| geneid | 150159 |
|---|---|
| ensemblid | ENSG00000164037.17 |
| hgncid | 24244 |
| symbol | SLC9B1 |
| name | solute carrier family 9 member B1 |
| refseq_nuc | NM_139173.4 |
| refseq_prot | NP_631912.3 |
| ensembl_nuc | ENST00000296422.12 |
| ensembl_prot | ENSP00000296422.7 |
| mane_status | MANE Select |
| chr | chr4 |
| start | 102900928 |
| end | 103019705 |
| strand | - |
| ver | v1.2 |
| region | chr4:102900928-103019705 |
| region5000 | chr4:102895928-103024705 |
| regionname0 | SLC9B1_chr4_102900928_103019705 |
| regionname5000 | SLC9B1_chr4_102895928_103024705 |
| 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 | 0/1 | 515 | 315 | 80 | 52 | 136 | 12 | 34 | 98 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | copy fasta | chr4 | 102895928 | 103024705 |
| a0002 | 0/0 | 515 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | copy fasta | chr4 | 102895928 | 103024705 |
| a0003 | 1/0 | 515 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | copy fasta | chr4 | 102895928 | 103024705 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/1 | 1548 | 313 | 80 | 52 | 135 | 12 | 33 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | copy fasta | chr4 | 102895928 | 103024705 |
| c0002 | 0/0 | 1548 | 2 | 2 | 0 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | copy fasta | chr4 | 102895928 | 103024705 |
| c0003 | 1/0 | 1548 | 1 | 0 | 0 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | copy fasta | chr4 | 102895928 | 103024705 |
| c0004 | 0/0 | 1548 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | copy fasta | chr4 | 102895928 | 103024705 |
| c0005 | 0/0 | 1548 | 1 | 0 | 0 | 0 | 0 | 1 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | copy fasta | chr4 | 102895928 | 103024705 |
| 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 | 297 | 315 | 82 | 52 | 133 | 12 | 34 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | copy fasta | chr4 | 102895928 | 103024705 |
| t0002 | 0/0 | 297 | 3 | 0 | 0 | 3 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | copy fasta | chr4 | 102895928 | 103024705 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0024 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0028 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0043 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0209 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0257 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0272 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0291 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0296 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 1548 | 313 | 80 | 52 | 135 | 12 | 33 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | copy fasta | chr4 | 102895928 | 103024705 |
| a0001c0004 | 0/0 | 1548 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | copy fasta | chr4 | 102895928 | 103024705 |
| a0001c0005 | 0/0 | 1548 | 1 | 0 | 0 | 0 | 0 | 1 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | copy fasta | chr4 | 102895928 | 103024705 |
| a0002c0002 | 0/0 | 1548 | 2 | 2 | 0 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | copy fasta | chr4 | 102895928 | 103024705 |
| a0003c0003 | 1/0 | 1548 | 1 | 0 | 0 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | copy fasta | chr4 | 102895928 | 103024705 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 1844 | 310 | 80 | 52 | 132 | 12 | 33 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | copy fasta | chr4 | 102895928 | 103024705 |
| a0001c0001t0002 | 0/0 | 1844 | 3 | 0 | 0 | 3 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | copy fasta | chr4 | 102895928 | 103024705 |
| a0001c0004t0001 | 0/0 | 1844 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | copy fasta | chr4 | 102895928 | 103024705 |
| a0001c0005t0001 | 0/0 | 1844 | 1 | 0 | 0 | 0 | 0 | 1 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | copy fasta | chr4 | 102895928 | 103024705 |
| a0002c0002t0001 | 0/0 | 1844 | 2 | 2 | 0 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | copy fasta | chr4 | 102895928 | 103024705 |
| a0003c0003t0001 | 1/0 | 1844 | 1 | 0 | 0 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | copy fasta | chr4 | 102895928 | 103024705 |
| 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 | 2 | 0 | 2 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0296 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0001g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0002g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0004t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0001c0005t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0002c0002t0001g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0002c0002t0001g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| a0003c0003t0001g0024 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0291 | EUR | GBR | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0057 | EUR | GBR | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0066 | EUR | GBR | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0257 | EUR | GBR | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0220 | EUR | FIN | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0060 | EUR | FIN | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0209 | EUR | FIN | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0106 | EUR | FIN | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | CHS | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | CHS | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | CHS | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0276 | EAS | CHS | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | CHS | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | CHS | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | CHS | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | CHS | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | CHS | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | CHS | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | CHS | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0270 | AMR | PUR | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0108 | AMR | PUR | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0088 | AMR | PUR | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0231 | AMR | PUR | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0267 | AMR | PUR | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0252 | AMR | PUR | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0119 | AMR | PUR | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0136 | AMR | PUR | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0278 | AMR | PUR | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0255 | AMR | PUR | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0162 | AMR | PUR | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0081 | AMR | PUR | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0199 | AMR | PUR | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0269 | AMR | PUR | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0218 | AMR | PUR | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | PUR | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0152 | AMR | PUR | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0284 | AMR | PUR | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0224 | AMR | PUR | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0217 | AMR | CLM | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0268 | AMR | CLM | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | CLM | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0059 | AMR | CLM | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0254 | AMR | CLM | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | CLM | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0058 | AMR | CLM | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0147 | AMR | CLM | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0064 | AMR | CLM | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0114 | AMR | CLM | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0170 | AMR | CLM | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0172 | AMR | CLM | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0043 | EUR | IBS | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0115 | EUR | IBS | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0289 | AFR | ACB | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0228 | AFR | ACB | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0312 | AFR | ACB | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0181 | AFR | ACB | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0197 | AMR | PEL | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0113 | AMR | PEL | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | PEL | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0256 | AMR | PEL | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0266 | AMR | PEL | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0160 | AMR | PEL | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0134 | AMR | PEL | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | PEL | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0265 | AMR | PEL | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | PEL | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0253 | AMR | PEL | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0153 | AMR | PEL | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | KHV | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | KHV | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | KHV | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | KHV | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | KHV | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | KHV | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | KHV | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | KHV | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | KHV | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0299 | EAS | KHV | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | KHV | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | KHV | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | KHV | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | KHV | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | KHV | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0309 | AFR | ACB | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0225 | AFR | ACB | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0298 | EAS | CDX | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | CDX | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0295 | EAS | CDX | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | CDX | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG02258 | hp1 | a0002 | c0002 | t0001 | g0317 | AFR | ACB | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | ACB | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | PEL | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0159 | AMR | PEL | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0184 | AFR | ACB | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | ACB | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | KHV | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | KHV | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0189 | AFR | GWD | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0283 | AFR | GWD | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0230 | AFR | GWD | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG02615 | hp2 | a0002 | c0002 | t0001 | g0316 | AFR | GWD | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0173 | AFR | GWD | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0093 | AFR | GWD | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0303 | AFR | GWD | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0307 | AFR | GWD | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0086 | AFR | GWD | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0290 | AFR | GWD | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0179 | SAS | PJL | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0102 | SAS | PJL | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0234 | AFR | GWD | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | GWD | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | GWD | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0282 | AFR | GWD | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0168 | SAS | PJL | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0087 | SAS | PJL | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0183 | SAS | PJL | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0097 | SAS | PJL | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0185 | AFR | GWD | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0285 | AFR | GWD | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0236 | AFR | GWD | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0274 | AFR | GWD | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0210 | AFR | GWD | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0232 | AFR | GWD | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0286 | AFR | GWD | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0305 | AFR | GWD | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0287 | AFR | GWD | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0130 | AFR | GWD | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0226 | AFR | ESN | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | ESN | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0238 | AFR | ESN | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | ESN | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0308 | AFR | ESN | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0294 | AFR | ESN | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0258 | SAS | PJL | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0038 | SAS | PJL | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | GWD | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0223 | AFR | GWD | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | MSL | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0292 | AFR | MSL | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0123 | AFR | ESN | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0235 | AFR | ESN | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0311 | AFR | MSL | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0302 | AFR | MSL | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | MSL | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0260 | AFR | MSL | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0310 | AFR | MSL | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0293 | AFR | MSL | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0273 | AFR | MSL | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0239 | AFR | MSL | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0219 | SAS | PJL | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0095 | SAS | PJL | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0096 | SAS | PJL | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0036 | SAS | PJL | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0196 | AFR | ESN | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0275 | AFR | ESN | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0288 | AFR | GWD | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0124 | AFR | GWD | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0227 | AFR | MSL | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | MSL | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0065 | SAS | PJL | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0121 | SAS | PJL | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0158 | SAS | PJL | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0161 | SAS | STU | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0042 | SAS | STU | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0101 | SAS | BEB | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0279 | SAS | BEB | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0040 | SAS | BEB | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0135 | SAS | BEB | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0213 | SAS | STU | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0105 | SAS | STU | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0204 | SAS | BEB | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0068 | SAS | BEB | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0140 | SAS | STU | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0050 | SAS | STU | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG04204 | hp1 | a0001 | c0005 | t0001 | g0205 | SAS | STU | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0094 | SAS | STU | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0259 | SAS | STU | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0054 | SAS | STU | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0306 | AFR | YRI | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0233 | AFR | YRI | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | CHB | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | CHB | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | CHB | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | CHB | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0090 | AFR | YRI | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0297 | AFR | YRI | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| NA18957 | hp2 | a0001 | c0001 | t0002 | g0107 | EAS | JPT | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0077 | EAS | JPT | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0314 | EAS | JPT | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0313 | EAS | JPT | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0229 | AFR | LWK | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0280 | AFR | LWK | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| NA19085 | hp2 | a0001 | c0004 | t0001 | g0053 | EAS | JPT | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0315 | AFR | YRI | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0222 | AFR | YRI | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0028 | EUR | TSI | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0272 | EUR | TSI | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0080 | SAS | GIH | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0169 | SAS | GIH | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0122 | AFR | ACB | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0112 | AFR | ACB | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0237 | AFR | ACB | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0092 | AFR | ACB | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0251 | AFR | ACB | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0304 | AFR | ACB | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0281 | AFR | MSL | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0186 | AFR | MSL | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | USA | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0240 | AFR | USA | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0056 | AFR | USA | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0177 | AFR | USA | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | LWK | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0174 | AFR | LWK | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0296 | REF | REF | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| homoSapiens_grch38 | hp1 | a0003 | c0003 | t0001 | g0024 | REF | REF | SLC9B1_chr4_102895928_103024705 | SLC9B1 | chr4 | 102895928 | 103024705 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:102901268
|
G | A | 1 | a0002 | 2 | HG02258.hp1 HG02615.hp2 |
missense_variant | MODERATE | c.1397C>T | p.Ala466Val | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 12/12 | 1505/1845 | 1397/1548 | 466/515 | chr4 | 102901268 | ||
| chr4:102989912
|
C | A | 2 | a0001a0002 | 317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
missense_variant | MODERATE | c.99G>T | p.Gln33His | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/12 | 207/1845 | 99/1548 | 33/515 | chr4 | 102989912 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:102905598
|
T | C | 1 | a0001c0004 | 1 | NA19085.hp2 | synonymous_variant | LOW | c.1248A>G | p.Thr416Thr | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 11/12 | 1356/1845 | 1248/1548 | 416/515 | chr4 | 102905598 | ||
| chr4:102911500
|
G | A | 1 | a0001c0005 | 1 | HG04204.hp1 | synonymous_variant | LOW | c.867C>T | p.Asn289Asn | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 8/12 | 975/1845 | 867/1548 | 289/515 | chr4 | 102911500 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:102901067
|
T | C | 1 | a0001c0001t0002 | 3 | NA18957.hp2 NA18980.hp1 NA19005.hp1 |
3_prime_UTR_variant | MODIFIER | c.*50A>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 12/12 | 50 | chr4 | 102901067 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:102901426
|
T | C | 10 | a0001c0001t0001g0226a0001c0001t0001g0227a0001c0001t0001g0228others(7): Show | 10 | HG00735.hp2 HG01884.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.1333-94A>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 11/11 | chr4 | 102901426 | ||||||
| chr4:102901430
|
A | G | 10 | a0001c0001t0001g0226a0001c0001t0001g0227a0001c0001t0001g0228others(7): Show | 10 | HG00735.hp2 HG01884.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.1333-98T>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 11/11 | chr4 | 102901430 | ||||||
| chr4:102901488
|
T | C | 3 | a0001c0001t0001g0112a0001c0001t0001g0302a0001c0001t0001g0315 | 3 | HG02109.hp2 HG03209.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1333-156A>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 11/11 | chr4 | 102901488 | ||||||
| chr4:102901530
|
C | G | 1 | a0001c0001t0001g0032 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1333-198G>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 11/11 | chr4 | 102901530 | ||||||
| chr4:102901654
|
G | C | 1 | a0001c0001t0001g0214 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1333-322C>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 11/11 | chr4 | 102901654 | ||||||
| chr4:102901660
|
CTTAGTTG others(2805): Show |
C | 1 | a0001c0001t0001g0120 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1332+1042_1333-329 others(3): Show |
SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 11/11 | chr4 | 102901660 | ||||||
| chr4:102901676
|
G | A | 209 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(206): Show | 210 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.1333-344C>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 11/11 | chr4 | 102901676 | ||||||
| chr4:102901897
|
C | A | 1 | a0001c0001t0001g0105 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1333-565G>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 11/11 | chr4 | 102901897 | ||||||
| chr4:102902012
|
T | C | 1 | a0001c0001t0001g0290 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1333-680A>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 11/11 | chr4 | 102902012 | ||||||
| chr4:102902543
|
A | C | 1 | a0001c0001t0001g0105 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1333-1211T>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 11/11 | chr4 | 102902543 | ||||||
| chr4:102902568
|
GA | G | 3 | a0001c0001t0001g0112a0001c0001t0001g0302a0001c0001t0001g0315 | 3 | HG02109.hp2 HG03209.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1333-1237delT | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 11/11 | chr4 | 102902568 | ||||||
| chr4:102902574
|
T | G | 209 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(206): Show | 210 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.1333-1242A>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 11/11 | chr4 | 102902574 | ||||||
| chr4:102902616
|
T | C | 1 | a0001c0001t0001g0012 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1333-1284A>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 11/11 | chr4 | 102902616 | ||||||
| chr4:102902840
|
C | G | 1 | a0001c0001t0001g0213 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1333-1508G>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 11/11 | chr4 | 102902840 | ||||||
| chr4:102903034
|
T | TATAAATA | 13 | a0001c0001t0001g0112a0001c0001t0001g0226a0001c0001t0001g0227others(10): Show | 13 | HG00735.hp2 HG01884.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.1333-1709_1333-170 others(11): Show |
SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 11/11 | chr4 | 102903034 | ||||||
| chr4:102903108
|
A | C | 1 | a0001c0001t0001g0008 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1333-1776T>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 11/11 | chr4 | 102903108 | ||||||
| chr4:102903160
|
G | A | 13 | a0001c0001t0001g0112a0001c0001t0001g0226a0001c0001t0001g0227others(10): Show | 13 | HG00735.hp2 HG01884.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.1333-1828C>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 11/11 | chr4 | 102903160 | ||||||
| chr4:102903921
|
G | C | 1 | a0001c0001t0001g0085 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1332+1593C>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 11/11 | chr4 | 102903921 | ||||||
| chr4:102904023
|
G | T | 1 | a0001c0001t0001g0119 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1332+1491C>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 11/11 | chr4 | 102904023 | ||||||
| chr4:102904091
|
T | C | 209 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(206): Show | 210 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.1332+1423A>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 11/11 | chr4 | 102904091 | ||||||
| chr4:102904452
|
T | C | 3 | a0001c0001t0001g0236a0001c0001t0001g0237a0001c0001t0001g0238 | 3 | HG02486.hp1 HG02818.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1332+1062A>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 11/11 | chr4 | 102904452 | ||||||
| chr4:102904470
|
C | CAT | 209 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(206): Show | 210 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.1332+1042_1332+104 others(6): Show |
SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 11/11 | chr4 | 102904470 | ||||||
| chr4:102904623
|
C | T | 1 | a0001c0001t0001g0217 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1332+891G>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 11/11 | chr4 | 102904623 | ||||||
| chr4:102904771
|
C | G | 1 | a0001c0001t0001g0243 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1332+743G>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 11/11 | chr4 | 102904771 | ||||||
| chr4:102904776
|
G | A | 1 | a0001c0001t0001g0181 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1332+738C>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 11/11 | chr4 | 102904776 | ||||||
| chr4:102904812
|
T | C | 8 | a0001c0001t0001g0138a0001c0001t0001g0152a0001c0001t0001g0153others(5): Show | 8 | HG01168.hp2 HG01169.hp2 HG01934.hp1 others(5): Show |
intron_variant | MODIFIER | c.1332+702A>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 11/11 | chr4 | 102904812 | ||||||
| chr4:102904856
|
C | G | 4 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0001g0224others(1): Show | 4 | HG01192.hp1 HG02145.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1332+658G>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 11/11 | chr4 | 102904856 | ||||||
| chr4:102904871
|
C | A | 13 | a0001c0001t0001g0112a0001c0001t0001g0226a0001c0001t0001g0227others(10): Show | 13 | HG00735.hp2 HG01884.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.1332+643G>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 11/11 | chr4 | 102904871 | ||||||
| chr4:102904879
|
A | G | 213 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(210): Show | 214 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.1332+635T>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 11/11 | chr4 | 102904879 | ||||||
| chr4:102904932
|
C | T | 1 | a0001c0001t0001g0012 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1332+582G>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 11/11 | chr4 | 102904932 | ||||||
| chr4:102904983
|
C | CA | 10 | a0001c0001t0001g0226a0001c0001t0001g0227a0001c0001t0001g0228others(7): Show | 10 | HG00735.hp2 HG01884.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.1332+530dupT | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 11/11 | chr4 | 102904983 | ||||||
| chr4:102904983
|
CA | C | 195 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(192): Show | 196 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.1332+530delT | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 11/11 | chr4 | 102904983 | ||||||
| chr4:102905122
|
C | A | 1 | a0001c0001t0001g0147 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1332+392G>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 11/11 | chr4 | 102905122 | ||||||
| chr4:102905209
|
G | GTTTATTT others(5): Show |
43 | a0001c0001t0001g0111a0001c0001t0001g0129a0001c0001t0001g0130others(40): Show | 43 | HG00140.hp2 HG00438.hp2 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.1332+293_1332+304d others(14): Show |
SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 11/11 | chr4 | 102905209 | ||||||
| chr4:102905209
|
G | GTTTATTT others(9): Show |
52 | a0001c0001t0001g0002a0001c0001t0001g0036a0001c0001t0001g0117others(49): Show | 52 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(49): Show |
intron_variant | MODIFIER | c.1332+289_1332+304d others(18): Show |
SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 11/11 | chr4 | 102905209 | ||||||
| chr4:102905209
|
G | GTTTATTT others(13): Show |
83 | a0001c0001t0001g0001a0001c0001t0001g0113a0001c0001t0001g0114others(80): Show | 84 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(81): Show |
intron_variant | MODIFIER | c.1332+285_1332+304d others(22): Show |
SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 11/11 | chr4 | 102905209 | ||||||
| chr4:102905209
|
G | GTTTATTT others(17): Show |
10 | a0001c0001t0001g0003a0001c0001t0001g0135a0001c0001t0001g0150others(7): Show | 10 | HG01192.hp1 HG02056.hp1 HG02132.hp2 others(7): Show |
intron_variant | MODIFIER | c.1332+281_1332+304d others(26): Show |
SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 11/11 | chr4 | 102905209 | ||||||
| chr4:102905209
|
G | GTTTATTT others(21): Show |
2 | a0001c0001t0001g0038a0001c0001t0001g0225 | 2 | HG02145.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.1332+304_1332+305i others(30): Show |
SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 11/11 | chr4 | 102905209 | ||||||
| chr4:102905209
|
G | GTTTGTTT others(13): Show |
4 | a0001c0001t0001g0132a0001c0001t0001g0133a0001c0001t0001g0191others(1): Show | 4 | NA18968.hp1 NA18972.hp1 NA18988.hp2 others(1): Show |
intron_variant | MODIFIER | c.1332+304_1332+305i others(22): Show |
SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 11/11 | chr4 | 102905209 | ||||||
| chr4:102905209
|
GTTTA | G | 13 | a0001c0001t0001g0112a0001c0001t0001g0226a0001c0001t0001g0227others(10): Show | 13 | HG00735.hp2 HG01884.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.1332+301_1332+304d others(6): Show |
SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 11/11 | chr4 | 102905209 | ||||||
| chr4:102905233
|
A | ATTTATTT others(13): Show |
1 | a0001c0001t0001g0222 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1332+280_1332+281i others(22): Show |
SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 11/11 | chr4 | 102905233 | ||||||
| chr4:102905233
|
A | ATTTATTT others(9): Show |
1 | a0001c0001t0001g0184 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1332+280_1332+281i others(18): Show |
SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 11/11 | chr4 | 102905233 | ||||||
| chr4:102905234
|
T | TTTATTTA others(16): Show |
1 | a0001c0001t0001g0174 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1332+279_1332+280i others(25): Show |
SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 11/11 | chr4 | 102905234 | ||||||
| chr4:102905330
|
C | T | 1 | a0001c0001t0001g0227 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1332+184G>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 11/11 | chr4 | 102905330 | ||||||
| chr4:102905478
|
T | C | 210 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(207): Show | 211 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.1332+36A>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 11/11 | chr4 | 102905478 | ||||||
| chr4:102905687
|
T | C | 1 | a0001c0001t0001g0087 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1196-37A>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 10/11 | chr4 | 102905687 | ||||||
| chr4:102905975
|
A | G | 211 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(208): Show | 212 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(209): Show |
intron_variant | MODIFIER | c.1196-325T>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 10/11 | chr4 | 102905975 | ||||||
| chr4:102906105
|
T | G | 1 | a0001c0001t0001g0174 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1195+431A>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 10/11 | chr4 | 102906105 | ||||||
| chr4:102906269
|
G | A | 3 | a0001c0001t0001g0272a0001c0001t0001g0282a0001c0001t0001g0291 | 3 | HG00099.hp1 HG02723.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.1195+267C>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 10/11 | chr4 | 102906269 | ||||||
| chr4:102906303
|
T | C | 2 | a0001c0001t0001g0193a0001c0001t0001g0194 | 2 | NA18979.hp2 NA18981.hp1 |
intron_variant | MODIFIER | c.1195+233A>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 10/11 | chr4 | 102906303 | ||||||
| chr4:102906331
|
T | G | 210 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(207): Show | 211 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.1195+205A>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 10/11 | chr4 | 102906331 | ||||||
| chr4:102906396
|
G | A | 9 | a0001c0001t0001g0304a0001c0001t0001g0305a0001c0001t0001g0306others(6): Show | 9 | HG01891.hp1 HG02145.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.1195+140C>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 10/11 | chr4 | 102906396 | ||||||
| chr4:102906443
|
A | C | 1 | a0001c0001t0001g0273 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1195+93T>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 10/11 | chr4 | 102906443 | ||||||
| chr4:102906450
|
G | T | 1 | a0001c0001t0001g0047 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1195+86C>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 10/11 | chr4 | 102906450 | ||||||
| chr4:102906454
|
T | C | 3 | a0001c0001t0001g0273a0001c0001t0001g0274a0001c0001t0001g0275 | 3 | HG02818.hp2 HG03486.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1195+82A>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 10/11 | chr4 | 102906454 | ||||||
| chr4:102906457
|
T | C | 1 | a0001c0001t0001g0119 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1195+79A>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 10/11 | chr4 | 102906457 | ||||||
| chr4:102906505
|
T | G | 15 | a0001c0001t0001g0002a0001c0001t0001g0239a0001c0001t0001g0240others(12): Show | 15 | HG01109.hp1 HG01175.hp2 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.1195+31A>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 10/11 | chr4 | 102906505 | ||||||
| chr4:102906712
|
TC | T | 181 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0036others(178): Show | 182 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.1087-69delG | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 9/11 | chr4 | 102906712 | ||||||
| chr4:102906809
|
T | C | 3 | a0001c0001t0001g0112a0001c0001t0001g0302a0001c0001t0001g0315 | 3 | HG02109.hp2 HG03209.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1087-165A>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 9/11 | chr4 | 102906809 | ||||||
| chr4:102906955
|
C | G | 1 | a0001c0001t0001g0168 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1087-311G>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 9/11 | chr4 | 102906955 | ||||||
| chr4:102907208
|
