Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 50508 |
|---|---|
| ensemblid | ENSG00000074771.4 |
| hgncid | 7890 |
| symbol | NOX3 |
| name | NADPH oxidase 3 |
| refseq_nuc | NM_015718.3 |
| refseq_prot | NP_056533.1 |
| ensembl_nuc | ENST00000159060.3 |
| ensembl_prot | ENSP00000159060.2 |
| mane_status | MANE Select |
| chr | chr6 |
| start | 155395368 |
| end | 155455839 |
| strand | - |
| ver | v1.2 |
| region | chr6:155395368-155455839 |
| region5000 | chr6:155390368-155460839 |
| regionname0 | NOX3_chr6_155395368_155455839 |
| regionname5000 | NOX3_chr6_155390368_155460839 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 568 | 260 | 82 | 60 | 78 | 10 | 28 | 63 | NOX3_chr6_155390368_155460839 | NOX3 | copy fasta | chr6 | 155390368 | 155460839 |
| a0002 | 0/0 | 568 | 89 | 6 | 12 | 60 | 0 | 11 | 45 | NOX3_chr6_155390368_155460839 | NOX3 | copy fasta | chr6 | 155390368 | 155460839 |
| a0003 | 0/0 | 568 | 5 | 0 | 0 | 5 | 0 | 0 | 2 | NOX3_chr6_155390368_155460839 | NOX3 | copy fasta | chr6 | 155390368 | 155460839 |
| a0004 | 0/0 | 568 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | copy fasta | chr6 | 155390368 | 155460839 |
| a0005 | 0/0 | 568 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | copy fasta | chr6 | 155390368 | 155460839 |
| a0006 | 0/0 | 568 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | copy fasta | chr6 | 155390368 | 155460839 |
| a0007 | 0/0 | 568 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NOX3_chr6_155390368_155460839 | NOX3 | copy fasta | chr6 | 155390368 | 155460839 |
| a0008 | 0/0 | 568 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | copy fasta | chr6 | 155390368 | 155460839 |
| a0009 | 0/0 | 568 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NOX3_chr6_155390368_155460839 | NOX3 | copy fasta | chr6 | 155390368 | 155460839 |
| a0010 | 0/0 | 568 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | copy fasta | chr6 | 155390368 | 155460839 |
| chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/1 | 1707 | 152 | 44 | 25 | 59 | 5 | 18 | NOX3_chr6_155390368_155460839 | NOX3 | copy fasta | chr6 | 155390368 | 155460839 |
| c0002 | 0/0 | 1707 | 76 | 4 | 11 | 52 | 0 | 9 | NOX3_chr6_155390368_155460839 | NOX3 | copy fasta | chr6 | 155390368 | 155460839 |
| c0003 | 1/0 | 1707 | 54 | 23 | 20 | 5 | 2 | 3 | NOX3_chr6_155390368_155460839 | NOX3 | copy fasta | chr6 | 155390368 | 155460839 |
| c0004 | 0/0 | 1707 | 24 | 4 | 7 | 8 | 2 | 3 | NOX3_chr6_155390368_155460839 | NOX3 | copy fasta | chr6 | 155390368 | 155460839 |
| c0005 | 0/0 | 1707 | 16 | 2 | 7 | 5 | 1 | 1 | NOX3_chr6_155390368_155460839 | NOX3 | copy fasta | chr6 | 155390368 | 155460839 |
| c0006 | 0/0 | 1707 | 12 | 9 | 1 | 0 | 0 | 2 | NOX3_chr6_155390368_155460839 | NOX3 | copy fasta | chr6 | 155390368 | 155460839 |
| c0007 | 0/0 | 1707 | 8 | 0 | 1 | 6 | 0 | 1 | NOX3_chr6_155390368_155460839 | NOX3 | copy fasta | chr6 | 155390368 | 155460839 |
| c0008 | 0/0 | 1707 | 3 | 0 | 0 | 3 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | copy fasta | chr6 | 155390368 | 155460839 |
| c0009 | 0/0 | 1707 | 2 | 2 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | copy fasta | chr6 | 155390368 | 155460839 |
| c0010 | 0/0 | 1707 | 2 | 2 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | copy fasta | chr6 | 155390368 | 155460839 |
| c0011 | 0/0 | 1707 | 2 | 0 | 0 | 1 | 0 | 1 | NOX3_chr6_155390368_155460839 | NOX3 | copy fasta | chr6 | 155390368 | 155460839 |
| c0012 | 0/0 | 1707 | 2 | 0 | 0 | 2 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | copy fasta | chr6 | 155390368 | 155460839 |
| c0013 | 0/0 | 1707 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | copy fasta | chr6 | 155390368 | 155460839 |
| c0014 | 0/0 | 1707 | 1 | 0 | 0 | 0 | 0 | 1 | NOX3_chr6_155390368_155460839 | NOX3 | copy fasta | chr6 | 155390368 | 155460839 |
| c0015 | 0/0 | 1707 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | copy fasta | chr6 | 155390368 | 155460839 |
| c0016 | 0/0 | 1707 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | copy fasta | chr6 | 155390368 | 155460839 |
| c0017 | 0/0 | 1707 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | copy fasta | chr6 | 155390368 | 155460839 |
| c0018 | 0/0 | 1707 | 1 | 1 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | copy fasta | chr6 | 155390368 | 155460839 |
| c0019 | 0/0 | 1707 | 1 | 1 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | copy fasta | chr6 | 155390368 | 155460839 |
| c0020 | 0/0 | 1707 | 1 | 0 | 0 | 0 | 0 | 1 | NOX3_chr6_155390368_155460839 | NOX3 | copy fasta | chr6 | 155390368 | 155460839 |
| c0021 | 0/0 | 1707 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | copy fasta | chr6 | 155390368 | 155460839 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/0 | 274 | 282 | 70 | 59 | 111 | 8 | 33 | NOX3_chr6_155390368_155460839 | NOX3 | copy fasta | chr6 | 155390368 | 155460839 |
| t0002 | 0/1 | 274 | 72 | 15 | 12 | 35 | 2 | 7 | NOX3_chr6_155390368_155460839 | NOX3 | copy fasta | chr6 | 155390368 | 155460839 |
| t0003 | 0/0 | 274 | 5 | 5 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | copy fasta | chr6 | 155390368 | 155460839 |
| t0004 | 0/0 | 274 | 2 | 1 | 1 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | copy fasta | chr6 | 155390368 | 155460839 |
| t0005 | 0/0 | 274 | 1 | 1 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | copy fasta | chr6 | 155390368 | 155460839 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 1/0 | 3 | 1 | 0 | 0 | 1 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0036 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0171 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0272 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0298 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0306 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0307 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0321 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0322 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0337 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0345 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0346 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| g0350 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 1707 | 152 | 44 | 25 | 59 | 5 | 18 | NOX3_chr6_155390368_155460839 | NOX3 | copy fasta | chr6 | 155390368 | 155460839 |
| a0001c0003 | 1/0 | 1707 | 54 | 23 | 20 | 5 | 2 | 3 | NOX3_chr6_155390368_155460839 | NOX3 | copy fasta | chr6 | 155390368 | 155460839 |
| a0001c0004 | 0/0 | 1707 | 24 | 4 | 7 | 8 | 2 | 3 | NOX3_chr6_155390368_155460839 | NOX3 | copy fasta | chr6 | 155390368 | 155460839 |
| a0001c0005 | 0/0 | 1707 | 16 | 2 | 7 | 5 | 1 | 1 | NOX3_chr6_155390368_155460839 | NOX3 | copy fasta | chr6 | 155390368 | 155460839 |
| a0001c0006 | 0/0 | 1707 | 12 | 9 | 1 | 0 | 0 | 2 | NOX3_chr6_155390368_155460839 | NOX3 | copy fasta | chr6 | 155390368 | 155460839 |
| a0001c0014 | 0/0 | 1707 | 1 | 0 | 0 | 0 | 0 | 1 | NOX3_chr6_155390368_155460839 | NOX3 | copy fasta | chr6 | 155390368 | 155460839 |
| a0001c0016 | 0/0 | 1707 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | copy fasta | chr6 | 155390368 | 155460839 |
| a0002c0002 | 0/0 | 1707 | 76 | 4 | 11 | 52 | 0 | 9 | NOX3_chr6_155390368_155460839 | NOX3 | copy fasta | chr6 | 155390368 | 155460839 |
| a0002c0007 | 0/0 | 1707 | 8 | 0 | 1 | 6 | 0 | 1 | NOX3_chr6_155390368_155460839 | NOX3 | copy fasta | chr6 | 155390368 | 155460839 |
| a0002c0009 | 0/0 | 1707 | 2 | 2 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | copy fasta | chr6 | 155390368 | 155460839 |
| a0002c0011 | 0/0 | 1707 | 2 | 0 | 0 | 1 | 0 | 1 | NOX3_chr6_155390368_155460839 | NOX3 | copy fasta | chr6 | 155390368 | 155460839 |
| a0002c0013 | 0/0 | 1707 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | copy fasta | chr6 | 155390368 | 155460839 |
| a0003c0008 | 0/0 | 1707 | 3 | 0 | 0 | 3 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | copy fasta | chr6 | 155390368 | 155460839 |
| a0003c0012 | 0/0 | 1707 | 2 | 0 | 0 | 2 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | copy fasta | chr6 | 155390368 | 155460839 |
| a0004c0010 | 0/0 | 1707 | 2 | 2 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | copy fasta | chr6 | 155390368 | 155460839 |
| a0005c0021 | 0/0 | 1707 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | copy fasta | chr6 | 155390368 | 155460839 |
| a0006c0020 | 0/0 | 1707 | 1 | 0 | 0 | 0 | 0 | 1 | NOX3_chr6_155390368_155460839 | NOX3 | copy fasta | chr6 | 155390368 | 155460839 |
| a0007c0017 | 0/0 | 1707 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | copy fasta | chr6 | 155390368 | 155460839 |
| a0008c0019 | 0/0 | 1707 | 1 | 1 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | copy fasta | chr6 | 155390368 | 155460839 |
| a0009c0015 | 0/0 | 1707 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | copy fasta | chr6 | 155390368 | 155460839 |
| a0010c0018 | 0/0 | 1707 | 1 | 1 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | copy fasta | chr6 | 155390368 | 155460839 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 1980 | 125 | 35 | 24 | 46 | 4 | 16 | NOX3_chr6_155390368_155460839 | NOX3 | copy fasta | chr6 | 155390368 | 155460839 |
| a0001c0001t0002 | 0/1 | 1980 | 27 | 9 | 1 | 13 | 1 | 2 | NOX3_chr6_155390368_155460839 | NOX3 | copy fasta | chr6 | 155390368 | 155460839 |
| a0001c0003t0001 | 1/0 | 1980 | 43 | 18 | 16 | 3 | 2 | 3 | NOX3_chr6_155390368_155460839 | NOX3 | copy fasta | chr6 | 155390368 | 155460839 |
| a0001c0003t0002 | 0/0 | 1980 | 10 | 4 | 4 | 2 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | copy fasta | chr6 | 155390368 | 155460839 |
| a0001c0003t0005 | 0/0 | 1980 | 1 | 1 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | copy fasta | chr6 | 155390368 | 155460839 |
| a0001c0004t0001 | 0/0 | 1980 | 19 | 2 | 6 | 6 | 2 | 3 | NOX3_chr6_155390368_155460839 | NOX3 | copy fasta | chr6 | 155390368 | 155460839 |
| a0001c0004t0002 | 0/0 | 1980 | 2 | 0 | 0 | 2 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | copy fasta | chr6 | 155390368 | 155460839 |
| a0001c0004t0003 | 0/0 | 1980 | 1 | 1 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | copy fasta | chr6 | 155390368 | 155460839 |
| a0001c0004t0004 | 0/0 | 1980 | 2 | 1 | 1 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | copy fasta | chr6 | 155390368 | 155460839 |
| a0001c0005t0001 | 0/0 | 1980 | 10 | 0 | 5 | 4 | 0 | 1 | NOX3_chr6_155390368_155460839 | NOX3 | copy fasta | chr6 | 155390368 | 155460839 |
| a0001c0005t0002 | 0/0 | 1980 | 4 | 0 | 2 | 1 | 1 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | copy fasta | chr6 | 155390368 | 155460839 |
| a0001c0005t0003 | 0/0 | 1980 | 2 | 2 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | copy fasta | chr6 | 155390368 | 155460839 |
| a0001c0006t0001 | 0/0 | 1980 | 10 | 7 | 1 | 0 | 0 | 2 | NOX3_chr6_155390368_155460839 | NOX3 | copy fasta | chr6 | 155390368 | 155460839 |
| a0001c0006t0002 | 0/0 | 1980 | 2 | 2 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | copy fasta | chr6 | 155390368 | 155460839 |
| a0001c0014t0002 | 0/0 | 1980 | 1 | 0 | 0 | 0 | 0 | 1 | NOX3_chr6_155390368_155460839 | NOX3 | copy fasta | chr6 | 155390368 | 155460839 |
| a0001c0016t0001 | 0/0 | 1980 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | copy fasta | chr6 | 155390368 | 155460839 |
| a0002c0002t0001 | 0/0 | 1980 | 55 | 4 | 6 | 39 | 0 | 6 | NOX3_chr6_155390368_155460839 | NOX3 | copy fasta | chr6 | 155390368 | 155460839 |
| a0002c0002t0002 | 0/0 | 1980 | 21 | 0 | 5 | 13 | 0 | 3 | NOX3_chr6_155390368_155460839 | NOX3 | copy fasta | chr6 | 155390368 | 155460839 |
| a0002c0007t0001 | 0/0 | 1980 | 6 | 0 | 1 | 4 | 0 | 1 | NOX3_chr6_155390368_155460839 | NOX3 | copy fasta | chr6 | 155390368 | 155460839 |
| a0002c0007t0002 | 0/0 | 1980 | 2 | 0 | 0 | 2 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | copy fasta | chr6 | 155390368 | 155460839 |
| a0002c0009t0003 | 0/0 | 1980 | 2 | 2 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | copy fasta | chr6 | 155390368 | 155460839 |
| a0002c0011t0001 | 0/0 | 1980 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | copy fasta | chr6 | 155390368 | 155460839 |
| a0002c0011t0002 | 0/0 | 1980 | 1 | 0 | 0 | 0 | 0 | 1 | NOX3_chr6_155390368_155460839 | NOX3 | copy fasta | chr6 | 155390368 | 155460839 |
| a0002c0013t0002 | 0/0 | 1980 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | copy fasta | chr6 | 155390368 | 155460839 |
| a0003c0008t0001 | 0/0 | 1980 | 3 | 0 | 0 | 3 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | copy fasta | chr6 | 155390368 | 155460839 |
| a0003c0012t0001 | 0/0 | 1980 | 2 | 0 | 0 | 2 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | copy fasta | chr6 | 155390368 | 155460839 |
| a0004c0010t0001 | 0/0 | 1980 | 2 | 2 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | copy fasta | chr6 | 155390368 | 155460839 |
| a0005c0021t0001 | 0/0 | 1980 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | copy fasta | chr6 | 155390368 | 155460839 |
| a0006c0020t0001 | 0/0 | 1980 | 1 | 0 | 0 | 0 | 0 | 1 | NOX3_chr6_155390368_155460839 | NOX3 | copy fasta | chr6 | 155390368 | 155460839 |
| a0007c0017t0002 | 0/0 | 1980 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | copy fasta | chr6 | 155390368 | 155460839 |
| a0008c0019t0001 | 0/0 | 1980 | 1 | 1 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | copy fasta | chr6 | 155390368 | 155460839 |
| a0009c0015t0001 | 0/0 | 1980 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | copy fasta | chr6 | 155390368 | 155460839 |
| a0010c0018t0001 | 0/0 | 1980 | 1 | 1 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | copy fasta | chr6 | 155390368 | 155460839 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0001t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0001t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0001t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0001t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0001t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0001t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0001t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0001t0002g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0001t0002g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0001t0002g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0001t0002g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0001t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0001t0002g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0001t0002g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0001t0002g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0001t0002g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0001t0002g0171 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0001t0002g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0001t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0001t0002g0272 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0001t0002g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0001t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0001t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0003t0001g0001 | 1/0 | 3 | 1 | 0 | 0 | 1 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0003t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0003t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0003t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0003t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0003t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0003t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0003t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0003t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0003t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0003t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0003t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0003t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0003t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0003t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0003t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0003t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0003t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0003t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0003t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0003t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0003t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0003t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0003t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0003t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0003t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0003t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0003t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0003t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0003t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0003t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0003t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0003t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0003t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0003t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0003t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0003t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0003t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0003t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0003t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0003t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0003t0002g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0003t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0003t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0003t0002g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0003t0002g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0003t0002g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0003t0002g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0003t0002g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0003t0002g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0003t0002g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0003t0005g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0004t0001g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0004t0001g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0004t0001g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0004t0001g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0004t0001g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0004t0001g0321 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0004t0001g0322 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0004t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0004t0001g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0004t0001g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0004t0001g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0004t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0004t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0004t0001g0337 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0004t0001g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0004t0001g0346 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0004t0002g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0004t0002g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0004t0003g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0004t0004g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0004t0004g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0005t0001g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0005t0001g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0005t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0005t0001g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0005t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0005t0001g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0005t0001g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0005t0001g0345 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0005t0001g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0005t0001g0350 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0005t0002g0036 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0005t0002g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0005t0002g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0005t0002g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0005t0003g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0006t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0006t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0006t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0006t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0006t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0006t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0006t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0006t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0006t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0006t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0006t0002g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0006t0002g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0014t0002g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0001c0016t0001g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0002c0002t0001g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0002c0002t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0002c0002t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0002c0002t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0002c0002t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0002c0002t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0002c0002t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0002c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0002c0002t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0002c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0002c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0002c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0002c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0002c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0002c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0002c0002t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0002c0002t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0002c0002t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0002c0002t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0002c0002t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0002c0002t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0002c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0002c0002t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0002c0002t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0002c0002t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0002c0002t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0002c0002t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0002c0002t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0002c0002t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0002c0002t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0002c0002t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0002c0002t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0002c0002t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0002c0002t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0002c0002t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0002c0002t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0002c0002t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0002c0002t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0002c0002t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0002c0002t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0002c0002t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0002c0002t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0002c0002t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0002c0002t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0002c0002t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0002c0002t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0002c0002t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0002c0002t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0002c0002t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0002c0002t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0002c0002t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0002c0002t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0002c0002t0001g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0002c0002t0002g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0002c0002t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0002c0002t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0002c0002t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0002c0002t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0002c0002t0002g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0002c0002t0002g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0002c0002t0002g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0002c0002t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0002c0002t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0002c0002t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0002c0002t0002g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0002c0002t0002g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0002c0002t0002g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0002c0002t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0002c0002t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0002c0002t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0002c0002t0002g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0002c0002t0002g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0002c0002t0002g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0002c0007t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0002c0007t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0002c0007t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0002c0007t0001g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0002c0007t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0002c0007t0001g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0002c0007t0002g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0002c0007t0002g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0002c0009t0003g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0002c0009t0003g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0002c0011t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0002c0011t0002g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0002c0013t0002g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0003c0008t0001g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0003c0008t0001g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0003c0008t0001g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0003c0012t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0003c0012t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0004c0010t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0004c0010t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0005c0021t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0006c0020t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0007c0017t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0008c0019t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0009c0015t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| a0010c0018t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0298 | EUR | FIN | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0272 | EUR | FIN | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | CHS | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG00423 | hp2 | a0002 | c0002 | t0001 | g0205 | EAS | CHS | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0293 | EAS | CHS | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | CHS | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG00558 | hp1 | a0002 | c0002 | t0001 | g0192 | EAS | CHS | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG00558 | hp2 | a0002 | c0002 | t0001 | g0112 | EAS | CHS | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG00609 | hp1 | a0002 | c0002 | t0001 | g0178 | EAS | CHS | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG00609 | hp2 | a0002 | c0002 | t0001 | g0193 | EAS | CHS | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG00621 | hp1 | a0002 | c0002 | t0001 | g0208 | EAS | CHS | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG00621 | hp2 | a0003 | c0008 | t0001 | g0340 | EAS | CHS | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG00639 | hp1 | a0001 | c0003 | t0002 | g0242 | AMR | PUR | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0175 | AMR | PUR | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG00642 | hp1 | a0001 | c0005 | t0001 | g0323 | AMR | PUR | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0235 | AMR | PUR | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | CHS | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | CHS | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG00735 | hp1 | a0002 | c0002 | t0002 | g0219 | AMR | PUR | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG00735 | hp2 | a0001 | c0003 | t0001 | g0246 | AMR | PUR | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG00738 | hp1 | a0001 | c0003 | t0001 | g0260 | AMR | PUR | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG00738 | hp2 | a0001 | c0006 | t0001 | g0170 | AMR | PUR | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG00741 | hp1 | a0002 | c0002 | t0001 | g0076 | AMR | PUR | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG00741 | hp2 | a0001 | c0003 | t0001 | g0184 | AMR | PUR | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0254 | AMR | PUR | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG01069 | hp2 | a0001 | c0003 | t0001 | g0162 | AMR | PUR | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0252 | AMR | PUR | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0294 | AMR | PUR | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0299 | AMR | PUR | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG01071 | hp2 | a0001 | c0003 | t0001 | g0163 | AMR | PUR | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0095 | AMR | PUR | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0173 | AMR | PUR | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG01081 | hp1 | a0002 | c0007 | t0001 | g0317 | AMR | PUR | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0082 | AMR | PUR | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0054 | AMR | PUR | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG01099 | hp2 | a0001 | c0003 | t0002 | g0243 | AMR | PUR | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0250 | AMR | PUR | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG01106 | hp2 | a0001 | c0003 | t0002 | g0241 | AMR | PUR | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG01109 | hp1 | a0001 | c0003 | t0001 | g0261 | AMR | PUR | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG01109 | hp2 | a0001 | c0003 | t0001 | g0144 | AMR | PUR | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0257 | AMR | PUR | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG01168 | hp2 | a0001 | c0001 | t0002 | g0231 | AMR | PUR | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG01169 | hp1 | a0001 | c0003 | t0001 | g0244 | AMR | PUR | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0258 | AMR | PUR | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0245 | AMR | PUR | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0234 | AMR | PUR | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG01192 | hp1 | a0002 | c0002 | t0001 | g0190 | AMR | PUR | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0249 | AMR | PUR | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG01243 | hp1 | a0001 | c0004 | t0004 | g0011 | AMR | PUR | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG01243 | hp2 | a0001 | c0003 | t0001 | g0161 | AMR | PUR | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG01255 | hp1 | a0001 | c0003 | t0001 | g0247 | AMR | CLM | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG01255 | hp2 | a0002 | c0002 | t0002 | g0158 | AMR | CLM | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG01256 | hp1 | a0001 | c0004 | t0001 | g0010 | AMR | CLM | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0229 | AMR | CLM | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | CLM | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0230 | AMR | CLM | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0232 | AMR | CLM | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG01261 | hp2 | a0001 | c0003 | t0001 | g0263 | AMR | CLM | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG01346 | hp1 | a0001 | c0003 | t0001 | g0248 | AMR | CLM | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG01346 | hp2 | a0001 | c0004 | t0001 | g0319 | AMR | CLM | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0255 | AMR | CLM | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG01361 | hp2 | a0001 | c0005 | t0001 | g0308 | AMR | CLM | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | CLM | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG01433 | hp2 | a0001 | c0003 | t0001 | g0259 | AMR | CLM | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG01496 | hp1 | a0001 | c0004 | t0001 | g0010 | AMR | CLM | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG01496 | hp2 | a0001 | c0003 | t0002 | g0148 | AMR | CLM | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG01515 | hp1 | a0001 | c0004 | t0001 | g0321 | EUR | IBS | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG01515 | hp2 | a0001 | c0003 | t0001 | g0067 | EUR | IBS | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0307 | EUR | IBS | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0106 | EUR | IBS | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0306 | EUR | IBS | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG01517 | hp2 | a0001 | c0004 | t0001 | g0322 | EUR | IBS | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG01884 | hp1 | a0001 | c0006 | t0001 | g0155 | AFR | ACB | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG01884 | hp2 | a0001 | c0003 | t0001 | g0160 | AFR | ACB | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0179 | AFR | ACB | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG01891 | hp2 | a0001 | c0003 | t0005 | g0038 | AFR | ACB | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG01943 | hp1 | a0001 | c0005 | t0001 | g0336 | AMR | PEL | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG01943 | hp2 | a0002 | c0002 | t0002 | g0220 | AMR | PEL | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG01975 | hp1 | a0001 | c0004 | t0001 | g0328 | AMR | PEL | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG01975 | hp2 | a0001 | c0003 | t0001 | g0045 | AMR | PEL | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG01978 | hp1 | a0002 | c0002 | t0001 | g0221 | AMR | PEL | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG01978 | hp2 | a0002 | c0002 | t0001 | g0006 | AMR | PEL | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG01981 | hp1 | a0001 | c0005 | t0001 | g0326 | AMR | PEL | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG01981 | hp2 | a0002 | c0002 | t0002 | g0271 | AMR | PEL | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG01993 | hp1 | a0001 | c0005 | t0001 | g0350 | AMR | PEL | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG01993 | hp2 | a0001 | c0005 | t0002 | g0329 | AMR | PEL | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG02004 | hp1 | a0001 | c0005 | t0002 | g0342 | AMR | PEL | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG02004 | hp2 | a0001 | c0004 | t0001 | g0327 | AMR | PEL | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG02015 | hp1 | a0002 | c0002 | t0002 | g0053 | EAS | KHV | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG02015 | hp2 | a0003 | c0008 | t0001 | g0338 | EAS | KHV | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG02027 | hp1 | a0002 | c0002 | t0002 | g0228 | EAS | KHV | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | KHV | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0285 | EAS | KHV | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | KHV | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0090 | AFR | ACB | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG02055 | hp2 | a0001 | c0003 | t0002 | g0279 | AFR | ACB | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | KHV | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0032 | EAS | KHV | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG02074 | hp1 | a0002 | c0002 | t0001 | g0157 | EAS | KHV | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG02074 | hp2 | a0002 | c0002 | t0002 | g0305 | EAS | KHV | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG02080 | hp1 | a0002 | c0002 | t0001 | g0034 | EAS | KHV | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0194 | EAS | KHV | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG02129 | hp1 | a0005 | c0021 | t0001 | g0156 | EAS | KHV | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG02129 | hp2 | a0003 | c0008 | t0001 | g0339 | EAS | KHV | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG02145 | hp1 | a0001 | c0004 | t0003 | g0015 | AFR | ACB | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0282 | AFR | ACB | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG02148 | hp1 | a0002 | c0002 | t0002 | g0218 | AMR | PEL | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG02148 | hp2 | a0002 | c0002 | t0001 | g0189 | AMR | PEL | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0027 | EAS | CDX | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG02155 | hp2 | a0002 | c0002 | t0001 | g0140 | EAS | CDX | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | CDX | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG02165 | hp2 | a0002 | c0002 | t0001 | g0086 | EAS | CDX | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0240 | AFR | ACB | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG02257 | hp2 | a0001 | c0003 | t0001 | g0068 | AFR | ACB | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | ACB | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG02258 | hp2 | a0001 | c0006 | t0001 | g0049 | AFR | ACB | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG02273 | hp1 | a0002 | c0002 | t0001 | g0006 | AMR | PEL | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG02273 | hp2 | a0001 | c0003 | t0001 | g0253 | AMR | PEL | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG02280 | hp1 | a0001 | c0003 | t0001 | g0039 | AFR | ACB | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG02280 | hp2 | a0001 | c0003 | t0001 | g0295 | AFR | ACB | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG02300 | hp1 | a0001 | c0004 | t0001 | g0330 | AMR | PEL | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG02300 | hp2 | a0001 | c0003 | t0001 | g0236 | AMR | PEL | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG02451 | hp1 | a0001 | c0001 | t0002 | g0019 | AFR | ACB | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0166 | AFR | ACB | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0064 | AFR | GWD | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0057 | SAS | PJL | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0303 | SAS | PJL | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0167 | AFR | GWD | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG02615 | hp2 | a0001 | c0003 | t0001 | g0050 | AFR | GWD | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG02622 | hp1 | a0001 | c0001 | t0002 | g0005 | AFR | GWD | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG02622 | hp2 | a0002 | c0009 | t0003 | g0012 | AFR | GWD | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0149 | AFR | GWD | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG02647 | hp1 | a0001 | c0003 | t0001 | g0051 | AFR | GWD | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0060 | AFR | GWD | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG02683 | hp1 | a0002 | c0002 | t0001 | g0300 | SAS | PJL | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0251 | SAS | PJL | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0023 | SAS | PJL | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0296 | SAS | PJL | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0153 | AFR | GWD | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | GWD | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG02723 | hp1 | a0002 | c0009 | t0003 | g0013 | AFR | GWD | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG02723 | hp2 | a0002 | c0002 | t0001 | g0021 | AFR | GWD | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG02809 | hp1 | a0001 | c0006 | t0001 | g0047 | AFR | GWD | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG02809 | hp2 | a0001 | c0006 | t0002 | g0059 | AFR | GWD | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0005 | AFR | GWD | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0281 | AFR | GWD | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | GWD | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | GWD | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0080 | AFR | GWD | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG02896 | hp1 | a0001 | c0001 | t0002 | g0061 | AFR | GWD | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG02896 | hp2 | a0001 | c0004 | t0001 | g0320 | AFR | GWD | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | GWD | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG02897 | hp2 | a0001 | c0001 | t0002 | g0062 | AFR | GWD | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0145 | AFR | ESN | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0150 | AFR | ESN | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG02965 | hp1 | a0001 | c0001 | t0002 | g0146 | AFR | ESN | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG02965 | hp2 | a0001 | c0001 | t0002 | g0004 | AFR | ESN | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG02976 | hp1 | a0001 | c0003 | t0001 | g0277 | AFR | ESN | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG02976 | hp2 | a0002 | c0002 | t0001 | g0029 | AFR | ESN | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0102 | SAS | PJL | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG03017 | hp2 | a0001 | c0006 | t0001 | g0126 | SAS | PJL | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0063 | AFR | GWD | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG03041 | hp2 | a0001 | c0001 | t0002 | g0046 | AFR | GWD | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG03098 | hp1 | a0001 | c0005 | t0003 | g0003 | AFR | MSL | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG03098 | hp2 | a0010 | c0018 | t0001 | g0275 | AFR | MSL | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG03130 | hp1 | a0002 | c0002 | t0001 | g0022 | AFR | ESN | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0304 | AFR | ESN | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG03139 | hp1 | a0001 | c0003 | t0001 | g0048 | AFR | ESN | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG03139 | hp2 | a0001 | c0003 | t0002 | g0256 | AFR | ESN | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG03195 | hp1 | a0001 | c0006 | t0001 | g0055 | AFR | ESN | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | ESN | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | MSL | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG03209 | hp2 | a0001 | c0003 | t0001 | g0040 | AFR | MSL | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0284 | AFR | MSL | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | MSL | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG03239 | hp1 | a0001 | c0003 | t0001 | g0172 | SAS | PJL | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG03239 | hp2 | a0001 | c0003 | t0001 | g0239 | SAS | PJL | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG03486 | hp1 | a0001 | c0006 | t0001 | g0154 | AFR | MSL | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0276 | AFR | MSL | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG03490 | hp1 | a0002 | c0002 | t0002 | g0176 | SAS | PJL | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0069 | SAS | PJL | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG03492 | hp1 | a0002 | c0002 | t0002 | g0177 | SAS | PJL | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG03492 | hp2 | a0001 | c0006 | t0001 | g0174 | SAS | PJL | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG03516 | hp1 | a0001 | c0006 | t0002 | g0058 | AFR | ESN | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG03516 | hp2 | a0002 | c0002 | t0001 | g0020 | AFR | ESN | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0238 | AFR | GWD | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0180 | AFR | GWD | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG03579 | hp1 | a0001 | c0003 | t0001 | g0164 | AFR | MSL | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG03579 | hp2 | a0001 | c0003 | t0001 | g0037 | AFR | MSL | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0291 | SAS | PJL | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0096 | SAS | PJL | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG03669 | hp1 | a0001 | c0004 | t0001 | g0337 | SAS | PJL | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG03669 | hp2 | a0001 | c0005 | t0001 | g0345 | SAS | PJL | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0286 | SAS | STU | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG03688 | hp2 | a0002 | c0002 | t0001 | g0072 | SAS | STU | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0290 | SAS | PJL | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0288 | SAS | PJL | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG03710 | hp1 | a0002 | c0011 | t0002 | g0078 | SAS | PJL | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG03710 | hp2 | a0001 | c0003 | t0001 | g0056 | SAS | PJL | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG03831 | hp1 | a0002 | c0002 | t0001 | g0188 | SAS | BEB | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG03831 | hp2 | a0002 | c0002 | t0001 | g0201 | SAS | BEB | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG03834 | hp1 | a0001 | c0004 | t0001 | g0309 | SAS | BEB | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG03834 | hp2 | a0002 | c0007 | t0001 | g0315 | SAS | BEB | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0122 | SAS | BEB | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG03927 | hp2 | a0002 | c0002 | t0001 | g0097 | SAS | BEB | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG03942 | hp1 | a0001 | c0004 | t0001 | g0346 | SAS | BEB | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0071 | SAS | BEB | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0287 | SAS | STU | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG04115 | hp2 | a0002 | c0002 | t0002 | g0302 | SAS | STU | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG04184 | hp1 | a0001 | c0014 | t0002 | g0035 | SAS | BEB | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG04184 | hp2 | a0002 | c0002 | t0001 | g0207 | SAS | BEB | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG04199 | hp1 | a0006 | c0020 | t0001 | g0274 | SAS | STU | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0127 | SAS | STU | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0289 | SAS | STU | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0283 | SAS | STU | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0165 | AFR | YRI | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| NA18522 | hp2 | a0001 | c0003 | t0001 | g0168 | AFR | YRI | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0292 | EAS | CHB | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| NA18612 | hp2 | a0002 | c0002 | t0001 | g0222 | EAS | CHB | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| NA18747 | hp1 | a0002 | c0002 | t0001 | g0087 | EAS | CHB | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | CHB | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| NA18906 | hp1 | a0001 | c0003 | t0001 | g0041 | AFR | YRI | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| NA18906 | hp2 | a0001 | c0006 | t0001 | g0181 | AFR | YRI | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| NA18939 | hp1 | a0002 | c0002 | t0002 | g0209 | EAS | JPT | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| NA18939 | hp2 | a0003 | c0012 | t0001 | g0070 | EAS | JPT | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| NA18940 | hp1 | a0001 | c0001 | t0002 | g0133 | EAS | JPT | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| NA18941 | hp1 | a0009 | c0015 | t0001 | g0332 | EAS | JPT | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| NA18941 | hp2 | a0001 | c0005 | t0001 | g0341 | EAS | JPT | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| NA18943 | hp1 | a0002 | c0002 | t0001 | g0210 | EAS | JPT | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| NA18943 | hp2 | a0001 | c0003 | t0001 | g0142 | EAS | JPT | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| NA18944 | hp2 | a0002 | c0002 | t0002 | g0085 | EAS | JPT | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| NA18945 | hp1 | a0001 | c0004 | t0001 | g0333 | EAS | JPT | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| NA18945 | hp2 | a0002 | c0002 | t0002 | g0199 | EAS | JPT | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| NA18946 | hp1 | a0002 | c0002 | t0002 | g0104 | EAS | JPT | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| NA18947 | hp2 | a0002 | c0007 | t0001 | g0314 | EAS | JPT | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| NA18948 | hp1 | a0002 | c0002 | t0001 | g0206 | EAS | JPT | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| NA18948 | hp2 | a0001 | c0005 | t0001 | g0347 | EAS | JPT | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| NA18951 | hp1 | a0002 | c0002 | t0001 | g0202 | EAS | JPT | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| NA18951 | hp2 | a0001 | c0004 | t0002 | g0349 | EAS | JPT | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| NA18952 | hp1 | a0002 | c0002 | t0001 | g0187 | EAS | JPT | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0265 | EAS | JPT | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| NA18954 | hp2 | a0002 | c0002 | t0002 | g0008 | EAS | JPT | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| NA18960 | hp2 | a0001 | c0005 | t0001 | g0324 | EAS | JPT | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| NA18961 | hp1 | a0002 | c0002 | t0001 | g0212 | EAS | JPT | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| NA18961 | hp2 | a0001 | c0001 | t0002 | g0117 | EAS | JPT | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| NA18963 | hp2 | a0002 | c0007 | t0002 | g0343 | EAS | JPT | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| NA18964 | hp1 | a0002 | c0002 | t0001 | g0204 | EAS | JPT | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| NA18965 | hp1 | a0001 | c0004 | t0001 | g0002 | EAS | JPT | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| NA18965 | hp2 | a0002 | c0002 | t0001 | g0186 | EAS | JPT | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| NA18968 | hp1 | a0001 | c0003 | t0002 | g0074 | EAS | JPT | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| NA18971 | hp1 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0094 | EAS | JPT | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| NA18983 | hp2 | a0002 | c0002 | t0001 | g0225 | EAS | JPT | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| NA18985 | hp1 | a0002 | c0002 | t0002 | g0008 | EAS | JPT | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| NA18986 | hp2 | a0001 | c0005 | t0002 | g0334 | EAS | JPT | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| NA18988 | hp1 | a0001 | c0001 | t0002 | g0297 | EAS | JPT | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| NA18988 | hp2 | a0002 | c0002 | t0001 | g0196 | EAS | JPT | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| NA18989 | hp1 | a0003 | c0012 | t0001 | g0138 | EAS | JPT | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| NA18989 | hp2 | a0002 | c0002 | t0002 | g0264 | EAS | JPT | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0143 | EAS | JPT | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| NA18990 | hp2 | a0001 | c0004 | t0001 | g0002 | EAS | JPT | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| NA18992 | hp2 | a0007 | c0017 | t0002 | g0237 | EAS | JPT | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| NA18993 | hp1 | a0001 | c0016 | t0001 | g0348 | EAS | JPT | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| NA18994 | hp2 | a0001 | c0001 | t0002 | g0101 | EAS | JPT | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| NA19000 | hp1 | a0002 | c0007 | t0002 | g0313 | EAS | JPT | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| NA19000 | hp2 | a0002 | c0002 | t0002 | g0079 | EAS | JPT | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| NA19001 | hp1 | a0001 | c0004 | t0001 | g0325 | EAS | JPT | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| NA19001 | hp2 | a0001 | c0001 | t0002 | g0110 | EAS | JPT | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| NA19005 | hp1 | a0002 | c0002 | t0001 | g0215 | EAS | JPT | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| NA19009 | hp1 | a0002 | c0002 | t0001 | g0185 | EAS | JPT | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| NA19009 | hp2 | a0002 | c0002 | t0002 | g0224 | EAS | JPT | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| NA19010 | hp1 | a0002 | c0002 | t0001 | g0216 | EAS | JPT | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| NA19010 | hp2 | a0002 | c0007 | t0001 | g0311 | EAS | JPT | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| NA19011 | hp1 | a0002 | c0002 | t0001 | g0269 | EAS | JPT | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| NA19011 | hp2 | a0002 | c0002 | t0001 | g0197 | EAS | JPT | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| NA19030 | hp1 | a0008 | c0019 | t0001 | g0033 | AFR | LWK | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| NA19030 | hp2 | a0001 | c0003 | t0002 | g0147 | AFR | LWK | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| NA19043 | hp1 | a0001 | c0003 | t0001 | g0169 | AFR | LWK | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| NA19043 | hp2 | a0001 | c0003 | t0001 | g0278 | AFR | LWK | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| NA19058 | hp1 | a0001 | c0004 | t0001 | g0335 | EAS | JPT | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| NA19060 | hp1 | a0001 | c0004 | t0002 | g0318 | EAS | JPT | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| NA19060 | hp2 | a0002 | c0002 | t0001 | g0084 | EAS | JPT | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| NA19063 | hp1 | a0002 | c0002 | t0001 | g0211 | EAS | JPT | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| NA19065 | hp1 | a0002 | c0002 | t0001 | g0217 | EAS | JPT | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| NA19065 | hp2 | a0002 | c0007 | t0001 | g0316 | EAS | JPT | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| NA19068 | hp2 | a0002 | c0002 | t0001 | g0213 | EAS | JPT | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| NA19070 | hp1 | a0001 | c0003 | t0001 | g0088 | EAS | JPT | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| NA19076 | hp1 | a0002 | c0002 | t0001 | g0198 | EAS | JPT | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| NA19077 | hp1 | a0002 | c0002 | t0001 | g0200 | EAS | JPT | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| NA19078 | hp1 | a0002 | c0002 | t0002 | g0191 | EAS | JPT | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| NA19079 | hp1 | a0002 | c0011 | t0001 | g0203 | EAS | JPT | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| NA19081 | hp1 | a0002 | c0002 | t0001 | g0139 | EAS | JPT | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| NA19081 | hp2 | a0002 | c0007 | t0001 | g0310 | EAS | JPT | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| NA19082 | hp2 | a0001 | c0004 | t0001 | g0002 | EAS | JPT | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| NA19085 | hp1 | a0002 | c0002 | t0001 | g0270 | EAS | JPT | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| NA19085 | hp2 | a0001 | c0005 | t0001 | g0331 | EAS | JPT | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| NA19087 | hp1 | a0001 | c0003 | t0002 | g0107 | EAS | JPT | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| NA19087 | hp2 | a0002 | c0002 | t0001 | g0214 | EAS | JPT | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| NA19090 | hp1 | a0002 | c0013 | t0002 | g0312 | EAS | JPT | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| NA19090 | hp2 | a0002 | c0002 | t0001 | g0227 | EAS | JPT | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| NA19091 | hp1 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| NA19240 | hp1 | a0004 | c0010 | t0001 | g0066 | AFR | YRI | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| NA19240 | hp2 | a0001 | c0004 | t0004 | g0014 | AFR | YRI | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| NA20129 | hp1 | a0001 | c0003 | t0001 | g0159 | AFR | ASW | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0280 | AFR | ASW | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| NA20752 | hp1 | a0001 | c0005 | t0002 | g0036 | EUR | TSI | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| NA20752 | hp2 | a0001 | c0003 | t0001 | g0001 | EUR | TSI | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG02486 | hp1 | a0001 | c0003 | t0001 | g0073 | AFR | ACB | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG02486 | hp2 | a0001 | c0003 | t0001 | g0001 | AFR | ACB | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG02559 | hp1 | a0001 | c0003 | t0002 | g0052 | AFR | ACB | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0152 | AFR | ACB | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG03471 | hp1 | a0004 | c0010 | t0001 | g0065 | AFR | MSL | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| HG03471 | hp2 | a0001 | c0005 | t0003 | g0003 | AFR | MSL | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| NA18955 | hp1 | a0002 | c0002 | t0001 | g0077 | EAS | JPT | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| NA18955 | hp2 | a0001 | c0003 | t0001 | g0105 | EAS | JPT | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0233 | AFR | USA | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0151 | AFR | USA | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| NA21309 | hp1 | a0001 | c0006 | t0001 | g0182 | AFR | LWK | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| NA21309 | hp2 | a0001 | c0004 | t0001 | g0344 | AFR | LWK | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0171 | REF | REF | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| homoSapiens_grch38 | hp1 | a0001 | c0003 | t0001 | g0001 | REF | REF | NOX3_chr6_155390368_155460839 | NOX3 | chr6 | 155390368 | 155460839 |
| chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:155428906
|
G | T | 1 | a0004 | 2 | HG03471.hp1 NA19240.hp1 |
missense_variant | MODERATE | c.1033C>A | p.Gln345Lys | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 9/14 | 1072/1980 | 1033/1707 | 345/568 | chr6 | 155428906 | ||
| chr6:155428941
|
A | C | 1 | a0007 | 1 | NA18992.hp2 | missense_variant | MODERATE | c.998T>G | p.Leu333Arg | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 9/14 | 1037/1980 | 998/1707 | 333/568 | chr6 | 155428941 | ||
| chr6:155429002
|
G | A | 1 | a0009 | 1 | NA18941.hp1 | missense_variant | MODERATE | c.937C>T | p.Arg313Cys | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 9/14 | 976/1980 | 937/1707 | 313/568 | chr6 | 155429002 | ||
| chr6:155436500
|
A | T | 1 | a0010 | 1 | HG03098.hp2 | missense_variant | MODERATE | c.716T>A | p.Ile239Asn | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 7/14 | 755/1980 | 716/1707 | 239/568 | chr6 | 155436500 | ||
| chr6:155439959
|
G | A | 1 | a0008 | 1 | NA19030.hp1 | missense_variant | MODERATE | c.665C>T | p.Thr222Met | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 6/14 | 704/1980 | 665/1707 | 222/568 | chr6 | 155439959 | ||
| chr6:155440032
|
C | T | 1 | a0003 | 5 | HG00621.hp2 HG02015.hp2 HG02129.hp2 others(2): Show |
missense_variant | MODERATE | c.592G>A | p.Ala198Thr | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 6/14 | 631/1980 | 592/1707 | 198/568 | chr6 | 155440032 | ||
| chr6:155440112
|
G | T | 4 | a0002a0004a0005others(1): Show | 93 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(90): Show |
missense_variant | MODERATE | c.512C>A | p.Thr171Lys | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 6/14 | 551/1980 | 512/1707 | 171/568 | chr6 | 155440112 | ||
| chr6:155453445
|
C | A | 1 | a0006 | 1 | HG04199.hp1 | missense_variant | MODERATE | c.299G>T | p.Arg100Ile | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 4/14 | 338/1980 | 299/1707 | 100/568 | chr6 | 155453445 | ||
| chr6:155453462
|
T | G | 1 | a0005 | 1 | HG02129.hp1 | missense_variant | MODERATE | c.282A>C | p.Gln94His | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 4/14 | 321/1980 | 282/1707 | 94/568 | chr6 | 155453462 |
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:155428901
|
C | T | 17 | a0001c0001a0001c0005a0001c0006others(14): Show | 281 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(278): Show |
synonymous_variant | LOW | c.1038G>A | p.Glu346Glu | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 9/14 | 1077/1980 | 1038/1707 | 346/568 | chr6 | 155428901 | ||
| chr6:155428904
|
C | T | 3 | a0001c0006a0001c0014a0002c0009 | 15 | HG00738.hp2 HG01884.hp1 HG02258.hp2 others(12): Show |
synonymous_variant | LOW | c.1035G>A | p.Gln345Gln | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 9/14 | 1074/1980 | 1035/1707 | 345/568 | chr6 | 155428904 | ||
| chr6:155453474
|
C | T | 8 | a0001c0004a0001c0005a0001c0014others(5): Show | 56 | HG00621.hp2 HG00642.hp1 HG01081.hp1 others(53): Show |
synonymous_variant | LOW | c.270G>A | p.Pro90Pro | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 4/14 | 309/1980 | 270/1707 | 90/568 | chr6 | 155453474 | ||
| chr6:155454846
|
G | T | 9 | a0001c0004a0001c0005a0001c0014others(6): Show | 57 | HG00621.hp2 HG00642.hp1 HG01081.hp1 others(54): Show |
synonymous_variant | LOW | c.220C>A | p.Arg74Arg | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 3/14 | 259/1980 | 220/1707 | 74/568 | chr6 | 155454846 |
| chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:155395413
|
G | T | 1 | a0001c0003t0005 | 1 | HG01891.hp2 | 3_prime_UTR_variant | MODIFIER | c.*189C>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 14/14 | 1423 | chr6 | 155395413 | |||||
| chr6:155395463
|
T | C | 13 | a0001c0001t0002a0001c0003t0002a0001c0003t0005others(10): Show | 75 | HG00280.hp2 HG00438.hp1 HG00639.hp1 others(72): Show |
3_prime_UTR_variant | MODIFIER | c.*139A>G | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 14/14 | 1373 | chr6 | 155395463 | |||||
| chr6:155455814
|
C | T | 4 | a0001c0004t0003a0001c0004t0004a0001c0005t0003others(1): Show | 7 | HG01243.hp1 HG02145.hp1 HG02622.hp2 others(4): Show |
5_prime_UTR_variant | MODIFIER | c.-14G>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 1/14 | 14 | chr6 | 155455814 |
| chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:155395614
|
G | A | 17 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0109others(14): Show | 19 | HG02074.hp1 HG03927.hp2 NA18943.hp1 others(16): Show |
intron_variant | MODIFIER | c.*28-40C>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 13/13 | chr6 | 155395614 | ||||||
| chr6:155395735
|
C | A | 123 | a0001c0001t0001g0024a0001c0001t0001g0060a0001c0001t0001g0063others(120): Show | 128 | HG00280.hp2 HG00438.hp1 HG00639.hp1 others(125): Show |
intron_variant | MODIFIER | c.*28-161G>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 13/13 | chr6 | 155395735 | ||||||
| chr6:155395803
|
A | G | 1 | a0008c0019t0001g0033 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.*28-229T>C | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 13/13 | chr6 | 155395803 | ||||||
| chr6:155396068
|
G | A | 18 | a0001c0001t0001g0075a0001c0001t0001g0083a0001c0001t0001g0103others(15): Show | 19 | HG00423.hp1 HG00558.hp2 HG00621.hp2 others(16): Show |
