | C | 2 | a0001c0001t0001g0310a0001c0002t0001g0067 | 2 | HG02258.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.485+4015T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22819110 | ||||||
| chr16:22819113
|
T | C | 15 | a0001c0001t0001g0216a0001c0001t0001g0286a0001c0001t0001g0287others(12): Show | 15 | HG01243.hp2 HG01884.hp2 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.485+4018T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22819113 | ||||||
| chr16:22819114
|
T | C | 3 | a0001c0001t0001g0310a0001c0002t0001g0008a0001c0002t0001g0067 | 3 | HG02258.hp2 HG03710.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.485+4019T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22819114 | ||||||
| chr16:22819117
|
T | C | 84 | a0001c0001t0001g0166a0001c0001t0001g0167a0001c0001t0001g0168others(81): Show | 84 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(81): Show |
intron_variant | MODIFIER | c.485+4022T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22819117 | ||||||
| chr16:22819118
|
T | C | 3 | a0001c0002t0001g0008a0001c0002t0001g0067a0001c0005t0002g0041 | 3 | HG03209.hp1 HG03710.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.485+4023T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22819118 | ||||||
| chr16:22819122
|
T | C | 2 | a0001c0002t0001g0008a0001c0002t0001g0067 | 2 | HG03710.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.485+4027T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22819122 | ||||||
| chr16:22819122
|
T | TCCTTCCC others(21): Show |
15 | a0001c0001t0001g0216a0001c0001t0001g0286a0001c0001t0001g0287others(12): Show | 15 | HG01243.hp2 HG01884.hp2 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.485+4033_485+4034i others(30): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22819122 | |||||
| chr16:22819125
|
T | C | 4 | a0001c0001t0001g0185a0001c0001t0001g0318a0001c0001t0001g0319others(1): Show | 4 | HG00544.hp1 HG00738.hp1 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.485+4030T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22819125 | ||||||
| chr16:22819126
|
T | C | 1 | a0001c0002t0001g0067 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.485+4031T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22819126 | ||||||
| chr16:22819126
|
T | TCCTCATT others(84): Show |
1 | a0001c0002t0001g0069 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.485+4034_485+4035i others(93): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22819126 | |||||
| chr16:22819130
|
T | C | 1 | a0001c0002t0001g0124 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.485+4035T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22819130 | ||||||
| chr16:22819132
|
A | C | 123 | a0001c0001t0001g0146a0001c0001t0001g0166a0001c0001t0001g0167others(120): Show | 123 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(120): Show |
intron_variant | MODIFIER | c.485+4037A>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22819132 | ||||||
| chr16:22819134
|
T | C | 4 | a0001c0001t0001g0217a0001c0001t0001g0218a0001c0001t0001g0299others(1): Show | 4 | HG01175.hp2 HG02109.hp1 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.485+4039T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22819134 | ||||||
| chr16:22819134
|
T | TCCCTCCT others(465): Show |
1 | a0001c0001t0001g0178 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.485+4041_485+4042i others(474): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22819134 | |||||
| chr16:22819134
|
T | TCCTTCCC others(466): Show |
1 | a0001c0005t0002g0009 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.485+4045_485+4046i others(475): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22819134 | |||||
| chr16:22819134
|
T | TCCTTCCC others(467): Show |
1 | a0001c0001t0001g0187 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.485+4045_485+4046i others(476): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22819134 | |||||
| chr16:22819134
|
T | TCCTTCCC others(465): Show |
2 | a0001c0002t0001g0063a0001c0004t0002g0183 | 2 | HG03017.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.485+4045_485+4046i others(474): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22819134 | |||||
| chr16:22819134
|
T | TCCTTCCC others(281): Show |
1 | a0001c0005t0002g0004 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.485+4045_485+4046i others(290): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22819134 | |||||
| chr16:22819134
|
T | TCCTTCCC others(465): Show |
2 | a0001c0001t0001g0320a0001c0001t0001g0321 | 2 | HG00323.hp2 HG01168.hp2 |
intron_variant | MODIFIER | c.485+4045_485+4046i others(474): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22819134 | |||||
| chr16:22819134
|
T | TCCTTCCC others(469): Show |
69 | a0001c0001t0001g0166a0001c0001t0001g0167a0001c0001t0001g0168others(66): Show | 69 | HG00140.hp2 HG01168.hp1 HG01169.hp1 others(66): Show |
intron_variant | MODIFIER | c.485+4045_485+4046i others(478): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22819134 | |||||
| chr16:22819134
|
T | TCCTTCCC others(468): Show |
1 | a0001c0001t0001g0350 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.485+4045_485+4046i others(477): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22819134 | |||||
| chr16:22819134
|
T | TCCTTCCC others(469): Show |
2 | a0001c0001t0001g0206a0001c0001t0001g0207 | 2 | NA18946.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.485+4045_485+4046i others(478): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22819134 | |||||
| chr16:22819134
|
T | TCCTTCCC others(449): Show |
2 | a0001c0002t0001g0105a0001c0002t0001g0106 | 2 | HG00323.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.485+4045_485+4046i others(458): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22819134 | |||||
| chr16:22819134
|
T | TCCTTCCT others(201): Show |
1 | a0001c0001t0001g0318 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.485+4053_485+4054i others(210): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22819134 | |||||
| chr16:22819134
|
T | TCCTTCCT others(205): Show |
3 | a0001c0001t0001g0185a0001c0001t0001g0319a0001c0002t0007g0044 | 3 | HG00544.hp1 HG01993.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.485+4053_485+4054i others(214): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22819134 | |||||
| chr16:22819134
|
T | TCCTTCCT others(65): Show |
9 | a0001c0001t0001g0302a0001c0001t0001g0303a0001c0001t0001g0305others(6): Show | 9 | HG01109.hp2 HG01256.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.485+4057_485+4058i others(74): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22819134 | |||||
| chr16:22819134
|
T | TCCTTCCT others(121): Show |
5 | a0001c0001t0001g0213a0001c0001t0001g0214a0001c0001t0001g0215others(2): Show | 5 | HG02258.hp1 HG02922.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.485+4057_485+4058i others(130): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22819134 | |||||
| chr16:22819134
|
T | TCCTTCCT others(300): Show |
1 | a0001c0001t0001g0150 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.485+4057_485+4058i others(309): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22819134 | |||||
| chr16:22819138
|
T | C | 1 | a0001c0002t0001g0124 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.485+4043T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22819138 | ||||||
| chr16:22819138
|
T | TCCTTCCT others(188): Show |
1 | a0001c0001t0001g0328 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.485+4061_485+4062i others(197): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22819138 | |||||
| chr16:22819141
|
T | C | 17 | a0001c0001t0001g0146a0001c0001t0001g0212a0001c0003t0003g0020others(14): Show | 17 | HG01496.hp2 HG01934.hp1 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.485+4046T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22819141 | ||||||
| chr16:22819142
|
T | C | 1 | a0001c0002t0001g0124 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.485+4047T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22819142 | ||||||
| chr16:22819142
|
T | TCCTTCCC others(57): Show |
1 | a0001c0005t0002g0041 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.485+4053_485+4054i others(66): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22819142 | |||||
| chr16:22819148
|
C | A | 16 | a0001c0001t0001g0216a0001c0001t0001g0286a0001c0001t0001g0287others(13): Show | 16 | HG01243.hp2 HG01884.hp2 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.485+4053C>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22819148 | ||||||
| chr16:22819151
|
C | CCTTCCTT others(468): Show |
1 | a0001c0001t0001g0212 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.485+4061_485+4062i others(477): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22819151 | |||||
| chr16:22819157
|
C | T | 69 | a0001c0001t0001g0001a0001c0001t0001g0161a0001c0001t0001g0216others(66): Show | 69 | HG00423.hp1 HG00438.hp1 HG00609.hp2 others(66): Show |
intron_variant | MODIFIER | c.485+4062C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22819157 | ||||||
| chr16:22819161
|
T | C | 2 | a0001c0002t0001g0067a0001c0002t0001g0069 | 2 | HG01081.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.485+4066T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22819161 | ||||||
| chr16:22819161
|
T | TTCCTTCA others(196): Show |
3 | a0001c0001t0001g0224a0001c0002t0001g0070a0001c0002t0001g0110 | 3 | HG01106.hp2 NA18953.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.485+4072_485+4073i others(205): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22819161 | |||||
| chr16:22819161
|
T | TTCCTTCC others(200): Show |
5 | a0001c0002t0001g0111a0001c0002t0001g0112a0001c0002t0001g0113others(2): Show | 5 | NA18979.hp1 NA18995.hp2 NA19005.hp2 others(2): Show |
intron_variant | MODIFIER | c.485+4076_485+4077i others(209): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22819161 | |||||
| chr16:22819161
|
T | TTCCTTCC others(200): Show |
10 | a0001c0001t0001g0161a0001c0001t0001g0326a0001c0001t0001g0327others(7): Show | 10 | HG00423.hp1 HG00438.hp1 HG00621.hp2 others(7): Show |
intron_variant | MODIFIER | c.485+4076_485+4077i others(209): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22819161 | |||||
| chr16:22819161
|
T | TTCCTTCC others(208): Show |
3 | a0001c0001t0001g0225a0001c0002t0001g0065a0001c0002t0001g0066 | 3 | HG02895.hp1 HG02897.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.485+4077_485+4078i others(217): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22819161 | |||||
| chr16:22819161
|
T | TTCCTTCC others(200): Show |
1 | a0001c0002t0001g0074 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.485+4077_485+4078i others(209): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22819161 | |||||
| chr16:22819161
|
T | TTCCTTCC others(204): Show |
24 | a0001c0001t0001g0001a0001c0001t0001g0226a0001c0001t0001g0227others(21): Show | 24 | HG00609.hp2 HG00639.hp2 HG01516.hp2 others(21): Show |
intron_variant | MODIFIER | c.485+4077_485+4078i others(213): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22819161 | |||||
| chr16:22819161
|
T | TTCCTTCC others(200): Show |
1 | a0001c0001t0001g0223 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.485+4077_485+4078i others(209): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22819161 | |||||
| chr16:22819161
|
T | TTCCTTCC others(208): Show |
1 | a0001c0002t0001g0079 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.485+4077_485+4078i others(217): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22819161 | |||||
| chr16:22819186
|
C | T | 1 | a0001c0001t0001g0310 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.485+4091C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22819186 | ||||||
| chr16:22819191
|
C | A | 10 | a0001c0003t0003g0024a0001c0003t0003g0027a0001c0003t0003g0028others(7): Show | 10 | HG01496.hp2 HG02615.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.485+4096C>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22819191 | ||||||
| chr16:22819293
|
T | C | 6 | a0001c0001t0001g0150a0001c0001t0001g0188a0001c0001t0001g0189others(3): Show | 6 | HG02165.hp1 NA18955.hp1 NA18959.hp1 others(3): Show |
intron_variant | MODIFIER | c.485+4198T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22819293 | ||||||
| chr16:22819587
|
A | G | 1 | a0001c0002t0001g0106 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.485+4492A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22819587 | ||||||
| chr16:22819769
|
C | T | 1 | a0001c0002t0001g0006 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.485+4674C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22819769 | ||||||
| chr16:22819781
|
G | A | 2 | a0001c0002t0001g0124a0001c0005t0002g0041 | 2 | HG02109.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.485+4686G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22819781 | ||||||
| chr16:22820100
|
C | A | 6 | a0001c0001t0001g0302a0001c0001t0001g0303a0001c0001t0001g0305others(3): Show | 6 | HG01109.hp2 HG02922.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.485+5005C>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22820100 | ||||||
| chr16:22820125
|
C | T | 3 | a0001c0001t0001g0298a0001c0003t0003g0036a0001c0003t0003g0037 | 3 | HG02559.hp2 HG03098.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.485+5030C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22820125 | ||||||
| chr16:22820137
|
A | G | 85 | a0001c0001t0001g0150a0001c0001t0001g0166a0001c0001t0001g0167others(82): Show | 85 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(82): Show |
intron_variant | MODIFIER | c.485+5042A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22820137 | ||||||
| chr16:22820169
|
A | C | 1 | a0001c0001t0001g0310 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.485+5074A>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22820169 | ||||||
| chr16:22820172
|
C | G | 3 | a0001c0001t0001g0349a0001c0002t0001g0062a0001c0005t0002g0060 | 3 | HG02486.hp2 HG03834.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.485+5077C>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22820172 | ||||||
| chr16:22820178
|
C | A | 1 | a0001c0001t0001g0306 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.485+5083C>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22820178 | ||||||
| chr16:22820392
|
A | G | 1 | a0001c0001t0001g0160 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.485+5297A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22820392 | ||||||
| chr16:22820583
|
A | T | 1 | a0001c0001t0001g0159 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.485+5488A>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22820583 | ||||||
| chr16:22820840
|
G | A | 65 | a0001c0001t0001g0146a0001c0001t0001g0151a0001c0001t0001g0153others(62): Show | 65 | HG00280.hp1 HG00280.hp2 HG00423.hp2 others(62): Show |
intron_variant | MODIFIER | c.485+5745G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22820840 | ||||||
| chr16:22821145
|
A | G | 2 | a0001c0002t0004g0096a0001c0002t0004g0097 | 2 | HG01071.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.485+6050A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22821145 | ||||||
| chr16:22821252
|
C | T | 1 | a0001c0003t0015g0032 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.485+6157C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22821252 | ||||||
| chr16:22821257
|
C | G | 1 | a0001c0002t0001g0006 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.485+6162C>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22821257 | ||||||
| chr16:22821284
|
G | A | 1 | a0001c0001t0001g0310 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.485+6189G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22821284 | ||||||
| chr16:22821456
|
G | A | 89 | a0001c0001t0001g0150a0001c0001t0001g0166a0001c0001t0001g0167others(86): Show | 89 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(86): Show |
intron_variant | MODIFIER | c.485+6361G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22821456 | ||||||
| chr16:22821640
|
A | C | 1 | a0001c0002t0001g0121 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.485+6545A>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22821640 | ||||||
| chr16:22821706
|
G | A | 143 | a0001c0001t0001g0001a0001c0001t0001g0150a0001c0001t0001g0161others(140): Show | 143 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(140): Show |
intron_variant | MODIFIER | c.485+6611G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22821706 | ||||||
| chr16:22822097
|
C | T | 43 | a0001c0001t0001g0146a0001c0001t0001g0151a0001c0001t0001g0153others(40): Show | 43 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(40): Show |
intron_variant | MODIFIER | c.485+7002C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22822097 | ||||||
| chr16:22822348
|
G | T | 2 | a0001c0002t0001g0124a0001c0005t0002g0041 | 2 | HG02109.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.485+7253G>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22822348 | ||||||
| chr16:22822377
|
A | G | 149 | a0001c0001t0001g0001a0001c0001t0001g0150a0001c0001t0001g0161others(146): Show | 149 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(146): Show |
intron_variant | MODIFIER | c.485+7282A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22822377 | ||||||
| chr16:22822384
|
T | C | 43 | a0001c0001t0001g0146a0001c0001t0001g0151a0001c0001t0001g0153others(40): Show | 43 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(40): Show |
intron_variant | MODIFIER | c.485+7289T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22822384 | ||||||
| chr16:22822416
|
C | T | 1 | a0001c0001t0001g0207 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.485+7321C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22822416 | ||||||
| chr16:22822438
|
G | A | 6 | a0001c0001t0001g0146a0001c0003t0003g0020a0001c0003t0003g0033others(3): Show | 6 | HG01934.hp1 HG02109.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.485+7343G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22822438 | ||||||
| chr16:22822443
|
C | T | 2 | a0001c0002t0005g0123a0001c0002t0005g0125 | 2 | HG01928.hp2 HG01952.hp1 |
intron_variant | MODIFIER | c.485+7348C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22822443 | ||||||
| chr16:22822449
|
T | G | 3 | a0001c0001t0001g0306a0001c0004t0002g0307a0001c0005t0002g0005 | 3 | HG01256.hp1 HG02572.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.485+7354T>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22822449 | ||||||
| chr16:22822482
|
G | C | 19 | a0001c0001t0001g0216a0001c0001t0001g0217a0001c0001t0001g0218others(16): Show | 19 | HG01175.hp2 HG01243.hp2 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.485+7387G>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22822482 | ||||||
| chr16:22822746
|
T | G | 1 | a0001c0002t0001g0124 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.485+7651T>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22822746 | ||||||
| chr16:22822767
|
G | A | 50 | a0001c0001t0001g0146a0001c0001t0001g0151a0001c0001t0001g0153others(47): Show | 50 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(47): Show |
intron_variant | MODIFIER | c.485+7672G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22822767 | ||||||
| chr16:22822856
|
G | GA | 23 | a0001c0001t0001g0146a0001c0001t0001g0225a0001c0001t0001g0298others(20): Show | 23 | HG00544.hp1 HG01261.hp2 HG01496.hp2 others(20): Show |
intron_variant | MODIFIER | c.485+7775dupA | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22822856 | |||||
| chr16:22822856
|
GA | G | 16 | a0001c0001t0001g0213a0001c0001t0001g0214a0001c0001t0001g0215others(13): Show | 16 | HG01934.hp1 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.485+7775delA | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22822856 | |||||
| chr16:22822875
|
G | A | 8 | a0001c0001t0001g0279a0001c0002t0001g0046a0001c0002t0001g0050others(5): Show | 8 | HG00741.hp1 HG01257.hp2 HG01993.hp2 others(5): Show |
intron_variant | MODIFIER | c.485+7780G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22822875 | ||||||
| chr16:22822957
|
C | T | 1 | a0001c0002t0001g0087 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.485+7862C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22822957 | ||||||
| chr16:22822986
|
A | G | 3 | a0001c0002t0001g0076a0001c0002t0001g0077a0001c0002t0001g0078 | 3 | NA18980.hp2 NA18990.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.485+7891A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22822986 | ||||||
| chr16:22823196
|
A | G | 33 | a0001c0001t0001g0151a0001c0001t0001g0153a0001c0001t0001g0154others(30): Show | 33 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(30): Show |
intron_variant | MODIFIER | c.485+8101A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22823196 | ||||||
| chr16:22823245
|
A | T | 59 | a0001c0001t0001g0146a0001c0001t0001g0151a0001c0001t0001g0153others(56): Show | 59 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(56): Show |
intron_variant | MODIFIER | c.485+8150A>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22823245 | ||||||
| chr16:22823558
|
G | A | 1 | a0001c0001t0001g0178 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.485+8463G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22823558 | ||||||
| chr16:22823568
|
C | A | 56 | a0001c0001t0001g0001a0001c0001t0001g0161a0001c0001t0001g0213others(53): Show | 56 | HG00423.hp1 HG00438.hp1 HG00621.hp2 others(53): Show |
intron_variant | MODIFIER | c.485+8473C>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22823568 | ||||||
| chr16:22823571
|
C | A | 1 | a0001c0001t0004g0193 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.485+8476C>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22823571 | ||||||
| chr16:22823618
|
T | TA | 8 | a0001c0001t0001g0243a0001c0001t0001g0244a0001c0001t0001g0269others(5): Show | 8 | HG01433.hp1 HG02080.hp1 HG02602.hp1 others(5): Show |
intron_variant | MODIFIER | c.485+8542dupA | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22823618 | |||||
| chr16:22823618
|
TA | T | 31 | a0001c0001t0001g0146a0001c0001t0001g0150a0001c0001t0001g0161others(28): Show | 31 | HG00323.hp1 HG00438.hp1 HG01106.hp1 others(28): Show |
intron_variant | MODIFIER | c.485+8542delA | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22823618 | |||||
| chr16:22823618
|
TAA | T | 174 | a0001c0001t0001g0001a0001c0001t0001g0151a0001c0001t0001g0153others(171): Show | 174 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(171): Show |
intron_variant | MODIFIER | c.485+8541_485+8542d others(4): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22823618 | |||||
| chr16:22823672
|
AACT | A | 8 | a0001c0001t0001g0146a0001c0003t0003g0024a0001c0003t0003g0027others(5): Show | 8 | HG02109.hp2 HG02486.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.485+8581_485+8583d others(5): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22823672 | |||||
| chr16:22823698
|
A | G | 56 | a0001c0001t0001g0001a0001c0001t0001g0161a0001c0001t0001g0213others(53): Show | 56 | HG00423.hp1 HG00438.hp1 HG00621.hp2 others(53): Show |
intron_variant | MODIFIER | c.485+8603A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22823698 | ||||||
| chr16:22823731
|
A | G | 56 | a0001c0001t0001g0001a0001c0001t0001g0161a0001c0001t0001g0213others(53): Show | 56 | HG00423.hp1 HG00438.hp1 HG00621.hp2 others(53): Show |
intron_variant | MODIFIER | c.485+8636A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22823731 | ||||||
| chr16:22824000
|
T | C | 1 | a0001c0005t0002g0060 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.485+8905T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22824000 | ||||||
| chr16:22824054
|
CACGTATC others(5): Show |
C | 1 | a0001c0002t0001g0064 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.485+8964_485+8975d others(14): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22824054 | |||||
| chr16:22824057
|
G | A | 97 | a0001c0001t0001g0150a0001c0001t0001g0166a0001c0001t0001g0167others(94): Show | 97 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.485+8962G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22824057 | ||||||
| chr16:22824068
|
C | T | 34 | a0001c0001t0001g0151a0001c0001t0001g0153a0001c0001t0001g0154others(31): Show | 34 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(31): Show |
intron_variant | MODIFIER | c.485+8973C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22824068 | ||||||
| chr16:22824142
|
G | C | 1 | a0001c0002t0001g0121 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.485+9047G>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22824142 | ||||||
| chr16:22824178
|
G | C | 56 | a0001c0001t0001g0001a0001c0001t0001g0161a0001c0001t0001g0213others(53): Show | 56 | HG00423.hp1 HG00438.hp1 HG00621.hp2 others(53): Show |
intron_variant | MODIFIER | c.485+9083G>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22824178 | ||||||
| chr16:22824213
|
A | C | 2 | a0001c0001t0001g0174a0001c0005t0002g0009 | 2 | HG03486.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.485+9118A>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22824213 | ||||||
| chr16:22824243
|
C | T | 1 | a0001c0001t0001g0288 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.485+9148C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22824243 | ||||||
| chr16:22824248
|
A | G | 56 | a0001c0001t0001g0001a0001c0001t0001g0161a0001c0001t0001g0213others(53): Show | 56 | HG00423.hp1 HG00438.hp1 HG00621.hp2 others(53): Show |
intron_variant | MODIFIER | c.485+9153A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22824248 | ||||||
| chr16:22824275
|
G | A | 36 | a0001c0001t0001g0151a0001c0001t0001g0153a0001c0001t0001g0154others(33): Show | 36 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(33): Show |
intron_variant | MODIFIER | c.485+9180G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22824275 | ||||||
| chr16:22824276
|
T | C | 56 | a0001c0001t0001g0001a0001c0001t0001g0161a0001c0001t0001g0213others(53): Show | 56 | HG00423.hp1 HG00438.hp1 HG00621.hp2 others(53): Show |
intron_variant | MODIFIER | c.485+9181T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22824276 | ||||||
| chr16:22824284
|
C | T | 6 | a0001c0001t0001g0216a0001c0001t0001g0294a0001c0001t0001g0295others(3): Show | 6 | HG01884.hp2 HG02145.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.485+9189C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22824284 | ||||||
| chr16:22824303
|
C | A | 18 | a0001c0001t0001g0151a0001c0001t0001g0153a0001c0001t0001g0154others(15): Show | 18 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(15): Show |
intron_variant | MODIFIER | c.485+9208C>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22824303 | ||||||
| chr16:22824325
|
G | T | 56 | a0001c0001t0001g0001a0001c0001t0001g0161a0001c0001t0001g0213others(53): Show | 56 | HG00423.hp1 HG00438.hp1 HG00621.hp2 others(53): Show |
intron_variant | MODIFIER | c.485+9230G>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22824325 | ||||||
| chr16:22824339
|
G | A | 1 | a0001c0001t0001g0306 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.485+9244G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22824339 | ||||||
| chr16:22824341
|
G | T | 1 | a0001c0001t0001g0310 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.485+9246G>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22824341 | ||||||
| chr16:22824471
|
C | T | 1 | a0001c0002t0001g0058 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.485+9376C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22824471 | ||||||
| chr16:22824542
|
G | A | 56 | a0001c0001t0001g0001a0001c0001t0001g0161a0001c0001t0001g0213others(53): Show | 56 | HG00423.hp1 HG00438.hp1 HG00621.hp2 others(53): Show |
intron_variant | MODIFIER | c.485+9447G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22824542 | ||||||
| chr16:22824547
|
A | AAAGC | 91 | a0001c0001t0001g0150a0001c0001t0001g0166a0001c0001t0001g0167others(88): Show | 91 | HG00140.hp2 HG00544.hp1 HG00738.hp1 others(88): Show |
intron_variant | MODIFIER | c.485+9459_485+9462d others(6): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22824547 | |||||
| chr16:22824558
|
A | G | 51 | a0001c0001t0001g0001a0001c0001t0001g0161a0001c0001t0001g0226others(48): Show | 51 | HG00423.hp1 HG00438.hp1 HG00621.hp2 others(48): Show |
intron_variant | MODIFIER | c.485+9463A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22824558 | ||||||
| chr16:22824629
|
C | T | 56 | a0001c0001t0001g0001a0001c0001t0001g0161a0001c0001t0001g0213others(53): Show | 56 | HG00423.hp1 HG00438.hp1 HG00621.hp2 others(53): Show |
intron_variant | MODIFIER | c.485+9534C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22824629 | ||||||
| chr16:22824634
|
G | A | 56 | a0001c0001t0001g0001a0001c0001t0001g0161a0001c0001t0001g0213others(53): Show | 56 | HG00423.hp1 HG00438.hp1 HG00621.hp2 others(53): Show |
intron_variant | MODIFIER | c.485+9539G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22824634 | ||||||
| chr16:22824743
|
G | T | 56 | a0001c0001t0001g0001a0001c0001t0001g0161a0001c0001t0001g0213others(53): Show | 56 | HG00423.hp1 HG00438.hp1 HG00621.hp2 others(53): Show |
intron_variant | MODIFIER | c.485+9648G>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22824743 | ||||||
| chr16:22824804
|
T | C | 51 | a0001c0001t0001g0001a0001c0001t0001g0161a0001c0001t0001g0226others(48): Show | 51 | HG00423.hp1 HG00438.hp1 HG00621.hp2 others(48): Show |
intron_variant | MODIFIER | c.485+9709T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22824804 | ||||||
| chr16:22824928
|
G | A | 56 | a0001c0001t0001g0001a0001c0001t0001g0161a0001c0001t0001g0213others(53): Show | 56 | HG00423.hp1 HG00438.hp1 HG00621.hp2 others(53): Show |
intron_variant | MODIFIER | c.485+9833G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22824928 | ||||||
| chr16:22824992
|
T | C | 1 | a0001c0001t0001g0287 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.485+9897T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22824992 | ||||||
| chr16:22825071
|
T | C | 56 | a0001c0001t0001g0001a0001c0001t0001g0161a0001c0001t0001g0213others(53): Show | 56 | HG00423.hp1 HG00438.hp1 HG00621.hp2 others(53): Show |
intron_variant | MODIFIER | c.485+9976T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22825071 | ||||||
| chr16:22825129
|
G | A | 57 | a0001c0001t0001g0001a0001c0001t0001g0161a0001c0001t0001g0210others(54): Show | 57 | HG00423.hp1 HG00438.hp1 HG00621.hp2 others(54): Show |
intron_variant | MODIFIER | c.485+10034G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22825129 | ||||||
| chr16:22825161
|
A | T | 56 | a0001c0001t0001g0001a0001c0001t0001g0161a0001c0001t0001g0213others(53): Show | 56 | HG00423.hp1 HG00438.hp1 HG00621.hp2 others(53): Show |
intron_variant | MODIFIER | c.485+10066A>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22825161 | ||||||
| chr16:22825253
|
A | G | 56 | a0001c0001t0001g0001a0001c0001t0001g0161a0001c0001t0001g0213others(53): Show | 56 | HG00423.hp1 HG00438.hp1 HG00621.hp2 others(53): Show |
intron_variant | MODIFIER | c.485+10158A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22825253 | ||||||
| chr16:22825322
|
G | C | 3 | a0001c0001t0001g0217a0001c0001t0001g0218a0001c0001t0001g0299 | 3 | HG01175.hp2 HG02451.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.485+10227G>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22825322 | ||||||
| chr16:22825440
|
T | C | 34 | a0001c0001t0001g0151a0001c0001t0001g0153a0001c0001t0001g0154others(31): Show | 34 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(31): Show |
intron_variant | MODIFIER | c.485+10345T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22825440 | ||||||
| chr16:22825639
|
T | A | 4 | a0001c0001t0001g0322a0001c0001t0001g0323a0001c0001t0001g0324others(1): Show | 4 | HG02132.hp1 NA18942.hp1 NA19088.hp2 others(1): Show |
intron_variant | MODIFIER | c.485+10544T>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22825639 | ||||||
| chr16:22825662
|
A | C | 56 | a0001c0001t0001g0001a0001c0001t0001g0161a0001c0001t0001g0213others(53): Show | 56 | HG00423.hp1 HG00438.hp1 HG00621.hp2 others(53): Show |
intron_variant | MODIFIER | c.485+10567A>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22825662 | ||||||
| chr16:22825741
|
T | C | 56 | a0001c0001t0001g0001a0001c0001t0001g0161a0001c0001t0001g0213others(53): Show | 56 | HG00423.hp1 HG00438.hp1 HG00621.hp2 others(53): Show |
intron_variant | MODIFIER | c.485+10646T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22825741 | ||||||
| chr16:22825762
|
A | C | 36 | a0001c0001t0001g0151a0001c0001t0001g0153a0001c0001t0001g0154others(33): Show | 36 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(33): Show |
intron_variant | MODIFIER | c.485+10667A>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22825762 | ||||||
| chr16:22825821
|
G | A | 56 | a0001c0001t0001g0001a0001c0001t0001g0161a0001c0001t0001g0213others(53): Show | 56 | HG00423.hp1 HG00438.hp1 HG00621.hp2 others(53): Show |
intron_variant | MODIFIER | c.485+10726G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22825821 | ||||||
| chr16:22825891
|
C | T | 1 | a0001c0002t0001g0112 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.485+10796C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22825891 | ||||||
| chr16:22825903
|
T | G | 56 | a0001c0001t0001g0001a0001c0001t0001g0161a0001c0001t0001g0213others(53): Show | 56 | HG00423.hp1 HG00438.hp1 HG00621.hp2 others(53): Show |
intron_variant | MODIFIER | c.485+10808T>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22825903 | ||||||
| chr16:22825962
|
G | T | 36 | a0001c0001t0001g0151a0001c0001t0001g0153a0001c0001t0001g0154others(33): Show | 36 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(33): Show |
intron_variant | MODIFIER | c.485+10867G>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22825962 | ||||||
| chr16:22826127
|
G | T | 56 | a0001c0001t0001g0001a0001c0001t0001g0161a0001c0001t0001g0213others(53): Show | 56 | HG00423.hp1 HG00438.hp1 HG00621.hp2 others(53): Show |
intron_variant | MODIFIER | c.485+11032G>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22826127 | ||||||
| chr16:22826169
|
G | C | 56 | a0001c0001t0001g0001a0001c0001t0001g0161a0001c0001t0001g0213others(53): Show | 56 | HG00423.hp1 HG00438.hp1 HG00621.hp2 others(53): Show |
intron_variant | MODIFIER | c.485+11074G>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22826169 | ||||||
| chr16:22826178
|
C | T | 56 | a0001c0001t0001g0001a0001c0001t0001g0161a0001c0001t0001g0213others(53): Show | 56 | HG00423.hp1 HG00438.hp1 HG00621.hp2 others(53): Show |
intron_variant | MODIFIER | c.485+11083C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22826178 | ||||||
| chr16:22826226
|
T | C | 56 | a0001c0001t0001g0001a0001c0001t0001g0161a0001c0001t0001g0213others(53): Show | 56 | HG00423.hp1 HG00438.hp1 HG00621.hp2 others(53): Show |
intron_variant | MODIFIER | c.485+11131T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22826226 | ||||||
| chr16:22826227
|
G | A | 56 | a0001c0001t0001g0001a0001c0001t0001g0161a0001c0001t0001g0213others(53): Show | 56 | HG00423.hp1 HG00438.hp1 HG00621.hp2 others(53): Show |
intron_variant | MODIFIER | c.485+11132G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22826227 | ||||||
| chr16:22826271
|
A | G | 2 | a0001c0001t0001g0320a0001c0001t0001g0321 | 2 | HG00323.hp2 HG01168.hp2 |
intron_variant | MODIFIER | c.485+11176A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22826271 | ||||||
| chr16:22826374
|
T | G | 90 | a0001c0001t0001g0001a0001c0001t0001g0151a0001c0001t0001g0153others(87): Show | 90 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.485+11279T>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22826374 | ||||||
| chr16:22826423
|
A | C | 1 | a0006c0012t0001g0347 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.485+11328A>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22826423 | ||||||
| chr16:22826608
|
C | T | 3 | a0001c0001t0001g0298a0001c0003t0003g0036a0001c0003t0003g0037 | 3 | HG02559.hp2 HG03098.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.485+11513C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22826608 | ||||||
| chr16:22826637
|
A | C | 210 | a0001c0001t0001g0001a0001c0001t0001g0146a0001c0001t0001g0150others(207): Show | 210 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(207): Show |
intron_variant | MODIFIER | c.485+11542A>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22826637 | ||||||
| chr16:22826680
|
A | G | 211 | a0001c0001t0001g0001a0001c0001t0001g0146a0001c0001t0001g0150others(208): Show | 211 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(208): Show |
intron_variant | MODIFIER | c.485+11585A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22826680 | ||||||
| chr16:22826837
|
C | T | 91 | a0001c0001t0001g0150a0001c0001t0001g0166a0001c0001t0001g0167others(88): Show | 91 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(88): Show |
intron_variant | MODIFIER | c.485+11742C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22826837 | ||||||
| chr16:22826887
|
G | T | 3 | a0001c0002t0001g0010a0001c0002t0001g0011a0001c0005t0002g0012 | 3 | HG02055.hp1 HG03098.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.485+11792G>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22826887 | ||||||
| chr16:22826955
|
T | C | 2 | a0001c0003t0003g0021a0007c0010t0001g0042 | 2 | HG01891.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.485+11860T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22826955 | ||||||
| chr16:22827000
|
C | T | 7 | a0001c0001t0001g0187a0001c0001t0001g0275a0001c0001t0001g0276others(4): Show | 7 | HG01433.hp1 HG01496.hp1 HG01934.hp2 others(4): Show |
intron_variant | MODIFIER | c.485+11905C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22827000 | ||||||
| chr16:22827334
|
T | C | 1 | a0001c0002t0001g0068 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.485+12239T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22827334 | ||||||
| chr16:22827411
|
T | A | 1 | a0001c0001t0001g0269 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.485+12316T>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22827411 | ||||||
| chr16:22827468
|
T | C | 3 | a0001c0001t0001g0298a0001c0003t0003g0036a0001c0003t0003g0037 | 3 | HG02559.hp2 HG03098.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.485+12373T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22827468 | ||||||
| chr16:22827469
|
G | A | 8 | a0001c0001t0001g0277a0001c0002t0001g0124a0001c0002t0003g0002others(5): Show | 8 | HG01496.hp2 HG02109.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.485+12374G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22827469 | ||||||
| chr16:22827607
|
C | T | 1 | a0001c0001t0001g0146 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.485+12512C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22827607 | ||||||
| chr16:22827686
|
G | A | 3 | a0001c0002t0001g0076a0001c0002t0001g0077a0001c0002t0001g0078 | 3 | NA18980.hp2 NA18990.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.485+12591G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22827686 | ||||||
| chr16:22827710
|
C | CT | 29 | a0001c0001t0001g0175a0001c0001t0001g0213a0001c0001t0001g0238others(26): Show | 29 | HG00323.hp1 HG00639.hp1 HG00735.hp1 others(26): Show |
intron_variant | MODIFIER | c.485+12634dupT | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22827710 | |||||
| chr16:22827710
|
C | CTT | 56 | a0001c0001t0001g0001a0001c0001t0001g0161a0001c0001t0001g0214others(53): Show | 56 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(53): Show |
intron_variant | MODIFIER | c.485+12633_485+1263 others(6): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22827710 | |||||
| chr16:22827710
|
CT | C | 116 | a0001c0001t0001g0146a0001c0001t0001g0151a0001c0001t0001g0166others(113): Show | 116 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(113): Show |
intron_variant | MODIFIER | c.485+12634delT | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22827710 | |||||
| chr16:22827710
|
CTT | C | 11 | a0001c0001t0001g0150a0001c0001t0001g0178a0001c0001t0001g0194others(8): Show | 11 | HG01169.hp1 HG02280.hp1 HG02698.hp1 others(8): Show |
intron_variant | MODIFIER | c.485+12633_485+1263 others(6): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22827710 | |||||
| chr16:22827721