G | A | 1 | a0001c0001t0001g0039 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1087-564C>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 9/11 | chr4 | 102907208 | ||||||
| chr4:102907249
|
A | G | 13 | a0001c0001t0001g0112a0001c0001t0001g0226a0001c0001t0001g0227others(10): Show | 13 | HG00735.hp2 HG01884.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.1087-605T>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 9/11 | chr4 | 102907249 | ||||||
| chr4:102907382
|
G | A | 1 | a0001c0001t0001g0151 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1087-738C>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 9/11 | chr4 | 102907382 | ||||||
| chr4:102907462
|
T | C | 1 | a0001c0001t0001g0008 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1087-818A>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 9/11 | chr4 | 102907462 | ||||||
| chr4:102907608
|
A | G | 1 | a0001c0001t0001g0209 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1087-964T>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 9/11 | chr4 | 102907608 | ||||||
| chr4:102907812
|
C | G | 210 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(207): Show | 211 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.1087-1168G>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 9/11 | chr4 | 102907812 | ||||||
| chr4:102908009
|
A | G | 1 | a0001c0001t0001g0315 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1087-1365T>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 9/11 | chr4 | 102908009 | ||||||
| chr4:102908186
|
T | C | 1 | a0001c0001t0001g0027 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1087-1542A>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 9/11 | chr4 | 102908186 | ||||||
| chr4:102908434
|
A | G | 1 | a0001c0001t0001g0308 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1087-1790T>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 9/11 | chr4 | 102908434 | ||||||
| chr4:102908625
|
T | C | 1 | a0001c0001t0001g0119 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1086+1814A>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 9/11 | chr4 | 102908625 | ||||||
| chr4:102908636
|
A | G | 10 | a0001c0001t0001g0226a0001c0001t0001g0227a0001c0001t0001g0228others(7): Show | 10 | HG00735.hp2 HG01884.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.1086+1803T>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 9/11 | chr4 | 102908636 | ||||||
| chr4:102908860
|
A | G | 1 | a0001c0001t0001g0008 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1086+1579T>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 9/11 | chr4 | 102908860 | ||||||
| chr4:102908942
|
C | T | 1 | a0001c0001t0001g0113 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1086+1497G>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 9/11 | chr4 | 102908942 | ||||||
| chr4:102909056
|
T | A | 4 | a0001c0001t0001g0257a0001c0001t0001g0258a0001c0001t0001g0267others(1): Show | 4 | HG00140.hp2 HG00738.hp2 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.1086+1383A>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 9/11 | chr4 | 102909056 | ||||||
| chr4:102909110
|
G | A | 1 | a0001c0001t0001g0188 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1086+1329C>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 9/11 | chr4 | 102909110 | ||||||
| chr4:102909296
|
C | CA | 193 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(190): Show | 194 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.1086+1142dupT | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 9/11 | chr4 | 102909296 | ||||||
| chr4:102909368
|
C | T | 197 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(194): Show | 198 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.1086+1071G>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 9/11 | chr4 | 102909368 | ||||||
| chr4:102909369
|
G | A | 3 | a0001c0001t0001g0112a0001c0001t0001g0302a0001c0001t0001g0315 | 3 | HG02109.hp2 HG03209.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1086+1070C>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 9/11 | chr4 | 102909369 | ||||||
| chr4:102909440
|
T | G | 1 | a0001c0001t0001g0052 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1086+999A>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 9/11 | chr4 | 102909440 | ||||||
| chr4:102909539
|
T | C | 197 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(194): Show | 198 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.1086+900A>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 9/11 | chr4 | 102909539 | ||||||
| chr4:102909591
|
G | A | 10 | a0001c0001t0001g0226a0001c0001t0001g0227a0001c0001t0001g0228others(7): Show | 10 | HG00735.hp2 HG01884.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.1086+848C>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 9/11 | chr4 | 102909591 | ||||||
| chr4:102909712
|
G | A | 1 | a0001c0001t0001g0246 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1086+727C>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 9/11 | chr4 | 102909712 | ||||||
| chr4:102909822
|
A | G | 1 | a0001c0001t0001g0061 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1086+617T>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 9/11 | chr4 | 102909822 | ||||||
| chr4:102910006
|
G | T | 1 | a0001c0001t0001g0232 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1086+433C>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 9/11 | chr4 | 102910006 | ||||||
| chr4:102910038
|
C | T | 42 | a0001c0001t0001g0111a0001c0001t0001g0221a0001c0001t0001g0241others(39): Show | 42 | HG00140.hp2 HG00438.hp2 HG00639.hp1 others(39): Show |
intron_variant | MODIFIER | c.1086+401G>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 9/11 | chr4 | 102910038 | ||||||
| chr4:102910055
|
T | C | 1 | a0001c0001t0001g0099 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1086+384A>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 9/11 | chr4 | 102910055 | ||||||
| chr4:102910069
|
C | T | 1 | a0001c0001t0001g0213 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1086+370G>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 9/11 | chr4 | 102910069 | ||||||
| chr4:102910126
|
T | A | 1 | a0001c0001t0001g0159 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1086+313A>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 9/11 | chr4 | 102910126 | ||||||
| chr4:102910128
|
T | C | 1 | a0001c0001t0001g0170 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1086+311A>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 9/11 | chr4 | 102910128 | ||||||
| chr4:102910165
|
T | A | 1 | a0001c0001t0001g0012 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1086+274A>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 9/11 | chr4 | 102910165 | ||||||
| chr4:102910202
|
T | C | 1 | a0001c0001t0001g0241 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.1086+237A>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 9/11 | chr4 | 102910202 | ||||||
| chr4:102910749
|
A | G | 11 | a0001c0001t0001g0111a0001c0001t0001g0221a0001c0001t0001g0242others(8): Show | 11 | HG00438.hp2 HG02056.hp2 HG02074.hp2 others(8): Show |
intron_variant | MODIFIER | c.937-161T>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 8/11 | chr4 | 102910749 | ||||||
| chr4:102910822
|
T | C | 1 | a0001c0001t0001g0012 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.937-234A>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 8/11 | chr4 | 102910822 | ||||||
| chr4:102910887
|
T | A | 119 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0036others(116): Show | 120 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.937-299A>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 8/11 | chr4 | 102910887 | ||||||
| chr4:102910975
|
C | A | 1 | a0001c0001t0001g0211 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.937-387G>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 8/11 | chr4 | 102910975 | ||||||
| chr4:102911156
|
T | C | 1 | a0001c0001t0001g0008 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.936+275A>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 8/11 | chr4 | 102911156 | ||||||
| chr4:102911423
|
G | A | 2 | a0001c0001t0001g0126a0001c0001t0001g0185 | 2 | HG02809.hp1 HG03041.hp1 |
splice_region_variant&intron_variant | LOW | c.936+8C>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 8/11 | chr4 | 102911423 | ||||||
| chr4:102911657
|
T | C | 1 | a0001c0001t0001g0225 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.830-120A>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102911657 | ||||||
| chr4:102911673
|
A | G | 2 | a0001c0001t0001g0112a0001c0001t0001g0302 | 2 | HG02109.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.830-136T>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102911673 | ||||||
| chr4:102911747
|
A | G | 1 | a0001c0001t0001g0062 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.830-210T>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102911747 | ||||||
| chr4:102911770
|
T | C | 18 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0013others(15): Show | 18 | HG00438.hp1 HG00597.hp2 HG01169.hp1 others(15): Show |
intron_variant | MODIFIER | c.830-233A>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102911770 | ||||||
| chr4:102911813
|
TC | T | 10 | a0001c0001t0001g0226a0001c0001t0001g0227a0001c0001t0001g0228others(7): Show | 10 | HG00735.hp2 HG01884.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.830-277delG | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102911813 | ||||||
| chr4:102911999
|
GGCACACA others(3): Show |
G | 1 | a0001c0001t0001g0124 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.830-472_830-463del others(10): Show |
SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102911999 | ||||||
| chr4:102912010
|
G | T | 1 | a0001c0001t0001g0124 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.830-473C>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102912010 | ||||||
| chr4:102912138
|
GA | G | 15 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0112others(12): Show | 15 | HG00735.hp2 HG01884.hp2 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.830-602delT | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102912138 | ||||||
| chr4:102912138
|
GAA | G | 197 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(194): Show | 198 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.830-603_830-602del others(2): Show |
SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102912138 | ||||||
| chr4:102912251
|
T | A | 1 | a0001c0001t0001g0282 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.830-714A>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102912251 | ||||||
| chr4:102912318
|
C | G | 1 | a0001c0001t0001g0027 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.830-781G>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102912318 | ||||||
| chr4:102912562
|
G | T | 1 | a0001c0001t0001g0039 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.830-1025C>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102912562 | ||||||
| chr4:102912693
|
C | A | 1 | a0001c0001t0001g0004 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.830-1156G>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102912693 | ||||||
| chr4:102912732
|
C | T | 197 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(194): Show | 198 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.830-1195G>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102912732 | ||||||
| chr4:102912734
|
AGCCCGGT others(35): Show |
A | 1 | a0001c0001t0001g0093 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.830-1239_830-1198d others(44): Show |
SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102912734 | ||||||
| chr4:102913241
|
A | G | 1 | a0001c0001t0001g0080 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.830-1704T>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102913241 | ||||||
| chr4:102913246
|
C | T | 10 | a0001c0001t0001g0226a0001c0001t0001g0227a0001c0001t0001g0228others(7): Show | 10 | HG00735.hp2 HG01884.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.830-1709G>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102913246 | ||||||
| chr4:102913321
|
G | A | 210 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(207): Show | 211 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.830-1784C>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102913321 | ||||||
| chr4:102913483
|
G | A | 197 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(194): Show | 198 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.830-1946C>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102913483 | ||||||
| chr4:102913592
|
G | T | 1 | a0001c0001t0001g0264 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.830-2055C>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102913592 | ||||||
| chr4:102913776
|
A | G | 10 | a0001c0001t0001g0226a0001c0001t0001g0227a0001c0001t0001g0228others(7): Show | 10 | HG00735.hp2 HG01884.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.830-2239T>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102913776 | ||||||
| chr4:102913785
|
G | C | 1 | a0001c0001t0001g0086 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.830-2248C>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102913785 | ||||||
| chr4:102913796
|
T | TA | 6 | a0001c0001t0001g0037a0001c0001t0001g0101a0001c0001t0001g0112others(3): Show | 6 | HG00609.hp1 HG02109.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.830-2260dupT | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102913796 | ||||||
| chr4:102913796
|
TA | T | 183 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(180): Show | 184 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(181): Show |
intron_variant | MODIFIER | c.830-2260delT | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102913796 | ||||||
| chr4:102913960
|
G | A | 5 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0091others(2): Show | 5 | HG02451.hp2 HG02486.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.830-2423C>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102913960 | ||||||
| chr4:102914190
|
C | T | 1 | a0001c0001t0001g0172 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.830-2653G>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102914190 | ||||||
| chr4:102914212
|
A | T | 1 | a0001c0001t0001g0240 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.830-2675T>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102914212 | ||||||
| chr4:102914225
|
C | G | 197 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(194): Show | 198 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.830-2688G>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102914225 | ||||||
| chr4:102914226
|
A | T | 197 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(194): Show | 198 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.830-2689T>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102914226 | ||||||
| chr4:102914227
|
C | G | 197 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(194): Show | 198 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.830-2690G>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102914227 | ||||||
| chr4:102914228
|
T | TC | 197 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(194): Show | 198 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.830-2692_830-2691i others(3): Show |
SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102914228 | ||||||
| chr4:102914229
|
G | A | 197 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(194): Show | 198 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.830-2692C>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102914229 | ||||||
| chr4:102914231
|
A | C | 197 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(194): Show | 198 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.830-2694T>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102914231 | ||||||
| chr4:102914235
|
A | T | 197 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(194): Show | 198 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.830-2698T>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102914235 | ||||||
| chr4:102914239
|
G | T | 197 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(194): Show | 198 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.830-2702C>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102914239 | ||||||
| chr4:102914249
|
G | C | 1 | a0001c0001t0001g0197 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.830-2712C>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102914249 | ||||||
| chr4:102914255
|
C | A | 1 | a0001c0001t0001g0139 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.830-2718G>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102914255 | ||||||
| chr4:102914546
|
T | C | 197 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(194): Show | 198 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.830-3009A>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102914546 | ||||||
| chr4:102914603
|
T | G | 3 | a0001c0001t0001g0112a0001c0001t0001g0302a0001c0001t0001g0315 | 3 | HG02109.hp2 HG03209.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.830-3066A>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102914603 | ||||||
| chr4:102914927
|
T | C | 196 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(193): Show | 197 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.830-3390A>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102914927 | ||||||
| chr4:102915076
|
T | C | 1 | a0001c0001t0001g0159 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.830-3539A>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102915076 | ||||||
| chr4:102915103
|
GA | G | 201 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(198): Show | 202 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.830-3567delT | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102915103 | ||||||
| chr4:102915111
|
A | G | 2 | a0001c0001t0001g0236a0001c0001t0001g0237 | 2 | HG02486.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.830-3574T>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102915111 | ||||||
| chr4:102915117
|
T | C | 1 | a0001c0001t0001g0258 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.830-3580A>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102915117 | ||||||
| chr4:102915484
|
G | T | 211 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(208): Show | 212 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(209): Show |
intron_variant | MODIFIER | c.830-3947C>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102915484 | ||||||
| chr4:102915665
|
A | G | 197 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(194): Show | 198 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.830-4128T>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102915665 | ||||||
| chr4:102915868
|
G | C | 10 | a0001c0001t0001g0226a0001c0001t0001g0227a0001c0001t0001g0228others(7): Show | 10 | HG00735.hp2 HG01884.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.830-4331C>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102915868 | ||||||
| chr4:102915970
|
G | T | 1 | a0001c0001t0001g0075 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.830-4433C>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102915970 | ||||||
| chr4:102916044
|
C | T | 13 | a0001c0001t0001g0112a0001c0001t0001g0226a0001c0001t0001g0227others(10): Show | 13 | HG00735.hp2 HG01884.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.830-4507G>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102916044 | ||||||
| chr4:102916054
|
A | G | 1 | a0001c0001t0001g0180 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.830-4517T>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102916054 | ||||||
| chr4:102916160
|
A | T | 1 | a0001c0001t0001g0204 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.830-4623T>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102916160 | ||||||
| chr4:102916335
|
G | A | 1 | a0001c0001t0001g0282 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.830-4798C>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102916335 | ||||||
| chr4:102916429
|
T | C | 1 | a0001c0001t0001g0269 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.830-4892A>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102916429 | ||||||
| chr4:102916530
|
G | C | 2 | a0001c0001t0001g0202a0001c0001t0001g0203 | 2 | NA18984.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.830-4993C>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102916530 | ||||||
| chr4:102917123
|
C | A | 1 | a0001c0001t0001g0027 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.830-5586G>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102917123 | ||||||
| chr4:102917320
|
G | A | 211 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(208): Show | 212 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(209): Show |
intron_variant | MODIFIER | c.830-5783C>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102917320 | ||||||
| chr4:102917429
|
G | GTATCTA | 34 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0014others(31): Show | 34 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(31): Show |
intron_variant | MODIFIER | c.830-5898_830-5893d others(8): Show |
SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102917429 | ||||||
| chr4:102917429
|
G | GTATCTAT others(5): Show |
9 | a0001c0001t0001g0028a0001c0001t0001g0030a0001c0001t0001g0040others(6): Show | 9 | HG00735.hp1 HG01168.hp1 HG01358.hp1 others(6): Show |
intron_variant | MODIFIER | c.830-5904_830-5893d others(14): Show |
SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102917429 | ||||||
| chr4:102917429
|
GTATCTA | G | 116 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0012others(113): Show | 117 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(114): Show |
intron_variant | MODIFIER | c.830-5898_830-5893d others(8): Show |
SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102917429 | ||||||
| chr4:102917429
|
GTATCTAT others(5): Show |
G | 55 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(52): Show | 55 | HG00423.hp2 HG00558.hp2 HG00621.hp2 others(52): Show |
intron_variant | MODIFIER | c.830-5904_830-5893d others(14): Show |
SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102917429 | ||||||
| chr4:102917429
|
GTATCTAT others(11): Show |
G | 22 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0039others(19): Show | 22 | HG00099.hp1 HG00597.hp1 HG00735.hp2 others(19): Show |
intron_variant | MODIFIER | c.830-5910_830-5893d others(20): Show |
SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102917429 | ||||||
| chr4:102917740
|
C | T | 5 | a0001c0001t0001g0165a0001c0001t0001g0166a0001c0001t0001g0167others(2): Show | 5 | HG00621.hp2 HG02083.hp2 NA18949.hp1 others(2): Show |
intron_variant | MODIFIER | c.830-6203G>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102917740 | ||||||
| chr4:102917876
|
C | A | 10 | a0001c0001t0001g0226a0001c0001t0001g0227a0001c0001t0001g0228others(7): Show | 10 | HG00735.hp2 HG01884.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.830-6339G>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102917876 | ||||||
| chr4:102918000
|
A | G | 197 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(194): Show | 198 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.830-6463T>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102918000 | ||||||
| chr4:102918013
|
A | T | 5 | a0001c0001t0001g0010a0001c0001t0001g0044a0001c0001t0001g0068others(2): Show | 5 | HG00438.hp1 HG04184.hp2 NA18968.hp2 others(2): Show |
intron_variant | MODIFIER | c.830-6476T>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102918013 | ||||||
| chr4:102918068
|
CA | C | 23 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0020others(20): Show | 23 | HG00735.hp2 HG01884.hp2 HG02451.hp2 others(20): Show |
intron_variant | MODIFIER | c.830-6532delT | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102918068 | ||||||
| chr4:102918096
|
G | GA | 197 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(194): Show | 198 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.830-6560dupT | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102918096 | ||||||
| chr4:102918111
|
A | G | 2 | a0002c0002t0001g0316a0002c0002t0001g0317 | 2 | HG02258.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.830-6574T>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102918111 | ||||||
| chr4:102918147
|
G | T | 1 | a0001c0001t0001g0003 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.830-6610C>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102918147 | ||||||
| chr4:102918497
|
C | T | 198 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(195): Show | 199 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.830-6960G>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102918497 | ||||||
| chr4:102918724
|
G | C | 1 | a0001c0001t0001g0042 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.830-7187C>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102918724 | ||||||
| chr4:102918858
|
T | A | 2 | a0001c0001t0001g0233a0001c0001t0001g0235 | 2 | HG03195.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.830-7321A>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102918858 | ||||||
| chr4:102918936
|
T | C | 210 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(207): Show | 211 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.830-7399A>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102918936 | ||||||
| chr4:102919212
|
G | A | 9 | a0001c0001t0001g0304a0001c0001t0001g0305a0001c0001t0001g0306others(6): Show | 9 | HG01891.hp1 HG02145.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.830-7675C>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102919212 | ||||||
| chr4:102919490
|
G | A | 4 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0001g0224others(1): Show | 4 | HG01192.hp1 HG02145.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.830-7953C>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102919490 | ||||||
| chr4:102919563
|
T | C | 1 | a0001c0001t0001g0315 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.830-8026A>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102919563 | ||||||
| chr4:102919616
|
C | T | 10 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0126others(7): Show | 10 | HG02572.hp1 HG02717.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.830-8079G>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102919616 | ||||||
| chr4:102919617
|
G | A | 1 | a0001c0001t0001g0142 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.830-8080C>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102919617 | ||||||
| chr4:102919723
|
GGTCTTAG others(5): Show |
G | 197 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(194): Show | 198 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.830-8198_830-8187d others(14): Show |
SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102919723 | ||||||
| chr4:102919736
|
A | T | 197 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(194): Show | 198 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.830-8199T>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102919736 | ||||||
| chr4:102919754
|
C | T | 2 | a0001c0001t0001g0101a0001c0001t0001g0102 | 2 | HG02698.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.830-8217G>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102919754 | ||||||
| chr4:102919808
|
C | T | 1 | a0001c0001t0001g0009 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.830-8271G>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102919808 | ||||||
| chr4:102919944
|
C | T | 10 | a0001c0001t0001g0226a0001c0001t0001g0227a0001c0001t0001g0228others(7): Show | 10 | HG00735.hp2 HG01884.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.830-8407G>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102919944 | ||||||
| chr4:102920048
|
G | C | 1 | a0001c0001t0001g0255 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.830-8511C>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102920048 | ||||||
| chr4:102920080
|
A | C | 1 | a0001c0001t0001g0309 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.830-8543T>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102920080 | ||||||
| chr4:102920096
|
A | G | 197 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(194): Show | 198 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.830-8559T>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102920096 | ||||||
| chr4:102920122
|
A | G | 10 | a0001c0001t0001g0226a0001c0001t0001g0227a0001c0001t0001g0228others(7): Show | 10 | HG00735.hp2 HG01884.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.830-8585T>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102920122 | ||||||
| chr4:102920277
|
G | T | 1 | a0001c0001t0001g0102 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.830-8740C>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102920277 | ||||||
| chr4:102920363
|
C | T | 1 | a0001c0001t0001g0175 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.830-8826G>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102920363 | ||||||
| chr4:102920413
|
G | A | 197 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(194): Show | 198 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.830-8876C>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102920413 | ||||||
| chr4:102920556
|
G | C | 1 | a0001c0001t0001g0042 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.830-9019C>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102920556 | ||||||
| chr4:102920847
|
G | A | 1 | a0001c0001t0001g0238 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.830-9310C>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102920847 | ||||||
| chr4:102920874
|
A | G | 197 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(194): Show | 198 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.830-9337T>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102920874 | ||||||
| chr4:102920983
|
C | G | 1 | a0001c0001t0001g0241 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.830-9446G>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102920983 | ||||||
| chr4:102920995
|
T | C | 10 | a0001c0001t0001g0226a0001c0001t0001g0227a0001c0001t0001g0228others(7): Show | 10 | HG00735.hp2 HG01884.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.830-9458A>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102920995 | ||||||
| chr4:102921262
|
C | T | 1 | a0001c0001t0001g0188 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.830-9725G>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102921262 | ||||||
| chr4:102921553
|
C | T | 210 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(207): Show | 211 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.830-10016G>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102921553 | ||||||
| chr4:102921594
|
C | A | 1 | a0001c0001t0001g0012 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.830-10057G>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102921594 | ||||||
| chr4:102921793
|
A | G | 197 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(194): Show | 198 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.830-10256T>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102921793 | ||||||
| chr4:102921913
|
G | A | 1 | a0001c0001t0001g0154 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.829+10211C>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102921913 | ||||||
| chr4:102921935
|
G | C | 1 | a0001c0001t0001g0002 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.829+10189C>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102921935 | ||||||
| chr4:102922082
|
C | G | 197 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(194): Show | 198 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.829+10042G>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102922082 | ||||||
| chr4:102922241
|
C | T | 1 | a0001c0001t0001g0131 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.829+9883G>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102922241 | ||||||
| chr4:102922279
|
A | G | 1 | a0001c0001t0001g0220 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.829+9845T>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102922279 | ||||||
| chr4:102922480
|
T | C | 1 | a0001c0001t0001g0036 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.829+9644A>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102922480 | ||||||
| chr4:102922596
|
C | CA | 13 | a0001c0001t0001g0111a0001c0001t0001g0221a0001c0001t0001g0242others(10): Show | 13 | HG00438.hp2 HG02056.hp2 HG02074.hp2 others(10): Show |
intron_variant | MODIFIER | c.829+9527dupT | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102922596 | ||||||
| chr4:102922602
|
G | A | 197 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(194): Show | 198 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.829+9522C>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102922602 | ||||||
| chr4:102922828
|
C | T | 1 | a0001c0001t0001g0154 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.829+9296G>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102922828 | ||||||
| chr4:102922873
|
G | T | 1 | a0001c0001t0001g0293 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.829+9251C>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102922873 | ||||||
| chr4:102923035
|
A | G | 2 | a0001c0001t0001g0112a0001c0001t0001g0302 | 2 | HG02109.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.829+9089T>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102923035 | ||||||
| chr4:102923198
|
A | T | 1 | a0001c0001t0001g0100 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.829+8926T>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102923198 | ||||||
| chr4:102923292
|
G | A | 197 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(194): Show | 198 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.829+8832C>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102923292 | ||||||
| chr4:102923312
|
C | T | 197 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(194): Show | 198 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.829+8812G>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102923312 | ||||||
| chr4:102923334
|
C | A | 1 | a0001c0001t0001g0242 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.829+8790G>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102923334 | ||||||
| chr4:102923386
|
T | A | 1 | a0001c0001t0001g0002 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.829+8738A>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102923386 | ||||||
| chr4:102923393
|
G | A | 10 | a0001c0001t0001g0226a0001c0001t0001g0227a0001c0001t0001g0228others(7): Show | 10 | HG00735.hp2 HG01884.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.829+8731C>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102923393 | ||||||
| chr4:102923401
|
T | C | 134 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(131): Show | 135 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.829+8723A>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102923401 | ||||||
| chr4:102923407
|
G | A | 1 | a0001c0001t0001g0187 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.829+8717C>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102923407 | ||||||
| chr4:102923560
|
C | A | 197 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(194): Show | 198 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.829+8564G>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102923560 | ||||||
| chr4:102923565
|
C | A | 1 | a0001c0001t0001g0020 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.829+8559G>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102923565 | ||||||
| chr4:102923644
|
T | G | 210 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(207): Show | 211 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.829+8480A>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102923644 | ||||||
| chr4:102923667
|
T | C | 1 | a0001c0001t0001g0288 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.829+8457A>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102923667 | ||||||
| chr4:102923693
|
C | CTGA | 197 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(194): Show | 198 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.829+8430_829+8431i others(5): Show |
SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102923693 | ||||||
| chr4:102923743
|
A | T | 1 | a0001c0001t0001g0037 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.829+8381T>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102923743 | ||||||
| chr4:102923884
|
C | G | 197 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(194): Show | 198 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.829+8240G>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102923884 | ||||||
| chr4:102923980
|
C | A | 1 | a0001c0001t0001g0137 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.829+8144G>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102923980 | ||||||
| chr4:102924274
|
T | A | 2 | a0001c0001t0001g0112a0001c0001t0001g0302 | 2 | HG02109.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.829+7850A>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102924274 | ||||||
| chr4:102924275
|
T | A | 2 | a0001c0001t0001g0112a0001c0001t0001g0302 | 2 | HG02109.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.829+7849A>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102924275 | ||||||
| chr4:102924343
|
G | A | 2 | a0001c0001t0001g0112a0001c0001t0001g0302 | 2 | HG02109.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.829+7781C>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102924343 | ||||||
| chr4:102924356
|
G | A | 1 | a0001c0001t0001g0235 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.829+7768C>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102924356 | ||||||
| chr4:102924485
|
C | A | 1 | a0001c0001t0001g0243 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.829+7639G>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102924485 | ||||||
| chr4:102924609
|
A | G | 1 | a0001c0001t0001g0242 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.829+7515T>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102924609 | ||||||
| chr4:102924723
|
C | A | 4 | a0001c0001t0001g0042a0001c0001t0001g0050a0001c0001t0001g0097others(1): Show | 4 | HG02738.hp2 HG03688.hp2 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.829+7401G>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102924723 | ||||||
| chr4:102924867
|
ACCAATTA others(2663): Show |
A | 1 | a0001c0001t0001g0169 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.829+4587_829+7256d others(2): Show |
SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102924867 | ||||||
| chr4:102924930
|
A | T | 1 | a0001c0001t0001g0147 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.829+7194T>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102924930 | ||||||
| chr4:102925000
|
T | C | 1 | a0001c0001t0001g0057 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.829+7124A>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102925000 | ||||||
| chr4:102925026
|
A | G | 1 | a0001c0001t0001g0031 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.829+7098T>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102925026 | ||||||
| chr4:102925035
|
C | T | 1 | a0001c0001t0001g0294 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.829+7089G>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102925035 | ||||||
| chr4:102925132
|
A | G | 3 | a0001c0001t0001g0112a0001c0001t0001g0302a0001c0001t0001g0315 | 3 | HG02109.hp2 HG03209.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.829+6992T>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102925132 | ||||||
| chr4:102925216
|
T | C | 1 | a0001c0001t0001g0238 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.829+6908A>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102925216 | ||||||
| chr4:102925217
|
A | T | 1 | a0001c0001t0001g0238 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.829+6907T>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102925217 | ||||||
| chr4:102925242
|
C | A | 196 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(193): Show | 197 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.829+6882G>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102925242 | ||||||
| chr4:102925267
|
A | G | 196 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(193): Show | 197 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.829+6857T>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102925267 | ||||||
| chr4:102925482
|
T | C | 18 | a0001c0001t0001g0002a0001c0001t0001g0239a0001c0001t0001g0240others(15): Show | 18 | HG00099.hp1 HG01109.hp1 HG01175.hp2 others(15): Show |
intron_variant | MODIFIER | c.829+6642A>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102925482 | ||||||
| chr4:102925594
|
C | G | 2 | a0001c0001t0001g0260a0001c0001t0001g0266 | 2 | HG01975.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.829+6530G>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102925594 | ||||||
| chr4:102925641
|
C | G | 196 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(193): Show | 197 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.829+6483G>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102925641 | ||||||
| chr4:102925699
|
C | CAAAAAA | 203 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(200): Show | 204 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(201): Show |
intron_variant | MODIFIER | c.829+6419_829+6424d others(8): Show |
SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102925699 | ||||||
| chr4:102925856
|
T | C | 4 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0001g0224others(1): Show | 4 | HG01192.hp1 HG02145.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.829+6268A>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102925856 | ||||||
| chr4:102926000
|
T | C | 3 | a0001c0001t0001g0112a0001c0001t0001g0302a0001c0001t0001g0315 | 3 | HG02109.hp2 HG03209.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.829+6124A>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102926000 | ||||||
| chr4:102926030
|
T | C | 1 | a0001c0001t0001g0003 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.829+6094A>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102926030 | ||||||
| chr4:102926110
|
G | A | 66 | a0001c0001t0001g0114a0001c0001t0001g0118a0001c0001t0001g0120others(63): Show | 66 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(63): Show |
intron_variant | MODIFIER | c.829+6014C>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102926110 | ||||||
| chr4:102926203
|
C | G | 3 | a0001c0001t0001g0236a0001c0001t0001g0237a0001c0001t0001g0238 | 3 | HG02486.hp1 HG02818.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.829+5921G>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102926203 | ||||||
| chr4:102926279
|
T | C | 1 | a0001c0001t0001g0217 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.829+5845A>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102926279 | ||||||
| chr4:102926325
|
C | T | 2 | a0001c0001t0001g0149a0001c0001t0001g0211 | 2 | HG00423.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.829+5799G>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102926325 | ||||||
| chr4:102926475
|
C | A | 1 | a0001c0001t0001g0272 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.829+5649G>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102926475 | ||||||
| chr4:102926671
|
C | T | 1 | a0001c0001t0001g0094 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.829+5453G>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102926671 | ||||||
| chr4:102926748
|
G | A | 209 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(206): Show | 210 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.829+5376C>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102926748 | ||||||
| chr4:102926849
|
G | A | 13 | a0001c0001t0001g0112a0001c0001t0001g0226a0001c0001t0001g0227others(10): Show | 13 | HG00735.hp2 HG01884.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.829+5275C>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102926849 | ||||||
| chr4:102926937
|
A | G | 196 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(193): Show | 197 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.829+5187T>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102926937 | ||||||
| chr4:102926976
|
A | C | 209 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(206): Show | 210 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.829+5148T>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102926976 | ||||||
| chr4:102927025
|
G | C | 10 | a0001c0001t0001g0226a0001c0001t0001g0227a0001c0001t0001g0228others(7): Show | 10 | HG00735.hp2 HG01884.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.829+5099C>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102927025 | ||||||
| chr4:102927188
|
G | T | 3 | a0001c0001t0001g0272a0001c0001t0001g0282a0001c0001t0001g0291 | 3 | HG00099.hp1 HG02723.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.829+4936C>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102927188 | ||||||
| chr4:102927259
|
C | T | 196 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(193): Show | 197 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.829+4865G>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102927259 | ||||||
| chr4:102927281
|
A | G | 196 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(193): Show | 197 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.829+4843T>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102927281 | ||||||
| chr4:102927300
|
A | G | 1 | a0001c0001t0001g0315 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.829+4824T>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102927300 | ||||||
| chr4:102927347
|
C | G | 1 | a0001c0001t0001g0029 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.829+4777G>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102927347 | ||||||
| chr4:102927484
|
T | A | 1 | a0001c0001t0001g0204 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.829+4640A>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102927484 | ||||||
| chr4:102927525
|
A | G | 1 | a0001c0001t0001g0227 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.829+4599T>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102927525 | ||||||
| chr4:102927736
|
A | G | 1 | a0001c0001t0001g0078 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.829+4388T>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102927736 | ||||||
| chr4:102927972
|
A | G | 1 | a0001c0001t0001g0307 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.829+4152T>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102927972 | ||||||
| chr4:102928160
|
G | A | 1 | a0001c0001t0001g0154 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.829+3964C>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102928160 | ||||||
| chr4:102928222
|
T | C | 1 | a0001c0001t0001g0052 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.829+3902A>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102928222 | ||||||
| chr4:102928227
|
A | C | 1 | a0001c0001t0001g0151 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.829+3897T>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102928227 | ||||||
| chr4:102928359
|
T | C | 197 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(194): Show | 198 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.829+3765A>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102928359 | ||||||
| chr4:102928385
|
A | G | 1 | a0001c0001t0001g0115 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.829+3739T>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102928385 | ||||||
| chr4:102928601
|
T | C | 210 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(207): Show | 211 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.829+3523A>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102928601 | ||||||
| chr4:102928637
|
G | C | 211 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(208): Show | 212 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(209): Show |
intron_variant | MODIFIER | c.829+3487C>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102928637 | ||||||
| chr4:102928691
|
T | C | 10 | a0001c0001t0001g0226a0001c0001t0001g0227a0001c0001t0001g0228others(7): Show | 10 | HG00735.hp2 HG01884.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.829+3433A>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102928691 | ||||||
| chr4:102928709
|
A | T | 10 | a0001c0001t0001g0226a0001c0001t0001g0227a0001c0001t0001g0228others(7): Show | 10 | HG00735.hp2 HG01884.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.829+3415T>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102928709 | ||||||
| chr4:102928748
|
G | A | 1 | a0001c0001t0001g0110 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.829+3376C>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102928748 | ||||||
| chr4:102928840
|
T | C | 210 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(207): Show | 211 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.829+3284A>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102928840 | ||||||
| chr4:102929227
|
A | G | 197 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(194): Show | 198 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.829+2897T>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102929227 | ||||||
| chr4:102929283
|
A | G | 1 | a0001c0001t0001g0272 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.829+2841T>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102929283 | ||||||
| chr4:102929325
|
A | T | 11 | a0001c0001t0001g0137a0001c0001t0001g0148a0001c0001t0001g0149others(8): Show | 11 | HG00423.hp1 HG00621.hp1 HG02071.hp2 others(8): Show |
intron_variant | MODIFIER | c.829+2799T>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102929325 | ||||||
| chr4:102929487
|
A | T | 1 | a0001c0001t0001g0238 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.829+2637T>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102929487 | ||||||
| chr4:102929522
|
A | AT | 10 | a0001c0001t0001g0226a0001c0001t0001g0227a0001c0001t0001g0228others(7): Show | 10 | HG00735.hp2 HG01884.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.829+2601dupA | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102929522 | ||||||
| chr4:102929772
|
T | C | 130 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(127): Show | 131 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(128): Show |
intron_variant | MODIFIER | c.829+2352A>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102929772 | ||||||
| chr4:102929922
|
C | T | 1 | a0001c0001t0001g0133 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.829+2202G>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102929922 | ||||||
| chr4:102929937
|
G | A | 1 | a0001c0001t0001g0162 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.829+2187C>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102929937 | ||||||
| chr4:102930222
|
T | A | 197 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(194): Show | 198 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.829+1902A>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102930222 | ||||||
| chr4:102930280
|
A | G | 1 | a0001c0001t0001g0122 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.829+1844T>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102930280 | ||||||
| chr4:102930355
|
T | C | 1 | a0001c0001t0001g0008 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.829+1769A>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102930355 | ||||||
| chr4:102930432
|
T | A | 1 | a0001c0001t0001g0309 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.829+1692A>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102930432 | ||||||
| chr4:102930491
|
G | A | 1 | a0001c0001t0001g0242 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.829+1633C>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102930491 | ||||||
| chr4:102930494
|
T | C | 3 | a0001c0001t0001g0273a0001c0001t0001g0274a0001c0001t0001g0275 | 3 | HG02818.hp2 HG03486.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.829+1630A>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102930494 | ||||||
| chr4:102930619
|
G | T | 197 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(194): Show | 198 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.829+1505C>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102930619 | ||||||
| chr4:102930644
|
A | G | 197 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(194): Show | 198 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.829+1480T>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102930644 | ||||||
| chr4:102930953
|
G | A | 197 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(194): Show | 198 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.829+1171C>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102930953 | ||||||
| chr4:102930990
|
C | T | 1 | a0001c0001t0001g0243 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.829+1134G>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102930990 | ||||||
| chr4:102930995
|
C | T | 197 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(194): Show | 198 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.829+1129G>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102930995 | ||||||
| chr4:102931082
|
C | T | 1 | a0001c0001t0001g0227 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.829+1042G>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102931082 | ||||||
| chr4:102931225
|
C | CA | 198 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(195): Show | 199 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.829+898dupT | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102931225 | ||||||
| chr4:102931340
|
AGAAGG | A | 13 | a0001c0001t0001g0112a0001c0001t0001g0226a0001c0001t0001g0227others(10): Show | 13 | HG00735.hp2 HG01884.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.829+779_829+783del others(5): Show |
SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102931340 | ||||||
| chr4:102931421
|
C | T | 197 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(194): Show | 198 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.829+703G>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102931421 | ||||||
| chr4:102931434
|
T | A | 12 | a0001c0001t0001g0118a0001c0001t0001g0120a0001c0001t0001g0139others(9): Show | 12 | HG00558.hp1 HG02056.hp1 HG02155.hp2 others(9): Show |
intron_variant | MODIFIER | c.829+690A>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102931434 | ||||||
| chr4:102931613
|
T | G | 1 | a0001c0001t0001g0184 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.829+511A>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102931613 | ||||||
| chr4:102931645
|
T | TG | 210 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(207): Show | 211 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.829+478dupC | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102931645 | ||||||
| chr4:102931818
|
G | A | 1 | a0001c0001t0001g0184 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.829+306C>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102931818 | ||||||
| chr4:102931878
|
A | G | 3 | a0001c0001t0001g0273a0001c0001t0001g0274a0001c0001t0001g0275 | 3 | HG02818.hp2 HG03486.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.829+246T>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102931878 | ||||||
| chr4:102932073
|
T | C | 1 | a0001c0001t0001g0315 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.829+51A>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 7/11 | chr4 | 102932073 | ||||||
| chr4:102932570
|
T | C | 1 | a0001c0001t0001g0094 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.654-271A>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 6/11 | chr4 | 102932570 | ||||||
| chr4:102932654
|
C | G | 1 | a0001c0001t0001g0187 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.654-355G>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 6/11 | chr4 | 102932654 | ||||||
| chr4:102932775
|
A | C | 13 | a0001c0001t0001g0241a0001c0001t0001g0243a0001c0001t0001g0244others(10): Show | 13 | HG02083.hp1 HG02155.hp1 HG02523.hp2 others(10): Show |
intron_variant | MODIFIER | c.654-476T>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 6/11 | chr4 | 102932775 | ||||||
| chr4:102932886
|
T | G | 197 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(194): Show | 198 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.654-587A>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 6/11 | chr4 | 102932886 | ||||||
| chr4:102933219
|
C | T | 1 | a0001c0001t0001g0292 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.654-920G>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 6/11 | chr4 | 102933219 | ||||||
| chr4:102933674
|
A | G | 1 | a0001c0001t0001g0246 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.654-1375T>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 6/11 | chr4 | 102933674 | ||||||
| chr4:102933792
|
A | T | 1 | a0001c0001t0001g0192 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.654-1493T>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 6/11 | chr4 | 102933792 | ||||||
| chr4:102933927
|
C | T | 4 | a0001c0001t0001g0003a0001c0001t0001g0173a0001c0001t0001g0174others(1): Show | 4 | HG02622.hp1 HG02886.hp1 NA21309.hp1 others(1): Show |
intron_variant | MODIFIER | c.654-1628G>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 6/11 | chr4 | 102933927 | ||||||
| chr4:102933928
|
G | A | 1 | a0001c0001t0001g0175 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.654-1629C>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 6/11 | chr4 | 102933928 | ||||||
| chr4:102934123
|
G | A | 9 | a0001c0001t0001g0304a0001c0001t0001g0305a0001c0001t0001g0306others(6): Show | 9 | HG01891.hp1 HG02145.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.654-1824C>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 6/11 | chr4 | 102934123 | ||||||
| chr4:102934318
|
G | C | 2 | a0001c0001t0001g0260a0001c0001t0001g0266 | 2 | HG01975.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.654-2019C>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 6/11 | chr4 | 102934318 | ||||||
| chr4:102934388
|
GAGAA | G | 3 | a0001c0001t0001g0112a0001c0001t0001g0302a0001c0001t0001g0315 | 3 | HG02109.hp2 HG03209.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.654-2093_654-2090d others(6): Show |
SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 6/11 | chr4 | 102934388 | ||||||
| chr4:102934409
|
T | C | 1 | a0001c0001t0001g0021 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.654-2110A>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 6/11 | chr4 | 102934409 | ||||||
| chr4:102934511
|
G | A | 44 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0038others(41): Show | 45 | HG00423.hp2 HG00597.hp1 HG00609.hp2 others(42): Show |
intron_variant | MODIFIER | c.654-2212C>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 6/11 | chr4 | 102934511 | ||||||
| chr4:102934690
|
C | T | 3 | a0001c0001t0001g0112a0001c0001t0001g0302a0001c0001t0001g0315 | 3 | HG02109.hp2 HG03209.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.654-2391G>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 6/11 | chr4 | 102934690 | ||||||
| chr4:102934691
|
G | A | 2 | a0001c0001t0001g0019a0001c0001t0001g0022 | 2 | HG00738.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.654-2392C>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 6/11 | chr4 | 102934691 | ||||||
| chr4:102934763
|
C | CA | 194 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(191): Show | 195 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.654-2465dupT | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 6/11 | chr4 | 102934763 | ||||||
| chr4:102934971
|
T | C | 197 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(194): Show | 198 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.654-2672A>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 6/11 | chr4 | 102934971 | ||||||
| chr4:102935389
|
T | C | 1 | a0001c0001t0001g0146 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.654-3090A>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 6/11 | chr4 | 102935389 | ||||||
| chr4:102935599
|
C | T | 1 | a0001c0001t0001g0051 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.654-3300G>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 6/11 | chr4 | 102935599 | ||||||
| chr4:102935714
|
CT | C | 197 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(194): Show | 198 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.654-3416delA | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 6/11 | chr4 | 102935714 | ||||||
| chr4:102935782
|
T | A | 1 | a0001c0001t0001g0121 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.654-3483A>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 6/11 | chr4 | 102935782 | ||||||
| chr4:102935843
|
C | T | 1 | a0001c0001t0001g0157 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.654-3544G>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 6/11 | chr4 | 102935843 | ||||||
| chr4:102935865
|
A | G | 197 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(194): Show | 198 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.654-3566T>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 6/11 | chr4 | 102935865 | ||||||
| chr4:102935906
|
G | A | 49 | a0001c0001t0001g0111a0001c0001t0001g0196a0001c0001t0001g0221others(46): Show | 49 | HG00140.hp2 HG00438.hp2 HG00639.hp1 others(46): Show |
intron_variant | MODIFIER | c.654-3607C>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 6/11 | chr4 | 102935906 | ||||||
| chr4:102936164
|
T | C | 3 | a0001c0001t0001g0236a0001c0001t0001g0237a0001c0001t0001g0238 | 3 | HG02486.hp1 HG02818.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.654-3865A>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 6/11 | chr4 | 102936164 | ||||||
| chr4:102936330
|
A | T | 2 | a0001c0001t0001g0236a0001c0001t0001g0237 | 2 | HG02486.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.654-4031T>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 6/11 | chr4 | 102936330 | ||||||
| chr4:102936332
|
A | C | 10 | a0001c0001t0001g0252a0001c0001t0001g0253a0001c0001t0001g0254others(7): Show | 10 | HG01069.hp1 HG01071.hp2 HG01074.hp1 others(7): Show |
intron_variant | MODIFIER | c.654-4033T>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 6/11 | chr4 | 102936332 | ||||||
| chr4:102936406
|
C | A | 1 | a0001c0001t0001g0140 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.654-4107G>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 6/11 | chr4 | 102936406 | ||||||
| chr4:102936459
|
T | C | 1 | a0001c0001t0001g0204 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.654-4160A>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 6/11 | chr4 | 102936459 | ||||||
| chr4:102936545
|
A | G | 197 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(194): Show | 198 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.654-4246T>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 6/11 | chr4 | 102936545 | ||||||
| chr4:102936774
|
C | G | 32 | a0001c0001t0001g0241a0001c0001t0001g0243a0001c0001t0001g0244others(29): Show | 32 | HG00140.hp2 HG00639.hp1 HG00738.hp2 others(29): Show |
intron_variant | MODIFIER | c.654-4475G>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 6/11 | chr4 | 102936774 | ||||||
| chr4:102936835
|
C | T | 2 | a0001c0001t0001g0193a0001c0001t0001g0194 | 2 | NA18979.hp2 NA18981.hp1 |
intron_variant | MODIFIER | c.654-4536G>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 6/11 | chr4 | 102936835 | ||||||
| chr4:102936865
|
G | A | 1 | a0001c0001t0001g0052 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.654-4566C>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 6/11 | chr4 | 102936865 | ||||||
| chr4:102936917
|
C | T | 3 | a0001c0001t0001g0112a0001c0001t0001g0302a0001c0001t0001g0315 | 3 | HG02109.hp2 HG03209.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.654-4618G>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 6/11 | chr4 | 102936917 | ||||||
| chr4:102936936
|
A | C | 1 | a0001c0001t0001g0008 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.654-4637T>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 6/11 | chr4 | 102936936 | ||||||
| chr4:102937126
|
G | A | 1 | a0001c0001t0001g0019 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.654-4827C>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 6/11 | chr4 | 102937126 | ||||||
| chr4:102937337
|
G | A | 45 | a0001c0001t0001g0111a0001c0001t0001g0221a0001c0001t0001g0241others(42): Show | 45 | HG00140.hp2 HG00438.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.654-5038C>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 6/11 | chr4 | 102937337 | ||||||
| chr4:102937412
|
T | TA | 19 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0020others(16): Show | 19 | HG00438.hp1 HG01361.hp1 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.654-5114dupT | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 6/11 | chr4 | 102937412 | ||||||
| chr4:102937412
|
TA | T | 26 | a0001c0001t0001g0005a0001c0001t0001g0017a0001c0001t0001g0019others(23): Show | 26 | HG00558.hp2 HG00621.hp2 HG00738.hp1 others(23): Show |
intron_variant | MODIFIER | c.654-5114delT | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 6/11 | chr4 | 102937412 | ||||||
| chr4:102937412
|
TAA | T | 179 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0036others(176): Show | 180 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(177): Show |
intron_variant | MODIFIER | c.654-5115_654-5114d others(4): Show |
SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 6/11 | chr4 | 102937412 | ||||||
| chr4:102937412
|
TAAA | T | 8 | a0001c0001t0001g0002a0001c0001t0001g0168a0001c0001t0001g0209others(5): Show | 8 | HG00323.hp1 HG01069.hp1 HG01074.hp1 others(5): Show |
intron_variant | MODIFIER | c.654-5116_654-5114d others(5): Show |
SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 6/11 | chr4 | 102937412 | ||||||
| chr4:102937437
|
A | C | 1 | a0001c0001t0001g0214 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.654-5138T>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 6/11 | chr4 | 102937437 | ||||||
| chr4:102937492
|
T | C | 1 | a0001c0001t0001g0302 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.654-5193A>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 6/11 | chr4 | 102937492 | ||||||
| chr4:102937723
|
C | CA | 36 | a0001c0001t0001g0007a0001c0001t0001g0026a0001c0001t0001g0039others(33): Show | 36 | HG00735.hp2 HG01261.hp1 HG01361.hp1 others(33): Show |
intron_variant | MODIFIER | c.654-5425dupT | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 6/11 | chr4 | 102937723 | ||||||
| chr4:102937723
|
CA | C | 133 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0036others(130): Show | 134 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(131): Show |
intron_variant | MODIFIER | c.654-5425delT | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 6/11 | chr4 | 102937723 | ||||||
| chr4:102937924
|
G | A | 197 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(194): Show | 198 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.654-5625C>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 6/11 | chr4 | 102937924 | ||||||
| chr4:102938135
|
C | G | 197 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(194): Show | 198 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.654-5836G>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 6/11 | chr4 | 102938135 | ||||||
| chr4:102938137
|
T | C | 1 | a0001c0001t0001g0047 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.654-5838A>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 6/11 | chr4 | 102938137 | ||||||
| chr4:102938241
|
T | C | 1 | a0001c0001t0001g0179 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.654-5942A>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 6/11 | chr4 | 102938241 | ||||||
| chr4:102938244
|
A | G | 197 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(194): Show | 198 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.654-5945T>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 6/11 | chr4 | 102938244 | ||||||
| chr4:102938381
|
A | G | 144 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(141): Show | 145 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(142): Show |
intron_variant | MODIFIER | c.654-6082T>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 6/11 | chr4 | 102938381 | ||||||
| chr4:102938388
|
C | T | 1 | a0001c0001t0001g0220 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.654-6089G>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 6/11 | chr4 | 102938388 | ||||||
| chr4:102938422
|
G | A | 1 | a0001c0001t0001g0108 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.654-6123C>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 6/11 | chr4 | 102938422 | ||||||
| chr4:102938648
|
G | A | 197 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(194): Show | 198 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.654-6349C>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 6/11 | chr4 | 102938648 | ||||||
| chr4:102938686
|
C | T | 1 | a0001c0001t0001g0119 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.654-6387G>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 6/11 | chr4 | 102938686 | ||||||
| chr4:102938720
|
C | T | 1 | a0001c0001t0001g0271 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.654-6421G>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 6/11 | chr4 | 102938720 | ||||||
| chr4:102938852
|
C | T | 13 | a0001c0001t0001g0112a0001c0001t0001g0226a0001c0001t0001g0227others(10): Show | 13 | HG00735.hp2 HG01884.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.653+6341G>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 6/11 | chr4 | 102938852 | ||||||
| chr4:102939130
|
C | G | 1 | a0001c0001t0001g0289 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.653+6063G>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 6/11 | chr4 | 102939130 | ||||||
| chr4:102939209
|
G | A | 1 | a0001c0001t0001g0315 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.653+5984C>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 6/11 | chr4 | 102939209 | ||||||
| chr4:102939406
|
C | CA | 187 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(184): Show | 188 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(185): Show |
intron_variant | MODIFIER | c.653+5786dupT | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 6/11 | chr4 | 102939406 | ||||||
| chr4:102939406
|
C | CAA | 12 | a0001c0001t0001g0114a0001c0001t0001g0138a0001c0001t0001g0157others(9): Show | 12 | HG00597.hp1 HG00738.hp2 HG01361.hp2 others(9): Show |
intron_variant | MODIFIER | c.653+5785_653+5786d others(4): Show |
SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 6/11 | chr4 | 102939406 | ||||||
| chr4:102939406
|
CA | C | 8 | a0001c0001t0001g0062a0001c0001t0001g0069a0001c0001t0001g0071others(5): Show | 8 | NA18747.hp2 NA18941.hp2 NA18969.hp2 others(5): Show |
intron_variant | MODIFIER | c.653+5786delT | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 6/11 | chr4 | 102939406 | ||||||
| chr4:102939598
|
C | T | 1 | a0001c0001t0001g0035 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.653+5595G>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 6/11 | chr4 | 102939598 | ||||||
| chr4:102939687
|
A | T | 1 | a0001c0001t0001g0060 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.653+5506T>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 6/11 | chr4 | 102939687 | ||||||
| chr4:102939718
|
G | C | 1 | a0001c0001t0001g0080 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.653+5475C>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 6/11 | chr4 | 102939718 | ||||||
| chr4:102940101
|
A | C | 4 | a0001c0001t0001g0046a0001c0001t0001g0048a0001c0001t0001g0070others(1): Show | 4 | NA18946.hp2 NA18979.hp1 NA19058.hp2 others(1): Show |
intron_variant | MODIFIER | c.653+5092T>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 6/11 | chr4 | 102940101 | ||||||
| chr4:102940223
|
A | G | 210 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(207): Show | 211 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.653+4970T>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 6/11 | chr4 | 102940223 | ||||||
| chr4:102940263
|
A | G | 1 | a0001c0001t0001g0176 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.653+4930T>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 6/11 | chr4 | 102940263 | ||||||
| chr4:102940283
|