intron_variant | MODIFIER | c.*28-494C>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 13/13 | chr6 | 155396068 | ||||||
| chr6:155396259
|
C | T | 2 | a0001c0001t0001g0042a0001c0001t0001g0043 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.*27+550G>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 13/13 | chr6 | 155396259 | ||||||
| chr6:155396272
|
A | G | 5 | a0001c0001t0001g0024a0001c0001t0001g0153a0001c0001t0001g0276others(2): Show | 5 | HG01257.hp1 HG02717.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.*27+537T>C | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 13/13 | chr6 | 155396272 | ||||||
| chr6:155396416
|
G | A | 1 | a0001c0001t0001g0090 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.*27+393C>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 13/13 | chr6 | 155396416 | ||||||
| chr6:155396528
|
T | A | 2 | a0001c0001t0001g0294a0001c0001t0001g0299 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.*27+281A>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 13/13 | chr6 | 155396528 | ||||||
| chr6:155396540
|
G | A | 2 | a0001c0003t0001g0073a0001c0004t0003g0015 | 2 | HG02145.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.*27+269C>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 13/13 | chr6 | 155396540 | ||||||
| chr6:155396722
|
C | G | 1 | a0008c0019t0001g0033 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.*27+87G>C | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 13/13 | chr6 | 155396722 | ||||||
| chr6:155396801
|
C | T | 1 | a0001c0001t0001g0254 | 1 | HG01069.hp1 | splice_region_variant&intron_variant | LOW | c.*27+8G>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 13/13 | chr6 | 155396801 | ||||||
| chr6:155396970
|
A | G | 5 | a0001c0001t0001g0081a0001c0001t0001g0266a0002c0007t0001g0310others(2): Show | 5 | HG02129.hp1 NA18954.hp1 NA19002.hp1 others(2): Show |
splice_region_variant&intron_variant | LOW | c.1581-8T>C | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 12/13 | chr6 | 155396970 | ||||||
| chr6:155397024
|
A | C | 3 | a0001c0001t0001g0282a0001c0003t0001g0169a0010c0018t0001g0275 | 3 | HG02145.hp2 HG03098.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1581-62T>G | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 12/13 | chr6 | 155397024 | ||||||
| chr6:155397049
|
G | A | 1 | a0001c0005t0001g0331 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1581-87C>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 12/13 | chr6 | 155397049 | ||||||
| chr6:155397066
|
T | C | 1 | a0002c0002t0002g0219 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1581-104A>G | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 12/13 | chr6 | 155397066 | ||||||
| chr6:155397254
|
G | A | 9 | a0001c0001t0001g0240a0001c0001t0001g0284a0001c0003t0001g0039others(6): Show | 9 | HG02257.hp1 HG02280.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.1581-292C>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 12/13 | chr6 | 155397254 | ||||||
| chr6:155397432
|
T | C | 18 | a0001c0001t0001g0075a0001c0001t0001g0083a0001c0001t0001g0103others(15): Show | 19 | HG00423.hp1 HG00558.hp2 HG00621.hp2 others(16): Show |
intron_variant | MODIFIER | c.1581-470A>G | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 12/13 | chr6 | 155397432 | ||||||
| chr6:155397473
|
C | T | 5 | a0001c0001t0001g0024a0001c0001t0001g0153a0001c0001t0001g0276others(2): Show | 5 | HG01257.hp1 HG02717.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.1581-511G>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 12/13 | chr6 | 155397473 | ||||||
| chr6:155397585
|
C | T | 9 | a0001c0001t0001g0063a0001c0001t0001g0089a0001c0001t0001g0165others(6): Show | 9 | HG01891.hp1 HG02040.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.1581-623G>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 12/13 | chr6 | 155397585 | ||||||
| chr6:155397609
|
C | T | 1 | a0001c0001t0001g0290 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1581-647G>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 12/13 | chr6 | 155397609 | ||||||
| chr6:155397634
|
T | C | 2 | a0001c0003t0002g0279a0001c0004t0004g0011 | 2 | HG01243.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.1581-672A>G | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 12/13 | chr6 | 155397634 | ||||||
| chr6:155397646
|
C | T | 1 | a0001c0001t0001g0121 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1581-684G>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 12/13 | chr6 | 155397646 | ||||||
| chr6:155397655
|
T | A | 1 | a0002c0009t0003g0012 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1581-693A>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 12/13 | chr6 | 155397655 | ||||||
| chr6:155397709
|
T | C | 1 | a0001c0005t0001g0308 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1581-747A>G | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 12/13 | chr6 | 155397709 | ||||||
| chr6:155397943
|
G | A | 166 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0024others(163): Show | 173 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(170): Show |
intron_variant | MODIFIER | c.1581-981C>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 12/13 | chr6 | 155397943 | ||||||
| chr6:155398235
|
C | A | 5 | a0001c0001t0001g0024a0001c0001t0001g0153a0001c0001t0001g0276others(2): Show | 5 | HG01257.hp1 HG02717.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.1581-1273G>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 12/13 | chr6 | 155398235 | ||||||
| chr6:155398285
|
C | T | 2 | a0001c0001t0001g0280a0004c0010t0001g0066 | 2 | NA19240.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1581-1323G>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 12/13 | chr6 | 155398285 | ||||||
| chr6:155398400
|
G | T | 166 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0024others(163): Show | 173 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(170): Show |
intron_variant | MODIFIER | c.1581-1438C>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 12/13 | chr6 | 155398400 | ||||||
| chr6:155398509
|
T | C | 2 | a0001c0001t0001g0024a0001c0001t0001g0153 | 2 | HG01257.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.1581-1547A>G | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 12/13 | chr6 | 155398509 | ||||||
| chr6:155398638
|
A | T | 8 | a0001c0001t0001g0024a0001c0001t0001g0153a0001c0001t0001g0276others(5): Show | 8 | HG01109.hp2 HG01257.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.1581-1676T>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 12/13 | chr6 | 155398638 | ||||||
| chr6:155398706
|
T | G | 2 | a0001c0003t0002g0107a0001c0004t0002g0349 | 2 | NA18951.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.1581-1744A>C | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 12/13 | chr6 | 155398706 | ||||||
| chr6:155398983
|
G | T | 24 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0026others(21): Show | 25 | HG01516.hp1 HG01517.hp1 HG02027.hp2 others(22): Show |
intron_variant | MODIFIER | c.1581-2021C>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 12/13 | chr6 | 155398983 | ||||||
| chr6:155399008
|
C | T | 1 | a0001c0001t0001g0254 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1581-2046G>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 12/13 | chr6 | 155399008 | ||||||
| chr6:155399107
|
G | A | 26 | a0001c0001t0001g0063a0001c0001t0001g0089a0001c0001t0001g0091others(23): Show | 28 | HG01891.hp1 HG02040.hp1 HG02074.hp1 others(25): Show |
intron_variant | MODIFIER | c.1581-2145C>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 12/13 | chr6 | 155399107 | ||||||
| chr6:155399213
|
T | A | 1 | a0002c0002t0001g0300 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1581-2251A>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 12/13 | chr6 | 155399213 | ||||||
| chr6:155399245
|
T | C | 28 | a0001c0001t0001g0063a0001c0001t0001g0089a0001c0001t0001g0091others(25): Show | 30 | HG01891.hp1 HG02040.hp1 HG02074.hp1 others(27): Show |
intron_variant | MODIFIER | c.1581-2283A>G | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 12/13 | chr6 | 155399245 | ||||||
| chr6:155399289
|
C | G | 1 | a0001c0004t0001g0319 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1581-2327G>C | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 12/13 | chr6 | 155399289 | ||||||
| chr6:155399474
|
C | T | 2 | a0002c0002t0001g0186a0002c0002t0001g0215 | 2 | NA18965.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.1581-2512G>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 12/13 | chr6 | 155399474 | ||||||
| chr6:155399478
|
G | A | 1 | a0001c0003t0001g0163 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.1581-2516C>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 12/13 | chr6 | 155399478 | ||||||
| chr6:155399634
|
T | C | 1 | a0001c0005t0003g0003 | 2 | HG03098.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1581-2672A>G | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 12/13 | chr6 | 155399634 | ||||||
| chr6:155399730
|
CT | C | 88 | a0001c0001t0001g0024a0001c0001t0001g0028a0001c0001t0001g0060others(85): Show | 91 | HG00280.hp2 HG00438.hp1 HG00639.hp1 others(88): Show |
intron_variant | MODIFIER | c.1581-2769delA | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 12/13 | chr6 | 155399730 | ||||||
| chr6:155399730
|
CTT | C | 28 | a0001c0001t0001g0063a0001c0001t0001g0089a0001c0001t0001g0091others(25): Show | 30 | HG01891.hp1 HG02040.hp1 HG02074.hp1 others(27): Show |
intron_variant | MODIFIER | c.1581-2770_1581-276 others(6): Show |
NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 12/13 | chr6 | 155399730 | ||||||
| chr6:155399743
|
C | G | 3 | a0001c0001t0001g0060a0001c0006t0001g0049a0002c0009t0003g0012 | 3 | HG02258.hp2 HG02622.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.1581-2781G>C | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 12/13 | chr6 | 155399743 | ||||||
| chr6:155399801
|
T | A | 2 | a0001c0001t0001g0280a0004c0010t0001g0066 | 2 | NA19240.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1581-2839A>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 12/13 | chr6 | 155399801 | ||||||
| chr6:155399857
|
C | A | 28 | a0001c0001t0001g0063a0001c0001t0001g0089a0001c0001t0001g0091others(25): Show | 30 | HG01891.hp1 HG02040.hp1 HG02074.hp1 others(27): Show |
intron_variant | MODIFIER | c.1581-2895G>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 12/13 | chr6 | 155399857 | ||||||
| chr6:155399908
|
G | A | 2 | a0001c0001t0001g0229a0001c0001t0001g0230 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.1581-2946C>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 12/13 | chr6 | 155399908 | ||||||
| chr6:155399913
|
A | G | 51 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0026others(48): Show | 53 | HG00423.hp1 HG00558.hp2 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.1581-2951T>C | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 12/13 | chr6 | 155399913 | ||||||
| chr6:155399960
|
G | A | 1 | a0002c0007t0001g0317 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1581-2998C>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 12/13 | chr6 | 155399960 | ||||||
| chr6:155399974
|
G | A | 1 | a0001c0001t0001g0234 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1581-3012C>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 12/13 | chr6 | 155399974 | ||||||
| chr6:155400355
|
C | T | 73 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0019others(70): Show | 76 | HG00280.hp2 HG00438.hp1 HG00639.hp1 others(73): Show |
intron_variant | MODIFIER | c.1581-3393G>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 12/13 | chr6 | 155400355 | ||||||
| chr6:155400382
|
T | TA | 27 | a0001c0001t0001g0075a0001c0001t0001g0083a0001c0001t0001g0103others(24): Show | 28 | HG00423.hp1 HG00558.hp2 HG00621.hp2 others(25): Show |
intron_variant | MODIFIER | c.1581-3421dupT | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 12/13 | chr6 | 155400382 | ||||||
| chr6:155400391
|
G | T | 51 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0026others(48): Show | 53 | HG00423.hp1 HG00558.hp2 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.1581-3429C>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 12/13 | chr6 | 155400391 | ||||||
| chr6:155400432
|
C | A | 1 | a0002c0011t0002g0078 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1581-3470G>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 12/13 | chr6 | 155400432 | ||||||
| chr6:155400451
|
G | A | 1 | a0002c0002t0001g0198 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1581-3489C>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 12/13 | chr6 | 155400451 | ||||||
| chr6:155400574
|
T | C | 1 | a0002c0002t0001g0022 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1581-3612A>G | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 12/13 | chr6 | 155400574 | ||||||
| chr6:155400633
|
C | T | 1 | a0001c0001t0002g0069 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1581-3671G>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 12/13 | chr6 | 155400633 | ||||||
| chr6:155400641
|
C | CT | 11 | a0001c0001t0001g0060a0001c0001t0001g0063a0001c0001t0001g0089others(8): Show | 11 | HG02040.hp1 HG02258.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.1581-3680dupA | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 12/13 | chr6 | 155400641 | ||||||
| chr6:155400641
|
CT | C | 251 | a0001c0001t0001g0009a0001c0001t0001g0016a0001c0001t0001g0017others(248): Show | 257 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(254): Show |
intron_variant | MODIFIER | c.1581-3680delA | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 12/13 | chr6 | 155400641 | ||||||
| chr6:155400731
|
G | A | 1 | a0001c0001t0002g0093 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1581-3769C>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 12/13 | chr6 | 155400731 | ||||||
| chr6:155400831
|
C | T | 4 | a0001c0001t0001g0149a0001c0006t0001g0154a0002c0009t0003g0013others(1): Show | 4 | HG02129.hp2 HG02630.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.1581-3869G>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 12/13 | chr6 | 155400831 | ||||||
| chr6:155400985
|
A | C | 147 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0024others(144): Show | 152 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(149): Show |
intron_variant | MODIFIER | c.1581-4023T>G | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 12/13 | chr6 | 155400985 | ||||||
| chr6:155401041
|
C | T | 8 | a0001c0001t0001g0149a0001c0003t0001g0037a0001c0003t0001g0040others(5): Show | 8 | HG02145.hp1 HG02486.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1581-4079G>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 12/13 | chr6 | 155401041 | ||||||
| chr6:155401100
|
C | T | 72 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0019others(69): Show | 75 | HG00280.hp2 HG00438.hp1 HG00639.hp1 others(72): Show |
intron_variant | MODIFIER | c.1581-4138G>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 12/13 | chr6 | 155401100 | ||||||
| chr6:155401238
|
C | T | 2 | a0001c0001t0001g0150a0001c0001t0001g0151 | 2 | HG02922.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1581-4276G>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 12/13 | chr6 | 155401238 | ||||||
| chr6:155401296
|
G | A | 1 | a0001c0003t0001g0056 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1581-4334C>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 12/13 | chr6 | 155401296 | ||||||
| chr6:155401355
|
T | G | 7 | a0001c0001t0001g0024a0001c0001t0001g0153a0001c0001t0001g0167others(4): Show | 7 | HG01257.hp1 HG02615.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1581-4393A>C | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 12/13 | chr6 | 155401355 | ||||||
| chr6:155401364
|
G | A | 2 | a0001c0003t0001g0073a0001c0004t0003g0015 | 2 | HG02145.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.1581-4402C>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 12/13 | chr6 | 155401364 | ||||||
| chr6:155401455
|
C | A | 3 | a0001c0003t0001g0051a0001c0003t0001g0144a0001c0003t0001g0168 | 3 | HG01109.hp2 HG02647.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1581-4493G>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 12/13 | chr6 | 155401455 | ||||||
| chr6:155401551
|
C | T | 9 | a0001c0001t0001g0063a0001c0001t0001g0089a0001c0001t0001g0165others(6): Show | 9 | HG01891.hp1 HG02040.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.1581-4589G>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 12/13 | chr6 | 155401551 | ||||||
| chr6:155401625
|
A | G | 146 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0024others(143): Show | 151 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(148): Show |
intron_variant | MODIFIER | c.1581-4663T>C | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 12/13 | chr6 | 155401625 | ||||||
| chr6:155401790
|
CA | C | 72 | a0001c0001t0001g0016a0001c0001t0001g0064a0001c0001t0001g0075others(69): Show | 75 | HG00423.hp1 HG00558.hp2 HG00621.hp2 others(72): Show |
intron_variant | MODIFIER | c.1581-4829delT | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 12/13 | chr6 | 155401790 | ||||||
| chr6:155401790
|
CAA | C | 76 | a0001c0001t0001g0063a0001c0001t0001g0089a0001c0001t0001g0165others(73): Show | 80 | HG00280.hp2 HG00438.hp1 HG00639.hp1 others(77): Show |
intron_variant | MODIFIER | c.1581-4830_1581-482 others(6): Show |
NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 12/13 | chr6 | 155401790 | ||||||
| chr6:155401865
|
C | T | 3 | a0001c0001t0001g0060a0001c0006t0001g0049a0002c0009t0003g0012 | 3 | HG02258.hp2 HG02622.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.1581-4903G>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 12/13 | chr6 | 155401865 | ||||||
| chr6:155401885
|
A | G | 1 | a0001c0001t0001g0167 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1581-4923T>C | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 12/13 | chr6 | 155401885 | ||||||
| chr6:155402020
|
G | A | 1 | a0001c0004t0001g0319 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1581-5058C>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 12/13 | chr6 | 155402020 | ||||||
| chr6:155402156
|
A | T | 7 | a0001c0001t0001g0024a0001c0001t0001g0153a0001c0001t0001g0167others(4): Show | 7 | HG01257.hp1 HG02615.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1580+4974T>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 12/13 | chr6 | 155402156 | ||||||
| chr6:155402165
|
A | G | 2 | a0002c0002t0001g0207a0003c0008t0001g0338 | 2 | HG02015.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.1580+4965T>C | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 12/13 | chr6 | 155402165 | ||||||
| chr6:155402197
|
A | G | 69 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0019others(66): Show | 72 | HG00280.hp2 HG00438.hp1 HG00639.hp1 others(69): Show |
intron_variant | MODIFIER | c.1580+4933T>C | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 12/13 | chr6 | 155402197 | ||||||
| chr6:155402300
|
C | T | 1 | a0002c0002t0001g0157 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1580+4830G>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 12/13 | chr6 | 155402300 | ||||||
| chr6:155402379
|
A | G | 2 | a0001c0001t0001g0306a0001c0001t0001g0307 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.1580+4751T>C | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 12/13 | chr6 | 155402379 | ||||||
| chr6:155402476
|
C | T | 8 | a0001c0001t0001g0092a0001c0001t0001g0123a0001c0001t0001g0124others(5): Show | 10 | HG03927.hp2 NA18943.hp1 NA18948.hp2 others(7): Show |
intron_variant | MODIFIER | c.1580+4654G>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 12/13 | chr6 | 155402476 | ||||||
| chr6:155402600
|
G | A | 1 | a0002c0002t0001g0300 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1580+4530C>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 12/13 | chr6 | 155402600 | ||||||
| chr6:155402790
|
C | T | 1 | a0001c0001t0001g0280 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1580+4340G>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 12/13 | chr6 | 155402790 | ||||||
| chr6:155402850
|
C | A | 3 | a0001c0003t0001g0051a0001c0003t0001g0144a0001c0003t0001g0168 | 3 | HG01109.hp2 HG02647.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1580+4280G>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 12/13 | chr6 | 155402850 | ||||||
| chr6:155402927
|
G | A | 7 | a0001c0001t0001g0024a0001c0001t0001g0153a0001c0001t0001g0167others(4): Show | 7 | HG01257.hp1 HG02615.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1580+4203C>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 12/13 | chr6 | 155402927 | ||||||
| chr6:155402949
|
G | A | 2 | a0001c0001t0001g0306a0001c0001t0001g0307 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.1580+4181C>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 12/13 | chr6 | 155402949 | ||||||
| chr6:155403157
|
G | A | 1 | a0002c0002t0001g0222 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1580+3973C>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 12/13 | chr6 | 155403157 | ||||||
| chr6:155403222
|
A | G | 1 | a0001c0001t0001g0134 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1580+3908T>C | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 12/13 | chr6 | 155403222 | ||||||
| chr6:155403351
|
C | T | 25 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0026others(22): Show | 26 | HG01516.hp1 HG01517.hp1 HG02027.hp2 others(23): Show |
intron_variant | MODIFIER | c.1580+3779G>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 12/13 | chr6 | 155403351 | ||||||
| chr6:155403442
|
C | G | 2 | a0001c0001t0001g0150a0001c0001t0001g0151 | 2 | HG02922.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1580+3688G>C | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 12/13 | chr6 | 155403442 | ||||||
| chr6:155403444
|
A | G | 12 | a0001c0001t0001g0245a0001c0001t0001g0296a0001c0003t0001g0236others(9): Show | 12 | HG00738.hp1 HG00741.hp1 HG01109.hp1 others(9): Show |
intron_variant | MODIFIER | c.1580+3686T>C | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 12/13 | chr6 | 155403444 | ||||||
| chr6:155403732
|
T | C | 2 | a0001c0005t0001g0341a0002c0002t0001g0204 | 2 | NA18941.hp2 NA18964.hp1 |
intron_variant | MODIFIER | c.1580+3398A>G | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 12/13 | chr6 | 155403732 | ||||||
| chr6:155403852
|
G | A | 7 | a0001c0001t0001g0024a0001c0001t0001g0153a0001c0001t0001g0167others(4): Show | 7 | HG01257.hp1 HG02615.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1580+3278C>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 12/13 | chr6 | 155403852 | ||||||
| chr6:155403912
|
G | A | 3 | a0001c0001t0002g0005a0001c0001t0002g0061a0001c0001t0002g0062 | 4 | HG02622.hp1 HG02818.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.1580+3218C>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 12/13 | chr6 | 155403912 | ||||||
| chr6:155404033
|
G | A | 5 | a0001c0001t0001g0030a0001c0001t0001g0044a0001c0001t0001g0090others(2): Show | 5 | HG01884.hp1 HG02055.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.1580+3097C>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 12/13 | chr6 | 155404033 | ||||||
| chr6:155404051
|
C | A | 1 | a0001c0003t0001g0161 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1580+3079G>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 12/13 | chr6 | 155404051 | ||||||
| chr6:155404051
|
C | T | 88 | a0001c0001t0001g0024a0001c0001t0001g0063a0001c0001t0001g0089others(85): Show | 91 | HG00280.hp2 HG00438.hp1 HG00639.hp1 others(88): Show |
intron_variant | MODIFIER | c.1580+3079G>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 12/13 | chr6 | 155404051 | ||||||
| chr6:155404091
|
C | T | 7 | a0001c0001t0001g0024a0001c0001t0001g0153a0001c0001t0001g0167others(4): Show | 7 | HG01257.hp1 HG02615.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1580+3039G>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 12/13 | chr6 | 155404091 | ||||||
| chr6:155404110
|
A | AAT | 35 | a0001c0001t0001g0017a0001c0001t0001g0026a0001c0001t0001g0075others(32): Show | 36 | HG00423.hp1 HG00558.hp2 HG00621.hp2 others(33): Show |
intron_variant | MODIFIER | c.1580+3018_1580+301 others(6): Show |
NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 12/13 | chr6 | 155404110 | ||||||
| chr6:155404110
|
A | AATAT | 10 | a0001c0001t0001g0016a0001c0001t0001g0064a0001c0001t0001g0149others(7): Show | 11 | HG02145.hp1 HG02486.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.1580+3016_1580+301 others(8): Show |
NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 12/13 | chr6 | 155404110 | ||||||
| chr6:155404110
|
A | AATATAT | 3 | a0001c0006t0001g0181a0004c0010t0001g0065a0004c0010t0001g0066 | 3 | HG03471.hp1 NA18906.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1580+3014_1580+301 others(10): Show |
NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 12/13 | chr6 | 155404110 | ||||||
| chr6:155404110
|
AATAT | A | 8 | a0001c0001t0001g0063a0001c0001t0001g0089a0001c0001t0001g0165others(5): Show | 8 | HG01891.hp1 HG02040.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.1580+3016_1580+301 others(8): Show |
NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 12/13 | chr6 | 155404110 | ||||||
| chr6:155404127
|
A | T | 4 | a0001c0001t0001g0100a0001c0001t0001g0135a0001c0005t0001g0324others(1): Show | 4 | NA18960.hp2 NA18971.hp2 NA18986.hp1 others(1): Show |
intron_variant | MODIFIER | c.1580+3003T>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 12/13 | chr6 | 155404127 | ||||||
| chr6:155404127
|
AT | A | 23 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0091others(20): Show | 25 | HG02074.hp1 HG02145.hp2 HG02895.hp1 others(22): Show |
intron_variant | MODIFIER | c.1580+3002delA | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 12/13 | chr6 | 155404127 | ||||||
| chr6:155404127
|
ATT | A | 9 | a0001c0001t0001g0240a0001c0001t0001g0284a0001c0003t0001g0039others(6): Show | 9 | HG01891.hp2 HG02257.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.1580+3001_1580+300 others(6): Show |
NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 12/13 | chr6 | 155404127 | ||||||
| chr6:155404127
|
ATTTT | A | 79 | a0001c0001t0001g0024a0001c0001t0001g0153a0001c0001t0001g0167others(76): Show | 82 | HG00280.hp2 HG00438.hp1 HG00639.hp1 others(79): Show |
intron_variant | MODIFIER | c.1580+2999_1580+300 others(8): Show |
NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 12/13 | chr6 | 155404127 | ||||||
| chr6:155404129
|
T | A | 46 | a0001c0001t0001g0009a0001c0001t0001g0016a0001c0001t0001g0017others(43): Show | 49 | HG00558.hp2 HG00621.hp2 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.1580+3001A>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 12/13 | chr6 | 155404129 | ||||||
| chr6:155404130
|
T | G | 1 | a0001c0001t0001g0303 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1580+3000A>C | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 12/13 | chr6 | 155404130 | ||||||
| chr6:155404131
|
T | A | 38 | a0001c0001t0001g0016a0001c0001t0001g0075a0001c0001t0001g0103others(35): Show | 39 | HG00558.hp2 HG00621.hp2 HG00673.hp2 others(36): Show |
intron_variant | MODIFIER | c.1580+2999A>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 12/13 | chr6 | 155404131 | ||||||
| chr6:155404236
|
C | T | 1 | a0001c0003t0001g0164 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1580+2894G>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 12/13 | chr6 | 155404236 | ||||||
| chr6:155404356
|
G | A | 4 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0003t0001g0045others(1): Show | 4 | HG01975.hp2 HG02922.hp2 HG04199.hp1 others(1): Show |
intron_variant | MODIFIER | c.1580+2774C>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 12/13 | chr6 | 155404356 | ||||||
| chr6:155404475
|
G | A | 3 | a0001c0001t0002g0004a0001c0003t0002g0052a0001c0003t0002g0148 | 4 | HG01496.hp2 HG02258.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1580+2655C>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 12/13 | chr6 | 155404475 | ||||||
| chr6:155404613
|
C | T | 1 | a0001c0001t0001g0167 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1580+2517G>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 12/13 | chr6 | 155404613 | ||||||
| chr6:155404621
|
C | A | 2 | a0001c0003t0001g0073a0001c0004t0003g0015 | 2 | HG02145.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.1580+2509G>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 12/13 | chr6 | 155404621 | ||||||
| chr6:155404778
|
G | A | 2 | a0002c0002t0001g0086a0003c0008t0001g0339 | 2 | HG02129.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.1580+2352C>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 12/13 | chr6 | 155404778 | ||||||
| chr6:155405273
|
A | G | 1 | a0001c0001t0001g0280 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1580+1857T>C | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 12/13 | chr6 | 155405273 | ||||||
| chr6:155405362
|
T | C | 9 | a0001c0001t0001g0063a0001c0001t0001g0089a0001c0001t0001g0165others(6): Show | 9 | HG01891.hp1 HG02040.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.1580+1768A>G | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 12/13 | chr6 | 155405362 | ||||||
| chr6:155405431
|
G | T | 2 | a0001c0001t0001g0153a0001c0003t0001g0050 | 2 | HG02615.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.1580+1699C>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 12/13 | chr6 | 155405431 | ||||||
| chr6:155405816
|
T | TCTCCACC others(8): Show |
1 | a0002c0011t0002g0078 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1580+1299_1580+131 others(19): Show |
NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 12/13 | chr6 | 155405816 | ||||||
| chr6:155405882
|
G | A | 23 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0026others(20): Show | 24 | HG01516.hp1 HG01517.hp1 HG02027.hp2 others(21): Show |
intron_variant | MODIFIER | c.1580+1248C>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 12/13 | chr6 | 155405882 | ||||||
| chr6:155406042
|
G | C | 1 | a0001c0005t0003g0003 | 2 | HG03098.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1580+1088C>G | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 12/13 | chr6 | 155406042 | ||||||
| chr6:155406047
|
T | C | 2 | a0001c0001t0001g0153a0001c0003t0001g0050 | 2 | HG02615.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.1580+1083A>G | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 12/13 | chr6 | 155406047 | ||||||
| chr6:155406165
|
G | A | 1 | a0003c0008t0001g0340 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1580+965C>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 12/13 | chr6 | 155406165 | ||||||
| chr6:155406198
|
T | G | 3 | a0001c0001t0001g0060a0001c0006t0001g0049a0002c0009t0003g0012 | 3 | HG02258.hp2 HG02622.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.1580+932A>C | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 12/13 | chr6 | 155406198 | ||||||
| chr6:155406247
|
C | A | 1 | a0008c0019t0001g0033 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1580+883G>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 12/13 | chr6 | 155406247 | ||||||
| chr6:155406259
|
C | T | 5 | a0001c0001t0001g0030a0001c0001t0001g0044a0001c0001t0001g0090others(2): Show | 5 | HG01884.hp1 HG02055.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.1580+871G>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 12/13 | chr6 | 155406259 | ||||||
| chr6:155406260
|
G | A | 1 | a0001c0001t0001g0127 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1580+870C>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 12/13 | chr6 | 155406260 | ||||||
| chr6:155406276
|
T | C | 1 | a0001c0001t0001g0116 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.1580+854A>G | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 12/13 | chr6 | 155406276 | ||||||
| chr6:155406316
|
G | A | 7 | a0001c0001t0001g0024a0001c0001t0001g0153a0001c0001t0001g0167others(4): Show | 7 | HG01257.hp1 HG02615.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1580+814C>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 12/13 | chr6 | 155406316 | ||||||
| chr6:155406465
|