|
T | C | 2 | a0001c0002t0001g0116a0001c0002t0001g0117 | 2 | NA18966.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.485+12626T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22827721 | ||||||
| chr16:22827932
|
A | G | 1 | a0001c0002t0001g0093 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.485+12837A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22827932 | ||||||
| chr16:22827996
|
C | T | 1 | a0001c0002t0001g0138 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.485+12901C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22827996 | ||||||
| chr16:22828065
|
A | C | 1 | a0001c0001t0001g0277 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.485+12970A>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22828065 | ||||||
| chr16:22828100
|
T | G | 54 | a0001c0001t0001g0001a0001c0001t0001g0220a0001c0001t0001g0226others(51): Show | 54 | HG00423.hp1 HG00544.hp2 HG00639.hp2 others(51): Show |
intron_variant | MODIFIER | c.485+13005T>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22828100 | ||||||
| chr16:22828378
|
A | G | 32 | a0001c0001t0001g0150a0001c0001t0001g0188a0001c0001t0001g0189others(29): Show | 32 | HG00280.hp1 HG00544.hp1 HG01106.hp1 others(29): Show |
intron_variant | MODIFIER | c.485+13283A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22828378 | ||||||
| chr16:22828554
|
C | T | 1 | a0001c0002t0001g0119 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.485+13459C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22828554 | ||||||
| chr16:22828672
|
C | A | 4 | a0001c0001t0001g0213a0001c0001t0001g0214a0001c0001t0001g0215others(1): Show | 4 | HG02922.hp2 HG02970.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.485+13577C>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22828672 | ||||||
| chr16:22828763
|
A | T | 1 | a0001c0002t0001g0119 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.485+13668A>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22828763 | ||||||
| chr16:22828798
|
C | T | 65 | a0001c0001t0001g0001a0001c0001t0001g0185a0001c0001t0001g0196others(62): Show | 65 | HG00423.hp1 HG00544.hp2 HG00639.hp2 others(62): Show |
intron_variant | MODIFIER | c.485+13703C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22828798 | ||||||
| chr16:22828799
|
G | A | 1 | a0001c0001t0001g0166 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.485+13704G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22828799 | ||||||
| chr16:22828806
|
C | A | 1 | a0001c0002t0001g0121 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.485+13711C>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22828806 | ||||||
| chr16:22828857
|
A | G | 2 | a0001c0001t0001g0194a0001c0001t0001g0195 | 2 | NA18955.hp2 NA18957.hp2 |
intron_variant | MODIFIER | c.485+13762A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22828857 | ||||||
| chr16:22828937
|
A | G | 1 | a0001c0002t0001g0117 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.485+13842A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22828937 | ||||||
| chr16:22829058
|
G | A | 5 | a0001c0001t0001g0293a0001c0001t0001g0306a0001c0002t0001g0007others(2): Show | 5 | HG02145.hp2 HG02572.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.485+13963G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22829058 | ||||||
| chr16:22829070
|
C | G | 3 | a0001c0001t0001g0265a0001c0002t0001g0064a0001c0002t0004g0059 | 3 | HG02071.hp1 HG04184.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.485+13975C>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22829070 | ||||||
| chr16:22829278
|
G | A | 1 | a0001c0004t0002g0144 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.485+14183G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22829278 | ||||||
| chr16:22829342
|
T | C | 4 | a0001c0002t0001g0124a0001c0003t0003g0028a0001c0003t0003g0029others(1): Show | 4 | HG01496.hp2 HG02109.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.485+14247T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22829342 | ||||||
| chr16:22829383
|
G | A | 137 | a0001c0001t0001g0001a0001c0001t0001g0150a0001c0001t0001g0166others(134): Show | 137 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.485+14288G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22829383 | ||||||
| chr16:22829425
|
C | T | 5 | a0001c0001t0001g0293a0001c0001t0001g0306a0001c0002t0001g0007others(2): Show | 5 | HG02145.hp2 HG02572.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.485+14330C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22829425 | ||||||
| chr16:22829479
|
C | CT | 10 | a0001c0001t0001g0216a0001c0001t0001g0294a0001c0001t0001g0295others(7): Show | 10 | HG01884.hp2 HG02145.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.485+14392dupT | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22829479 | |||||
| chr16:22829480
|
T | A | 1 | a0001c0001t0001g0218 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.485+14385T>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22829480 | ||||||
| chr16:22829487
|
T | A | 67 | a0001c0001t0001g0150a0001c0001t0001g0176a0001c0001t0001g0177others(64): Show | 67 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(64): Show |
intron_variant | MODIFIER | c.485+14392T>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22829487 | ||||||
| chr16:22829487
|
T | TA | 7 | a0001c0002t0001g0111a0001c0002t0001g0112a0001c0002t0001g0113others(4): Show | 7 | HG02451.hp2 HG02615.hp2 NA18979.hp1 others(4): Show |
intron_variant | MODIFIER | c.485+14397dupA | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22829487 | |||||
| chr16:22829506
|
A | G | 51 | a0001c0001t0001g0146a0001c0001t0001g0150a0001c0001t0001g0176others(48): Show | 51 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(48): Show |
intron_variant | MODIFIER | c.485+14411A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22829506 | ||||||
| chr16:22829534
|
A | G | 17 | a0001c0001t0001g0216a0001c0001t0001g0294a0001c0001t0001g0295others(14): Show | 17 | HG01884.hp2 HG02145.hp1 HG02280.hp1 others(14): Show |
intron_variant | MODIFIER | c.485+14439A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22829534 | ||||||
| chr16:22829603
|
G | T | 1 | a0001c0001t0013g0264 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.485+14508G>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22829603 | ||||||
| chr16:22829622
|
A | C | 2 | a0001c0003t0003g0017a0001c0004t0014g0242 | 2 | HG03041.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.485+14527A>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22829622 | ||||||
| chr16:22829626
|
G | T | 1 | a0001c0002t0003g0039 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.485+14531G>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22829626 | ||||||
| chr16:22829670
|
A | G | 1 | a0001c0002t0001g0007 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.485+14575A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22829670 | ||||||
| chr16:22829674
|
G | C | 10 | a0001c0001t0001g0297a0001c0001t0001g0302a0001c0001t0001g0303others(7): Show | 10 | HG02886.hp1 HG02922.hp1 HG03130.hp2 others(7): Show |
intron_variant | MODIFIER | c.485+14579G>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22829674 | ||||||
| chr16:22829738
|
C | G | 1 | a0001c0002t0004g0137 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.485+14643C>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22829738 | ||||||
| chr16:22829787
|
C | T | 49 | a0001c0001t0001g0150a0001c0001t0001g0176a0001c0001t0001g0177others(46): Show | 49 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(46): Show |
intron_variant | MODIFIER | c.485+14692C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22829787 | ||||||
| chr16:22829882
|
G | A | 2 | a0001c0001t0001g0316a0001c0002t0001g0122 | 2 | HG00280.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.485+14787G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22829882 | ||||||
| chr16:22830112
|
GACTCGCT others(59): Show |
G | 1 | a0001c0002t0001g0067 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.485+15021_485+1508 others(70): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22830112 | |||||
| chr16:22830135
|
T | G | 1 | a0001c0002t0008g0143 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.485+15040T>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22830135 | ||||||
| chr16:22830171
|
T | G | 50 | a0001c0001t0001g0150a0001c0001t0001g0176a0001c0001t0001g0177others(47): Show | 50 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(47): Show |
intron_variant | MODIFIER | c.485+15076T>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22830171 | ||||||
| chr16:22830181
|
T | A | 1 | a0001c0002t0001g0067 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.485+15086T>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22830181 | ||||||
| chr16:22830184
|
G | T | 1 | a0001c0002t0001g0067 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.485+15089G>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22830184 | ||||||
| chr16:22830188
|
T | A | 1 | a0001c0002t0001g0067 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.485+15093T>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22830188 | ||||||
| chr16:22830189
|
T | C | 1 | a0001c0002t0001g0067 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.485+15094T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22830189 | ||||||
| chr16:22830191
|
C | T | 1 | a0001c0002t0001g0067 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.485+15096C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22830191 | ||||||
| chr16:22830192
|
C | A | 1 | a0001c0002t0001g0067 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.485+15097C>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22830192 | ||||||
| chr16:22830194
|
C | T | 1 | a0001c0002t0001g0067 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.485+15099C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22830194 | ||||||
| chr16:22830198
|
C | A | 1 | a0001c0002t0001g0067 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.485+15103C>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22830198 | ||||||
| chr16:22830199
|
T | A | 1 | a0001c0002t0001g0067 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.485+15104T>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22830199 | ||||||
| chr16:22830236
|
A | G | 4 | a0001c0002t0001g0124a0001c0003t0003g0028a0001c0003t0003g0029others(1): Show | 4 | HG01496.hp2 HG02109.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.485+15141A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22830236 | ||||||
| chr16:22830275
|
G | A | 49 | a0001c0001t0001g0001a0001c0001t0001g0185a0001c0001t0001g0226others(46): Show | 49 | HG00423.hp1 HG00639.hp2 HG00738.hp1 others(46): Show |
intron_variant | MODIFIER | c.485+15180G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22830275 | ||||||
| chr16:22830371
|
A | C | 1 | a0001c0004t0002g0266 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.485+15276A>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22830371 | ||||||
| chr16:22830402
|
G | A | 2 | a0001c0001t0001g0238a0001c0001t0001g0281 | 2 | HG02523.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.485+15307G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22830402 | ||||||
| chr16:22830403
|
G | A | 50 | a0001c0001t0001g0150a0001c0001t0001g0176a0001c0001t0001g0177others(47): Show | 50 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(47): Show |
intron_variant | MODIFIER | c.485+15308G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22830403 | ||||||
| chr16:22830487
|
G | A | 50 | a0001c0001t0001g0150a0001c0001t0001g0176a0001c0001t0001g0177others(47): Show | 50 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(47): Show |
intron_variant | MODIFIER | c.485+15392G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22830487 | ||||||
| chr16:22830490
|
A | G | 1 | a0001c0005t0002g0014 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.485+15395A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22830490 | ||||||
| chr16:22830537
|
A | G | 4 | a0001c0001t0001g0250a0001c0001t0001g0251a0001c0001t0001g0252others(1): Show | 4 | NA18966.hp2 NA18995.hp1 NA19011.hp2 others(1): Show |
intron_variant | MODIFIER | c.485+15442A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22830537 | ||||||
| chr16:22830627
|
A | G | 50 | a0001c0001t0001g0150a0001c0001t0001g0176a0001c0001t0001g0177others(47): Show | 50 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(47): Show |
intron_variant | MODIFIER | c.485+15532A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22830627 | ||||||
| chr16:22830722
|
A | G | 4 | a0001c0001t0001g0293a0001c0002t0001g0007a0001c0004t0002g0144others(1): Show | 4 | HG02145.hp2 HG03209.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.485+15627A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22830722 | ||||||
| chr16:22830948
|
A | G | 2 | a0001c0001t0001g0331a0001c0001t0001g0332 | 2 | HG01099.hp2 HG01109.hp1 |
intron_variant | MODIFIER | c.485+15853A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22830948 | ||||||
| chr16:22831042
|
G | T | 1 | a0001c0002t0005g0141 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.485+15947G>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22831042 | ||||||
| chr16:22831104
|
A | C | 166 | a0001c0001t0001g0001a0001c0001t0001g0150a0001c0001t0001g0166others(163): Show | 166 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(163): Show |
intron_variant | MODIFIER | c.485+16009A>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22831104 | ||||||
| chr16:22831107
|
C | T | 1 | a0001c0001t0001g0277 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.485+16012C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22831107 | ||||||
| chr16:22831160
|
G | A | 1 | a0001c0002t0003g0039 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.485+16065G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22831160 | ||||||
| chr16:22831224
|
A | C | 2 | a0001c0001t0004g0340a0001c0002t0001g0121 | 2 | HG03927.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.485+16129A>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22831224 | ||||||
| chr16:22831282
|
A | C | 2 | a0001c0003t0003g0027a0001c0006t0006g0026 | 2 | HG02615.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.485+16187A>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22831282 | ||||||
| chr16:22831481
|
G | A | 1 | a0001c0001t0001g0178 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.485+16386G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22831481 | ||||||
| chr16:22831537
|
G | A | 1 | a0001c0001t0001g0277 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.485+16442G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22831537 | ||||||
| chr16:22831593
|
A | AT | 105 | a0001c0001t0001g0001a0001c0001t0001g0150a0001c0001t0001g0166others(102): Show | 105 | HG00423.hp1 HG00639.hp2 HG00738.hp1 others(102): Show |
intron_variant | MODIFIER | c.485+16510dupT | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22831593 | |||||
| chr16:22831593
|
A | ATT | 55 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0178others(52): Show | 55 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(52): Show |
intron_variant | MODIFIER | c.485+16509_485+1651 others(6): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22831593 | |||||
| chr16:22831615
|
G | A | 161 | a0001c0001t0001g0001a0001c0001t0001g0150a0001c0001t0001g0166others(158): Show | 161 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(158): Show |
intron_variant | MODIFIER | c.485+16520G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22831615 | ||||||
| chr16:22831627
|
G | A | 1 | a0001c0001t0001g0237 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.485+16532G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22831627 | ||||||
| chr16:22831690
|
T | A | 5 | a0001c0002t0001g0010a0001c0003t0003g0020a0001c0003t0003g0033others(2): Show | 5 | HG01934.hp1 HG02055.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.485+16595T>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22831690 | ||||||
| chr16:22831879
|
T | C | 5 | a0001c0002t0001g0010a0001c0003t0003g0020a0001c0003t0003g0033others(2): Show | 5 | HG01934.hp1 HG02055.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.485+16784T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22831879 | ||||||
| chr16:22832004
|
A | G | 10 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170others(7): Show | 10 | HG01884.hp1 HG02280.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.485+16909A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22832004 | ||||||
| chr16:22832151
|
C | CT | 38 | a0001c0001t0001g0175a0001c0001t0001g0185a0001c0001t0001g0195others(35): Show | 38 | HG00738.hp1 HG01175.hp2 HG01261.hp2 others(35): Show |
intron_variant | MODIFIER | c.485+17074dupT | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22832151 | |||||
| chr16:22832151
|
C | CTTTTTTT others(3): Show |
4 | a0001c0001t0001g0178a0001c0001t0001g0321a0001c0002t0001g0121others(1): Show | 4 | HG01168.hp2 HG02965.hp1 NA20905.hp1 others(1): Show |
intron_variant | MODIFIER | c.485+17065_485+1707 others(14): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22832151 | |||||
| chr16:22832151
|
C | CTTTTTTT others(4): Show |
28 | a0001c0001t0001g0150a0001c0001t0001g0176a0001c0001t0001g0177others(25): Show | 28 | HG00140.hp2 HG00323.hp2 HG01256.hp2 others(25): Show |
intron_variant | MODIFIER | c.485+17064_485+1707 others(15): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22832151 | |||||
| chr16:22832151
|
C | CTTTTTTT others(5): Show |
15 | a0001c0001t0001g0192a0001c0001t0001g0198a0001c0001t0001g0199others(12): Show | 15 | HG00544.hp1 HG01109.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.485+17063_485+1707 others(16): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22832151 | |||||
| chr16:22832151
|
C | CTTTTTTT others(6): Show |
2 | a0001c0001t0001g0212a0001c0002t0001g0348 | 2 | HG02074.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.485+17062_485+1707 others(17): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22832151 | |||||
| chr16:22832151
|
CT | C | 21 | a0001c0001t0001g0148a0001c0001t0001g0153a0001c0001t0001g0160others(18): Show | 21 | HG00323.hp1 HG01070.hp1 HG01070.hp2 others(18): Show |
intron_variant | MODIFIER | c.485+17074delT | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22832151 | |||||
| chr16:22832169
|
T | A | 1 | a0001c0002t0003g0002 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.485+17074T>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22832169 | ||||||
| chr16:22832175
|
T | G | 1 | a0001c0001t0001g0277 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.485+17080T>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22832175 | ||||||
| chr16:22832181
|
G | C | 3 | a0001c0001t0001g0224a0001c0001t0001g0228a0001c0002t0001g0062 | 3 | NA18953.hp2 NA19054.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.485+17086G>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22832181 | ||||||
| chr16:22832208
|
G | A | 49 | a0001c0001t0001g0150a0001c0001t0001g0176a0001c0001t0001g0177others(46): Show | 49 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(46): Show |
intron_variant | MODIFIER | c.485+17113G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22832208 | ||||||
| chr16:22832257
|
A | G | 2 | a0001c0004t0002g0266a0001c0011t0011g0003 | 2 | HG02451.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.485+17162A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22832257 | ||||||
| chr16:22832343
|
A | G | 5 | a0001c0002t0001g0010a0001c0003t0003g0020a0001c0003t0003g0033others(2): Show | 5 | HG01934.hp1 HG02055.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.485+17248A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22832343 | ||||||
| chr16:22832435
|
G | C | 49 | a0001c0001t0001g0150a0001c0001t0001g0176a0001c0001t0001g0177others(46): Show | 49 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(46): Show |
intron_variant | MODIFIER | c.485+17340G>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22832435 | ||||||
| chr16:22832522
|
C | T | 4 | a0001c0001t0001g0167a0001c0001t0001g0175a0001c0001t0001g0217others(1): Show | 4 | HG01175.hp2 HG02451.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.485+17427C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22832522 | ||||||
| chr16:22832526
|
C | T | 1 | a0001c0002t0001g0067 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.485+17431C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22832526 | ||||||
| chr16:22832733
|
G | C | 95 | a0001c0001t0001g0001a0001c0001t0001g0166a0001c0001t0001g0167others(92): Show | 95 | HG00423.hp1 HG00639.hp2 HG00738.hp1 others(92): Show |
intron_variant | MODIFIER | c.485+17638G>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22832733 | ||||||
| chr16:22832780
|
G | A | 1 | a0001c0004t0002g0184 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.485+17685G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22832780 | ||||||
| chr16:22832922
|
G | A | 1 | a0001c0001t0001g0310 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.485+17827G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22832922 | ||||||
| chr16:22832932
|
A | T | 49 | a0001c0001t0001g0150a0001c0001t0001g0176a0001c0001t0001g0177others(46): Show | 49 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(46): Show |
intron_variant | MODIFIER | c.485+17837A>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22832932 | ||||||
| chr16:22832998
|
C | T | 49 | a0001c0001t0001g0150a0001c0001t0001g0176a0001c0001t0001g0177others(46): Show | 49 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(46): Show |
intron_variant | MODIFIER | c.485+17903C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22832998 | ||||||
| chr16:22833062
|
G | C | 49 | a0001c0001t0001g0150a0001c0001t0001g0176a0001c0001t0001g0177others(46): Show | 49 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(46): Show |
intron_variant | MODIFIER | c.485+17967G>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22833062 | ||||||
| chr16:22833294
|
G | T | 6 | a0001c0001t0001g0213a0001c0001t0001g0214a0001c0001t0001g0215others(3): Show | 6 | HG02486.hp2 HG02922.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.485+18199G>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22833294 | ||||||
| chr16:22833304
|
C | T | 2 | a0001c0001t0001g0310a0001c0001t0001g0336 | 2 | HG01433.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.485+18209C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22833304 | ||||||
| chr16:22833323
|
A | G | 2 | a0001c0001t0001g0284a0001c0001t0007g0208 | 2 | NA18942.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.485+18228A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22833323 | ||||||
| chr16:22833372
|
A | C | 150 | a0001c0001t0001g0001a0001c0001t0001g0150a0001c0001t0001g0166others(147): Show | 150 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(147): Show |
intron_variant | MODIFIER | c.485+18277A>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22833372 | ||||||
| chr16:22833374
|
T | C | 145 | a0001c0001t0001g0001a0001c0001t0001g0150a0001c0001t0001g0166others(142): Show | 145 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(142): Show |
intron_variant | MODIFIER | c.485+18279T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22833374 | ||||||
| chr16:22833406
|
G | A | 1 | a0001c0006t0006g0022 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.485+18311G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22833406 | ||||||
| chr16:22833424
|
G | A | 56 | a0001c0001t0001g0001a0001c0001t0001g0185a0001c0001t0001g0226others(53): Show | 56 | HG00423.hp1 HG00639.hp2 HG00738.hp1 others(53): Show |
intron_variant | MODIFIER | c.485+18329G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22833424 | ||||||
| chr16:22833656
|
A | G | 5 | a0001c0002t0001g0010a0001c0003t0003g0020a0001c0003t0003g0033others(2): Show | 5 | HG01934.hp1 HG02055.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.485+18561A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22833656 | ||||||
| chr16:22833662
|
G | T | 2 | a0001c0001t0001g0316a0001c0002t0001g0122 | 2 | HG00280.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.485+18567G>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22833662 | ||||||
| chr16:22833711
|
A | G | 1 | a0001c0002t0001g0053 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.485+18616A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22833711 | ||||||
| chr16:22833852
|
C | T | 1 | a0001c0002t0003g0002 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.485+18757C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22833852 | ||||||
| chr16:22833910
|
A | G | 75 | a0001c0001t0001g0001a0001c0001t0001g0168a0001c0001t0001g0169others(72): Show | 75 | HG00423.hp1 HG00639.hp2 HG00738.hp1 others(72): Show |
intron_variant | MODIFIER | c.485+18815A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22833910 | ||||||
| chr16:22833920
|
G | A | 1 | a0001c0001t0001g0336 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.485+18825G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22833920 | ||||||
| chr16:22833934
|
AC | A | 10 | a0001c0001t0001g0167a0001c0001t0001g0175a0001c0001t0001g0213others(7): Show | 10 | HG01175.hp2 HG02451.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.485+18840delC | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22833934 | ||||||
| chr16:22834107
|
A | G | 4 | a0001c0001t0001g0286a0001c0003t0003g0019a0001c0004t0002g0267others(1): Show | 4 | HG01891.hp2 HG02647.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.485+19012A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22834107 | ||||||
| chr16:22834195
|
C | G | 1 | a0001c0005t0002g0014 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.485+19100C>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22834195 | ||||||
| chr16:22834211
|
A | G | 49 | a0001c0001t0001g0150a0001c0001t0001g0176a0001c0001t0001g0177others(46): Show | 49 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(46): Show |
intron_variant | MODIFIER | c.485+19116A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22834211 | ||||||
| chr16:22834323
|
T | G | 1 | a0001c0001t0001g0226 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.485+19228T>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22834323 | ||||||
| chr16:22834423
|
G | A | 138 | a0001c0001t0001g0001a0001c0001t0001g0150a0001c0001t0001g0166others(135): Show | 138 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(135): Show |
intron_variant | MODIFIER | c.485+19328G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22834423 | ||||||
| chr16:22834538
|
G | A | 95 | a0001c0001t0001g0001a0001c0001t0001g0166a0001c0001t0001g0167others(92): Show | 95 | HG00423.hp1 HG00639.hp2 HG00738.hp1 others(92): Show |
intron_variant | MODIFIER | c.485+19443G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22834538 | ||||||
| chr16:22834677
|
T | TAAAAAGT others(307): Show |
43 | a0001c0001t0001g0150a0001c0001t0001g0176a0001c0001t0001g0177others(40): Show | 43 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(40): Show |
intron_variant | MODIFIER | c.485+19601_485+1960 others(318): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22834677 | |||||
| chr16:22834677
|
T | TAAAAAGT others(308): Show |
1 | a0005c0013t0002g0263 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.485+19601_485+1960 others(319): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22834677 | |||||
| chr16:22834677
|
T | TAAAAAGT others(312): Show |
4 | a0001c0003t0003g0020a0001c0003t0003g0033a0001c0003t0003g0034others(1): Show | 4 | HG01934.hp1 HG02818.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.485+19601_485+1960 others(323): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22834677 | |||||
| chr16:22834677
|
T | TAAAAAGT others(313): Show |
1 | a0001c0002t0001g0010 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.485+19601_485+1960 others(324): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22834677 | |||||
| chr16:22834717
|
C | T | 3 | a0001c0001t0001g0230a0001c0001t0001g0270a0001c0001t0001g0350 | 3 | NA18969.hp1 NA19006.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.485+19622C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22834717 | ||||||
| chr16:22834724
|
C | T | 5 | a0001c0002t0001g0010a0001c0003t0003g0020a0001c0003t0003g0033others(2): Show | 5 | HG01934.hp1 HG02055.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.485+19629C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22834724 | ||||||
| chr16:22834742
|
A | T | 1 | a0001c0004t0002g0267 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.485+19647A>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22834742 | ||||||
| chr16:22834752
|
C | T | 5 | a0001c0001t0001g0293a0001c0001t0001g0306a0001c0002t0001g0007others(2): Show | 5 | HG02145.hp2 HG02572.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.485+19657C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22834752 | ||||||
| chr16:22834929
|
G | C | 165 | a0001c0001t0001g0001a0001c0001t0001g0150a0001c0001t0001g0166others(162): Show | 165 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(162): Show |
intron_variant | MODIFIER | c.485+19834G>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22834929 | ||||||
| chr16:22834953
|
A | ATTTC | 91 | a0001c0001t0001g0001a0001c0001t0001g0166a0001c0001t0001g0167others(88): Show | 91 | HG00423.hp1 HG00639.hp2 HG00738.hp1 others(88): Show |
intron_variant | MODIFIER | c.485+19863_485+1986 others(8): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22834953 | |||||
| chr16:22834955
|
T | TTCTG | 4 | a0001c0001t0001g0286a0001c0003t0003g0019a0001c0004t0002g0267others(1): Show | 4 | HG01891.hp2 HG02647.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.485+19863_485+1986 others(8): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22834955 | |||||
| chr16:22835043
|
G | A | 1 | a0001c0001t0001g0306 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.485+19948G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22835043 | ||||||
| chr16:22835091
|
G | A | 1 | a0001c0003t0003g0018 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.485+19996G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22835091 | ||||||
| chr16:22835115
|
A | AAGTCTTA others(186): Show |
1 | a0001c0001t0001g0277 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.485+20034_485+2003 others(197): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22835115 | |||||
| chr16:22835138
|
G | A | 1 | a0001c0001t0001g0271 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.485+20043G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22835138 | ||||||
| chr16:22835180
|
A | AT | 20 | a0001c0001t0001g0166a0001c0001t0001g0167a0001c0001t0001g0175others(17): Show | 20 | HG01175.hp2 HG02451.hp1 HG02451.hp2 others(17): Show |
intron_variant | MODIFIER | c.485+20094dupT | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22835180 | |||||
| chr16:22835255
|
C | T | 1 | a0001c0002t0001g0013 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.485+20160C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22835255 | ||||||
| chr16:22835280
|
A | G | 1 | a0001c0001t0001g0289 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.485+20185A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22835280 | ||||||
| chr16:22835296
|
T | TTTTG | 102 | a0001c0001t0001g0001a0001c0001t0001g0166a0001c0001t0001g0167others(99): Show | 102 | HG00423.hp1 HG00639.hp2 HG00738.hp1 others(99): Show |
intron_variant | MODIFIER | c.485+20209_485+2021 others(8): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22835296 | |||||
| chr16:22835378
|
C | T | 1 | a0001c0002t0004g0072 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.485+20283C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22835378 | ||||||
| chr16:22835485
|
G | A | 1 | a0001c0001t0001g0175 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.485+20390G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22835485 | ||||||
| chr16:22835637
|
C | T | 102 | a0001c0001t0001g0001a0001c0001t0001g0166a0001c0001t0001g0167others(99): Show | 102 | HG00423.hp1 HG00639.hp2 HG00738.hp1 others(99): Show |
intron_variant | MODIFIER | c.485+20542C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22835637 | ||||||
| chr16:22835677
|
A | G | 1 | a0001c0001t0001g0262 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.485+20582A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22835677 | ||||||
| chr16:22835692
|
C | G | 3 | a0001c0001t0001g0302a0001c0001t0001g0303a0001c0001t0001g0305 | 3 | HG02922.hp1 HG03453.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.485+20597C>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22835692 | ||||||
| chr16:22835854
|
T | A | 1 | a0001c0001t0001g0313 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.485+20759T>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22835854 | ||||||
| chr16:22835886
|
A | G | 1 | a0001c0002t0003g0002 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.485+20791A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22835886 | ||||||
| chr16:22836025
|
A | C | 1 | a0001c0001t0001g0277 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.485+20930A>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22836025 | ||||||
| chr16:22836467
|
C | T | 10 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170others(7): Show | 10 | HG01884.hp1 HG02280.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.485+21372C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22836467 | ||||||
| chr16:22836535
|
T | C | 10 | a0001c0001t0001g0166a0001c0001t0001g0181a0001c0001t0001g0182others(7): Show | 10 | HG02486.hp1 HG02559.hp1 HG03453.hp1 others(7): Show |
intron_variant | MODIFIER | c.485+21440T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22836535 | ||||||
| chr16:22836619
|
A | C | 1 | a0001c0001t0001g0162 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.485+21524A>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22836619 | ||||||
| chr16:22836620
|
G | A | 2 | a0001c0002t0001g0065a0001c0002t0001g0066 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.485+21525G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22836620 | ||||||
| chr16:22836640
|
T | G | 4 | a0001c0001t0001g0320a0001c0001t0001g0321a0001c0004t0002g0179others(1): Show | 4 | HG00323.hp2 HG01168.hp2 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.485+21545T>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22836640 | ||||||
| chr16:22836738
|
G | A | 4 | a0001c0001t0001g0286a0001c0003t0003g0019a0001c0004t0002g0267others(1): Show | 4 | HG01891.hp2 HG02647.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.485+21643G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22836738 | ||||||
| chr16:22836797
|
C | T | 1 | a0001c0004t0002g0261 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.485+21702C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22836797 | ||||||
| chr16:22836801
|
G | A | 2 | a0003c0008t0002g0231a0003c0008t0002g0232 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.485+21706G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22836801 | ||||||
| chr16:22836872
|
A | G | 103 | a0001c0001t0001g0001a0001c0001t0001g0166a0001c0001t0001g0167others(100): Show | 103 | HG00423.hp1 HG00639.hp1 HG00639.hp2 others(100): Show |
intron_variant | MODIFIER | c.485+21777A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22836872 | ||||||
| chr16:22837119
|
G | GT | 238 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0147others(235): Show | 238 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(235): Show |
intron_variant | MODIFIER | c.485+22036dupT | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22837119 | |||||
| chr16:22837119
|
G | GTT | 11 | a0001c0001t0001g0187a0001c0001t0001g0203a0001c0001t0001g0260others(8): Show | 11 | HG01256.hp1 HG02074.hp2 HG02965.hp2 others(8): Show |
intron_variant | MODIFIER | c.485+22035_485+2203 others(6): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22837119 | |||||
| chr16:22837119
|
GT | G | 81 | a0001c0001t0001g0001a0001c0001t0001g0166a0001c0001t0001g0168others(78): Show | 81 | HG00423.hp1 HG00639.hp2 HG00738.hp1 others(78): Show |
intron_variant | MODIFIER | c.485+22036delT | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22837119 | |||||
| chr16:22837172
|
T | C | 2 | a0001c0001t0001g0287a0001c0001t0001g0288 | 2 | HG06807.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.485+22077T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22837172 | ||||||
| chr16:22837327
|
T | G | 3 | a0001c0001t0001g0300a0001c0003t0003g0017a0001c0004t0014g0242 | 3 | HG02965.hp2 HG03041.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.485+22232T>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22837327 | ||||||
| chr16:22837358
|
T | C | 1 | a0001c0002t0001g0081 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.485+22263T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22837358 | ||||||
| chr16:22837405
|
G | A | 15 | a0001c0001t0001g0167a0001c0001t0001g0175a0001c0001t0001g0213others(12): Show | 15 | HG01934.hp1 HG02055.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.485+22310G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22837405 | ||||||
| chr16:22837410
|
T | C | 2 | a0001c0002t0001g0093a0001c0004t0002g0272 | 2 | HG01255.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.485+22315T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22837410 | ||||||
| chr16:22837446
|
C | T | 1 | a0001c0002t0001g0086 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.485+22351C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22837446 | ||||||
| chr16:22837473
|
T | G | 7 | a0001c0001t0001g0194a0001c0001t0001g0195a0001c0001t0001g0277others(4): Show | 7 | NA18955.hp2 NA18957.hp2 NA18967.hp1 others(4): Show |
intron_variant | MODIFIER | c.485+22378T>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22837473 | ||||||
| chr16:22837479
|
TC | T | 10 | a0001c0001t0001g0167a0001c0001t0001g0175a0001c0001t0001g0213others(7): Show | 10 | HG02451.hp1 HG02451.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.485+22386delC | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22837479 | |||||
| chr16:22837483
|
A | ATG | 8 | a0001c0001t0001g0194a0001c0001t0001g0195a0001c0001t0001g0277others(5): Show | 8 | HG02129.hp1 NA18955.hp2 NA18957.hp2 others(5): Show |
intron_variant | MODIFIER | c.485+22404_485+2240 others(6): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22837483 | |||||
| chr16:22837483
|
A | ATGTG | 57 | a0001c0001t0001g0001a0001c0001t0001g0204a0001c0001t0001g0226others(54): Show | 57 | HG00423.hp1 HG00639.hp2 HG00738.hp1 others(54): Show |
intron_variant | MODIFIER | c.485+22402_485+2240 others(8): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22837483 | |||||
| chr16:22837483
|
A | ATGTGTG | 13 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170others(10): Show | 13 | HG01884.hp1 HG01891.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.485+22400_485+2240 others(10): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22837483 | |||||
| chr16:22837501
|
A | G | 3 | a0001c0001t0001g0300a0001c0003t0003g0017a0001c0004t0014g0242 | 3 | HG02965.hp2 HG03041.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.485+22406A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22837501 | ||||||
| chr16:22837509
|
G | GTGTATAT others(37): Show |
1 | a0001c0005t0002g0014 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.485+22429_485+2247 others(48): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22837509 | |||||
| chr16:22837513
|
A | G | 16 | a0001c0001t0001g0166a0001c0001t0001g0181a0001c0001t0001g0182others(13): Show | 16 | HG02486.hp1 HG02559.hp1 HG03453.hp1 others(13): Show |
intron_variant | MODIFIER | c.485+22418A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22837513 | ||||||
| chr16:22837538
|
GATATATG others(3): Show |
G | 2 | a0001c0001t0001g0310a0001c0002t0001g0013 | 2 | HG02258.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.485+22460_485+2246 others(14): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22837538 | |||||
| chr16:22837544
|