G | C | 1 | a0001c0001t0001g0256 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.653+4910C>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 6/11 | chr4 | 102940283 | ||||||
| chr4:102940395
|
G | A | 1 | a0001c0001t0001g0246 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.653+4798C>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 6/11 | chr4 | 102940395 | ||||||
| chr4:102940408
|
T | C | 1 | a0001c0001t0001g0174 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.653+4785A>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 6/11 | chr4 | 102940408 | ||||||
| chr4:102940467
|
C | G | 32 | a0001c0001t0001g0241a0001c0001t0001g0243a0001c0001t0001g0244others(29): Show | 32 | HG00140.hp2 HG00639.hp1 HG00738.hp2 others(29): Show |
intron_variant | MODIFIER | c.653+4726G>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 6/11 | chr4 | 102940467 | ||||||
| chr4:102940527
|
A | C | 197 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(194): Show | 198 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.653+4666T>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 6/11 | chr4 | 102940527 | ||||||
| chr4:102940554
|
T | C | 1 | a0001c0001t0001g0008 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.653+4639A>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 6/11 | chr4 | 102940554 | ||||||
| chr4:102940625
|
A | G | 1 | a0001c0001t0001g0206 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.653+4568T>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 6/11 | chr4 | 102940625 | ||||||
| chr4:102940651
|
G | T | 1 | a0001c0001t0001g0040 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.653+4542C>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 6/11 | chr4 | 102940651 | ||||||
| chr4:102940671
|
T | C | 1 | a0001c0001t0001g0012 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.653+4522A>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 6/11 | chr4 | 102940671 | ||||||
| chr4:102940858
|
A | G | 1 | a0001c0001t0001g0061 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.653+4335T>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 6/11 | chr4 | 102940858 | ||||||
| chr4:102940889
|
C | T | 1 | a0001c0001t0001g0211 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.653+4304G>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 6/11 | chr4 | 102940889 | ||||||
| chr4:102940972
|
C | A | 197 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(194): Show | 198 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.653+4221G>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 6/11 | chr4 | 102940972 | ||||||
| chr4:102941116
|
C | T | 1 | a0001c0001t0001g0276 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.653+4077G>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 6/11 | chr4 | 102941116 | ||||||
| chr4:102941411
|
A | G | 3 | a0001c0001t0001g0236a0001c0001t0001g0237a0001c0001t0001g0238 | 3 | HG02486.hp1 HG02818.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.653+3782T>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 6/11 | chr4 | 102941411 | ||||||
| chr4:102941413
|
T | C | 1 | a0001c0001t0001g0315 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.653+3780A>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 6/11 | chr4 | 102941413 | ||||||
| chr4:102941635
|
G | A | 197 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(194): Show | 198 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.653+3558C>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 6/11 | chr4 | 102941635 | ||||||
| chr4:102941639
|
C | CA | 9 | a0001c0001t0001g0009a0001c0001t0001g0021a0001c0001t0001g0033others(6): Show | 9 | HG01169.hp1 HG01261.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.653+3553dupT | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 6/11 | chr4 | 102941639 | ||||||
| chr4:102941639
|
CA | C | 17 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0069others(14): Show | 17 | HG00735.hp2 HG01884.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.653+3553delT | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 6/11 | chr4 | 102941639 | ||||||
| chr4:102941639
|
CAA | C | 13 | a0001c0001t0001g0001a0001c0001t0001g0122a0001c0001t0001g0149others(10): Show | 14 | HG00323.hp1 HG01192.hp1 HG01257.hp1 others(11): Show |
intron_variant | MODIFIER | c.653+3552_653+3553d others(4): Show |
SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 6/11 | chr4 | 102941639 | ||||||
| chr4:102941639
|
CAAA | C | 136 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0036others(133): Show | 136 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(133): Show |
intron_variant | MODIFIER | c.653+3551_653+3553d others(5): Show |
SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 6/11 | chr4 | 102941639 | ||||||
| chr4:102941639
|
CAAAA | C | 48 | a0001c0001t0001g0111a0001c0001t0001g0118a0001c0001t0001g0128others(45): Show | 48 | HG00140.hp2 HG00438.hp2 HG00639.hp1 others(45): Show |
intron_variant | MODIFIER | c.653+3550_653+3553d others(6): Show |
SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 6/11 | chr4 | 102941639 | ||||||
| chr4:102941654
|
A | C | 1 | a0001c0001t0001g0284 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.653+3539T>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 6/11 | chr4 | 102941654 | ||||||
| chr4:102941664
|
C | CGA | 197 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(194): Show | 198 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.653+3527_653+3528d others(4): Show |
SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 6/11 | chr4 | 102941664 | ||||||
| chr4:102941697
|
G | A | 316 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(313): Show | 317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.653+3496C>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 6/11 | chr4 | 102941697 | ||||||
| chr4:102941770
|
C | T | 13 | a0001c0001t0001g0112a0001c0001t0001g0226a0001c0001t0001g0227others(10): Show | 13 | HG00735.hp2 HG01884.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.653+3423G>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 6/11 | chr4 | 102941770 | ||||||
| chr4:102941869
|
T | C | 13 | a0001c0001t0001g0112a0001c0001t0001g0226a0001c0001t0001g0227others(10): Show | 13 | HG00735.hp2 HG01884.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.653+3324A>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 6/11 | chr4 | 102941869 | ||||||
| chr4:102941895
|
T | C | 1 | a0001c0001t0001g0059 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.653+3298A>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 6/11 | chr4 | 102941895 | ||||||
| chr4:102942000
|
G | C | 3 | a0001c0001t0001g0273a0001c0001t0001g0274a0001c0001t0001g0275 | 3 | HG02818.hp2 HG03486.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.653+3193C>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 6/11 | chr4 | 102942000 | ||||||
| chr4:102942012
|
G | A | 3 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0001g0313 | 3 | HG01496.hp1 NA19009.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.653+3181C>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 6/11 | chr4 | 102942012 | ||||||
| chr4:102942019
|
G | T | 44 | a0001c0001t0001g0111a0001c0001t0001g0221a0001c0001t0001g0241others(41): Show | 44 | HG00140.hp2 HG00438.hp2 HG00639.hp1 others(41): Show |
intron_variant | MODIFIER | c.653+3174C>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 6/11 | chr4 | 102942019 | ||||||
| chr4:102942033
|
G | A | 197 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(194): Show | 198 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.653+3160C>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 6/11 | chr4 | 102942033 | ||||||
| chr4:102942116
|
C | T | 4 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0001g0183others(1): Show | 4 | HG01496.hp1 HG02738.hp1 NA19009.hp2 others(1): Show |
intron_variant | MODIFIER | c.653+3077G>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 6/11 | chr4 | 102942116 | ||||||
| chr4:102942360
|
G | A | 1 | a0001c0001t0001g0016 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.653+2833C>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 6/11 | chr4 | 102942360 | ||||||
| chr4:102942533
|
G | C | 1 | a0001c0001t0001g0008 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.653+2660C>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 6/11 | chr4 | 102942533 | ||||||
| chr4:102943080
|
C | T | 1 | a0001c0001t0001g0304 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.653+2113G>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 6/11 | chr4 | 102943080 | ||||||
| chr4:102943158
|
C | CA | 5 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0001g0224others(2): Show | 5 | HG00099.hp1 HG01192.hp1 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.653+2034dupT | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 6/11 | chr4 | 102943158 | ||||||
| chr4:102943158
|
C | CAA | 15 | a0001c0001t0001g0002a0001c0001t0001g0239a0001c0001t0001g0240others(12): Show | 15 | HG01109.hp1 HG01175.hp2 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.653+2033_653+2034d others(4): Show |
SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 6/11 | chr4 | 102943158 | ||||||
| chr4:102943166
|
T | A | 21 | a0001c0001t0001g0002a0001c0001t0001g0222a0001c0001t0001g0223others(18): Show | 21 | HG00099.hp1 HG01109.hp1 HG01175.hp2 others(18): Show |
intron_variant | MODIFIER | c.653+2027A>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 6/11 | chr4 | 102943166 | ||||||
| chr4:102943166
|
T | TA | 166 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0036others(163): Show | 167 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.653+2026dupT | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 6/11 | chr4 | 102943166 | ||||||
| chr4:102943270
|
G | T | 1 | a0001c0001t0001g0102 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.653+1923C>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 6/11 | chr4 | 102943270 | ||||||
| chr4:102943418
|
G | A | 1 | a0001c0001t0001g0100 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.653+1775C>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 6/11 | chr4 | 102943418 | ||||||
| chr4:102943502
|
T | TACACACA others(1): Show |
6 | a0001c0001t0001g0257a0001c0001t0001g0279a0001c0001t0001g0282others(3): Show | 6 | HG00099.hp1 HG00140.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.653+1690_653+1691i others(10): Show |
SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 6/11 | chr4 | 102943502 | ||||||
| chr4:102943502
|
T | TACACACA others(3): Show |
14 | a0001c0001t0001g0002a0001c0001t0001g0239a0001c0001t0001g0240others(11): Show | 14 | HG01109.hp1 HG01175.hp2 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.653+1690_653+1691i others(12): Show |
SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 6/11 | chr4 | 102943502 | ||||||
| chr4:102943503
|
G | A | 197 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(194): Show | 198 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.653+1690C>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 6/11 | chr4 | 102943503 | ||||||
| chr4:102943504
|
T | C | 20 | a0001c0001t0001g0002a0001c0001t0001g0239a0001c0001t0001g0240others(17): Show | 20 | HG00099.hp1 HG00140.hp2 HG01109.hp1 others(17): Show |
intron_variant | MODIFIER | c.653+1689A>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 6/11 | chr4 | 102943504 | ||||||
| chr4:102943504
|
T | TACACACA others(1): Show |
4 | a0001c0001t0001g0253a0001c0001t0001g0254a0001c0001t0001g0256others(1): Show | 4 | HG01261.hp1 HG01943.hp2 HG02004.hp1 others(1): Show |
intron_variant | MODIFIER | c.653+1688_653+1689i others(10): Show |
SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 6/11 | chr4 | 102943504 | ||||||
| chr4:102943504
|
T | TACACACA others(3): Show |
22 | a0001c0001t0001g0221a0001c0001t0001g0241a0001c0001t0001g0243others(19): Show | 22 | HG00438.hp2 HG01069.hp1 HG01071.hp2 others(19): Show |
intron_variant | MODIFIER | c.653+1688_653+1689i others(12): Show |
SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 6/11 | chr4 | 102943504 | ||||||
| chr4:102943504
|
T | TACACACA others(5): Show |
18 | a0001c0001t0001g0111a0001c0001t0001g0175a0001c0001t0001g0242others(15): Show | 18 | HG00639.hp1 HG00738.hp2 HG02056.hp2 others(15): Show |
intron_variant | MODIFIER | c.653+1688_653+1689i others(14): Show |
SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 6/11 | chr4 | 102943504 | ||||||
| chr4:102943504
|
T | TACACACA others(7): Show |
4 | a0001c0001t0001g0236a0001c0001t0001g0246a0001c0001t0001g0296others(1): Show | 4 | HG02523.hp2 HG02818.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.653+1688_653+1689i others(16): Show |
SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 6/11 | chr4 | 102943504 | ||||||
| chr4:102943504
|
T | TACACACA others(9): Show |
2 | a0001c0001t0001g0148a0001c0001t0001g0237 | 2 | HG02486.hp1 NA18969.hp1 |
intron_variant | MODIFIER | c.653+1688_653+1689i others(18): Show |
SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 6/11 | chr4 | 102943504 | ||||||
| chr4:102943506
|
T | C | 71 | a0001c0001t0001g0002a0001c0001t0001g0111a0001c0001t0001g0148others(68): Show | 71 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(68): Show |
intron_variant | MODIFIER | c.653+1687A>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 6/11 | chr4 | 102943506 | ||||||
| chr4:102943506
|
T | TACAC | 10 | a0001c0001t0001g0008a0001c0001t0001g0112a0001c0001t0001g0123others(7): Show | 10 | HG02109.hp2 HG02723.hp1 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.653+1683_653+1686d others(6): Show |
SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 6/11 | chr4 | 102943506 | ||||||
| chr4:102943506
|
T | TACACAC | 9 | a0001c0001t0001g0226a0001c0001t0001g0227a0001c0001t0001g0228others(6): Show | 9 | HG00735.hp2 HG01884.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.653+1681_653+1686d others(8): Show |
SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 6/11 | chr4 | 102943506 | ||||||
| chr4:102943506
|
T | TACACACA others(1): Show |
9 | a0001c0001t0001g0124a0001c0001t0001g0129a0001c0001t0001g0171others(6): Show | 9 | HG01192.hp1 HG02145.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.653+1679_653+1686d others(10): Show |
SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 6/11 | chr4 | 102943506 | ||||||
| chr4:102943506
|
T | TACACACA others(3): Show |
36 | a0001c0001t0001g0121a0001c0001t0001g0130a0001c0001t0001g0131others(33): Show | 36 | HG00323.hp1 HG00621.hp1 HG01099.hp2 others(33): Show |
intron_variant | MODIFIER | c.653+1677_653+1686d others(12): Show |
SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 6/11 | chr4 | 102943506 | ||||||
| chr4:102943506
|
T | TACACACA others(5): Show |
48 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0036others(45): Show | 49 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(46): Show |
intron_variant | MODIFIER | c.653+1675_653+1686d others(14): Show |
SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 6/11 | chr4 | 102943506 | ||||||
| chr4:102943506
|
T | TACACACA others(7): Show |
21 | a0001c0001t0001g0118a0001c0001t0001g0139a0001c0001t0001g0141others(18): Show | 21 | HG00558.hp1 HG01074.hp2 HG02083.hp2 others(18): Show |
intron_variant | MODIFIER | c.653+1673_653+1686d others(16): Show |
SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 6/11 | chr4 | 102943506 | ||||||
| chr4:102943506
|
T | TACACACA others(9): Show |
4 | a0001c0001t0001g0120a0001c0001t0001g0146a0001c0001t0001g0179others(1): Show | 4 | HG02056.hp1 HG02698.hp1 NA18975.hp2 others(1): Show |
intron_variant | MODIFIER | c.653+1671_653+1686d others(18): Show |
SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 6/11 | chr4 | 102943506 | ||||||
| chr4:102943506
|
T | TACACACA others(11): Show |
1 | a0001c0001t0001g0163 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.653+1669_653+1686d others(20): Show |
SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 6/11 | chr4 | 102943506 | ||||||
| chr4:102943506
|
T | TATACACA others(7): Show |
1 | a0001c0001t0001g0166 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.653+1686_653+1687i others(16): Show |
SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 6/11 | chr4 | 102943506 | ||||||
| chr4:102943538
|
C | CACACACA others(6): Show |
1 | a0001c0001t0001g0145 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.653+1654_653+1655i others(15): Show |
SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 6/11 | chr4 | 102943538 | ||||||
| chr4:102943741
|
G | C | 1 | a0001c0001t0001g0171 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.653+1452C>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 6/11 | chr4 | 102943741 | ||||||
| chr4:102944060
|
C | T | 48 | a0001c0001t0001g0111a0001c0001t0001g0221a0001c0001t0001g0241others(45): Show | 48 | HG00140.hp2 HG00438.hp2 HG00639.hp1 others(45): Show |
intron_variant | MODIFIER | c.653+1133G>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 6/11 | chr4 | 102944060 | ||||||
| chr4:102944085
|
T | C | 1 | a0001c0001t0001g0117 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.653+1108A>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 6/11 | chr4 | 102944085 | ||||||
| chr4:102944102
|
A | G | 3 | a0001c0001t0001g0273a0001c0001t0001g0274a0001c0001t0001g0275 | 3 | HG02818.hp2 HG03486.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.653+1091T>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 6/11 | chr4 | 102944102 | ||||||
| chr4:102944188
|
T | C | 2 | a0001c0001t0001g0112a0001c0001t0001g0302 | 2 | HG02109.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.653+1005A>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 6/11 | chr4 | 102944188 | ||||||
| chr4:102944396
|
A | G | 197 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(194): Show | 198 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.653+797T>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 6/11 | chr4 | 102944396 | ||||||
| chr4:102944433
|
T | C | 5 | a0001c0001t0001g0165a0001c0001t0001g0166a0001c0001t0001g0167others(2): Show | 5 | HG00621.hp2 HG02083.hp2 NA18949.hp1 others(2): Show |
intron_variant | MODIFIER | c.653+760A>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 6/11 | chr4 | 102944433 | ||||||
| chr4:102944508
|
G | A | 1 | a0001c0001t0001g0125 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.653+685C>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 6/11 | chr4 | 102944508 | ||||||
| chr4:102944611
|
A | G | 2 | a0001c0001t0001g0162a0001c0001t0001g0163 | 2 | HG01074.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.653+582T>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 6/11 | chr4 | 102944611 | ||||||
| chr4:102944814
|
T | C | 130 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(127): Show | 131 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(128): Show |
intron_variant | MODIFIER | c.653+379A>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 6/11 | chr4 | 102944814 | ||||||
| chr4:102944944
|
G | A | 9 | a0001c0001t0001g0304a0001c0001t0001g0305a0001c0001t0001g0306others(6): Show | 9 | HG01891.hp1 HG02145.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.653+249C>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 6/11 | chr4 | 102944944 | ||||||
| chr4:102945024
|
C | G | 1 | a0001c0001t0001g0273 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.653+169G>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 6/11 | chr4 | 102945024 | ||||||
| chr4:102945025
|
G | A | 3 | a0001c0001t0001g0041a0001c0001t0001g0075a0001c0001t0001g0083 | 3 | NA18943.hp2 NA18952.hp1 NA18978.hp1 |
intron_variant | MODIFIER | c.653+168C>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 6/11 | chr4 | 102945025 | ||||||
| chr4:102945087
|
C | T | 1 | a0001c0001t0001g0066 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.653+106G>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 6/11 | chr4 | 102945087 | ||||||
| chr4:102945323
|
G | A | 197 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(194): Show | 198 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(195): Show |
splice_region_variant&intron_variant | LOW | c.526-3C>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 5/11 | chr4 | 102945323 | ||||||
| chr4:102945638
|
T | A | 1 | a0001c0001t0001g0086 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.526-318A>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 5/11 | chr4 | 102945638 | ||||||
| chr4:102945729
|
C | G | 5 | a0001c0001t0001g0003a0001c0001t0001g0173a0001c0001t0001g0174others(2): Show | 5 | HG02622.hp1 HG02698.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.526-409G>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 5/11 | chr4 | 102945729 | ||||||
| chr4:102945744
|
T | C | 4 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0001g0224others(1): Show | 4 | HG01192.hp1 HG02145.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.526-424A>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 5/11 | chr4 | 102945744 | ||||||
| chr4:102945863
|
T | G | 1 | a0001c0001t0001g0237 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.526-543A>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 5/11 | chr4 | 102945863 | ||||||
| chr4:102945969
|
CA | C | 10 | a0001c0001t0001g0226a0001c0001t0001g0227a0001c0001t0001g0228others(7): Show | 10 | HG00735.hp2 HG01884.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.526-650delT | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 5/11 | chr4 | 102945969 | ||||||
| chr4:102946067
|
T | C | 8 | a0001c0001t0001g0241a0001c0001t0001g0243a0001c0001t0001g0244others(5): Show | 8 | NA18943.hp1 NA18945.hp2 NA18951.hp1 others(5): Show |
intron_variant | MODIFIER | c.525+580A>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 5/11 | chr4 | 102946067 | ||||||
| chr4:102946149
|
T | C | 1 | a0001c0001t0001g0043 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.525+498A>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 5/11 | chr4 | 102946149 | ||||||
| chr4:102946452
|
T | G | 2 | a0001c0001t0001g0236a0001c0001t0001g0237 | 2 | HG02486.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.525+195A>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 5/11 | chr4 | 102946452 | ||||||
| chr4:102946467
|
A | AC | 195 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(192): Show | 196 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.525+179_525+180ins others(1): Show |
SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 5/11 | chr4 | 102946467 | ||||||
| chr4:102947106
|
G | A | 1 | a0001c0001t0001g0100 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.383-317C>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 4/11 | chr4 | 102947106 | ||||||
| chr4:102947233
|
T | C | 4 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(1): Show | 4 | HG01169.hp1 HG01943.hp1 HG01978.hp2 others(1): Show |
intron_variant | MODIFIER | c.383-444A>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 4/11 | chr4 | 102947233 | ||||||
| chr4:102947592
|
G | T | 195 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(192): Show | 196 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.383-803C>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 4/11 | chr4 | 102947592 | ||||||
| chr4:102947643
|
G | A | 1 | a0001c0004t0001g0053 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.383-854C>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 4/11 | chr4 | 102947643 | ||||||
| chr4:102947907
|
T | C | 1 | a0001c0001t0001g0216 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.383-1118A>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 4/11 | chr4 | 102947907 | ||||||
| chr4:102947966
|
A | AGTGATGG others(11): Show |
195 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(192): Show | 196 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.383-1195_383-1178d others(20): Show |
SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 4/11 | chr4 | 102947966 | ||||||
| chr4:102948055
|
A | C | 132 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(129): Show | 133 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(130): Show |
intron_variant | MODIFIER | c.382+1202T>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 4/11 | chr4 | 102948055 | ||||||
| chr4:102948193
|
C | T | 211 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(208): Show | 212 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(209): Show |
intron_variant | MODIFIER | c.382+1064G>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 4/11 | chr4 | 102948193 | ||||||
| chr4:102948294
|
A | G | 2 | a0001c0001t0001g0099a0001c0001t0001g0100 | 2 | HG02132.hp1 NA18950.hp2 |
intron_variant | MODIFIER | c.382+963T>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 4/11 | chr4 | 102948294 | ||||||
| chr4:102948325
|
T | TAC | 82 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(79): Show | 83 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(80): Show |
intron_variant | MODIFIER | c.382+930_382+931dup others(2): Show |
SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 4/11 | chr4 | 102948325 | ||||||
| chr4:102948325
|
T | TACAC | 47 | a0001c0001t0001g0011a0001c0001t0001g0019a0001c0001t0001g0029others(44): Show | 47 | HG00099.hp2 HG00423.hp2 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.382+928_382+931dup others(4): Show |
SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 4/11 | chr4 | 102948325 | ||||||
| chr4:102948325
|
T | TACACAC | 44 | a0001c0001t0001g0022a0001c0001t0001g0037a0001c0001t0001g0071others(41): Show | 44 | HG00280.hp1 HG00423.hp1 HG00597.hp1 others(41): Show |
intron_variant | MODIFIER | c.382+926_382+931dup others(6): Show |
SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 4/11 | chr4 | 102948325 | ||||||
| chr4:102948325
|
T | TACACACA others(1): Show |
8 | a0001c0001t0001g0003a0001c0001t0001g0020a0001c0001t0001g0121others(5): Show | 8 | HG00558.hp1 HG01255.hp1 HG02080.hp2 others(5): Show |
intron_variant | MODIFIER | c.382+924_382+931dup others(8): Show |
SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 4/11 | chr4 | 102948325 | ||||||
| chr4:102948325
|
T | TACACACA others(3): Show |
1 | a0001c0001t0001g0074 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.382+922_382+931dup others(10): Show |
SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 4/11 | chr4 | 102948325 | ||||||
| chr4:102948325
|
T | TACACACA others(5): Show |
2 | a0001c0001t0001g0132a0001c0001t0001g0303 | 2 | HG02630.hp1 NA18988.hp2 |
intron_variant | MODIFIER | c.382+920_382+931dup others(12): Show |
SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 4/11 | chr4 | 102948325 | ||||||
| chr4:102948325
|
TAC | T | 15 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0012others(12): Show | 15 | HG02615.hp1 HG02717.hp2 HG03225.hp1 others(12): Show |
intron_variant | MODIFIER | c.382+930_382+931del others(2): Show |
SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 4/11 | chr4 | 102948325 | ||||||
| chr4:102948366
|
A | ACACG | 13 | a0001c0001t0001g0002a0001c0001t0001g0239a0001c0001t0001g0240others(10): Show | 13 | HG01109.hp1 HG01175.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.382+890_382+891ins others(4): Show |
SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 4/11 | chr4 | 102948366 | ||||||
| chr4:102948366
|
A | G | 1 | a0001c0001t0001g0283 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.382+891T>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 4/11 | chr4 | 102948366 | ||||||
| chr4:102948439
|
A | G | 1 | a0001c0001t0001g0284 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.382+818T>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 4/11 | chr4 | 102948439 | ||||||
| chr4:102948785
|
A | G | 1 | a0001c0001t0001g0015 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.382+472T>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 4/11 | chr4 | 102948785 | ||||||
| chr4:102948903
|
G | C | 208 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(205): Show | 209 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(206): Show |
intron_variant | MODIFIER | c.382+354C>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 4/11 | chr4 | 102948903 | ||||||
| chr4:102948934
|
A | G | 7 | a0001c0001t0001g0117a0001c0001t0001g0119a0001c0001t0001g0122others(4): Show | 7 | HG01069.hp2 HG01891.hp2 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.382+323T>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 4/11 | chr4 | 102948934 | ||||||
| chr4:102949002
|
A | G | 1 | a0001c0001t0001g0116 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.382+255T>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 4/11 | chr4 | 102949002 | ||||||
| chr4:102949557
|
T | G | 5 | a0001c0001t0001g0029a0001c0001t0001g0061a0001c0001t0001g0062others(2): Show | 5 | HG02074.hp1 HG02080.hp1 NA18941.hp2 others(2): Show |
intron_variant | MODIFIER | c.212-130A>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102949557 | ||||||
| chr4:102949674
|
T | C | 1 | a0001c0001t0001g0073 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.212-247A>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102949674 | ||||||
| chr4:102949812
|
T | C | 1 | a0001c0001t0001g0106 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.212-385A>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102949812 | ||||||
| chr4:102949973
|
A | G | 1 | a0001c0001t0001g0061 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.212-546T>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102949973 | ||||||
| chr4:102950000
|
C | T | 1 | a0001c0001t0001g0125 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.212-573G>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102950000 | ||||||
| chr4:102950388
|
G | A | 1 | a0002c0002t0001g0317 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.212-961C>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102950388 | ||||||
| chr4:102950864
|
G | A | 8 | a0001c0001t0001g0117a0001c0001t0001g0119a0001c0001t0001g0122others(5): Show | 8 | HG01069.hp2 HG01496.hp2 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.212-1437C>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102950864 | ||||||
| chr4:102950996
|
AAGAAAAC others(15): Show |
A | 2 | a0001c0001t0001g0233a0001c0001t0001g0235 | 2 | HG03195.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.212-1591_212-1570d others(24): Show |
SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102950996 | ||||||
| chr4:102951186
|
T | C | 195 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(192): Show | 196 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.212-1759A>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102951186 | ||||||
| chr4:102951376
|
T | C | 2 | a0001c0001t0001g0127a0001c0001t0001g0128 | 2 | HG02723.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.212-1949A>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102951376 | ||||||
| chr4:102951421
|
G | A | 212 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(209): Show | 213 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.212-1994C>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102951421 | ||||||
| chr4:102951615
|
C | T | 195 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(192): Show | 196 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.212-2188G>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102951615 | ||||||
| chr4:102951697
|
C | A | 200 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(197): Show | 201 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(198): Show |
intron_variant | MODIFIER | c.212-2270G>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102951697 | ||||||
| chr4:102951944
|
AAGGCAAA others(2499): Show |
A | 195 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(192): Show | 196 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.212-5023_212-2518d others(2): Show |
SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102951944 | ||||||
| chr4:102951958
|
A | ATTTTT | 7 | a0001c0001t0001g0226a0001c0001t0001g0227a0001c0001t0001g0228others(4): Show | 7 | HG00735.hp2 HG01884.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.212-2532_212-2531i others(7): Show |
SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102951958 | ||||||
| chr4:102951960
|
C | CTTTTTTT others(3): Show |
2 | a0001c0001t0001g0012a0001c0001t0001g0027 | 2 | HG02965.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.212-2543_212-2534d others(12): Show |
SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102951960 | ||||||
| chr4:102951960
|
C | CTTTTTTT others(4): Show |
18 | a0001c0001t0001g0008a0001c0001t0001g0017a0001c0001t0001g0034others(15): Show | 18 | HG00323.hp2 HG01943.hp1 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.212-2544_212-2534d others(13): Show |
SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102951960 | ||||||
| chr4:102951960
|
C | CTTTTTTT others(5): Show |
65 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(62): Show | 65 | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(62): Show |
intron_variant | MODIFIER | c.212-2545_212-2534d others(14): Show |
SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102951960 | ||||||
| chr4:102951960
|
C | CTTTTTTT others(6): Show |
17 | a0001c0001t0001g0011a0001c0001t0001g0014a0001c0001t0001g0020others(14): Show | 17 | HG00735.hp1 HG01099.hp1 HG01175.hp1 others(14): Show |
intron_variant | MODIFIER | c.212-2546_212-2534d others(15): Show |
SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102951960 | ||||||
| chr4:102951960
|
C | CTTTTTTT others(7): Show |
2 | a0001c0001t0001g0063a0001c0001t0001g0098 | 2 | HG02074.hp1 HG02080.hp1 |
intron_variant | MODIFIER | c.212-2547_212-2534d others(16): Show |
SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102951960 | ||||||
| chr4:102951960
|
C | T | 8 | a0001c0001t0001g0226a0001c0001t0001g0227a0001c0001t0001g0228others(5): Show | 8 | HG00735.hp2 HG01884.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.212-2533G>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102951960 | ||||||
| chr4:102952303
|
A | C | 3 | a0001c0001t0001g0112a0001c0001t0001g0302a0001c0001t0001g0315 | 3 | HG02109.hp2 HG03209.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.212-2876T>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102952303 | ||||||
| chr4:102952417
|
C | T | 1 | a0001c0001t0001g0016 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.212-2990G>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102952417 | ||||||
| chr4:102952424
|
A | T | 1 | a0001c0001t0001g0020 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.212-2997T>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102952424 | ||||||
| chr4:102952522
|
T | G | 9 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(6): Show | 9 | HG00558.hp2 HG02015.hp2 HG02071.hp1 others(6): Show |
intron_variant | MODIFIER | c.212-3095A>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102952522 | ||||||
| chr4:102952530
|
T | C | 1 | a0002c0002t0001g0317 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.212-3103A>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102952530 | ||||||
| chr4:102952592
|
A | C | 13 | a0001c0001t0001g0112a0001c0001t0001g0226a0001c0001t0001g0227others(10): Show | 13 | HG00735.hp2 HG01884.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.212-3165T>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102952592 | ||||||
| chr4:102952612
|
G | A | 3 | a0001c0001t0001g0112a0001c0001t0001g0302a0001c0001t0001g0315 | 3 | HG02109.hp2 HG03209.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.212-3185C>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102952612 | ||||||
| chr4:102952654
|
C | T | 121 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(118): Show | 121 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(118): Show |
intron_variant | MODIFIER | c.212-3227G>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102952654 | ||||||
| chr4:102952797
|
G | A | 1 | a0001c0001t0001g0233 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.212-3370C>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102952797 | ||||||
| chr4:102953392
|
A | G | 1 | a0001c0001t0001g0049 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.212-3965T>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102953392 | ||||||
| chr4:102953630
|