G | A | 5 | a0001c0003t0001g0051a0001c0003t0001g0073a0001c0003t0001g0144others(2): Show | 5 | HG01109.hp2 HG02145.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1580+665C>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 12/13 | chr6 | 155406465 | ||||||
| chr6:155406791
|
T | G | 30 | a0001c0001t0001g0075a0001c0001t0001g0083a0001c0001t0001g0103others(27): Show | 31 | HG00423.hp1 HG00558.hp2 HG00621.hp2 others(28): Show |
intron_variant | MODIFIER | c.1580+339A>C | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 12/13 | chr6 | 155406791 | ||||||
| chr6:155406998
|
T | C | 30 | a0001c0001t0001g0075a0001c0001t0001g0083a0001c0001t0001g0103others(27): Show | 31 | HG00423.hp1 HG00558.hp2 HG00621.hp2 others(28): Show |
intron_variant | MODIFIER | c.1580+132A>G | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 12/13 | chr6 | 155406998 | ||||||
| chr6:155407073
|
C | T | 2 | a0001c0003t0001g0073a0001c0004t0003g0015 | 2 | HG02145.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.1580+57G>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 12/13 | chr6 | 155407073 | ||||||
| chr6:155407098
|
C | T | 69 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0019others(66): Show | 72 | HG00280.hp2 HG00438.hp1 HG00639.hp1 others(69): Show |
intron_variant | MODIFIER | c.1580+32G>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 12/13 | chr6 | 155407098 | ||||||
| chr6:155407299
|
T | A | 9 | a0001c0001t0001g0240a0001c0001t0001g0284a0001c0003t0001g0039others(6): Show | 9 | HG01891.hp2 HG02257.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.1456-45A>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 11/13 | chr6 | 155407299 | ||||||
| chr6:155407546
|
T | C | 3 | a0001c0003t0001g0051a0001c0003t0001g0144a0001c0003t0001g0168 | 3 | HG01109.hp2 HG02647.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1456-292A>G | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 11/13 | chr6 | 155407546 | ||||||
| chr6:155407577
|
A | G | 2 | a0001c0001t0001g0096a0001c0005t0001g0345 | 2 | HG03654.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.1456-323T>C | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 11/13 | chr6 | 155407577 | ||||||
| chr6:155407730
|
G | T | 2 | a0001c0001t0001g0145a0001c0006t0001g0055 | 2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1456-476C>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 11/13 | chr6 | 155407730 | ||||||
| chr6:155407840
|
T | C | 2 | a0001c0001t0001g0145a0001c0006t0001g0055 | 2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1456-586A>G | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 11/13 | chr6 | 155407840 | ||||||
| chr6:155407851
|
C | G | 3 | a0002c0002t0002g0104a0002c0002t0002g0228a0002c0002t0002g0264 | 3 | HG02027.hp1 NA18946.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.1456-597G>C | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 11/13 | chr6 | 155407851 | ||||||
| chr6:155407896
|
G | A | 1 | a0002c0002t0001g0201 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1456-642C>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 11/13 | chr6 | 155407896 | ||||||
| chr6:155408040
|
G | A | 1 | a0001c0001t0001g0238 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1456-786C>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 11/13 | chr6 | 155408040 | ||||||
| chr6:155408046
|
T | C | 2 | a0002c0002t0001g0020a0002c0002t0001g0029 | 2 | HG02976.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1456-792A>G | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 11/13 | chr6 | 155408046 | ||||||
| chr6:155408061
|
C | T | 1 | a0001c0001t0001g0080 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1456-807G>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 11/13 | chr6 | 155408061 | ||||||
| chr6:155408062
|
T | C | 1 | a0001c0001t0001g0116 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.1456-808A>G | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 11/13 | chr6 | 155408062 | ||||||
| chr6:155408110
|
C | T | 1 | a0002c0002t0002g0158 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1456-856G>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 11/13 | chr6 | 155408110 | ||||||
| chr6:155408152
|
T | G | 6 | a0001c0001t0001g0149a0001c0003t0001g0037a0001c0003t0001g0040others(3): Show | 6 | HG02630.hp2 HG02723.hp1 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.1456-898A>C | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 11/13 | chr6 | 155408152 | ||||||
| chr6:155408154
|
G | T | 8 | a0001c0001t0001g0063a0001c0001t0001g0089a0001c0001t0001g0165others(5): Show | 8 | HG01891.hp1 HG02040.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.1456-900C>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 11/13 | chr6 | 155408154 | ||||||
| chr6:155408169
|
T | A | 30 | a0001c0001t0001g0075a0001c0001t0001g0083a0001c0001t0001g0103others(27): Show | 31 | HG00423.hp1 HG00558.hp2 HG00621.hp2 others(28): Show |
intron_variant | MODIFIER | c.1456-915A>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 11/13 | chr6 | 155408169 | ||||||
| chr6:155408169
|
T | C | 5 | a0001c0003t0001g0051a0001c0003t0001g0073a0001c0003t0001g0144others(2): Show | 5 | HG01109.hp2 HG02145.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1456-915A>G | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 11/13 | chr6 | 155408169 | ||||||
| chr6:155408291
|
C | T | 1 | a0001c0001t0001g0167 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1456-1037G>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 11/13 | chr6 | 155408291 | ||||||
| chr6:155408292
|
A | T | 1 | a0001c0006t0001g0049 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1456-1038T>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 11/13 | chr6 | 155408292 | ||||||
| chr6:155408394
|
C | A | 3 | a0001c0001t0001g0082a0001c0005t0001g0323a0002c0002t0001g0300 | 3 | HG00642.hp1 HG01081.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.1456-1140G>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 11/13 | chr6 | 155408394 | ||||||
| chr6:155408399
|
A | G | 1 | a0001c0001t0001g0179 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1456-1145T>C | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 11/13 | chr6 | 155408399 | ||||||
| chr6:155408462
|
C | A | 9 | a0001c0001t0001g0063a0001c0001t0001g0089a0001c0001t0001g0165others(6): Show | 9 | HG01891.hp1 HG02040.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.1456-1208G>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 11/13 | chr6 | 155408462 | ||||||
| chr6:155408517
|
C | G | 5 | a0001c0003t0001g0051a0001c0003t0001g0073a0001c0003t0001g0144others(2): Show | 5 | HG01109.hp2 HG02145.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1456-1263G>C | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 11/13 | chr6 | 155408517 | ||||||
| chr6:155408580
|
A | T | 3 | a0001c0001t0002g0004a0001c0003t0002g0052a0001c0003t0002g0148 | 4 | HG01496.hp2 HG02258.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1456-1326T>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 11/13 | chr6 | 155408580 | ||||||
| chr6:155408593
|
G | A | 3 | a0001c0001t0002g0101a0002c0002t0002g0079a0002c0007t0002g0343 | 3 | NA18963.hp2 NA18994.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.1456-1339C>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 11/13 | chr6 | 155408593 | ||||||
| chr6:155408595
|
C | T | 21 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0109others(18): Show | 23 | HG02074.hp1 HG02145.hp2 HG03098.hp2 others(20): Show |
intron_variant | MODIFIER | c.1456-1341G>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 11/13 | chr6 | 155408595 | ||||||
| chr6:155408631
|
G | A | 8 | a0001c0001t0001g0063a0001c0001t0001g0089a0001c0001t0001g0165others(5): Show | 8 | HG01891.hp1 HG02040.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.1456-1377C>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 11/13 | chr6 | 155408631 | ||||||
| chr6:155408749
|
A | G | 9 | a0001c0001t0001g0024a0001c0001t0001g0153a0001c0001t0001g0167others(6): Show | 9 | HG01257.hp1 HG02615.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.1456-1495T>C | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 11/13 | chr6 | 155408749 | ||||||
| chr6:155408868
|
C | G | 1 | a0001c0001t0001g0291 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1456-1614G>C | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 11/13 | chr6 | 155408868 | ||||||
| chr6:155408947
|
C | T | 1 | a0001c0003t0002g0241 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1456-1693G>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 11/13 | chr6 | 155408947 | ||||||
| chr6:155408954
|
G | C | 4 | a0001c0001t0001g0119a0001c0001t0001g0128a0001c0001t0001g0132others(1): Show | 4 | NA18963.hp1 NA18982.hp2 NA18994.hp1 others(1): Show |
intron_variant | MODIFIER | c.1456-1700C>G | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 11/13 | chr6 | 155408954 | ||||||
| chr6:155408954
|
G | T | 26 | a0001c0001t0001g0024a0001c0001t0001g0091a0001c0001t0001g0092others(23): Show | 28 | HG01257.hp1 HG02074.hp1 HG02615.hp1 others(25): Show |
intron_variant | MODIFIER | c.1456-1700C>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 11/13 | chr6 | 155408954 | ||||||
| chr6:155408992
|
C | T | 4 | a0001c0001t0001g0232a0001c0001t0001g0234a0001c0003t0001g0162others(1): Show | 4 | HG01069.hp2 HG01071.hp2 HG01175.hp2 others(1): Show |
intron_variant | MODIFIER | c.1456-1738G>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 11/13 | chr6 | 155408992 | ||||||
| chr6:155409054
|
A | G | 1 | a0001c0003t0001g0144 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1456-1800T>C | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 11/13 | chr6 | 155409054 | ||||||
| chr6:155409082
|
G | C | 1 | a0001c0003t0001g0172 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1456-1828C>G | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 11/13 | chr6 | 155409082 | ||||||
| chr6:155409246
|
C | T | 1 | a0001c0001t0001g0023 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1455+1968G>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 11/13 | chr6 | 155409246 | ||||||
| chr6:155409252
|
G | A | 9 | a0001c0001t0001g0240a0001c0001t0001g0284a0001c0003t0001g0039others(6): Show | 9 | HG01891.hp2 HG02257.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.1455+1962C>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 11/13 | chr6 | 155409252 | ||||||
| chr6:155409446
|
G | A | 22 | a0001c0001t0001g0075a0001c0001t0001g0083a0001c0001t0001g0103others(19): Show | 23 | HG00423.hp1 HG00558.hp2 HG00621.hp2 others(20): Show |
intron_variant | MODIFIER | c.1455+1768C>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 11/13 | chr6 | 155409446 | ||||||
| chr6:155409678
|
C | T | 39 | a0001c0001t0001g0063a0001c0001t0001g0075a0001c0001t0001g0083others(36): Show | 40 | HG00423.hp1 HG00558.hp2 HG00621.hp2 others(37): Show |
intron_variant | MODIFIER | c.1455+1536G>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 11/13 | chr6 | 155409678 | ||||||
| chr6:155409682
|
A | G | 1 | a0001c0006t0001g0126 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1455+1532T>C | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 11/13 | chr6 | 155409682 | ||||||
| chr6:155409683
|
G | A | 1 | a0001c0003t0001g0161 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1455+1531C>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 11/13 | chr6 | 155409683 | ||||||
| chr6:155409792
|
A | G | 1 | a0001c0003t0001g0253 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1455+1422T>C | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 11/13 | chr6 | 155409792 | ||||||
| chr6:155409808
|
G | A | 3 | a0001c0001t0001g0060a0001c0006t0001g0049a0002c0009t0003g0012 | 3 | HG02258.hp2 HG02622.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.1455+1406C>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 11/13 | chr6 | 155409808 | ||||||
| chr6:155409823
|
A | G | 1 | a0001c0003t0002g0074 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1455+1391T>C | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 11/13 | chr6 | 155409823 | ||||||
| chr6:155409929
|
G | T | 9 | a0001c0001t0001g0240a0001c0001t0001g0284a0001c0003t0001g0039others(6): Show | 9 | HG01891.hp2 HG02257.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.1455+1285C>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 11/13 | chr6 | 155409929 | ||||||
| chr6:155410106
|
A | G | 31 | a0001c0001t0001g0075a0001c0001t0001g0083a0001c0001t0001g0103others(28): Show | 32 | HG00423.hp1 HG00558.hp2 HG00621.hp2 others(29): Show |
intron_variant | MODIFIER | c.1455+1108T>C | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 11/13 | chr6 | 155410106 | ||||||
| chr6:155410151
|
C | T | 1 | a0001c0001t0001g0280 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1455+1063G>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 11/13 | chr6 | 155410151 | ||||||
| chr6:155410180
|
A | G | 8 | a0001c0001t0001g0063a0001c0001t0001g0089a0001c0001t0001g0165others(5): Show | 8 | HG01891.hp1 HG02040.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.1455+1034T>C | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 11/13 | chr6 | 155410180 | ||||||
| chr6:155410258
|
A | C | 1 | a0001c0004t0001g0333 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1455+956T>G | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 11/13 | chr6 | 155410258 | ||||||
| chr6:155410296
|
A | AGT | 60 | a0001c0001t0001g0116a0001c0001t0001g0183a0001c0001t0001g0280others(57): Show | 61 | HG00280.hp2 HG00438.hp1 HG00609.hp2 others(58): Show |
intron_variant | MODIFIER | c.1455+916_1455+917d others(4): Show |
NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 11/13 | chr6 | 155410296 | ||||||
| chr6:155410296
|
A | AGTGT | 22 | a0001c0001t0001g0075a0001c0001t0001g0083a0001c0001t0001g0103others(19): Show | 23 | HG00423.hp1 HG00558.hp2 HG00621.hp2 others(20): Show |
intron_variant | MODIFIER | c.1455+914_1455+917d others(6): Show |
NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 11/13 | chr6 | 155410296 | ||||||
| chr6:155410296
|
A | AGTGTGT | 22 | a0001c0001t0001g0060a0001c0001t0001g0285a0001c0001t0002g0004others(19): Show | 24 | HG00639.hp1 HG01099.hp2 HG01109.hp2 others(21): Show |
intron_variant | MODIFIER | c.1455+912_1455+917d others(8): Show |
NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 11/13 | chr6 | 155410296 | ||||||
| chr6:155410296
|
A | AGTGTGTG others(1): Show |
10 | a0001c0001t0001g0063a0001c0001t0001g0089a0001c0001t0001g0165others(7): Show | 10 | HG01891.hp1 HG02145.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.1455+910_1455+917d others(10): Show |
NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 11/13 | chr6 | 155410296 | ||||||
| chr6:155410296
|
A | AGTGTGTG others(3): Show |
1 | a0001c0006t0001g0181 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1455+908_1455+917d others(12): Show |
NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 11/13 | chr6 | 155410296 | ||||||
| chr6:155410296
|
A | AGTGTGTG others(5): Show |
7 | a0001c0001t0001g0024a0001c0001t0001g0153a0001c0001t0001g0167others(4): Show | 7 | HG01257.hp1 HG02615.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1455+906_1455+917d others(14): Show |
NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 11/13 | chr6 | 155410296 | ||||||
| chr6:155410296
|
AGT | A | 17 | a0001c0001t0001g0017a0001c0001t0001g0026a0001c0001t0001g0080others(14): Show | 17 | HG01516.hp1 HG01517.hp1 HG02027.hp2 others(14): Show |
intron_variant | MODIFIER | c.1455+916_1455+917d others(4): Show |
NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 11/13 | chr6 | 155410296 | ||||||
| chr6:155410316
|
T | C | 1 | a0001c0001t0001g0124 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1455+898A>G | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 11/13 | chr6 | 155410316 | ||||||
| chr6:155410318
|
T | C | 21 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0109others(18): Show | 23 | HG02074.hp1 HG02145.hp2 HG03098.hp2 others(20): Show |
intron_variant | MODIFIER | c.1455+896A>G | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 11/13 | chr6 | 155410318 | ||||||
| chr6:155410320
|
C | T | 110 | a0001c0001t0001g0024a0001c0001t0001g0060a0001c0001t0001g0075others(107): Show | 114 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.1455+894G>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 11/13 | chr6 | 155410320 | ||||||
| chr6:155410321
|
G | A | 1 | a0002c0007t0001g0315 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1455+893C>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 11/13 | chr6 | 155410321 | ||||||
| chr6:155410324
|
C | T | 1 | a0002c0002t0002g0220 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1455+890G>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 11/13 | chr6 | 155410324 | ||||||
| chr6:155410335
|
G | A | 1 | a0001c0001t0001g0280 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1455+879C>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 11/13 | chr6 | 155410335 | ||||||
| chr6:155410337
|
A | G | 3 | a0001c0001t0002g0110a0002c0002t0002g0008a0002c0013t0002g0312 | 4 | NA18954.hp2 NA18985.hp1 NA19001.hp2 others(1): Show |
intron_variant | MODIFIER | c.1455+877T>C | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 11/13 | chr6 | 155410337 | ||||||
| chr6:155410485
|
G | T | 9 | a0001c0001t0001g0240a0001c0001t0001g0284a0001c0003t0001g0039others(6): Show | 9 | HG01891.hp2 HG02257.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.1455+729C>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 11/13 | chr6 | 155410485 | ||||||
| chr6:155410532
|
T | C | 1 | a0002c0002t0002g0191 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1455+682A>G | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 11/13 | chr6 | 155410532 | ||||||
| chr6:155410679
|
A | G | 22 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0026others(19): Show | 23 | HG01516.hp1 HG01517.hp1 HG02027.hp2 others(20): Show |
intron_variant | MODIFIER | c.1455+535T>C | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 11/13 | chr6 | 155410679 | ||||||
| chr6:155410688
|
C | G | 5 | a0001c0003t0001g0051a0001c0003t0001g0073a0001c0003t0001g0144others(2): Show | 5 | HG01109.hp2 HG02145.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1455+526G>C | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 11/13 | chr6 | 155410688 | ||||||
| chr6:155410940
|
T | C | 36 | a0001c0001t0001g0075a0001c0001t0001g0083a0001c0001t0001g0103others(33): Show | 37 | HG00423.hp1 HG00558.hp2 HG00621.hp2 others(34): Show |
intron_variant | MODIFIER | c.1455+274A>G | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 11/13 | chr6 | 155410940 | ||||||
| chr6:155411066
|
G | C | 8 | a0001c0001t0001g0063a0001c0001t0001g0089a0001c0001t0001g0165others(5): Show | 8 | HG01891.hp1 HG02040.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.1455+148C>G | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 11/13 | chr6 | 155411066 | ||||||
| chr6:155411118
|
G | T | 9 | a0001c0001t0001g0024a0001c0001t0001g0153a0001c0001t0001g0167others(6): Show | 9 | HG01257.hp1 HG02615.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.1455+96C>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 11/13 | chr6 | 155411118 | ||||||
| chr6:155411153
|
G | T | 3 | a0001c0003t0001g0051a0001c0003t0001g0144a0001c0003t0001g0168 | 3 | HG01109.hp2 HG02647.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1455+61C>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 11/13 | chr6 | 155411153 | ||||||
| chr6:155411390
|
C | T | 22 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0026others(19): Show | 23 | HG01516.hp1 HG01517.hp1 HG02027.hp2 others(20): Show |
intron_variant | MODIFIER | c.1309-30G>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 10/13 | chr6 | 155411390 | ||||||
| chr6:155411482
|
C | CT | 79 | a0001c0001t0001g0024a0001c0001t0001g0153a0001c0001t0001g0167others(76): Show | 82 | HG00280.hp2 HG00438.hp1 HG00639.hp1 others(79): Show |
intron_variant | MODIFIER | c.1309-123dupA | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 10/13 | chr6 | 155411482 | ||||||
| chr6:155411489
|
T | TG | 3 | a0001c0001t0001g0060a0001c0006t0001g0049a0002c0009t0003g0012 | 3 | HG02258.hp2 HG02622.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.1309-130_1309-129i others(3): Show |
NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 10/13 | chr6 | 155411489 | ||||||
| chr6:155411623
|
A | G | 2 | a0001c0003t0001g0073a0001c0004t0003g0015 | 2 | HG02145.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.1309-263T>C | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 10/13 | chr6 | 155411623 | ||||||
| chr6:155411688
|
C | T | 1 | a0001c0001t0001g0280 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1309-328G>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 10/13 | chr6 | 155411688 | ||||||
| chr6:155411713
|
G | A | 1 | a0001c0001t0001g0233 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1309-353C>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 10/13 | chr6 | 155411713 | ||||||
| chr6:155411730
|
A | T | 4 | a0001c0001t0002g0046a0001c0001t0002g0146a0001c0004t0004g0014others(1): Show | 4 | HG02965.hp1 HG03041.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1309-370T>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 10/13 | chr6 | 155411730 | ||||||
| chr6:155411890
|
C | T | 6 | a0001c0001t0001g0280a0001c0003t0001g0051a0001c0003t0001g0073others(3): Show | 6 | HG01109.hp2 HG02145.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.1309-530G>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 10/13 | chr6 | 155411890 | ||||||
| chr6:155411896
|
G | A | 22 | a0001c0001t0001g0075a0001c0001t0001g0083a0001c0001t0001g0103others(19): Show | 23 | HG00423.hp1 HG00558.hp2 HG00621.hp2 others(20): Show |
intron_variant | MODIFIER | c.1309-536C>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 10/13 | chr6 | 155411896 | ||||||
| chr6:155411922
|
G | A | 1 | a0001c0001t0002g0046 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1309-562C>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 10/13 | chr6 | 155411922 | ||||||
| chr6:155411958
|
T | C | 8 | a0001c0001t0001g0063a0001c0001t0001g0089a0001c0001t0001g0165others(5): Show | 8 | HG01891.hp1 HG02040.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.1309-598A>G | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 10/13 | chr6 | 155411958 | ||||||
| chr6:155412011
|
CAAA | C | 8 | a0001c0001t0001g0063a0001c0001t0001g0089a0001c0001t0001g0165others(5): Show | 8 | HG01891.hp1 HG02040.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.1309-654_1309-652d others(5): Show |
NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 10/13 | chr6 | 155412011 | ||||||
| chr6:155412018
|
T | A | 8 | a0001c0001t0001g0063a0001c0001t0001g0089a0001c0001t0001g0165others(5): Show | 8 | HG01891.hp1 HG02040.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.1309-658A>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 10/13 | chr6 | 155412018 | ||||||
| chr6:155412279
|
T | C | 22 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0026others(19): Show | 23 | HG01516.hp1 HG01517.hp1 HG02027.hp2 others(20): Show |
intron_variant | MODIFIER | c.1309-919A>G | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 10/13 | chr6 | 155412279 | ||||||
| chr6:155412311
|
T | G | 12 | a0001c0001t0001g0017a0001c0001t0001g0026a0001c0001t0001g0080others(9): Show | 12 | HG01516.hp1 HG01517.hp1 HG02027.hp2 others(9): Show |
intron_variant | MODIFIER | c.1309-951A>C | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 10/13 | chr6 | 155412311 | ||||||
| chr6:155412348
|
G | A | 2 | a0001c0001t0001g0306a0001c0001t0001g0307 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.1309-988C>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 10/13 | chr6 | 155412348 | ||||||
| chr6:155412423
|
C | T | 81 | a0001c0001t0001g0024a0001c0001t0001g0060a0001c0001t0001g0153others(78): Show | 84 | HG00280.hp2 HG00438.hp1 HG00639.hp1 others(81): Show |
intron_variant | MODIFIER | c.1309-1063G>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 10/13 | chr6 | 155412423 | ||||||
| chr6:155412488
|
G | A | 8 | a0001c0001t0001g0063a0001c0001t0001g0089a0001c0001t0001g0165others(5): Show | 8 | HG01891.hp1 HG02040.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.1309-1128C>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 10/13 | chr6 | 155412488 | ||||||
| chr6:155412502
|
A | G | 118 | a0001c0001t0001g0024a0001c0001t0001g0060a0001c0001t0001g0075others(115): Show | 122 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(119): Show |
intron_variant | MODIFIER | c.1309-1142T>C | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 10/13 | chr6 | 155412502 | ||||||
| chr6:155412593
|
A | G | 118 | a0001c0001t0001g0024a0001c0001t0001g0060a0001c0001t0001g0075others(115): Show | 122 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(119): Show |
intron_variant | MODIFIER | c.1309-1233T>C | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 10/13 | chr6 | 155412593 | ||||||
| chr6:155412595
|
A | G | 2 | a0001c0006t0001g0049a0002c0009t0003g0012 | 2 | HG02258.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.1309-1235T>C | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 10/13 | chr6 | 155412595 | ||||||
| chr6:155412679
|
C | T | 1 | a0002c0002t0001g0300 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1309-1319G>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 10/13 | chr6 | 155412679 | ||||||
| chr6:155412760
|
C | T | 5 | a0001c0003t0001g0051a0001c0003t0001g0073a0001c0003t0001g0144others(2): Show | 5 | HG01109.hp2 HG02145.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1309-1400G>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 10/13 | chr6 | 155412760 | ||||||
| chr6:155412849
|
G | A | 22 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0026others(19): Show | 23 | HG01516.hp1 HG01517.hp1 HG02027.hp2 others(20): Show |
intron_variant | MODIFIER | c.1309-1489C>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 10/13 | chr6 | 155412849 | ||||||
| chr6:155413066
|
G | T | 1 | a0001c0001t0002g0032 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1309-1706C>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 10/13 | chr6 | 155413066 | ||||||
| chr6:155413138
|
T | C | 1 | a0001c0004t0001g0325 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1309-1778A>G | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 10/13 | chr6 | 155413138 | ||||||
| chr6:155413198
|
G | A | 1 | a0001c0001t0001g0017 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1309-1838C>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 10/13 | chr6 | 155413198 | ||||||
| chr6:155413258
|
G | A | 80 | a0001c0001t0001g0024a0001c0001t0001g0060a0001c0001t0001g0153others(77): Show | 83 | HG00280.hp2 HG00438.hp1 HG00639.hp1 others(80): Show |
intron_variant | MODIFIER | c.1309-1898C>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 10/13 | chr6 | 155413258 | ||||||
| chr6:155413391
|
G | A | 1 | a0002c0002t0001g0140 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1309-2031C>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 10/13 | chr6 | 155413391 | ||||||
| chr6:155413393
|
T | C | 148 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0024others(145): Show | 153 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(150): Show |
intron_variant | MODIFIER | c.1309-2033A>G | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 10/13 | chr6 | 155413393 | ||||||
| chr6:155413409
|
G | A | 1 | a0002c0002t0001g0193 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1309-2049C>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 10/13 | chr6 | 155413409 | ||||||
| chr6:155413436
|
C | T | 1 | a0001c0014t0002g0035 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1309-2076G>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 10/13 | chr6 | 155413436 | ||||||
| chr6:155413520
|
G | A | 167 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0024others(164): Show | 174 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(171): Show |
intron_variant | MODIFIER | c.1309-2160C>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 10/13 | chr6 | 155413520 | ||||||
| chr6:155413537
|
A | G | 167 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0024others(164): Show | 174 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(171): Show |
intron_variant | MODIFIER | c.1309-2177T>C | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 10/13 | chr6 | 155413537 | ||||||
| chr6:155413563
|
G | A | 4 | a0001c0001t0001g0266a0002c0007t0001g0310a0002c0007t0001g0311others(1): Show | 4 | HG02129.hp1 NA18954.hp1 NA19010.hp2 others(1): Show |
intron_variant | MODIFIER | c.1309-2203C>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 10/13 | chr6 | 155413563 | ||||||
| chr6:155413620
|
T | C | 327 | a0001c0001t0001g0009a0001c0001t0001g0016a0001c0001t0001g0017others(324): Show | 336 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(333): Show |
intron_variant | MODIFIER | c.1309-2260A>G | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 10/13 | chr6 | 155413620 | ||||||
| chr6:155413655
|
C | T | 1 | a0001c0004t0001g0346 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1309-2295G>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 10/13 | chr6 | 155413655 | ||||||
| chr6:155413665
|
C | T | 1 | a0001c0001t0001g0023 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1309-2305G>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 10/13 | chr6 | 155413665 | ||||||
| chr6:155413669
|
G | T | 45 | a0001c0001t0002g0027a0001c0001t0002g0032a0001c0001t0002g0093others(42): Show | 46 | HG00280.hp2 HG00438.hp1 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.1309-2309C>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 10/13 | chr6 | 155413669 | ||||||
| chr6:155413701
|
A | G | 20 | a0001c0001t0001g0075a0001c0001t0001g0083a0001c0001t0001g0103others(17): Show | 21 | HG00423.hp1 HG00558.hp2 HG00621.hp2 others(18): Show |
intron_variant | MODIFIER | c.1309-2341T>C | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 10/13 | chr6 | 155413701 | ||||||
| chr6:155413721
|
T | C | 146 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0024others(143): Show | 151 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(148): Show |
intron_variant | MODIFIER | c.1309-2361A>G | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 10/13 | chr6 | 155413721 | ||||||
| chr6:155413724
|
C | A | 2 | a0002c0002t0001g0217a0002c0002t0001g0225 | 2 | NA18983.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.1309-2364G>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 10/13 | chr6 | 155413724 | ||||||
| chr6:155413735
|
C | T | 1 | a0001c0001t0001g0167 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1309-2375G>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 10/13 | chr6 | 155413735 | ||||||
| chr6:155413774
|
G | C | 80 | a0001c0001t0001g0024a0001c0001t0001g0060a0001c0001t0001g0153others(77): Show | 83 | HG00280.hp2 HG00438.hp1 HG00639.hp1 others(80): Show |
intron_variant | MODIFIER | c.1309-2414C>G | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 10/13 | chr6 | 155413774 | ||||||
| chr6:155414001
|
G | A | 1 | a0002c0002t0002g0271 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1309-2641C>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 10/13 | chr6 | 155414001 | ||||||
| chr6:155414064
|
G | T | 1 | a0002c0002t0002g0085 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1309-2704C>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 10/13 | chr6 | 155414064 | ||||||
| chr6:155414086
|
C | T | 20 | a0001c0001t0001g0075a0001c0001t0001g0083a0001c0001t0001g0103others(17): Show | 21 | HG00423.hp1 HG00558.hp2 HG00621.hp2 others(18): Show |
intron_variant | MODIFIER | c.1309-2726G>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 10/13 | chr6 | 155414086 | ||||||
| chr6:155414090
|
C | T | 5 | a0001c0003t0001g0051a0001c0003t0001g0073a0001c0003t0001g0144others(2): Show | 5 | HG01109.hp2 HG02145.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1309-2730G>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 10/13 | chr6 | 155414090 | ||||||
| chr6:155414226
|