T | G | 16 | a0001c0001t0001g0318a0001c0001t0001g0319a0001c0001t0004g0193others(13): Show | 16 | HG00423.hp1 HG00738.hp1 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.485+22449T>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22837544 | ||||||
| chr16:22837566
|
CAT | C | 14 | a0001c0001t0001g0166a0001c0001t0001g0181a0001c0001t0001g0182others(11): Show | 14 | HG01934.hp1 HG02055.hp1 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.485+22483_485+2248 others(6): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22837566 | |||||
| chr16:22837566
|
CATAT | C | 10 | a0001c0001t0001g0167a0001c0001t0001g0175a0001c0001t0001g0213others(7): Show | 10 | HG02451.hp1 HG02451.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.485+22481_485+2248 others(8): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22837566 | |||||
| chr16:22837576
|
TATAC | T | 7 | a0001c0001t0001g0194a0001c0001t0001g0195a0001c0001t0001g0277others(4): Show | 7 | NA18955.hp2 NA18957.hp2 NA18967.hp1 others(4): Show |
intron_variant | MODIFIER | c.485+22483_485+2248 others(8): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22837576 | |||||
| chr16:22837578
|
T | C | 57 | a0001c0001t0001g0001a0001c0001t0001g0204a0001c0001t0001g0226others(54): Show | 57 | HG00423.hp1 HG00639.hp2 HG00738.hp1 others(54): Show |
intron_variant | MODIFIER | c.485+22483T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22837578 | ||||||
| chr16:22837590
|
C | CAT | 57 | a0001c0001t0001g0001a0001c0001t0001g0204a0001c0001t0001g0226others(54): Show | 57 | HG00423.hp1 HG00639.hp2 HG00738.hp1 others(54): Show |
intron_variant | MODIFIER | c.485+22495_485+2249 others(6): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22837590 | ||||||
| chr16:22837590
|
C | T | 14 | a0001c0001t0001g0166a0001c0001t0001g0181a0001c0001t0001g0182others(11): Show | 14 | HG01934.hp1 HG02055.hp1 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.485+22495C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22837590 | ||||||
| chr16:22837591
|
G | A | 2 | a0002c0009t0001g0342a0002c0009t0001g0344 | 2 | NA18962.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.485+22496G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22837591 | ||||||
| chr16:22837630
|
A | AAC | 103 | a0001c0001t0001g0001a0001c0001t0001g0166a0001c0001t0001g0167others(100): Show | 103 | HG00423.hp1 HG00639.hp2 HG00738.hp1 others(100): Show |
intron_variant | MODIFIER | c.485+22545_485+2254 others(6): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22837630 | |||||
| chr16:22837630
|
A | AACAC | 5 | a0001c0002t0001g0124a0001c0003t0003g0028a0001c0003t0003g0029others(2): Show | 5 | HG00639.hp1 HG01496.hp2 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.485+22543_485+2254 others(8): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22837630 | |||||
| chr16:22837834
|
G | A | 1 | a0001c0001t0001g0268 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.485+22739G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22837834 | ||||||
| chr16:22837845
|
G | A | 16 | a0001c0001t0001g0166a0001c0001t0001g0181a0001c0001t0001g0182others(13): Show | 16 | HG02486.hp1 HG02559.hp1 HG03453.hp1 others(13): Show |
intron_variant | MODIFIER | c.485+22750G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22837845 | ||||||
| chr16:22837878
|
G | A | 9 | a0001c0001t0001g0166a0001c0001t0001g0181a0001c0001t0001g0182others(6): Show | 9 | HG02486.hp1 HG02559.hp1 HG03453.hp1 others(6): Show |
intron_variant | MODIFIER | c.485+22783G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22837878 | ||||||
| chr16:22837879
|
A | G | 15 | a0001c0001t0001g0167a0001c0001t0001g0175a0001c0001t0001g0213others(12): Show | 15 | HG01934.hp1 HG02055.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.485+22784A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22837879 | ||||||
| chr16:22838024
|
G | GA | 16 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170others(13): Show | 16 | HG01884.hp1 HG01891.hp2 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.485+22938dupA | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22838024 | |||||
| chr16:22838177
|
C | T | 8 | a0001c0001t0001g0166a0001c0001t0001g0181a0001c0001t0001g0182others(5): Show | 8 | HG02486.hp1 HG02559.hp1 HG03453.hp1 others(5): Show |
intron_variant | MODIFIER | c.485+23082C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22838177 | ||||||
| chr16:22838256
|
G | C | 1 | a0001c0001t0001g0203 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.485+23161G>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22838256 | ||||||
| chr16:22838276
|
C | T | 2 | a0001c0004t0002g0183a0001c0005t0002g0098 | 2 | NA20752.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.485+23181C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22838276 | ||||||
| chr16:22838280
|
G | A | 1 | a0001c0002t0008g0139 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.485+23185G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22838280 | ||||||
| chr16:22838338
|
C | T | 2 | a0001c0002t0001g0077a0001c0002t0001g0078 | 2 | NA18980.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.485+23243C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22838338 | ||||||
| chr16:22838352
|
G | A | 16 | a0001c0001t0001g0166a0001c0001t0001g0181a0001c0001t0001g0182others(13): Show | 16 | HG02486.hp1 HG02559.hp1 HG03453.hp1 others(13): Show |
intron_variant | MODIFIER | c.485+23257G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22838352 | ||||||
| chr16:22838379
|
G | A | 4 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0186others(1): Show | 4 | HG02559.hp1 HG03453.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.485+23284G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22838379 | ||||||
| chr16:22838401
|
G | A | 9 | a0001c0001t0001g0166a0001c0001t0001g0181a0001c0001t0001g0182others(6): Show | 9 | HG02486.hp1 HG02559.hp1 HG03453.hp1 others(6): Show |
intron_variant | MODIFIER | c.485+23306G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22838401 | ||||||
| chr16:22838522
|
G | A | 1 | a0001c0005t0002g0009 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.485+23427G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22838522 | ||||||
| chr16:22838620
|
T | C | 152 | a0001c0001t0001g0001a0001c0001t0001g0150a0001c0001t0001g0166others(149): Show | 152 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(149): Show |
intron_variant | MODIFIER | c.485+23525T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22838620 | ||||||
| chr16:22838810
|
G | A | 4 | a0001c0002t0001g0124a0001c0003t0003g0028a0001c0003t0003g0029others(1): Show | 4 | HG01496.hp2 HG02109.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.485+23715G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22838810 | ||||||
| chr16:22838908
|
A | T | 1 | a0001c0001t0001g0204 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.485+23813A>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22838908 | ||||||
| chr16:22839175
|
G | A | 1 | a0001c0002t0001g0055 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.485+24080G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22839175 | ||||||
| chr16:22839193
|
T | C | 8 | a0001c0001t0001g0166a0001c0001t0001g0181a0001c0001t0001g0182others(5): Show | 8 | HG02486.hp1 HG02559.hp1 HG03453.hp1 others(5): Show |
intron_variant | MODIFIER | c.485+24098T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22839193 | ||||||
| chr16:22839406
|
T | G | 5 | a0001c0001t0001g0293a0001c0001t0001g0306a0001c0002t0001g0007others(2): Show | 5 | HG02145.hp2 HG02572.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.485+24311T>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22839406 | ||||||
| chr16:22839615
|
T | G | 72 | a0001c0001t0001g0001a0001c0001t0001g0167a0001c0001t0001g0175others(69): Show | 72 | HG00423.hp1 HG00639.hp2 HG00738.hp1 others(69): Show |
intron_variant | MODIFIER | c.485+24520T>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22839615 | ||||||
| chr16:22839663
|
A | G | 14 | a0001c0001t0001g0166a0001c0001t0001g0181a0001c0001t0001g0182others(11): Show | 14 | HG02486.hp1 HG02559.hp1 HG03453.hp1 others(11): Show |
intron_variant | MODIFIER | c.485+24568A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22839663 | ||||||
| chr16:22839677
|
A | G | 2 | a0001c0001t0001g0153a0001c0001t0001g0158 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.485+24582A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22839677 | ||||||
| chr16:22839727
|
C | T | 46 | a0001c0001t0001g0150a0001c0001t0001g0176a0001c0001t0001g0177others(43): Show | 46 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(43): Show |
intron_variant | MODIFIER | c.485+24632C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22839727 | ||||||
| chr16:22839852
|
C | T | 7 | a0001c0001t0001g0166a0001c0001t0001g0181a0001c0001t0001g0182others(4): Show | 7 | HG02486.hp1 HG02559.hp1 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.485+24757C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22839852 | ||||||
| chr16:22839914
|
A | G | 5 | a0001c0002t0001g0010a0001c0003t0003g0020a0001c0003t0003g0033others(2): Show | 5 | HG01934.hp1 HG02055.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.485+24819A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22839914 | ||||||
| chr16:22839978
|
T | C | 5 | a0001c0001t0001g0293a0001c0001t0001g0306a0001c0002t0001g0007others(2): Show | 5 | HG02145.hp2 HG02572.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.485+24883T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22839978 | ||||||
| chr16:22840139
|
G | T | 3 | a0001c0001t0001g0300a0001c0003t0003g0017a0001c0004t0014g0242 | 3 | HG02965.hp2 HG03041.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.485+25044G>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22840139 | ||||||
| chr16:22840155
|
G | A | 45 | a0001c0001t0001g0150a0001c0001t0001g0176a0001c0001t0001g0177others(42): Show | 45 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(42): Show |
intron_variant | MODIFIER | c.485+25060G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22840155 | ||||||
| chr16:22840384
|
C | CT | 15 | a0001c0001t0001g0166a0001c0001t0001g0181a0001c0001t0001g0182others(12): Show | 15 | HG02486.hp1 HG02559.hp1 HG03225.hp2 others(12): Show |
intron_variant | MODIFIER | c.485+25302dupT | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22840384 | |||||
| chr16:22840515
|
T | G | 13 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170others(10): Show | 13 | HG01884.hp1 HG01891.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.485+25420T>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22840515 | ||||||
| chr16:22840556
|
T | G | 14 | a0001c0001t0001g0166a0001c0001t0001g0181a0001c0001t0001g0182others(11): Show | 14 | HG02486.hp1 HG02559.hp1 HG03453.hp1 others(11): Show |
intron_variant | MODIFIER | c.485+25461T>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22840556 | ||||||
| chr16:22840727
|
T | C | 1 | a0001c0002t0001g0117 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.485+25632T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22840727 | ||||||
| chr16:22840754
|
G | A | 4 | a0001c0002t0001g0124a0001c0003t0003g0028a0001c0003t0003g0029others(1): Show | 4 | HG01496.hp2 HG02109.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.485+25659G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22840754 | ||||||
| chr16:22840903
|
T | C | 14 | a0001c0001t0001g0166a0001c0001t0001g0181a0001c0001t0001g0182others(11): Show | 14 | HG02486.hp1 HG02559.hp1 HG03453.hp1 others(11): Show |
intron_variant | MODIFIER | c.485+25808T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22840903 | ||||||
| chr16:22840938
|
A | G | 1 | a0001c0001t0001g0212 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.485+25843A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22840938 | ||||||
| chr16:22840962
|
C | T | 6 | a0001c0001t0001g0166a0001c0001t0001g0181a0001c0001t0001g0182others(3): Show | 6 | HG02486.hp1 HG02559.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.485+25867C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22840962 | ||||||
| chr16:22840963
|
C | A | 3 | a0001c0002t0001g0110a0001c0002t0001g0308a0001c0002t0001g0309 | 3 | HG01106.hp2 HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.485+25868C>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22840963 | ||||||
| chr16:22840981
|
C | T | 1 | a0001c0002t0004g0095 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.485+25886C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22840981 | ||||||
| chr16:22840994
|
G | A | 5 | a0001c0002t0001g0010a0001c0003t0003g0020a0001c0003t0003g0033others(2): Show | 5 | HG01934.hp1 HG02055.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.485+25899G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22840994 | ||||||
| chr16:22841003
|
C | T | 1 | a0001c0001t0001g0249 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.485+25908C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22841003 | ||||||
| chr16:22841125
|
G | A | 1 | a0001c0002t0001g0058 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.485+26030G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22841125 | ||||||
| chr16:22841164
|
C | T | 4 | a0001c0002t0001g0124a0001c0003t0003g0028a0001c0003t0003g0029others(1): Show | 4 | HG01496.hp2 HG02109.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.485+26069C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22841164 | ||||||
| chr16:22841175
|
C | T | 1 | a0001c0001t0001g0253 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.485+26080C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22841175 | ||||||
| chr16:22841215
|
G | A | 1 | a0001c0004t0002g0179 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.485+26120G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22841215 | ||||||
| chr16:22841254
|
C | G | 1 | a0001c0002t0001g0138 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.485+26159C>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22841254 | ||||||
| chr16:22841274
|
G | A | 1 | a0001c0001t0001g0243 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.485+26179G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22841274 | ||||||
| chr16:22841330
|
G | C | 7 | a0001c0001t0001g0194a0001c0001t0001g0195a0001c0001t0001g0277others(4): Show | 7 | NA18955.hp2 NA18957.hp2 NA18967.hp1 others(4): Show |
intron_variant | MODIFIER | c.485+26235G>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22841330 | ||||||
| chr16:22841368
|
C | A | 12 | a0001c0001t0001g0167a0001c0001t0001g0175a0001c0001t0001g0213others(9): Show | 12 | HG02451.hp1 HG02451.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.485+26273C>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22841368 | ||||||
| chr16:22841627
|
T | G | 7 | a0001c0001t0001g0213a0001c0001t0001g0214a0001c0001t0001g0215others(4): Show | 7 | HG02451.hp2 HG02486.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.485+26532T>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22841627 | ||||||
| chr16:22841793
|
T | C | 7 | a0001c0001t0001g0194a0001c0001t0001g0195a0001c0001t0001g0277others(4): Show | 7 | NA18955.hp2 NA18957.hp2 NA18967.hp1 others(4): Show |
intron_variant | MODIFIER | c.485+26698T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22841793 | ||||||
| chr16:22841824
|
A | G | 15 | a0001c0001t0001g0166a0001c0001t0001g0181a0001c0001t0001g0182others(12): Show | 15 | HG02486.hp1 HG02559.hp1 HG02809.hp1 others(12): Show |
intron_variant | MODIFIER | c.485+26729A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22841824 | ||||||
| chr16:22841850
|
C | T | 12 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170others(9): Show | 12 | HG01884.hp1 HG01891.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.485+26755C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22841850 | ||||||
| chr16:22842062
|
CT | C | 68 | a0001c0001t0001g0145a0001c0001t0001g0167a0001c0001t0001g0168others(65): Show | 68 | HG00323.hp1 HG00423.hp2 HG00639.hp1 others(65): Show |
intron_variant | MODIFIER | c.485+26986delT | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22842062 | |||||
| chr16:22842062
|
CTT | C | 76 | a0001c0001t0001g0001a0001c0001t0001g0166a0001c0001t0001g0181others(73): Show | 76 | HG00423.hp1 HG00639.hp2 HG00738.hp1 others(73): Show |
intron_variant | MODIFIER | c.485+26985_485+2698 others(6): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22842062 | |||||
| chr16:22842062
|
CTTT | C | 42 | a0001c0001t0001g0146a0001c0001t0001g0150a0001c0001t0001g0176others(39): Show | 42 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(39): Show |
intron_variant | MODIFIER | c.485+26984_485+2698 others(7): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22842062 | |||||
| chr16:22842068
|
T | C | 14 | a0001c0001t0001g0166a0001c0001t0001g0181a0001c0001t0001g0182others(11): Show | 14 | HG02486.hp1 HG02559.hp1 HG03453.hp1 others(11): Show |
intron_variant | MODIFIER | c.485+26973T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22842068 | ||||||
| chr16:22842187
|
G | A | 11 | a0001c0001t0001g0151a0001c0001t0001g0153a0001c0001t0001g0154others(8): Show | 11 | HG00280.hp2 HG01070.hp1 HG01257.hp1 others(8): Show |
intron_variant | MODIFIER | c.485+27092G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22842187 | ||||||
| chr16:22842244
|
C | T | 5 | a0001c0002t0001g0110a0001c0002t0001g0308a0001c0002t0001g0309others(2): Show | 5 | HG00639.hp2 HG01106.hp2 HG01516.hp2 others(2): Show |
intron_variant | MODIFIER | c.485+27149C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22842244 | ||||||
| chr16:22842295
|
T | C | 1 | a0001c0002t0001g0076 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.485+27200T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22842295 | ||||||
| chr16:22842309
|
C | T | 7 | a0001c0001t0001g0213a0001c0001t0001g0214a0001c0001t0001g0215others(4): Show | 7 | HG02451.hp2 HG02486.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.485+27214C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22842309 | ||||||
| chr16:22842345
|
G | A | 1 | a0001c0002t0001g0084 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.485+27250G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22842345 | ||||||
| chr16:22842398
|
T | C | 1 | a0001c0001t0001g0286 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.485+27303T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22842398 | ||||||
| chr16:22842525
|
C | T | 1 | a0001c0011t0011g0003 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.485+27430C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22842525 | ||||||
| chr16:22842553
|
G | A | 157 | a0001c0001t0001g0001a0001c0001t0001g0146a0001c0001t0001g0150others(154): Show | 157 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(154): Show |
intron_variant | MODIFIER | c.485+27458G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22842553 | ||||||
| chr16:22842555
|
C | A | 13 | a0001c0001t0001g0151a0001c0001t0001g0153a0001c0001t0001g0154others(10): Show | 13 | HG00280.hp2 HG01070.hp1 HG01257.hp1 others(10): Show |
intron_variant | MODIFIER | c.485+27460C>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22842555 | ||||||
| chr16:22842621
|
C | T | 1 | a0001c0005t0002g0041 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.485+27526C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22842621 | ||||||
| chr16:22842704
|
C | T | 1 | a0001c0001t0001g0162 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.485+27609C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22842704 | ||||||
| chr16:22842810
|
C | T | 1 | a0001c0001t0001g0248 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.485+27715C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22842810 | ||||||
| chr16:22842921
|
T | C | 15 | a0001c0001t0001g0166a0001c0001t0001g0181a0001c0001t0001g0182others(12): Show | 15 | HG02486.hp1 HG02559.hp1 HG02809.hp1 others(12): Show |
intron_variant | MODIFIER | c.485+27826T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22842921 | ||||||
| chr16:22843138
|
CTG | C | 42 | a0001c0001t0001g0150a0001c0001t0001g0176a0001c0001t0001g0177others(39): Show | 42 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(39): Show |
intron_variant | MODIFIER | c.485+28046_485+2804 others(6): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22843138 | |||||
| chr16:22843154
|
G | GCA | 3 | a0001c0003t0003g0028a0001c0003t0003g0029a0001c0003t0003g0030 | 3 | HG01496.hp2 HG02622.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.485+28059_485+2806 others(6): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22843154 | ||||||
| chr16:22843155
|
T | C | 1 | a0001c0002t0001g0124 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.485+28060T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22843155 | ||||||
| chr16:22843156
|
A | ATG | 62 | a0001c0001t0001g0150a0001c0001t0001g0167a0001c0001t0001g0175others(59): Show | 62 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(59): Show |
intron_variant | MODIFIER | c.485+28080_485+2808 others(6): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22843156 | |||||
| chr16:22843156
|
A | G | 3 | a0001c0003t0003g0028a0001c0003t0003g0029a0001c0003t0003g0030 | 3 | HG01496.hp2 HG02622.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.485+28061A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22843156 | ||||||
| chr16:22843156
|
ATG | A | 5 | a0001c0001t0001g0293a0001c0001t0001g0306a0001c0002t0001g0007others(2): Show | 5 | HG02145.hp2 HG02572.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.485+28080_485+2808 others(6): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22843156 | |||||
| chr16:22843236
|
A | G | 15 | a0001c0001t0001g0166a0001c0001t0001g0181a0001c0001t0001g0182others(12): Show | 15 | HG02486.hp1 HG02559.hp1 HG02809.hp1 others(12): Show |
intron_variant | MODIFIER | c.485+28141A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22843236 | ||||||
| chr16:22843284
|
A | G | 4 | a0001c0001t0001g0172a0001c0001t0001g0218a0001c0005t0006g0040others(1): Show | 4 | HG01167.hp2 HG02647.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.485+28189A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22843284 | ||||||
| chr16:22843362
|
G | A | 1 | a0001c0001t0001g0255 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.485+28267G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22843362 | ||||||
| chr16:22843402
|
G | A | 52 | a0001c0001t0001g0001a0001c0001t0001g0201a0001c0001t0001g0226others(49): Show | 52 | HG00423.hp1 HG00639.hp2 HG00738.hp1 others(49): Show |
intron_variant | MODIFIER | c.485+28307G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22843402 | ||||||
| chr16:22843574
|
T | G | 1 | a0001c0001t0001g0146 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.485+28479T>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22843574 | ||||||
| chr16:22843609
|
T | G | 2 | a0001c0001t0001g0194a0001c0001t0001g0195 | 2 | NA18955.hp2 NA18957.hp2 |
intron_variant | MODIFIER | c.485+28514T>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22843609 | ||||||
| chr16:22843621
|
G | A | 1 | a0001c0001t0001g0227 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.485+28526G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22843621 | ||||||
| chr16:22843621
|
G | T | 1 | a0001c0004t0002g0179 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.485+28526G>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22843621 | ||||||
| chr16:22843647
|
T | G | 157 | a0001c0001t0001g0001a0001c0001t0001g0146a0001c0001t0001g0150others(154): Show | 157 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(154): Show |
intron_variant | MODIFIER | c.485+28552T>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22843647 | ||||||
| chr16:22843806
|
A | C | 3 | a0001c0001t0001g0217a0001c0001t0001g0271a0001c0003t0003g0015 | 3 | HG01175.hp2 HG02897.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.485+28711A>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22843806 | ||||||
| chr16:22843906
|
AAGAAAC | A | 42 | a0001c0001t0001g0150a0001c0001t0001g0176a0001c0001t0001g0177others(39): Show | 42 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(39): Show |
intron_variant | MODIFIER | c.485+28815_485+2882 others(10): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22843906 | |||||
| chr16:22843958
|
C | T | 52 | a0001c0001t0001g0001a0001c0001t0001g0201a0001c0001t0001g0226others(49): Show | 52 | HG00423.hp1 HG00639.hp2 HG00738.hp1 others(49): Show |
intron_variant | MODIFIER | c.485+28863C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22843958 | ||||||
| chr16:22844008
|
T | TAC | 21 | a0001c0001t0001g0162a0001c0001t0001g0237a0001c0001t0001g0240others(18): Show | 21 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(18): Show |
intron_variant | MODIFIER | c.485+28940_485+2894 others(6): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22844008 | |||||
| chr16:22844008
|
TAC | T | 11 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170others(8): Show | 11 | HG01884.hp1 HG02280.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.485+28940_485+2894 others(6): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22844008 | |||||
| chr16:22844008
|
TACAC | T | 10 | a0001c0001t0001g0166a0001c0001t0001g0173a0001c0001t0001g0181others(7): Show | 10 | HG02486.hp1 HG02559.hp1 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.485+28938_485+2894 others(8): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22844008 | |||||
| chr16:22844008
|
TACACAC | T | 108 | a0001c0001t0001g0001a0001c0001t0001g0146a0001c0001t0001g0150others(105): Show | 108 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(105): Show |
intron_variant | MODIFIER | c.485+28936_485+2894 others(10): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22844008 | |||||
| chr16:22844008
|
TACACACA others(1): Show |
T | 7 | a0001c0001t0001g0213a0001c0001t0001g0214a0001c0001t0001g0215others(4): Show | 7 | HG02451.hp2 HG02486.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.485+28934_485+2894 others(12): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22844008 | |||||
| chr16:22844029
|
ACACACAC others(1): Show |
A | 5 | a0001c0001t0001g0293a0001c0001t0001g0306a0001c0002t0001g0007others(2): Show | 5 | HG02145.hp2 HG02572.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.485+28942_485+2894 others(12): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22844029 | |||||
| chr16:22844039
|
A | G | 6 | a0001c0001t0001g0254a0001c0001t0001g0293a0001c0001t0001g0306others(3): Show | 6 | HG02145.hp2 HG02572.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.485+28944A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22844039 | ||||||
| chr16:22844356
|
C | A | 32 | a0001c0001t0001g0166a0001c0001t0001g0167a0001c0001t0001g0175others(29): Show | 32 | HG02145.hp2 HG02451.hp1 HG02451.hp2 others(29): Show |
intron_variant | MODIFIER | c.485+29261C>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22844356 | ||||||
| chr16:22844410
|
G | A | 1 | a0002c0009t0001g0342 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.485+29315G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22844410 | ||||||
| chr16:22844859
|
CT | C | 6 | a0001c0001t0001g0168a0001c0001t0001g0250a0001c0001t0001g0300others(3): Show | 6 | HG01257.hp2 HG01516.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.485+29777delT | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22844859 | |||||
| chr16:22844980
|
AAGTAGCT others(490): Show |
A | 33 | a0001c0001t0001g0146a0001c0001t0001g0166a0001c0001t0001g0167others(30): Show | 33 | HG02109.hp2 HG02145.hp2 HG02451.hp1 others(30): Show |
intron_variant | MODIFIER | c.485+29904_485+3040 others(4): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22844980 | |||||
| chr16:22845001
|
C | T | 2 | a0001c0001t0001g0164a0001c0002t0001g0104 | 2 | HG01123.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.485+29906C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22845001 | ||||||
| chr16:22845058
|
G | A | 1 | a0001c0002t0001g0104 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.485+29963G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22845058 | ||||||
| chr16:22845083
|
T | C | 51 | a0001c0001t0001g0001a0001c0001t0001g0201a0001c0001t0001g0226others(48): Show | 51 | HG00423.hp1 HG00639.hp2 HG00738.hp1 others(48): Show |
intron_variant | MODIFIER | c.485+29988T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22845083 | ||||||
| chr16:22845354
|
A | AT | 113 | a0001c0001t0001g0001a0001c0001t0001g0150a0001c0001t0001g0168others(110): Show | 113 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(110): Show |
intron_variant | MODIFIER | c.485+30274dupT | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22845354 | |||||
| chr16:22845354
|
A | ATT | 16 | a0001c0001t0004g0193a0001c0002t0001g0063a0001c0002t0001g0069others(13): Show | 16 | HG01071.hp2 HG01081.hp2 HG01192.hp1 others(13): Show |
intron_variant | MODIFIER | c.485+30273_485+3027 others(6): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22845354 | |||||
| chr16:22845624
|
TA | T | 5 | a0001c0002t0001g0010a0001c0003t0003g0020a0001c0003t0003g0033others(2): Show | 5 | HG01934.hp1 HG02055.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.485+30530delA | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22845624 | ||||||
| chr16:22845630
|
C | T | 1 | a0001c0002t0001g0048 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.485+30535C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22845630 | ||||||
| chr16:22845641
|
C | T | 8 | a0001c0001t0001g0166a0001c0001t0001g0181a0001c0001t0001g0182others(5): Show | 8 | HG02486.hp1 HG02559.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.485+30546C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22845641 | ||||||
| chr16:22845671
|
C | T | 1 | a0001c0001t0001g0305 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.485+30576C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22845671 | ||||||
| chr16:22845733
|
T | C | 3 | a0001c0003t0003g0028a0001c0003t0003g0029a0001c0003t0003g0030 | 3 | HG01496.hp2 HG02622.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.485+30638T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22845733 | ||||||
| chr16:22845761
|
G | A | 8 | a0001c0001t0001g0166a0001c0001t0001g0181a0001c0001t0001g0182others(5): Show | 8 | HG02486.hp1 HG02559.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.485+30666G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22845761 | ||||||
| chr16:22846017
|
C | A | 13 | a0001c0001t0001g0146a0001c0001t0001g0167a0001c0001t0001g0175others(10): Show | 13 | HG02109.hp2 HG02451.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.485+30922C>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22846017 | ||||||
| chr16:22846027
|
C | T | 1 | a0001c0002t0001g0119 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.485+30932C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22846027 | ||||||
| chr16:22846059
|
C | T | 1 | a0001c0004t0002g0149 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.485+30964C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22846059 | ||||||
| chr16:22846138
|
A | G | 1 | a0001c0002t0001g0085 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.485+31043A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22846138 | ||||||
| chr16:22846214
|
T | C | 11 | a0001c0001t0001g0216a0001c0001t0001g0294a0001c0001t0001g0295others(8): Show | 11 | HG01106.hp1 HG01884.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.485+31119T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22846214 | ||||||
| chr16:22846275
|
T | TA | 119 | a0001c0001t0001g0001a0001c0001t0001g0150a0001c0001t0001g0166others(116): Show | 119 | HG00140.hp2 HG00423.hp1 HG00544.hp1 others(116): Show |
intron_variant | MODIFIER | c.485+31194dupA | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22846275 | |||||
| chr16:22846275
|
TA | T | 9 | a0001c0001t0001g0268a0001c0001t0001g0293a0001c0001t0001g0306others(6): Show | 9 | HG00323.hp1 HG01243.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.485+31194delA | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22846275 | |||||
| chr16:22846391
|
C | G | 4 | a0001c0002t0001g0124a0001c0003t0003g0028a0001c0003t0003g0029others(1): Show | 4 | HG01496.hp2 HG02109.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.485+31296C>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22846391 | ||||||
| chr16:22846415
|
A | C | 1 | a0001c0001t0001g0148 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.485+31320A>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22846415 | ||||||
| chr16:22846600
|
G | A | 1 | a0001c0002t0001g0111 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.485+31505G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22846600 | ||||||
| chr16:22846630
|
G | A | 2 | a0001c0001t0001g0279a0001c0002t0001g0053 | 2 | NA19011.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.485+31535G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22846630 | ||||||
| chr16:22846798
|
G | T | 155 | a0001c0001t0001g0001a0001c0001t0001g0146a0001c0001t0001g0150others(152): Show | 155 | HG00140.hp2 HG00423.hp1 HG00544.hp1 others(152): Show |
intron_variant | MODIFIER | c.485+31703G>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22846798 | ||||||
| chr16:22846799
|
T | A | 53 | a0001c0001t0001g0150a0001c0001t0001g0166a0001c0001t0001g0176others(50): Show | 53 | HG00140.hp2 HG00544.hp1 HG01109.hp2 others(50): Show |
intron_variant | MODIFIER | c.485+31704T>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22846799 | ||||||
| chr16:22846914
|
G | A | 1 | a0001c0001t0004g0340 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.485+31819G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22846914 | ||||||
| chr16:22846975
|
G | C | 60 | a0001c0001t0001g0150a0001c0001t0001g0166a0001c0001t0001g0176others(57): Show | 60 | HG00140.hp2 HG00544.hp1 HG01109.hp2 others(57): Show |
intron_variant | MODIFIER | c.485+31880G>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22846975 | ||||||
| chr16:22847001
|
T | C | 78 | a0001c0001t0001g0001a0001c0001t0001g0168a0001c0001t0001g0169others(75): Show | 78 | HG00423.hp1 HG00639.hp2 HG00738.hp1 others(75): Show |
intron_variant | MODIFIER | c.485+31906T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22847001 | ||||||
| chr16:22847038
|
C | T | 21 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170others(18): Show | 21 | HG01884.hp1 HG01891.hp2 HG02258.hp2 others(18): Show |
intron_variant | MODIFIER | c.485+31943C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22847038 | ||||||
| chr16:22847045
|
T | C | 64 | a0001c0001t0001g0150a0001c0001t0001g0166a0001c0001t0001g0176others(61): Show | 64 | HG00140.hp2 HG00544.hp1 HG01109.hp2 others(61): Show |
intron_variant | MODIFIER | c.485+31950T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22847045 | ||||||
| chr16:22847045
|
T | G | 21 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170others(18): Show | 21 | HG01884.hp1 HG01891.hp2 HG02258.hp2 others(18): Show |
intron_variant | MODIFIER | c.485+31950T>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22847045 | ||||||
| chr16:22847050
|
G | A | 4 | a0001c0001t0001g0297a0001c0001t0001g0302a0001c0001t0001g0303others(1): Show | 4 | HG02922.hp1 HG03130.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.485+31955G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22847050 | ||||||
| chr16:22847258
|
G | A | 1 | a0001c0005t0002g0004 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.485+32163G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22847258 | ||||||
| chr16:22847531
|
A | G | 1 | a0001c0001t0001g0254 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.485+32436A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22847531 | ||||||
| chr16:22847546
|
T | G | 1 | a0001c0001t0001g0315 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.485+32451T>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22847546 | ||||||
| chr16:22847598
|
C | G | 3 | a0001c0001t0001g0302a0001c0001t0001g0303a0001c0001t0001g0305 | 3 | HG02922.hp1 HG03453.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.485+32503C>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22847598 | ||||||
| chr16:22847661
|
T | A | 5 | a0001c0002t0001g0010a0001c0003t0003g0020a0001c0003t0003g0033others(2): Show | 5 | HG01934.hp1 HG02055.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.485+32566T>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22847661 | ||||||
| chr16:22847681
|
C | T | 1 | a0001c0004t0002g0202 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.485+32586C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22847681 | ||||||
| chr16:22847682
|
G | A | 140 | a0001c0001t0001g0145a0001c0001t0001g0150a0001c0001t0001g0151others(137): Show | 140 | HG00140.hp2 HG00280.hp2 HG00544.hp1 others(137): Show |
intron_variant | MODIFIER | c.485+32587G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22847682 | ||||||
| chr16:22847840
|
AAAGG | A | 8 | a0001c0001t0001g0166a0001c0001t0001g0181a0001c0001t0001g0182others(5): Show | 8 | HG02486.hp1 HG02559.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.485+32759_485+3276 others(8): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22847840 | |||||
| chr16:22847864
|
GA | G | 6 | a0001c0001t0001g0302a0001c0001t0001g0303a0001c0001t0001g0305others(3): Show | 6 | HG02040.hp2 HG02109.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.485+32778delA | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22847864 | |||||
| chr16:22847903
|
A | G | 2 | a0001c0002t0001g0011a0001c0005t0002g0012 | 2 | HG03098.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.485+32808A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22847903 | ||||||
| chr16:22848142
|
TA | T | 149 | a0001c0001t0001g0001a0001c0001t0001g0145a0001c0001t0001g0146others(146): Show | 149 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(146): Show |
intron_variant | MODIFIER | c.485+33049delA | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22848142 | |||||
| chr16:22848300
|
A | G | 281 | a0001c0001t0001g0001a0001c0001t0001g0145a0001c0001t0001g0146others(278): Show | 281 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(278): Show |
intron_variant | MODIFIER | c.485+33205A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22848300 | ||||||
| chr16:22848363
|
A | G | 2 | a0001c0001t0001g0218a0001c0006t0006g0016 | 2 | HG02717.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.485+33268A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22848363 | ||||||
| chr16:22848521
|
AT | A | 95 | a0001c0001t0001g0001a0001c0001t0001g0145a0001c0001t0001g0146others(92): Show | 95 | HG00140.hp2 HG00558.hp1 HG00609.hp1 others(92): Show |
intron_variant | MODIFIER | c.485+33433delT | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22848521 | |||||
| chr16:22848722
|
C | T | 1 | a0001c0004t0002g0307 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.485+33627C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22848722 | ||||||
| chr16:22848803
|
T | C | 5 | a0001c0001t0001g0175a0001c0001t0001g0294a0001c0001t0001g0295others(2): Show | 5 | HG01884.hp2 HG02280.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.485+33708T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22848803 | ||||||
| chr16:22848829
|
G | A | 5 | a0001c0001t0001g0300a0001c0003t0003g0017a0001c0004t0002g0307others(2): Show | 5 | HG01167.hp2 HG02965.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.485+33734G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22848829 | ||||||
| chr16:22849076
|
G | A | 1 | a0001c0001t0001g0160 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.485+33981G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22849076 | ||||||
| chr16:22849089
|
G | A | 1 | a0001c0001t0001g0339 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.485+33994G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22849089 | ||||||
| chr16:22849097
|
T | C | 29 | a0001c0001t0001g0150a0001c0001t0001g0172a0001c0001t0001g0188others(26): Show | 29 | HG00140.hp2 HG01109.hp2 HG01891.hp1 others(26): Show |
intron_variant | MODIFIER | c.485+34002T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22849097 | ||||||
| chr16:22849377
|
T | C | 10 | a0001c0001t0001g0145a0001c0001t0001g0292a0001c0002t0003g0039others(7): Show | 10 | HG01243.hp2 HG02451.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.485+34282T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22849377 | ||||||