G | C | 13 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0086others(10): Show | 13 | HG00735.hp2 HG01884.hp2 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.212-4203C>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102953630 | ||||||
| chr4:102953862
|
A | G | 4 | a0001c0001t0001g0069a0001c0001t0001g0071a0001c0001t0001g0072others(1): Show | 4 | NA18969.hp2 NA18988.hp1 NA19002.hp1 others(1): Show |
intron_variant | MODIFIER | c.212-4435T>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102953862 | ||||||
| chr4:102953879
|
G | A | 10 | a0001c0001t0001g0226a0001c0001t0001g0227a0001c0001t0001g0228others(7): Show | 10 | HG00735.hp2 HG01884.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.212-4452C>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102953879 | ||||||
| chr4:102953948
|
T | C | 1 | a0001c0001t0001g0229 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.212-4521A>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102953948 | ||||||
| chr4:102954049
|
T | C | 13 | a0001c0001t0001g0112a0001c0001t0001g0226a0001c0001t0001g0227others(10): Show | 13 | HG00735.hp2 HG01884.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.212-4622A>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102954049 | ||||||
| chr4:102954641
|
A | G | 1 | a0001c0001t0001g0227 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.212-5214T>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102954641 | ||||||
| chr4:102954855
|
T | C | 10 | a0001c0001t0001g0226a0001c0001t0001g0227a0001c0001t0001g0228others(7): Show | 10 | HG00735.hp2 HG01884.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.212-5428A>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102954855 | ||||||
| chr4:102955130
|
C | T | 208 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(205): Show | 209 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(206): Show |
intron_variant | MODIFIER | c.212-5703G>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102955130 | ||||||
| chr4:102955235
|
G | C | 6 | a0001c0001t0001g0123a0001c0001t0001g0126a0001c0001t0001g0127others(3): Show | 6 | HG02723.hp1 HG02809.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.212-5808C>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102955235 | ||||||
| chr4:102955360
|
T | C | 1 | a0001c0001t0001g0122 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.212-5933A>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102955360 | ||||||
| chr4:102955432
|
A | G | 3 | a0001c0001t0001g0112a0001c0001t0001g0302a0001c0001t0001g0315 | 3 | HG02109.hp2 HG03209.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.212-6005T>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102955432 | ||||||
| chr4:102955457
|
A | G | 208 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(205): Show | 209 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(206): Show |
intron_variant | MODIFIER | c.212-6030T>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102955457 | ||||||
| chr4:102955550
|
G | T | 1 | a0001c0001t0001g0315 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.212-6123C>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102955550 | ||||||
| chr4:102955757
|
A | G | 9 | a0001c0001t0001g0304a0001c0001t0001g0305a0001c0001t0001g0306others(6): Show | 9 | HG01891.hp1 HG02145.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.212-6330T>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102955757 | ||||||
| chr4:102955796
|
AAG | A | 3 | a0001c0001t0001g0251a0001c0001t0001g0280a0001c0001t0001g0281 | 3 | HG02559.hp1 HG03471.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.212-6371_212-6370d others(4): Show |
SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102955796 | ||||||
| chr4:102955841
|
GAGAGAAA others(27): Show |
G | 2 | a0001c0001t0001g0112a0001c0001t0001g0302 | 2 | HG02109.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.212-6448_212-6415d others(36): Show |
SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102955841 | ||||||
| chr4:102955843
|
G | GAGAA | 29 | a0001c0001t0001g0011a0001c0001t0001g0020a0001c0001t0001g0025others(26): Show | 29 | HG00099.hp1 HG00323.hp2 HG00558.hp1 others(26): Show |
intron_variant | MODIFIER | c.212-6420_212-6417d others(6): Show |
SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102955843 | ||||||
| chr4:102955843
|
G | GAGAAAGA others(1): Show |
9 | a0001c0001t0001g0059a0001c0001t0001g0108a0001c0001t0001g0128others(6): Show | 9 | HG00639.hp2 HG01258.hp2 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.212-6424_212-6417d others(10): Show |
SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102955843 | ||||||
| chr4:102955843
|
G | GAGAAAGA others(5): Show |
1 | a0001c0001t0001g0270 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.212-6428_212-6417d others(14): Show |
SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102955843 | ||||||
| chr4:102955843
|
G | GAGAAAGA others(9): Show |
1 | a0001c0001t0001g0060 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.212-6432_212-6417d others(18): Show |
SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102955843 | ||||||
| chr4:102955843
|
G | GAGAAGAA others(4): Show |
1 | a0001c0001t0001g0300 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.212-6417_212-6416i others(13): Show |
SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102955843 | ||||||
| chr4:102955843
|
GAGAA | G | 29 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0008others(26): Show | 29 | HG00140.hp1 HG00735.hp2 HG01168.hp1 others(26): Show |
intron_variant | MODIFIER | c.212-6420_212-6417d others(6): Show |
SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102955843 | ||||||
| chr4:102955843
|
GAGAAAGA others(1): Show |
G | 3 | a0001c0001t0001g0029a0001c0001t0001g0067a0001c0001t0001g0101 | 3 | HG03831.hp1 NA18954.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.212-6424_212-6417d others(10): Show |
SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102955843 | ||||||
| chr4:102955843
|
GAGAAAGA others(5): Show |
G | 3 | a0001c0001t0001g0228a0001c0001t0001g0232a0001c0001t0001g0234 | 3 | HG01884.hp2 HG02717.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.212-6428_212-6417d others(14): Show |
SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102955843 | ||||||
| chr4:102955847
|
A | G | 2 | a0001c0001t0001g0127a0001c0001t0001g0249 | 2 | HG06807.hp1 NA18945.hp2 |
intron_variant | MODIFIER | c.212-6420T>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102955847 | ||||||
| chr4:102955879
|
AAGAAAGA others(17): Show |
A | 1 | a0001c0001t0001g0305 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.212-6476_212-6453d others(26): Show |
SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102955879 | ||||||
| chr4:102955883
|
AAGAAAGA others(13): Show |
A | 10 | a0001c0001t0001g0286a0001c0001t0001g0287a0001c0001t0001g0304others(7): Show | 10 | HG01891.hp1 HG02145.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.212-6476_212-6457d others(22): Show |
SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102955883 | ||||||
| chr4:102955887
|
AAGAAAGA others(9): Show |
A | 8 | a0001c0001t0001g0002a0001c0001t0001g0187a0001c0001t0001g0239others(5): Show | 8 | HG01109.hp1 HG02572.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.212-6476_212-6461d others(18): Show |
SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102955887 | ||||||
| chr4:102955891
|
AAGAAAGA others(5): Show |
A | 8 | a0001c0001t0001g0160a0001c0001t0001g0178a0001c0001t0001g0236others(5): Show | 8 | HG01175.hp2 HG01884.hp1 HG01975.hp2 others(5): Show |
intron_variant | MODIFIER | c.212-6476_212-6465d others(14): Show |
SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102955891 | ||||||
| chr4:102955895
|
AAGAAAGA others(1): Show |
A | 33 | a0001c0001t0001g0111a0001c0001t0001g0114a0001c0001t0001g0116others(30): Show | 33 | HG00323.hp1 HG00438.hp2 HG00609.hp2 others(30): Show |
intron_variant | MODIFIER | c.212-6476_212-6469d others(10): Show |
SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102955895 | ||||||
| chr4:102955899
|
A | AAGAAAG | 5 | a0001c0001t0001g0069a0001c0001t0001g0071a0001c0001t0001g0072others(2): Show | 5 | NA18969.hp2 NA18988.hp1 NA19002.hp1 others(2): Show |
intron_variant | MODIFIER | c.212-6473_212-6472i others(8): Show |
SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102955899 | ||||||
| chr4:102955899
|
A | AAGAAAGA others(3): Show |
1 | a0001c0001t0001g0084 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.212-6473_212-6472i others(12): Show |
SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102955899 | ||||||
| chr4:102955899
|
A | AAGAAAGA others(5): Show |
6 | a0001c0001t0001g0037a0001c0001t0001g0052a0001c0001t0001g0079others(3): Show | 6 | HG00609.hp1 HG03491.hp2 HG03492.hp1 others(3): Show |
intron_variant | MODIFIER | c.212-6473_212-6472i others(14): Show |
SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102955899 | ||||||
| chr4:102955899
|
A | AAGAAAGA others(1): Show |
9 | a0001c0001t0001g0035a0001c0001t0001g0042a0001c0001t0001g0049others(6): Show | 9 | HG02135.hp2 HG02738.hp2 HG03688.hp2 others(6): Show |
intron_variant | MODIFIER | c.212-6473_212-6472i others(10): Show |
SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102955899 | ||||||
| chr4:102955899
|
A | AAGAG | 15 | a0001c0001t0001g0019a0001c0001t0001g0031a0001c0001t0001g0032others(12): Show | 15 | HG01169.hp1 HG01192.hp2 HG01943.hp1 others(12): Show |
intron_variant | MODIFIER | c.212-6476_212-6473d others(6): Show |
SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102955899 | ||||||
| chr4:102955899
|
A | G | 16 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0013others(13): Show | 16 | HG00438.hp1 HG00597.hp2 HG00738.hp1 others(13): Show |
intron_variant | MODIFIER | c.212-6472T>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102955899 | ||||||
| chr4:102955899
|
AAGAG | A | 48 | a0001c0001t0001g0003a0001c0001t0001g0117a0001c0001t0001g0121others(45): Show | 48 | HG00280.hp1 HG01069.hp1 HG01071.hp2 others(45): Show |
intron_variant | MODIFIER | c.212-6476_212-6473d others(6): Show |
SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102955899 | ||||||
| chr4:102955903
|
G | A | 87 | a0001c0001t0001g0001a0001c0001t0001g0113a0001c0001t0001g0115others(84): Show | 88 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(85): Show |
intron_variant | MODIFIER | c.212-6476C>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102955903 | ||||||
| chr4:102955907
|
G | A | 1 | a0001c0001t0001g0243 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.212-6480C>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102955907 | ||||||
| chr4:102955909
|
A | G | 1 | a0001c0001t0001g0036 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.212-6482T>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102955909 | ||||||
| chr4:102955979
|
G | T | 195 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(192): Show | 196 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.212-6552C>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102955979 | ||||||
| chr4:102956033
|
T | G | 3 | a0001c0001t0001g0236a0001c0001t0001g0237a0001c0001t0001g0238 | 3 | HG02486.hp1 HG02818.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.212-6606A>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102956033 | ||||||
| chr4:102956074
|
C | T | 1 | a0001c0001t0001g0125 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.212-6647G>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102956074 | ||||||
| chr4:102956217
|
C | T | 1 | a0001c0001t0001g0267 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.212-6790G>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102956217 | ||||||
| chr4:102956314
|
TA | T | 187 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0111others(184): Show | 188 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(185): Show |
intron_variant | MODIFIER | c.212-6888delT | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102956314 | ||||||
| chr4:102956314
|
TAA | T | 11 | a0001c0001t0001g0134a0001c0001t0001g0159a0001c0001t0001g0160others(8): Show | 11 | HG01192.hp1 HG01975.hp2 HG01978.hp1 others(8): Show |
intron_variant | MODIFIER | c.212-6889_212-6888d others(4): Show |
SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102956314 | ||||||
| chr4:102956394
|
C | T | 1 | a0001c0001t0001g0296 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.212-6967G>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102956394 | ||||||
| chr4:102956834
|
T | C | 195 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(192): Show | 196 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.212-7407A>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102956834 | ||||||
| chr4:102957010
|
C | T | 195 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(192): Show | 196 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.212-7583G>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102957010 | ||||||
| chr4:102957243
|
A | G | 1 | a0001c0001t0001g0315 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.212-7816T>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102957243 | ||||||
| chr4:102957331
|
A | G | 45 | a0001c0001t0001g0111a0001c0001t0001g0221a0001c0001t0001g0241others(42): Show | 45 | HG00140.hp2 HG00438.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.212-7904T>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102957331 | ||||||
| chr4:102957366
|
C | T | 10 | a0001c0001t0001g0226a0001c0001t0001g0227a0001c0001t0001g0228others(7): Show | 10 | HG00735.hp2 HG01884.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.212-7939G>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102957366 | ||||||
| chr4:102957501
|
C | G | 1 | a0001c0001t0001g0012 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.212-8074G>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102957501 | ||||||
| chr4:102957720
|
C | T | 196 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(193): Show | 197 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.212-8293G>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102957720 | ||||||
| chr4:102957722
|
G | T | 1 | a0001c0001t0001g0108 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.212-8295C>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102957722 | ||||||
| chr4:102957780
|
A | G | 8 | a0001c0001t0001g0304a0001c0001t0001g0305a0001c0001t0001g0306others(5): Show | 8 | HG01891.hp1 HG02145.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.212-8353T>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102957780 | ||||||
| chr4:102957782
|
A | ATG | 4 | a0001c0001t0001g0010a0001c0001t0001g0082a0001c0001t0001g0170others(1): Show | 4 | HG00438.hp1 HG01496.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.212-8357_212-8356d others(4): Show |
SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102957782 | ||||||
| chr4:102957786
|
G | A | 1 | a0001c0001t0001g0308 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.212-8359C>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102957786 | ||||||
| chr4:102957922
|
C | T | 11 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0126others(8): Show | 11 | HG02572.hp1 HG02717.hp2 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.212-8495G>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102957922 | ||||||
| chr4:102957991
|
C | T | 195 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(192): Show | 196 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.212-8564G>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102957991 | ||||||
| chr4:102958135
|
A | G | 4 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0197others(1): Show | 4 | HG01168.hp2 HG01169.hp2 HG01934.hp1 others(1): Show |
intron_variant | MODIFIER | c.212-8708T>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102958135 | ||||||
| chr4:102958255
|
G | A | 52 | a0001c0001t0001g0114a0001c0001t0001g0118a0001c0001t0001g0120others(49): Show | 52 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(49): Show |
intron_variant | MODIFIER | c.212-8828C>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102958255 | ||||||
| chr4:102958304
|
C | T | 1 | a0001c0001t0001g0161 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.212-8877G>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102958304 | ||||||
| chr4:102958332
|
C | T | 1 | a0001c0001t0001g0043 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.212-8905G>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102958332 | ||||||
| chr4:102958354
|
C | A | 195 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(192): Show | 196 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.212-8927G>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102958354 | ||||||
| chr4:102958383
|
C | T | 2 | a0001c0001t0001g0199a0001c0001t0001g0209 | 2 | HG00323.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.212-8956G>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102958383 | ||||||
| chr4:102958499
|
A | G | 1 | a0001c0001t0001g0209 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.212-9072T>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102958499 | ||||||
| chr4:102958648
|
C | T | 10 | a0001c0001t0001g0226a0001c0001t0001g0227a0001c0001t0001g0228others(7): Show | 10 | HG00735.hp2 HG01884.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.212-9221G>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102958648 | ||||||
| chr4:102958689
|
G | A | 9 | a0001c0001t0001g0138a0001c0001t0001g0152a0001c0001t0001g0153others(6): Show | 9 | HG01168.hp2 HG01169.hp2 HG01934.hp1 others(6): Show |
intron_variant | MODIFIER | c.212-9262C>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102958689 | ||||||
| chr4:102958779
|
C | T | 2 | a0001c0001t0001g0019a0001c0001t0001g0022 | 2 | HG00738.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.212-9352G>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102958779 | ||||||
| chr4:102958781
|
G | A | 3 | a0001c0001t0001g0272a0001c0001t0001g0282a0001c0001t0001g0291 | 3 | HG00099.hp1 HG02723.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.212-9354C>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102958781 | ||||||
| chr4:102959087
|
A | C | 13 | a0001c0001t0001g0112a0001c0001t0001g0226a0001c0001t0001g0227others(10): Show | 13 | HG00735.hp2 HG01884.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.212-9660T>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102959087 | ||||||
| chr4:102959225
|
CAT | C | 3 | a0001c0001t0001g0063a0001c0001t0001g0240a0001c0001t0001g0256 | 3 | HG01943.hp2 HG02080.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.212-9800_212-9799d others(4): Show |
SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102959225 | ||||||
| chr4:102959225
|
CATAT | C | 9 | a0001c0001t0001g0304a0001c0001t0001g0305a0001c0001t0001g0306others(6): Show | 9 | HG01891.hp1 HG02145.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.212-9802_212-9799d others(6): Show |
SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102959225 | ||||||
| chr4:102959235
|
T | C | 1 | a0001c0001t0001g0020 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.212-9808A>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102959235 | ||||||
| chr4:102959235
|
TAC | T | 184 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(181): Show | 185 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.212-9810_212-9809d others(4): Show |
SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102959235 | ||||||
| chr4:102959237
|
C | T | 11 | a0001c0001t0001g0203a0001c0001t0001g0226a0001c0001t0001g0227others(8): Show | 11 | HG00735.hp2 HG01884.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.212-9810G>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102959237 | ||||||
| chr4:102959239
|
C | T | 46 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0113others(43): Show | 47 | HG00423.hp2 HG00597.hp1 HG00609.hp2 others(44): Show |
intron_variant | MODIFIER | c.212-9812G>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102959239 | ||||||
| chr4:102959294
|
T | C | 195 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(192): Show | 196 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.212-9867A>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102959294 | ||||||
| chr4:102959530
|
TA | T | 48 | a0001c0001t0001g0111a0001c0001t0001g0221a0001c0001t0001g0241others(45): Show | 48 | HG00140.hp2 HG00438.hp2 HG00639.hp1 others(45): Show |
intron_variant | MODIFIER | c.212-10104delT | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102959530 | ||||||
| chr4:102959554
|
G | C | 117 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0113others(114): Show | 118 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(115): Show |
intron_variant | MODIFIER | c.212-10127C>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102959554 | ||||||
| chr4:102959623
|
A | G | 1 | a0001c0001t0001g0090 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.212-10196T>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102959623 | ||||||
| chr4:102959663
|
C | T | 1 | a0001c0001t0001g0022 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.212-10236G>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102959663 | ||||||
| chr4:102959677
|
G | T | 13 | a0001c0001t0001g0112a0001c0001t0001g0226a0001c0001t0001g0227others(10): Show | 13 | HG00735.hp2 HG01884.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.212-10250C>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102959677 | ||||||
| chr4:102959729
|
TGGCTGGT others(5): Show |
T | 1 | a0001c0001t0001g0042 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.212-10314_212-1030 others(16): Show |
SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102959729 | ||||||
| chr4:102959922
|
G | A | 195 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(192): Show | 196 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.212-10495C>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102959922 | ||||||
| chr4:102960203
|
T | TTA | 191 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(188): Show | 192 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.212-10778_212-1077 others(6): Show |
SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102960203 | ||||||
| chr4:102960203
|
T | TTATA | 4 | a0001c0001t0001g0236a0001c0001t0001g0237a0001c0001t0001g0238others(1): Show | 4 | HG02486.hp1 HG02818.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.212-10780_212-1077 others(8): Show |
SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102960203 | ||||||
| chr4:102960368
|
G | T | 1 | a0001c0001t0001g0089 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.212-10941C>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102960368 | ||||||
| chr4:102960419
|
A | T | 10 | a0001c0001t0001g0226a0001c0001t0001g0227a0001c0001t0001g0228others(7): Show | 10 | HG00735.hp2 HG01884.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.212-10992T>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102960419 | ||||||
| chr4:102960575
|
T | G | 1 | a0001c0001t0001g0121 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.212-11148A>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102960575 | ||||||
| chr4:102960665
|
G | C | 1 | a0001c0001t0001g0003 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.212-11238C>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102960665 | ||||||
| chr4:102960806
|
C | T | 3 | a0001c0001t0001g0272a0001c0001t0001g0282a0001c0001t0001g0291 | 3 | HG00099.hp1 HG02723.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.212-11379G>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102960806 | ||||||
| chr4:102960973
|
C | A | 195 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(192): Show | 196 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.212-11546G>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102960973 | ||||||
| chr4:102960974
|
C | T | 195 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(192): Show | 196 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.212-11547G>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102960974 | ||||||
| chr4:102961049
|
A | C | 195 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(192): Show | 196 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.212-11622T>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102961049 | ||||||
| chr4:102961209
|
A | G | 1 | a0001c0001t0001g0203 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.212-11782T>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102961209 | ||||||
| chr4:102961210
|
G | A | 1 | a0001c0001t0001g0203 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.212-11783C>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102961210 | ||||||
| chr4:102961313
|
T | C | 128 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(125): Show | 129 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(126): Show |
intron_variant | MODIFIER | c.212-11886A>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102961313 | ||||||
| chr4:102961355
|
T | G | 1 | a0001c0001t0001g0066 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.212-11928A>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102961355 | ||||||
| chr4:102961380
|
A | G | 1 | a0001c0001t0001g0008 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.212-11953T>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102961380 | ||||||
| chr4:102961386
|
G | A | 1 | a0001c0001t0001g0265 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.212-11959C>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102961386 | ||||||
| chr4:102961621
|
A | C | 312 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(309): Show | 313 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(310): Show |
intron_variant | MODIFIER | c.212-12194T>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102961621 | ||||||
| chr4:102961721
|
C | T | 45 | a0001c0001t0001g0111a0001c0001t0001g0221a0001c0001t0001g0241others(42): Show | 45 | HG00140.hp2 HG00438.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.212-12294G>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102961721 | ||||||
| chr4:102961886
|
G | C | 1 | a0001c0001t0001g0180 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.212-12459C>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102961886 | ||||||
| chr4:102961913
|
G | A | 2 | a0001c0001t0001g0161a0001c0001t0001g0303 | 2 | HG02630.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.212-12486C>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102961913 | ||||||
| chr4:102962086
|
C | T | 1 | a0001c0001t0001g0303 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.212-12659G>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102962086 | ||||||
| chr4:102962159
|
G | A | 1 | a0001c0001t0001g0136 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.212-12732C>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102962159 | ||||||
| chr4:102962267
|
A | G | 1 | a0001c0001t0001g0128 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.212-12840T>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102962267 | ||||||
| chr4:102962418
|
G | C | 1 | a0001c0001t0001g0006 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.212-12991C>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102962418 | ||||||
| chr4:102962451
|
A | G | 45 | a0001c0001t0001g0111a0001c0001t0001g0221a0001c0001t0001g0241others(42): Show | 45 | HG00140.hp2 HG00438.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.212-13024T>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102962451 | ||||||
| chr4:102963166
|
G | T | 1 | a0001c0001t0001g0115 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.212-13739C>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102963166 | ||||||
| chr4:102963502
|
C | T | 3 | a0001c0001t0001g0112a0001c0001t0001g0302a0001c0001t0001g0315 | 3 | HG02109.hp2 HG03209.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.212-14075G>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102963502 | ||||||
| chr4:102963510
|
GT | G | 51 | a0001c0001t0001g0111a0001c0001t0001g0221a0001c0001t0001g0241others(48): Show | 51 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(48): Show |
intron_variant | MODIFIER | c.212-14084delA | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102963510 | ||||||
| chr4:102963564
|
C | T | 1 | a0001c0001t0001g0012 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.212-14137G>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102963564 | ||||||
| chr4:102963607
|
A | G | 1 | a0001c0001t0001g0315 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.212-14180T>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102963607 | ||||||
| chr4:102963692
|
C | T | 2 | a0001c0001t0001g0262a0001c0001t0001g0263 | 2 | NA18950.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.212-14265G>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102963692 | ||||||
| chr4:102963775
|
C | G | 13 | a0001c0001t0001g0112a0001c0001t0001g0226a0001c0001t0001g0227others(10): Show | 13 | HG00735.hp2 HG01884.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.212-14348G>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102963775 | ||||||
| chr4:102964173
|
T | C | 8 | a0001c0001t0001g0117a0001c0001t0001g0119a0001c0001t0001g0122others(5): Show | 8 | HG01069.hp2 HG01496.hp2 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.212-14746A>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102964173 | ||||||
| chr4:102964347
|
C | T | 200 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(197): Show | 201 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(198): Show |
intron_variant | MODIFIER | c.212-14920G>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102964347 | ||||||
| chr4:102964399
|
T | TA | 10 | a0001c0001t0001g0226a0001c0001t0001g0227a0001c0001t0001g0228others(7): Show | 10 | HG00735.hp2 HG01884.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.212-14973dupT | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102964399 | ||||||
| chr4:102964411
|
T | G | 204 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(201): Show | 205 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(202): Show |
intron_variant | MODIFIER | c.212-14984A>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102964411 | ||||||
| chr4:102964634
|
G | C | 3 | a0001c0001t0001g0112a0001c0001t0001g0302a0001c0001t0001g0315 | 3 | HG02109.hp2 HG03209.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.212-15207C>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102964634 | ||||||
| chr4:102965261
|
C | T | 195 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(192): Show | 196 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.212-15834G>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102965261 | ||||||
| chr4:102965265
|
A | T | 195 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(192): Show | 196 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.212-15838T>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102965265 | ||||||
| chr4:102965336
|
C | T | 3 | a0001c0001t0001g0236a0001c0001t0001g0237a0001c0001t0001g0238 | 3 | HG02486.hp1 HG02818.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.212-15909G>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102965336 | ||||||
| chr4:102965481
|
T | C | 5 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0091others(2): Show | 5 | HG02451.hp2 HG02486.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.212-16054A>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102965481 | ||||||
| chr4:102965505
|
C | G | 10 | a0001c0001t0001g0226a0001c0001t0001g0227a0001c0001t0001g0228others(7): Show | 10 | HG00735.hp2 HG01884.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.212-16078G>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102965505 | ||||||
| chr4:102965527
|
C | T | 18 | a0001c0001t0001g0002a0001c0001t0001g0239a0001c0001t0001g0240others(15): Show | 18 | HG00099.hp1 HG01109.hp1 HG01175.hp2 others(15): Show |
intron_variant | MODIFIER | c.212-16100G>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102965527 | ||||||
| chr4:102965540
|
A | G | 1 | a0001c0001t0001g0171 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.212-16113T>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102965540 | ||||||
| chr4:102965773
|
C | T | 1 | a0001c0001t0001g0217 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.212-16346G>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102965773 | ||||||
| chr4:102965784
|
TA | T | 206 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(203): Show | 207 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.212-16358delT | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102965784 | ||||||
| chr4:102965917
|
G | C | 208 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(205): Show | 209 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(206): Show |
intron_variant | MODIFIER | c.212-16490C>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102965917 | ||||||
| chr4:102965934
|
T | C | 6 | a0001c0001t0001g0123a0001c0001t0001g0126a0001c0001t0001g0127others(3): Show | 6 | HG02723.hp1 HG02809.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.212-16507A>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102965934 | ||||||
| chr4:102965969
|
C | T | 1 | a0001c0001t0001g0315 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.212-16542G>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102965969 | ||||||
| chr4:102966148
|
G | T | 3 | a0001c0001t0001g0112a0001c0001t0001g0302a0001c0001t0001g0315 | 3 | HG02109.hp2 HG03209.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.212-16721C>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102966148 | ||||||
| chr4:102966174
|
G | A | 195 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(192): Show | 196 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.212-16747C>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102966174 | ||||||
| chr4:102966235
|
C | T | 2 | a0001c0001t0001g0112a0001c0001t0001g0302 | 2 | HG02109.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.212-16808G>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102966235 | ||||||
| chr4:102966396
|
G | A | 10 | a0001c0001t0001g0226a0001c0001t0001g0227a0001c0001t0001g0228others(7): Show | 10 | HG00735.hp2 HG01884.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.212-16969C>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102966396 | ||||||
| chr4:102966404
|
G | C | 195 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(192): Show | 196 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.212-16977C>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102966404 | ||||||
| chr4:102966985
|
C | A | 3 | a0001c0001t0001g0236a0001c0001t0001g0237a0001c0001t0001g0238 | 3 | HG02486.hp1 HG02818.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.212-17558G>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102966985 | ||||||
| chr4:102966987
|
A | G | 1 | a0001c0001t0001g0027 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.212-17560T>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102966987 | ||||||
| chr4:102967096
|
A | C | 195 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(192): Show | 196 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.212-17669T>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102967096 | ||||||
| chr4:102967138
|
C | A | 13 | a0001c0001t0001g0112a0001c0001t0001g0226a0001c0001t0001g0227others(10): Show | 13 | HG00735.hp2 HG01884.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.212-17711G>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102967138 | ||||||
| chr4:102967286
|
C | T | 1 | a0001c0001t0001g0176 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.212-17859G>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102967286 | ||||||
| chr4:102967365
|
C | T | 2 | a0001c0001t0001g0236a0001c0001t0001g0237 | 2 | HG02486.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.212-17938G>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102967365 | ||||||
| chr4:102967411
|
G | A | 3 | a0001c0001t0001g0272a0001c0001t0001g0282a0001c0001t0001g0291 | 3 | HG00099.hp1 HG02723.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.212-17984C>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102967411 | ||||||
| chr4:102967591
|
G | A | 1 | a0001c0001t0001g0285 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.212-18164C>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102967591 | ||||||