T | C | 9 | a0001c0001t0001g0240a0001c0001t0001g0284a0001c0003t0001g0039others(6): Show | 9 | HG01891.hp2 HG02257.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.1309-2866A>G | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 10/13 | chr6 | 155414226 | ||||||
| chr6:155414233
|
C | T | 20 | a0001c0001t0001g0075a0001c0001t0001g0083a0001c0001t0001g0103others(17): Show | 21 | HG00423.hp1 HG00558.hp2 HG00621.hp2 others(18): Show |
intron_variant | MODIFIER | c.1309-2873G>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 10/13 | chr6 | 155414233 | ||||||
| chr6:155414285
|
C | T | 1 | a0001c0001t0001g0111 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1309-2925G>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 10/13 | chr6 | 155414285 | ||||||
| chr6:155414510
|
A | C | 4 | a0001c0001t0001g0294a0001c0001t0001g0298a0001c0001t0001g0299others(1): Show | 4 | HG00280.hp1 HG01070.hp2 HG01071.hp1 others(1): Show |
intron_variant | MODIFIER | c.1309-3150T>G | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 10/13 | chr6 | 155414510 | ||||||
| chr6:155414528
|
C | G | 5 | a0001c0003t0001g0051a0001c0003t0001g0073a0001c0003t0001g0144others(2): Show | 5 | HG01109.hp2 HG02145.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1309-3168G>C | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 10/13 | chr6 | 155414528 | ||||||
| chr6:155414562
|
G | A | 2 | a0002c0002t0001g0186a0002c0002t0001g0215 | 2 | NA18965.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.1309-3202C>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 10/13 | chr6 | 155414562 | ||||||
| chr6:155414622
|
T | C | 12 | a0001c0001t0001g0063a0001c0001t0001g0082a0001c0001t0001g0089others(9): Show | 12 | HG00642.hp1 HG01081.hp2 HG01261.hp1 others(9): Show |
intron_variant | MODIFIER | c.1309-3262A>G | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 10/13 | chr6 | 155414622 | ||||||
| chr6:155414623
|
C | CT | 10 | a0001c0001t0001g0016a0001c0001t0001g0180a0001c0003t0001g0039others(7): Show | 10 | HG01891.hp2 HG02280.hp1 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.1309-3264dupA | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 10/13 | chr6 | 155414623 | ||||||
| chr6:155414623
|
CT | C | 38 | a0001c0001t0001g0024a0001c0001t0001g0075a0001c0001t0001g0080others(35): Show | 40 | HG00280.hp1 HG00423.hp1 HG00558.hp2 others(37): Show |
intron_variant | MODIFIER | c.1309-3264delA | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 10/13 | chr6 | 155414623 | ||||||
| chr6:155414623
|
CTT | C | 78 | a0001c0001t0001g0153a0001c0001t0001g0167a0001c0001t0001g0238others(75): Show | 80 | HG00280.hp2 HG00438.hp1 HG00639.hp1 others(77): Show |
intron_variant | MODIFIER | c.1309-3265_1309-326 others(6): Show |
NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 10/13 | chr6 | 155414623 | ||||||
| chr6:155414625
|
T | C | 3 | a0001c0006t0001g0049a0002c0009t0003g0012a0008c0019t0001g0033 | 3 | HG02258.hp2 HG02622.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1309-3265A>G | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 10/13 | chr6 | 155414625 | ||||||
| chr6:155414626
|
T | C | 23 | a0001c0001t0001g0024a0001c0001t0001g0075a0001c0001t0001g0083others(20): Show | 25 | HG00423.hp1 HG00558.hp2 HG00621.hp2 others(22): Show |
intron_variant | MODIFIER | c.1309-3266A>G | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 10/13 | chr6 | 155414626 | ||||||
| chr6:155414627
|
T | C | 78 | a0001c0001t0001g0153a0001c0001t0001g0167a0001c0001t0001g0238others(75): Show | 80 | HG00280.hp2 HG00438.hp1 HG00639.hp1 others(77): Show |
intron_variant | MODIFIER | c.1309-3267A>G | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 10/13 | chr6 | 155414627 | ||||||
| chr6:155414628
|
T | C | 21 | a0001c0001t0001g0075a0001c0001t0001g0083a0001c0001t0001g0103others(18): Show | 22 | HG00423.hp1 HG00558.hp2 HG00621.hp2 others(19): Show |
intron_variant | MODIFIER | c.1309-3268A>G | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 10/13 | chr6 | 155414628 | ||||||
| chr6:155414668
|
C | A | 1 | a0001c0001t0001g0292 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1309-3308G>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 10/13 | chr6 | 155414668 | ||||||
| chr6:155414789
|
G | A | 1 | a0001c0001t0001g0153 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1309-3429C>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 10/13 | chr6 | 155414789 | ||||||
| chr6:155414801
|
A | G | 2 | a0001c0003t0001g0073a0001c0004t0003g0015 | 2 | HG02145.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.1309-3441T>C | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 10/13 | chr6 | 155414801 | ||||||
| chr6:155414832
|
T | C | 1 | a0002c0009t0003g0012 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1309-3472A>G | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 10/13 | chr6 | 155414832 | ||||||
| chr6:155414845
|
C | T | 1 | a0001c0003t0001g0239 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1309-3485G>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 10/13 | chr6 | 155414845 | ||||||
| chr6:155414856
|
G | C | 12 | a0001c0001t0001g0063a0001c0001t0001g0082a0001c0001t0001g0089others(9): Show | 12 | HG00642.hp1 HG01081.hp2 HG01261.hp1 others(9): Show |
intron_variant | MODIFIER | c.1309-3496C>G | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 10/13 | chr6 | 155414856 | ||||||
| chr6:155414877
|
C | T | 3 | a0001c0001t0002g0004a0001c0003t0002g0052a0001c0003t0002g0148 | 4 | HG01496.hp2 HG02258.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1309-3517G>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 10/13 | chr6 | 155414877 | ||||||
| chr6:155414880
|
G | A | 10 | a0001c0001t0001g0240a0001c0001t0001g0284a0001c0003t0001g0039others(7): Show | 10 | HG00609.hp2 HG01891.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.1309-3520C>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 10/13 | chr6 | 155414880 | ||||||
| chr6:155415052
|
G | A | 20 | a0001c0001t0001g0075a0001c0001t0001g0083a0001c0001t0001g0103others(17): Show | 21 | HG00423.hp1 HG00558.hp2 HG00621.hp2 others(18): Show |
intron_variant | MODIFIER | c.1309-3692C>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 10/13 | chr6 | 155415052 | ||||||
| chr6:155415192
|
G | A | 1 | a0001c0001t0001g0292 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1309-3832C>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 10/13 | chr6 | 155415192 | ||||||
| chr6:155415427
|
A | G | 3 | a0001c0001t0001g0098a0001c0001t0001g0099a0001c0004t0001g0325 | 3 | NA18982.hp1 NA19001.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.1309-4067T>C | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 10/13 | chr6 | 155415427 | ||||||
| chr6:155415774
|
A | ATGTTT | 12 | a0001c0001t0001g0017a0001c0001t0001g0026a0001c0001t0001g0080others(9): Show | 12 | HG01516.hp1 HG01517.hp1 HG02027.hp2 others(9): Show |
intron_variant | MODIFIER | c.1309-4419_1309-441 others(9): Show |
NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 10/13 | chr6 | 155415774 | ||||||
| chr6:155415795
|
T | C | 1 | a0001c0001t0001g0108 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.1309-4435A>G | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 10/13 | chr6 | 155415795 | ||||||
| chr6:155415819
|
G | A | 2 | a0002c0002t0001g0020a0002c0002t0001g0029 | 2 | HG02976.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1309-4459C>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 10/13 | chr6 | 155415819 | ||||||
| chr6:155416273
|
T | C | 2 | a0001c0001t0001g0145a0001c0006t0001g0055 | 2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1309-4913A>G | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 10/13 | chr6 | 155416273 | ||||||
| chr6:155416291
|
A | G | 14 | a0001c0001t0001g0024a0001c0001t0001g0060a0001c0001t0001g0153others(11): Show | 15 | HG01257.hp1 HG01496.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.1309-4931T>C | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 10/13 | chr6 | 155416291 | ||||||
| chr6:155416350
|
A | G | 3 | a0001c0001t0002g0004a0001c0003t0002g0052a0001c0003t0002g0148 | 4 | HG01496.hp2 HG02258.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1309-4990T>C | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 10/13 | chr6 | 155416350 | ||||||
| chr6:155416398
|
G | A | 11 | a0001c0001t0001g0063a0001c0001t0001g0089a0001c0001t0001g0095others(8): Show | 11 | HG01074.hp1 HG01261.hp1 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.1309-5038C>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 10/13 | chr6 | 155416398 | ||||||
| chr6:155416408
|
A | G | 23 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0026others(20): Show | 24 | HG01516.hp1 HG01517.hp1 HG02027.hp2 others(21): Show |
intron_variant | MODIFIER | c.1309-5048T>C | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 10/13 | chr6 | 155416408 | ||||||
| chr6:155416554
|
C | T | 3 | a0001c0001t0002g0004a0001c0003t0002g0052a0001c0003t0002g0148 | 4 | HG01496.hp2 HG02258.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1309-5194G>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 10/13 | chr6 | 155416554 | ||||||
| chr6:155416651
|
G | A | 1 | a0002c0002t0001g0196 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.1309-5291C>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 10/13 | chr6 | 155416651 | ||||||
| chr6:155416661
|
T | C | 19 | a0001c0001t0001g0075a0001c0001t0001g0083a0001c0001t0001g0103others(16): Show | 20 | HG00423.hp1 HG00558.hp2 HG00621.hp2 others(17): Show |
intron_variant | MODIFIER | c.1309-5301A>G | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 10/13 | chr6 | 155416661 | ||||||
| chr6:155416744
|
C | CT | 81 | a0001c0001t0001g0026a0001c0001t0001g0080a0001c0001t0001g0081others(78): Show | 82 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(79): Show |
intron_variant | MODIFIER | c.1309-5385dupA | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 10/13 | chr6 | 155416744 | ||||||
| chr6:155416744
|
C | CTT | 23 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0063others(20): Show | 24 | HG01074.hp1 HG01261.hp1 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.1309-5386_1309-538 others(6): Show |
NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 10/13 | chr6 | 155416744 | ||||||
| chr6:155416744
|
C | CTTTTTTT | 33 | a0001c0001t0002g0005a0001c0001t0002g0019a0001c0001t0002g0027others(30): Show | 35 | HG00280.hp2 HG00438.hp1 HG00735.hp1 others(32): Show |
intron_variant | MODIFIER | c.1309-5391_1309-538 others(11): Show |
NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 10/13 | chr6 | 155416744 | ||||||
| chr6:155416744
|
C | CTTTTTTT others(1): Show |
22 | a0001c0001t0001g0280a0001c0001t0002g0069a0001c0001t0002g0101others(19): Show | 22 | HG00639.hp1 HG01099.hp2 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.1309-5392_1309-538 others(12): Show |
NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 10/13 | chr6 | 155416744 | ||||||
| chr6:155416744
|
C | CTTTTTTT others(3): Show |
2 | a0001c0001t0002g0046a0001c0003t0002g0107 | 2 | HG03041.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.1309-5394_1309-538 others(14): Show |
NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 10/13 | chr6 | 155416744 | ||||||
| chr6:155416744
|
C | CTTTTTTT others(4): Show |
2 | a0001c0001t0002g0146a0001c0006t0002g0058 | 2 | HG02965.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1309-5395_1309-538 others(15): Show |
NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 10/13 | chr6 | 155416744 | ||||||
| chr6:155416744
|
C | CTTTTTTT others(10): Show |
2 | a0001c0003t0001g0073a0001c0004t0003g0015 | 2 | HG02145.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.1309-5401_1309-538 others(21): Show |
NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 10/13 | chr6 | 155416744 | ||||||
| chr6:155416744
|
C | CTTTTTTT others(19): Show |
1 | a0001c0003t0001g0168 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1309-5385_1309-538 others(30): Show |
NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 10/13 | chr6 | 155416744 | ||||||
| chr6:155416744
|
C | CTTTTTTT others(20): Show |
2 | a0001c0003t0001g0051a0001c0003t0001g0144 | 2 | HG01109.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.1309-5385_1309-538 others(31): Show |
NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 10/13 | chr6 | 155416744 | ||||||
| chr6:155416744
|
CTTTTTTT | C | 9 | a0001c0001t0001g0240a0001c0001t0001g0284a0001c0003t0001g0039others(6): Show | 9 | HG01891.hp2 HG02257.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.1309-5391_1309-538 others(11): Show |
NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 10/13 | chr6 | 155416744 | ||||||
| chr6:155416744
|
CTTTTTTT others(1): Show |
C | 7 | a0001c0001t0001g0024a0001c0001t0001g0153a0001c0001t0001g0167others(4): Show | 7 | HG01257.hp1 HG02615.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1309-5392_1309-538 others(12): Show |
NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 10/13 | chr6 | 155416744 | ||||||
| chr6:155416744
|
CTTTTTTT others(4): Show |
C | 20 | a0001c0001t0001g0075a0001c0001t0001g0083a0001c0001t0001g0103others(17): Show | 21 | HG00423.hp1 HG00558.hp2 HG00621.hp2 others(18): Show |
intron_variant | MODIFIER | c.1309-5395_1309-538 others(15): Show |
NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 10/13 | chr6 | 155416744 | ||||||
| chr6:155416744
|
CTTTTTTT others(5): Show |
C | 6 | a0001c0001t0001g0060a0001c0001t0002g0004a0001c0003t0002g0052others(3): Show | 7 | HG01496.hp2 HG02258.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.1309-5396_1309-538 others(16): Show |
NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 10/13 | chr6 | 155416744 | ||||||
| chr6:155416772
|
A | C | 2 | a0001c0001t0001g0298a0001c0004t0001g0309 | 2 | HG00280.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.1309-5412T>G | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 10/13 | chr6 | 155416772 | ||||||
| chr6:155416820
|
A | G | 1 | a0001c0004t0004g0014 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1309-5460T>C | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 10/13 | chr6 | 155416820 | ||||||
| chr6:155416822
|
T | C | 1 | a0001c0004t0004g0014 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1309-5462A>G | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 10/13 | chr6 | 155416822 | ||||||
| chr6:155416827
|
T | C | 9 | a0001c0001t0001g0301a0001c0004t0001g0328a0001c0005t0001g0326others(6): Show | 10 | HG01081.hp1 HG01192.hp1 HG01943.hp1 others(7): Show |
intron_variant | MODIFIER | c.1309-5467A>G | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 10/13 | chr6 | 155416827 | ||||||
| chr6:155416882
|
C | T | 2 | a0001c0001t0001g0091a0002c0002t0001g0077 | 2 | NA18953.hp1 NA18955.hp1 |
intron_variant | MODIFIER | c.1309-5522G>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 10/13 | chr6 | 155416882 | ||||||
| chr6:155416887
|
A | G | 14 | a0001c0001t0001g0024a0001c0001t0001g0060a0001c0001t0001g0153others(11): Show | 15 | HG01257.hp1 HG01496.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.1309-5527T>C | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 10/13 | chr6 | 155416887 | ||||||
| chr6:155416907
|
C | T | 5 | a0001c0001t0001g0149a0001c0003t0001g0037a0001c0003t0001g0040others(2): Show | 5 | HG02630.hp2 HG02723.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.1309-5547G>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 10/13 | chr6 | 155416907 | ||||||
| chr6:155416911
|
C | T | 72 | a0001c0001t0001g0280a0001c0001t0002g0005a0001c0001t0002g0019others(69): Show | 74 | HG00280.hp2 HG00438.hp1 HG00639.hp1 others(71): Show |
intron_variant | MODIFIER | c.1309-5551G>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 10/13 | chr6 | 155416911 | ||||||
| chr6:155416994
|
G | A | 20 | a0001c0001t0001g0075a0001c0001t0001g0083a0001c0001t0001g0103others(17): Show | 21 | HG00423.hp1 HG00558.hp2 HG00621.hp2 others(18): Show |
intron_variant | MODIFIER | c.1309-5634C>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 10/13 | chr6 | 155416994 | ||||||
| chr6:155417002
|
C | T | 2 | a0001c0001t0001g0285a0001c0003t0001g0142 | 2 | HG02040.hp1 NA18943.hp2 |
intron_variant | MODIFIER | c.1309-5642G>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 10/13 | chr6 | 155417002 | ||||||
| chr6:155417004
|
A | G | 106 | a0001c0001t0001g0024a0001c0001t0001g0060a0001c0001t0001g0075others(103): Show | 110 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.1309-5644T>C | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 10/13 | chr6 | 155417004 | ||||||
| chr6:155417040
|
C | T | 1 | a0001c0001t0001g0082 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1308+5654G>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 10/13 | chr6 | 155417040 | ||||||
| chr6:155417169
|
C | T | 3 | a0001c0003t0001g0039a0001c0003t0001g0041a0001c0003t0005g0038 | 3 | HG01891.hp2 HG02280.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1308+5525G>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 10/13 | chr6 | 155417169 | ||||||
| chr6:155417185
|
T | A | 1 | a0002c0002t0002g0305 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1308+5509A>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 10/13 | chr6 | 155417185 | ||||||
| chr6:155417446
|
T | C | 8 | a0001c0001t0001g0229a0001c0001t0001g0230a0001c0001t0001g0234others(5): Show | 8 | HG01069.hp2 HG01071.hp2 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.1308+5248A>G | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 10/13 | chr6 | 155417446 | ||||||
| chr6:155417512
|
T | C | 34 | a0001c0001t0001g0063a0001c0001t0001g0075a0001c0001t0001g0082others(31): Show | 35 | HG00423.hp1 HG00558.hp2 HG00621.hp2 others(32): Show |
intron_variant | MODIFIER | c.1308+5182A>G | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 10/13 | chr6 | 155417512 | ||||||
| chr6:155417572
|
G | C | 53 | a0001c0001t0002g0019a0001c0001t0002g0027a0001c0001t0002g0032others(50): Show | 54 | HG00280.hp2 HG00438.hp1 HG00735.hp1 others(51): Show |
intron_variant | MODIFIER | c.1308+5122C>G | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 10/13 | chr6 | 155417572 | ||||||
| chr6:155417654
|
T | A | 1 | a0001c0004t0001g0337 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1308+5040A>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 10/13 | chr6 | 155417654 | ||||||
| chr6:155417793
|
A | AT | 32 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0026others(29): Show | 33 | HG01516.hp1 HG01517.hp1 HG01891.hp2 others(30): Show |
intron_variant | MODIFIER | c.1308+4900dupA | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 10/13 | chr6 | 155417793 | ||||||
| chr6:155417794
|
T | G | 22 | a0001c0001t0001g0024a0001c0001t0001g0091a0001c0001t0001g0092others(19): Show | 24 | HG01257.hp1 HG02074.hp1 HG02615.hp1 others(21): Show |
intron_variant | MODIFIER | c.1308+4900A>C | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 10/13 | chr6 | 155417794 | ||||||
| chr6:155417858
|
T | G | 77 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0026others(74): Show | 80 | HG00423.hp1 HG00558.hp2 HG00621.hp2 others(77): Show |
intron_variant | MODIFIER | c.1308+4836A>C | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 10/13 | chr6 | 155417858 | ||||||
| chr6:155417941
|
T | C | 1 | a0002c0002t0002g0079 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1308+4753A>G | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 10/13 | chr6 | 155417941 | ||||||
| chr6:155418153
|
C | T | 12 | a0001c0001t0001g0063a0001c0001t0001g0089a0001c0001t0001g0165others(9): Show | 12 | HG01891.hp1 HG02040.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.1308+4541G>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 10/13 | chr6 | 155418153 | ||||||
| chr6:155418197
|
A | G | 1 | a0001c0003t0001g0067 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1308+4497T>C | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 10/13 | chr6 | 155418197 | ||||||
| chr6:155418280
|
G | A | 1 | a0002c0007t0001g0315 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1308+4414C>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 10/13 | chr6 | 155418280 | ||||||
| chr6:155418343
|
C | T | 1 | a0001c0006t0001g0126 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1308+4351G>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 10/13 | chr6 | 155418343 | ||||||
| chr6:155418453
|
G | C | 1 | a0002c0002t0001g0192 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1308+4241C>G | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 10/13 | chr6 | 155418453 | ||||||
| chr6:155418528
|
T | C | 24 | a0001c0001t0001g0016a0001c0001t0001g0028a0001c0001t0001g0064others(21): Show | 25 | HG01109.hp2 HG01891.hp2 HG02257.hp1 others(22): Show |
intron_variant | MODIFIER | c.1308+4166A>G | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 10/13 | chr6 | 155418528 | ||||||
| chr6:155418530
|
A | G | 3 | a0001c0001t0001g0153a0001c0001t0001g0238a0001c0003t0001g0050 | 3 | HG02615.hp2 HG02717.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1308+4164T>C | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 10/13 | chr6 | 155418530 | ||||||
| chr6:155418592
|
C | T | 15 | a0001c0001t0001g0063a0001c0001t0001g0089a0001c0001t0001g0095others(12): Show | 15 | HG01074.hp1 HG01884.hp1 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.1308+4102G>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 10/13 | chr6 | 155418592 | ||||||
| chr6:155418634
|
T | G | 168 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0024others(165): Show | 174 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(171): Show |
intron_variant | MODIFIER | c.1308+4060A>C | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 10/13 | chr6 | 155418634 | ||||||
| chr6:155418768
|
G | A | 3 | a0001c0001t0001g0179a0001c0001t0001g0180a0001c0001t0001g0304 | 3 | HG01891.hp1 HG03130.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1308+3926C>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 10/13 | chr6 | 155418768 | ||||||
| chr6:155418790
|
C | T | 41 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0026others(38): Show | 42 | HG01109.hp2 HG01516.hp1 HG01517.hp1 others(39): Show |
intron_variant | MODIFIER | c.1308+3904G>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 10/13 | chr6 | 155418790 | ||||||
| chr6:155418799
|
T | C | 2 | a0001c0001t0001g0167a0001c0001t0001g0276 | 2 | HG02615.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1308+3895A>G | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 10/13 | chr6 | 155418799 | ||||||
| chr6:155418819
|
A | G | 20 | a0001c0001t0001g0063a0001c0001t0001g0082a0001c0001t0001g0089others(17): Show | 20 | HG00642.hp1 HG01074.hp1 HG01081.hp2 others(17): Show |
intron_variant | MODIFIER | c.1308+3875T>C | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 10/13 | chr6 | 155418819 | ||||||
| chr6:155418890
|
A | G | 24 | a0001c0001t0001g0016a0001c0001t0001g0028a0001c0001t0001g0064others(21): Show | 25 | HG01109.hp2 HG01891.hp2 HG02257.hp1 others(22): Show |
intron_variant | MODIFIER | c.1308+3804T>C | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 10/13 | chr6 | 155418890 | ||||||
| chr6:155418959
|
C | G | 1 | a0001c0001t0001g0103 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1308+3735G>C | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 10/13 | chr6 | 155418959 | ||||||
| chr6:155419068
|
G | T | 1 | a0001c0001t0001g0304 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1308+3626C>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 10/13 | chr6 | 155419068 | ||||||
| chr6:155419151
|
C | A | 60 | a0001c0001t0001g0016a0001c0001t0001g0028a0001c0001t0001g0063others(57): Show | 63 | HG01074.hp1 HG01109.hp2 HG01884.hp1 others(60): Show |
intron_variant | MODIFIER | c.1308+3543G>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 10/13 | chr6 | 155419151 | ||||||
| chr6:155419227
|
A | G | 69 | a0001c0001t0001g0280a0001c0001t0002g0005a0001c0001t0002g0019others(66): Show | 71 | HG00280.hp2 HG00438.hp1 HG00639.hp1 others(68): Show |
intron_variant | MODIFIER | c.1308+3467T>C | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 10/13 | chr6 | 155419227 | ||||||
| chr6:155419394
|
T | G | 67 | a0001c0001t0002g0005a0001c0001t0002g0019a0001c0001t0002g0027others(64): Show | 69 | HG00280.hp2 HG00438.hp1 HG00639.hp1 others(66): Show |
intron_variant | MODIFIER | c.1308+3300A>C | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 10/13 | chr6 | 155419394 | ||||||
| chr6:155419445
|
A | T | 2 | a0001c0006t0001g0049a0002c0009t0003g0012 | 2 | HG02258.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.1308+3249T>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 10/13 | chr6 | 155419445 | ||||||
| chr6:155419452
|
T | A | 84 | a0001c0001t0001g0075a0001c0001t0001g0081a0001c0001t0001g0083others(81): Show | 86 | HG00423.hp1 HG00438.hp2 HG00558.hp1 others(83): Show |
intron_variant | MODIFIER | c.1308+3242A>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 10/13 | chr6 | 155419452 | ||||||
| chr6:155419468
|
A | G | 15 | a0001c0001t0001g0017a0001c0001t0001g0026a0001c0001t0001g0060others(12): Show | 15 | HG01516.hp1 HG01517.hp1 HG02027.hp2 others(12): Show |
intron_variant | MODIFIER | c.1308+3226T>C | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 10/13 | chr6 | 155419468 | ||||||
| chr6:155419484
|
T | C | 1 | a0002c0011t0002g0078 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1308+3210A>G | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 10/13 | chr6 | 155419484 | ||||||
| chr6:155419570
|
C | A | 66 | a0001c0001t0001g0280a0001c0001t0002g0005a0001c0001t0002g0019others(63): Show | 68 | HG00280.hp2 HG00438.hp1 HG00639.hp1 others(65): Show |
intron_variant | MODIFIER | c.1308+3124G>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 10/13 | chr6 | 155419570 | ||||||
| chr6:155419598
|
A | G | 1 | a0001c0003t0001g0105 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1308+3096T>C | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 10/13 | chr6 | 155419598 | ||||||
| chr6:155419740
|
G | A | 1 | a0001c0001t0001g0276 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1308+2954C>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 10/13 | chr6 | 155419740 | ||||||
| chr6:155419868
|
T | A | 1 | a0001c0006t0001g0047 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1308+2826A>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 10/13 | chr6 | 155419868 | ||||||
| chr6:155419941
|
A | G | 1 | a0001c0001t0001g0091 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1308+2753T>C | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 10/13 | chr6 | 155419941 | ||||||
| chr6:155420026
|
G | GTA | 20 | a0001c0001t0001g0017a0001c0001t0001g0026a0001c0001t0001g0060others(17): Show | 20 | HG00438.hp2 HG00673.hp2 HG00735.hp2 others(17): Show |
intron_variant | MODIFIER | c.1308+2666_1308+266 others(6): Show |
NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 10/13 | chr6 | 155420026 | ||||||
| chr6:155420028
|
A | G | 1 | a0001c0005t0003g0003 | 2 | HG03098.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1308+2666T>C | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 10/13 | chr6 | 155420028 | ||||||
| chr6:155420158
|
G | A | 1 | a0001c0001t0002g0110 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1308+2536C>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 10/13 | chr6 | 155420158 | ||||||
| chr6:155420240
|
C | A | 3 | a0001c0001t0001g0280a0001c0001t0002g0061a0001c0001t0002g0062 | 3 | HG02896.hp1 HG02897.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1308+2454G>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 10/13 | chr6 | 155420240 | ||||||
| chr6:155420373
|
T | C | 1 | a0002c0002t0001g0196 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.1308+2321A>G | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 10/13 | chr6 | 155420373 | ||||||
| chr6:155420386
|
A | G | 220 | a0001c0001t0001g0016a0001c0001t0001g0023a0001c0001t0001g0024others(217): Show | 223 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(220): Show |
intron_variant | MODIFIER | c.1308+2308T>C | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 10/13 | chr6 | 155420386 | ||||||
| chr6:155420429
|
C | T | 1 | a0001c0001t0001g0238 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1308+2265G>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 10/13 | chr6 | 155420429 | ||||||
| chr6:155420503
|
T | C | 159 | a0001c0001t0001g0024a0001c0001t0001g0026a0001c0001t0001g0031others(156): Show | 162 | HG00423.hp2 HG00438.hp2 HG00558.hp1 others(159): Show |
intron_variant | MODIFIER | c.1308+2191A>G | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 10/13 | chr6 | 155420503 | ||||||
| chr6:155420733
|
C | T | 12 | a0001c0001t0001g0017a0001c0001t0001g0060a0001c0001t0001g0281others(9): Show | 13 | HG02145.hp1 HG02145.hp2 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.1308+1961G>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 10/13 | chr6 | 155420733 | ||||||
| chr6:155420758
|
T | G | 16 | a0001c0001t0001g0018a0001c0001t0001g0145a0001c0001t0001g0152others(13): Show | 16 | HG01069.hp1 HG01070.hp1 HG01169.hp1 others(13): Show |
intron_variant | MODIFIER | c.1308+1936A>C | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 10/13 | chr6 | 155420758 | ||||||
| chr6:155420860
|
C | A | 2 | a0001c0003t0001g0050a0001c0006t0001g0181 | 2 | HG02615.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1308+1834G>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 10/13 | chr6 | 155420860 | ||||||
| chr6:155420979
|
G | A | 242 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0018others(239): Show | 248 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(245): Show |
intron_variant | MODIFIER | c.1308+1715C>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 10/13 | chr6 | 155420979 | ||||||
| chr6:155421052
|
T | C | 7 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0238others(4): Show | 8 | HG02257.hp1 HG02895.hp1 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.1308+1642A>G | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 10/13 | chr6 | 155421052 | ||||||
| chr6:155421443
|
GC | G | 6 | a0001c0001t0001g0017a0001c0001t0001g0060a0001c0001t0001g0281others(3): Show | 7 | HG02145.hp2 HG02572.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1308+1250delG | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 10/13 | chr6 | 155421443 | ||||||
| chr6:155421512
|
A | G | 66 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0064others(63): Show | 68 | HG00621.hp2 HG00738.hp1 HG00741.hp2 others(65): Show |
intron_variant | MODIFIER | c.1308+1182T>C | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 10/13 | chr6 | 155421512 | ||||||
| chr6:155421558
|
A | C | 6 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0179others(3): Show | 6 | HG01891.hp1 HG02818.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.1308+1136T>G | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 10/13 | chr6 | 155421558 | ||||||
| chr6:155421576
|
T | C | 1 | a0001c0004t0001g0337 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1308+1118A>G | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 10/13 | chr6 | 155421576 | ||||||
| chr6:155421657
|
T | C | 1 | a0002c0002t0002g0305 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1308+1037A>G | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 10/13 | chr6 | 155421657 | ||||||
| chr6:155421693
|
C | T | 6 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0179others(3): Show | 6 | HG01891.hp1 HG02818.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.1308+1001G>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 10/13 | chr6 | 155421693 | ||||||
| chr6:155421711
|
C | T | 200 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0042others(197): Show | 205 | HG00423.hp2 HG00438.hp2 HG00558.hp1 others(202): Show |
intron_variant | MODIFIER | c.1308+983G>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 10/13 | chr6 | 155421711 | ||||||
| chr6:155421720
|
C | T | 7 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0238others(4): Show | 8 | HG02257.hp1 HG02895.hp1 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.1308+974G>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 10/13 | chr6 | 155421720 | ||||||
| chr6:155421758
|