| chr16:22849479
|
G | A | 2 | a0001c0002t0001g0007a0001c0005t0002g0041 | 2 | HG02145.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.485+34384G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22849479 | ||||||
| chr16:22849581
|
C | T | 3 | a0001c0001t0001g0170a0001c0001t0001g0289a0001c0004t0002g0171 | 3 | HG02280.hp2 HG03139.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.485+34486C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22849581 | ||||||
| chr16:22849605
|
T | C | 8 | a0001c0001t0001g0252a0001c0001t0001g0314a0001c0001t0001g0341others(5): Show | 8 | NA18747.hp1 NA18968.hp2 NA18973.hp1 others(5): Show |
intron_variant | MODIFIER | c.485+34510T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22849605 | ||||||
| chr16:22849651
|
A | C | 2 | a0001c0002t0001g0065a0001c0002t0001g0066 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.485+34556A>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22849651 | ||||||
| chr16:22849654
|
A | G | 116 | a0001c0001t0001g0001a0001c0001t0001g0145a0001c0001t0001g0146others(113): Show | 116 | HG00140.hp2 HG00558.hp1 HG00609.hp1 others(113): Show |
intron_variant | MODIFIER | c.485+34559A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22849654 | ||||||
| chr16:22849692
|
T | A | 6 | a0001c0001t0001g0175a0001c0001t0001g0294a0001c0001t0001g0295others(3): Show | 6 | HG01884.hp2 HG02280.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.485+34597T>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22849692 | ||||||
| chr16:22849704
|
A | G | 4 | a0001c0001t0001g0257a0001c0004t0002g0202a0001c0005t0002g0098others(1): Show | 4 | HG01099.hp1 HG03942.hp1 HG04204.hp1 others(1): Show |
intron_variant | MODIFIER | c.485+34609A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22849704 | ||||||
| chr16:22849872
|
C | T | 5 | a0001c0001t0001g0300a0001c0003t0003g0017a0001c0004t0002g0307others(2): Show | 5 | HG01167.hp2 HG02965.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.485+34777C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22849872 | ||||||
| chr16:22849888
|
T | C | 116 | a0001c0001t0001g0001a0001c0001t0001g0145a0001c0001t0001g0146others(113): Show | 116 | HG00140.hp2 HG00558.hp1 HG00609.hp1 others(113): Show |
intron_variant | MODIFIER | c.485+34793T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22849888 | ||||||
| chr16:22849899
|
G | A | 1 | a0001c0001t0001g0329 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.485+34804G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22849899 | ||||||
| chr16:22850021
|
C | T | 30 | a0001c0001t0001g0150a0001c0001t0001g0172a0001c0001t0001g0188others(27): Show | 30 | HG00140.hp2 HG01109.hp2 HG01891.hp1 others(27): Show |
intron_variant | MODIFIER | c.485+34926C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22850021 | ||||||
| chr16:22850070
|
A | AG | 19 | a0001c0001t0001g0146a0001c0001t0001g0178a0001c0001t0001g0223others(16): Show | 19 | HG01106.hp1 HG01175.hp1 HG01256.hp1 others(16): Show |
intron_variant | MODIFIER | c.485+34975_485+3497 others(5): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22850070 | ||||||
| chr16:22850120
|
C | T | 6 | a0001c0001t0001g0174a0001c0001t0001g0217a0001c0001t0001g0271others(3): Show | 6 | HG01175.hp2 HG02572.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.485+35025C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22850120 | ||||||
| chr16:22850185
|
A | C | 1 | a0001c0001t0001g0300 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.485+35090A>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22850185 | ||||||
| chr16:22850252
|
C | T | 4 | a0001c0001t0001g0186a0001c0003t0003g0028a0001c0003t0003g0029others(1): Show | 4 | HG01496.hp2 HG02622.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.485+35157C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22850252 | ||||||
| chr16:22850320
|
G | A | 6 | a0001c0001t0001g0216a0001c0002t0001g0010a0001c0003t0003g0020others(3): Show | 6 | HG01934.hp1 HG02055.hp1 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.485+35225G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22850320 | ||||||
| chr16:22850343
|
C | T | 3 | a0001c0001t0001g0274a0001c0002t0001g0045a0001c0002t0001g0107 | 3 | HG00558.hp2 NA19056.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.485+35248C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22850343 | ||||||
| chr16:22850429
|
G | A | 2 | a0001c0001t0001g0197a0001c0006t0006g0023 | 2 | HG02735.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.485+35334G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22850429 | ||||||
| chr16:22850512
|
C | T | 1 | a0001c0001t0001g0220 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.485+35417C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22850512 | ||||||
| chr16:22850842
|
A | C | 1 | a0001c0001t0001g0218 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.485+35747A>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22850842 | ||||||
| chr16:22851014
|
G | A | 68 | a0001c0001t0001g0147a0001c0001t0001g0151a0001c0001t0001g0153others(65): Show | 68 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(65): Show |
intron_variant | MODIFIER | c.485+35919G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22851014 | ||||||
| chr16:22851178
|
G | A | 1 | a0001c0001t0001g0265 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.485+36083G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22851178 | ||||||
| chr16:22851248
|
G | A | 1 | a0001c0002t0003g0002 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.485+36153G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22851248 | ||||||
| chr16:22851278
|
A | G | 1 | a0001c0002t0003g0002 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.485+36183A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22851278 | ||||||
| chr16:22851293
|
C | A | 1 | a0007c0010t0001g0042 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.485+36198C>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22851293 | ||||||
| chr16:22851414
|
C | T | 40 | a0001c0001t0001g0145a0001c0001t0001g0150a0001c0001t0001g0172others(37): Show | 40 | HG00140.hp2 HG01109.hp2 HG01243.hp2 others(37): Show |
intron_variant | MODIFIER | c.485+36319C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22851414 | ||||||
| chr16:22851426
|
G | A | 5 | a0001c0001t0001g0175a0001c0001t0001g0294a0001c0001t0001g0295others(2): Show | 5 | HG01884.hp2 HG02280.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.485+36331G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22851426 | ||||||
| chr16:22851441
|
A | G | 1 | a0001c0004t0002g0241 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.485+36346A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22851441 | ||||||
| chr16:22851584
|
G | A | 11 | a0001c0001t0001g0145a0001c0001t0001g0292a0001c0001t0001g0310others(8): Show | 11 | HG01243.hp2 HG02258.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.485+36489G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22851584 | ||||||
| chr16:22851607
|
C | G | 5 | a0001c0001t0001g0175a0001c0001t0001g0294a0001c0001t0001g0295others(2): Show | 5 | HG01884.hp2 HG02280.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.485+36512C>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22851607 | ||||||
| chr16:22851655
|
T | C | 1 | a0001c0002t0001g0348 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.485+36560T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22851655 | ||||||
| chr16:22851956
|
A | G | 1 | a0001c0004t0002g0171 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.485+36861A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22851956 | ||||||
| chr16:22852096
|
G | C | 5 | a0001c0001t0001g0175a0001c0001t0001g0294a0001c0001t0001g0295others(2): Show | 5 | HG01884.hp2 HG02280.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.485+37001G>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22852096 | ||||||
| chr16:22852153
|
A | G | 1 | a0001c0001t0001g0001 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.485+37058A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22852153 | ||||||
| chr16:22852226
|
G | A | 5 | a0001c0001t0001g0175a0001c0001t0001g0294a0001c0001t0001g0295others(2): Show | 5 | HG01884.hp2 HG02280.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.485+37131G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22852226 | ||||||
| chr16:22852263
|
T | C | 5 | a0001c0001t0001g0174a0001c0001t0001g0217a0001c0001t0001g0271others(2): Show | 5 | HG01175.hp2 HG02572.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.485+37168T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22852263 | ||||||
| chr16:22852294
|
T | C | 3 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0003t0003g0018 | 3 | HG02559.hp1 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.485+37199T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22852294 | ||||||
| chr16:22852362
|
A | G | 12 | a0001c0001t0001g0175a0001c0001t0001g0252a0001c0001t0001g0294others(9): Show | 12 | HG01884.hp2 HG02280.hp1 HG02723.hp1 others(9): Show |
intron_variant | MODIFIER | c.485+37267A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22852362 | ||||||
| chr16:22852406
|
A | G | 6 | a0001c0001t0001g0216a0001c0002t0001g0010a0001c0003t0003g0020others(3): Show | 6 | HG01934.hp1 HG02055.hp1 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.485+37311A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22852406 | ||||||
| chr16:22852451
|
T | C | 1 | a0001c0011t0011g0003 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.485+37356T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22852451 | ||||||
| chr16:22852453
|
T | C | 2 | a0001c0001t0001g0321a0001c0002t0001g0110 | 2 | HG01106.hp2 HG01168.hp2 |
intron_variant | MODIFIER | c.485+37358T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22852453 | ||||||
| chr16:22852544
|
C | T | 3 | a0001c0001t0001g0233a0001c0001t0001g0316a0001c0002t0001g0138 | 3 | HG01261.hp2 HG02683.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.485+37449C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22852544 | ||||||
| chr16:22852671
|
G | A | 19 | a0001c0001t0001g0146a0001c0001t0001g0178a0001c0001t0001g0223others(16): Show | 19 | HG01106.hp1 HG01175.hp1 HG01256.hp1 others(16): Show |
intron_variant | MODIFIER | c.485+37576G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22852671 | ||||||
| chr16:22852771
|
C | A | 29 | a0001c0001t0001g0150a0001c0001t0001g0172a0001c0001t0001g0188others(26): Show | 29 | HG00140.hp2 HG01109.hp2 HG01891.hp1 others(26): Show |
intron_variant | MODIFIER | c.485+37676C>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22852771 | ||||||
| chr16:22852897
|
C | T | 29 | a0001c0001t0001g0150a0001c0001t0001g0172a0001c0001t0001g0188others(26): Show | 29 | HG00140.hp2 HG01109.hp2 HG01891.hp1 others(26): Show |
intron_variant | MODIFIER | c.485+37802C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22852897 | ||||||
| chr16:22852945
|
T | TA | 114 | a0001c0001t0001g0001a0001c0001t0001g0145a0001c0001t0001g0146others(111): Show | 114 | HG00140.hp2 HG00558.hp1 HG00609.hp1 others(111): Show |
intron_variant | MODIFIER | c.485+37850_485+3785 others(5): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22852945 | ||||||
| chr16:22852949
|
G | A | 29 | a0001c0001t0001g0150a0001c0001t0001g0172a0001c0001t0001g0188others(26): Show | 29 | HG00140.hp2 HG01109.hp2 HG01891.hp1 others(26): Show |
intron_variant | MODIFIER | c.485+37854G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22852949 | ||||||
| chr16:22852985
|
C | T | 5 | a0001c0001t0001g0175a0001c0001t0001g0294a0001c0001t0001g0295others(2): Show | 5 | HG01884.hp2 HG02280.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.485+37890C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22852985 | ||||||
| chr16:22853005
|
C | T | 1 | a0001c0001t0001g0310 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.485+37910C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22853005 | ||||||
| chr16:22853087
|
T | G | 140 | a0001c0001t0001g0001a0001c0001t0001g0145a0001c0001t0001g0146others(137): Show | 140 | HG00140.hp2 HG00558.hp1 HG00609.hp1 others(137): Show |
intron_variant | MODIFIER | c.485+37992T>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22853087 | ||||||
| chr16:22853088
|
G | A | 5 | a0001c0001t0001g0223a0001c0003t0015g0032a0001c0004t0002g0183others(2): Show | 5 | HG01106.hp1 HG01175.hp1 HG01346.hp1 others(2): Show |
intron_variant | MODIFIER | c.485+37993G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22853088 | ||||||
| chr16:22853231
|
C | A | 10 | a0001c0001t0001g0145a0001c0001t0001g0292a0001c0002t0003g0039others(7): Show | 10 | HG01243.hp2 HG02451.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.485+38136C>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22853231 | ||||||
| chr16:22853561
|
A | G | 1 | a0001c0002t0003g0002 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.485+38466A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22853561 | ||||||
| chr16:22853651
|
C | T | 16 | a0001c0001t0001g0166a0001c0001t0001g0170a0001c0001t0001g0173others(13): Show | 16 | HG00639.hp1 HG02280.hp2 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.485+38556C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22853651 | ||||||
| chr16:22853815
|
C | T | 15 | a0001c0001t0001g0172a0001c0001t0001g0213a0001c0001t0001g0215others(12): Show | 15 | HG02258.hp1 HG02647.hp2 HG02717.hp1 others(12): Show |
intron_variant | MODIFIER | c.485+38720C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22853815 | ||||||
| chr16:22853913
|
G | T | 5 | a0001c0001t0001g0175a0001c0001t0001g0294a0001c0001t0001g0295others(2): Show | 5 | HG01884.hp2 HG02280.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.485+38818G>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22853913 | ||||||
| chr16:22854135
|
G | A | 6 | a0001c0001t0001g0174a0001c0001t0001g0217a0001c0001t0001g0271others(3): Show | 6 | HG01175.hp2 HG02572.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.485+39040G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22854135 | ||||||
| chr16:22854290
|
A | C | 1 | a0001c0001t0001g0349 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.485+39195A>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22854290 | ||||||
| chr16:22854619
|
ATC | A | 7 | a0001c0001t0001g0252a0001c0001t0001g0314a0001c0001t0001g0341others(4): Show | 7 | NA18968.hp2 NA18973.hp1 NA19009.hp1 others(4): Show |
intron_variant | MODIFIER | c.485+39526_485+3952 others(6): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22854619 | |||||
| chr16:22854639
|
CT | C | 135 | a0001c0001t0001g0001a0001c0001t0001g0146a0001c0001t0001g0150others(132): Show | 135 | HG00140.hp2 HG00558.hp1 HG00609.hp1 others(132): Show |
intron_variant | MODIFIER | c.485+39561delT | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22854639 | |||||
| chr16:22854664
|
G | A | 1 | a0001c0001t0001g0234 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.485+39569G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22854664 | ||||||
| chr16:22854742
|
G | A | 1 | a0001c0001t0001g0278 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.485+39647G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22854742 | ||||||
| chr16:22854884
|
C | T | 7 | a0001c0001t0001g0252a0001c0001t0001g0314a0001c0001t0001g0341others(4): Show | 7 | NA18968.hp2 NA18973.hp1 NA19009.hp1 others(4): Show |
intron_variant | MODIFIER | c.485+39789C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22854884 | ||||||
| chr16:22854903
|
G | A | 1 | a0001c0005t0002g0014 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.485+39808G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22854903 | ||||||
| chr16:22855043
|
G | A | 26 | a0001c0001t0001g0166a0001c0001t0001g0167a0001c0001t0001g0170others(23): Show | 26 | HG00639.hp1 HG01891.hp2 HG02055.hp2 others(23): Show |
intron_variant | MODIFIER | c.485+39948G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22855043 | ||||||
| chr16:22855283
|
G | A | 1 | a0001c0002t0001g0053 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.485+40188G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22855283 | ||||||
| chr16:22855362
|
T | C | 112 | a0001c0001t0001g0001a0001c0001t0001g0145a0001c0001t0001g0146others(109): Show | 112 | HG00140.hp2 HG00558.hp1 HG00609.hp1 others(109): Show |
intron_variant | MODIFIER | c.485+40267T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22855362 | ||||||
| chr16:22855372
|
C | A | 10 | a0001c0001t0001g0167a0001c0001t0001g0214a0001c0001t0001g0286others(7): Show | 10 | HG01891.hp2 HG02055.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.485+40277C>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22855372 | ||||||
| chr16:22855581
|
T | C | 1 | a0001c0001t0001g0250 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.485+40486T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22855581 | ||||||
| chr16:22855696
|
G | C | 1 | a0001c0001t0001g0288 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.485+40601G>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22855696 | ||||||
| chr16:22855696
|
G | GTC | 28 | a0001c0001t0001g0150a0001c0001t0001g0174a0001c0001t0001g0188others(25): Show | 28 | HG00438.hp2 HG01167.hp2 HG01175.hp2 others(25): Show |
intron_variant | MODIFIER | c.485+40633_485+4063 others(6): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22855696 | |||||
| chr16:22855696
|
G | GTCTC | 47 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0151others(44): Show | 47 | HG00280.hp2 HG00323.hp2 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.485+40631_485+4063 others(8): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22855696 | |||||
| chr16:22855696
|
G | GTCTCTC | 46 | a0001c0001t0001g0001a0001c0001t0001g0166a0001c0001t0001g0167others(43): Show | 46 | HG00609.hp1 HG00639.hp1 HG01106.hp1 others(43): Show |
intron_variant | MODIFIER | c.485+40629_485+4063 others(10): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22855696 | |||||
| chr16:22855696
|
G | GTCTCTCT others(1): Show |
18 | a0001c0001t0001g0145a0001c0001t0001g0277a0001c0001t0001g0337others(15): Show | 18 | HG00423.hp1 HG00558.hp1 HG02071.hp1 others(15): Show |
intron_variant | MODIFIER | c.485+40627_485+4063 others(12): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22855696 | |||||
| chr16:22855696
|
G | GTCTCTCT others(3): Show |
18 | a0001c0001t0001g0196a0001c0001t0001g0214a0001c0001t0001g0256others(15): Show | 18 | HG01070.hp2 HG01071.hp1 HG01167.hp1 others(15): Show |
intron_variant | MODIFIER | c.485+40625_485+4063 others(14): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22855696 | |||||
| chr16:22855696
|
G | GTCTCTCT others(5): Show |
20 | a0001c0001t0001g0161a0001c0001t0001g0205a0001c0001t0001g0226others(17): Show | 20 | HG00423.hp2 HG00438.hp1 HG00558.hp2 others(17): Show |
intron_variant | MODIFIER | c.485+40623_485+4063 others(16): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22855696 | |||||
| chr16:22855696
|
G | GTCTCTCT others(7): Show |
9 | a0001c0001t0001g0220a0001c0001t0001g0269a0001c0001t0001g0273others(6): Show | 9 | HG01099.hp2 HG02040.hp2 HG02080.hp1 others(6): Show |
intron_variant | MODIFIER | c.485+40621_485+4063 others(18): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22855696 | |||||
| chr16:22855696
|
G | GTCTCTCT others(9): Show |
1 | a0001c0001t0013g0264 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.485+40619_485+4063 others(20): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22855696 | |||||
| chr16:22855696
|
G | GTCTCTCT others(13): Show |
1 | a0001c0001t0001g0206 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.485+40615_485+4063 others(24): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22855696 | |||||
| chr16:22855696
|
GTC | G | 10 | a0001c0001t0001g0210a0001c0001t0001g0234a0001c0001t0001g0260others(7): Show | 10 | HG01516.hp1 HG02109.hp1 HG03225.hp1 others(7): Show |
intron_variant | MODIFIER | c.485+40633_485+4063 others(6): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22855696 | |||||
| chr16:22855696
|
GTCTC | G | 6 | a0001c0001t0001g0180a0001c0001t0001g0186a0001c0002t0001g0122others(3): Show | 6 | HG00280.hp1 HG01496.hp2 HG02602.hp2 others(3): Show |
intron_variant | MODIFIER | c.485+40631_485+4063 others(8): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22855696 | |||||
| chr16:22855696
|
GTCTCTCT others(3): Show |
G | 7 | a0001c0001t0001g0252a0001c0001t0001g0314a0001c0001t0001g0341others(4): Show | 7 | NA18968.hp2 NA18973.hp1 NA19009.hp1 others(4): Show |
intron_variant | MODIFIER | c.485+40625_485+4063 others(14): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22855696 | |||||
| chr16:22855729
|
T | TCTCTCTC others(6): Show |
2 | a0001c0001t0001g0204a0001c0001t0001g0280 | 2 | HG02155.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.485+40634_485+4063 others(17): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22855729 | ||||||
| chr16:22855729
|
T | TCTCTCTC others(8): Show |
1 | a0005c0013t0002g0263 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.485+40634_485+4063 others(19): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22855729 | ||||||
| chr16:22855729
|
T | TCTCTCTC others(12): Show |
1 | a0001c0002t0001g0081 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.485+40634_485+4063 others(23): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22855729 | ||||||
| chr16:22855879
|
T | A | 1 | a0001c0003t0003g0020 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.485+40784T>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22855879 | ||||||
| chr16:22855978
|
C | T | 7 | a0001c0001t0001g0252a0001c0001t0001g0314a0001c0001t0001g0341others(4): Show | 7 | NA18968.hp2 NA18973.hp1 NA19009.hp1 others(4): Show |
intron_variant | MODIFIER | c.485+40883C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22855978 | ||||||
| chr16:22856009
|
A | G | 4 | a0001c0001t0001g0214a0001c0001t0001g0286a0001c0001t0001g0290others(1): Show | 4 | HG01891.hp2 HG02055.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.485+40914A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22856009 | ||||||
| chr16:22856162
|
G | A | 6 | a0001c0001t0001g0178a0001c0001t0001g0223a0001c0003t0015g0032others(3): Show | 6 | HG01106.hp1 HG01175.hp1 HG01346.hp1 others(3): Show |
intron_variant | MODIFIER | c.485+41067G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22856162 | ||||||
| chr16:22856188
|
T | G | 2 | a0001c0001t0001g0213a0001c0001t0001g0215 | 2 | HG02922.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.485+41093T>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22856188 | ||||||
| chr16:22856296
|
G | A | 1 | a0001c0002t0001g0008 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.485+41201G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22856296 | ||||||
| chr16:22856317
|
G | A | 190 | a0001c0001t0001g0001a0001c0001t0001g0145a0001c0001t0001g0146others(187): Show | 190 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(187): Show |
intron_variant | MODIFIER | c.485+41222G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22856317 | ||||||
| chr16:22856387
|
G | A | 6 | a0001c0001t0001g0201a0001c0001t0001g0322a0001c0001t0001g0323others(3): Show | 6 | HG00544.hp2 HG02132.hp1 NA18942.hp1 others(3): Show |
intron_variant | MODIFIER | c.485+41292G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22856387 | ||||||
| chr16:22856500
|
A | G | 46 | a0001c0001t0001g0001a0001c0001t0001g0146a0001c0001t0001g0175others(43): Show | 46 | HG00558.hp1 HG00609.hp1 HG01106.hp1 others(43): Show |
intron_variant | MODIFIER | c.485+41405A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22856500 | ||||||
| chr16:22856548
|
C | T | 3 | a0001c0003t0003g0017a0001c0004t0014g0242a0001c0005t0006g0040 | 3 | HG01167.hp2 HG03041.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.485+41453C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22856548 | ||||||
| chr16:22856714
|
T | C | 21 | a0001c0001t0001g0163a0001c0001t0001g0164a0001c0001t0001g0197others(18): Show | 21 | HG00140.hp1 HG00738.hp1 HG01071.hp2 others(18): Show |
intron_variant | MODIFIER | c.485+41619T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22856714 | ||||||
| chr16:22856721
|
A | C | 10 | a0001c0001t0001g0145a0001c0001t0001g0292a0001c0002t0003g0039others(7): Show | 10 | HG01243.hp2 HG02451.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.485+41626A>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22856721 | ||||||
| chr16:22856817
|
C | T | 7 | a0001c0001t0001g0252a0001c0001t0001g0314a0001c0001t0001g0341others(4): Show | 7 | NA18968.hp2 NA18973.hp1 NA19009.hp1 others(4): Show |
intron_variant | MODIFIER | c.485+41722C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22856817 | ||||||
| chr16:22856866
|
G | A | 21 | a0001c0001t0001g0174a0001c0001t0001g0186a0001c0001t0001g0217others(18): Show | 21 | HG01167.hp2 HG01175.hp2 HG01496.hp2 others(18): Show |
intron_variant | MODIFIER | c.485+41771G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22856866 | ||||||
| chr16:22857005
|
C | T | 1 | a0001c0001t0004g0193 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.485+41910C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22857005 | ||||||
| chr16:22857089
|
G | A | 5 | a0001c0001t0001g0300a0001c0003t0003g0017a0001c0004t0002g0307others(2): Show | 5 | HG01167.hp2 HG02965.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.485+41994G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22857089 | ||||||
| chr16:22857137
|
G | A | 1 | a0001c0002t0003g0002 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.485+42042G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22857137 | ||||||
| chr16:22857282
|
G | A | 6 | a0001c0001t0001g0252a0001c0001t0001g0314a0001c0001t0001g0341others(3): Show | 6 | NA18968.hp2 NA18973.hp1 NA19011.hp2 others(3): Show |
intron_variant | MODIFIER | c.485+42187G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22857282 | ||||||
| chr16:22857303
|
G | A | 4 | a0001c0001t0001g0214a0001c0001t0001g0286a0001c0001t0001g0290others(1): Show | 4 | HG01891.hp2 HG02055.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.485+42208G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22857303 | ||||||
| chr16:22857444
|
C | A | 1 | a0001c0001t0001g0298 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.485+42349C>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22857444 | ||||||
| chr16:22857444
|
C | T | 5 | a0001c0001t0001g0194a0001c0001t0001g0195a0001c0002t0001g0091others(2): Show | 5 | NA18955.hp2 NA18957.hp2 NA18967.hp1 others(2): Show |
intron_variant | MODIFIER | c.485+42349C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22857444 | ||||||
| chr16:22857655
|
C | G | 7 | a0001c0001t0001g0252a0001c0001t0001g0314a0001c0001t0001g0341others(4): Show | 7 | NA18968.hp2 NA18973.hp1 NA19009.hp1 others(4): Show |
intron_variant | MODIFIER | c.485+42560C>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22857655 | ||||||
| chr16:22857697
|
T | A | 1 | a0001c0011t0011g0003 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.485+42602T>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22857697 | ||||||
| chr16:22857706
|
C | T | 185 | a0001c0001t0001g0001a0001c0001t0001g0145a0001c0001t0001g0146others(182): Show | 185 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(182): Show |
intron_variant | MODIFIER | c.485+42611C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22857706 | ||||||
| chr16:22857860
|
C | T | 7 | a0001c0001t0001g0252a0001c0001t0001g0314a0001c0001t0001g0341others(4): Show | 7 | NA18968.hp2 NA18973.hp1 NA19009.hp1 others(4): Show |
intron_variant | MODIFIER | c.485+42765C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22857860 | ||||||
| chr16:22857990
|
A | G | 2 | a0001c0001t0001g0167a0001c0001t0001g0299 | 2 | HG02451.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.485+42895A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22857990 | ||||||
| chr16:22857999
|
A | G | 4 | a0001c0001t0001g0186a0001c0003t0003g0028a0001c0003t0003g0029others(1): Show | 4 | HG01496.hp2 HG02622.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.485+42904A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22857999 | ||||||
| chr16:22858094
|
AT | A | 163 | a0001c0001t0001g0001a0001c0001t0001g0145a0001c0001t0001g0146others(160): Show | 163 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(160): Show |
intron_variant | MODIFIER | c.485+43003delT | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22858094 | |||||
| chr16:22858183
|
C | A | 5 | a0001c0001t0001g0300a0001c0003t0003g0017a0001c0004t0002g0307others(2): Show | 5 | HG01167.hp2 HG02965.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.485+43088C>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22858183 | ||||||
| chr16:22858191
|
G | T | 1 | a0001c0005t0002g0014 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.485+43096G>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22858191 | ||||||
| chr16:22858344
|
T | C | 136 | a0001c0001t0001g0001a0001c0001t0001g0145a0001c0001t0001g0146others(133): Show | 136 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.485+43249T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22858344 | ||||||
| chr16:22858345
|
T | A | 5 | a0001c0001t0001g0234a0001c0001t0001g0260a0001c0001t0001g0333others(2): Show | 5 | HG01516.hp1 HG02109.hp1 HG03710.hp1 others(2): Show |
intron_variant | MODIFIER | c.485+43250T>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22858345 | ||||||
| chr16:22858346
|
A | T | 1 | a0001c0001t0001g0243 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.485+43251A>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22858346 | ||||||
| chr16:22858555
|
T | TTTTG | 119 | a0001c0001t0001g0001a0001c0001t0001g0146a0001c0001t0001g0157others(116): Show | 119 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(116): Show |
intron_variant | MODIFIER | c.485+43485_485+4348 others(8): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22858555 | |||||
| chr16:22858555
|
T | TTTTGTTT others(1): Show |
12 | a0001c0001t0001g0145a0001c0001t0001g0260a0001c0001t0001g0292others(9): Show | 12 | HG01243.hp2 HG02451.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.485+43481_485+4348 others(12): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22858555 | |||||
| chr16:22858632
|
A | G | 1 | a0001c0001t0001g0314 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.485+43537A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22858632 | ||||||
| chr16:22858633
|
G | A | 7 | a0001c0001t0001g0252a0001c0001t0001g0314a0001c0001t0001g0341others(4): Show | 7 | NA18968.hp2 NA18973.hp1 NA19009.hp1 others(4): Show |
intron_variant | MODIFIER | c.485+43538G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22858633 | ||||||
| chr16:22858639
|
A | G | 7 | a0001c0001t0001g0252a0001c0001t0001g0314a0001c0001t0001g0341others(4): Show | 7 | NA18968.hp2 NA18973.hp1 NA19009.hp1 others(4): Show |
intron_variant | MODIFIER | c.485+43544A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22858639 | ||||||
| chr16:22858937
|
G | C | 6 | a0001c0001t0001g0170a0001c0001t0001g0181a0001c0001t0001g0182others(3): Show | 6 | HG02280.hp2 HG02559.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.485+43842G>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22858937 | ||||||
| chr16:22859276
|
A | G | 5 | a0001c0001t0001g0175a0001c0001t0001g0294a0001c0001t0001g0295others(2): Show | 5 | HG01884.hp2 HG02280.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.485+44181A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22859276 | ||||||
| chr16:22859387
|
T | C | 161 | a0001c0001t0001g0001a0001c0001t0001g0145a0001c0001t0001g0146others(158): Show | 161 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(158): Show |
intron_variant | MODIFIER | c.485+44292T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22859387 | ||||||
| chr16:22859415
|
C | G | 16 | a0001c0001t0001g0146a0001c0001t0001g0213a0001c0001t0001g0215others(13): Show | 16 | HG01106.hp1 HG01175.hp1 HG01256.hp1 others(13): Show |
intron_variant | MODIFIER | c.485+44320C>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22859415 | ||||||
| chr16:22859534
|
T | C | 1 | a0001c0006t0006g0026 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.485+44439T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22859534 | ||||||
| chr16:22859589
|
C | A | 34 | a0001c0001t0001g0170a0001c0001t0001g0173a0001c0001t0001g0181others(31): Show | 34 | HG01167.hp2 HG01496.hp2 HG02280.hp2 others(31): Show |
intron_variant | MODIFIER | c.485+44494C>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22859589 | ||||||
| chr16:22859820
|
T | A | 20 | a0001c0001t0001g0170a0001c0001t0001g0173a0001c0001t0001g0181others(17): Show | 20 | HG01516.hp1 HG02280.hp2 HG02559.hp1 others(17): Show |
intron_variant | MODIFIER | c.485+44725T>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22859820 | ||||||
| chr16:22859841
|
T | C | 8 | a0001c0001t0001g0216a0001c0002t0001g0010a0001c0002t0001g0013others(5): Show | 8 | HG01934.hp1 HG02055.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.485+44746T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22859841 | ||||||
| chr16:22859868
|
A | G | 1 | a0001c0006t0006g0025 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.485+44773A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22859868 | ||||||
| chr16:22859902
|
A | C | 1 | a0001c0005t0002g0090 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.485+44807A>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22859902 | ||||||
| chr16:22859940
|
C | A | 90 | a0001c0001t0001g0147a0001c0001t0001g0150a0001c0001t0001g0163others(87): Show | 90 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(87): Show |
intron_variant | MODIFIER | c.485+44845C>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22859940 | ||||||
| chr16:22859991
|
G | A | 169 | a0001c0001t0001g0147a0001c0001t0001g0150a0001c0001t0001g0151others(166): Show | 169 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(166): Show |
intron_variant | MODIFIER | c.485+44896G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22859991 | ||||||
| chr16:22860072
|
G | A | 169 | a0001c0001t0001g0147a0001c0001t0001g0150a0001c0001t0001g0151others(166): Show | 169 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(166): Show |
intron_variant | MODIFIER | c.485+44977G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22860072 | ||||||
| chr16:22860105
|
T | A | 1 | a0001c0001t0001g0224 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.485+45010T>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22860105 | ||||||
| chr16:22860226
|
A | G | 5 | a0001c0001t0001g0300a0001c0003t0003g0017a0001c0004t0002g0307others(2): Show | 5 | HG01167.hp2 HG02965.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.485+45131A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22860226 | ||||||
| chr16:22860246
|
G | A | 4 | a0001c0001t0001g0224a0001c0001t0007g0208a0002c0009t0001g0342others(1): Show | 4 | NA18953.hp2 NA18962.hp2 NA19065.hp2 others(1): Show |
intron_variant | MODIFIER | c.485+45151G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22860246 | ||||||
| chr16:22860284
|
G | A | 42 | a0001c0001t0001g0161a0001c0001t0001g0178a0001c0001t0001g0194others(39): Show | 42 | HG00438.hp1 HG00558.hp2 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.485+45189G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22860284 | ||||||
| chr16:22860317
|
G | A | 1 | a0001c0005t0002g0014 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.485+45222G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22860317 | ||||||
| chr16:22860425
|
A | G | 1 | a0001c0001t0001g0305 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.485+45330A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22860425 | ||||||
| chr16:22860468
|
G | A | 5 | a0001c0001t0001g0186a0001c0002t0001g0011a0001c0003t0003g0028others(2): Show | 5 | HG01496.hp2 HG02622.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.485+45373G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22860468 | ||||||
| chr16:22860735
|
T | C | 2 | a0001c0002t0001g0013a0001c0002t0003g0002 | 2 | HG02615.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.485+45640T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22860735 | ||||||
| chr16:22860745
|
A | G | 1 | a0001c0001t0001g0166 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.485+45650A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22860745 | ||||||
| chr16:22860750
|
A | G | 1 | a0001c0001t0001g0145 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.485+45655A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22860750 | ||||||
| chr16:22860817
|
C | T | 104 | a0001c0001t0001g0001a0001c0001t0001g0145a0001c0001t0001g0161others(101): Show | 104 | HG00438.hp1 HG00558.hp2 HG00609.hp2 others(101): Show |
intron_variant | MODIFIER | c.485+45722C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22860817 | ||||||
| chr16:22860826
|
G | A | 43 | a0001c0001t0001g0161a0001c0001t0001g0164a0001c0001t0001g0166others(40): Show | 43 | HG00438.hp1 HG00558.hp2 HG00609.hp2 others(40): Show |
intron_variant | MODIFIER | c.485+45731G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22860826 | ||||||
| chr16:22860856
|
T | C | 2 | a0001c0001t0001g0293a0001c0003t0003g0021 | 2 | HG01891.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.485+45761T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22860856 | ||||||
| chr16:22860867
|
G | A | 111 | a0001c0001t0001g0001a0001c0001t0001g0145a0001c0001t0001g0161others(108): Show | 111 | HG00438.hp1 HG00558.hp2 HG00609.hp2 others(108): Show |
intron_variant | MODIFIER | c.485+45772G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22860867 | ||||||
| chr16:22860912
|
G | A | 32 | a0001c0001t0001g0001a0001c0001t0001g0167a0001c0001t0001g0168others(29): Show | 32 | HG00621.hp2 HG01099.hp2 HG01109.hp1 others(29): Show |
intron_variant | MODIFIER | c.485+45817G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22860912 | ||||||
| chr16:22860964
|
C | T | 2 | a0001c0002t0001g0013a0001c0002t0003g0002 | 2 | HG02615.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.485+45869C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22860964 | ||||||
| chr16:22861173
|
G | A | 5 | a0001c0002t0001g0099a0001c0002t0001g0100a0001c0002t0001g0101others(2): Show | 5 | HG01070.hp2 HG01071.hp1 HG01167.hp1 others(2): Show |
intron_variant | MODIFIER | c.485+46078G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22861173 | ||||||
| chr16:22861229
|
G | A | 5 | a0001c0001t0001g0186a0001c0002t0001g0011a0001c0003t0003g0028others(2): Show | 5 | HG01496.hp2 HG02622.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.485+46134G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22861229 | ||||||
| chr16:22861399
|
G | T | 7 | a0001c0001t0001g0223a0001c0003t0015g0032a0001c0004t0002g0241others(4): Show | 7 | HG00735.hp2 HG01081.hp1 HG01106.hp1 others(4): Show |
intron_variant | MODIFIER | c.485+46304G>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22861399 | ||||||
| chr16:22861404
|
T | C | 48 | a0001c0001t0001g0145a0001c0001t0001g0147a0001c0001t0001g0157others(45): Show | 48 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(45): Show |
intron_variant | MODIFIER | c.485+46309T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22861404 | ||||||
| chr16:22861702
|
C | A | 4 | a0001c0001t0001g0341a0001c0002t0001g0054a0001c0002t0001g0058others(1): Show | 4 | NA18973.hp1 NA19065.hp1 NA19079.hp2 others(1): Show |
intron_variant | MODIFIER | c.485+46607C>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22861702 | ||||||
| chr16:22861729
|
G | C | 1 | a0001c0001t0001g0275 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.485+46634G>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22861729 | ||||||
| chr16:22861774
|
A | G | 1 | a0001c0001t0001g0204 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.485+46679A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22861774 | ||||||
| chr16:22861838
|
G | A | 7 | a0001c0001t0001g0201a0001c0001t0001g0281a0001c0001t0001g0323others(4): Show | 7 | HG02132.hp1 HG02523.hp2 NA18973.hp1 others(4): Show |
intron_variant | MODIFIER | c.485+46743G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22861838 | ||||||
| chr16:22861926