| chr4:102967760
|
A | G | 9 | a0001c0001t0001g0304a0001c0001t0001g0305a0001c0001t0001g0306others(6): Show | 9 | HG01891.hp1 HG02145.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.212-18333T>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102967760 | ||||||
| chr4:102967812
|
A | G | 1 | a0001c0001t0001g0012 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.212-18385T>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102967812 | ||||||
| chr4:102967828
|
A | T | 45 | a0001c0001t0001g0111a0001c0001t0001g0221a0001c0001t0001g0241others(42): Show | 45 | HG00140.hp2 HG00438.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.212-18401T>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102967828 | ||||||
| chr4:102968044
|
A | C | 1 | a0001c0001t0001g0001 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.212-18617T>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102968044 | ||||||
| chr4:102968117
|
C | A | 3 | a0001c0001t0001g0112a0001c0001t0001g0302a0001c0001t0001g0315 | 3 | HG02109.hp2 HG03209.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.212-18690G>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102968117 | ||||||
| chr4:102968155
|
T | G | 1 | a0001c0001t0001g0022 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.212-18728A>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102968155 | ||||||
| chr4:102968169
|
G | C | 5 | a0001c0001t0001g0029a0001c0001t0001g0061a0001c0001t0001g0062others(2): Show | 5 | HG02074.hp1 HG02080.hp1 NA18941.hp2 others(2): Show |
intron_variant | MODIFIER | c.212-18742C>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102968169 | ||||||
| chr4:102968380
|
A | G | 208 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(205): Show | 209 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(206): Show |
intron_variant | MODIFIER | c.212-18953T>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102968380 | ||||||
| chr4:102968404
|
A | G | 1 | a0001c0001t0001g0282 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.212-18977T>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102968404 | ||||||
| chr4:102968434
|
C | G | 1 | a0001c0001t0001g0180 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.212-19007G>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102968434 | ||||||
| chr4:102968582
|
A | C | 1 | a0001c0001t0001g0306 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.212-19155T>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102968582 | ||||||
| chr4:102968657
|
G | T | 195 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(192): Show | 196 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.212-19230C>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102968657 | ||||||
| chr4:102968817
|
G | A | 1 | a0001c0001t0001g0017 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.212-19390C>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102968817 | ||||||
| chr4:102968897
|
G | A | 1 | a0001c0001t0001g0148 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.212-19470C>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102968897 | ||||||
| chr4:102968908
|
C | T | 195 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(192): Show | 196 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.212-19481G>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102968908 | ||||||
| chr4:102969100
|
G | T | 2 | a0001c0001t0001g0095a0001c0001t0001g0096 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.212-19673C>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102969100 | ||||||
| chr4:102969201
|
C | T | 312 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(309): Show | 313 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(310): Show |
intron_variant | MODIFIER | c.212-19774G>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102969201 | ||||||
| chr4:102969273
|
T | G | 208 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(205): Show | 209 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(206): Show |
intron_variant | MODIFIER | c.212-19846A>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102969273 | ||||||
| chr4:102969292
|
G | A | 195 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(192): Show | 196 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.212-19865C>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102969292 | ||||||
| chr4:102969603
|
G | A | 10 | a0001c0001t0001g0226a0001c0001t0001g0227a0001c0001t0001g0228others(7): Show | 10 | HG00735.hp2 HG01884.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.212-20176C>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102969603 | ||||||
| chr4:102969751
|
G | C | 1 | a0001c0001t0001g0022 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.211+20049C>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102969751 | ||||||
| chr4:102969823
|
T | C | 212 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(209): Show | 213 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.211+19977A>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102969823 | ||||||
| chr4:102969872
|
T | C | 1 | a0001c0001t0001g0194 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.211+19928A>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102969872 | ||||||
| chr4:102969946
|
T | TA | 10 | a0001c0001t0001g0164a0001c0001t0001g0304a0001c0001t0001g0305others(7): Show | 10 | HG01891.hp1 HG02145.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.211+19853dupT | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102969946 | ||||||
| chr4:102970022
|
T | A | 1 | a0001c0001t0001g0134 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.211+19778A>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102970022 | ||||||
| chr4:102970077
|
CAGG | C | 3 | a0001c0001t0001g0272a0001c0001t0001g0282a0001c0001t0001g0291 | 3 | HG00099.hp1 HG02723.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.211+19720_211+1972 others(7): Show |
SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102970077 | ||||||
| chr4:102970130
|
AC | A | 3 | a0001c0001t0001g0251a0001c0001t0001g0280a0001c0001t0001g0281 | 3 | HG02559.hp1 HG03471.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.211+19669delG | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102970130 | ||||||
| chr4:102970264
|
A | G | 2 | a0001c0001t0001g0112a0001c0001t0001g0302 | 2 | HG02109.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.211+19536T>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102970264 | ||||||
| chr4:102970317
|
G | C | 51 | a0001c0001t0001g0111a0001c0001t0001g0221a0001c0001t0001g0241others(48): Show | 51 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(48): Show |
intron_variant | MODIFIER | c.211+19483C>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102970317 | ||||||
| chr4:102970339
|
T | A | 1 | a0001c0001t0001g0120 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.211+19461A>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102970339 | ||||||
| chr4:102970583
|
C | T | 1 | a0001c0001t0001g0291 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.211+19217G>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102970583 | ||||||
| chr4:102970677
|
A | G | 1 | a0001c0001t0001g0199 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.211+19123T>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102970677 | ||||||
| chr4:102970717
|
A | T | 13 | a0001c0001t0001g0112a0001c0001t0001g0226a0001c0001t0001g0227others(10): Show | 13 | HG00735.hp2 HG01884.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.211+19083T>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102970717 | ||||||
| chr4:102970820
|
A | C | 1 | a0001c0001t0001g0220 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.211+18980T>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102970820 | ||||||
| chr4:102970996
|
T | C | 1 | a0001c0001t0001g0184 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.211+18804A>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102970996 | ||||||
| chr4:102971084
|
C | G | 1 | a0001c0001t0001g0041 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.211+18716G>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102971084 | ||||||
| chr4:102971225
|
C | T | 10 | a0001c0001t0001g0226a0001c0001t0001g0227a0001c0001t0001g0228others(7): Show | 10 | HG00735.hp2 HG01884.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.211+18575G>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102971225 | ||||||
| chr4:102971445
|
A | G | 3 | a0001c0001t0001g0112a0001c0001t0001g0302a0001c0001t0001g0315 | 3 | HG02109.hp2 HG03209.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.211+18355T>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102971445 | ||||||
| chr4:102971626
|
A | G | 1 | a0001c0001t0001g0296 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.211+18174T>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102971626 | ||||||
| chr4:102971666
|
T | C | 208 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(205): Show | 209 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(206): Show |
intron_variant | MODIFIER | c.211+18134A>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102971666 | ||||||
| chr4:102971710
|
T | C | 1 | a0001c0001t0001g0277 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.211+18090A>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102971710 | ||||||
| chr4:102971754
|
A | G | 10 | a0001c0001t0001g0226a0001c0001t0001g0227a0001c0001t0001g0228others(7): Show | 10 | HG00735.hp2 HG01884.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.211+18046T>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102971754 | ||||||
| chr4:102971925
|
T | C | 212 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(209): Show | 213 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.211+17875A>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102971925 | ||||||
| chr4:102972000
|
T | G | 4 | a0001c0001t0001g0076a0001c0001t0002g0018a0001c0001t0002g0077others(1): Show | 4 | NA18946.hp2 NA18957.hp2 NA18980.hp1 others(1): Show |
intron_variant | MODIFIER | c.211+17800A>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102972000 | ||||||
| chr4:102972221
|
C | T | 1 | a0001c0001t0001g0086 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.211+17579G>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102972221 | ||||||
| chr4:102972232
|
A | C | 1 | a0001c0001t0001g0235 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.211+17568T>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102972232 | ||||||
| chr4:102972303
|
G | A | 10 | a0001c0001t0001g0226a0001c0001t0001g0227a0001c0001t0001g0228others(7): Show | 10 | HG00735.hp2 HG01884.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.211+17497C>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102972303 | ||||||
| chr4:102972399
|
C | A | 48 | a0001c0001t0001g0111a0001c0001t0001g0221a0001c0001t0001g0241others(45): Show | 48 | HG00140.hp2 HG00438.hp2 HG00639.hp1 others(45): Show |
intron_variant | MODIFIER | c.211+17401G>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102972399 | ||||||
| chr4:102972413
|
T | C | 2 | a0001c0001t0001g0236a0001c0001t0001g0237 | 2 | HG02486.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.211+17387A>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102972413 | ||||||
| chr4:102972451
|
G | A | 10 | a0001c0001t0001g0226a0001c0001t0001g0227a0001c0001t0001g0228others(7): Show | 10 | HG00735.hp2 HG01884.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.211+17349C>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102972451 | ||||||
| chr4:102972487
|
C | G | 1 | a0002c0002t0001g0316 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.211+17313G>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102972487 | ||||||
| chr4:102972524
|
G | A | 4 | a0001c0001t0001g0103a0001c0001t0001g0104a0001c0001t0001g0109others(1): Show | 4 | NA18962.hp2 NA18970.hp1 NA18975.hp1 others(1): Show |
intron_variant | MODIFIER | c.211+17276C>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102972524 | ||||||
| chr4:102972674
|
G | A | 1 | a0001c0001t0001g0280 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.211+17126C>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102972674 | ||||||
| chr4:102972745
|
T | G | 1 | a0001c0001t0001g0315 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.211+17055A>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102972745 | ||||||
| chr4:102972856
|
T | C | 1 | a0001c0001t0001g0312 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.211+16944A>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102972856 | ||||||
| chr4:102972886
|
G | A | 1 | a0001c0001t0001g0280 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.211+16914C>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102972886 | ||||||
| chr4:102972991
|
T | A | 1 | a0001c0001t0001g0227 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.211+16809A>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102972991 | ||||||
| chr4:102973149
|
T | A | 2 | a0001c0001t0001g0200a0001c0001t0001g0212 | 2 | NA18991.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.211+16651A>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102973149 | ||||||
| chr4:102973356
|
T | C | 2 | a0001c0001t0001g0127a0001c0001t0001g0128 | 2 | HG02723.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.211+16444A>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102973356 | ||||||
| chr4:102973399
|
T | C | 1 | a0001c0001t0001g0235 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.211+16401A>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102973399 | ||||||
| chr4:102973598
|
G | T | 1 | a0001c0001t0001g0003 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.211+16202C>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102973598 | ||||||
| chr4:102973921
|
G | A | 1 | a0001c0001t0001g0295 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.211+15879C>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102973921 | ||||||
| chr4:102973995
|
G | T | 1 | a0001c0001t0001g0039 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.211+15805C>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102973995 | ||||||
| chr4:102974011
|
G | A | 1 | a0001c0001t0001g0194 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.211+15789C>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102974011 | ||||||
| chr4:102974025
|
C | T | 1 | a0001c0001t0001g0242 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.211+15775G>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102974025 | ||||||
| chr4:102974066
|
A | G | 208 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(205): Show | 209 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(206): Show |
intron_variant | MODIFIER | c.211+15734T>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102974066 | ||||||
| chr4:102974159
|
C | T | 3 | a0001c0001t0001g0120a0001c0001t0001g0139a0001c0001t0001g0192 | 3 | HG00558.hp1 NA18983.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.211+15641G>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102974159 | ||||||
| chr4:102974160
|
T | G | 195 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(192): Show | 196 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.211+15640A>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102974160 | ||||||
| chr4:102974240
|
T | TAA | 7 | a0001c0001t0001g0236a0001c0001t0001g0237a0001c0001t0001g0241others(4): Show | 7 | HG00639.hp1 HG01109.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.211+15559_211+1556 others(6): Show |
SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102974240 | ||||||
| chr4:102974240
|
T | TAAA | 60 | a0001c0001t0001g0002a0001c0001t0001g0111a0001c0001t0001g0130others(57): Show | 60 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(57): Show |
intron_variant | MODIFIER | c.211+15559_211+1556 others(7): Show |
SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102974240 | ||||||
| chr4:102974240
|
T | TAAAA | 79 | a0001c0001t0001g0003a0001c0001t0001g0115a0001c0001t0001g0117others(76): Show | 79 | HG00438.hp2 HG00558.hp1 HG00597.hp1 others(76): Show |
intron_variant | MODIFIER | c.211+15559_211+1556 others(8): Show |
SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102974240 | ||||||
| chr4:102974240
|
T | TAAAAA | 34 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0116others(31): Show | 34 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(31): Show |
intron_variant | MODIFIER | c.211+15559_211+1556 others(9): Show |
SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102974240 | ||||||
| chr4:102974240
|
T | TAAAAAA | 15 | a0001c0001t0001g0001a0001c0001t0001g0134a0001c0001t0001g0136others(12): Show | 16 | HG01071.hp1 HG01257.hp1 HG01258.hp1 others(13): Show |
intron_variant | MODIFIER | c.211+15559_211+1556 others(10): Show |
SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102974240 | ||||||
| chr4:102974241
|
T | A | 195 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(192): Show | 196 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.211+15559A>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102974241 | ||||||
| chr4:102974241
|
TGAAAAAA others(2): Show |
T | 10 | a0001c0001t0001g0226a0001c0001t0001g0227a0001c0001t0001g0228others(7): Show | 10 | HG00735.hp2 HG01884.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.211+15550_211+1555 others(13): Show |
SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102974241 | ||||||
| chr4:102974242
|
G | A | 199 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(196): Show | 200 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.211+15558C>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102974242 | ||||||
| chr4:102974242
|
G | GA | 10 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0013others(7): Show | 10 | HG00438.hp1 HG00597.hp2 HG01981.hp2 others(7): Show |
intron_variant | MODIFIER | c.211+15557dupT | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102974242 | ||||||
| chr4:102974242
|
GA | G | 18 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(15): Show | 18 | HG00558.hp2 HG01099.hp1 HG02071.hp1 others(15): Show |
intron_variant | MODIFIER | c.211+15557delT | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102974242 | ||||||
| chr4:102974407
|
A | G | 208 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(205): Show | 209 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(206): Show |
intron_variant | MODIFIER | c.211+15393T>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102974407 | ||||||
| chr4:102974636
|
T | C | 1 | a0001c0001t0001g0086 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.211+15164A>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102974636 | ||||||
| chr4:102974679
|
C | T | 3 | a0001c0001t0001g0236a0001c0001t0001g0237a0001c0001t0001g0238 | 3 | HG02486.hp1 HG02818.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.211+15121G>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102974679 | ||||||
| chr4:102974952
|
C | T | 208 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(205): Show | 209 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(206): Show |
intron_variant | MODIFIER | c.211+14848G>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102974952 | ||||||
| chr4:102975235
|
T | C | 1 | a0001c0001t0001g0174 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.211+14565A>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102975235 | ||||||
| chr4:102975256
|
A | T | 195 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(192): Show | 196 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.211+14544T>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102975256 | ||||||
| chr4:102975434
|
G | A | 1 | a0001c0001t0001g0277 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.211+14366C>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102975434 | ||||||
| chr4:102975550
|
T | C | 10 | a0001c0001t0001g0226a0001c0001t0001g0227a0001c0001t0001g0228others(7): Show | 10 | HG00735.hp2 HG01884.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.211+14250A>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102975550 | ||||||
| chr4:102975565
|
C | CAT | 5 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(2): Show | 5 | HG00609.hp1 HG02132.hp1 HG03017.hp2 others(2): Show |
intron_variant | MODIFIER | c.211+14233_211+1423 others(6): Show |
SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102975565 | ||||||
| chr4:102975565
|
CAT | C | 3 | a0001c0001t0001g0012a0001c0001t0001g0021a0001c0001t0001g0232 | 3 | HG01261.hp2 HG02886.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.211+14233_211+1423 others(6): Show |
SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102975565 | ||||||
| chr4:102975567
|
T | TATAC | 3 | a0001c0001t0001g0131a0001c0001t0001g0272a0001c0001t0001g0280 | 3 | HG02015.hp1 NA19030.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.211+14232_211+1423 others(8): Show |
SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102975567 | ||||||
| chr4:102975569
|
T | TAC | 14 | a0001c0001t0001g0241a0001c0001t0001g0251a0001c0001t0001g0261others(11): Show | 14 | HG00438.hp2 HG01975.hp1 HG02056.hp2 others(11): Show |
intron_variant | MODIFIER | c.211+14230_211+1423 others(6): Show |
SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102975569 | ||||||
| chr4:102975571
|
T | C | 177 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(174): Show | 178 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.211+14229A>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102975571 | ||||||
| chr4:102975582
|
A | T | 1 | a0001c0001t0001g0235 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.211+14218T>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102975582 | ||||||
| chr4:102975584
|
A | ATTT | 3 | a0001c0001t0001g0121a0001c0001t0001g0245a0001c0001t0001g0250 | 3 | HG03654.hp2 NA19004.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.211+14215_211+1421 others(7): Show |
SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102975584 | ||||||
| chr4:102975584
|
A | ATTTT | 10 | a0001c0001t0001g0003a0001c0001t0001g0154a0001c0001t0001g0174others(7): Show | 10 | HG00280.hp1 HG01168.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.211+14215_211+1421 others(8): Show |
SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102975584 | ||||||
| chr4:102975584
|
A | ATTTTT | 21 | a0001c0001t0001g0002a0001c0001t0001g0086a0001c0001t0001g0120others(18): Show | 21 | HG00323.hp1 HG00558.hp1 HG01074.hp2 others(18): Show |
intron_variant | MODIFIER | c.211+14215_211+1421 others(9): Show |
SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102975584 | ||||||
| chr4:102975584
|
A | ATTTTTT | 7 | a0001c0001t0001g0114a0001c0001t0001g0126a0001c0001t0001g0138others(4): Show | 7 | HG01361.hp2 HG02622.hp1 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.211+14215_211+1421 others(10): Show |
SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102975584 | ||||||
| chr4:102975584
|
A | ATTTTTTT | 12 | a0001c0001t0001g0123a0001c0001t0001g0128a0001c0001t0001g0149others(9): Show | 12 | HG00621.hp1 HG02071.hp2 HG02132.hp2 others(9): Show |
intron_variant | MODIFIER | c.211+14215_211+1421 others(11): Show |
SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102975584 | ||||||
| chr4:102975584
|
A | ATTTTTTT others(1): Show |
17 | a0001c0001t0001g0113a0001c0001t0001g0116a0001c0001t0001g0125others(14): Show | 17 | HG00423.hp1 HG00423.hp2 HG00609.hp2 others(14): Show |
intron_variant | MODIFIER | c.211+14215_211+1421 others(12): Show |
SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102975584 | ||||||
| chr4:102975584
|
A | ATTTTTTT others(4): Show |
2 | a0001c0001t0001g0158a0001c0001t0001g0183 | 2 | HG02738.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.211+14215_211+1421 others(15): Show |
SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102975584 | ||||||
| chr4:102975584
|
A | T | 13 | a0001c0001t0001g0115a0001c0001t0001g0157a0001c0001t0001g0175others(10): Show | 13 | HG00597.hp1 HG00735.hp2 HG01515.hp2 others(10): Show |
intron_variant | MODIFIER | c.211+14216T>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102975584 | ||||||
| chr4:102975586
|
A | AT | 10 | a0001c0001t0001g0013a0001c0001t0001g0027a0001c0001t0001g0031others(7): Show | 10 | HG00597.hp2 HG01169.hp1 HG01943.hp1 others(7): Show |
intron_variant | MODIFIER | c.211+14213dupA | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102975586 | ||||||
| chr4:102975586
|
A | ATATTTTT others(3): Show |
1 | a0001c0001t0001g0213 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.211+14213_211+1421 others(14): Show |
SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102975586 | ||||||
| chr4:102975586
|
A | ATTT | 22 | a0001c0001t0001g0111a0001c0001t0001g0141a0001c0001t0001g0221others(19): Show | 22 | HG00140.hp2 HG00639.hp1 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.211+14211_211+1421 others(7): Show |
SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102975586 | ||||||
| chr4:102975586
|
A | ATTTT | 12 | a0001c0001t0001g0140a0001c0001t0001g0252a0001c0001t0001g0253others(9): Show | 12 | HG01069.hp1 HG01071.hp2 HG01074.hp1 others(9): Show |
intron_variant | MODIFIER | c.211+14210_211+1421 others(8): Show |
SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102975586 | ||||||
| chr4:102975586
|
A | ATTTTT | 11 | a0001c0001t0001g0132a0001c0001t0001g0133a0001c0001t0001g0176others(8): Show | 11 | HG01255.hp1 HG02080.hp2 HG02165.hp2 others(8): Show |
intron_variant | MODIFIER | c.211+14209_211+1421 others(9): Show |
SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102975586 | ||||||
| chr4:102975586
|
A | ATTTTTT | 7 | a0001c0001t0001g0117a0001c0001t0001g0124a0001c0001t0001g0180others(4): Show | 7 | HG01192.hp1 HG02145.hp2 HG03540.hp2 others(4): Show |
intron_variant | MODIFIER | c.211+14208_211+1421 others(10): Show |
SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102975586 | ||||||
| chr4:102975586
|
A | ATTTTTTT | 10 | a0001c0001t0001g0119a0001c0001t0001g0122a0001c0001t0001g0129others(7): Show | 10 | HG01069.hp2 HG01496.hp1 HG01496.hp2 others(7): Show |
intron_variant | MODIFIER | c.211+14207_211+1421 others(11): Show |
SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102975586 | ||||||
| chr4:102975586
|
A | ATTTTTTT others(1): Show |
8 | a0001c0001t0001g0136a0001c0001t0001g0165a0001c0001t0001g0166others(5): Show | 8 | HG00621.hp2 HG01071.hp1 HG02083.hp2 others(5): Show |
intron_variant | MODIFIER | c.211+14206_211+1421 others(12): Show |
SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102975586 | ||||||
| chr4:102975586
|
A | T | 108 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0012others(105): Show | 108 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(105): Show |
intron_variant | MODIFIER | c.211+14214T>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102975586 | ||||||
| chr4:102975586
|
ATTTTT | A | 9 | a0001c0001t0001g0304a0001c0001t0001g0305a0001c0001t0001g0306others(6): Show | 9 | HG01891.hp1 HG02145.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.211+14209_211+1421 others(9): Show |
SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102975586 | ||||||
| chr4:102975587
|
T | TA | 6 | a0001c0001t0001g0010a0001c0001t0001g0068a0001c0001t0001g0069others(3): Show | 6 | HG00438.hp1 HG04184.hp2 NA18747.hp2 others(3): Show |
intron_variant | MODIFIER | c.211+14212_211+1421 others(5): Show |
SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102975587 | ||||||
| chr4:102975588
|
T | A | 10 | a0001c0001t0001g0016a0001c0001t0001g0070a0001c0001t0001g0071others(7): Show | 10 | HG01099.hp1 HG02818.hp2 HG03486.hp1 others(7): Show |
intron_variant | MODIFIER | c.211+14212A>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102975588 | ||||||
| chr4:102975589
|
T | A | 1 | a0001c0001t0001g0074 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.211+14211A>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102975589 | ||||||
| chr4:102975593
|
T | A | 1 | a0001c0001t0001g0309 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.211+14207A>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102975593 | ||||||
| chr4:102975621
|
G | T | 1 | a0001c0001t0001g0102 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.211+14179C>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102975621 | ||||||
| chr4:102975634
|
A | C | 209 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(206): Show | 210 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.211+14166T>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102975634 | ||||||
| chr4:102976084
|
A | C | 1 | a0001c0001t0001g0266 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.211+13716T>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102976084 | ||||||
| chr4:102976120
|
T | G | 1 | a0001c0005t0001g0205 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.211+13680A>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102976120 | ||||||
| chr4:102976130
|
T | C | 1 | a0001c0001t0001g0308 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.211+13670A>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102976130 | ||||||
| chr4:102976549
|
T | C | 1 | a0001c0001t0001g0235 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.211+13251A>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102976549 | ||||||
| chr4:102976818
|
A | G | 48 | a0001c0001t0001g0111a0001c0001t0001g0221a0001c0001t0001g0241others(45): Show | 48 | HG00140.hp2 HG00438.hp2 HG00639.hp1 others(45): Show |
intron_variant | MODIFIER | c.211+12982T>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102976818 | ||||||
| chr4:102976938
|
C | G | 4 | a0001c0001t0001g0157a0001c0001t0001g0202a0001c0001t0001g0203others(1): Show | 4 | HG00597.hp1 NA18984.hp1 NA19005.hp2 others(1): Show |
intron_variant | MODIFIER | c.211+12862G>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102976938 | ||||||
| chr4:102976939
|
A | G | 208 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(205): Show | 209 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(206): Show |
intron_variant | MODIFIER | c.211+12861T>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102976939 | ||||||
| chr4:102977009
|
A | C | 208 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(205): Show | 209 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(206): Show |
intron_variant | MODIFIER | c.211+12791T>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102977009 | ||||||
| chr4:102977025
|
C | A | 1 | a0001c0001t0001g0161 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.211+12775G>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102977025 | ||||||
| chr4:102977161
|
A | G | 3 | a0001c0001t0001g0236a0001c0001t0001g0237a0001c0001t0001g0238 | 3 | HG02486.hp1 HG02818.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.211+12639T>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102977161 | ||||||
| chr4:102977269
|
G | A | 1 | a0001c0001t0001g0075 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.211+12531C>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102977269 | ||||||
| chr4:102977297
|
TA | T | 8 | a0001c0001t0001g0027a0001c0001t0001g0030a0001c0001t0001g0085others(5): Show | 8 | HG00735.hp1 HG01168.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.211+12502delT | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102977297 | ||||||
| chr4:102977297
|
TAAA | T | 24 | a0001c0001t0001g0112a0001c0001t0001g0132a0001c0001t0001g0133others(21): Show | 24 | HG00558.hp1 HG00735.hp2 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.211+12500_211+1250 others(7): Show |
SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102977297 | ||||||
| chr4:102977297
|
TAAAA | T | 174 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(171): Show | 175 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(172): Show |
intron_variant | MODIFIER | c.211+12499_211+1250 others(8): Show |
SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102977297 | ||||||
| chr4:102977297
|
TAAAAA | T | 10 | a0001c0001t0001g0126a0001c0001t0001g0147a0001c0001t0001g0184others(7): Show | 10 | HG00099.hp1 HG01358.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.211+12498_211+1250 others(9): Show |
SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102977297 | ||||||
| chr4:102977308
|
A | G | 2 | a0001c0001t0001g0112a0001c0001t0001g0302 | 2 | HG02109.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.211+12492T>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102977308 | ||||||
| chr4:102977724
|
G | A | 1 | a0001c0001t0001g0169 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.211+12076C>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102977724 | ||||||
| chr4:102977915
|
G | A | 1 | a0001c0001t0001g0012 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.211+11885C>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102977915 | ||||||
| chr4:102977942
|
A | C | 2 | a0001c0001t0001g0227a0001c0001t0001g0230 | 2 | HG02615.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.211+11858T>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102977942 | ||||||
| chr4:102977991
|
A | T | 1 | a0001c0001t0001g0008 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.211+11809T>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102977991 | ||||||
| chr4:102978012
|
T | C | 1 | a0001c0001t0001g0026 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.211+11788A>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102978012 | ||||||
| chr4:102978078
|
G | A | 4 | a0001c0001t0001g0076a0001c0001t0002g0018a0001c0001t0002g0077others(1): Show | 4 | NA18946.hp2 NA18957.hp2 NA18980.hp1 others(1): Show |
intron_variant | MODIFIER | c.211+11722C>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102978078 | ||||||
| chr4:102978110
|
C | T | 1 | a0001c0001t0001g0303 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.211+11690G>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102978110 | ||||||
| chr4:102978255
|
G | A | 2 | a0001c0001t0001g0002a0001c0001t0001g0263 | 2 | HG01109.hp1 NA18950.hp1 |
intron_variant | MODIFIER | c.211+11545C>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102978255 | ||||||
| chr4:102978353
|
G | T | 51 | a0001c0001t0001g0111a0001c0001t0001g0221a0001c0001t0001g0241others(48): Show | 51 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(48): Show |
intron_variant | MODIFIER | c.211+11447C>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102978353 | ||||||
| chr4:102978797
|
G | A | 52 | a0001c0001t0001g0114a0001c0001t0001g0118a0001c0001t0001g0120others(49): Show | 52 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(49): Show |
intron_variant | MODIFIER | c.211+11003C>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102978797 | ||||||
| chr4:102978844
|
T | C | 1 | a0001c0001t0001g0078 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.211+10956A>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102978844 | ||||||
| chr4:102978933
|
T | A | 115 | a0001c0001t0001g0003a0001c0001t0001g0113a0001c0001t0001g0114others(112): Show | 115 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(112): Show |
intron_variant | MODIFIER | c.211+10867A>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102978933 | ||||||
| chr4:102979044
|
G | T | 195 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(192): Show | 196 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.211+10756C>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102979044 | ||||||
| chr4:102979503
|
C | T | 1 | a0001c0001t0001g0235 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.211+10297G>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102979503 | ||||||
| chr4:102979506
|
A | C | 9 | a0001c0001t0001g0304a0001c0001t0001g0305a0001c0001t0001g0306others(6): Show | 9 | HG01891.hp1 HG02145.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.211+10294T>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102979506 | ||||||
| chr4:102979797
|
C | T | 1 | a0001c0001t0001g0029 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.211+10003G>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102979797 | ||||||
| chr4:102979829
|
T | G | 2 | a0001c0001t0001g0112a0001c0001t0001g0302 | 2 | HG02109.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.211+9971A>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102979829 | ||||||
| chr4:102979939
|