G | A | 2 | a0001c0004t0001g0325a0001c0004t0001g0333 | 2 | NA18945.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.1308+936C>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 10/13 | chr6 | 155421758 | ||||||
| chr6:155421786
|
C | T | 1 | a0001c0001t0001g0280 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1308+908G>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 10/13 | chr6 | 155421786 | ||||||
| chr6:155421787
|
G | A | 2 | a0001c0001t0001g0064a0008c0019t0001g0033 | 2 | HG02572.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1308+907C>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 10/13 | chr6 | 155421787 | ||||||
| chr6:155421878
|
C | T | 1 | a0001c0001t0001g0106 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1308+816G>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 10/13 | chr6 | 155421878 | ||||||
| chr6:155422018
|
C | T | 7 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0179others(4): Show | 7 | HG01109.hp2 HG01891.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1308+676G>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 10/13 | chr6 | 155422018 | ||||||
| chr6:155422111
|
C | T | 58 | a0001c0003t0001g0037a0001c0003t0001g0039a0001c0003t0001g0040others(55): Show | 60 | HG00621.hp2 HG00738.hp1 HG00741.hp2 others(57): Show |
intron_variant | MODIFIER | c.1308+583G>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 10/13 | chr6 | 155422111 | ||||||
| chr6:155422207
|
T | C | 1 | a0001c0001t0001g0016 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1308+487A>G | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 10/13 | chr6 | 155422207 | ||||||
| chr6:155422369
|
G | C | 130 | a0001c0001t0001g0064a0001c0001t0001g0081a0001c0001t0001g0091others(127): Show | 132 | HG00423.hp2 HG00438.hp2 HG00558.hp1 others(129): Show |
intron_variant | MODIFIER | c.1308+325C>G | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 10/13 | chr6 | 155422369 | ||||||
| chr6:155422477
|
T | C | 7 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0238others(4): Show | 8 | HG02257.hp1 HG02895.hp1 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.1308+217A>G | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 10/13 | chr6 | 155422477 | ||||||
| chr6:155422673
|
G | C | 1 | a0001c0001t0001g0063 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1308+21C>G | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 10/13 | chr6 | 155422673 | ||||||
| chr6:155422879
|
C | G | 26 | a0001c0003t0001g0045a0001c0003t0001g0056a0001c0003t0001g0105others(23): Show | 28 | HG00738.hp1 HG00741.hp2 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.1146-23G>C | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 9/13 | chr6 | 155422879 | ||||||
| chr6:155422946
|
A | G | 7 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0238others(4): Show | 8 | HG02257.hp1 HG02895.hp1 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.1146-90T>C | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 9/13 | chr6 | 155422946 | ||||||
| chr6:155423069
|
C | T | 1 | a0001c0001t0001g0283 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1146-213G>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 9/13 | chr6 | 155423069 | ||||||
| chr6:155423216
|
C | G | 1 | a0001c0001t0002g0110 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1146-360G>C | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 9/13 | chr6 | 155423216 | ||||||
| chr6:155423485
|
T | C | 55 | a0001c0001t0001g0017a0001c0001t0001g0060a0001c0001t0001g0281others(52): Show | 58 | HG00738.hp1 HG00741.hp2 HG01106.hp2 others(55): Show |
intron_variant | MODIFIER | c.1146-629A>G | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 9/13 | chr6 | 155423485 | ||||||
| chr6:155423526
|
T | C | 1 | a0001c0005t0001g0308 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1146-670A>G | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 9/13 | chr6 | 155423526 | ||||||
| chr6:155423654
|
T | C | 1 | a0001c0001t0001g0016 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1146-798A>G | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 9/13 | chr6 | 155423654 | ||||||
| chr6:155423663
|
C | T | 14 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0179others(11): Show | 14 | HG00621.hp2 HG01891.hp1 HG02015.hp2 others(11): Show |
intron_variant | MODIFIER | c.1146-807G>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 9/13 | chr6 | 155423663 | ||||||
| chr6:155423681
|
A | G | 7 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0238others(4): Show | 8 | HG02257.hp1 HG02895.hp1 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.1146-825T>C | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 9/13 | chr6 | 155423681 | ||||||
| chr6:155423702
|
G | C | 14 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0179others(11): Show | 14 | HG00621.hp2 HG01891.hp1 HG02015.hp2 others(11): Show |
intron_variant | MODIFIER | c.1146-846C>G | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 9/13 | chr6 | 155423702 | ||||||
| chr6:155423743
|
CT | C | 10 | a0001c0001t0001g0016a0001c0001t0001g0118a0001c0001t0001g0252others(7): Show | 10 | HG01070.hp1 HG01109.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.1146-888delA | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 9/13 | chr6 | 155423743 | ||||||
| chr6:155423897
|
C | T | 2 | a0001c0001t0001g0064a0008c0019t0001g0033 | 2 | HG02572.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1146-1041G>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 9/13 | chr6 | 155423897 | ||||||
| chr6:155423908
|
T | A | 1 | a0001c0004t0001g0346 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1146-1052A>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 9/13 | chr6 | 155423908 | ||||||
| chr6:155423932
|
G | A | 3 | a0002c0002t0001g0084a0002c0002t0002g0085a0002c0002t0002g0224 | 3 | NA18944.hp2 NA19009.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.1146-1076C>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 9/13 | chr6 | 155423932 | ||||||
| chr6:155423993
|
G | A | 5 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0238others(2): Show | 6 | HG01978.hp1 HG02895.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1146-1137C>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 9/13 | chr6 | 155423993 | ||||||
| chr6:155424019
|
G | A | 1 | a0001c0004t0002g0349 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1146-1163C>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 9/13 | chr6 | 155424019 | ||||||
| chr6:155424053
|
C | T | 63 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0042others(60): Show | 66 | HG00738.hp1 HG00741.hp2 HG01106.hp2 others(63): Show |
intron_variant | MODIFIER | c.1146-1197G>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 9/13 | chr6 | 155424053 | ||||||
| chr6:155424246
|
G | A | 2 | a0001c0001t0001g0064a0008c0019t0001g0033 | 2 | HG02572.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1146-1390C>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 9/13 | chr6 | 155424246 | ||||||
| chr6:155424394
|
A | T | 113 | a0001c0001t0001g0081a0001c0001t0001g0091a0001c0001t0001g0092others(110): Show | 115 | HG00423.hp2 HG00438.hp2 HG00558.hp1 others(112): Show |
intron_variant | MODIFIER | c.1146-1538T>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 9/13 | chr6 | 155424394 | ||||||
| chr6:155424415
|
A | G | 1 | a0001c0003t0002g0107 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1146-1559T>C | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 9/13 | chr6 | 155424415 | ||||||
| chr6:155424531
|
C | T | 5 | a0001c0003t0001g0169a0001c0003t0002g0147a0001c0003t0002g0148others(2): Show | 5 | HG01106.hp2 HG01243.hp1 HG01496.hp2 others(2): Show |
intron_variant | MODIFIER | c.1146-1675G>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 9/13 | chr6 | 155424531 | ||||||
| chr6:155424577
|
A | G | 1 | a0001c0006t0002g0059 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1146-1721T>C | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 9/13 | chr6 | 155424577 | ||||||
| chr6:155424615
|
C | A | 1 | a0001c0001t0001g0016 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1146-1759G>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 9/13 | chr6 | 155424615 | ||||||
| chr6:155425178
|
A | T | 1 | a0001c0003t0001g0260 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1146-2322T>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 9/13 | chr6 | 155425178 | ||||||
| chr6:155425380
|
G | A | 4 | a0001c0001t0001g0018a0001c0001t0001g0152a0001c0001t0001g0153others(1): Show | 4 | HG02451.hp1 HG02559.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.1146-2524C>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 9/13 | chr6 | 155425380 | ||||||
| chr6:155425609
|
C | T | 1 | a0001c0001t0001g0025 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1146-2753G>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 9/13 | chr6 | 155425609 | ||||||
| chr6:155425779
|
C | T | 5 | a0001c0003t0001g0048a0001c0003t0001g0164a0001c0003t0001g0277others(2): Show | 5 | HG02055.hp2 HG02976.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1146-2923G>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 9/13 | chr6 | 155425779 | ||||||
| chr6:155425887
|
T | G | 1 | a0001c0001t0001g0267 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.1145+2907A>C | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 9/13 | chr6 | 155425887 | ||||||
| chr6:155426173
|
T | C | 50 | a0001c0003t0001g0037a0001c0003t0001g0039a0001c0003t0001g0040others(47): Show | 52 | HG00738.hp1 HG00741.hp2 HG01106.hp2 others(49): Show |
intron_variant | MODIFIER | c.1145+2621A>G | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 9/13 | chr6 | 155426173 | ||||||
| chr6:155426298
|
G | C | 3 | a0001c0003t0001g0051a0001c0003t0001g0144a0001c0003t0001g0168 | 3 | HG01109.hp2 HG02647.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1145+2496C>G | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 9/13 | chr6 | 155426298 | ||||||
| chr6:155426337
|
G | C | 328 | a0001c0001t0001g0009a0001c0001t0001g0016a0001c0001t0001g0017others(325): Show | 337 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(334): Show |
intron_variant | MODIFIER | c.1145+2457C>G | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 9/13 | chr6 | 155426337 | ||||||
| chr6:155426499
|
T | C | 2 | a0001c0001t0001g0064a0008c0019t0001g0033 | 2 | HG02572.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1145+2295A>G | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 9/13 | chr6 | 155426499 | ||||||
| chr6:155426591
|
C | T | 7 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0238others(4): Show | 8 | HG02257.hp1 HG02895.hp1 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.1145+2203G>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 9/13 | chr6 | 155426591 | ||||||
| chr6:155426982
|
G | GGCGTGT | 13 | a0001c0001t0001g0024a0001c0001t0001g0083a0001c0001t0001g0175others(10): Show | 13 | HG00423.hp1 HG00639.hp2 HG00642.hp1 others(10): Show |
intron_variant | MODIFIER | c.1145+1806_1145+181 others(10): Show |
NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 9/13 | chr6 | 155426982 | ||||||
| chr6:155426984
|
C | CGTGT | 7 | a0001c0001t0001g0120a0001c0005t0001g0331a0002c0002t0001g0217others(4): Show | 7 | HG02015.hp2 HG02129.hp2 NA18983.hp2 others(4): Show |
intron_variant | MODIFIER | c.1145+1806_1145+180 others(8): Show |
NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 9/13 | chr6 | 155426984 | ||||||
| chr6:155426984
|
C | CGTGTGCG others(1): Show |
57 | a0001c0001t0001g0018a0001c0001t0001g0028a0001c0001t0001g0063others(54): Show | 58 | HG00280.hp1 HG00280.hp2 HG00642.hp2 others(55): Show |
intron_variant | MODIFIER | c.1145+1809_1145+181 others(12): Show |
NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 9/13 | chr6 | 155426984 | ||||||
| chr6:155426984
|
C | CGTGTGCG others(3): Show |
33 | a0001c0001t0001g0009a0001c0001t0001g0023a0001c0001t0001g0025others(30): Show | 35 | HG00673.hp2 HG01070.hp1 HG01074.hp1 others(32): Show |
intron_variant | MODIFIER | c.1145+1809_1145+181 others(14): Show |
NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 9/13 | chr6 | 155426984 | ||||||
| chr6:155426984
|
C | CGTGTGCG others(5): Show |
4 | a0001c0001t0001g0266a0001c0001t0002g0293a0002c0007t0001g0311others(1): Show | 4 | HG00438.hp1 NA18954.hp1 NA19010.hp2 others(1): Show |
intron_variant | MODIFIER | c.1145+1809_1145+181 others(16): Show |
NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 9/13 | chr6 | 155426984 | ||||||
| chr6:155426984
|
C | CGTGTGCG others(7): Show |
4 | a0001c0001t0001g0098a0001c0001t0001g0099a0001c0001t0001g0149others(1): Show | 4 | HG02630.hp2 NA18982.hp1 NA19081.hp2 others(1): Show |
intron_variant | MODIFIER | c.1145+1809_1145+181 others(18): Show |
NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 9/13 | chr6 | 155426984 | ||||||
| chr6:155426984
|
C | CGTGTGCG others(11): Show |
1 | a0001c0005t0001g0326 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1145+1809_1145+181 others(22): Show |
NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 9/13 | chr6 | 155426984 | ||||||
| chr6:155426984
|
C | CGTGTGT | 3 | a0001c0001t0001g0017a0002c0002t0002g0220a0003c0012t0001g0070 | 3 | HG01943.hp2 HG02572.hp2 NA18939.hp2 |
intron_variant | MODIFIER | c.1145+1804_1145+180 others(10): Show |
NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 9/13 | chr6 | 155426984 | ||||||
| chr6:155426984
|
C | CGTGTGTG others(1): Show |
13 | a0001c0001t0001g0060a0001c0001t0001g0141a0001c0001t0001g0183others(10): Show | 13 | HG00438.hp2 HG01978.hp1 HG02080.hp1 others(10): Show |
intron_variant | MODIFIER | c.1145+1802_1145+180 others(12): Show |
NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 9/13 | chr6 | 155426984 | ||||||
| chr6:155426984
|
C | CGTGTGTG others(3): Show |
19 | a0001c0001t0001g0081a0001c0001t0001g0108a0001c0001t0001g0113others(16): Show | 20 | HG00558.hp2 HG00609.hp2 HG02145.hp2 others(17): Show |
intron_variant | MODIFIER | c.1145+1800_1145+180 others(14): Show |
NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 9/13 | chr6 | 155426984 | ||||||
| chr6:155426984
|
C | CGTGTGTG others(5): Show |
23 | a0001c0001t0001g0092a0001c0001t0001g0109a0001c0001t0001g0119others(20): Show | 24 | HG00558.hp1 HG00609.hp1 HG00735.hp1 others(21): Show |
intron_variant | MODIFIER | c.1145+1798_1145+180 others(16): Show |
NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 9/13 | chr6 | 155426984 | ||||||
| chr6:155426984
|
C | CGTGTGTG others(7): Show |
13 | a0001c0001t0001g0100a0001c0001t0001g0114a0001c0001t0001g0131others(10): Show | 13 | HG00621.hp1 HG00673.hp1 HG01069.hp1 others(10): Show |
intron_variant | MODIFIER | c.1145+1796_1145+180 others(18): Show |
NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 9/13 | chr6 | 155426984 | ||||||
| chr6:155426984
|
C | CGTGTGTG others(9): Show |
18 | a0001c0001t0001g0115a0001c0001t0001g0130a0001c0001t0001g0135others(15): Show | 19 | HG00423.hp2 HG00741.hp1 HG02056.hp2 others(16): Show |
intron_variant | MODIFIER | c.1145+1794_1145+180 others(20): Show |
NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 9/13 | chr6 | 155426984 | ||||||
| chr6:155426984
|
C | CGTGTGTG others(11): Show |
12 | a0001c0001t0002g0110a0002c0002t0001g0077a0002c0002t0001g0086others(9): Show | 12 | HG02129.hp1 HG02165.hp2 HG03831.hp2 others(9): Show |
intron_variant | MODIFIER | c.1145+1792_1145+180 others(22): Show |
NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 9/13 | chr6 | 155426984 | ||||||
| chr6:155426984
|
C | CGTGTGTG others(13): Show |
8 | a0001c0001t0001g0091a0001c0001t0001g0132a0002c0002t0001g0140others(5): Show | 8 | HG02015.hp1 HG02155.hp2 NA18944.hp2 others(5): Show |
intron_variant | MODIFIER | c.1145+1790_1145+180 others(24): Show |
NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 9/13 | chr6 | 155426984 | ||||||
| chr6:155426984
|
C | CGTGTGTG others(15): Show |
3 | a0002c0002t0001g0084a0002c0002t0001g0139a0002c0002t0001g0157 | 3 | HG02074.hp1 NA19060.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.1145+1788_1145+180 others(26): Show |
NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 9/13 | chr6 | 155426984 | ||||||
| chr6:155426984
|
C | CGTGTGTG others(19): Show |
1 | a0001c0001t0001g0129 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.1145+1784_1145+180 others(30): Show |
NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 9/13 | chr6 | 155426984 | ||||||
| chr6:155426984
|
C | CGTGTGTG others(21): Show |
1 | a0002c0002t0001g0200 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1145+1782_1145+180 others(32): Show |
NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 9/13 | chr6 | 155426984 | ||||||
| chr6:155426984
|
CGTGT | C | 8 | a0001c0001t0001g0043a0001c0001t0001g0103a0001c0001t0001g0165others(5): Show | 9 | HG02451.hp2 HG02895.hp1 HG03098.hp1 others(6): Show |
intron_variant | MODIFIER | c.1145+1806_1145+180 others(8): Show |
NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 9/13 | chr6 | 155426984 | ||||||
| chr6:155426984
|
CGTGTGTG others(3): Show |
C | 1 | a0001c0001t0001g0238 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1145+1800_1145+180 others(14): Show |
NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 9/13 | chr6 | 155426984 | ||||||
| chr6:155426984
|
CGTGTGTG others(5): Show |
C | 1 | a0001c0006t0001g0047 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1145+1798_1145+180 others(16): Show |
NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 9/13 | chr6 | 155426984 | ||||||
| chr6:155426984
|
CGTGTGTG others(7): Show |
C | 14 | a0001c0006t0001g0049a0001c0006t0001g0055a0001c0006t0001g0126others(11): Show | 14 | HG00738.hp2 HG01884.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.1145+1796_1145+180 others(18): Show |
NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 9/13 | chr6 | 155426984 | ||||||
| chr6:155426986
|
T | TGTGC | 6 | a0001c0001t0001g0057a0001c0001t0001g0127a0001c0001t0001g0151others(3): Show | 6 | HG02602.hp1 HG04199.hp2 NA18992.hp2 others(3): Show |
intron_variant | MODIFIER | c.1145+1807_1145+180 others(8): Show |
NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 9/13 | chr6 | 155426986 | ||||||
| chr6:155426986
|
T | TGTGCGTG others(3): Show |
1 | a0001c0001t0001g0153 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1145+1807_1145+180 others(14): Show |
NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 9/13 | chr6 | 155426986 | ||||||
| chr6:155426989
|
G | A | 4 | a0001c0001t0001g0043a0001c0005t0003g0003a0004c0010t0001g0065others(1): Show | 5 | HG02895.hp1 HG03098.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.1145+1805C>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 9/13 | chr6 | 155426989 | ||||||
| chr6:155426991
|
G | A | 2 | a0001c0001t0001g0042a0001c0001t0001g0240 | 2 | HG02257.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1145+1803C>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 9/13 | chr6 | 155426991 | ||||||
| chr6:155426993
|
G | GTGTGTGT others(9): Show |
5 | a0001c0003t0001g0037a0001c0003t0001g0039a0001c0003t0001g0041others(2): Show | 5 | HG01109.hp2 HG01891.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.1145+1800_1145+180 others(20): Show |
NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 9/13 | chr6 | 155426993 | ||||||
| chr6:155426994
|
T | C | 2 | a0001c0001t0001g0165a0001c0001t0001g0166 | 2 | HG02451.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1145+1800A>G | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 9/13 | chr6 | 155426994 | ||||||
| chr6:155426995
|
G | A | 1 | a0001c0001t0001g0238 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1145+1799C>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 9/13 | chr6 | 155426995 | ||||||
| chr6:155426995
|
G | GTGTGTGT others(7): Show |
4 | a0001c0003t0001g0050a0001c0003t0001g0051a0001c0003t0001g0168others(1): Show | 4 | HG02615.hp2 HG02647.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1145+1798_1145+179 others(18): Show |
NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 9/13 | chr6 | 155426995 | ||||||
| chr6:155426995
|
G | GTGTGTGT others(9): Show |
3 | a0001c0003t0001g0073a0001c0004t0003g0015a0001c0004t0004g0014 | 3 | HG02145.hp1 HG02486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1145+1798_1145+179 others(20): Show |
NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 9/13 | chr6 | 155426995 | ||||||
| chr6:155426997
|
G | GTGTGTGT others(5): Show |
8 | a0001c0003t0001g0040a0001c0003t0001g0056a0001c0004t0001g0002others(5): Show | 10 | HG01975.hp1 HG02004.hp2 HG02300.hp1 others(7): Show |
intron_variant | MODIFIER | c.1145+1796_1145+179 others(16): Show |
NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 9/13 | chr6 | 155426997 | ||||||
| chr6:155426999
|
G | GTGTGTGT others(3): Show |
30 | a0001c0003t0001g0045a0001c0003t0001g0048a0001c0003t0001g0105others(27): Show | 30 | HG00738.hp1 HG00741.hp2 HG01106.hp2 others(27): Show |
intron_variant | MODIFIER | c.1145+1794_1145+179 others(14): Show |
NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 9/13 | chr6 | 155426999 | ||||||
| chr6:155427028
|
T | C | 17 | a0001c0001t0001g0165a0001c0001t0001g0166a0001c0006t0001g0047others(14): Show | 17 | HG00738.hp2 HG01884.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.1145+1766A>G | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 9/13 | chr6 | 155427028 | ||||||
| chr6:155427028
|
T | TGTGTGTG others(5): Show |
1 | a0001c0001t0001g0064 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1145+1765_1145+176 others(16): Show |
NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 9/13 | chr6 | 155427028 | ||||||
| chr6:155427043
|
T | G | 1 | a0001c0003t0002g0074 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1145+1751A>C | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 9/13 | chr6 | 155427043 | ||||||
| chr6:155427051
|
G | A | 1 | a0003c0012t0001g0138 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1145+1743C>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 9/13 | chr6 | 155427051 | ||||||
| chr6:155427078
|
A | C | 166 | a0001c0001t0001g0081a0001c0001t0001g0091a0001c0001t0001g0092others(163): Show | 170 | HG00423.hp2 HG00438.hp2 HG00558.hp1 others(167): Show |
intron_variant | MODIFIER | c.1145+1716T>G | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 9/13 | chr6 | 155427078 | ||||||
| chr6:155427262
|
T | C | 2 | a0001c0001t0002g0046a0001c0001t0002g0146 | 2 | HG02965.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1145+1532A>G | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 9/13 | chr6 | 155427262 | ||||||
| chr6:155427553
|
C | T | 1 | a0001c0003t0001g0040 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1145+1241G>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 9/13 | chr6 | 155427553 | ||||||
| chr6:155427625
|
G | T | 5 | a0001c0001t0001g0017a0001c0001t0001g0060a0001c0001t0001g0281others(2): Show | 6 | HG02145.hp2 HG02572.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.1145+1169C>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 9/13 | chr6 | 155427625 | ||||||
| chr6:155427961
|
C | T | 1 | a0001c0001t0001g0129 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.1145+833G>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 9/13 | chr6 | 155427961 | ||||||
| chr6:155428027
|
G | A | 119 | a0001c0001t0001g0009a0001c0001t0001g0016a0001c0001t0001g0018others(116): Show | 122 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(119): Show |
intron_variant | MODIFIER | c.1145+767C>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 9/13 | chr6 | 155428027 | ||||||
| chr6:155428073
|
G | A | 1 | a0001c0003t0001g0045 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1145+721C>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 9/13 | chr6 | 155428073 | ||||||
| chr6:155428076
|
TTTTTAGT others(10): Show |
T | 118 | a0001c0001t0001g0009a0001c0001t0001g0018a0001c0001t0001g0023others(115): Show | 121 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(118): Show |
intron_variant | MODIFIER | c.1145+701_1145+717d others(19): Show |
NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 9/13 | chr6 | 155428076 | ||||||
| chr6:155428270
|
T | C | 328 | a0001c0001t0001g0009a0001c0001t0001g0016a0001c0001t0001g0017others(325): Show | 337 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(334): Show |
intron_variant | MODIFIER | c.1145+524A>G | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 9/13 | chr6 | 155428270 | ||||||
| chr6:155428275
|
C | T | 1 | a0002c0002t0001g0205 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1145+519G>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 9/13 | chr6 | 155428275 | ||||||
| chr6:155428360
|
T | C | 314 | a0001c0001t0001g0009a0001c0001t0001g0016a0001c0001t0001g0018others(311): Show | 321 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(318): Show |
intron_variant | MODIFIER | c.1145+434A>G | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 9/13 | chr6 | 155428360 | ||||||
| chr6:155428494
|
C | G | 2 | a0001c0005t0001g0336a0001c0005t0002g0342 | 2 | HG01943.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.1145+300G>C | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 9/13 | chr6 | 155428494 | ||||||
| chr6:155428579
|
T | C | 47 | a0001c0003t0001g0037a0001c0003t0001g0039a0001c0003t0001g0040others(44): Show | 49 | HG00738.hp1 HG00741.hp2 HG01106.hp2 others(46): Show |
intron_variant | MODIFIER | c.1145+215A>G | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 9/13 | chr6 | 155428579 | ||||||
| chr6:155428586
|
C | CT | 111 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0081others(108): Show | 113 | HG00423.hp2 HG00438.hp2 HG00558.hp1 others(110): Show |
intron_variant | MODIFIER | c.1145+207dupA | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 9/13 | chr6 | 155428586 | ||||||
| chr6:155428586
|
CT | C | 77 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0064others(74): Show | 79 | HG00738.hp1 HG00738.hp2 HG00741.hp2 others(76): Show |
intron_variant | MODIFIER | c.1145+207delA | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 9/13 | chr6 | 155428586 | ||||||
| chr6:155428589
|
T | TC | 4 | a0001c0001t0001g0071a0001c0001t0002g0032a0002c0002t0002g0264others(1): Show | 4 | HG02056.hp2 HG03098.hp2 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.1145+204_1145+205i others(3): Show |
NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 9/13 | chr6 | 155428589 | ||||||
| chr6:155428590
|
T | C | 115 | a0001c0001t0001g0009a0001c0001t0001g0018a0001c0001t0001g0023others(112): Show | 118 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(115): Show |
intron_variant | MODIFIER | c.1145+204A>G | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 9/13 | chr6 | 155428590 | ||||||
| chr6:155428591
|
T | C | 8 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0064others(5): Show | 8 | HG01891.hp1 HG02572.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.1145+203A>G | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 9/13 | chr6 | 155428591 | ||||||
| chr6:155428593
|
T | C | 1 | a0001c0001t0001g0016 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1145+201A>G | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 9/13 | chr6 | 155428593 | ||||||
| chr6:155429085
|
G | A | 328 | a0001c0001t0001g0009a0001c0001t0001g0016a0001c0001t0001g0017others(325): Show | 337 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(334): Show |
intron_variant | MODIFIER | c.892-38C>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 8/13 | chr6 | 155429085 | ||||||
| chr6:155429124
|
T | C | 7 | a0001c0001t0001g0017a0001c0001t0001g0060a0001c0001t0001g0064others(4): Show | 8 | HG02145.hp2 HG02572.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.892-77A>G | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 8/13 | chr6 | 155429124 | ||||||
| chr6:155429385
|
G | T | 1 | a0002c0002t0001g0072 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.892-338C>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 8/13 | chr6 | 155429385 | ||||||
| chr6:155429529
|
A | G | 12 | a0001c0001t0001g0017a0001c0001t0001g0060a0001c0001t0001g0064others(9): Show | 13 | HG02145.hp2 HG02572.hp1 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.892-482T>C | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 8/13 | chr6 | 155429529 | ||||||
| chr6:155429619
|
T | C | 4 | a0001c0001t0001g0132a0001c0001t0001g0135a0001c0001t0001g0136others(1): Show | 4 | NA18944.hp1 NA18953.hp2 NA18971.hp2 others(1): Show |
intron_variant | MODIFIER | c.892-572A>G | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 8/13 | chr6 | 155429619 | ||||||
| chr6:155429647
|
G | A | 1 | a0001c0006t0001g0174 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.892-600C>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 8/13 | chr6 | 155429647 | ||||||
| chr6:155429821
|
C | T | 3 | a0001c0001t0001g0245a0001c0001t0001g0251a0001c0001t0001g0252 | 3 | HG01070.hp1 HG01175.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.892-774G>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 8/13 | chr6 | 155429821 | ||||||
| chr6:155429823
|
G | A | 14 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0179others(11): Show | 14 | HG00621.hp2 HG01891.hp1 HG02015.hp2 others(11): Show |
intron_variant | MODIFIER | c.892-776C>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 8/13 | chr6 | 155429823 | ||||||
| chr6:155429878
|
C | G | 15 | a0001c0006t0001g0047a0001c0006t0001g0049a0001c0006t0001g0055others(12): Show | 15 | HG00738.hp2 HG01884.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.892-831G>C | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 8/13 | chr6 | 155429878 | ||||||
| chr6:155429951
|
T | C | 1 | a0001c0004t0001g0344 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.891+892A>G | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 8/13 | chr6 | 155429951 | ||||||
| chr6:155430103
|
A | T | 1 | a0001c0001t0002g0004 | 2 | HG02258.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.891+740T>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 8/13 | chr6 | 155430103 | ||||||
| chr6:155430191
|
C | G | 1 | a0001c0001t0001g0018 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.891+652G>C | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 8/13 | chr6 | 155430191 | ||||||
| chr6:155430224
|
C | G | 3 | a0001c0003t0001g0105a0001c0004t0001g0325a0001c0004t0001g0333 | 3 | NA18945.hp1 NA18955.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.891+619G>C | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 8/13 | chr6 | 155430224 | ||||||
| chr6:155430275
|
T | C | 2 | a0001c0001t0001g0064a0008c0019t0001g0033 | 2 | HG02572.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.891+568A>G | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 8/13 | chr6 | 155430275 | ||||||
| chr6:155430371
|
C | T | 1 | a0001c0001t0001g0080 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.891+472G>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 8/13 | chr6 | 155430371 | ||||||
| chr6:155430625
|
T | C | 17 | a0001c0001t0001g0018a0001c0001t0001g0023a0001c0001t0001g0025others(14): Show | 17 | HG00673.hp2 HG01099.hp1 HG01433.hp1 others(14): Show |
intron_variant | MODIFIER | c.891+218A>G | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 8/13 | chr6 | 155430625 | ||||||
| chr6:155430680
|
T | C | 123 | a0001c0001t0001g0009a0001c0001t0001g0018a0001c0001t0001g0023others(120): Show | 126 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(123): Show |
intron_variant | MODIFIER | c.891+163A>G | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 8/13 | chr6 | 155430680 | ||||||
| chr6:155430954
|
A | T | 1 | a0001c0004t0001g0321 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.799-19T>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 7/13 | chr6 | 155430954 | ||||||
| chr6:155431228
|
A | C | 112 | a0001c0001t0001g0081a0001c0001t0001g0091a0001c0001t0001g0092others(109): Show | 114 | HG00423.hp2 HG00438.hp2 HG00558.hp1 others(111): Show |
intron_variant | MODIFIER | c.799-293T>G | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 7/13 | chr6 | 155431228 | ||||||
| chr6:155431254
|
A | G | 1 | a0001c0001t0001g0115 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.799-319T>C | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 7/13 | chr6 | 155431254 | ||||||