|
A | G | 1 | a0001c0001t0001g0305 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.485+46831A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22861926 | ||||||
| chr16:22862118
|
C | T | 25 | a0001c0001t0001g0155a0001c0001t0001g0157a0001c0001t0001g0196others(22): Show | 25 | HG00423.hp2 HG00609.hp2 HG00741.hp1 others(22): Show |
intron_variant | MODIFIER | c.485+47023C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22862118 | ||||||
| chr16:22862190
|
C | T | 24 | a0001c0001t0001g0155a0001c0001t0001g0157a0001c0001t0001g0196others(21): Show | 24 | HG00423.hp2 HG00609.hp2 HG00741.hp1 others(21): Show |
intron_variant | MODIFIER | c.485+47095C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22862190 | ||||||
| chr16:22862263
|
G | C | 24 | a0001c0001t0001g0155a0001c0001t0001g0157a0001c0001t0001g0160others(21): Show | 24 | HG00423.hp2 HG00741.hp1 HG01070.hp1 others(21): Show |
intron_variant | MODIFIER | c.485+47168G>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22862263 | ||||||
| chr16:22862275
|
C | CT | 56 | a0001c0001t0001g0001a0001c0001t0001g0146a0001c0001t0001g0151others(53): Show | 56 | HG00544.hp2 HG01099.hp2 HG01109.hp1 others(53): Show |
intron_variant | MODIFIER | c.485+47199dupT | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22862275 | |||||
| chr16:22862275
|
CT | C | 35 | a0001c0001t0001g0164a0001c0001t0001g0168a0001c0001t0001g0169others(32): Show | 35 | HG00323.hp1 HG01106.hp1 HG01175.hp1 others(32): Show |
intron_variant | MODIFIER | c.485+47199delT | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22862275 | |||||
| chr16:22862275
|
CTT | C | 24 | a0001c0001t0001g0155a0001c0001t0001g0157a0001c0001t0001g0160others(21): Show | 24 | HG00423.hp2 HG00741.hp1 HG01070.hp1 others(21): Show |
intron_variant | MODIFIER | c.485+47198_485+4719 others(6): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22862275 | |||||
| chr16:22862348
|
G | T | 3 | a0001c0001t0001g0341a0001c0002t0001g0058a0001c0002t0001g0092 | 3 | NA19065.hp1 NA19079.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.485+47253G>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22862348 | ||||||
| chr16:22862418
|
G | C | 1 | a0001c0002t0001g0089 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.485+47323G>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22862418 | ||||||
| chr16:22862493
|
C | T | 165 | a0001c0001t0001g0001a0001c0001t0001g0145a0001c0001t0001g0155others(162): Show | 165 | HG00423.hp2 HG00544.hp2 HG00558.hp2 others(162): Show |
intron_variant | MODIFIER | c.485+47398C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22862493 | ||||||
| chr16:22862510
|
G | A | 29 | a0001c0001t0001g0167a0001c0001t0001g0214a0001c0001t0001g0271others(26): Show | 29 | HG00735.hp2 HG01081.hp1 HG01256.hp1 others(26): Show |
intron_variant | MODIFIER | c.485+47415G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22862510 | ||||||
| chr16:22862521
|
G | A | 3 | a0001c0001t0001g0320a0004c0007t0001g0221a0004c0007t0001g0222 | 3 | HG00323.hp2 HG00639.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.485+47426G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22862521 | ||||||
| chr16:22862550
|
G | A | 6 | a0001c0001t0001g0186a0001c0002t0001g0011a0001c0003t0003g0028others(3): Show | 6 | HG01496.hp2 HG02622.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.485+47455G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22862550 | ||||||
| chr16:22862787
|
T | A | 1 | a0001c0003t0003g0021 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.485+47692T>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22862787 | ||||||
| chr16:22862847
|
G | A | 1 | a0001c0002t0001g0013 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.485+47752G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22862847 | ||||||
| chr16:22863006
|
C | T | 1 | a0001c0001t0001g0257 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.485+47911C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22863006 | ||||||
| chr16:22863047
|
C | T | 1 | a0001c0002t0001g0008 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.485+47952C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22863047 | ||||||
| chr16:22863079
|
T | C | 59 | a0001c0001t0001g0155a0001c0001t0001g0156a0001c0001t0001g0157others(56): Show | 59 | HG00423.hp2 HG00544.hp2 HG00558.hp2 others(56): Show |
intron_variant | MODIFIER | c.485+47984T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22863079 | ||||||
| chr16:22863204
|
T | C | 59 | a0001c0001t0001g0155a0001c0001t0001g0156a0001c0001t0001g0157others(56): Show | 59 | HG00423.hp2 HG00544.hp2 HG00558.hp2 others(56): Show |
intron_variant | MODIFIER | c.485+48109T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22863204 | ||||||
| chr16:22863242
|
C | G | 1 | a0001c0001t0001g0287 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.485+48147C>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22863242 | ||||||
| chr16:22863271
|
A | G | 4 | a0001c0001t0001g0293a0001c0001t0001g0301a0001c0003t0003g0024others(1): Show | 4 | HG02717.hp2 HG02895.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.485+48176A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22863271 | ||||||
| chr16:22863292
|
G | A | 2 | a0001c0004t0002g0267a0001c0006t0006g0016 | 2 | HG02809.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.485+48197G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22863292 | ||||||
| chr16:22863375
|
C | G | 4 | a0001c0002t0001g0065a0001c0002t0001g0066a0001c0005t0002g0009others(1): Show | 4 | HG02895.hp1 HG02897.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.485+48280C>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22863375 | ||||||
| chr16:22863467
|
G | A | 1 | a0001c0002t0001g0113 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.485+48372G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22863467 | ||||||
| chr16:22863470
|
C | T | 1 | a0001c0001t0001g0280 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.485+48375C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22863470 | ||||||
| chr16:22863477
|
G | T | 18 | a0001c0001t0001g0318a0001c0001t0004g0193a0001c0002t0001g0083others(15): Show | 18 | HG00738.hp1 HG01071.hp2 HG01192.hp1 others(15): Show |
intron_variant | MODIFIER | c.485+48382G>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22863477 | ||||||
| chr16:22863607
|
T | C | 49 | a0001c0001t0001g0145a0001c0001t0001g0166a0001c0001t0001g0167others(46): Show | 49 | HG00735.hp2 HG01081.hp1 HG01106.hp1 others(46): Show |
intron_variant | MODIFIER | c.485+48512T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22863607 | ||||||
| chr16:22863706
|
G | A | 6 | a0001c0001t0001g0186a0001c0002t0001g0011a0001c0003t0003g0028others(3): Show | 6 | HG01496.hp2 HG02622.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.485+48611G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22863706 | ||||||
| chr16:22863752
|
C | A | 2 | a0001c0001t0001g0230a0001c0001t0001g0350 | 2 | NA18969.hp1 NA19006.hp2 |
intron_variant | MODIFIER | c.485+48657C>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22863752 | ||||||
| chr16:22863807
|
G | A | 5 | a0001c0001t0001g0341a0001c0002t0001g0007a0001c0002t0001g0058others(2): Show | 5 | HG02109.hp1 HG02145.hp2 NA19065.hp1 others(2): Show |
intron_variant | MODIFIER | c.485+48712G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22863807 | ||||||
| chr16:22863832
|
C | T | 4 | a0001c0001t0001g0293a0001c0001t0001g0301a0001c0003t0003g0024others(1): Show | 4 | HG02717.hp2 HG02895.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.485+48737C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22863832 | ||||||
| chr16:22863917
|
G | A | 132 | a0001c0001t0001g0145a0001c0001t0001g0155a0001c0001t0001g0156others(129): Show | 132 | HG00423.hp2 HG00544.hp2 HG00558.hp2 others(129): Show |
intron_variant | MODIFIER | c.485+48822G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22863917 | ||||||
| chr16:22863975
|
A | G | 343 | a0001c0001t0001g0001a0001c0001t0001g0145a0001c0001t0001g0146others(340): Show | 343 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(340): Show |
intron_variant | MODIFIER | c.485+48880A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22863975 | ||||||
| chr16:22864062
|
G | A | 1 | a0001c0003t0003g0021 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.485+48967G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22864062 | ||||||
| chr16:22864079
|
C | A | 1 | a0001c0001t0001g0288 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.485+48984C>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22864079 | ||||||
| chr16:22864113
|
T | G | 1 | a0001c0001t0001g0287 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.485+49018T>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22864113 | ||||||
| chr16:22864165
|
A | G | 1 | a0001c0001t0001g0259 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.485+49070A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22864165 | ||||||
| chr16:22864262
|
C | T | 5 | a0001c0001t0001g0150a0001c0001t0001g0188a0001c0001t0001g0190others(2): Show | 5 | NA18955.hp1 NA18961.hp1 NA19054.hp1 others(2): Show |
intron_variant | MODIFIER | c.485+49167C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22864262 | ||||||
| chr16:22864329
|
C | T | 3 | a0001c0001t0001g0341a0001c0002t0001g0058a0001c0002t0001g0092 | 3 | NA19065.hp1 NA19079.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.485+49234C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22864329 | ||||||
| chr16:22864421
|
A | G | 73 | a0001c0001t0001g0155a0001c0001t0001g0156a0001c0001t0001g0157others(70): Show | 73 | HG00423.hp2 HG00544.hp2 HG00558.hp2 others(70): Show |
intron_variant | MODIFIER | c.485+49326A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22864421 | ||||||
| chr16:22864479
|
C | T | 165 | a0001c0001t0001g0001a0001c0001t0001g0145a0001c0001t0001g0155others(162): Show | 165 | HG00423.hp2 HG00544.hp2 HG00558.hp2 others(162): Show |
intron_variant | MODIFIER | c.485+49384C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22864479 | ||||||
| chr16:22864577
|
G | A | 3 | a0001c0001t0001g0341a0001c0002t0001g0058a0001c0002t0001g0092 | 3 | NA19065.hp1 NA19079.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.485+49482G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22864577 | ||||||
| chr16:22864720
|
T | C | 168 | a0001c0001t0001g0001a0001c0001t0001g0145a0001c0001t0001g0155others(165): Show | 168 | HG00423.hp2 HG00544.hp2 HG00558.hp2 others(165): Show |
intron_variant | MODIFIER | c.485+49625T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22864720 | ||||||
| chr16:22864855
|
A | G | 25 | a0001c0001t0001g0001a0001c0001t0001g0195a0001c0001t0001g0201others(22): Show | 25 | HG01081.hp2 HG02074.hp1 HG02132.hp1 others(22): Show |
intron_variant | MODIFIER | c.485+49760A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22864855 | ||||||
| chr16:22864871
|
C | A | 1 | a0001c0002t0001g0077 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.485+49776C>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22864871 | ||||||
| chr16:22864882
|
C | CA | 14 | a0001c0001t0001g0163a0001c0001t0001g0198a0001c0001t0001g0205others(11): Show | 14 | HG01123.hp2 HG02145.hp2 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.485+49807dupA | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22864882 | |||||
| chr16:22864882
|
C | CAAAAAAA others(1): Show |
49 | a0001c0001t0001g0166a0001c0001t0001g0167a0001c0001t0001g0181others(46): Show | 49 | HG00735.hp2 HG01081.hp1 HG01081.hp2 others(46): Show |
intron_variant | MODIFIER | c.485+49800_485+4980 others(12): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22864882 | |||||
| chr16:22864882
|
C | CAAAAAAA others(2): Show |
36 | a0001c0001t0001g0001a0001c0001t0001g0145a0001c0001t0001g0174others(33): Show | 36 | HG01175.hp1 HG01361.hp2 HG01884.hp1 others(33): Show |
intron_variant | MODIFIER | c.485+49799_485+4980 others(13): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22864882 | |||||
| chr16:22864882
|
C | CAAAAAAA others(3): Show |
42 | a0001c0001t0001g0155a0001c0001t0001g0156a0001c0001t0001g0160others(39): Show | 42 | HG00558.hp2 HG00741.hp1 HG01070.hp1 others(39): Show |
intron_variant | MODIFIER | c.485+49798_485+4980 others(14): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22864882 | |||||
| chr16:22864882
|
C | CAAAAAAA others(4): Show |
26 | a0001c0001t0001g0157a0001c0001t0001g0162a0001c0001t0001g0180others(23): Show | 26 | HG00423.hp2 HG00544.hp2 HG00621.hp2 others(23): Show |
intron_variant | MODIFIER | c.485+49797_485+4980 others(15): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22864882 | |||||
| chr16:22864882
|
C | CAAAAAAA others(7): Show |
2 | a0001c0001t0001g0287a0001c0005t0002g0014 | 2 | HG00639.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.485+49794_485+4980 others(18): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22864882 | |||||
| chr16:22864882
|
CAAAAA | C | 7 | a0001c0001t0001g0173a0001c0001t0001g0175a0001c0001t0001g0294others(4): Show | 7 | HG01884.hp2 HG02280.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.485+49803_485+4980 others(9): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22864882 | |||||
| chr16:22864928
|
G | A | 3 | a0001c0001t0001g0288a0001c0004t0002g0307a0001c0006t0006g0023 | 3 | HG02970.hp2 HG03195.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.485+49833G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22864928 | ||||||
| chr16:22864970
|
G | A | 2 | a0001c0001t0001g0330a0001c0002t0001g0118 | 2 | NA18612.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.485+49875G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22864970 | ||||||
| chr16:22865004
|
C | G | 67 | a0001c0001t0001g0145a0001c0001t0001g0166a0001c0001t0001g0167others(64): Show | 67 | HG00735.hp2 HG01081.hp1 HG01106.hp1 others(64): Show |
intron_variant | MODIFIER | c.485+49909C>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22865004 | ||||||
| chr16:22865010
|
C | T | 1 | a0001c0002t0001g0119 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.485+49915C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22865010 | ||||||
| chr16:22865028
|
G | A | 4 | a0001c0001t0001g0161a0001c0001t0001g0317a0001c0002t0001g0078others(1): Show | 4 | HG00438.hp1 HG02165.hp2 NA18612.hp2 others(1): Show |
intron_variant | MODIFIER | c.486-49916G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22865028 | ||||||
| chr16:22865049
|
C | CA | 7 | a0001c0001t0001g0270a0001c0001t0001g0287a0001c0001t0001g0327others(4): Show | 7 | HG00639.hp1 HG01261.hp2 HG03831.hp1 others(4): Show |
intron_variant | MODIFIER | c.486-49873dupA | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22865049 | |||||
| chr16:22865049
|
CA | C | 66 | a0001c0001t0001g0001a0001c0001t0001g0162a0001c0001t0001g0166others(63): Show | 66 | HG00323.hp2 HG00544.hp2 HG01070.hp2 others(63): Show |
intron_variant | MODIFIER | c.486-49873delA | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22865049 | |||||
| chr16:22865049
|
CAA | C | 83 | a0001c0001t0001g0145a0001c0001t0001g0155a0001c0001t0001g0156others(80): Show | 83 | HG00423.hp2 HG00558.hp2 HG00621.hp2 others(80): Show |
intron_variant | MODIFIER | c.486-49874_486-4987 others(6): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22865049 | |||||
| chr16:22865049
|
CAAAA | C | 9 | a0001c0001t0001g0186a0001c0001t0001g0293a0001c0002t0001g0011others(6): Show | 9 | HG01496.hp2 HG02622.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.486-49876_486-4987 others(8): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22865049 | |||||
| chr16:22865087
|
C | A | 55 | a0001c0001t0001g0145a0001c0001t0001g0166a0001c0001t0001g0167others(52): Show | 55 | HG00735.hp2 HG01081.hp1 HG01106.hp1 others(52): Show |
intron_variant | MODIFIER | c.486-49857C>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22865087 | ||||||
| chr16:22865185
|
C | G | 4 | a0001c0001t0001g0195a0001c0001t0001g0258a0001c0002t0001g0074others(1): Show | 4 | NA18947.hp2 NA18955.hp2 NA18960.hp1 others(1): Show |
intron_variant | MODIFIER | c.486-49759C>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22865185 | ||||||
| chr16:22865232
|
T | C | 1 | a0001c0001t0001g0315 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.486-49712T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22865232 | ||||||
| chr16:22865261
|
A | C | 1 | a0001c0002t0001g0063 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.486-49683A>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22865261 | ||||||
| chr16:22865339
|
G | T | 93 | a0001c0001t0001g0001a0001c0001t0001g0155a0001c0001t0001g0156others(90): Show | 93 | HG00423.hp2 HG00544.hp2 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.486-49605G>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22865339 | ||||||
| chr16:22865488
|
G | A | 1 | a0001c0001t0001g0287 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.486-49456G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22865488 | ||||||
| chr16:22865527
|
G | C | 1 | a0001c0001t0001g0210 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.486-49417G>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22865527 | ||||||
| chr16:22865758
|
G | T | 1 | a0001c0001t0001g0287 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.486-49186G>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22865758 | ||||||
| chr16:22865889
|
A | G | 1 | a0001c0001t0001g0279 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.486-49055A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22865889 | ||||||
| chr16:22865961
|
A | G | 1 | a0001c0002t0001g0013 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.486-48983A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22865961 | ||||||
| chr16:22865996
|
C | G | 1 | a0001c0002t0001g0063 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.486-48948C>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22865996 | ||||||
| chr16:22866142
|
C | G | 1 | a0001c0002t0001g0104 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.486-48802C>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22866142 | ||||||
| chr16:22866201
|
GT | G | 93 | a0001c0001t0001g0001a0001c0001t0001g0155a0001c0001t0001g0156others(90): Show | 93 | HG00423.hp2 HG00544.hp2 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.486-48739delT | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22866201 | |||||
| chr16:22866291
|
A | G | 1 | a0001c0001t0001g0321 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.486-48653A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22866291 | ||||||
| chr16:22866302
|
T | C | 4 | a0001c0002t0001g0065a0001c0002t0001g0066a0001c0005t0002g0009others(1): Show | 4 | HG02895.hp1 HG02897.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.486-48642T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22866302 | ||||||
| chr16:22866306
|
C | T | 1 | a0001c0005t0002g0014 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.486-48638C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22866306 | ||||||
| chr16:22866314
|
C | T | 15 | a0001c0001t0001g0169a0001c0001t0001g0174a0001c0001t0001g0217others(12): Show | 15 | HG01175.hp2 HG01243.hp2 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.486-48630C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22866314 | ||||||
| chr16:22866316
|
T | TGC | 17 | a0001c0001t0001g0155a0001c0001t0001g0162a0001c0001t0001g0196others(14): Show | 17 | HG01099.hp2 HG01496.hp1 HG01993.hp2 others(14): Show |
intron_variant | MODIFIER | c.486-48617_486-4861 others(6): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22866316 | |||||
| chr16:22866318
|
C | T | 2 | a0001c0004t0002g0307a0001c0006t0006g0023 | 2 | HG02970.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.486-48626C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22866318 | ||||||
| chr16:22866321
|
G | A | 7 | a0001c0004t0002g0183a0001c0004t0002g0184a0001c0004t0002g0261others(4): Show | 7 | HG00735.hp2 HG01081.hp1 HG01256.hp1 others(4): Show |
intron_variant | MODIFIER | c.486-48623G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22866321 | ||||||
| chr16:22866323
|
G | A | 8 | a0001c0001t0001g0173a0001c0001t0001g0175a0001c0001t0001g0294others(5): Show | 8 | HG01884.hp2 HG02280.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.486-48621G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22866323 | ||||||
| chr16:22866325
|
G | GCA | 5 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0003t0003g0018others(2): Show | 5 | HG01109.hp2 HG02559.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.486-48618_486-4861 others(6): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22866325 | |||||
| chr16:22866325
|
G | T | 1 | a0001c0002t0001g0108 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.486-48619G>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22866325 | ||||||
| chr16:22866326
|
C | A | 1 | a0001c0002t0001g0108 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.486-48618C>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22866326 | ||||||
| chr16:22866326
|
C | T | 1 | a0001c0003t0003g0021 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.486-48618C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22866326 | ||||||
| chr16:22866327
|
G | A | 43 | a0001c0001t0001g0145a0001c0001t0001g0167a0001c0001t0001g0169others(40): Show | 43 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(40): Show |
intron_variant | MODIFIER | c.486-48617G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22866327 | ||||||
| chr16:22866327
|
GCA | G | 39 | a0001c0001t0001g0001a0001c0001t0001g0166a0001c0001t0001g0186others(36): Show | 39 | HG01081.hp2 HG01496.hp2 HG01943.hp2 others(36): Show |
intron_variant | MODIFIER | c.486-48601_486-4860 others(6): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22866327 | |||||
| chr16:22866329
|
A | G | 69 | a0001c0001t0001g0155a0001c0001t0001g0156a0001c0001t0001g0157others(66): Show | 69 | HG00423.hp2 HG00544.hp2 HG00558.hp2 others(66): Show |
intron_variant | MODIFIER | c.486-48615A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22866329 | ||||||
| chr16:22866331
|
A | G | 34 | a0001c0001t0001g0001a0001c0001t0001g0186a0001c0001t0001g0195others(31): Show | 34 | HG01081.hp2 HG01496.hp2 HG02074.hp1 others(31): Show |
intron_variant | MODIFIER | c.486-48613A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22866331 | ||||||
| chr16:22866333
|
A | G | 1 | a0001c0005t0002g0014 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.486-48611A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22866333 | ||||||
| chr16:22866369
|
C | CGT | 62 | a0001c0001t0001g0148a0001c0001t0001g0151a0001c0001t0001g0153others(59): Show | 62 | HG00280.hp1 HG00323.hp1 HG00438.hp1 others(59): Show |
intron_variant | MODIFIER | c.486-48538_486-4853 others(6): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22866369 | |||||
| chr16:22866369
|
C | CGTGT | 11 | a0001c0001t0001g0172a0001c0001t0001g0225a0001c0002t0001g0006others(8): Show | 11 | HG00639.hp1 HG02622.hp1 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.486-48540_486-4853 others(8): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22866369 | |||||
| chr16:22866369
|
C | CGTGTGTG others(3): Show |
2 | a0001c0004t0002g0267a0001c0006t0006g0016 | 2 | HG02809.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.486-48546_486-4853 others(14): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22866369 | |||||
| chr16:22866369
|
C | T | 1 | a0001c0003t0003g0021 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.486-48575C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22866369 | ||||||
| chr16:22866369
|
CGT | C | 61 | a0001c0001t0001g0147a0001c0001t0001g0159a0001c0001t0001g0162others(58): Show | 61 | HG00280.hp2 HG00323.hp2 HG00639.hp2 others(58): Show |
intron_variant | MODIFIER | c.486-48538_486-4853 others(6): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22866369 | |||||
| chr16:22866369
|
CGTGT | C | 56 | a0001c0001t0001g0150a0001c0001t0001g0163a0001c0001t0001g0164others(53): Show | 56 | HG00140.hp1 HG00544.hp1 HG00558.hp1 others(53): Show |
intron_variant | MODIFIER | c.486-48540_486-4853 others(8): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22866369 | |||||
| chr16:22866373
|
T | C | 1 | a0001c0001t0001g0287 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.486-48571T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22866373 | ||||||
| chr16:22866386
|
G | A | 1 | a0001c0001t0001g0210 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.486-48558G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22866386 | ||||||
| chr16:22866388
|
G | A | 91 | a0001c0001t0001g0001a0001c0001t0001g0155a0001c0001t0001g0156others(88): Show | 91 | HG00423.hp2 HG00544.hp2 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.486-48556G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22866388 | ||||||
| chr16:22866408
|
T | C | 1 | a0001c0005t0002g0041 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.486-48536T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22866408 | ||||||
| chr16:22866409
|
G | T | 1 | a0001c0002t0001g0118 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.486-48535G>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22866409 | ||||||
| chr16:22866577
|
C | G | 1 | a0001c0001t0001g0316 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.486-48367C>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22866577 | ||||||
| chr16:22866614
|
A | G | 1 | a0001c0005t0002g0014 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.486-48330A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22866614 | ||||||
| chr16:22866621
|
C | A | 4 | a0001c0001t0001g0293a0001c0001t0001g0301a0001c0003t0003g0024others(1): Show | 4 | HG02717.hp2 HG02895.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.486-48323C>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22866621 | ||||||
| chr16:22866849
|
A | G | 8 | a0001c0001t0001g0173a0001c0001t0001g0175a0001c0001t0001g0294others(5): Show | 8 | HG01884.hp2 HG02280.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.486-48095A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22866849 | ||||||
| chr16:22866883
|
C | T | 1 | a0001c0002t0001g0048 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.486-48061C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22866883 | ||||||
| chr16:22867102
|
G | A | 1 | a0001c0001t0001g0218 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.486-47842G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22867102 | ||||||
| chr16:22867107
|
G | T | 49 | a0001c0001t0001g0145a0001c0001t0001g0166a0001c0001t0001g0167others(46): Show | 49 | HG00735.hp2 HG01081.hp1 HG01106.hp1 others(46): Show |
intron_variant | MODIFIER | c.486-47837G>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22867107 | ||||||
| chr16:22867324
|
T | C | 1 | a0001c0005t0002g0014 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.486-47620T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22867324 | ||||||
| chr16:22867419
|
A | G | 1 | a0001c0001t0001g0276 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.486-47525A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22867419 | ||||||
| chr16:22867538
|
A | G | 1 | a0001c0001t0001g0274 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.486-47406A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22867538 | ||||||
| chr16:22867562
|
C | T | 1 | a0001c0002t0001g0013 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.486-47382C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22867562 | ||||||
| chr16:22867663
|
G | A | 3 | a0001c0001t0001g0341a0001c0002t0001g0058a0001c0002t0001g0092 | 3 | NA19065.hp1 NA19079.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.486-47281G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22867663 | ||||||
| chr16:22868074
|
C | T | 32 | a0001c0001t0001g0145a0001c0001t0001g0166a0001c0001t0001g0167others(29): Show | 32 | HG00735.hp2 HG01081.hp1 HG01106.hp1 others(29): Show |
intron_variant | MODIFIER | c.486-46870C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22868074 | ||||||
| chr16:22868134
|
A | G | 12 | a0001c0001t0001g0173a0001c0001t0001g0175a0001c0001t0001g0185others(9): Show | 12 | HG00280.hp1 HG01168.hp1 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.486-46810A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22868134 | ||||||
| chr16:22868160
|
C | T | 1 | a0001c0002t0001g0076 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.486-46784C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22868160 | ||||||
| chr16:22868317
|
G | A | 27 | a0001c0001t0001g0156a0001c0001t0001g0162a0001c0001t0001g0180others(24): Show | 27 | HG00544.hp2 HG00558.hp2 HG00621.hp2 others(24): Show |
intron_variant | MODIFIER | c.486-46627G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22868317 | ||||||
| chr16:22868405
|
C | CA | 36 | a0001c0001t0001g0168a0001c0001t0001g0198a0001c0001t0001g0199others(33): Show | 36 | HG00735.hp2 HG01081.hp1 HG01106.hp1 others(33): Show |
intron_variant | MODIFIER | c.486-46514dupA | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22868405 | |||||
| chr16:22868405
|
C | CAA | 39 | a0001c0001t0001g0001a0001c0001t0001g0145a0001c0001t0001g0166others(36): Show | 39 | HG01081.hp2 HG01109.hp2 HG01167.hp2 others(36): Show |
intron_variant | MODIFIER | c.486-46515_486-4651 others(6): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22868405 | |||||
| chr16:22868405
|
C | CAAA | 55 | a0001c0001t0001g0155a0001c0001t0001g0156a0001c0001t0001g0157others(52): Show | 55 | HG00423.hp2 HG00558.hp2 HG00741.hp1 others(52): Show |
intron_variant | MODIFIER | c.486-46516_486-4651 others(7): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22868405 | |||||
| chr16:22868405
|
C | CAAAA | 12 | a0001c0001t0001g0162a0001c0001t0001g0170a0001c0001t0001g0224others(9): Show | 12 | HG00544.hp2 HG00621.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.486-46517_486-4651 others(8): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22868405 | |||||
| chr16:22868405
|
CAAAAAAA others(2): Show |
C | 6 | a0001c0001t0001g0186a0001c0002t0001g0011a0001c0003t0003g0028others(3): Show | 6 | HG01496.hp2 HG02622.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.486-46522_486-4651 others(13): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22868405 | |||||
| chr16:22868526
|
C | T | 3 | a0001c0001t0001g0341a0001c0002t0001g0058a0001c0002t0001g0092 | 3 | NA19065.hp1 NA19079.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.486-46418C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22868526 | ||||||
| chr16:22868596
|
G | A | 97 | a0001c0001t0001g0001a0001c0001t0001g0155a0001c0001t0001g0156others(94): Show | 97 | HG00423.hp2 HG00544.hp2 HG00558.hp2 others(94): Show |
intron_variant | MODIFIER | c.486-46348G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22868596 | ||||||
| chr16:22868606
|
C | T | 3 | a0001c0001t0001g0298a0001c0003t0003g0036a0001c0003t0003g0037 | 3 | HG02559.hp2 HG03098.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.486-46338C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22868606 | ||||||
| chr16:22868715
|
T | G | 1 | a0001c0002t0001g0107 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.486-46229T>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22868715 | ||||||
| chr16:22868742
|
G | A | 1 | a0001c0001t0001g0229 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.486-46202G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22868742 | ||||||
| chr16:22868759
|
G | A | 1 | a0001c0002t0005g0123 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.486-46185G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22868759 | ||||||
| chr16:22869021
|
T | C | 96 | a0001c0001t0001g0001a0001c0001t0001g0155a0001c0001t0001g0156others(93): Show | 96 | HG00423.hp2 HG00544.hp2 HG00558.hp2 others(93): Show |
intron_variant | MODIFIER | c.486-45923T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22869021 | ||||||
| chr16:22869055
|
T | C | 6 | a0001c0001t0001g0212a0001c0001t0001g0219a0001c0001t0001g0275others(3): Show | 6 | HG01934.hp2 NA18962.hp1 NA18993.hp2 others(3): Show |
intron_variant | MODIFIER | c.486-45889T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22869055 | ||||||
| chr16:22869066
|
G | T | 8 | a0001c0001t0001g0173a0001c0001t0001g0175a0001c0001t0001g0294others(5): Show | 8 | HG01884.hp2 HG02280.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.486-45878G>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22869066 | ||||||
| chr16:22869382
|
C | T | 4 | a0001c0001t0001g0293a0001c0001t0001g0301a0001c0003t0003g0024others(1): Show | 4 | HG02717.hp2 HG02895.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.486-45562C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22869382 | ||||||
| chr16:22869601
|
A | C | 91 | a0001c0001t0001g0001a0001c0001t0001g0155a0001c0001t0001g0156others(88): Show | 91 | HG00423.hp2 HG00544.hp2 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.486-45343A>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22869601 | ||||||
| chr16:22869691
|
C | T | 86 | a0001c0001t0001g0001a0001c0001t0001g0155a0001c0001t0001g0156others(83): Show | 86 | HG00423.hp2 HG00544.hp2 HG00558.hp2 others(83): Show |
intron_variant | MODIFIER | c.486-45253C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22869691 | ||||||
| chr16:22869990
|
T | C | 4 | a0001c0001t0001g0298a0001c0003t0003g0021a0001c0003t0003g0036others(1): Show | 4 | HG01891.hp1 HG02559.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.486-44954T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22869990 | ||||||
| chr16:22870035
|
A | G | 4 | a0001c0001t0001g0298a0001c0003t0003g0021a0001c0003t0003g0036others(1): Show | 4 | HG01891.hp1 HG02559.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.486-44909A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22870035 | ||||||
| chr16:22870122
|
G | A | 1 | a0001c0002t0001g0092 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.486-44822G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22870122 | ||||||
| chr16:22870125
|
G | A | 43 | a0001c0001t0001g0001a0001c0001t0001g0181a0001c0001t0001g0182others(40): Show | 43 | HG01081.hp2 HG01109.hp2 HG01167.hp2 others(40): Show |
intron_variant | MODIFIER | c.486-44819G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22870125 | ||||||
| chr16:22870257
|
A | G | 156 | a0001c0001t0001g0001a0001c0001t0001g0145a0001c0001t0001g0147others(153): Show | 156 | HG00423.hp2 HG00544.hp2 HG00558.hp2 others(153): Show |
intron_variant | MODIFIER | c.486-44687A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22870257 | ||||||
| chr16:22870276
|
G | C | 1 | a0001c0001t0001g0269 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.486-44668G>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22870276 | ||||||
| chr16:22870318
|
C | T | 1 | a0001c0002t0001g0013 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.486-44626C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22870318 | ||||||
| chr16:22870319
|
G | A | 54 | a0001c0001t0001g0001a0001c0001t0001g0147a0001c0001t0001g0182others(51): Show | 54 | HG00735.hp2 HG00741.hp2 HG01081.hp1 others(51): Show |
intron_variant | MODIFIER | c.486-44625G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22870319 | ||||||
| chr16:22870499
|
A | G | 2 | a0001c0001t0001g0301a0001c0003t0003g0024 | 2 | HG02717.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.486-44445A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22870499 | ||||||
| chr16:22870544
|
A | G | 3 | a0001c0001t0001g0224a0002c0009t0001g0342a0002c0009t0001g0344 | 3 | NA18953.hp2 NA18962.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.486-44400A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22870544 | ||||||
| chr16:22870628
|
T | C | 2 | a0001c0001t0001g0301a0001c0003t0003g0024 | 2 | HG02717.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.486-44316T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22870628 | ||||||
| chr16:22870878
|
C | G | 2 | a0001c0001t0001g0194a0001c0001t0001g0254 | 2 | NA18957.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.486-44066C>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22870878 | ||||||
| chr16:22870897
|
C | T | 2 | a0001c0001t0001g0287a0001c0011t0011g0003 | 2 | HG03471.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.486-44047C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22870897 | ||||||
| chr16:22870898
|
G | A | 1 | a0001c0004t0002g0241 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.486-44046G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22870898 | ||||||
| chr16:22870929
|
C | T | 1 | a0001c0002t0001g0121 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.486-44015C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22870929 | ||||||
| chr16:22871058
|
T | C | 2 | a0001c0001t0001g0287a0001c0011t0011g0003 | 2 | HG03471.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.486-43886T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22871058 | ||||||
| chr16:22871138
|
A | G | 91 | a0001c0001t0001g0145a0001c0001t0001g0147a0001c0001t0001g0155others(88): Show | 91 | HG00423.hp2 HG00544.hp2 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.486-43806A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22871138 | ||||||
| chr16:22871211
|
C | T | 3 | a0001c0001t0001g0265a0001c0001t0001g0313a0001c0002t0001g0071 | 3 | HG00423.hp1 HG04184.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.486-43733C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22871211 | ||||||
| chr16:22871354
|
CA | C | 198 | a0001c0001t0001g0001a0001c0001t0001g0146a0001c0001t0001g0147others(195): Show | 198 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(195): Show |
intron_variant | MODIFIER | c.486-43576delA | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22871354 | |||||
| chr16:22871680
|
C | G | 3 | a0001c0001t0001g0201a0001c0001t0001g0323a0001c0002t0001g0348 | 3 | HG02074.hp1 HG02132.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.486-43264C>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22871680 | ||||||
| chr16:22871981
|
G | A | 2 | a0001c0001t0001g0287a0001c0011t0011g0003 | 2 | HG03471.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.486-42963G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22871981 | ||||||
| chr16:22871987
|
C | T | 1 | a0001c0001t0001g0328 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.486-42957C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22871987 | ||||||
| chr16:22872161
|
T | C | 2 | a0001c0001t0001g0287a0001c0011t0011g0003 | 2 | HG03471.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.486-42783T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22872161 | ||||||
| chr16:22872249
|
A | G | 1 | a0001c0005t0002g0041 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.486-42695A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22872249 | ||||||
| chr16:22872530
|
T | C | 90 | a0001c0001t0001g0145a0001c0001t0001g0147a0001c0001t0001g0155others(87): Show | 90 | HG00423.hp2 HG00544.hp2 HG00558.hp2 others(87): Show |
intron_variant | MODIFIER | c.486-42414T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22872530 | ||||||
| chr16:22872655
|
C | T | 2 | a0001c0001t0001g0287a0001c0011t0011g0003 | 2 | HG03471.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.486-42289C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22872655 | ||||||
| chr16:22872683
|
G | A | 1 | a0001c0001t0001g0287 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.486-42261G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22872683 | ||||||
| chr16:22872690
|
G | A | 94 | a0001c0001t0001g0145a0001c0001t0001g0147a0001c0001t0001g0155others(91): Show | 94 | HG00423.hp2 HG00544.hp2 HG00558.hp2 others(91): Show |
intron_variant | MODIFIER | c.486-42254G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22872690 | ||||||
| chr16:22872732
|
T | C | 283 | a0001c0001t0001g0001a0001c0001t0001g0145a0001c0001t0001g0147others(280): Show | 283 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(280): Show |
intron_variant | MODIFIER | c.486-42212T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22872732 | ||||||
| chr16:22872906
|
T | C | 3 | a0001c0001t0001g0146a0001c0002t0003g0002a0001c0003t0003g0015 | 3 | HG02109.hp2 HG02615.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.486-42038T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22872906 | ||||||