A | G | 13 | a0001c0001t0001g0112a0001c0001t0001g0226a0001c0001t0001g0227others(10): Show | 13 | HG00735.hp2 HG01884.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.211+9861T>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102979939 | ||||||
| chr4:102980351
|
C | T | 1 | a0001c0001t0001g0303 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.211+9449G>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102980351 | ||||||
| chr4:102980538
|
A | C | 195 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(192): Show | 196 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.211+9262T>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102980538 | ||||||
| chr4:102980615
|
A | C | 2 | a0001c0001t0001g0121a0001c0001t0001g0140 | 2 | HG03654.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.211+9185T>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102980615 | ||||||
| chr4:102980629
|
C | T | 195 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(192): Show | 196 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.211+9171G>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102980629 | ||||||
| chr4:102980711
|
T | A | 1 | a0001c0001t0001g0315 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.211+9089A>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102980711 | ||||||
| chr4:102980747
|
G | A | 1 | a0001c0001t0001g0008 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.211+9053C>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102980747 | ||||||
| chr4:102980904
|
A | G | 1 | a0001c0001t0001g0139 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.211+8896T>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102980904 | ||||||
| chr4:102980948
|
T | C | 1 | a0001c0001t0001g0308 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.211+8852A>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102980948 | ||||||
| chr4:102981009
|
C | T | 1 | a0001c0001t0001g0028 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.211+8791G>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102981009 | ||||||
| chr4:102981137
|
T | C | 10 | a0001c0001t0001g0226a0001c0001t0001g0227a0001c0001t0001g0228others(7): Show | 10 | HG00735.hp2 HG01884.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.211+8663A>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102981137 | ||||||
| chr4:102981356
|
T | A | 4 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0001g0224others(1): Show | 4 | HG01192.hp1 HG02145.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.211+8444A>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102981356 | ||||||
| chr4:102981591
|
T | C | 1 | a0001c0001t0001g0088 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.211+8209A>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102981591 | ||||||
| chr4:102981959
|
C | T | 194 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(191): Show | 195 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.211+7841G>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102981959 | ||||||
| chr4:102982052
|
G | A | 7 | a0001c0001t0001g0117a0001c0001t0001g0119a0001c0001t0001g0122others(4): Show | 7 | HG01069.hp2 HG01891.hp2 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.211+7748C>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102982052 | ||||||
| chr4:102982242
|
T | C | 1 | a0001c0001t0001g0155 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.211+7558A>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102982242 | ||||||
| chr4:102982303
|
G | A | 1 | a0001c0001t0001g0086 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.211+7497C>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102982303 | ||||||
| chr4:102982397
|
C | T | 6 | a0001c0001t0001g0131a0001c0001t0001g0132a0001c0001t0001g0133others(3): Show | 6 | HG02015.hp1 HG02080.hp2 HG02165.hp2 others(3): Show |
intron_variant | MODIFIER | c.211+7403G>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102982397 | ||||||
| chr4:102982443
|
A | T | 18 | a0001c0001t0001g0118a0001c0001t0001g0120a0001c0001t0001g0121others(15): Show | 18 | HG00558.hp1 HG01074.hp2 HG02056.hp1 others(15): Show |
intron_variant | MODIFIER | c.211+7357T>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102982443 | ||||||
| chr4:102982595
|
T | G | 1 | a0001c0001t0001g0297 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.211+7205A>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102982595 | ||||||
| chr4:102982834
|
G | C | 1 | a0001c0001t0001g0008 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.211+6966C>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102982834 | ||||||
| chr4:102983013
|
T | C | 195 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(192): Show | 196 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.211+6787A>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102983013 | ||||||
| chr4:102983084
|
T | A | 195 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(192): Show | 196 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.211+6716A>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102983084 | ||||||
| chr4:102983502
|
G | A | 1 | a0001c0001t0001g0315 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.211+6298C>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102983502 | ||||||
| chr4:102983598
|
C | G | 211 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(208): Show | 212 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(209): Show |
intron_variant | MODIFIER | c.211+6202G>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102983598 | ||||||
| chr4:102983665
|
A | C | 212 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(209): Show | 213 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.211+6135T>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102983665 | ||||||
| chr4:102983877
|
C | T | 195 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(192): Show | 196 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.211+5923G>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102983877 | ||||||
| chr4:102984025
|
A | G | 1 | a0001c0001t0001g0086 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.211+5775T>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102984025 | ||||||
| chr4:102984034
|
C | T | 1 | a0001c0001t0001g0008 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.211+5766G>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102984034 | ||||||
| chr4:102984212
|
G | C | 9 | a0001c0001t0001g0125a0001c0001t0001g0164a0001c0001t0001g0170others(6): Show | 9 | HG00423.hp2 HG00609.hp2 HG01496.hp1 others(6): Show |
intron_variant | MODIFIER | c.211+5588C>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102984212 | ||||||
| chr4:102984213
|
G | A | 2 | a0001c0001t0001g0112a0001c0001t0001g0302 | 2 | HG02109.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.211+5587C>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102984213 | ||||||
| chr4:102984252
|
A | T | 1 | a0001c0001t0001g0012 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.211+5548T>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102984252 | ||||||
| chr4:102984363
|
G | C | 1 | a0001c0001t0001g0281 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.211+5437C>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102984363 | ||||||
| chr4:102984446
|
G | A | 1 | a0001c0001t0001g0025 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.211+5354C>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102984446 | ||||||
| chr4:102984567
|
T | C | 1 | a0001c0001t0001g0079 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.211+5233A>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102984567 | ||||||
| chr4:102984956
|
A | C | 209 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(206): Show | 210 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.211+4844T>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102984956 | ||||||
| chr4:102985203
|
T | C | 1 | a0001c0001t0001g0161 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.211+4597A>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102985203 | ||||||
| chr4:102985229
|
G | A | 5 | a0001c0001t0001g0165a0001c0001t0001g0166a0001c0001t0001g0167others(2): Show | 5 | HG00621.hp2 HG02083.hp2 NA18949.hp1 others(2): Show |
intron_variant | MODIFIER | c.211+4571C>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102985229 | ||||||
| chr4:102985507
|
C | T | 1 | a0001c0001t0001g0294 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.211+4293G>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102985507 | ||||||
| chr4:102985508
|
G | A | 3 | a0001c0001t0001g0112a0001c0001t0001g0302a0001c0001t0001g0315 | 3 | HG02109.hp2 HG03209.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.211+4292C>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102985508 | ||||||
| chr4:102985525
|
A | T | 195 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(192): Show | 196 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.211+4275T>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102985525 | ||||||
| chr4:102985539
|
CT | C | 211 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(208): Show | 212 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(209): Show |
intron_variant | MODIFIER | c.211+4260delA | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102985539 | ||||||
| chr4:102985550
|
T | A | 1 | a0001c0001t0001g0242 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.211+4250A>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102985550 | ||||||
| chr4:102985853
|
G | T | 1 | a0001c0001t0001g0270 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.211+3947C>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102985853 | ||||||
| chr4:102986209
|
T | C | 2 | a0001c0001t0001g0112a0001c0001t0001g0302 | 2 | HG02109.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.211+3591A>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102986209 | ||||||
| chr4:102986254
|
G | GT | 15 | a0001c0001t0001g0017a0001c0001t0001g0026a0001c0001t0001g0112others(12): Show | 15 | HG00735.hp2 HG01884.hp2 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.211+3545dupA | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102986254 | ||||||
| chr4:102986266
|
T | C | 9 | a0001c0001t0001g0120a0001c0001t0001g0305a0001c0001t0001g0306others(6): Show | 9 | HG01891.hp1 HG02145.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.211+3534A>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102986266 | ||||||
| chr4:102986266
|
T | TC | 186 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(183): Show | 187 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.211+3533_211+3534i others(3): Show |
SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102986266 | ||||||
| chr4:102986339
|
T | C | 3 | a0001c0001t0001g0112a0001c0001t0001g0302a0001c0001t0001g0315 | 3 | HG02109.hp2 HG03209.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.211+3461A>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102986339 | ||||||
| chr4:102986439
|
G | C | 209 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(206): Show | 210 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.211+3361C>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102986439 | ||||||
| chr4:102986455
|
T | C | 3 | a0001c0001t0001g0236a0001c0001t0001g0237a0001c0001t0001g0238 | 3 | HG02486.hp1 HG02818.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.211+3345A>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102986455 | ||||||
| chr4:102986546
|
G | A | 2 | a0001c0001t0001g0200a0001c0001t0001g0212 | 2 | NA18991.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.211+3254C>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102986546 | ||||||
| chr4:102986881
|
G | A | 209 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(206): Show | 210 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.211+2919C>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102986881 | ||||||
| chr4:102986905
|
A | G | 1 | a0001c0001t0001g0291 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.211+2895T>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102986905 | ||||||
| chr4:102987023
|
T | G | 2 | a0001c0001t0001g0232a0001c0001t0001g0234 | 2 | HG02717.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.211+2777A>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102987023 | ||||||
| chr4:102987210
|
T | C | 1 | a0001c0001t0001g0267 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.211+2590A>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102987210 | ||||||
| chr4:102987338
|
A | G | 1 | a0001c0001t0001g0285 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.211+2462T>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102987338 | ||||||
| chr4:102987551
|
G | A | 1 | a0001c0001t0001g0303 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.211+2249C>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102987551 | ||||||
| chr4:102987573
|
T | G | 2 | a0001c0001t0001g0086a0001c0001t0001g0088 | 2 | HG00735.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.211+2227A>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102987573 | ||||||
| chr4:102987574
|
G | T | 206 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(203): Show | 207 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.211+2226C>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102987574 | ||||||
| chr4:102987770
|
T | C | 10 | a0001c0001t0001g0226a0001c0001t0001g0227a0001c0001t0001g0228others(7): Show | 10 | HG00735.hp2 HG01884.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.211+2030A>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102987770 | ||||||
| chr4:102987859
|
C | G | 3 | a0001c0001t0001g0120a0001c0001t0001g0139a0001c0001t0001g0192 | 3 | HG00558.hp1 NA18983.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.211+1941G>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102987859 | ||||||
| chr4:102987964
|
G | C | 4 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0001g0224others(1): Show | 4 | HG01192.hp1 HG02145.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.211+1836C>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102987964 | ||||||
| chr4:102988385
|
G | T | 10 | a0001c0001t0001g0226a0001c0001t0001g0227a0001c0001t0001g0228others(7): Show | 10 | HG00735.hp2 HG01884.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.211+1415C>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102988385 | ||||||
| chr4:102988867
|
C | T | 1 | a0001c0001t0001g0025 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.211+933G>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102988867 | ||||||
| chr4:102988986
|
T | C | 3 | a0001c0001t0001g0112a0001c0001t0001g0302a0001c0001t0001g0315 | 3 | HG02109.hp2 HG03209.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.211+814A>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102988986 | ||||||
| chr4:102988989
|
A | T | 2 | a0001c0001t0001g0130a0001c0001t0001g0189 | 2 | HG02572.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.211+811T>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102988989 | ||||||
| chr4:102989001
|
G | A | 10 | a0001c0001t0001g0226a0001c0001t0001g0227a0001c0001t0001g0228others(7): Show | 10 | HG00735.hp2 HG01884.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.211+799C>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102989001 | ||||||
| chr4:102989106
|
G | GA | 44 | a0001c0001t0001g0111a0001c0001t0001g0201a0001c0001t0001g0221others(41): Show | 44 | HG00140.hp2 HG00438.hp2 HG00639.hp1 others(41): Show |
intron_variant | MODIFIER | c.211+693dupT | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102989106 | ||||||
| chr4:102989117
|
A | T | 1 | a0001c0001t0001g0008 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.211+683T>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102989117 | ||||||
| chr4:102989414
|
G | C | 1 | a0001c0001t0001g0156 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.211+386C>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102989414 | ||||||
| chr4:102989580
|
A | G | 2 | a0001c0001t0001g0111a0001c0001t0001g0276 | 2 | HG00438.hp2 HG02074.hp2 |
intron_variant | MODIFIER | c.211+220T>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102989580 | ||||||
| chr4:102989631
|
T | C | 1 | a0001c0001t0001g0008 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.211+169A>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 3/11 | chr4 | 102989631 | ||||||
| chr4:102990002
|
A | C | 195 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(192): Show | 196 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.70-61T>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 2/11 | chr4 | 102990002 | ||||||
| chr4:102990065
|
C | G | 195 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(192): Show | 196 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.70-124G>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 2/11 | chr4 | 102990065 | ||||||
| chr4:102990349
|
A | G | 1 | a0001c0001t0001g0291 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.70-408T>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 2/11 | chr4 | 102990349 | ||||||
| chr4:102990559
|
A | G | 1 | a0001c0001t0001g0101 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.70-618T>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 2/11 | chr4 | 102990559 | ||||||
| chr4:102990624
|
G | A | 194 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(191): Show | 195 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.70-683C>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 2/11 | chr4 | 102990624 | ||||||
| chr4:102990686
|
C | G | 1 | a0001c0001t0001g0224 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.70-745G>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 2/11 | chr4 | 102990686 | ||||||
| chr4:102990783
|
T | C | 1 | a0001c0001t0001g0021 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.70-842A>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 2/11 | chr4 | 102990783 | ||||||
| chr4:102991042
|
T | C | 1 | a0001c0001t0001g0008 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.69+601A>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 2/11 | chr4 | 102991042 | ||||||
| chr4:102991324
|
T | C | 1 | a0001c0001t0001g0190 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.69+319A>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 2/11 | chr4 | 102991324 | ||||||
| chr4:102991563
|
T | A | 3 | a0001c0001t0001g0273a0001c0001t0001g0274a0001c0001t0001g0275 | 3 | HG02818.hp2 HG03486.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.69+80A>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 2/11 | chr4 | 102991563 | ||||||
| chr4:102991567
|
A | G | 3 | a0001c0001t0001g0112a0001c0001t0001g0302a0001c0001t0001g0315 | 3 | HG02109.hp2 HG03209.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.69+76T>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 2/11 | chr4 | 102991567 | ||||||
| chr4:102991579
|
G | A | 1 | a0001c0001t0001g0088 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.69+64C>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 2/11 | chr4 | 102991579 | ||||||
| chr4:102991926
|
A | G | 195 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(192): Show | 196 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.-1-214T>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 102991926 | ||||||
| chr4:102992104
|
T | G | 1 | a0001c0001t0001g0220 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-1-392A>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 102992104 | ||||||
| chr4:102992223
|
G | A | 1 | a0001c0001t0001g0315 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-1-511C>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 102992223 | ||||||
| chr4:102992240
|
A | C | 1 | a0001c0001t0001g0023 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.-1-528T>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 102992240 | ||||||
| chr4:102992344
|
G | A | 1 | a0001c0001t0001g0080 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-1-632C>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 102992344 | ||||||
| chr4:102992498
|
T | A | 1 | a0001c0001t0001g0008 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-1-786A>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 102992498 | ||||||
| chr4:102992511
|
C | T | 1 | a0001c0001t0001g0188 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.-1-799G>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 102992511 | ||||||
| chr4:102992574
|
C | T | 1 | a0001c0001t0001g0086 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-1-862G>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 102992574 | ||||||
| chr4:102992591
|
A | G | 3 | a0001c0001t0001g0112a0001c0001t0001g0302a0001c0001t0001g0315 | 3 | HG02109.hp2 HG03209.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-1-879T>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 102992591 | ||||||
| chr4:102992849
|
A | G | 1 | a0001c0001t0001g0022 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-1-1137T>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 102992849 | ||||||
| chr4:102993033
|
G | T | 1 | a0001c0001t0001g0008 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-1-1321C>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 102993033 | ||||||
| chr4:102993053
|
T | G | 1 | a0001c0001t0001g0235 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-1-1341A>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 102993053 | ||||||
| chr4:102993090
|
C | CT | 195 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(192): Show | 196 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.-1-1379_-1-1378ins others(1): Show |
SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 102993090 | ||||||
| chr4:102993224
|
C | T | 1 | a0001c0001t0001g0220 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-1-1512G>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 102993224 | ||||||
| chr4:102993283
|
A | G | 195 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(192): Show | 196 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.-1-1571T>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 102993283 | ||||||
| chr4:102993352
|
C | G | 1 | a0001c0001t0001g0021 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-1-1640G>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 102993352 | ||||||
| chr4:102993481
|
A | G | 195 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(192): Show | 196 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.-1-1769T>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 102993481 | ||||||
| chr4:102993594
|
C | G | 1 | a0001c0001t0001g0113 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-1-1882G>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 102993594 | ||||||
| chr4:102993663
|
T | C | 209 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(206): Show | 210 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.-1-1951A>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 102993663 | ||||||
| chr4:102994153
|
T | G | 192 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(189): Show | 193 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(190): Show |
intron_variant | MODIFIER | c.-1-2441A>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 102994153 | ||||||
| chr4:102994166
|
T | G | 1 | a0001c0001t0001g0008 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-1-2454A>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 102994166 | ||||||
| chr4:102994201
|
G | C | 1 | a0001c0001t0001g0295 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-1-2489C>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 102994201 | ||||||
| chr4:102994253
|
T | C | 18 | a0001c0001t0001g0002a0001c0001t0001g0239a0001c0001t0001g0240others(15): Show | 18 | HG00099.hp1 HG01109.hp1 HG01175.hp2 others(15): Show |
intron_variant | MODIFIER | c.-1-2541A>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 102994253 | ||||||
| chr4:102994461
|
T | C | 201 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(198): Show | 202 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.-1-2749A>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 102994461 | ||||||
| chr4:102994888
|
T | A | 208 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(205): Show | 209 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(206): Show |
intron_variant | MODIFIER | c.-1-3176A>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 102994888 | ||||||
| chr4:102995297
|
C | T | 194 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(191): Show | 195 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.-1-3585G>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 102995297 | ||||||
| chr4:102995560
|
A | G | 32 | a0001c0001t0001g0241a0001c0001t0001g0243a0001c0001t0001g0244others(29): Show | 32 | HG00140.hp2 HG00639.hp1 HG00738.hp2 others(29): Show |
intron_variant | MODIFIER | c.-1-3848T>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 102995560 | ||||||
| chr4:102995595
|
C | A | 13 | a0001c0001t0001g0112a0001c0001t0001g0226a0001c0001t0001g0227others(10): Show | 13 | HG00735.hp2 HG01884.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.-1-3883G>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 102995595 | ||||||
| chr4:102995896
|
C | T | 1 | a0001c0001t0001g0138 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.-1-4184G>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 102995896 | ||||||
| chr4:102996351
|
G | A | 1 | a0001c0001t0001g0289 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-1-4639C>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 102996351 | ||||||
| chr4:102996374
|
A | C | 1 | a0001c0001t0001g0105 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-1-4662T>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 102996374 | ||||||
| chr4:102996388
|
C | T | 3 | a0001c0001t0001g0272a0001c0001t0001g0282a0001c0001t0001g0291 | 3 | HG00099.hp1 HG02723.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.-1-4676G>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 102996388 | ||||||
| chr4:102996626
|
T | C | 3 | a0001c0001t0001g0112a0001c0001t0001g0302a0001c0001t0001g0315 | 3 | HG02109.hp2 HG03209.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-1-4914A>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 102996626 | ||||||
| chr4:102996749
|
G | C | 1 | a0001c0001t0001g0002 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-1-5037C>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 102996749 | ||||||
| chr4:102996873
|
A | G | 1 | a0001c0001t0001g0175 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.-1-5161T>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 102996873 | ||||||
| chr4:102996952
|
A | AT | 191 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(188): Show | 192 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.-1-5241dupA | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 102996952 | ||||||
| chr4:102996966
|
A | T | 208 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(205): Show | 209 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(206): Show |
intron_variant | MODIFIER | c.-1-5254T>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 102996966 | ||||||
| chr4:102996996
|
A | T | 1 | a0001c0001t0001g0020 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-1-5284T>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 102996996 | ||||||
| chr4:102997109
|
C | T | 1 | a0001c0001t0001g0191 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.-1-5397G>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 102997109 | ||||||
| chr4:102997430
|
G | A | 1 | a0001c0001t0001g0265 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.-1-5718C>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 102997430 | ||||||
| chr4:102997541
|
C | T | 3 | a0001c0001t0001g0112a0001c0001t0001g0302a0001c0001t0001g0315 | 3 | HG02109.hp2 HG03209.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-1-5829G>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 102997541 | ||||||
| chr4:102997908
|
A | C | 65 | a0001c0001t0001g0114a0001c0001t0001g0118a0001c0001t0001g0120others(62): Show | 65 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(62): Show |
intron_variant | MODIFIER | c.-1-6196T>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 102997908 | ||||||
| chr4:102998304
|
A | G | 1 | a0002c0002t0001g0316 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-1-6592T>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 102998304 | ||||||
| chr4:102998364
|
A | G | 1 | a0001c0001t0001g0315 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-1-6652T>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 102998364 | ||||||
| chr4:102998403
|
T | C | 2 | a0001c0001t0001g0161a0001c0001t0001g0303 | 2 | HG02630.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.-1-6691A>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 102998403 | ||||||
| chr4:102998430
|
A | G | 1 | a0001c0001t0001g0175 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.-1-6718T>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 102998430 | ||||||
| chr4:102998474
|
T | A | 1 | a0001c0001t0001g0238 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-1-6762A>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 102998474 | ||||||
| chr4:102998513
|
T | G | 2 | a0001c0001t0001g0236a0001c0001t0001g0237 | 2 | HG02486.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.-1-6801A>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 102998513 | ||||||
| chr4:102998604
|
G | GT | 145 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(142): Show | 146 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(143): Show |
intron_variant | MODIFIER | c.-1-6893dupA | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 102998604 | ||||||
| chr4:102998706
|
T | C | 10 | a0001c0001t0001g0226a0001c0001t0001g0227a0001c0001t0001g0228others(7): Show | 10 | HG00735.hp2 HG01884.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.-1-6994A>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 102998706 | ||||||
| chr4:102998734
|
T | C | 2 | a0001c0001t0001g0162a0001c0001t0001g0163 | 2 | HG01074.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.-1-7022A>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 102998734 | ||||||
| chr4:102998756
|
T | C | 4 | a0001c0001t0001g0003a0001c0001t0001g0173a0001c0001t0001g0174others(1): Show | 4 | HG02622.hp1 HG02886.hp1 NA21309.hp1 others(1): Show |
intron_variant | MODIFIER | c.-1-7044A>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 102998756 | ||||||
| chr4:102998759
|
T | A | 9 | a0001c0001t0001g0304a0001c0001t0001g0305a0001c0001t0001g0306others(6): Show | 9 | HG01891.hp1 HG02145.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.-1-7047A>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 102998759 | ||||||
| chr4:102998887
|
G | A | 1 | a0001c0001t0001g0227 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-1-7175C>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 102998887 | ||||||
| chr4:102999121
|
C | A | 1 | a0001c0001t0001g0012 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-1-7409G>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 102999121 | ||||||
| chr4:102999156
|
T | A | 14 | a0001c0001t0001g0125a0001c0001t0001g0164a0001c0001t0001g0165others(11): Show | 14 | HG00423.hp2 HG00609.hp2 HG00621.hp2 others(11): Show |
intron_variant | MODIFIER | c.-1-7444A>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 102999156 | ||||||
| chr4:102999166
|
C | T | 1 | a0001c0001t0001g0184 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-1-7454G>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 102999166 | ||||||
| chr4:102999270
|
C | T | 3 | a0001c0001t0001g0112a0001c0001t0001g0302a0001c0001t0001g0315 | 3 | HG02109.hp2 HG03209.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-1-7558G>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 102999270 | ||||||
| chr4:102999274
|
T | C | 1 | a0001c0001t0001g0081 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-1-7562A>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 102999274 | ||||||
| chr4:102999579
|
T | C | 1 | a0001c0001t0001g0008 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-1-7867A>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 102999579 | ||||||
| chr4:102999660
|
T | G | 1 | a0001c0001t0001g0082 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.-1-7948A>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 102999660 | ||||||
| chr4:103000141
|
C | A | 194 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(191): Show | 195 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.-1-8429G>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 103000141 | ||||||
| chr4:103000234
|
C | A | 2 | a0001c0001t0001g0112a0001c0001t0001g0302 | 2 | HG02109.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-1-8522G>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 103000234 | ||||||
| chr4:103000265
|
A | T | 1 | a0001c0001t0001g0302 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-1-8553T>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 103000265 | ||||||
| chr4:103000428
|
C | T | 13 | a0001c0001t0001g0112a0001c0001t0001g0226a0001c0001t0001g0227others(10): Show | 13 | HG00735.hp2 HG01884.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.-1-8716G>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 103000428 | ||||||
| chr4:103000724
|
C | A | 1 | a0001c0001t0001g0213 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-1-9012G>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 103000724 | ||||||
| chr4:103000787
|
T | C | 18 | a0001c0001t0001g0002a0001c0001t0001g0239a0001c0001t0001g0240others(15): Show | 18 | HG00099.hp1 HG01109.hp1 HG01175.hp2 others(15): Show |
intron_variant | MODIFIER | c.-1-9075A>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 103000787 | ||||||
| chr4:103000813
|
A | G | 1 | a0001c0001t0001g0012 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-1-9101T>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 103000813 | ||||||
| chr4:103000952
|
G | A | 8 | a0001c0001t0001g0117a0001c0001t0001g0119a0001c0001t0001g0122others(5): Show | 8 | HG01069.hp2 HG01496.hp2 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.-1-9240C>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 103000952 | ||||||
| chr4:103000959
|
T | C | 10 | a0001c0001t0001g0226a0001c0001t0001g0227a0001c0001t0001g0228others(7): Show | 10 | HG00735.hp2 HG01884.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.-1-9247A>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 103000959 | ||||||
| chr4:103001087
|
G | A | 1 | a0001c0001t0001g0296 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.-1-9375C>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 103001087 | ||||||
| chr4:103001320
|
C | T | 2 | a0001c0001t0001g0236a0001c0001t0001g0237 | 2 | HG02486.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.-1-9608G>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 103001320 | ||||||
| chr4:103001336
|
C | A | 11 | a0001c0001t0001g0226a0001c0001t0001g0227a0001c0001t0001g0228others(8): Show | 11 | HG00735.hp2 HG01884.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.-1-9624G>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 103001336 | ||||||
| chr4:103001752
|
C | T | 2 | a0001c0001t0001g0112a0001c0001t0001g0302 | 2 | HG02109.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-1-10040G>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 103001752 | ||||||
| chr4:103001810
|
C | T | 1 | a0001c0001t0001g0187 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.-1-10098G>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 103001810 | ||||||
| chr4:103001864
|
A | G | 208 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(205): Show | 209 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(206): Show |
intron_variant | MODIFIER | c.-1-10152T>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 103001864 | ||||||
| chr4:103002016
|
C | T | 2 | a0001c0001t0001g0112a0001c0001t0001g0302 | 2 | HG02109.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-1-10304G>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 103002016 | ||||||
| chr4:103002258
|
C | T | 1 | a0001c0001t0001g0011 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-1-10546G>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 103002258 | ||||||
| chr4:103002267
|