| chr6:155431403
|
T | G | 1 | a0001c0001t0001g0016 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.799-468A>C | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 7/13 | chr6 | 155431403 | ||||||
| chr6:155431413
|
A | AAAAC | 3 | a0001c0001t0001g0042a0004c0010t0001g0065a0004c0010t0001g0066 | 3 | HG02897.hp1 HG03471.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.799-479_799-478ins others(4): Show |
NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 7/13 | chr6 | 155431413 | ||||||
| chr6:155431413
|
A | AAAACACA others(1): Show |
2 | a0001c0001t0001g0238a0001c0005t0003g0003 | 3 | HG03098.hp1 HG03471.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.799-479_799-478ins others(8): Show |
NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 7/13 | chr6 | 155431413 | ||||||
| chr6:155431413
|
A | AAAACACA others(3): Show |
4 | a0001c0005t0001g0331a0003c0008t0001g0338a0003c0008t0001g0339others(1): Show | 4 | HG00621.hp2 HG02015.hp2 HG02129.hp2 others(1): Show |
intron_variant | MODIFIER | c.799-479_799-478ins others(10): Show |
NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 7/13 | chr6 | 155431413 | ||||||
| chr6:155431413
|
A | AAAACACA others(5): Show |
7 | a0001c0001t0001g0016a0001c0001t0001g0254a0001c0001t0001g0255others(4): Show | 7 | HG01069.hp1 HG01361.hp1 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.799-479_799-478ins others(12): Show |
NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 7/13 | chr6 | 155431413 | ||||||
| chr6:155431413
|
A | AAC | 16 | a0001c0001t0001g0071a0001c0001t0001g0095a0001c0001t0001g0096others(13): Show | 16 | HG01070.hp1 HG01074.hp1 HG01175.hp1 others(13): Show |
intron_variant | MODIFIER | c.799-480_799-479dup others(2): Show |
NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 7/13 | chr6 | 155431413 | ||||||
| chr6:155431413
|
A | AACAC | 59 | a0001c0001t0001g0009a0001c0001t0001g0024a0001c0001t0001g0025others(56): Show | 61 | HG00642.hp1 HG01106.hp1 HG01168.hp1 others(58): Show |
intron_variant | MODIFIER | c.799-482_799-479dup others(4): Show |
NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 7/13 | chr6 | 155431413 | ||||||
| chr6:155431413
|
A | AACACAC | 55 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0023others(52): Show | 57 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(54): Show |
intron_variant | MODIFIER | c.799-484_799-479dup others(6): Show |
NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 7/13 | chr6 | 155431413 | ||||||
| chr6:155431413
|
A | AACACACA others(1): Show |
24 | a0001c0001t0001g0075a0001c0001t0001g0089a0001c0001t0001g0134others(21): Show | 24 | HG00673.hp2 HG01168.hp2 HG01243.hp1 others(21): Show |
intron_variant | MODIFIER | c.799-486_799-479dup others(8): Show |
NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 7/13 | chr6 | 155431413 | ||||||
| chr6:155431413
|
A | AACACACA others(3): Show |
56 | a0001c0001t0001g0060a0001c0001t0001g0080a0001c0001t0001g0109others(53): Show | 59 | HG00558.hp2 HG00609.hp1 HG00738.hp1 others(56): Show |
intron_variant | MODIFIER | c.799-488_799-479dup others(10): Show |
NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 7/13 | chr6 | 155431413 | ||||||
| chr6:155431413
|
A | AACACACA others(5): Show |
62 | a0001c0001t0001g0064a0001c0001t0001g0081a0001c0001t0001g0103others(59): Show | 63 | HG00423.hp2 HG00558.hp1 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.799-490_799-479dup others(12): Show |
NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 7/13 | chr6 | 155431413 | ||||||
| chr6:155431413
|
A | AACACACA others(7): Show |
15 | a0001c0001t0001g0083a0001c0001t0001g0108a0001c0001t0001g0118others(12): Show | 15 | HG00423.hp1 HG00438.hp2 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.799-492_799-479dup others(14): Show |
NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 7/13 | chr6 | 155431413 | ||||||
| chr6:155431413
|
A | AACACACA others(9): Show |
12 | a0001c0001t0001g0091a0001c0001t0001g0100a0001c0001t0001g0141others(9): Show | 12 | HG00609.hp2 HG00735.hp1 HG01943.hp2 others(9): Show |
intron_variant | MODIFIER | c.799-494_799-479dup others(16): Show |
NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 7/13 | chr6 | 155431413 | ||||||
| chr6:155431413
|
A | ACACACAC others(4): Show |
1 | a0002c0002t0001g0204 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.799-479_799-478ins others(11): Show |
NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 7/13 | chr6 | 155431413 | ||||||
| chr6:155431413
|
A | ACACACAC others(6): Show |
4 | a0001c0001t0001g0092a0001c0001t0001g0115a0002c0002t0002g0079others(1): Show | 4 | NA18969.hp2 NA19000.hp1 NA19000.hp2 others(1): Show |
intron_variant | MODIFIER | c.799-479_799-478ins others(13): Show |
NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 7/13 | chr6 | 155431413 | ||||||
| chr6:155431413
|
A | ACACACAC others(12): Show |
1 | a0001c0004t0001g0319 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.799-479_799-478ins others(19): Show |
NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 7/13 | chr6 | 155431413 | ||||||
| chr6:155431558
|
T | C | 1 | a0001c0001t0001g0127 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.799-623A>G | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 7/13 | chr6 | 155431558 | ||||||
| chr6:155431606
|
G | A | 1 | a0001c0001t0001g0016 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.799-671C>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 7/13 | chr6 | 155431606 | ||||||
| chr6:155431755
|
A | G | 8 | a0001c0005t0001g0331a0002c0002t0001g0217a0002c0002t0001g0225others(5): Show | 8 | HG00621.hp2 HG02015.hp2 HG02129.hp2 others(5): Show |
intron_variant | MODIFIER | c.799-820T>C | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 7/13 | chr6 | 155431755 | ||||||
| chr6:155431757
|
T | C | 4 | a0001c0006t0001g0055a0001c0006t0001g0154a0001c0006t0001g0155others(1): Show | 4 | HG01884.hp1 HG03195.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.799-822A>G | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 7/13 | chr6 | 155431757 | ||||||
| chr6:155431829
|
G | A | 1 | a0001c0005t0001g0336 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.799-894C>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 7/13 | chr6 | 155431829 | ||||||
| chr6:155431891
|
G | A | 1 | a0001c0005t0001g0336 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.799-956C>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 7/13 | chr6 | 155431891 | ||||||
| chr6:155432080
|
A | G | 1 | a0001c0001t0002g0117 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.799-1145T>C | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 7/13 | chr6 | 155432080 | ||||||
| chr6:155432108
|
C | T | 30 | a0001c0001t0001g0009a0001c0001t0001g0044a0001c0001t0001g0090others(27): Show | 31 | HG00642.hp1 HG01070.hp1 HG01074.hp1 others(28): Show |
intron_variant | MODIFIER | c.799-1173G>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 7/13 | chr6 | 155432108 | ||||||
| chr6:155432159
|
G | C | 1 | a0001c0006t0001g0174 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.799-1224C>G | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 7/13 | chr6 | 155432159 | ||||||
| chr6:155432179
|
A | G | 5 | a0001c0001t0001g0017a0001c0001t0001g0060a0001c0001t0001g0281others(2): Show | 6 | HG02145.hp2 HG02572.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.799-1244T>C | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 7/13 | chr6 | 155432179 | ||||||
| chr6:155432283
|
T | C | 39 | a0001c0001t0001g0018a0001c0001t0001g0023a0001c0001t0001g0024others(36): Show | 40 | HG00621.hp2 HG00673.hp2 HG01099.hp1 others(37): Show |
intron_variant | MODIFIER | c.799-1348A>G | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 7/13 | chr6 | 155432283 | ||||||
| chr6:155432409
|
G | C | 2 | a0002c0002t0001g0087a0002c0002t0001g0193 | 2 | HG00609.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.799-1474C>G | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 7/13 | chr6 | 155432409 | ||||||
| chr6:155432409
|
G | T | 6 | a0001c0001t0001g0064a0001c0003t0001g0051a0001c0003t0001g0144others(3): Show | 6 | HG01109.hp2 HG01243.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.799-1474C>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 7/13 | chr6 | 155432409 | ||||||
| chr6:155432473
|
T | C | 1 | a0002c0009t0003g0013 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.799-1538A>G | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 7/13 | chr6 | 155432473 | ||||||
| chr6:155432632
|
T | C | 1 | a0002c0007t0001g0314 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.799-1697A>G | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 7/13 | chr6 | 155432632 | ||||||
| chr6:155432683
|
C | T | 28 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0028others(25): Show | 30 | HG00741.hp2 HG01175.hp2 HG01192.hp2 others(27): Show |
intron_variant | MODIFIER | c.799-1748G>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 7/13 | chr6 | 155432683 | ||||||
| chr6:155432885
|
C | T | 1 | a0002c0002t0001g0190 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.799-1950G>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 7/13 | chr6 | 155432885 | ||||||
| chr6:155432908
|
CT | C | 8 | a0001c0005t0001g0331a0002c0007t0001g0310a0002c0007t0001g0311others(5): Show | 8 | HG00621.hp2 HG02015.hp2 HG02129.hp2 others(5): Show |
intron_variant | MODIFIER | c.799-1974delA | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 7/13 | chr6 | 155432908 | ||||||
| chr6:155433024
|
A | T | 2 | a0001c0003t0001g0088a0001c0003t0001g0142 | 2 | NA18943.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.799-2089T>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 7/13 | chr6 | 155433024 | ||||||
| chr6:155433086
|
A | C | 1 | a0002c0002t0001g0269 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.799-2151T>G | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 7/13 | chr6 | 155433086 | ||||||
| chr6:155433189
|
T | C | 38 | a0001c0001t0001g0063a0001c0001t0001g0071a0001c0001t0001g0082others(35): Show | 38 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(35): Show |
intron_variant | MODIFIER | c.799-2254A>G | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 7/13 | chr6 | 155433189 | ||||||
| chr6:155433239
|
G | A | 9 | a0002c0002t0001g0020a0002c0002t0001g0021a0002c0002t0001g0022others(6): Show | 9 | HG02622.hp2 HG02683.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.799-2304C>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 7/13 | chr6 | 155433239 | ||||||
| chr6:155433252
|
C | T | 3 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0276 | 3 | HG02818.hp2 HG03195.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.799-2317G>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 7/13 | chr6 | 155433252 | ||||||
| chr6:155433303
|
G | A | 1 | a0001c0006t0001g0174 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.799-2368C>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 7/13 | chr6 | 155433303 | ||||||
| chr6:155433407
|
C | T | 3 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0002g0005 | 4 | HG02145.hp2 HG02622.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.799-2472G>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 7/13 | chr6 | 155433407 | ||||||
| chr6:155433419
|
G | A | 11 | a0001c0001t0001g0080a0001c0001t0001g0145a0001c0001t0001g0149others(8): Show | 11 | HG02055.hp2 HG02258.hp2 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.799-2484C>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 7/13 | chr6 | 155433419 | ||||||
| chr6:155433474
|
C | A | 1 | a0001c0001t0001g0291 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.799-2539G>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 7/13 | chr6 | 155433474 | ||||||
| chr6:155433572
|
C | T | 9 | a0002c0002t0001g0020a0002c0002t0001g0021a0002c0002t0001g0022others(6): Show | 9 | HG02622.hp2 HG02683.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.799-2637G>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 7/13 | chr6 | 155433572 | ||||||
| chr6:155433584
|
TTAAA | T | 4 | a0002c0002t0001g0178a0002c0002t0001g0186a0002c0002t0002g0176others(1): Show | 4 | HG00609.hp1 HG03490.hp1 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.799-2653_799-2650d others(6): Show |
NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 7/13 | chr6 | 155433584 | ||||||
| chr6:155433640
|
TAGC | T | 115 | a0001c0001t0001g0017a0001c0001t0001g0080a0001c0001t0001g0091others(112): Show | 119 | HG00423.hp2 HG00558.hp1 HG00609.hp1 others(116): Show |
intron_variant | MODIFIER | c.799-2708_799-2706d others(5): Show |
NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 7/13 | chr6 | 155433640 | ||||||
| chr6:155433668
|
A | T | 4 | a0001c0001t0001g0245a0001c0001t0001g0250a0001c0001t0001g0251others(1): Show | 4 | HG01070.hp1 HG01106.hp1 HG01175.hp1 others(1): Show |
intron_variant | MODIFIER | c.799-2733T>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 7/13 | chr6 | 155433668 | ||||||
| chr6:155433733
|
CAG | C | 98 | a0001c0001t0001g0017a0001c0001t0001g0080a0001c0001t0001g0091others(95): Show | 101 | HG00423.hp2 HG00558.hp1 HG00609.hp1 others(98): Show |
intron_variant | MODIFIER | c.798+2683_798+2684d others(4): Show |
NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 7/13 | chr6 | 155433733 | ||||||
| chr6:155434002
|
T | A | 116 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(113): Show | 118 | HG00438.hp2 HG00621.hp2 HG00673.hp2 others(115): Show |
intron_variant | MODIFIER | c.798+2416A>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 7/13 | chr6 | 155434002 | ||||||
| chr6:155434125
|
T | C | 1 | a0001c0001t0001g0301 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.798+2293A>G | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 7/13 | chr6 | 155434125 | ||||||
| chr6:155434270
|
A | G | 159 | a0001c0001t0001g0017a0001c0001t0001g0063a0001c0001t0001g0071others(156): Show | 163 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(160): Show |
intron_variant | MODIFIER | c.798+2148T>C | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 7/13 | chr6 | 155434270 | ||||||
| chr6:155434277
|
C | G | 1 | a0001c0001t0001g0017 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.798+2141G>C | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 7/13 | chr6 | 155434277 | ||||||
| chr6:155434343
|
C | T | 1 | a0001c0001t0001g0071 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.798+2075G>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 7/13 | chr6 | 155434343 | ||||||
| chr6:155434599
|
A | G | 7 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0002g0005others(4): Show | 8 | HG01109.hp2 HG01243.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.798+1819T>C | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 7/13 | chr6 | 155434599 | ||||||
| chr6:155434600
|
T | A | 1 | a0001c0001t0001g0063 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.798+1818A>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 7/13 | chr6 | 155434600 | ||||||
| chr6:155434785
|
G | T | 2 | a0004c0010t0001g0065a0004c0010t0001g0066 | 2 | HG03471.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.798+1633C>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 7/13 | chr6 | 155434785 | ||||||
| chr6:155434840
|
A | G | 160 | a0001c0001t0001g0017a0001c0001t0001g0063a0001c0001t0001g0071others(157): Show | 164 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(161): Show |
intron_variant | MODIFIER | c.798+1578T>C | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 7/13 | chr6 | 155434840 | ||||||
| chr6:155434883
|
G | A | 4 | a0002c0002t0001g0221a0002c0002t0002g0218a0002c0002t0002g0219others(1): Show | 4 | HG00735.hp1 HG01943.hp2 HG01978.hp1 others(1): Show |
intron_variant | MODIFIER | c.798+1535C>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 7/13 | chr6 | 155434883 | ||||||
| chr6:155435079
|
A | G | 1 | a0001c0001t0001g0116 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.798+1339T>C | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 7/13 | chr6 | 155435079 | ||||||
| chr6:155435080
|
G | C | 1 | a0001c0001t0001g0116 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.798+1338C>G | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 7/13 | chr6 | 155435080 | ||||||
| chr6:155435081
|
C | G | 1 | a0001c0001t0001g0116 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.798+1337G>C | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 7/13 | chr6 | 155435081 | ||||||
| chr6:155435231
|
C | T | 101 | a0001c0001t0001g0017a0001c0001t0001g0080a0001c0001t0001g0091others(98): Show | 104 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(101): Show |
intron_variant | MODIFIER | c.798+1187G>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 7/13 | chr6 | 155435231 | ||||||
| chr6:155435258
|
G | C | 1 | a0001c0001t0001g0060 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.798+1160C>G | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 7/13 | chr6 | 155435258 | ||||||
| chr6:155435265
|
A | G | 11 | a0001c0001t0001g0080a0001c0001t0001g0145a0001c0001t0001g0149others(8): Show | 11 | HG02055.hp2 HG02258.hp2 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.798+1153T>C | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 7/13 | chr6 | 155435265 | ||||||
| chr6:155435270
|
T | C | 9 | a0002c0002t0001g0020a0002c0002t0001g0021a0002c0002t0001g0022others(6): Show | 9 | HG02622.hp2 HG02683.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.798+1148A>G | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 7/13 | chr6 | 155435270 | ||||||
| chr6:155435285
|
T | C | 1 | a0001c0004t0001g0330 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.798+1133A>G | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 7/13 | chr6 | 155435285 | ||||||
| chr6:155435352
|
T | C | 10 | a0001c0001t0001g0280a0002c0002t0001g0020a0002c0002t0001g0021others(7): Show | 10 | HG02622.hp2 HG02683.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.798+1066A>G | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 7/13 | chr6 | 155435352 | ||||||
| chr6:155435389
|
G | C | 1 | a0001c0001t0001g0280 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.798+1029C>G | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 7/13 | chr6 | 155435389 | ||||||
| chr6:155435409
|
G | C | 9 | a0001c0001t0001g0018a0001c0001t0001g0089a0001c0001t0001g0179others(6): Show | 9 | HG01884.hp1 HG01891.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.798+1009C>G | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 7/13 | chr6 | 155435409 | ||||||
| chr6:155435433
|
T | C | 160 | a0001c0001t0001g0017a0001c0001t0001g0063a0001c0001t0001g0071others(157): Show | 164 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(161): Show |
intron_variant | MODIFIER | c.798+985A>G | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 7/13 | chr6 | 155435433 | ||||||
| chr6:155435445
|
T | A | 1 | a0001c0001t0001g0116 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.798+973A>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 7/13 | chr6 | 155435445 | ||||||
| chr6:155435447
|
C | T | 1 | a0001c0001t0001g0116 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.798+971G>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 7/13 | chr6 | 155435447 | ||||||
| chr6:155435458
|
G | C | 1 | a0001c0005t0001g0323 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.798+960C>G | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 7/13 | chr6 | 155435458 | ||||||
| chr6:155435471
|
C | A | 2 | a0001c0003t0001g0263a0001c0003t0002g0242 | 2 | HG00639.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.798+947G>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 7/13 | chr6 | 155435471 | ||||||
| chr6:155435524
|
GT | G | 162 | a0001c0001t0001g0017a0001c0001t0001g0028a0001c0001t0001g0063others(159): Show | 166 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(163): Show |
intron_variant | MODIFIER | c.798+893delA | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 7/13 | chr6 | 155435524 | ||||||
| chr6:155435534
|
T | A | 6 | a0002c0002t0001g0006a0002c0002t0001g0189a0002c0002t0001g0190others(3): Show | 7 | HG01081.hp1 HG01192.hp1 HG01255.hp2 others(4): Show |
intron_variant | MODIFIER | c.798+884A>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 7/13 | chr6 | 155435534 | ||||||
| chr6:155435716
|
C | T | 1 | a0001c0001t0001g0054 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.798+702G>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 7/13 | chr6 | 155435716 | ||||||
| chr6:155435813
|
G | A | 11 | a0001c0001t0001g0254a0001c0001t0001g0255a0001c0001t0001g0281others(8): Show | 12 | HG00639.hp1 HG01069.hp1 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.798+605C>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 7/13 | chr6 | 155435813 | ||||||
| chr6:155435920
|
C | G | 1 | a0001c0001t0001g0280 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.798+498G>C | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 7/13 | chr6 | 155435920 | ||||||
| chr6:155435934
|
G | A | 1 | a0002c0002t0001g0300 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.798+484C>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 7/13 | chr6 | 155435934 | ||||||
| chr6:155435970
|
A | G | 2 | a0004c0010t0001g0065a0004c0010t0001g0066 | 2 | HG03471.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.798+448T>C | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 7/13 | chr6 | 155435970 | ||||||
| chr6:155436010
|
A | C | 1 | a0002c0011t0002g0078 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.798+408T>G | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 7/13 | chr6 | 155436010 | ||||||
| chr6:155436288
|
A | G | 4 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0002g0027others(1): Show | 4 | HG02027.hp2 HG02155.hp1 NA19063.hp2 others(1): Show |
intron_variant | MODIFIER | c.798+130T>C | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 7/13 | chr6 | 155436288 | ||||||
| chr6:155436647
|
T | A | 38 | a0001c0001t0001g0063a0001c0001t0001g0071a0001c0001t0001g0082others(35): Show | 38 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(35): Show |
intron_variant | MODIFIER | c.669-100A>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 6/13 | chr6 | 155436647 | ||||||
| chr6:155436677
|
C | T | 4 | a0001c0001t0001g0254a0001c0001t0001g0255a0001c0003t0001g0263others(1): Show | 4 | HG00639.hp1 HG01069.hp1 HG01261.hp2 others(1): Show |
intron_variant | MODIFIER | c.669-130G>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 6/13 | chr6 | 155436677 | ||||||
| chr6:155436694
|
C | T | 79 | a0001c0001t0001g0091a0001c0001t0001g0103a0001c0001t0001g0129others(76): Show | 81 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(78): Show |
intron_variant | MODIFIER | c.669-147G>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 6/13 | chr6 | 155436694 | ||||||
| chr6:155436718
|
A | C | 1 | a0001c0001t0002g0171 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.669-171T>G | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 6/13 | chr6 | 155436718 | ||||||
| chr6:155436854
|
T | A | 4 | a0001c0001t0002g0046a0001c0004t0003g0015a0001c0004t0004g0014others(1): Show | 5 | HG02145.hp1 HG03041.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.669-307A>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 6/13 | chr6 | 155436854 | ||||||
| chr6:155437043
|
C | G | 1 | a0001c0001t0001g0280 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.669-496G>C | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 6/13 | chr6 | 155437043 | ||||||
| chr6:155437101
|
C | T | 150 | a0001c0001t0001g0017a0001c0001t0001g0063a0001c0001t0001g0071others(147): Show | 154 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(151): Show |
intron_variant | MODIFIER | c.669-554G>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 6/13 | chr6 | 155437101 | ||||||
| chr6:155437116
|
T | C | 1 | a0001c0001t0001g0280 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.669-569A>G | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 6/13 | chr6 | 155437116 | ||||||
| chr6:155437149
|
G | A | 1 | a0001c0001t0001g0280 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.669-602C>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 6/13 | chr6 | 155437149 | ||||||
| chr6:155437207
|
C | G | 2 | a0001c0001t0001g0150a0001c0001t0001g0151 | 2 | HG02922.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.669-660G>C | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 6/13 | chr6 | 155437207 | ||||||
| chr6:155437254
|
C | T | 29 | a0001c0001t0001g0127a0001c0001t0001g0150a0001c0001t0001g0151others(26): Show | 30 | HG00738.hp2 HG01081.hp1 HG01175.hp2 others(27): Show |
intron_variant | MODIFIER | c.669-707G>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 6/13 | chr6 | 155437254 | ||||||
| chr6:155437311
|
G | A | 1 | a0001c0001t0001g0280 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.669-764C>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 6/13 | chr6 | 155437311 | ||||||
| chr6:155437476
|
C | T | 110 | a0001c0001t0001g0018a0001c0001t0001g0023a0001c0001t0001g0024others(107): Show | 111 | HG00438.hp2 HG00621.hp2 HG00673.hp2 others(108): Show |
intron_variant | MODIFIER | c.669-929G>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 6/13 | chr6 | 155437476 | ||||||
| chr6:155437548
|
C | G | 1 | a0001c0001t0001g0064 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.669-1001G>C | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 6/13 | chr6 | 155437548 | ||||||
| chr6:155437968
|
A | G | 1 | a0001c0001t0001g0232 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.669-1421T>C | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 6/13 | chr6 | 155437968 | ||||||
| chr6:155438066
|
T | C | 47 | a0001c0001t0001g0026a0001c0001t0001g0063a0001c0001t0001g0071others(44): Show | 47 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(44): Show |
intron_variant | MODIFIER | c.669-1519A>G | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 6/13 | chr6 | 155438066 | ||||||
| chr6:155438077
|
C | T | 1 | a0001c0001t0002g0146 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.669-1530G>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 6/13 | chr6 | 155438077 | ||||||
| chr6:155438189
|
G | T | 1 | a0001c0001t0002g0005 | 2 | HG02622.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.669-1642C>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 6/13 | chr6 | 155438189 | ||||||
| chr6:155438203
|
C | T | 1 | a0001c0003t0001g0050 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.669-1656G>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 6/13 | chr6 | 155438203 | ||||||
| chr6:155438381
|
C | A | 1 | a0002c0007t0001g0315 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.668+1575G>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 6/13 | chr6 | 155438381 | ||||||
| chr6:155438626
|
T | C | 1 | a0001c0001t0001g0057 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.668+1330A>G | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 6/13 | chr6 | 155438626 | ||||||
| chr6:155438644
|
T | C | 40 | a0001c0001t0001g0127a0001c0001t0001g0153a0001c0001t0001g0165others(37): Show | 40 | HG00642.hp2 HG00738.hp2 HG01069.hp2 others(37): Show |
intron_variant | MODIFIER | c.668+1312A>G | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 6/13 | chr6 | 155438644 | ||||||
| chr6:155438660
|
C | T | 1 | a0001c0003t0002g0241 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.668+1296G>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 6/13 | chr6 | 155438660 | ||||||
| chr6:155438765
|
G | A | 1 | a0001c0001t0001g0044 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.668+1191C>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 6/13 | chr6 | 155438765 | ||||||
| chr6:155438783
|
C | G | 3 | a0001c0001t0001g0060a0001c0006t0001g0154a0001c0006t0001g0155 | 3 | HG01884.hp1 HG02647.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.668+1173G>C | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 6/13 | chr6 | 155438783 | ||||||
| chr6:155438881
|
T | C | 1 | a0001c0001t0001g0280 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.668+1075A>G | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 6/13 | chr6 | 155438881 | ||||||
| chr6:155438950
|
C | T | 91 | a0001c0001t0001g0114a0001c0001t0001g0283a0001c0001t0001g0301others(88): Show | 94 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(91): Show |
intron_variant | MODIFIER | c.668+1006G>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 6/13 | chr6 | 155438950 | ||||||
| chr6:155439050
|
T | C | 1 | a0001c0001t0001g0096 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.668+906A>G | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 6/13 | chr6 | 155439050 | ||||||
| chr6:155439061
|
C | T | 93 | a0001c0001t0001g0017a0001c0001t0001g0023a0001c0001t0001g0024others(90): Show | 95 | HG00438.hp2 HG00673.hp1 HG00673.hp2 others(92): Show |
intron_variant | MODIFIER | c.668+895G>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 6/13 | chr6 | 155439061 | ||||||
| chr6:155439062
|
C | CT | 5 | a0001c0003t0001g0037a0001c0003t0001g0039a0001c0003t0001g0040others(2): Show | 5 | HG01891.hp2 HG02280.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.668+893dupA | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 6/13 | chr6 | 155439062 | ||||||
| chr6:155439082
|
C | T | 1 | a0001c0006t0001g0055 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.668+874G>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 6/13 | chr6 | 155439082 | ||||||
| chr6:155439251
|
C | T | 20 | a0001c0001t0001g0018a0001c0001t0001g0028a0001c0001t0001g0060others(17): Show | 21 | HG01109.hp2 HG01243.hp1 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.668+705G>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 6/13 | chr6 | 155439251 | ||||||
| chr6:155439521
|
C | T | 31 | a0001c0001t0001g0127a0001c0001t0001g0165a0001c0001t0001g0166others(28): Show | 31 | HG00642.hp2 HG00738.hp2 HG01069.hp2 others(28): Show |
intron_variant | MODIFIER | c.668+435G>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 6/13 | chr6 | 155439521 | ||||||
| chr6:155439569
|
A | C | 1 | a0003c0008t0001g0338 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.668+387T>G | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 6/13 | chr6 | 155439569 | ||||||
| chr6:155439653
|
A | T | 2 | a0003c0012t0001g0070a0003c0012t0001g0138 | 2 | NA18939.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.668+303T>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 6/13 | chr6 | 155439653 | ||||||
| chr6:155439677
|
T | A | 1 | a0001c0001t0001g0031 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.668+279A>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 6/13 | chr6 | 155439677 | ||||||
| chr6:155439847
|
C | A | 1 | a0001c0004t0001g0344 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.668+109G>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 6/13 | chr6 | 155439847 | ||||||
| chr6:155439857
|
A | G | 1 | a0001c0004t0001g0344 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.668+99T>C | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 6/13 | chr6 | 155439857 | ||||||
| chr6:155439871
|
G | A | 1 | a0001c0005t0002g0334 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.668+85C>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 6/13 | chr6 | 155439871 | ||||||
| chr6:155440145
|
A | C | 1 | a0001c0004t0001g0344 | 1 | NA21309.hp2 | splice_region_variant&intron_variant | LOW | c.487-8T>G | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 5/13 | chr6 | 155440145 | ||||||
| chr6:155440185
|
C | T | 4 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0042others(1): Show | 4 | HG02818.hp2 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.487-48G>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 5/13 | chr6 | 155440185 | ||||||
| chr6:155440196
|
A | C | 2 | a0001c0004t0003g0015a0001c0004t0004g0014 | 2 | HG02145.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.487-59T>G | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 5/13 | chr6 | 155440196 | ||||||
| chr6:155440261
|
G | A | 2 | a0001c0001t0001g0128a0001c0003t0002g0052 | 2 | HG02559.hp1 NA18963.hp1 |