| chr16:22872923
|
A | G | 103 | a0001c0001t0001g0145a0001c0001t0001g0147a0001c0001t0001g0155others(100): Show | 103 | HG00423.hp2 HG00544.hp2 HG00558.hp2 others(100): Show |
intron_variant | MODIFIER | c.486-42021A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22872923 | ||||||
| chr16:22872969
|
T | TC | 3 | a0001c0001t0001g0301a0001c0003t0003g0024a0001c0004t0002g0171 | 3 | HG02717.hp2 HG02895.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.486-41974dupC | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22872969 | |||||
| chr16:22872995
|
T | G | 96 | a0001c0001t0001g0145a0001c0001t0001g0147a0001c0001t0001g0155others(93): Show | 96 | HG00423.hp2 HG00544.hp2 HG00558.hp2 others(93): Show |
intron_variant | MODIFIER | c.486-41949T>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22872995 | ||||||
| chr16:22873188
|
C | T | 7 | a0001c0001t0001g0223a0001c0002t0001g0006a0001c0004t0002g0241others(4): Show | 7 | HG01070.hp2 HG01071.hp1 HG01106.hp1 others(4): Show |
intron_variant | MODIFIER | c.486-41756C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22873188 | ||||||
| chr16:22873247
|
C | A | 1 | a0001c0001t0001g0270 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.486-41697C>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22873247 | ||||||
| chr16:22873275
|
C | A | 2 | a0004c0007t0001g0221a0004c0007t0001g0222 | 2 | HG00639.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.486-41669C>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22873275 | ||||||
| chr16:22873276
|
G | A | 4 | a0001c0001t0001g0170a0001c0001t0001g0181a0001c0001t0001g0292others(1): Show | 4 | HG01243.hp2 HG02280.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.486-41668G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22873276 | ||||||
| chr16:22873326
|
A | G | 7 | a0001c0001t0001g0173a0001c0001t0001g0175a0001c0001t0001g0294others(4): Show | 7 | HG01884.hp2 HG02280.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.486-41618A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22873326 | ||||||
| chr16:22873493
|
T | C | 2 | a0001c0001t0001g0287a0001c0011t0011g0003 | 2 | HG03471.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.486-41451T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22873493 | ||||||
| chr16:22873678
|
G | A | 1 | a0001c0001t0001g0287 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.486-41266G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22873678 | ||||||
| chr16:22873827
|
A | G | 2 | a0001c0001t0001g0287a0001c0011t0011g0003 | 2 | HG03471.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.486-41117A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22873827 | ||||||
| chr16:22873977
|
G | A | 3 | a0001c0001t0001g0341a0001c0002t0001g0058a0001c0002t0001g0092 | 3 | NA19065.hp1 NA19079.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.486-40967G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22873977 | ||||||
| chr16:22873982
|
T | C | 283 | a0001c0001t0001g0001a0001c0001t0001g0145a0001c0001t0001g0147others(280): Show | 283 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(280): Show |
intron_variant | MODIFIER | c.486-40962T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22873982 | ||||||
| chr16:22874100
|
G | A | 130 | a0001c0001t0001g0148a0001c0001t0001g0150a0001c0001t0001g0151others(127): Show | 130 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(127): Show |
intron_variant | MODIFIER | c.486-40844G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22874100 | ||||||
| chr16:22874130
|
G | A | 2 | a0001c0001t0001g0216a0001c0003t0003g0034 | 2 | HG02145.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.486-40814G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22874130 | ||||||
| chr16:22874196
|
TTCC | T | 3 | a0001c0001t0001g0341a0001c0002t0001g0058a0001c0002t0001g0092 | 3 | NA19065.hp1 NA19079.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.486-40746_486-4074 others(7): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22874196 | |||||
| chr16:22874214
|
G | T | 2 | a0001c0001t0001g0287a0001c0011t0011g0003 | 2 | HG03471.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.486-40730G>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22874214 | ||||||
| chr16:22874374
|
C | T | 4 | a0001c0001t0001g0201a0001c0001t0001g0323a0001c0002t0001g0348others(1): Show | 4 | HG02074.hp1 HG02132.hp1 NA18962.hp2 others(1): Show |
intron_variant | MODIFIER | c.486-40570C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22874374 | ||||||
| chr16:22874442
|
A | G | 1 | a0001c0002t0001g0073 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.486-40502A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22874442 | ||||||
| chr16:22874617
|
C | A | 2 | a0001c0001t0001g0287a0001c0011t0011g0003 | 2 | HG03471.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.486-40327C>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22874617 | ||||||
| chr16:22874658
|
C | A | 7 | a0001c0004t0002g0183a0001c0004t0002g0184a0001c0004t0002g0261others(4): Show | 7 | HG00735.hp2 HG01081.hp1 HG01256.hp1 others(4): Show |
intron_variant | MODIFIER | c.486-40286C>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22874658 | ||||||
| chr16:22874847
|
G | A | 1 | a0001c0005t0002g0090 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.486-40097G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22874847 | ||||||
| chr16:22874919
|
C | G | 132 | a0001c0001t0001g0148a0001c0001t0001g0150a0001c0001t0001g0151others(129): Show | 132 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(129): Show |
intron_variant | MODIFIER | c.486-40025C>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22874919 | ||||||
| chr16:22875369
|
A | AATTTATT others(5): Show |
5 | a0001c0001t0001g0287a0001c0001t0001g0341a0001c0002t0001g0058others(2): Show | 5 | HG03471.hp1 NA19065.hp1 NA19079.hp2 others(2): Show |
intron_variant | MODIFIER | c.486-39557_486-3954 others(16): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22875369 | |||||
| chr16:22875369
|
A | C | 2 | a0001c0001t0001g0230a0001c0001t0001g0350 | 2 | NA18969.hp1 NA19006.hp2 |
intron_variant | MODIFIER | c.486-39575A>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22875369 | ||||||
| chr16:22875419
|
C | T | 2 | a0001c0001t0001g0287a0001c0011t0011g0003 | 2 | HG03471.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.486-39525C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22875419 | ||||||
| chr16:22875488
|
C | T | 1 | a0001c0004t0002g0266 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.486-39456C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22875488 | ||||||
| chr16:22875539
|
C | T | 1 | a0001c0005t0002g0014 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.486-39405C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22875539 | ||||||
| chr16:22875574
|
G | A | 2 | a0001c0001t0001g0328a0001c0002t0001g0111 | 2 | NA18980.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.486-39370G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22875574 | ||||||
| chr16:22875612
|
ACCT | A | 3 | a0001c0003t0003g0027a0001c0004t0002g0266a0001c0006t0006g0026 | 3 | HG02451.hp2 HG02615.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.486-39330_486-3932 others(7): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22875612 | |||||
| chr16:22875694
|
T | G | 3 | a0001c0005t0002g0102a0003c0008t0002g0231a0003c0008t0002g0232 | 3 | HG01070.hp2 HG01071.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.486-39250T>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22875694 | ||||||
| chr16:22875831
|
C | A | 1 | a0001c0001t0001g0346 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.486-39113C>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22875831 | ||||||
| chr16:22875875
|
C | T | 1 | a0001c0002t0004g0059 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.486-39069C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22875875 | ||||||
| chr16:22875981
|
G | A | 99 | a0001c0001t0001g0148a0001c0001t0001g0150a0001c0001t0001g0151others(96): Show | 99 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(96): Show |
intron_variant | MODIFIER | c.486-38963G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22875981 | ||||||
| chr16:22876002
|
G | T | 3 | a0001c0001t0001g0341a0001c0002t0001g0058a0001c0002t0001g0092 | 3 | NA19065.hp1 NA19079.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.486-38942G>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22876002 | ||||||
| chr16:22876035
|
A | G | 1 | a0001c0002t0001g0068 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.486-38909A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22876035 | ||||||
| chr16:22876048
|
T | A | 95 | a0001c0001t0001g0145a0001c0001t0001g0147a0001c0001t0001g0155others(92): Show | 95 | HG00544.hp2 HG00558.hp2 HG00621.hp2 others(92): Show |
intron_variant | MODIFIER | c.486-38896T>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22876048 | ||||||
| chr16:22876185
|
T | C | 96 | a0001c0001t0001g0145a0001c0001t0001g0147a0001c0001t0001g0155others(93): Show | 96 | HG00544.hp2 HG00558.hp2 HG00621.hp2 others(93): Show |
intron_variant | MODIFIER | c.486-38759T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22876185 | ||||||
| chr16:22876201
|
C | T | 64 | a0001c0001t0001g0145a0001c0001t0001g0147a0001c0001t0001g0156others(61): Show | 64 | HG00544.hp2 HG00558.hp2 HG00621.hp2 others(61): Show |
intron_variant | MODIFIER | c.486-38743C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22876201 | ||||||
| chr16:22876269
|
C | T | 1 | a0001c0002t0001g0107 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.486-38675C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22876269 | ||||||
| chr16:22876278
|
G | C | 4 | a0001c0001t0001g0157a0001c0001t0001g0224a0002c0009t0001g0342others(1): Show | 4 | HG01943.hp1 NA18953.hp2 NA18962.hp2 others(1): Show |
intron_variant | MODIFIER | c.486-38666G>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22876278 | ||||||
| chr16:22876308
|
G | A | 1 | a0001c0001t0001g0283 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.486-38636G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22876308 | ||||||
| chr16:22876397
|
A | G | 2 | a0001c0001t0001g0287a0001c0011t0011g0003 | 2 | HG03471.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.486-38547A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22876397 | ||||||
| chr16:22876437
|
T | A | 1 | a0001c0002t0012g0080 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.486-38507T>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22876437 | ||||||
| chr16:22876488
|
A | G | 1 | a0001c0002t0010g0043 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.486-38456A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22876488 | ||||||
| chr16:22876516
|
G | A | 1 | a0001c0003t0003g0017 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.486-38428G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22876516 | ||||||
| chr16:22876551
|
C | T | 2 | a0001c0004t0002g0179a0001c0004t0002g0272 | 2 | HG03831.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.486-38393C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22876551 | ||||||
| chr16:22876558
|
A | G | 1 | a0001c0002t0001g0085 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.486-38386A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22876558 | ||||||
| chr16:22876724
|
C | T | 2 | a0001c0001t0001g0287a0001c0011t0011g0003 | 2 | HG03471.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.486-38220C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22876724 | ||||||
| chr16:22877108
|
G | A | 89 | a0001c0001t0001g0145a0001c0001t0001g0147a0001c0001t0001g0155others(86): Show | 89 | HG00544.hp2 HG00558.hp2 HG00621.hp2 others(86): Show |
intron_variant | MODIFIER | c.486-37836G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22877108 | ||||||
| chr16:22877197
|
A | C | 1 | a0001c0001t0001g0252 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.486-37747A>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22877197 | ||||||
| chr16:22877278
|
G | A | 1 | a0001c0001t0001g0148 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.486-37666G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22877278 | ||||||
| chr16:22877363
|
C | T | 2 | a0001c0001t0001g0287a0001c0011t0011g0003 | 2 | HG03471.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.486-37581C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22877363 | ||||||
| chr16:22877428
|
A | G | 1 | a0001c0002t0001g0069 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.486-37516A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22877428 | ||||||
| chr16:22877480
|
G | T | 1 | a0001c0003t0003g0029 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.486-37464G>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22877480 | ||||||
| chr16:22877495
|
G | A | 9 | a0001c0004t0002g0183a0001c0004t0002g0184a0001c0004t0002g0261others(6): Show | 9 | HG00735.hp2 HG01081.hp1 HG01256.hp1 others(6): Show |
intron_variant | MODIFIER | c.486-37449G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22877495 | ||||||
| chr16:22877819
|
G | T | 14 | a0001c0001t0001g0178a0001c0001t0001g0185a0001c0001t0001g0197others(11): Show | 14 | HG00280.hp1 HG00323.hp1 HG01168.hp1 others(11): Show |
intron_variant | MODIFIER | c.486-37125G>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22877819 | ||||||
| chr16:22877865
|
G | A | 110 | a0001c0001t0001g0148a0001c0001t0001g0150a0001c0001t0001g0151others(107): Show | 110 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.486-37079G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22877865 | ||||||
| chr16:22877909
|
G | T | 1 | a0001c0005t0002g0009 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.486-37035G>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22877909 | ||||||
| chr16:22877919
|
G | A | 1 | a0001c0002t0004g0140 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.486-37025G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22877919 | ||||||
| chr16:22877987
|
T | C | 1 | a0001c0005t0002g0014 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.486-36957T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22877987 | ||||||
| chr16:22878086
|
G | A | 1 | a0001c0004t0002g0179 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.486-36858G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22878086 | ||||||
| chr16:22878106
|
A | G | 8 | a0001c0001t0001g0186a0001c0001t0001g0293a0001c0001t0001g0298others(5): Show | 8 | HG01496.hp2 HG02559.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.486-36838A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22878106 | ||||||
| chr16:22878135
|
G | A | 2 | a0001c0001t0001g0287a0001c0011t0011g0003 | 2 | HG03471.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.486-36809G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22878135 | ||||||
| chr16:22878199
|
T | C | 1 | a0001c0004t0002g0179 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.486-36745T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22878199 | ||||||
| chr16:22878609
|
T | TA | 3 | a0001c0001t0001g0169a0001c0005t0006g0038a0007c0010t0001g0042 | 3 | HG01884.hp1 HG02647.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.486-36335_486-3633 others(5): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22878609 | ||||||
| chr16:22878610
|
C | A | 3 | a0001c0001t0001g0169a0001c0005t0006g0038a0007c0010t0001g0042 | 3 | HG01884.hp1 HG02647.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.486-36334C>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22878610 | ||||||
| chr16:22878610
|
C | CA | 87 | a0001c0001t0001g0145a0001c0001t0001g0147a0001c0001t0001g0155others(84): Show | 87 | HG00544.hp2 HG00558.hp2 HG00621.hp2 others(84): Show |
intron_variant | MODIFIER | c.486-36325dupA | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22878610 | |||||
| chr16:22878612
|
A | C | 6 | a0001c0001t0001g0315a0001c0001t0004g0200a0001c0001t0004g0340others(3): Show | 6 | HG00423.hp2 HG02071.hp1 HG02080.hp2 others(3): Show |
intron_variant | MODIFIER | c.486-36332A>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22878612 | ||||||
| chr16:22878713
|
T | C | 3 | a0001c0003t0003g0027a0001c0004t0002g0266a0001c0006t0006g0026 | 3 | HG02451.hp2 HG02615.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.486-36231T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22878713 | ||||||
| chr16:22878748
|
C | T | 2 | a0001c0001t0001g0174a0001c0001t0001g0217 | 2 | HG01175.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.486-36196C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22878748 | ||||||
| chr16:22878797
|
G | A | 1 | a0001c0001t0001g0160 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.486-36147G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22878797 | ||||||
| chr16:22878893
|
T | A | 1 | a0001c0001t0001g0159 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.486-36051T>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22878893 | ||||||
| chr16:22878921
|
G | A | 1 | a0001c0001t0001g0148 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.486-36023G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22878921 | ||||||
| chr16:22878982
|
G | A | 1 | a0001c0001t0001g0203 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.486-35962G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22878982 | ||||||
| chr16:22879242
|
T | A | 89 | a0001c0001t0001g0145a0001c0001t0001g0147a0001c0001t0001g0155others(86): Show | 89 | HG00544.hp2 HG00558.hp2 HG00621.hp2 others(86): Show |
intron_variant | MODIFIER | c.486-35702T>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22879242 | ||||||
| chr16:22879259
|
T | C | 3 | a0001c0001t0001g0297a0001c0002t0001g0010a0001c0003t0003g0020 | 3 | HG02055.hp1 HG02965.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.486-35685T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22879259 | ||||||
| chr16:22879408
|
C | T | 1 | a0001c0001t0001g0253 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.486-35536C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22879408 | ||||||
| chr16:22879481
|
G | A | 1 | a0001c0002t0001g0074 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.486-35463G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22879481 | ||||||
| chr16:22879544
|
G | T | 3 | a0001c0003t0003g0027a0001c0004t0002g0266a0001c0006t0006g0026 | 3 | HG02451.hp2 HG02615.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.486-35400G>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22879544 | ||||||
| chr16:22879563
|
C | T | 1 | a0001c0002t0008g0139 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.486-35381C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22879563 | ||||||
| chr16:22879676
|
G | A | 86 | a0001c0001t0001g0145a0001c0001t0001g0147a0001c0001t0001g0155others(83): Show | 86 | HG00544.hp2 HG00558.hp2 HG00621.hp2 others(83): Show |
intron_variant | MODIFIER | c.486-35268G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22879676 | ||||||
| chr16:22879732
|
G | T | 2 | a0001c0001t0001g0314a0001c0001t0001g0324 | 2 | NA18968.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.486-35212G>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22879732 | ||||||
| chr16:22879753
|
G | A | 1 | a0001c0001t0001g0218 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.486-35191G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22879753 | ||||||
| chr16:22879763
|
C | T | 93 | a0001c0001t0001g0145a0001c0001t0001g0147a0001c0001t0001g0155others(90): Show | 93 | HG00544.hp2 HG00558.hp2 HG00621.hp2 others(90): Show |
intron_variant | MODIFIER | c.486-35181C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22879763 | ||||||
| chr16:22879807
|
G | T | 3 | a0001c0002t0001g0099a0001c0002t0001g0100a0001c0002t0001g0101 | 3 | HG01167.hp1 HG01169.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.486-35137G>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22879807 | ||||||
| chr16:22879880
|
A | C | 3 | a0001c0001t0001g0341a0001c0002t0001g0058a0001c0002t0001g0092 | 3 | NA19065.hp1 NA19079.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.486-35064A>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22879880 | ||||||
| chr16:22880103
|
C | G | 86 | a0001c0001t0001g0145a0001c0001t0001g0147a0001c0001t0001g0155others(83): Show | 86 | HG00544.hp2 HG00558.hp2 HG00621.hp2 others(83): Show |
intron_variant | MODIFIER | c.486-34841C>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22880103 | ||||||
| chr16:22880117
|
CTTCTTTC others(3): Show |
C | 8 | a0001c0001t0001g0186a0001c0001t0001g0293a0001c0001t0001g0298others(5): Show | 8 | HG01496.hp2 HG02559.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.486-34825_486-3481 others(14): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22880117 | |||||
| chr16:22880140
|
G | A | 8 | a0001c0001t0001g0186a0001c0001t0001g0293a0001c0001t0001g0298others(5): Show | 8 | HG01496.hp2 HG02559.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.486-34804G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22880140 | ||||||
| chr16:22880144
|
G | A | 1 | a0001c0001t0001g0001 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.486-34800G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22880144 | ||||||
| chr16:22880188
|
G | C | 1 | a0001c0002t0004g0059 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.486-34756G>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22880188 | ||||||
| chr16:22880226
|
A | G | 1 | a0001c0002t0001g0006 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.486-34718A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22880226 | ||||||
| chr16:22880254
|
A | C | 1 | a0001c0002t0008g0143 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.486-34690A>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22880254 | ||||||
| chr16:22880285
|
G | A | 14 | a0001c0001t0001g0178a0001c0001t0001g0185a0001c0001t0001g0197others(11): Show | 14 | HG00280.hp1 HG00323.hp1 HG01168.hp1 others(11): Show |
intron_variant | MODIFIER | c.486-34659G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22880285 | ||||||
| chr16:22880381
|
T | C | 240 | a0001c0001t0001g0145a0001c0001t0001g0147a0001c0001t0001g0148others(237): Show | 240 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(237): Show |
intron_variant | MODIFIER | c.486-34563T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22880381 | ||||||
| chr16:22880528
|
T | C | 13 | a0001c0001t0001g0170a0001c0001t0001g0181a0001c0001t0001g0182others(10): Show | 13 | HG01109.hp2 HG01167.hp2 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.486-34416T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22880528 | ||||||
| chr16:22880552
|
C | T | 2 | a0001c0001t0001g0312a0001c0002t0007g0056 | 2 | HG02071.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.486-34392C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22880552 | ||||||
| chr16:22880556
|
C | T | 1 | a0001c0002t0001g0063 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.486-34388C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22880556 | ||||||
| chr16:22880565
|
G | T | 2 | a0001c0001t0001g0147a0001c0002t0001g0104 | 2 | HG00741.hp2 HG01123.hp1 |
intron_variant | MODIFIER | c.486-34379G>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22880565 | ||||||
| chr16:22880598
|
C | T | 1 | a0001c0002t0001g0063 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.486-34346C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22880598 | ||||||
| chr16:22880647
|
C | G | 2 | a0001c0001t0001g0287a0001c0011t0011g0003 | 2 | HG03471.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.486-34297C>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22880647 | ||||||
| chr16:22880648
|
C | A | 1 | a0001c0001t0001g0178 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.486-34296C>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22880648 | ||||||
| chr16:22880811
|
G | A | 1 | a0001c0001t0001g0283 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.486-34133G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22880811 | ||||||
| chr16:22880832
|
G | A | 2 | a0001c0001t0001g0306a0001c0003t0003g0035 | 2 | HG02572.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.486-34112G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22880832 | ||||||
| chr16:22880834
|
A | T | 2 | a0001c0001t0001g0306a0001c0003t0003g0035 | 2 | HG02572.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.486-34110A>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22880834 | ||||||
| chr16:22880841
|
G | A | 1 | a0001c0002t0001g0006 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.486-34103G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22880841 | ||||||
| chr16:22880845
|
C | T | 2 | a0001c0001t0001g0306a0001c0003t0003g0035 | 2 | HG02572.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.486-34099C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22880845 | ||||||
| chr16:22880846
|
A | T | 2 | a0001c0001t0001g0306a0001c0003t0003g0035 | 2 | HG02572.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.486-34098A>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22880846 | ||||||
| chr16:22881214
|
A | C | 4 | a0001c0001t0001g0301a0001c0003t0003g0024a0001c0004t0002g0171others(1): Show | 4 | HG02717.hp2 HG02723.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.486-33730A>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22881214 | ||||||
| chr16:22881323
|
C | T | 2 | a0001c0001t0001g0341a0001c0002t0001g0058 | 2 | NA19065.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.486-33621C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22881323 | ||||||
| chr16:22881349
|
C | T | 1 | a0001c0001t0001g0199 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.486-33595C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22881349 | ||||||
| chr16:22881362
|
A | G | 2 | a0001c0004t0002g0266a0001c0006t0006g0026 | 2 | HG02451.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.486-33582A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22881362 | ||||||
| chr16:22881586
|
A | G | 229 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0147others(226): Show | 229 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(226): Show |
intron_variant | MODIFIER | c.486-33358A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22881586 | ||||||
| chr16:22881644
|
T | C | 126 | a0001c0001t0001g0148a0001c0001t0001g0150a0001c0001t0001g0151others(123): Show | 126 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(123): Show |
intron_variant | MODIFIER | c.486-33300T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22881644 | ||||||
| chr16:22881770
|
C | A | 1 | a0001c0001t0001g0244 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.486-33174C>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22881770 | ||||||
| chr16:22881956
|
A | ATGTT | 7 | a0001c0001t0001g0167a0001c0001t0001g0214a0001c0001t0001g0286others(4): Show | 7 | HG01891.hp2 HG01934.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.486-32972_486-3296 others(8): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22881956 | |||||
| chr16:22882126
|
G | A | 1 | a0001c0001t0001g0197 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.486-32818G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22882126 | ||||||
| chr16:22882170
|
A | G | 255 | a0001c0001t0001g0001a0001c0001t0001g0145a0001c0001t0001g0146others(252): Show | 255 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(252): Show |
intron_variant | MODIFIER | c.486-32774A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22882170 | ||||||
| chr16:22882424
|
G | A | 14 | a0001c0004t0002g0144a0001c0004t0002g0183a0001c0004t0002g0184others(11): Show | 14 | HG00735.hp2 HG01081.hp1 HG01256.hp1 others(11): Show |
intron_variant | MODIFIER | c.486-32520G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22882424 | ||||||
| chr16:22882554
|
C | T | 1 | a0001c0006t0006g0016 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.486-32390C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22882554 | ||||||
| chr16:22882716
|
G | C | 1 | a0001c0006t0006g0026 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.486-32228G>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22882716 | ||||||
| chr16:22882761
|
G | C | 1 | a0001c0001t0001g0257 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.486-32183G>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22882761 | ||||||
| chr16:22883274
|
C | G | 3 | a0001c0002t0001g0099a0001c0002t0001g0100a0001c0002t0001g0101 | 3 | HG01167.hp1 HG01169.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.486-31670C>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22883274 | ||||||
| chr16:22883277
|
C | T | 1 | a0001c0001t0001g0289 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.486-31667C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22883277 | ||||||
| chr16:22883308
|
C | T | 1 | a0001c0001t0001g0203 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.486-31636C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22883308 | ||||||
| chr16:22883319
|
C | T | 1 | a0001c0001t0004g0200 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.486-31625C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22883319 | ||||||
| chr16:22883633
|
G | A | 1 | a0001c0002t0001g0006 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.486-31311G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22883633 | ||||||
| chr16:22883649
|
A | G | 1 | a0001c0002t0001g0006 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.486-31295A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22883649 | ||||||
| chr16:22883688
|
T | C | 155 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0153others(152): Show | 155 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(152): Show |
intron_variant | MODIFIER | c.486-31256T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22883688 | ||||||
| chr16:22883718
|
T | TA | 4 | a0001c0004t0002g0171a0001c0004t0002g0266a0001c0004t0002g0267others(1): Show | 4 | HG02451.hp2 HG02809.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.486-31219dupA | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22883718 | |||||
| chr16:22883936
|
G | A | 2 | a0001c0001t0001g0341a0001c0002t0001g0058 | 2 | NA19065.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.486-31008G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22883936 | ||||||
| chr16:22884077
|
C | A | 1 | a0001c0006t0006g0025 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.486-30867C>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22884077 | ||||||
| chr16:22884077
|
C | T | 1 | a0001c0002t0001g0048 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.486-30867C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22884077 | ||||||
| chr16:22884101
|
C | T | 1 | a0001c0004t0002g0267 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.486-30843C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22884101 | ||||||
| chr16:22884129
|
T | C | 1 | a0001c0001t0001g0198 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.486-30815T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22884129 | ||||||
| chr16:22884141
|
A | G | 247 | a0001c0001t0001g0001a0001c0001t0001g0145a0001c0001t0001g0146others(244): Show | 247 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(244): Show |
intron_variant | MODIFIER | c.486-30803A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22884141 | ||||||
| chr16:22884188
|
G | A | 1 | a0001c0001t0001g0185 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.486-30756G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22884188 | ||||||
| chr16:22884406
|
T | C | 154 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0153others(151): Show | 154 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(151): Show |
intron_variant | MODIFIER | c.486-30538T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22884406 | ||||||
| chr16:22884458
|
T | C | 4 | a0001c0001t0001g0182a0001c0001t0001g0301a0001c0003t0003g0018others(1): Show | 4 | HG02559.hp1 HG02717.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.486-30486T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22884458 | ||||||
| chr16:22884653
|
G | GA | 9 | a0001c0001t0001g0145a0001c0001t0001g0195a0001c0001t0001g0204others(6): Show | 9 | HG02155.hp2 HG02809.hp2 HG03139.hp2 others(6): Show |
intron_variant | MODIFIER | c.486-30284dupA | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22884653 | |||||
| chr16:22884658
|
AAATATAT others(12): Show |
A | 6 | a0001c0004t0002g0241a0001c0005t0002g0004a0001c0005t0002g0090others(3): Show | 6 | HG00738.hp2 HG01070.hp2 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.486-30285_486-3026 others(23): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22884658 | ||||||
| chr16:22884659
|
A | T | 9 | a0001c0001t0001g0288a0001c0004t0002g0144a0001c0004t0002g0179others(6): Show | 9 | HG00639.hp1 HG01109.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.486-30285A>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22884659 | ||||||
| chr16:22884660
|
AT | A | 12 | a0001c0001t0001g0148a0001c0001t0001g0156a0001c0001t0001g0189others(9): Show | 12 | HG01516.hp1 HG02040.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.486-30283delT | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22884660 | ||||||
| chr16:22884661
|
T | A | 111 | a0001c0001t0001g0145a0001c0001t0001g0161a0001c0001t0001g0162others(108): Show | 111 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.486-30283T>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22884661 | ||||||
| chr16:22884663
|
T | A | 33 | a0001c0001t0001g0148a0001c0001t0001g0162a0001c0001t0001g0169others(30): Show | 33 | HG00544.hp2 HG00621.hp2 HG00735.hp1 others(30): Show |
intron_variant | MODIFIER | c.486-30281T>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22884663 | ||||||
| chr16:22884665
|
T | A | 1 | a0001c0002t0001g0107 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.486-30279T>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22884665 | ||||||
| chr16:22884677
|
T | TTA | 6 | a0001c0001t0001g0172a0001c0001t0001g0215a0001c0002t0001g0008others(3): Show | 6 | HG01884.hp1 HG02647.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.486-30251_486-3025 others(6): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22884677 | |||||
| chr16:22884677
|
TTA | T | 9 | a0001c0004t0002g0149a0001c0004t0002g0179a0001c0004t0002g0291others(6): Show | 9 | HG01109.hp2 HG01167.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.486-30251_486-3025 others(6): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22884677 | |||||
| chr16:22884846
|
C | CT | 135 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0153others(132): Show | 135 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(132): Show |
intron_variant | MODIFIER | c.486-30085dupT | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22884846 | |||||
| chr16:22885158
|
T | C | 1 | a0001c0001t0001g0164 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.486-29786T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22885158 | ||||||
| chr16:22885333
|
G | GA | 13 | a0001c0004t0002g0149a0001c0004t0002g0171a0001c0004t0002g0179others(10): Show | 13 | HG01109.hp2 HG01167.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.486-29602dupA | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22885333 | |||||
| chr16:22885373
|
A | C | 2 | a0001c0001t0001g0288a0001c0011t0011g0003 | 2 | HG03471.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.486-29571A>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22885373 | ||||||
| chr16:22885389
|
A | G | 10 | a0001c0001t0001g0199a0001c0001t0001g0315a0001c0001t0004g0200others(7): Show | 10 | HG00423.hp2 HG02071.hp1 HG02080.hp2 others(7): Show |
intron_variant | MODIFIER | c.486-29555A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22885389 | ||||||
| chr16:22885502
|
C | G | 1 | a0001c0011t0011g0003 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.486-29442C>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22885502 | ||||||
| chr16:22885580
|
C | T | 11 | a0001c0001t0001g0168a0001c0001t0001g0186a0001c0001t0001g0293others(8): Show | 11 | HG02559.hp2 HG02572.hp2 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.486-29364C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22885580 | ||||||
| chr16:22885655
|
C | A | 2 | a0001c0001t0001g0288a0001c0011t0011g0003 | 2 | HG03471.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.486-29289C>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22885655 | ||||||
| chr16:22885656
|
G | A | 1 | a0001c0001t0004g0193 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.486-29288G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22885656 | ||||||
| chr16:22885708
|
G | A | 116 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0153others(113): Show | 116 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(113): Show |
intron_variant | MODIFIER | c.486-29236G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22885708 | ||||||
| chr16:22886047
|
G | A | 1 | a0001c0001t0001g0312 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.486-28897G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22886047 | ||||||
| chr16:22886064
|
C | T | 2 | a0001c0001t0001g0341a0001c0002t0001g0058 | 2 | NA19065.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.486-28880C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22886064 | ||||||
| chr16:22886075
|
A | G | 1 | a0001c0001t0001g0280 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.486-28869A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22886075 | ||||||
| chr16:22886244
|
C | T | 1 | a0001c0011t0011g0003 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.486-28700C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22886244 | ||||||
| chr16:22886474
|
G | A | 78 | a0001c0001t0001g0001a0001c0001t0001g0145a0001c0001t0001g0146others(75): Show | 78 | HG00544.hp2 HG00609.hp2 HG00621.hp2 others(75): Show |
intron_variant | MODIFIER | c.486-28470G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22886474 | ||||||
| chr16:22886476
|
G | A | 2 | a0001c0001t0001g0288a0001c0002t0001g0138 | 2 | HG01261.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.486-28468G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22886476 | ||||||
| chr16:22886586
|
C | T | 7 | a0001c0001t0001g0225a0001c0001t0001g0244a0001c0001t0001g0246others(4): Show | 7 | NA18979.hp1 NA18979.hp2 NA18982.hp1 others(4): Show |
intron_variant | MODIFIER | c.486-28358C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22886586 | ||||||
| chr16:22886627
|
A | G | 2 | a0001c0002t0001g0006a0001c0002t0001g0013 | 2 | HG03225.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.486-28317A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22886627 | ||||||
| chr16:22886776
|
T | C | 1 | a0001c0001t0001g0146 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.486-28168T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22886776 | ||||||
| chr16:22887569
|
G | C | 2 | a0001c0001t0001g0341a0001c0002t0001g0058 | 2 | NA19065.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.486-27375G>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22887569 | ||||||
| chr16:22887606
|
G | A | 118 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0153others(115): Show | 118 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(115): Show |
intron_variant | MODIFIER | c.486-27338G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22887606 | ||||||
| chr16:22887623
|
G | A | 1 | a0001c0005t0002g0014 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.486-27321G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22887623 | ||||||
| chr16:22887638
|
C | T | 1 | a0001c0001t0001g0259 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.486-27306C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22887638 | ||||||
| chr16:22887712
|
C | T | 3 | a0001c0001t0001g0240a0001c0001t0001g0314a0001c0001t0001g0324 | 3 | HG02129.hp2 NA18968.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.486-27232C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22887712 | ||||||
| chr16:22887786
|
G | GA | 122 | a0001c0001t0001g0001a0001c0001t0001g0145a0001c0001t0001g0146others(119): Show | 122 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(119): Show |