A | C | 2 | a0002c0002t0001g0316a0002c0002t0001g0317 | 2 | HG02258.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.-1-10555T>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 103002267 | ||||||
| chr4:103002401
|
C | T | 194 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(191): Show | 195 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.-1-10689G>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 103002401 | ||||||
| chr4:103002507
|
C | A | 194 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(191): Show | 195 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.-1-10795G>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 103002507 | ||||||
| chr4:103002790
|
C | T | 1 | a0001c0001t0001g0137 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.-1-11078G>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 103002790 | ||||||
| chr4:103003168
|
T | C | 1 | a0001c0001t0001g0174 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-1-11456A>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 103003168 | ||||||
| chr4:103003360
|
T | C | 1 | a0001c0001t0001g0266 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.-1-11648A>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 103003360 | ||||||
| chr4:103003392
|
TA | T | 7 | a0001c0001t0001g0123a0001c0001t0001g0126a0001c0001t0001g0127others(4): Show | 7 | HG02717.hp2 HG02723.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.-1-11681delT | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 103003392 | ||||||
| chr4:103003780
|
A | G | 1 | a0001c0001t0001g0251 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-1-12068T>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 103003780 | ||||||
| chr4:103003800
|
C | G | 1 | a0001c0001t0001g0125 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.-1-12088G>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 103003800 | ||||||
| chr4:103003981
|
G | C | 195 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(192): Show | 196 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.-1-12269C>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 103003981 | ||||||
| chr4:103004009
|
A | T | 2 | a0001c0001t0001g0001a0001c0001t0001g0136 | 3 | HG01071.hp1 HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.-1-12297T>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 103004009 | ||||||
| chr4:103004032
|
T | A | 195 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(192): Show | 196 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.-1-12320A>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 103004032 | ||||||
| chr4:103004203
|
T | C | 1 | a0001c0001t0001g0217 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-1-12491A>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 103004203 | ||||||
| chr4:103004350
|
A | G | 2 | a0001c0001t0001g0001a0001c0001t0001g0136 | 3 | HG01071.hp1 HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.-1-12638T>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 103004350 | ||||||
| chr4:103004432
|
T | G | 13 | a0001c0001t0001g0112a0001c0001t0001g0226a0001c0001t0001g0227others(10): Show | 13 | HG00735.hp2 HG01884.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.-1-12720A>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 103004432 | ||||||
| chr4:103004514
|
G | A | 194 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(191): Show | 195 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.-1-12802C>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 103004514 | ||||||
| chr4:103004782
|
C | G | 1 | a0001c0001t0001g0124 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-1-13070G>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 103004782 | ||||||
| chr4:103004895
|
T | C | 8 | a0001c0001t0001g0117a0001c0001t0001g0119a0001c0001t0001g0122others(5): Show | 8 | HG01069.hp2 HG01496.hp2 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.-1-13183A>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 103004895 | ||||||
| chr4:103005059
|
T | C | 3 | a0001c0001t0001g0236a0001c0001t0001g0237a0001c0001t0001g0238 | 3 | HG02486.hp1 HG02818.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.-1-13347A>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 103005059 | ||||||
| chr4:103005261
|
T | TA | 12 | a0001c0001t0001g0083a0001c0001t0001g0084a0001c0001t0001g0105others(9): Show | 12 | HG00735.hp2 HG01884.hp2 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.-1-13550dupT | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 103005261 | ||||||
| chr4:103005261
|
TAAA | T | 189 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(186): Show | 190 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(187): Show |
intron_variant | MODIFIER | c.-1-13552_-1-13550d others(5): Show |
SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 103005261 | ||||||
| chr4:103005277
|
A | C | 3 | a0001c0001t0001g0273a0001c0001t0001g0274a0001c0001t0001g0275 | 3 | HG02818.hp2 HG03486.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-1-13565T>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 103005277 | ||||||
| chr4:103005385
|
C | T | 194 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(191): Show | 195 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.-1-13673G>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 103005385 | ||||||
| chr4:103005570
|
A | G | 141 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(138): Show | 142 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(139): Show |
intron_variant | MODIFIER | c.-1-13858T>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 103005570 | ||||||
| chr4:103005678
|
A | G | 45 | a0001c0001t0001g0111a0001c0001t0001g0221a0001c0001t0001g0241others(42): Show | 45 | HG00140.hp2 HG00438.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.-2+13921T>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 103005678 | ||||||
| chr4:103005797
|
C | G | 1 | a0001c0001t0001g0121 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-2+13802G>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 103005797 | ||||||
| chr4:103005805
|
T | C | 1 | a0001c0001t0001g0219 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.-2+13794A>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 103005805 | ||||||
| chr4:103006324
|
A | G | 1 | a0001c0001t0001g0008 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-2+13275T>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 103006324 | ||||||
| chr4:103006416
|
A | G | 194 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(191): Show | 195 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.-2+13183T>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 103006416 | ||||||
| chr4:103006522
|
A | G | 1 | a0001c0001t0001g0191 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.-2+13077T>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 103006522 | ||||||
| chr4:103006524
|
C | G | 3 | a0001c0001t0001g0273a0001c0001t0001g0274a0001c0001t0001g0275 | 3 | HG02818.hp2 HG03486.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-2+13075G>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 103006524 | ||||||
| chr4:103006643
|
A | T | 1 | a0001c0001t0001g0294 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-2+12956T>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 103006643 | ||||||
| chr4:103006847
|
T | A | 1 | a0001c0001t0001g0108 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-2+12752A>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 103006847 | ||||||
| chr4:103006890
|
A | G | 128 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(125): Show | 129 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(126): Show |
intron_variant | MODIFIER | c.-2+12709T>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 103006890 | ||||||
| chr4:103006969
|
G | T | 1 | a0001c0001t0001g0017 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.-2+12630C>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 103006969 | ||||||
| chr4:103006991
|
G | A | 194 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(191): Show | 195 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.-2+12608C>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 103006991 | ||||||
| chr4:103007102
|
A | G | 1 | a0001c0001t0001g0019 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.-2+12497T>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 103007102 | ||||||
| chr4:103007174
|
G | C | 1 | a0001c0001t0001g0290 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-2+12425C>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 103007174 | ||||||
| chr4:103007177
|
G | C | 1 | a0001c0001t0001g0267 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-2+12422C>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 103007177 | ||||||
| chr4:103007229
|
T | C | 1 | a0001c0001t0001g0085 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.-2+12370A>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 103007229 | ||||||
| chr4:103007359
|
A | C | 1 | a0001c0001t0001g0315 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-2+12240T>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 103007359 | ||||||
| chr4:103007591
|
CT | C | 14 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0086others(11): Show | 14 | HG00735.hp2 HG01884.hp2 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.-2+12007delA | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 103007591 | ||||||
| chr4:103007591
|
CTTT | C | 188 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(185): Show | 189 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(186): Show |
intron_variant | MODIFIER | c.-2+12005_-2+12007d others(5): Show |
SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 103007591 | ||||||
| chr4:103007591
|
CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0001g0227 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-2+11998_-2+12007d others(12): Show |
SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 103007591 | ||||||
| chr4:103007907
|
G | T | 1 | a0001c0001t0002g0018 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.-2+11692C>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 103007907 | ||||||
| chr4:103007929
|
T | C | 1 | a0001c0001t0001g0088 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-2+11670A>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 103007929 | ||||||
| chr4:103008027
|
T | C | 1 | a0001c0001t0001g0315 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-2+11572A>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 103008027 | ||||||
| chr4:103008142
|
A | G | 1 | a0001c0001t0001g0017 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.-2+11457T>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 103008142 | ||||||
| chr4:103008233
|
T | C | 1 | a0001c0001t0001g0172 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-2+11366A>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 103008233 | ||||||
| chr4:103008422
|
CTT | C | 178 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0113others(175): Show | 179 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(176): Show |
intron_variant | MODIFIER | c.-2+11175_-2+11176d others(4): Show |
SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 103008422 | ||||||
| chr4:103008422
|
CTTT | C | 16 | a0001c0001t0001g0003a0001c0001t0001g0173a0001c0001t0001g0174others(13): Show | 16 | HG00323.hp1 HG01891.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.-2+11174_-2+11176d others(5): Show |
SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 103008422 | ||||||
| chr4:103008663
|
ATGAGACA others(7): Show |
A | 5 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0091others(2): Show | 5 | HG02451.hp2 HG02486.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.-2+10922_-2+10935d others(16): Show |
SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 103008663 | ||||||
| chr4:103008672
|
C | T | 190 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(187): Show | 191 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.-2+10927G>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 103008672 | ||||||
| chr4:103008685
|
G | T | 1 | a0001c0001t0001g0012 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-2+10914C>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 103008685 | ||||||
| chr4:103008795
|
TTC | T | 31 | a0001c0001t0001g0011a0001c0001t0001g0221a0001c0001t0001g0242others(28): Show | 31 | HG00140.hp2 HG00639.hp1 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.-2+10802_-2+10803d others(4): Show |
SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 103008795 | ||||||
| chr4:103008796
|
TC | T | 13 | a0001c0001t0001g0241a0001c0001t0001g0244a0001c0001t0001g0245others(10): Show | 13 | HG00438.hp2 HG02056.hp2 HG02155.hp1 others(10): Show |
intron_variant | MODIFIER | c.-2+10802delG | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 103008796 | ||||||
| chr4:103008797
|
C | CT | 126 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0012others(123): Show | 127 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(124): Show |
intron_variant | MODIFIER | c.-2+10801dupA | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 103008797 | ||||||
| chr4:103008797
|
C | CTT | 24 | a0001c0001t0001g0003a0001c0001t0001g0123a0001c0001t0001g0124others(21): Show | 24 | HG00609.hp2 HG01175.hp2 HG01978.hp1 others(21): Show |
intron_variant | MODIFIER | c.-2+10800_-2+10801d others(4): Show |
SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 103008797 | ||||||
| chr4:103008797
|
C | T | 1 | a0001c0001t0001g0243 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.-2+10802G>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 103008797 | ||||||
| chr4:103008801
|
T | TC | 7 | a0001c0001t0001g0226a0001c0001t0001g0227a0001c0001t0001g0229others(4): Show | 7 | HG00735.hp2 HG02615.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.-2+10797_-2+10798i others(3): Show |
SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 103008801 | ||||||
| chr4:103008900
|
A | G | 1 | a0001c0001t0001g0123 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-2+10699T>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 103008900 | ||||||
| chr4:103008905
|
T | C | 1 | a0001c0001t0001g0094 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-2+10694A>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 103008905 | ||||||
| chr4:103009063
|
A | G | 130 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(127): Show | 131 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(128): Show |
intron_variant | MODIFIER | c.-2+10536T>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 103009063 | ||||||
| chr4:103009088
|
G | A | 144 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(141): Show | 145 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(142): Show |
intron_variant | MODIFIER | c.-2+10511C>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 103009088 | ||||||
| chr4:103009201
|
A | C | 1 | a0001c0001t0001g0242 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-2+10398T>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 103009201 | ||||||
| chr4:103009289
|
T | C | 1 | a0001c0001t0001g0315 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-2+10310A>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 103009289 | ||||||
| chr4:103009324
|
C | T | 1 | a0001c0001t0001g0300 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.-2+10275G>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 103009324 | ||||||
| chr4:103009354
|
T | C | 195 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(192): Show | 196 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.-2+10245A>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 103009354 | ||||||
| chr4:103009456
|
C | T | 4 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0001g0224others(1): Show | 4 | HG01192.hp1 HG02145.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.-2+10143G>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 103009456 | ||||||
| chr4:103009555
|
A | G | 1 | a0001c0001t0001g0214 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.-2+10044T>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 103009555 | ||||||
| chr4:103009918
|
A | AT | 194 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(191): Show | 195 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.-2+9680dupA | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 103009918 | ||||||
| chr4:103010149
|
T | C | 207 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(204): Show | 208 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(205): Show |
intron_variant | MODIFIER | c.-2+9450A>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 103010149 | ||||||
| chr4:103010206
|
T | C | 194 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(191): Show | 195 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.-2+9393A>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 103010206 | ||||||
| chr4:103010240
|
ACC | A | 194 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(191): Show | 195 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.-2+9357_-2+9358del others(2): Show |
SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 103010240 | ||||||
| chr4:103010332
|
G | T | 1 | a0001c0001t0001g0182 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-2+9267C>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 103010332 | ||||||
| chr4:103010334
|
C | T | 1 | a0001c0001t0001g0008 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-2+9265G>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 103010334 | ||||||
| chr4:103010336
|
C | A | 1 | a0001c0001t0001g0097 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-2+9263G>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 103010336 | ||||||
| chr4:103010694
|
A | G | 2 | a0001c0001t0001g0112a0001c0001t0001g0302 | 2 | HG02109.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-2+8905T>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 103010694 | ||||||
| chr4:103010900
|
T | C | 1 | a0001c0001t0001g0008 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-2+8699A>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 103010900 | ||||||
| chr4:103010913
|
A | G | 207 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(204): Show | 208 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(205): Show |
intron_variant | MODIFIER | c.-2+8686T>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 103010913 | ||||||
| chr4:103011391
|
G | T | 2 | a0001c0001t0001g0117a0001c0001t0001g0181 | 2 | HG01891.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.-2+8208C>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 103011391 | ||||||
| chr4:103011399
|
C | T | 194 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(191): Show | 195 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.-2+8200G>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 103011399 | ||||||
| chr4:103011660
|
T | A | 1 | a0001c0001t0001g0098 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-2+7939A>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 103011660 | ||||||
| chr4:103011670
|
G | A | 1 | a0001c0001t0001g0315 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-2+7929C>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 103011670 | ||||||
| chr4:103011793
|
G | A | 1 | a0001c0001t0001g0292 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-2+7806C>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 103011793 | ||||||
| chr4:103011818
|
T | G | 70 | a0001c0001t0001g0002a0001c0001t0001g0099a0001c0001t0001g0100others(67): Show | 70 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(67): Show |
intron_variant | MODIFIER | c.-2+7781A>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 103011818 | ||||||
| chr4:103011846
|
T | C | 2 | a0001c0001t0001g0101a0001c0001t0001g0102 | 2 | HG02698.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.-2+7753A>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 103011846 | ||||||
| chr4:103012119
|
T | C | 1 | a0001c0001t0001g0238 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-2+7480A>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 103012119 | ||||||
| chr4:103012211
|
T | C | 113 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0113others(110): Show | 114 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(111): Show |
intron_variant | MODIFIER | c.-2+7388A>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 103012211 | ||||||
| chr4:103012410
|
T | G | 132 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(129): Show | 133 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(130): Show |
intron_variant | MODIFIER | c.-2+7189A>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 103012410 | ||||||
| chr4:103012819
|
G | T | 1 | a0001c0001t0001g0213 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-2+6780C>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 103012819 | ||||||
| chr4:103012895
|
A | G | 1 | a0001c0001t0001g0292 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-2+6704T>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 103012895 | ||||||
| chr4:103012919
|
C | T | 1 | a0001c0001t0001g0272 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-2+6680G>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 103012919 | ||||||
| chr4:103013004
|
A | C | 1 | a0001c0001t0001g0300 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.-2+6595T>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 103013004 | ||||||
| chr4:103013153
|
A | C | 3 | a0001c0001t0001g0236a0001c0001t0001g0237a0001c0001t0001g0238 | 3 | HG02486.hp1 HG02818.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.-2+6446T>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 103013153 | ||||||
| chr4:103013280
|
T | C | 1 | a0001c0001t0001g0179 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-2+6319A>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 103013280 | ||||||
| chr4:103013386
|
C | T | 2 | a0001c0001t0001g0112a0001c0001t0001g0302 | 2 | HG02109.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-2+6213G>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 103013386 | ||||||
| chr4:103013431
|
C | T | 1 | a0001c0001t0001g0122 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-2+6168G>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 103013431 | ||||||
| chr4:103013555
|
A | C | 9 | a0001c0001t0001g0304a0001c0001t0001g0305a0001c0001t0001g0306others(6): Show | 9 | HG01891.hp1 HG02145.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.-2+6044T>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 103013555 | ||||||
| chr4:103013596
|
T | C | 1 | a0001c0001t0001g0268 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-2+6003A>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 103013596 | ||||||
| chr4:103013743
|
C | T | 194 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(191): Show | 195 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.-2+5856G>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 103013743 | ||||||
| chr4:103013871
|
T | G | 4 | a0001c0001t0001g0103a0001c0001t0001g0104a0001c0001t0001g0109others(1): Show | 4 | NA18962.hp2 NA18970.hp1 NA18975.hp1 others(1): Show |
intron_variant | MODIFIER | c.-2+5728A>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 103013871 | ||||||
| chr4:103014012
|
T | C | 1 | a0001c0001t0001g0269 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-2+5587A>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 103014012 | ||||||
| chr4:103014361
|
C | T | 1 | a0001c0001t0001g0008 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-2+5238G>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 103014361 | ||||||
| chr4:103014522
|
G | A | 1 | a0001c0001t0001g0270 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-2+5077C>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 103014522 | ||||||
| chr4:103014603
|
T | C | 2 | a0001c0001t0001g0112a0001c0001t0001g0302 | 2 | HG02109.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-2+4996A>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 103014603 | ||||||
| chr4:103014732
|
T | A | 2 | a0001c0001t0001g0112a0001c0001t0001g0302 | 2 | HG02109.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-2+4867A>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 103014732 | ||||||
| chr4:103014844
|
G | A | 113 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0113others(110): Show | 114 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(111): Show |
intron_variant | MODIFIER | c.-2+4755C>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 103014844 | ||||||
| chr4:103014874
|
T | C | 1 | a0001c0001t0001g0112 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-2+4725A>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 103014874 | ||||||
| chr4:103015016
|
T | C | 1 | a0001c0001t0001g0234 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-2+4583A>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 103015016 | ||||||
| chr4:103015280
|
C | T | 1 | a0001c0001t0001g0121 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-2+4319G>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 103015280 | ||||||
| chr4:103015281
|
C | CA | 9 | a0001c0001t0001g0105a0001c0001t0001g0180a0001c0001t0001g0212others(6): Show | 9 | HG01192.hp1 HG02135.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.-2+4317dupT | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 103015281 | ||||||
| chr4:103015392
|
C | T | 1 | a0001c0001t0001g0241 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.-2+4207G>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 103015392 | ||||||
| chr4:103015491
|
T | C | 132 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(129): Show | 133 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(130): Show |
intron_variant | MODIFIER | c.-2+4108A>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 103015491 | ||||||
| chr4:103015693
|
A | G | 3 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007 | 3 | HG00558.hp2 HG02071.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.-2+3906T>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 103015693 | ||||||
| chr4:103015751
|
G | T | 1 | a0001c0001t0001g0120 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.-2+3848C>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 103015751 | ||||||
| chr4:103015838
|
T | C | 1 | a0001c0001t0001g0271 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.-2+3761A>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 103015838 | ||||||
| chr4:103016006
|
C | T | 44 | a0001c0001t0001g0221a0001c0001t0001g0241a0001c0001t0001g0242others(41): Show | 44 | HG00140.hp2 HG00438.hp2 HG00639.hp1 others(41): Show |
intron_variant | MODIFIER | c.-2+3593G>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 103016006 | ||||||
| chr4:103016007
|
G | A | 1 | a0001c0001t0001g0291 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-2+3592C>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 103016007 | ||||||
| chr4:103016134
|
C | CAAAAAAA others(5): Show |
43 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0119others(40): Show | 43 | HG00140.hp2 HG00639.hp1 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.-2+3453_-2+3464dup others(12): Show |
SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 103016134 | ||||||
| chr4:103016134
|
C | CAAAAAAA others(6): Show |
95 | a0001c0001t0001g0003a0001c0001t0001g0113a0001c0001t0001g0115others(92): Show | 95 | HG00099.hp1 HG00438.hp2 HG00558.hp1 others(92): Show |
intron_variant | MODIFIER | c.-2+3452_-2+3464dup others(13): Show |
SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 103016134 | ||||||
| chr4:103016134
|
C | CAAAAAAA others(7): Show |
47 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0114others(44): Show | 48 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(45): Show |
intron_variant | MODIFIER | c.-2+3451_-2+3464dup others(14): Show |
SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 103016134 | ||||||
| chr4:103016134
|
C | CAAAAAAA others(8): Show |
9 | a0001c0001t0001g0116a0001c0001t0001g0213a0001c0001t0001g0214others(6): Show | 9 | HG00735.hp2 HG01884.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.-2+3450_-2+3464dup others(15): Show |
SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 103016134 | ||||||
| chr4:103016134
|
C | CAAAAAAA others(9): Show |
4 | a0001c0001t0001g0217a0001c0001t0001g0232a0001c0001t0001g0233others(1): Show | 4 | HG01255.hp1 HG02717.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.-2+3449_-2+3464dup others(16): Show |
SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 103016134 | ||||||
| chr4:103016134
|
C | CAAAAAAA others(10): Show |
2 | a0001c0001t0001g0235a0001c0001t0001g0313 | 2 | HG03195.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.-2+3448_-2+3464dup others(17): Show |
SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 103016134 | ||||||
| chr4:103016204
|
A | G | 1 | a0001c0001t0001g0116 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.-2+3395T>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 103016204 | ||||||
| chr4:103016317
|
C | T | 1 | a0001c0001t0001g0115 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.-2+3282G>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 103016317 | ||||||
| chr4:103016335
|
C | T | 1 | a0001c0001t0001g0114 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-2+3264G>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 103016335 | ||||||
| chr4:103016438
|
G | A | 194 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(191): Show | 195 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.-2+3161C>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 103016438 | ||||||
| chr4:103016616
|
CT | C | 8 | a0001c0001t0001g0106a0001c0001t0001g0108a0001c0001t0001g0109others(5): Show | 8 | HG00323.hp2 HG00639.hp2 HG01168.hp2 others(5): Show |
intron_variant | MODIFIER | c.-2+2982delA | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 103016616 | ||||||
| chr4:103016640
|
G | A | 1 | a0001c0001t0001g0220 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-2+2959C>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 103016640 | ||||||
| chr4:103016658
|
G | A | 1 | a0001c0001t0001g0296 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.-2+2941C>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 103016658 | ||||||
| chr4:103016729
|
T | A | 194 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(191): Show | 195 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.-2+2870A>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 103016729 | ||||||
| chr4:103016738
|
G | A | 1 | a0001c0001t0001g0315 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-2+2861C>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 103016738 | ||||||
| chr4:103016776
|
T | C | 208 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(205): Show | 209 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(206): Show |
intron_variant | MODIFIER | c.-2+2823A>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 103016776 | ||||||
| chr4:103016805
|
T | G | 1 | a0001c0001t0001g0295 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-2+2794A>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 103016805 | ||||||
| chr4:103016817
|
C | A | 194 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(191): Show | 195 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.-2+2782G>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 103016817 | ||||||
| chr4:103016873
|
C | T | 1 | a0001c0001t0001g0113 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-2+2726G>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 103016873 | ||||||
| chr4:103016960
|
G | A | 1 | a0001c0001t0001g0296 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.-2+2639C>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 103016960 | ||||||
| chr4:103017039
|
C | T | 1 | a0001c0001t0001g0004 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.-2+2560G>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 103017039 | ||||||
| chr4:103017131
|
G | A | 1 | a0001c0001t0001g0297 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-2+2468C>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 103017131 | ||||||
| chr4:103017334
|
C | T | 4 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0001g0224others(1): Show | 4 | HG01192.hp1 HG02145.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.-2+2265G>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 103017334 | ||||||
| chr4:103017583
|
T | C | 4 | a0001c0001t0001g0298a0001c0001t0001g0299a0001c0001t0001g0300others(1): Show | 4 | HG02083.hp1 HG02155.hp1 NA18995.hp2 others(1): Show |
intron_variant | MODIFIER | c.-2+2016A>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 103017583 | ||||||
| chr4:103017627
|
A | G | 2 | a0001c0001t0001g0112a0001c0001t0001g0302 | 2 | HG02109.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-2+1972T>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 103017627 | ||||||
| chr4:103017703
|
A | ACT | 207 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(204): Show | 208 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(205): Show |
intron_variant | MODIFIER | c.-2+1895_-2+1896ins others(2): Show |
SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 103017703 | ||||||
| chr4:103017856
|
C | T | 2 | a0001c0001t0001g0112a0001c0001t0001g0302 | 2 | HG02109.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-2+1743G>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 103017856 | ||||||
| chr4:103018198
|
C | T | 1 | a0001c0001t0001g0221 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-2+1401G>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 103018198 | ||||||
| chr4:103018276
|
C | T | 113 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0113others(110): Show | 114 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(111): Show |
intron_variant | MODIFIER | c.-2+1323G>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 103018276 | ||||||
| chr4:103018363
|
T | G | 205 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(202): Show | 206 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.-2+1236A>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 103018363 | ||||||
| chr4:103018535
|
G | A | 1 | a0001c0001t0001g0302 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-2+1064C>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 103018535 | ||||||
| chr4:103018664
|
AG | A | 207 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(204): Show | 208 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(205): Show |
intron_variant | MODIFIER | c.-2+934delC | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 103018664 | ||||||
| chr4:103018706
|
G | A | 1 | a0001c0001t0001g0303 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-2+893C>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 103018706 | ||||||
| chr4:103018720
|
T | A | 9 | a0001c0001t0001g0304a0001c0001t0001g0305a0001c0001t0001g0306others(6): Show | 9 | HG01891.hp1 HG02145.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.-2+879A>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 103018720 | ||||||
| chr4:103018902
|
G | A | 1 | a0001c0001t0001g0313 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.-2+697C>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 103018902 | ||||||
| chr4:103019174
|
G | C | 1 | a0001c0001t0001g0314 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.-2+425C>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 103019174 | ||||||
| chr4:103019401
|
G | A | 1 | a0001c0001t0001g0315 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-2+198C>T | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 103019401 | ||||||
| chr4:103019504
|
C | G | 1 | a0001c0001t0001g0003 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-2+95G>C | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 103019504 | ||||||
| chr4:103019591
|
G | C | 2 | a0002c0002t0001g0316a0002c0002t0001g0317 | 2 | HG02258.hp1 HG02615.hp2 |
splice_region_variant&intron_variant | LOW | c.-2+8C>G | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 103019591 | ||||||
| chr4:103019594
|
C | T | 1 | a0001c0001t0001g0002 | 1 | HG01109.hp1 | splice_region_variant&intron_variant | LOW | c.-2+5G>A | SLC9B1 | ENSG00000164037.17 | transcript | ENST00000296422.12 | protein_coding | 1/11 | chr4 | 103019594 |