intron_variant | MODIFIER | c.486-27145dupA | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22887786 | |||||
| chr16:22887786
|
G | GAA | 122 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0153others(119): Show | 122 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(119): Show |
intron_variant | MODIFIER | c.486-27146_486-2714 others(6): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22887786 | |||||
| chr16:22887787
|
A | G | 1 | a0001c0001t0001g0174 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.486-27157A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22887787 | ||||||
| chr16:22887803
|
G | T | 1 | a0001c0006t0006g0026 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.486-27141G>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22887803 | ||||||
| chr16:22888030
|
G | C | 152 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0153others(149): Show | 152 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(149): Show |
intron_variant | MODIFIER | c.486-26914G>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22888030 | ||||||
| chr16:22888373
|
C | CT | 34 | a0001c0001t0001g0167a0001c0001t0001g0168a0001c0001t0001g0173others(31): Show | 34 | HG00140.hp2 HG01099.hp2 HG01109.hp1 others(31): Show |
intron_variant | MODIFIER | c.486-26552dupT | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22888373 | |||||
| chr16:22888378
|
T | C | 29 | a0001c0001t0001g0170a0001c0001t0001g0175a0001c0001t0001g0181others(26): Show | 29 | HG01081.hp2 HG01243.hp2 HG01943.hp2 others(26): Show |
intron_variant | MODIFIER | c.486-26566T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22888378 | ||||||
| chr16:22888384
|
T | TTC | 115 | a0001c0001t0001g0001a0001c0001t0001g0145a0001c0001t0001g0146others(112): Show | 115 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(112): Show |
intron_variant | MODIFIER | c.486-26559_486-2655 others(6): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22888384 | |||||
| chr16:22888384
|
T | TTCTTTTT others(4): Show |
128 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0153others(125): Show | 128 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(125): Show |
intron_variant | MODIFIER | c.486-26559_486-2655 others(15): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22888384 | |||||
| chr16:22888384
|
T | TTTCTTTT others(5): Show |
4 | a0001c0001t0001g0225a0001c0001t0001g0246a0001c0002t0001g0115others(1): Show | 4 | NA18953.hp1 NA18979.hp1 NA18979.hp2 others(1): Show |
intron_variant | MODIFIER | c.486-26558_486-2655 others(16): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22888384 | |||||
| chr16:22888392
|
T | C | 3 | a0001c0001t0001g0161a0001c0002t0001g0078a0001c0002t0001g0084 | 3 | HG00438.hp1 NA18612.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.486-26552T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22888392 | ||||||
| chr16:22888393
|
C | CT | 11 | a0001c0001t0001g0234a0001c0001t0001g0238a0001c0001t0001g0252others(8): Show | 11 | HG00735.hp1 HG01099.hp1 HG01167.hp1 others(8): Show |
intron_variant | MODIFIER | c.486-26540dupT | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22888393 | |||||
| chr16:22888393
|
C | T | 3 | a0001c0001t0001g0161a0001c0002t0001g0078a0001c0002t0001g0084 | 3 | HG00438.hp1 NA18612.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.486-26551C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22888393 | ||||||
| chr16:22888411
|
G | A | 1 | a0001c0001t0001g0334 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.486-26533G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22888411 | ||||||
| chr16:22888438
|
G | T | 10 | a0001c0001t0001g0199a0001c0001t0001g0315a0001c0001t0004g0200others(7): Show | 10 | HG00423.hp2 HG02071.hp1 HG02080.hp2 others(7): Show |
intron_variant | MODIFIER | c.486-26506G>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22888438 | ||||||
| chr16:22888531
|
C | T | 2 | a0001c0001t0001g0230a0001c0001t0001g0350 | 2 | NA18969.hp1 NA19006.hp2 |
intron_variant | MODIFIER | c.486-26413C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22888531 | ||||||
| chr16:22888533
|
T | A | 1 | a0001c0002t0001g0124 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.486-26411T>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22888533 | ||||||
| chr16:22888547
|
T | C | 75 | a0001c0001t0001g0001a0001c0001t0001g0145a0001c0001t0001g0146others(72): Show | 75 | HG00544.hp2 HG00609.hp2 HG00621.hp2 others(72): Show |
intron_variant | MODIFIER | c.486-26397T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22888547 | ||||||
| chr16:22888653
|
G | A | 1 | a0001c0002t0007g0056 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.486-26291G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22888653 | ||||||
| chr16:22888678
|
C | T | 1 | a0001c0001t0001g0316 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.486-26266C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22888678 | ||||||
| chr16:22888686
|
C | T | 1 | a0001c0001t0001g0281 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.486-26258C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22888686 | ||||||
| chr16:22888687
|
G | A | 2 | a0001c0001t0001g0341a0001c0002t0001g0058 | 2 | NA19065.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.486-26257G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22888687 | ||||||
| chr16:22888786
|
G | A | 1 | a0001c0003t0003g0021 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.486-26158G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22888786 | ||||||
| chr16:22888812
|
G | T | 1 | a0001c0001t0001g0317 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.486-26132G>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22888812 | ||||||
| chr16:22889123
|
C | T | 1 | a0001c0001t0001g0217 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.486-25821C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22889123 | ||||||
| chr16:22889303
|
C | T | 2 | a0001c0001t0001g0288a0001c0011t0011g0003 | 2 | HG03471.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.486-25641C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22889303 | ||||||
| chr16:22889350
|
T | C | 1 | a0001c0001t0001g0278 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.486-25594T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22889350 | ||||||
| chr16:22889543
|
G | A | 1 | a0001c0002t0001g0075 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.486-25401G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22889543 | ||||||
| chr16:22889590
|
A | G | 1 | a0001c0011t0011g0003 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.486-25354A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22889590 | ||||||
| chr16:22889595
|
C | T | 1 | a0001c0001t0001g0181 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.486-25349C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22889595 | ||||||
| chr16:22890100
|
C | T | 1 | a0001c0002t0001g0118 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.486-24844C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22890100 | ||||||
| chr16:22890305
|
AT | A | 118 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0153others(115): Show | 118 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(115): Show |
intron_variant | MODIFIER | c.486-24632delT | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22890305 | |||||
| chr16:22890393
|
A | C | 2 | a0001c0001t0001g0341a0001c0002t0001g0058 | 2 | NA19065.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.486-24551A>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22890393 | ||||||
| chr16:22890462
|
T | TTAAAGCT others(356): Show |
1 | a0001c0004t0002g0267 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.486-24469_486-2446 others(367): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22890462 | |||||
| chr16:22890493
|
A | G | 7 | a0001c0001t0001g0194a0001c0001t0001g0212a0001c0001t0001g0219others(4): Show | 7 | HG02523.hp2 NA18957.hp2 NA18962.hp1 others(4): Show |
intron_variant | MODIFIER | c.486-24451A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22890493 | ||||||
| chr16:22890530
|
G | C | 152 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0153others(149): Show | 152 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(149): Show |
intron_variant | MODIFIER | c.486-24414G>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22890530 | ||||||
| chr16:22890746
|
T | G | 148 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0153others(145): Show | 148 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(145): Show |
intron_variant | MODIFIER | c.486-24198T>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22890746 | ||||||
| chr16:22890861
|
G | A | 15 | a0001c0001t0001g0151a0001c0001t0001g0153a0001c0001t0001g0154others(12): Show | 15 | HG01106.hp2 HG01168.hp2 HG01255.hp1 others(12): Show |
intron_variant | MODIFIER | c.486-24083G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22890861 | ||||||
| chr16:22890954
|
C | T | 1 | a0001c0002t0001g0103 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.486-23990C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22890954 | ||||||
| chr16:22891072
|
G | C | 3 | a0001c0001t0001g0271a0001c0001t0001g0288a0001c0011t0011g0003 | 3 | HG03471.hp1 HG06807.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.486-23872G>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22891072 | ||||||
| chr16:22891156
|
G | T | 1 | a0001c0001t0001g0233 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.486-23788G>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22891156 | ||||||
| chr16:22891173
|
C | T | 1 | a0001c0001t0001g0172 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.486-23771C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22891173 | ||||||
| chr16:22891477
|
GA | G | 164 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0153others(161): Show | 164 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(161): Show |
intron_variant | MODIFIER | c.486-23456delA | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22891477 | |||||
| chr16:22891572
|
A | C | 2 | a0001c0001t0001g0166a0001c0001t0001g0299 | 2 | HG02451.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.486-23372A>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22891572 | ||||||
| chr16:22891573
|
C | T | 1 | a0001c0002t0001g0124 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.486-23371C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22891573 | ||||||
| chr16:22891699
|
G | A | 29 | a0001c0001t0001g0170a0001c0001t0001g0175a0001c0001t0001g0181others(26): Show | 29 | HG01081.hp2 HG01243.hp2 HG01943.hp2 others(26): Show |
intron_variant | MODIFIER | c.486-23245G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22891699 | ||||||
| chr16:22891701
|
A | T | 36 | a0001c0001t0001g0167a0001c0001t0001g0168a0001c0001t0001g0173others(33): Show | 36 | HG00140.hp2 HG01099.hp2 HG01109.hp1 others(33): Show |
intron_variant | MODIFIER | c.486-23243A>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22891701 | ||||||
| chr16:22891886
|
G | A | 1 | a0001c0001t0001g0255 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.486-23058G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22891886 | ||||||
| chr16:22892090
|
C | T | 152 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0153others(149): Show | 152 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(149): Show |
intron_variant | MODIFIER | c.486-22854C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22892090 | ||||||
| chr16:22892110
|
T | TA | 10 | a0001c0001t0001g0216a0001c0001t0001g0223a0001c0001t0001g0226others(7): Show | 10 | HG01175.hp1 HG02145.hp1 HG04204.hp1 others(7): Show |
intron_variant | MODIFIER | c.486-22813dupA | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22892110 | |||||
| chr16:22892110
|
TA | T | 153 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0153others(150): Show | 153 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(150): Show |
intron_variant | MODIFIER | c.486-22813delA | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22892110 | |||||
| chr16:22892110
|
TAA | T | 14 | a0001c0001t0001g0199a0001c0001t0001g0315a0001c0001t0004g0200others(11): Show | 14 | HG00423.hp2 HG01257.hp2 HG02071.hp1 others(11): Show |
intron_variant | MODIFIER | c.486-22814_486-2281 others(6): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22892110 | |||||
| chr16:22892111
|
A | G | 4 | a0001c0001t0001g0197a0001c0001t0001g0233a0001c0002t0001g0105others(1): Show | 4 | HG00323.hp1 HG01243.hp1 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.486-22833A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22892111 | ||||||
| chr16:22892147
|
G | A | 1 | a0001c0002t0005g0131 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.486-22797G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22892147 | ||||||
| chr16:22892156
|
G | A | 1 | a0001c0006t0006g0026 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.486-22788G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22892156 | ||||||
| chr16:22892167
|
A | G | 168 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0153others(165): Show | 168 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(165): Show |
intron_variant | MODIFIER | c.486-22777A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22892167 | ||||||
| chr16:22892397
|
A | C | 1 | a0001c0011t0011g0003 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.486-22547A>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22892397 | ||||||
| chr16:22892453
|
C | T | 331 | a0001c0001t0001g0001a0001c0001t0001g0145a0001c0001t0001g0146others(328): Show | 331 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(328): Show |
intron_variant | MODIFIER | c.486-22491C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22892453 | ||||||
| chr16:22892468
|
A | G | 2 | a0001c0001t0001g0194a0001c0001t0001g0254 | 2 | NA18957.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.486-22476A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22892468 | ||||||
| chr16:22892750
|
A | G | 1 | a0001c0001t0001g0203 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.486-22194A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22892750 | ||||||
| chr16:22892800
|
T | C | 16 | a0001c0004t0002g0149a0001c0004t0002g0179a0001c0004t0002g0241others(13): Show | 16 | HG00639.hp1 HG00738.hp2 HG01070.hp2 others(13): Show |
intron_variant | MODIFIER | c.486-22144T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22892800 | ||||||
| chr16:22892834
|
G | A | 15 | a0001c0001t0001g0178a0001c0001t0001g0185a0001c0001t0001g0197others(12): Show | 15 | HG00280.hp1 HG00323.hp1 HG01168.hp1 others(12): Show |
intron_variant | MODIFIER | c.486-22110G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22892834 | ||||||
| chr16:22892864
|
A | G | 1 | a0001c0001t0001g0191 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.486-22080A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22892864 | ||||||
| chr16:22893040
|
C | T | 1 | a0001c0002t0001g0071 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.486-21904C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22893040 | ||||||
| chr16:22893171
|
A | T | 1 | a0001c0001t0001g0300 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.486-21773A>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22893171 | ||||||
| chr16:22893191
|
G | A | 1 | a0001c0001t0001g0327 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.486-21753G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22893191 | ||||||
| chr16:22893254
|
T | C | 1 | a0001c0001t0001g0186 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.486-21690T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22893254 | ||||||
| chr16:22893258
|
A | G | 1 | a0001c0001t0001g0279 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.486-21686A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22893258 | ||||||
| chr16:22893284
|
T | C | 1 | a0001c0006t0006g0025 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.486-21660T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22893284 | ||||||
| chr16:22893340
|
C | T | 4 | a0001c0001t0001g0182a0001c0001t0001g0301a0001c0003t0003g0018others(1): Show | 4 | HG02559.hp1 HG02717.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.486-21604C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22893340 | ||||||
| chr16:22893436
|
C | T | 1 | a0001c0001t0001g0349 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.486-21508C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22893436 | ||||||
| chr16:22893634
|
C | CT | 325 | a0001c0001t0001g0001a0001c0001t0001g0145a0001c0001t0001g0146others(322): Show | 325 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(322): Show |
intron_variant | MODIFIER | c.486-21295dupT | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22893634 | |||||
| chr16:22893650
|
A | T | 3 | a0001c0001t0001g0204a0001c0002t0001g0308a0001c0002t0001g0309 | 3 | HG01516.hp2 HG01517.hp2 HG02155.hp2 |
intron_variant | MODIFIER | c.486-21294A>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22893650 | ||||||
| chr16:22893709
|
A | G | 1 | a0001c0004t0014g0242 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.486-21235A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22893709 | ||||||
| chr16:22893723
|
C | A | 1 | a0001c0006t0006g0025 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.486-21221C>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22893723 | ||||||
| chr16:22894093
|
T | C | 1 | a0001c0002t0001g0110 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.486-20851T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22894093 | ||||||
| chr16:22894256
|
C | T | 1 | a0001c0002t0001g0079 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.486-20688C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22894256 | ||||||
| chr16:22894302
|
C | G | 7 | a0001c0004t0002g0183a0001c0004t0002g0184a0001c0004t0002g0261others(4): Show | 7 | HG00735.hp2 HG01081.hp1 HG01256.hp1 others(4): Show |
intron_variant | MODIFIER | c.486-20642C>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22894302 | ||||||
| chr16:22894592
|
A | G | 3 | a0001c0001t0001g0218a0001c0001t0001g0288a0001c0011t0011g0003 | 3 | HG02717.hp1 HG03471.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.486-20352A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22894592 | ||||||
| chr16:22894735
|
T | TA | 7 | a0001c0001t0001g0350a0001c0001t0004g0235a0001c0001t0009g0209others(4): Show | 7 | HG00438.hp2 HG02040.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.486-20192dupA | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22894735 | |||||
| chr16:22894959
|
T | C | 1 | a0001c0001t0001g0163 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.486-19985T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22894959 | ||||||
| chr16:22895017
|
G | A | 2 | a0002c0009t0001g0342a0002c0009t0001g0344 | 2 | NA18962.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.486-19927G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22895017 | ||||||
| chr16:22895070
|
CT | C | 175 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0153others(172): Show | 175 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(172): Show |
intron_variant | MODIFIER | c.486-19858delT | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22895070 | |||||
| chr16:22895135
|
A | G | 247 | a0001c0001t0001g0001a0001c0001t0001g0145a0001c0001t0001g0146others(244): Show | 247 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(244): Show |
intron_variant | MODIFIER | c.486-19809A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22895135 | ||||||
| chr16:22895215
|
G | A | 1 | a0001c0001t0001g0280 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.486-19729G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22895215 | ||||||
| chr16:22895328
|
G | C | 152 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0153others(149): Show | 152 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(149): Show |
intron_variant | MODIFIER | c.486-19616G>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22895328 | ||||||
| chr16:22895343
|
G | C | 3 | a0001c0001t0001g0306a0001c0003t0003g0027a0001c0003t0003g0035 | 3 | HG02572.hp1 HG02615.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.486-19601G>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22895343 | ||||||
| chr16:22895769
|
T | G | 1 | a0001c0001t0001g0220 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.486-19175T>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22895769 | ||||||
| chr16:22896061
|
C | T | 1 | a0001c0006t0006g0025 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.486-18883C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22896061 | ||||||
| chr16:22896867
|
C | T | 1 | a0001c0001t0001g0204 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.486-18077C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22896867 | ||||||
| chr16:22896933
|
A | T | 2 | a0001c0001t0001g0271a0001c0001t0001g0288 | 2 | HG06807.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.486-18011A>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22896933 | ||||||
| chr16:22896975
|
T | C | 3 | a0001c0001t0001g0271a0001c0001t0001g0288a0001c0011t0011g0003 | 3 | HG03471.hp1 HG06807.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.486-17969T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22896975 | ||||||
| chr16:22896982
|
A | AT | 5 | a0001c0001t0001g0223a0001c0001t0001g0310a0001c0001t0001g0331others(2): Show | 5 | HG01099.hp2 HG01109.hp1 HG01175.hp1 others(2): Show |
intron_variant | MODIFIER | c.486-17955dupT | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22896982 | |||||
| chr16:22897106
|
C | A | 1 | a0001c0001t0001g0283 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.486-17838C>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22897106 | ||||||
| chr16:22897152
|
C | T | 148 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0153others(145): Show | 148 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(145): Show |
intron_variant | MODIFIER | c.486-17792C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22897152 | ||||||
| chr16:22897201
|
A | G | 167 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0153others(164): Show | 167 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(164): Show |
intron_variant | MODIFIER | c.486-17743A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22897201 | ||||||
| chr16:22897230
|
G | A | 2 | a0001c0001t0001g0341a0001c0002t0001g0058 | 2 | NA19065.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.486-17714G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22897230 | ||||||
| chr16:22897347
|
G | T | 1 | a0001c0006t0006g0025 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.486-17597G>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22897347 | ||||||
| chr16:22897562
|
T | C | 8 | a0001c0001t0001g0315a0001c0001t0004g0200a0001c0001t0004g0235others(5): Show | 8 | HG00423.hp2 HG02071.hp1 HG02080.hp2 others(5): Show |
intron_variant | MODIFIER | c.486-17382T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22897562 | ||||||
| chr16:22897650
|
CATCTTTG others(270): Show |
C | 248 | a0001c0001t0001g0001a0001c0001t0001g0145a0001c0001t0001g0146others(245): Show | 248 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(245): Show |
intron_variant | MODIFIER | c.486-17291_486-1701 others(4): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22897650 | |||||
| chr16:22897748
|
A | G | 4 | a0001c0001t0001g0237a0001c0001t0001g0260a0001c0002t0001g0079others(1): Show | 4 | HG00140.hp2 HG02683.hp1 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.486-17196A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22897748 | ||||||
| chr16:22897930
|
G | A | 248 | a0001c0001t0001g0001a0001c0001t0001g0145a0001c0001t0001g0146others(245): Show | 248 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(245): Show |
intron_variant | MODIFIER | c.486-17014G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22897930 | ||||||
| chr16:22898240
|
G | A | 1 | a0001c0002t0007g0056 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.486-16704G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22898240 | ||||||
| chr16:22899008
|
G | A | 30 | a0001c0001t0001g0167a0001c0001t0001g0168a0001c0001t0001g0174others(27): Show | 30 | HG00140.hp2 HG01099.hp2 HG01109.hp1 others(27): Show |
intron_variant | MODIFIER | c.486-15936G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22899008 | ||||||
| chr16:22899052
|
C | A | 1 | a0001c0003t0003g0021 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.486-15892C>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22899052 | ||||||
| chr16:22899117
|
A | C | 1 | a0001c0002t0001g0068 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.486-15827A>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22899117 | ||||||
| chr16:22899647
|
A | G | 1 | a0001c0005t0002g0014 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.486-15297A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22899647 | ||||||
| chr16:22899747
|
G | A | 24 | a0001c0001t0001g0148a0001c0001t0001g0156a0001c0001t0001g0189others(21): Show | 24 | HG00544.hp2 HG00621.hp2 HG02040.hp1 others(21): Show |
intron_variant | MODIFIER | c.486-15197G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22899747 | ||||||
| chr16:22899950
|
A | G | 241 | a0001c0001t0001g0001a0001c0001t0001g0145a0001c0001t0001g0146others(238): Show | 241 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(238): Show |
intron_variant | MODIFIER | c.486-14994A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22899950 | ||||||
| chr16:22900232
|
G | C | 80 | a0001c0001t0001g0001a0001c0001t0001g0145a0001c0001t0001g0146others(77): Show | 80 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(77): Show |
intron_variant | MODIFIER | c.486-14712G>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22900232 | ||||||
| chr16:22900401
|
G | A | 2 | a0001c0005t0002g0090a0001c0005t0002g0102 | 2 | HG00738.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.486-14543G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22900401 | ||||||
| chr16:22900424
|
A | G | 1 | a0001c0001t0001g0271 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.486-14520A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22900424 | ||||||
| chr16:22900427
|
C | T | 164 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0153others(161): Show | 164 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(161): Show |
intron_variant | MODIFIER | c.486-14517C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22900427 | ||||||
| chr16:22900485
|
C | T | 1 | a0001c0001t0001g0251 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.486-14459C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22900485 | ||||||
| chr16:22900487
|
G | A | 1 | a0001c0001t0001g0198 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.486-14457G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22900487 | ||||||
| chr16:22900718
|
C | T | 1 | a0001c0002t0001g0114 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.486-14226C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22900718 | ||||||
| chr16:22900754
|
G | A | 1 | a0001c0001t0001g0217 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.486-14190G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22900754 | ||||||
| chr16:22901085
|
G | A | 1 | a0001c0001t0001g0237 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.486-13859G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22901085 | ||||||
| chr16:22901183
|
A | G | 4 | a0001c0001t0001g0212a0001c0001t0001g0219a0001c0001t0001g0281others(1): Show | 4 | HG02523.hp2 NA18962.hp1 NA19086.hp1 others(1): Show |
intron_variant | MODIFIER | c.486-13761A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22901183 | ||||||
| chr16:22901453
|
A | G | 4 | a0001c0001t0001g0182a0001c0001t0001g0301a0001c0003t0003g0018others(1): Show | 4 | HG02559.hp1 HG02717.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.486-13491A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22901453 | ||||||
| chr16:22901549
|
A | G | 248 | a0001c0001t0001g0001a0001c0001t0001g0145a0001c0001t0001g0146others(245): Show | 248 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(245): Show |
intron_variant | MODIFIER | c.486-13395A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22901549 | ||||||
| chr16:22901714
|
G | A | 1 | a0001c0011t0011g0003 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.486-13230G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22901714 | ||||||
| chr16:22901906
|
A | T | 1 | a0001c0005t0002g0014 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.486-13038A>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22901906 | ||||||
| chr16:22902046
|
A | G | 1 | a0001c0011t0011g0003 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.486-12898A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22902046 | ||||||
| chr16:22902146
|
T | C | 11 | a0001c0001t0001g0199a0001c0001t0001g0271a0001c0001t0004g0200others(8): Show | 11 | HG00639.hp1 HG02071.hp1 HG02080.hp2 others(8): Show |
intron_variant | MODIFIER | c.486-12798T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22902146 | ||||||
| chr16:22902246
|
T | C | 4 | a0001c0001t0001g0265a0001c0002t0001g0054a0001c0002t0001g0055others(1): Show | 4 | HG00558.hp1 HG04184.hp1 NA18957.hp1 others(1): Show |
intron_variant | MODIFIER | c.486-12698T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22902246 | ||||||
| chr16:22902277
|
G | A | 14 | a0001c0004t0002g0144a0001c0004t0002g0183a0001c0004t0002g0184others(11): Show | 14 | HG00735.hp2 HG01081.hp1 HG01256.hp1 others(11): Show |
intron_variant | MODIFIER | c.486-12667G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22902277 | ||||||
| chr16:22902526
|
A | T | 9 | a0001c0001t0001g0199a0001c0001t0004g0200a0001c0001t0004g0235others(6): Show | 9 | HG02071.hp1 HG02080.hp2 HG02698.hp2 others(6): Show |
intron_variant | MODIFIER | c.486-12418A>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22902526 | ||||||
| chr16:22902620
|
T | C | 2 | a0001c0001t0001g0218a0001c0001t0001g0303 | 2 | HG02717.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.486-12324T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22902620 | ||||||
| chr16:22902666
|
T | C | 10 | a0001c0001t0001g0145a0001c0001t0001g0169a0001c0001t0001g0287others(7): Show | 10 | HG02055.hp1 HG02647.hp1 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.486-12278T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22902666 | ||||||
| chr16:22902721
|
A | T | 154 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0153others(151): Show | 154 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(151): Show |
intron_variant | MODIFIER | c.486-12223A>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22902721 | ||||||
| chr16:22902721
|
AT | A | 12 | a0001c0001t0001g0199a0001c0001t0001g0271a0001c0001t0004g0200others(9): Show | 12 | HG00639.hp1 HG02071.hp1 HG02080.hp2 others(9): Show |
intron_variant | MODIFIER | c.486-12215delT | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22902721 | |||||
| chr16:22902722
|
T | C | 4 | a0001c0001t0001g0170a0001c0001t0001g0175a0001c0001t0001g0181others(1): Show | 4 | HG01243.hp2 HG02280.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.486-12222T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22902722 | ||||||
| chr16:22902990
|
C | T | 1 | a0001c0004t0002g0267 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.486-11954C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22902990 | ||||||
| chr16:22903339
|
G | A | 79 | a0001c0001t0001g0001a0001c0001t0001g0145a0001c0001t0001g0146others(76): Show | 79 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(76): Show |
intron_variant | MODIFIER | c.486-11605G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22903339 | ||||||
| chr16:22903387
|
G | A | 1 | a0001c0001t0001g0283 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.486-11557G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22903387 | ||||||
| chr16:22903568
|
G | A | 1 | a0001c0001t0001g0233 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.486-11376G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22903568 | ||||||
| chr16:22903605
|
T | C | 34 | a0001c0001t0001g0167a0001c0001t0001g0168a0001c0001t0001g0173others(31): Show | 34 | HG00140.hp2 HG01175.hp1 HG01175.hp2 others(31): Show |
intron_variant | MODIFIER | c.486-11339T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22903605 | ||||||
| chr16:22903627
|
A | G | 156 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0153others(153): Show | 156 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(153): Show |
intron_variant | MODIFIER | c.486-11317A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22903627 | ||||||
| chr16:22903638
|
A | G | 1 | a0001c0001t0001g0271 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.486-11306A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22903638 | ||||||
| chr16:22903644
|
C | T | 1 | a0001c0001t0001g0146 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.486-11300C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22903644 | ||||||
| chr16:22903819
|
G | A | 1 | a0001c0006t0006g0016 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.486-11125G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22903819 | ||||||
| chr16:22903825
|
C | T | 158 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0153others(155): Show | 158 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(155): Show |
intron_variant | MODIFIER | c.486-11119C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22903825 | ||||||
| chr16:22903911
|
A | G | 1 | a0001c0011t0011g0003 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.486-11033A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22903911 | ||||||
| chr16:22903924
|
T | C | 248 | a0001c0001t0001g0001a0001c0001t0001g0145a0001c0001t0001g0146others(245): Show | 248 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(245): Show |
intron_variant | MODIFIER | c.486-11020T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22903924 | ||||||
| chr16:22904006
|
A | G | 346 | a0001c0001t0001g0001a0001c0001t0001g0145a0001c0001t0001g0146others(343): Show | 346 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(343): Show |
intron_variant | MODIFIER | c.486-10938A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22904006 | ||||||
| chr16:22904293
|
C | T | 1 | a0001c0001t0004g0235 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.486-10651C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22904293 | ||||||
| chr16:22904298
|
C | A | 2 | a0001c0004t0002g0307a0001c0006t0006g0023 | 2 | HG02970.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.486-10646C>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22904298 | ||||||
| chr16:22904320
|
C | T | 9 | a0001c0001t0001g0199a0001c0001t0004g0200a0001c0001t0004g0235others(6): Show | 9 | HG02071.hp1 HG02080.hp2 HG02698.hp2 others(6): Show |
intron_variant | MODIFIER | c.486-10624C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22904320 | ||||||
| chr16:22904321
|
G | A | 1 | a0001c0004t0002g0171 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.486-10623G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22904321 | ||||||
| chr16:22904431
|
G | A | 1 | a0001c0006t0006g0025 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.486-10513G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22904431 | ||||||
| chr16:22904468
|
T | C | 173 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0153others(170): Show | 173 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(170): Show |
intron_variant | MODIFIER | c.486-10476T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22904468 | ||||||
| chr16:22904511
|
C | T | 1 | a0001c0006t0006g0025 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.486-10433C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22904511 | ||||||
| chr16:22904545
|
A | T | 1 | a0001c0001t0001g0316 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.486-10399A>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22904545 | ||||||
| chr16:22904603
|
C | T | 149 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0153others(146): Show | 149 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(146): Show |
intron_variant | MODIFIER | c.486-10341C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22904603 | ||||||
| chr16:22904889
|
C | T | 1 | a0001c0011t0011g0003 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.486-10055C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22904889 | ||||||
| chr16:22904926
|
C | A | 10 | a0001c0001t0001g0155a0001c0001t0001g0160a0001c0001t0001g0275others(7): Show | 10 | HG00741.hp1 HG01070.hp1 HG01257.hp2 others(7): Show |
intron_variant | MODIFIER | c.486-10018C>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22904926 | ||||||
| chr16:22904941
|
A | G | 3 | a0001c0001t0001g0161a0001c0002t0001g0078a0001c0002t0001g0084 | 3 | HG00438.hp1 NA18612.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.486-10003A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22904941 | ||||||
| chr16:22904980
|
T | C | 1 | a0001c0002t0004g0072 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.486-9964T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22904980 | ||||||
| chr16:22905162
|
T | C | 1 | a0001c0006t0006g0025 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.486-9782T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22905162 | ||||||
| chr16:22905241
|
G | A | 1 | a0001c0001t0001g0223 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.486-9703G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22905241 | ||||||
| chr16:22905251
|
C | T | 1 | a0001c0001t0001g0256 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.486-9693C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22905251 | ||||||
| chr16:22905330
|
C | T | 1 | a0001c0006t0006g0025 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.486-9614C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22905330 | ||||||
| chr16:22905343
|
C | T | 1 | a0001c0006t0006g0025 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.486-9601C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22905343 | ||||||
| chr16:22905369
|
A | G | 1 | a0001c0006t0006g0025 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.486-9575A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22905369 | ||||||
| chr16:22905424
|
G | T | 1 | a0001c0001t0009g0209 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.486-9520G>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22905424 | ||||||
| chr16:22905459
|
C | A | 1 | a0007c0010t0001g0042 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.486-9485C>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22905459 | ||||||
| chr16:22905623
|
C | T | 2 | a0001c0002t0001g0006a0001c0002t0001g0013 | 2 | HG03225.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.486-9321C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22905623 | ||||||
| chr16:22905624
|
G | C | 1 | a0001c0001t0001g0288 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.486-9320G>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22905624 | ||||||
| chr16:22905730
|
G | A | 1 | a0001c0001t0001g0233 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.486-9214G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22905730 | ||||||
| chr16:22905866
|
G | A | 1 | a0001c0002t0004g0072 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.486-9078G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22905866 | ||||||
| chr16:22905880
|
T | C | 1 | a0001c0001t0001g0172 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.486-9064T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22905880 | ||||||
| chr16:22905998
|
C | T | 2 | a0001c0002t0001g0006a0001c0002t0001g0013 | 2 | HG03225.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.486-8946C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22905998 | ||||||
| chr16:22906095
|
G | A | 1 | a0001c0006t0006g0025 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.486-8849G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22906095 | ||||||
| chr16:22906113
|
C | T | 151 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0153others(148): Show | 151 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(148): Show |
intron_variant | MODIFIER | c.486-8831C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22906113 | ||||||
| chr16:22906197
|
C | T | 1 | a0001c0001t0001g0336 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.486-8747C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22906197 | ||||||
| chr16:22906268
|
G | A | 1 | a0001c0001t0001g0313 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.486-8676G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22906268 | ||||||
| chr16:22906367
|
C | CTAAA | 3 | a0001c0001t0001g0288a0001c0002t0001g0006a0001c0002t0001g0013 | 3 | HG03225.hp2 HG06807.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.486-8552_486-8549d others(6): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22906367 | |||||
| chr16:22906367
|
C | CTAAATAA others(1): Show |
4 | a0001c0001t0001g0302a0001c0002t0001g0113a0001c0002t0001g0116others(1): Show | 4 | HG02886.hp1 HG03453.hp2 NA19005.hp2 others(1): Show |
intron_variant | MODIFIER | c.486-8556_486-8549d others(10): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22906367 | |||||
| chr16:22906367
|
C | CTAAATAA others(5): Show |
14 | a0001c0001t0001g0162a0001c0001t0001g0166a0001c0001t0001g0224others(11): Show | 14 | HG01952.hp2 HG01975.hp2 HG02132.hp2 others(11): Show |
intron_variant | MODIFIER | c.486-8560_486-8549d others(14): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22906367 | |||||
| chr16:22906367
|
C | CTAAATAA others(9): Show |
244 | a0001c0001t0001g0001a0001c0001t0001g0145a0001c0001t0001g0146others(241): Show | 244 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(241): Show |
intron_variant | MODIFIER | c.486-8564_486-8549d others(18): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22906367 | |||||
| chr16:22906367
|
C | CTAAATAA others(13): Show |
63 | a0001c0001t0001g0161a0001c0001t0001g0163a0001c0001t0001g0170others(60): Show | 63 | HG00438.hp1 HG00558.hp2 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.486-8568_486-8549d others(22): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22906367 | |||||
| chr16:22906379
|
A | ATAAATAA others(9): Show |
1 | a0001c0006t0006g0025 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.486-8550_486-8549i others(18): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22906379 | |||||
| chr16:22906461
|
T | A | 1 | a0001c0006t0006g0025 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.486-8483T>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22906461 | ||||||
| chr16:22906573
|
G | A | 2 | a0001c0001t0001g0147a0001c0002t0001g0104 | 2 | HG00741.hp2 HG01123.hp1 |
intron_variant | MODIFIER | c.486-8371G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22906573 | ||||||
| chr16:22906585
|
T | C | 2 | a0001c0001t0001g0166a0001c0001t0001g0299 | 2 | HG02451.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.486-8359T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22906585 | ||||||
| chr16:22906595
|
C | T | 1 | a0001c0011t0011g0003 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.486-8349C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22906595 | ||||||
| chr16:22906662
|
C | G | 4 | a0001c0001t0001g0322a0001c0001t0001g0325a0001c0002t0001g0092others(1): Show | 4 | NA18942.hp1 NA19009.hp1 NA19083.hp1 others(1): Show |
intron_variant | MODIFIER | c.486-8282C>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22906662 | ||||||
| chr16:22906818
|
C | A | 2 | a0001c0001t0001g0341a0001c0002t0001g0058 | 2 | NA19065.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.486-8126C>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22906818 | ||||||
| chr16:22906826
|
G | T | 2 | a0001c0001t0001g0341a0001c0002t0001g0058 | 2 | NA19065.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.486-8118G>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22906826 | ||||||
| chr16:22906876
|
T | C | 3 | a0001c0001t0001g0288a0001c0002t0001g0006a0001c0002t0001g0013 | 3 | HG03225.hp2 HG06807.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.486-8068T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22906876 | ||||||
| chr16:22907036
|
G | T | 1 | a0001c0004t0002g0171 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.486-7908G>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22907036 | ||||||
| chr16:22907427
|
A | G | 152 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0153others(149): Show | 152 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(149): Show |
intron_variant | MODIFIER | c.486-7517A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22907427 | ||||||
| chr16:22907472
|
T | A | 14 | a0001c0001t0001g0182a0001c0001t0001g0199a0001c0001t0001g0271others(11): Show | 14 | HG02071.hp1 HG02080.hp2 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.486-7472T>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22907472 | ||||||
| chr16:22907531
|
G | GT | 3 | a0001c0001t0001g0288a0001c0002t0001g0006a0001c0002t0001g0013 | 3 | HG03225.hp2 HG06807.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.486-7411dupT | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22907531 | |||||
| chr16:22907943
|
G | C | 6 | a0001c0001t0001g0173a0001c0001t0001g0294a0001c0001t0001g0295others(3): Show | 6 | HG01884.hp2 HG02280.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.486-7001G>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22907943 | ||||||
| chr16:22908031
|
G | C | 1 | a0001c0006t0006g0025 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.486-6913G>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22908031 | ||||||
| chr16:22908059
|
C | T | 1 | a0001c0001t0004g0340 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.486-6885C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22908059 | ||||||
| chr16:22908075
|
T | C | 1 | a0001c0001t0001g0297 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.486-6869T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22908075 | ||||||
| chr16:22908142
|
A | G | 152 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0153others(149): Show | 152 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(149): Show |
intron_variant | MODIFIER | c.486-6802A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22908142 | ||||||
| chr16:22908227
|
G | A | 1 | a0001c0002t0001g0120 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.486-6717G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22908227 | ||||||
| chr16:22908385
|
GTGGGGTG others(4): Show |
G | 1 | a0001c0001t0001g0288 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.486-6557_486-6547d others(13): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22908385 | |||||
| chr16:22908461
|
T | G | 19 | a0001c0001t0001g0150a0001c0001t0001g0187a0001c0001t0001g0188others(16): Show | 19 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(16): Show |
intron_variant | MODIFIER | c.486-6483T>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22908461 | ||||||
| chr16:22908496
|
C | G | 2 | a0001c0002t0001g0006a0001c0002t0001g0013 | 2 | HG03225.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.486-6448C>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22908496 | ||||||
| chr16:22908565
|
C | G | 1 | a0001c0002t0001g0113 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.486-6379C>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22908565 | ||||||
| chr16:22908657
|
C | T | 1 | a0001c0006t0006g0025 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.486-6287C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22908657 | ||||||
| chr16:22908771
|
A | G | 2 | a0001c0001t0001g0153a0001c0001t0001g0176 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.486-6173A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22908771 | ||||||
| chr16:22908810
|
G | C | 2 | a0001c0001t0001g0166a0001c0001t0001g0299 | 2 | HG02451.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.486-6134G>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22908810 | ||||||
| chr16:22908825
|
A | C | 14 | a0001c0004t0002g0144a0001c0004t0002g0183a0001c0004t0002g0184others(11): Show | 14 | HG00735.hp2 HG01081.hp1 HG01256.hp1 others(11): Show |
intron_variant | MODIFIER | c.486-6119A>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22908825 | ||||||
| chr16:22908844
|
A | G | 1 | a0001c0001t0001g0186 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.486-6100A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22908844 | ||||||
| chr16:22908990
|
G | A | 4 | a0001c0004t0002g0171a0001c0004t0002g0266a0001c0004t0002g0267others(1): Show | 4 | HG02451.hp2 HG02809.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.486-5954G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22908990 | ||||||
| chr16:22909148
|
C | G | 1 | a0001c0002t0001g0116 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.486-5796C>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22909148 | ||||||
| chr16:22909183
|
T | C | 152 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0153others(149): Show | 152 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(149): Show |
intron_variant | MODIFIER | c.486-5761T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22909183 | ||||||
| chr16:22909283
|
G | A | 281 | a0001c0001t0001g0001a0001c0001t0001g0145a0001c0001t0001g0146others(278): Show | 281 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(278): Show |
intron_variant | MODIFIER | c.486-5661G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22909283 | ||||||
| chr16:22909380
|
G | T | 1 | a0001c0002t0001g0118 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.486-5564G>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22909380 | ||||||
| chr16:22909483
|
T | C | 2 | a0001c0002t0001g0007a0001c0002t0001g0124 | 2 | HG02109.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.486-5461T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22909483 | ||||||
| chr16:22909531
|
C | A | 75 | a0001c0001t0001g0001a0001c0001t0001g0145a0001c0001t0001g0146others(72): Show | 75 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(72): Show |
intron_variant | MODIFIER | c.486-5413C>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22909531 | ||||||
| chr16:22909740
|
A | C | 1 | a0001c0001t0004g0200 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.486-5204A>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22909740 | ||||||
| chr16:22909898
|
G | A | 1 | a0001c0001t0001g0324 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.486-5046G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22909898 | ||||||
| chr16:22909953
|
C | T | 1 | a0001c0001t0001g0154 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.486-4991C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22909953 | ||||||
| chr16:22910037
|
C | CA | 11 | a0001c0001t0001g0182a0001c0001t0001g0224a0001c0001t0001g0259others(8): Show | 11 | HG02559.hp1 HG02717.hp2 HG02895.hp2 others(8): Show |
intron_variant | MODIFIER | c.486-4890dupA | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22910037 | |||||
| chr16:22910037
|
C | CAA | 83 | a0001c0001t0001g0001a0001c0001t0001g0145a0001c0001t0001g0146others(80): Show | 83 | HG00323.hp2 HG00423.hp2 HG00544.hp2 others(80): Show |
intron_variant | MODIFIER | c.486-4891_486-4890d others(4): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22910037 | |||||
| chr16:22910037
|
C | CAAA | 132 | a0001c0001t0001g0151a0001c0001t0001g0153a0001c0001t0001g0155others(129): Show | 132 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(129): Show |
intron_variant | MODIFIER | c.486-4892_486-4890d others(5): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22910037 | |||||
| chr16:22910037
|
C | CAAAA | 11 | a0001c0001t0001g0350a0001c0001t0009g0209a0001c0002t0001g0054others(8): Show | 11 | HG00639.hp1 HG01361.hp2 HG02040.hp2 others(8): Show |
intron_variant | MODIFIER | c.486-4893_486-4890d others(6): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22910037 | |||||
| chr16:22910159
|
A | G | 2 | a0001c0001t0001g0178a0001c0001t0001g0316 | 2 | HG02683.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.486-4785A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22910159 | ||||||
| chr16:22910258
|
T | C | 8 | a0001c0001t0001g0160a0001c0001t0001g0275a0001c0002t0001g0046others(5): Show | 8 | HG00741.hp1 HG01070.hp1 HG01257.hp2 others(5): Show |
intron_variant | MODIFIER | c.486-4686T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22910258 | ||||||
| chr16:22910277
|
A | G | 1 | a0001c0001t0001g0259 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.486-4667A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22910277 | ||||||
| chr16:22910376
|
A | C | 2 | a0001c0001t0001g0216a0001c0003t0003g0034 | 2 | HG02145.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.486-4568A>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22910376 | ||||||
| chr16:22910575
|
T | C | 15 | a0001c0001t0001g0159a0001c0001t0001g0318a0001c0001t0004g0152others(12): Show | 15 | HG00280.hp2 HG00738.hp1 HG01071.hp2 others(12): Show |
intron_variant | MODIFIER | c.486-4369T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22910575 | ||||||
| chr16:22910690
|
A | T | 2 | a0001c0001t0001g0341a0001c0002t0001g0058 | 2 | NA19065.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.486-4254A>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22910690 | ||||||
| chr16:22910846
|
C | T | 1 | a0001c0004t0002g0144 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.486-4098C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22910846 | ||||||
| chr16:22910897
|
T | C | 5 | a0001c0001t0001g0182a0001c0001t0001g0288a0001c0001t0001g0301others(2): Show | 5 | HG02559.hp1 HG02717.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.486-4047T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22910897 | ||||||
| chr16:22911059
|
G | T | 1 | a0001c0001t0001g0319 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.486-3885G>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22911059 | ||||||
| chr16:22911241
|
A | G | 1 | a0001c0002t0001g0058 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.486-3703A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22911241 | ||||||
| chr16:22911257
|
T | C | 13 | a0001c0001t0001g0161a0001c0001t0001g0163a0001c0001t0001g0201others(10): Show | 13 | HG00438.hp1 HG00735.hp1 HG01099.hp1 others(10): Show |
intron_variant | MODIFIER | c.486-3687T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22911257 | ||||||
| chr16:22911343
|
A | G | 1 | a0001c0001t0001g0271 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.486-3601A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22911343 | ||||||
| chr16:22911530
|
A | G | 1 | a0001c0006t0006g0025 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.486-3414A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22911530 | ||||||
| chr16:22911579
|
C | T | 4 | a0001c0001t0001g0206a0001c0001t0001g0207a0001c0001t0001g0228others(1): Show | 4 | NA18946.hp1 NA18960.hp2 NA19054.hp2 others(1): Show |
intron_variant | MODIFIER | c.486-3365C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22911579 | ||||||
| chr16:22911592
|
C | T | 5 | a0001c0001t0001g0182a0001c0001t0001g0288a0001c0001t0001g0301others(2): Show | 5 | HG02559.hp1 HG02717.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.486-3352C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22911592 | ||||||
| chr16:22911657
|
C | A | 1 | a0001c0002t0001g0081 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.486-3287C>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22911657 | ||||||
| chr16:22911695
|
A | G | 1 | a0001c0001t0001g0283 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.486-3249A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22911695 | ||||||
| chr16:22911771
|
C | G | 1 | a0001c0011t0011g0003 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.486-3173C>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22911771 | ||||||
| chr16:22911924
|
C | T | 25 | a0001c0001t0001g0001a0001c0001t0001g0147a0001c0001t0001g0196others(22): Show | 25 | HG00423.hp2 HG00609.hp2 HG00741.hp2 others(22): Show |
intron_variant | MODIFIER | c.486-3020C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22911924 | ||||||
| chr16:22911948
|
C | A | 1 | a0001c0001t0001g0145 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.486-2996C>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22911948 | ||||||
| chr16:22911990
|
T | C | 77 | a0001c0001t0001g0001a0001c0001t0001g0145a0001c0001t0001g0146others(74): Show | 77 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(74): Show |
intron_variant | MODIFIER | c.486-2954T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22911990 | ||||||
| chr16:22911996
|
C | A | 14 | a0001c0004t0002g0144a0001c0004t0002g0183a0001c0004t0002g0184others(11): Show | 14 | HG00735.hp2 HG01081.hp1 HG01256.hp1 others(11): Show |
intron_variant | MODIFIER | c.486-2948C>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22911996 | ||||||
| chr16:22912144
|
A | C | 229 | a0001c0001t0001g0001a0001c0001t0001g0145a0001c0001t0001g0146others(226): Show | 229 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(226): Show |
intron_variant | MODIFIER | c.486-2800A>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22912144 | ||||||
| chr16:22912372
|
T | C | 33 | a0001c0001t0001g0167a0001c0001t0001g0168a0001c0001t0001g0173others(30): Show | 33 | HG00140.hp2 HG01175.hp1 HG01175.hp2 others(30): Show |
intron_variant | MODIFIER | c.486-2572T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22912372 | ||||||
| chr16:22912464
|
A | G | 10 | a0001c0001t0001g0199a0001c0001t0001g0271a0001c0001t0004g0200others(7): Show | 10 | HG02071.hp1 HG02080.hp2 HG02698.hp2 others(7): Show |
intron_variant | MODIFIER | c.486-2480A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22912464 | ||||||
| chr16:22912486
|
C | G | 2 | a0001c0002t0001g0006a0001c0002t0001g0013 | 2 | HG03225.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.486-2458C>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22912486 | ||||||
| chr16:22912530
|
G | A | 1 | a0001c0006t0006g0025 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.486-2414G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22912530 | ||||||
| chr16:22912538
|
G | A | 14 | a0001c0004t0002g0144a0001c0004t0002g0183a0001c0004t0002g0184others(11): Show | 14 | HG00735.hp2 HG01081.hp1 HG01256.hp1 others(11): Show |
intron_variant | MODIFIER | c.486-2406G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22912538 | ||||||
| chr16:22912664
|
G | A | 1 | a0001c0001t0001g0217 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.486-2280G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22912664 | ||||||
| chr16:22912771
|
T | A | 1 | a0001c0001t0001g0287 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.486-2173T>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22912771 | ||||||
| chr16:22912807
|
C | T | 2 | a0001c0001t0001g0174a0001c0001t0001g0217 | 2 | HG01175.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.486-2137C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22912807 | ||||||
| chr16:22912951
|
G | A | 1 | a0001c0001t0001g0147 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.486-1993G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22912951 | ||||||
| chr16:22913066
|
T | C | 1 | a0001c0006t0006g0025 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.486-1878T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22913066 | ||||||
| chr16:22913123
|
A | AAAGG | 26 | a0001c0001t0001g0159a0001c0001t0001g0162a0001c0001t0001g0248others(23): Show | 26 | HG00280.hp2 HG00438.hp2 HG00639.hp1 others(23): Show |
intron_variant | MODIFIER | c.486-1796_486-1793d others(6): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22913123 | |||||
| chr16:22913123
|
A | AAAGGAAG others(1): Show |
74 | a0001c0001t0001g0151a0001c0001t0001g0153a0001c0001t0001g0154others(71): Show | 74 | HG00140.hp1 HG00323.hp2 HG00558.hp1 others(71): Show |
intron_variant | MODIFIER | c.486-1800_486-1793d others(10): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22913123 | |||||
| chr16:22913123
|
A | AAAGGAAG others(5): Show |
24 | a0001c0001t0001g0150a0001c0001t0001g0180a0001c0001t0001g0188others(21): Show | 24 | HG00423.hp1 HG00609.hp1 HG01070.hp2 others(21): Show |
intron_variant | MODIFIER | c.486-1804_486-1793d others(14): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22913123 | |||||
| chr16:22913123
|
A | AAAGGAAG others(9): Show |
7 | a0001c0001t0001g0225a0001c0001t0001g0245a0001c0001t0001g0333others(4): Show | 7 | HG00544.hp1 HG02451.hp2 NA18967.hp2 others(4): Show |
intron_variant | MODIFIER | c.486-1808_486-1793d others(18): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22913123 | |||||
| chr16:22913123
|
A | AAAGGAAG others(13): Show |
2 | a0001c0004t0002g0267a0001c0005t0002g0041 | 2 | HG02809.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.486-1812_486-1793d others(22): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22913123 | |||||
| chr16:22913123
|
A | AAAGGAAG others(17): Show |
1 | a0001c0006t0006g0026 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.486-1816_486-1793d others(26): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22913123 | |||||
| chr16:22913123
|
AAAGG | A | 3 | a0001c0001t0001g0167a0001c0001t0001g0257a0001c0002t0001g0007 | 3 | HG01099.hp1 HG02145.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.486-1796_486-1793d others(6): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22913123 | |||||
| chr16:22913131
|
G | T | 1 | a0001c0002t0001g0075 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.486-1813G>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22913131 | ||||||
| chr16:22913144
|
A | AAGGGAGG others(1): Show |
16 | a0001c0001t0001g0148a0001c0001t0001g0191a0001c0001t0001g0195others(13): Show | 16 | HG00544.hp2 HG02040.hp1 HG02071.hp2 others(13): Show |
intron_variant | MODIFIER | c.486-1797_486-1796i others(10): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22913144 | |||||
| chr16:22913144
|
A | AAGGGAGG others(5): Show |
3 | a0001c0001t0001g0156a0001c0001t0001g0189a0001c0001t0001g0227 | 3 | HG03704.hp1 HG03710.hp2 NA18959.hp1 |
intron_variant | MODIFIER | c.486-1797_486-1796i others(14): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22913144 | |||||
| chr16:22913144
|
A | AAGGGAGG others(9): Show |
4 | a0001c0001t0001g0145a0001c0001t0001g0326a0001c0002t0001g0053others(1): Show | 4 | HG02809.hp2 NA19004.hp1 NA19011.hp1 others(1): Show |
intron_variant | MODIFIER | c.486-1797_486-1796i others(18): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22913144 | |||||
| chr16:22913144
|
A | G | 1 | a0001c0002t0001g0006 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.486-1800A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22913144 | ||||||
| chr16:22913148
|
A | AAGGAAGG others(8): Show |
1 | a0001c0002t0001g0093 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.486-1793_486-1792i others(17): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22913148 | |||||
| chr16:22913148
|
A | AAGGAAGG others(29): Show |
1 | a0001c0006t0006g0025 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.486-1793_486-1792i others(38): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22913148 | |||||
| chr16:22913148
|
A | AAGGAAGG others(13): Show |
1 | a0001c0004t0002g0171 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.486-1793_486-1792i others(22): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22913148 | |||||
| chr16:22913148
|
A | AAGGAAGG others(5): Show |
1 | a0001c0001t0001g0271 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.486-1793_486-1792i others(14): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22913148 | |||||
| chr16:22913148
|
A | AAGGG | 6 | a0001c0001t0001g0170a0001c0001t0001g0175a0001c0001t0001g0181others(3): Show | 6 | HG01243.hp2 HG02280.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.486-1763_486-1760d others(6): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22913148 | |||||
| chr16:22913148
|
A | AAGGGAGG others(1): Show |
4 | a0001c0001t0001g0306a0001c0002t0003g0039a0001c0003t0003g0027others(1): Show | 4 | HG02572.hp1 HG02615.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.486-1767_486-1760d others(10): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22913148 | |||||
| chr16:22913148
|
A | AAGGGAGG others(5): Show |
3 | a0001c0001t0001g0238a0001c0003t0003g0019a0001c0003t0003g0021 | 3 | HG01891.hp1 HG02523.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.486-1771_486-1760d others(14): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22913148 | |||||
| chr16:22913148
|
A | AAGGGAGG others(9): Show |
10 | a0001c0001t0001g0201a0001c0001t0001g0213a0001c0001t0001g0215others(7): Show | 10 | HG02055.hp1 HG02258.hp1 HG02922.hp2 others(7): Show |
intron_variant | MODIFIER | c.486-1775_486-1760d others(18): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22913148 | |||||
| chr16:22913148
|
A | AAGGGAGG others(13): Show |
2 | a0001c0001t0001g0169a0001c0001t0001g0287 | 2 | HG02818.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.486-1779_486-1760d others(22): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22913148 | |||||
| chr16:22913148
|
A | AAGGGAGG others(17): Show |
1 | a0001c0002t0001g0011 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.486-1783_486-1760d others(26): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22913148 | |||||
| chr16:22913148
|
A | AAGGGAGG others(21): Show |
1 | a0007c0010t0001g0042 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.486-1787_486-1760d others(30): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22913148 | |||||
| chr16:22913148
|
A | G | 36 | a0001c0001t0001g0145a0001c0001t0001g0148a0001c0001t0001g0156others(33): Show | 36 | HG00544.hp2 HG00621.hp2 HG01884.hp1 others(33): Show |
intron_variant | MODIFIER | c.486-1796A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22913148 | ||||||
| chr16:22913148
|
AAGGG | A | 19 | a0001c0001t0001g0161a0001c0001t0001g0168a0001c0001t0001g0186others(16): Show | 19 | HG00438.hp1 HG01261.hp2 HG02559.hp2 others(16): Show |
intron_variant | MODIFIER | c.486-1763_486-1760d others(6): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22913148 | |||||
| chr16:22913152
|
G | A | 114 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0153others(111): Show | 114 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(111): Show |
intron_variant | MODIFIER | c.486-1792G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22913152 | ||||||
| chr16:22913156
|
G | A | 24 | a0001c0001t0001g0162a0001c0001t0001g0262a0001c0004t0002g0144others(21): Show | 24 | HG00639.hp1 HG00738.hp2 HG01070.hp2 others(21): Show |
intron_variant | MODIFIER | c.486-1788G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22913156 | ||||||
| chr16:22913160
|
G | A | 4 | a0001c0004t0002g0144a0001c0004t0002g0307a0001c0006t0006g0016others(1): Show | 4 | HG02970.hp2 HG02976.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.486-1784G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22913160 | ||||||
| chr16:22913172
|
GAGGGAGG others(9): Show |
G | 2 | a0001c0005t0002g0009a0001c0005t0006g0038 | 2 | HG01884.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.486-1768_486-1753d others(18): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22913172 | |||||
| chr16:22913176
|
GAGGGAGG others(5): Show |
G | 2 | a0001c0001t0001g0288a0001c0004t0014g0242 | 2 | HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.486-1764_486-1753d others(14): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22913176 | |||||
| chr16:22913180
|
GAGGGCGG others(1): Show |
G | 11 | a0001c0001t0001g0301a0001c0001t0007g0165a0001c0003t0003g0024others(8): Show | 11 | HG01109.hp2 HG01167.hp2 HG02698.hp1 others(8): Show |
intron_variant | MODIFIER | c.486-1760_486-1753d others(10): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22913180 | |||||
| chr16:22913181
|
AGGGC | A | 3 | a0001c0001t0001g0166a0001c0001t0001g0299a0001c0001t0001g0302 | 3 | HG02451.hp1 HG02486.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.486-1760_486-1757d others(6): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22913181 | |||||
| chr16:22913185
|
C | A | 214 | a0001c0001t0001g0001a0001c0001t0001g0145a0001c0001t0001g0146others(211): Show | 214 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(211): Show |
intron_variant | MODIFIER | c.486-1759C>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22913185 | ||||||
| chr16:22913188
|
A | G | 140 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0153others(137): Show | 140 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.486-1756A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22913188 | ||||||
| chr16:22913220
|
C | T | 79 | a0001c0001t0001g0001a0001c0001t0001g0145a0001c0001t0001g0146others(76): Show | 79 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(76): Show |
intron_variant | MODIFIER | c.486-1724C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22913220 | ||||||
| chr16:22913253
|
G | A | 9 | a0001c0004t0002g0149a0001c0004t0002g0179a0001c0004t0002g0291others(6): Show | 9 | HG01109.hp2 HG01167.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.486-1691G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22913253 | ||||||
| chr16:22913298
|
A | G | 229 | a0001c0001t0001g0001a0001c0001t0001g0145a0001c0001t0001g0146others(226): Show | 229 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(226): Show |
intron_variant | MODIFIER | c.486-1646A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22913298 | ||||||
| chr16:22913381
|
G | T | 1 | a0001c0004t0002g0266 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.486-1563G>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22913381 | ||||||
| chr16:22913394
|
A | T | 1 | a0001c0004t0002g0266 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.486-1550A>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22913394 | ||||||
| chr16:22913399
|
A | T | 1 | a0001c0011t0011g0003 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.486-1545A>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22913399 | ||||||
| chr16:22913424
|
A | T | 1 | a0001c0004t0002g0266 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.486-1520A>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22913424 | ||||||
| chr16:22913426
|
C | A | 1 | a0001c0004t0002g0266 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.486-1518C>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22913426 | ||||||
| chr16:22913427
|
C | A | 1 | a0001c0004t0002g0266 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.486-1517C>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22913427 | ||||||
| chr16:22913431
|
C | G | 1 | a0001c0004t0002g0266 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.486-1513C>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22913431 | ||||||
| chr16:22913433
|
C | G | 1 | a0001c0004t0002g0266 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.486-1511C>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22913433 | ||||||
| chr16:22913435
|
T | A | 1 | a0001c0004t0002g0266 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.486-1509T>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22913435 | ||||||
| chr16:22913445
|
C | T | 1 | a0001c0004t0002g0266 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.486-1499C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22913445 | ||||||
| chr16:22913446
|
C | A | 1 | a0001c0004t0002g0266 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.486-1498C>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22913446 | ||||||
| chr16:22913503
|
G | A | 5 | a0001c0004t0002g0144a0001c0005t0002g0009a0001c0005t0002g0060others(2): Show | 5 | HG01884.hp1 HG02486.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.486-1441G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22913503 | ||||||
| chr16:22913575
|
A | C | 1 | a0001c0004t0002g0267 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.486-1369A>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22913575 | ||||||
| chr16:22913637
|
T | A | 2 | a0001c0005t0002g0012a0001c0005t0006g0040 | 2 | HG01167.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.486-1307T>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22913637 | ||||||
| chr16:22913870
|
C | G | 4 | a0001c0001t0001g0182a0001c0001t0001g0301a0001c0003t0003g0018others(1): Show | 4 | HG02559.hp1 HG02717.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.486-1074C>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22913870 | ||||||
| chr16:22913892
|
C | T | 5 | a0001c0004t0002g0144a0001c0005t0002g0009a0001c0005t0002g0060others(2): Show | 5 | HG01884.hp1 HG02486.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.486-1052C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22913892 | ||||||
| chr16:22913900
|
G | A | 39 | a0001c0004t0002g0144a0001c0004t0002g0149a0001c0004t0002g0171others(36): Show | 39 | HG00639.hp1 HG00735.hp2 HG00738.hp2 others(36): Show |
intron_variant | MODIFIER | c.486-1044G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22913900 | ||||||
| chr16:22913961
|
A | C | 77 | a0001c0001t0001g0001a0001c0001t0001g0145a0001c0001t0001g0146others(74): Show | 77 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(74): Show |
intron_variant | MODIFIER | c.486-983A>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22913961 | ||||||
| chr16:22914022
|
C | T | 1 | a0001c0006t0006g0025 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.486-922C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22914022 | ||||||
| chr16:22914486
|
G | T | 10 | a0001c0001t0001g0199a0001c0001t0001g0271a0001c0001t0004g0200others(7): Show | 10 | HG02071.hp1 HG02080.hp2 HG02698.hp2 others(7): Show |
intron_variant | MODIFIER | c.486-458G>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22914486 | ||||||
| chr16:22914606
|
G | GAGATGGG others(1): Show |
94 | a0001c0001t0001g0001a0001c0001t0001g0145a0001c0001t0001g0146others(91): Show | 94 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(91): Show |
intron_variant | MODIFIER | c.486-301_486-294dup others(8): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22914606 | |||||
| chr16:22914606
|
G | GAGATGGG others(9): Show |
2 | a0001c0006t0006g0025a0001c0006t0006g0026 | 2 | HG03486.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.486-309_486-294dup others(16): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22914606 | |||||
| chr16:22914615
|
A | T | 7 | a0001c0001t0001g0167a0001c0001t0001g0214a0001c0001t0001g0286others(4): Show | 7 | HG01891.hp2 HG01934.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.486-329A>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22914615 | ||||||
| chr16:22914649
|
A | G | 2 | a0001c0002t0001g0006a0001c0002t0001g0013 | 2 | HG03225.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.486-295A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22914649 | ||||||
| chr16:22914716
|
G | A | 20 | a0001c0004t0002g0149a0001c0004t0002g0179a0001c0004t0002g0202others(17): Show | 20 | HG00639.hp1 HG00738.hp2 HG01070.hp2 others(17): Show |
intron_variant | MODIFIER | c.486-228G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22914716 | ||||||
| chr16:22914736
|
C | CA | 17 | a0001c0001t0001g0199a0001c0001t0001g0205a0001c0001t0001g0218others(14): Show | 17 | HG00735.hp1 HG01943.hp2 HG02080.hp2 others(14): Show |
intron_variant | MODIFIER | c.486-180dupA | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22914736 | |||||
| chr16:22914736
|
C | CAAAAAAA others(2): Show |
8 | a0001c0001t0001g0189a0001c0001t0001g0195a0001c0001t0001g0297others(5): Show | 8 | HG00544.hp2 HG02965.hp1 HG03130.hp2 others(5): Show |
intron_variant | MODIFIER | c.486-188_486-180dup others(9): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22914736 | |||||
| chr16:22914736
|
C | CAAAAAAA others(3): Show |
18 | a0001c0001t0001g0148a0001c0001t0001g0156a0001c0001t0001g0169others(15): Show | 18 | HG02040.hp1 HG02055.hp1 HG02129.hp2 others(15): Show |
intron_variant | MODIFIER | c.486-189_486-180dup others(10): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22914736 | |||||
| chr16:22914736
|
C | CAAAAAAA others(4): Show |
3 | a0001c0001t0001g0287a0001c0001t0001g0343a0001c0002t0001g0011 | 3 | HG03098.hp1 NA19006.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.486-190_486-180dup others(11): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22914736 | |||||
| chr16:22914736
|
C | CAAAAAAA others(5): Show |
1 | a0001c0001t0001g0145 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.486-191_486-180dup others(12): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22914736 | |||||
| chr16:22914736
|
CA | C | 108 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0153others(105): Show | 108 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(105): Show |
intron_variant | MODIFIER | c.486-180delA | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22914736 | |||||
| chr16:22914736
|
CAA | C | 8 | a0001c0001t0001g0157a0001c0001t0001g0166a0001c0001t0001g0172others(5): Show | 8 | HG00738.hp1 HG01943.hp1 HG01975.hp2 others(5): Show |
intron_variant | MODIFIER | c.486-181_486-180del others(2): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22914736 | |||||
| chr16:22914736
|
CAAA | C | 6 | a0001c0001t0001g0206a0001c0001t0001g0284a0001c0001t0007g0208others(3): Show | 6 | HG03225.hp2 NA18942.hp2 NA18946.hp1 others(3): Show |
intron_variant | MODIFIER | c.486-182_486-180del others(3): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22914736 | |||||
| chr16:22914736
|
CAAAA | C | 31 | a0001c0001t0001g0001a0001c0001t0001g0146a0001c0001t0001g0147others(28): Show | 31 | HG00423.hp2 HG00609.hp2 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.486-183_486-180del others(4): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22914736 | |||||
| chr16:22914736
|
CAAAAAAA others(1): Show |
C | 11 | a0001c0001t0001g0173a0001c0001t0001g0294a0001c0001t0001g0295others(8): Show | 11 | HG00621.hp2 HG01884.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.486-187_486-180del others(8): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22914736 | |||||
| chr16:22914763
|
A | AAAAAAAA others(5): Show |
2 | a0001c0004t0002g0171a0001c0004t0002g0266 | 2 | HG02451.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.486-180_486-179ins others(12): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22914763 | |||||
| chr16:22914763
|
A | AAAAAAAA others(4): Show |
3 | a0001c0004t0002g0267a0001c0004t0002g0272a0001c0006t0006g0026 | 3 | HG02809.hp1 HG03486.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.486-180_486-179ins others(11): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22914763 | |||||
| chr16:22914763
|
A | AAAAAAAA others(3): Show |
6 | a0001c0004t0002g0291a0001c0004t0002g0304a0001c0004t0014g0242others(3): Show | 6 | HG01109.hp2 HG02486.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.486-180_486-179ins others(10): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22914763 | |||||
| chr16:22914763
|
A | AAAAAAAA others(3): Show |
1 | a0001c0005t0006g0040 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.486-180_486-179ins others(10): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22914763 | |||||
| chr16:22914763
|
A | AAAAAAG | 7 | a0001c0004t0002g0202a0001c0005t0002g0004a0001c0005t0002g0098others(4): Show | 7 | HG01070.hp2 HG01071.hp1 HG01346.hp1 others(4): Show |
intron_variant | MODIFIER | c.486-180_486-179ins others(6): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22914763 | |||||
| chr16:22914763
|
A | G | 4 | a0001c0004t0002g0144a0001c0006t0006g0016a0001c0006t0006g0022others(1): Show | 4 | HG02970.hp1 HG02976.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.486-181A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22914763 | ||||||
| chr16:22914894
|
C | T | 2 | a0001c0001t0004g0235a0001c0001t0004g0236 | 2 | HG03492.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.486-50C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22914894 | ||||||
| chr16:22914936
|
C | T | 13 | a0001c0001t0001g0161a0001c0001t0001g0163a0001c0001t0001g0201others(10): Show | 13 | HG00438.hp1 HG00735.hp1 HG01099.hp1 others(10): Show |
splice_region_variant&intron_variant | LOW | c.486-8C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22914936 |