intron_variant | MODIFIER | c.487-124C>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 5/13 | chr6 | 155440261 | ||||||
| chr6:155440283
|
G | A | 7 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0003t0001g0050others(4): Show | 7 | HG01109.hp2 HG01243.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.487-146C>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 5/13 | chr6 | 155440283 | ||||||
| chr6:155440306
|
C | G | 1 | a0001c0004t0001g0344 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.487-169G>C | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 5/13 | chr6 | 155440306 | ||||||
| chr6:155440324
|
C | T | 1 | a0001c0001t0001g0240 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.487-187G>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 5/13 | chr6 | 155440324 | ||||||
| chr6:155440360
|
G | A | 91 | a0002c0002t0001g0006a0002c0002t0001g0007a0002c0002t0001g0020others(88): Show | 94 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(91): Show |
intron_variant | MODIFIER | c.487-223C>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 5/13 | chr6 | 155440360 | ||||||
| chr6:155440387
|
G | A | 34 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0028others(31): Show | 34 | HG00639.hp1 HG01099.hp2 HG01106.hp2 others(31): Show |
intron_variant | MODIFIER | c.487-250C>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 5/13 | chr6 | 155440387 | ||||||
| chr6:155440410
|
C | G | 4 | a0001c0004t0001g0327a0001c0004t0001g0328a0001c0004t0001g0330others(1): Show | 4 | HG01975.hp1 HG01993.hp2 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.487-273G>C | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 5/13 | chr6 | 155440410 | ||||||
| chr6:155440431
|
A | G | 90 | a0002c0002t0001g0006a0002c0002t0001g0007a0002c0002t0001g0020others(87): Show | 93 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.487-294T>C | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 5/13 | chr6 | 155440431 | ||||||
| chr6:155440467
|
A | C | 33 | a0001c0001t0001g0127a0001c0001t0001g0165a0001c0001t0001g0166others(30): Show | 33 | HG00642.hp2 HG00738.hp2 HG01069.hp2 others(30): Show |
intron_variant | MODIFIER | c.487-330T>G | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 5/13 | chr6 | 155440467 | ||||||
| chr6:155440480
|
A | C | 94 | a0001c0001t0001g0017a0001c0001t0001g0023a0001c0001t0001g0024others(91): Show | 96 | HG00438.hp2 HG00673.hp1 HG00673.hp2 others(93): Show |
intron_variant | MODIFIER | c.487-343T>G | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 5/13 | chr6 | 155440480 | ||||||
| chr6:155440484
|
A | T | 276 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(273): Show | 282 | HG00423.hp2 HG00438.hp2 HG00558.hp1 others(279): Show |
intron_variant | MODIFIER | c.487-347T>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 5/13 | chr6 | 155440484 | ||||||
| chr6:155440485
|
A | T | 36 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0042others(33): Show | 36 | HG00642.hp2 HG00738.hp2 HG01069.hp2 others(33): Show |
intron_variant | MODIFIER | c.487-348T>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 5/13 | chr6 | 155440485 | ||||||
| chr6:155440535
|
G | A | 91 | a0002c0002t0001g0006a0002c0002t0001g0007a0002c0002t0001g0020others(88): Show | 94 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(91): Show |
intron_variant | MODIFIER | c.487-398C>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 5/13 | chr6 | 155440535 | ||||||
| chr6:155440545
|
G | A | 308 | a0001c0001t0001g0009a0001c0001t0001g0016a0001c0001t0001g0017others(305): Show | 317 | HG00423.hp2 HG00438.hp2 HG00558.hp1 others(314): Show |
intron_variant | MODIFIER | c.487-408C>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 5/13 | chr6 | 155440545 | ||||||
| chr6:155440585
|
G | A | 1 | a0001c0001t0001g0280 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.487-448C>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 5/13 | chr6 | 155440585 | ||||||
| chr6:155440604
|
G | C | 1 | a0001c0004t0001g0344 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.487-467C>G | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 5/13 | chr6 | 155440604 | ||||||
| chr6:155440683
|
CA | C | 41 | a0001c0001t0001g0064a0001c0001t0001g0127a0001c0001t0001g0153others(38): Show | 41 | HG00642.hp2 HG00738.hp2 HG01069.hp2 others(38): Show |
intron_variant | MODIFIER | c.487-547delT | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 5/13 | chr6 | 155440683 | ||||||
| chr6:155440686
|
A | C | 5 | a0003c0008t0001g0338a0003c0008t0001g0339a0003c0008t0001g0340others(2): Show | 5 | HG00621.hp2 HG02015.hp2 HG02129.hp2 others(2): Show |
intron_variant | MODIFIER | c.487-549T>G | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 5/13 | chr6 | 155440686 | ||||||
| chr6:155440687
|
A | AC | 3 | a0001c0001t0001g0292a0001c0001t0002g0293a0001c0001t0002g0297 | 3 | HG00438.hp1 NA18612.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.487-551_487-550ins others(1): Show |
NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 5/13 | chr6 | 155440687 | ||||||
| chr6:155440687
|
A | C | 30 | a0001c0001t0001g0018a0001c0001t0001g0028a0001c0001t0001g0030others(27): Show | 31 | HG00609.hp2 HG01884.hp1 HG01891.hp1 others(28): Show |
intron_variant | MODIFIER | c.487-550T>G | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 5/13 | chr6 | 155440687 | ||||||
| chr6:155440688
|
A | C | 4 | a0001c0004t0001g0344a0002c0002t0001g0007a0002c0002t0001g0196others(1): Show | 5 | NA18971.hp1 NA18988.hp2 NA19011.hp2 others(2): Show |
intron_variant | MODIFIER | c.487-551T>G | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 5/13 | chr6 | 155440688 | ||||||
| chr6:155440689
|
A | C | 8 | a0001c0001t0001g0113a0001c0001t0001g0183a0001c0001t0002g0194others(5): Show | 8 | HG00621.hp2 HG02015.hp2 HG02080.hp2 others(5): Show |
intron_variant | MODIFIER | c.487-552T>G | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 5/13 | chr6 | 155440689 | ||||||
| chr6:155440690
|
A | AC | 8 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0003t0001g0050others(5): Show | 9 | HG01109.hp2 HG01243.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.487-554_487-553ins others(1): Show |
NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 5/13 | chr6 | 155440690 | ||||||
| chr6:155440691
|
A | C | 1 | a0010c0018t0001g0275 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.487-554T>G | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 5/13 | chr6 | 155440691 | ||||||
| chr6:155440760
|
T | C | 1 | a0008c0019t0001g0033 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.487-623A>G | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 5/13 | chr6 | 155440760 | ||||||
| chr6:155440850
|
A | AT | 94 | a0001c0001t0001g0017a0001c0001t0001g0023a0001c0001t0001g0024others(91): Show | 96 | HG00438.hp2 HG00673.hp1 HG00673.hp2 others(93): Show |
intron_variant | MODIFIER | c.487-714dupA | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 5/13 | chr6 | 155440850 | ||||||
| chr6:155440874
|
C | T | 1 | a0001c0003t0002g0052 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.487-737G>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 5/13 | chr6 | 155440874 | ||||||
| chr6:155440931
|
C | T | 8 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0003t0001g0050others(5): Show | 9 | HG01109.hp2 HG01243.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.487-794G>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 5/13 | chr6 | 155440931 | ||||||
| chr6:155441046
|
G | C | 1 | a0001c0004t0001g0344 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.487-909C>G | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 5/13 | chr6 | 155441046 | ||||||
| chr6:155441051
|
G | T | 166 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(163): Show | 168 | HG00438.hp2 HG00639.hp1 HG00642.hp2 others(165): Show |
intron_variant | MODIFIER | c.487-914C>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 5/13 | chr6 | 155441051 | ||||||
| chr6:155441053
|
C | G | 81 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(78): Show | 82 | HG00438.hp2 HG00673.hp1 HG00673.hp2 others(79): Show |
intron_variant | MODIFIER | c.487-916G>C | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 5/13 | chr6 | 155441053 | ||||||
| chr6:155441133
|
T | C | 4 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0042others(1): Show | 4 | HG02818.hp2 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.487-996A>G | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 5/13 | chr6 | 155441133 | ||||||
| chr6:155441201
|
C | T | 1 | a0002c0002t0001g0193 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.487-1064G>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 5/13 | chr6 | 155441201 | ||||||
| chr6:155441285
|
G | A | 32 | a0001c0001t0001g0127a0001c0001t0001g0165a0001c0001t0001g0166others(29): Show | 32 | HG00642.hp2 HG00738.hp2 HG01069.hp2 others(29): Show |
intron_variant | MODIFIER | c.487-1148C>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 5/13 | chr6 | 155441285 | ||||||
| chr6:155441301
|
A | ATTGT | 278 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(275): Show | 284 | HG00423.hp2 HG00438.hp2 HG00558.hp1 others(281): Show |
intron_variant | MODIFIER | c.487-1165_487-1164i others(6): Show |
NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 5/13 | chr6 | 155441301 | ||||||
| chr6:155441319
|
A | C | 1 | a0001c0001t0001g0098 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.487-1182T>G | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 5/13 | chr6 | 155441319 | ||||||
| chr6:155441329
|
G | A | 1 | a0001c0004t0001g0344 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.487-1192C>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 5/13 | chr6 | 155441329 | ||||||
| chr6:155441534
|
C | T | 1 | a0001c0001t0001g0280 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.487-1397G>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 5/13 | chr6 | 155441534 | ||||||
| chr6:155441676
|
C | T | 1 | a0001c0001t0001g0095 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.487-1539G>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 5/13 | chr6 | 155441676 | ||||||
| chr6:155441923
|
C | A | 1 | a0001c0003t0001g0236 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.486+1350G>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 5/13 | chr6 | 155441923 | ||||||
| chr6:155441986
|
C | T | 13 | a0001c0001t0001g0229a0001c0001t0001g0230a0001c0001t0001g0232others(10): Show | 13 | HG00642.hp2 HG01175.hp2 HG01256.hp2 others(10): Show |
intron_variant | MODIFIER | c.486+1287G>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 5/13 | chr6 | 155441986 | ||||||
| chr6:155441992
|
C | T | 9 | a0001c0001t0001g0106a0001c0001t0001g0229a0001c0001t0001g0230others(6): Show | 9 | HG00642.hp2 HG01175.hp2 HG01256.hp2 others(6): Show |
intron_variant | MODIFIER | c.486+1281G>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 5/13 | chr6 | 155441992 | ||||||
| chr6:155441995
|
T | G | 1 | a0001c0003t0001g0073 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.486+1278A>C | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 5/13 | chr6 | 155441995 | ||||||
| chr6:155442035
|
T | C | 102 | a0001c0001t0001g0092a0001c0001t0001g0127a0001c0001t0001g0195others(99): Show | 107 | HG00423.hp2 HG00558.hp2 HG00609.hp1 others(104): Show |
intron_variant | MODIFIER | c.486+1238A>G | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 5/13 | chr6 | 155442035 | ||||||
| chr6:155442039
|
C | T | 8 | a0001c0003t0001g0259a0001c0003t0001g0260a0001c0003t0001g0261others(5): Show | 8 | HG00642.hp1 HG00738.hp1 HG01109.hp1 others(5): Show |
intron_variant | MODIFIER | c.486+1234G>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 5/13 | chr6 | 155442039 | ||||||
| chr6:155442046
|
C | T | 2 | a0001c0001t0001g0091a0001c0001t0002g0143 | 2 | NA18953.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.486+1227G>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 5/13 | chr6 | 155442046 | ||||||
| chr6:155442075
|
T | C | 88 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(85): Show | 88 | HG00438.hp2 HG00673.hp1 HG00673.hp2 others(85): Show |
intron_variant | MODIFIER | c.486+1198A>G | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 5/13 | chr6 | 155442075 | ||||||
| chr6:155442081
|
A | G | 1 | a0001c0001t0001g0284 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.486+1192T>C | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 5/13 | chr6 | 155442081 | ||||||
| chr6:155442136
|
T | C | 2 | a0001c0001t0002g0272a0001c0005t0002g0036 | 2 | HG00280.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.486+1137A>G | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 5/13 | chr6 | 155442136 | ||||||
| chr6:155442213
|
G | A | 3 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137 | 3 | NA18944.hp1 NA18953.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.486+1060C>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 5/13 | chr6 | 155442213 | ||||||
| chr6:155442214
|
T | A | 3 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137 | 3 | NA18944.hp1 NA18953.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.486+1059A>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 5/13 | chr6 | 155442214 | ||||||
| chr6:155442230
|
C | G | 1 | a0001c0001t0002g0019 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.486+1043G>C | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 5/13 | chr6 | 155442230 | ||||||
| chr6:155442237
|
T | C | 1 | a0001c0001t0001g0044 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.486+1036A>G | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 5/13 | chr6 | 155442237 | ||||||
| chr6:155442238
|
C | T | 1 | a0001c0001t0001g0044 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.486+1035G>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 5/13 | chr6 | 155442238 | ||||||
| chr6:155442239
|
T | G | 1 | a0001c0001t0001g0044 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.486+1034A>C | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 5/13 | chr6 | 155442239 | ||||||
| chr6:155442327
|
T | C | 4 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0042others(1): Show | 4 | HG02818.hp2 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.486+946A>G | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 5/13 | chr6 | 155442327 | ||||||
| chr6:155442330
|
C | T | 112 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(109): Show | 116 | HG00423.hp2 HG00558.hp1 HG00609.hp1 others(113): Show |
intron_variant | MODIFIER | c.486+943G>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 5/13 | chr6 | 155442330 | ||||||
| chr6:155442337
|
T | C | 5 | a0001c0003t0001g0037a0001c0003t0001g0039a0001c0003t0001g0040others(2): Show | 5 | HG01891.hp2 HG02280.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.486+936A>G | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 5/13 | chr6 | 155442337 | ||||||
| chr6:155442374
|
G | T | 108 | a0001c0001t0001g0057a0001c0001t0001g0064a0001c0001t0001g0075others(105): Show | 111 | HG00438.hp2 HG00558.hp2 HG00642.hp1 others(108): Show |
intron_variant | MODIFIER | c.486+899C>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 5/13 | chr6 | 155442374 | ||||||
| chr6:155442420
|
A | G | 2 | a0001c0003t0001g0073a0010c0018t0001g0275 | 2 | HG02486.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.486+853T>C | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 5/13 | chr6 | 155442420 | ||||||
| chr6:155442490
|
G | C | 1 | a0001c0001t0001g0044 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.486+783C>G | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 5/13 | chr6 | 155442490 | ||||||
| chr6:155442495
|
T | C | 1 | a0001c0001t0001g0044 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.486+778A>G | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 5/13 | chr6 | 155442495 | ||||||
| chr6:155442503
|
C | T | 6 | a0001c0001t0001g0017a0001c0001t0001g0089a0001c0001t0001g0179others(3): Show | 7 | HG01891.hp1 HG02572.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.486+770G>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 5/13 | chr6 | 155442503 | ||||||
| chr6:155442535
|
T | C | 4 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0042others(1): Show | 4 | HG02818.hp2 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.486+738A>G | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 5/13 | chr6 | 155442535 | ||||||
| chr6:155442782
|
G | T | 1 | a0002c0002t0002g0191 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.486+491C>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 5/13 | chr6 | 155442782 | ||||||
| chr6:155442783
|
C | G | 1 | a0002c0002t0002g0191 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.486+490G>C | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 5/13 | chr6 | 155442783 | ||||||
| chr6:155443026
|
A | G | 3 | a0001c0001t0001g0145a0001c0001t0002g0004a0001c0001t0002g0146 | 4 | HG02258.hp1 HG02922.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.486+247T>C | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 5/13 | chr6 | 155443026 | ||||||
| chr6:155443039
|
A | G | 2 | a0001c0001t0001g0238a0001c0001t0001g0240 | 2 | HG02257.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.486+234T>C | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 5/13 | chr6 | 155443039 | ||||||
| chr6:155443201
|
G | A | 1 | a0002c0002t0001g0072 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.486+72C>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 5/13 | chr6 | 155443201 | ||||||
| chr6:155443478
|
A | G | 1 | a0001c0001t0001g0167 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.341-60T>C | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 4/13 | chr6 | 155443478 | ||||||
| chr6:155443569
|
C | T | 12 | a0001c0001t0002g0046a0001c0003t0001g0048a0001c0003t0001g0050others(9): Show | 12 | HG01109.hp2 HG01243.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.341-151G>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 4/13 | chr6 | 155443569 | ||||||
| chr6:155443781
|
G | A | 1 | a0001c0001t0001g0288 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.341-363C>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 4/13 | chr6 | 155443781 | ||||||
| chr6:155443794
|
G | A | 1 | a0002c0002t0001g0072 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.341-376C>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 4/13 | chr6 | 155443794 | ||||||
| chr6:155443803
|
A | C | 2 | a0001c0001t0001g0111a0001c0001t0002g0110 | 2 | HG02040.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.341-385T>G | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 4/13 | chr6 | 155443803 | ||||||
| chr6:155443869
|
TAATA | T | 4 | a0001c0001t0001g0044a0001c0001t0001g0281a0001c0001t0001g0282others(1): Show | 4 | HG02145.hp2 HG02886.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.341-455_341-452del others(4): Show |
NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 4/13 | chr6 | 155443869 | ||||||
| chr6:155443871
|
A | G | 1 | a0001c0003t0001g0259 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.341-453T>C | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 4/13 | chr6 | 155443871 | ||||||
| chr6:155443894
|
A | T | 6 | a0002c0002t0001g0006a0002c0002t0001g0189a0002c0002t0001g0190others(3): Show | 7 | HG01081.hp1 HG01192.hp1 HG01255.hp2 others(4): Show |
intron_variant | MODIFIER | c.341-476T>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 4/13 | chr6 | 155443894 | ||||||
| chr6:155443947
|
C | A | 1 | a0001c0001t0001g0280 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.341-529G>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 4/13 | chr6 | 155443947 | ||||||
| chr6:155444065
|
A | G | 212 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0028others(209): Show | 215 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(212): Show |
intron_variant | MODIFIER | c.341-647T>C | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 4/13 | chr6 | 155444065 | ||||||
| chr6:155444212
|
C | A | 3 | a0001c0001t0001g0238a0001c0001t0001g0240a0002c0002t0001g0185 | 3 | HG02257.hp1 HG03540.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.341-794G>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 4/13 | chr6 | 155444212 | ||||||
| chr6:155444569
|
A | G | 1 | a0001c0001t0002g0069 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.341-1151T>C | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 4/13 | chr6 | 155444569 | ||||||
| chr6:155444617
|
A | G | 1 | a0001c0001t0001g0089 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.341-1199T>C | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 4/13 | chr6 | 155444617 | ||||||
| chr6:155444638
|
C | A | 1 | a0001c0003t0001g0051 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.341-1220G>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 4/13 | chr6 | 155444638 | ||||||
| chr6:155444646
|
G | A | 1 | a0001c0003t0001g0051 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.341-1228C>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 4/13 | chr6 | 155444646 | ||||||
| chr6:155444720
|
A | G | 2 | a0001c0001t0001g0238a0001c0001t0001g0240 | 2 | HG02257.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.341-1302T>C | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 4/13 | chr6 | 155444720 | ||||||
| chr6:155444780
|
T | C | 3 | a0003c0008t0001g0338a0003c0008t0001g0339a0003c0008t0001g0340 | 3 | HG00621.hp2 HG02015.hp2 HG02129.hp2 |
intron_variant | MODIFIER | c.341-1362A>G | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 4/13 | chr6 | 155444780 | ||||||
| chr6:155445041
|
A | C | 1 | a0001c0006t0001g0055 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.341-1623T>G | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 4/13 | chr6 | 155445041 | ||||||
| chr6:155445051
|
G | A | 2 | a0002c0002t0001g0020a0002c0002t0001g0021 | 2 | HG02723.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.341-1633C>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 4/13 | chr6 | 155445051 | ||||||
| chr6:155445213
|
G | T | 1 | a0001c0001t0001g0284 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.341-1795C>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 4/13 | chr6 | 155445213 | ||||||
| chr6:155445228
|
G | A | 212 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0028others(209): Show | 215 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(212): Show |
intron_variant | MODIFIER | c.341-1810C>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 4/13 | chr6 | 155445228 | ||||||
| chr6:155445337
|
G | A | 1 | a0001c0003t0001g0073 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.341-1919C>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 4/13 | chr6 | 155445337 | ||||||
| chr6:155445392
|
G | A | 1 | a0002c0002t0001g0087 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.341-1974C>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 4/13 | chr6 | 155445392 | ||||||
| chr6:155445553
|
G | T | 135 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0042others(132): Show | 138 | HG00438.hp2 HG00558.hp2 HG00621.hp2 others(135): Show |
intron_variant | MODIFIER | c.341-2135C>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 4/13 | chr6 | 155445553 | ||||||
| chr6:155445708
|
G | A | 1 | a0001c0005t0001g0341 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.341-2290C>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 4/13 | chr6 | 155445708 | ||||||
| chr6:155445772
|
A | G | 5 | a0001c0001t0001g0017a0001c0001t0001g0089a0001c0001t0001g0179others(2): Show | 5 | HG01891.hp1 HG02572.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.341-2354T>C | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 4/13 | chr6 | 155445772 | ||||||
| chr6:155445810
|
A | C | 212 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0028others(209): Show | 215 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(212): Show |
intron_variant | MODIFIER | c.341-2392T>G | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 4/13 | chr6 | 155445810 | ||||||
| chr6:155445824
|
A | G | 1 | a0001c0001t0001g0028 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.341-2406T>C | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 4/13 | chr6 | 155445824 | ||||||
| chr6:155445869
|
CAT | C | 213 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0028others(210): Show | 218 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(215): Show |
intron_variant | MODIFIER | c.341-2453_341-2452d others(4): Show |
NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 4/13 | chr6 | 155445869 | ||||||
| chr6:155445869
|
CATAT | C | 6 | a0001c0001t0001g0016a0001c0001t0001g0150a0001c0001t0001g0151others(3): Show | 6 | HG02257.hp1 HG02559.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.341-2455_341-2452d others(6): Show |
NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 4/13 | chr6 | 155445869 | ||||||
| chr6:155445869
|
CATATATA others(62): Show |
C | 1 | a0002c0007t0001g0317 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.341-2520_341-2452d others(71): Show |
NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 4/13 | chr6 | 155445869 | ||||||
| chr6:155445874
|
A | ATATATAT others(16): Show |
1 | a0001c0001t0001g0280 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.341-2457_341-2456i others(25): Show |
NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 4/13 | chr6 | 155445874 | ||||||
| chr6:155445874
|
ATATATAT others(19): Show |
A | 1 | a0001c0001t0001g0128 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.341-2482_341-2457d others(28): Show |
NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 4/13 | chr6 | 155445874 | ||||||
| chr6:155445876
|
A | ATATATAT others(15): Show |
2 | a0001c0001t0001g0179a0001c0001t0001g0180 | 2 | HG01891.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.341-2459_341-2458i others(24): Show |
NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 4/13 | chr6 | 155445876 | ||||||
| chr6:155445887
|
CTA | C | 89 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(86): Show | 92 | HG00423.hp2 HG00558.hp1 HG00609.hp1 others(89): Show |
intron_variant | MODIFIER | c.341-2471_341-2470d others(4): Show |
NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 4/13 | chr6 | 155445887 | ||||||
| chr6:155445892
|
T | G | 5 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0042others(2): Show | 5 | HG02486.hp1 HG02818.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.341-2474A>C | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 4/13 | chr6 | 155445892 | ||||||
| chr6:155445897
|
A | T | 1 | a0002c0002t0002g0264 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.341-2479T>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 4/13 | chr6 | 155445897 | ||||||
| chr6:155445898
|
TA | T | 130 | a0001c0001t0001g0057a0001c0001t0001g0060a0001c0001t0001g0063others(127): Show | 133 | HG00438.hp2 HG00558.hp2 HG00621.hp2 others(130): Show |
intron_variant | MODIFIER | c.341-2481delT | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 4/13 | chr6 | 155445898 | ||||||
| chr6:155445903
|
TATATATG others(13): Show |
T | 4 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0042others(1): Show | 4 | HG02818.hp2 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.341-2505_341-2486d others(22): Show |
NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 4/13 | chr6 | 155445903 | ||||||
| chr6:155445919
|
A | G | 1 | a0001c0003t0001g0056 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.341-2501T>C | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 4/13 | chr6 | 155445919 | ||||||
| chr6:155445923
|
A | G | 1 | a0001c0001t0001g0280 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.341-2505T>C | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 4/13 | chr6 | 155445923 | ||||||
| chr6:155445957
|
C | CTATATAT others(17): Show |
1 | a0001c0006t0001g0047 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.341-2540_341-2539i others(26): Show |
NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 4/13 | chr6 | 155445957 | ||||||
| chr6:155445957
|
C | CTATATAT others(19): Show |
10 | a0001c0001t0002g0046a0001c0003t0001g0048a0001c0003t0001g0050others(7): Show | 10 | HG01243.hp1 HG02055.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.341-2540_341-2539i others(28): Show |
NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 4/13 | chr6 | 155445957 | ||||||
| chr6:155445957
|
C | CTATATAT others(21): Show |
1 | a0001c0001t0001g0016 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.341-2540_341-2539i others(30): Show |
NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 4/13 | chr6 | 155445957 | ||||||
| chr6:155445957
|
CTA | C | 3 | a0001c0001t0001g0109a0001c0001t0001g0280a0001c0003t0001g0144 | 3 | HG01109.hp2 NA19078.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.341-2541_341-2540d others(4): Show |
NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 4/13 | chr6 | 155445957 | ||||||
| chr6:155445960
|
TA | T | 4 | a0001c0001t0001g0286a0001c0001t0001g0287a0001c0001t0001g0288others(1): Show | 4 | HG03688.hp1 HG03704.hp2 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.341-2543delT | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 4/13 | chr6 | 155445960 | ||||||
| chr6:155445961
|
ATATATAT others(13): Show |
A | 14 | a0001c0001t0001g0060a0001c0001t0001g0063a0001c0001t0001g0071others(11): Show | 14 | HG01515.hp2 HG01516.hp1 HG01517.hp1 others(11): Show |
intron_variant | MODIFIER | c.341-2563_341-2544d others(22): Show |
NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 4/13 | chr6 | 155445961 | ||||||
| chr6:155445962
|
T | G | 47 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0042others(44): Show | 49 | HG00621.hp2 HG00642.hp1 HG00738.hp1 others(46): Show |
intron_variant | MODIFIER | c.341-2544A>C | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 4/13 | chr6 | 155445962 | ||||||
| chr6:155445969
|
A | AATATATA others(14): Show |
6 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0266others(3): Show | 6 | NA18953.hp1 NA18954.hp1 NA18969.hp2 others(3): Show |
intron_variant | MODIFIER | c.341-2572_341-2552d others(23): Show |
NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 4/13 | chr6 | 155445969 | ||||||
| chr6:155445981
|
C | CTA | 96 | a0001c0001t0001g0017a0001c0001t0001g0023a0001c0001t0001g0024others(93): Show | 100 | HG00423.hp2 HG00558.hp1 HG00609.hp1 others(97): Show |
intron_variant | MODIFIER | c.341-2565_341-2564d others(4): Show |
NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 4/13 | chr6 | 155445981 | ||||||
| chr6:155445981
|
C | CTATA | 122 | a0001c0001t0001g0016a0001c0001t0001g0064a0001c0001t0001g0075others(119): Show | 126 | HG00438.hp2 HG00558.hp2 HG00621.hp2 others(123): Show |
intron_variant | MODIFIER | c.341-2567_341-2564d others(6): Show |
NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 4/13 | chr6 | 155445981 | ||||||
| chr6:155445981
|
C | CTATATA | 12 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0131others(9): Show | 12 | HG00673.hp1 HG02165.hp1 NA18940.hp1 others(9): Show |
intron_variant | MODIFIER | c.341-2569_341-2564d others(8): Show |
NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 4/13 | chr6 | 155445981 | ||||||
| chr6:155445981
|
C | CTATATAT others(21): Show |
1 | a0001c0001t0002g0272 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.341-2564_341-2563i others(30): Show |
NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 4/13 | chr6 | 155445981 | ||||||
| chr6:155445981
|
C | CTATATAT others(21): Show |
1 | a0001c0001t0001g0255 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.341-2564_341-2563i others(30): Show |
NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 4/13 | chr6 | 155445981 | ||||||
| chr6:155445981
|
C | CTATATAT others(23): Show |
5 | a0001c0001t0001g0080a0001c0001t0001g0165a0001c0001t0001g0166others(2): Show | 5 | HG00639.hp2 HG02451.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.341-2564_341-2563i others(32): Show |
NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 4/13 | chr6 | 155445981 | ||||||
| chr6:155445981
|
C | CTATATAT others(25): Show |
1 | a0001c0006t0001g0174 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.341-2564_341-2563i others(34): Show |
NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 4/13 | chr6 | 155445981 | ||||||
| chr6:155445981
|
C | CTATATAT others(21): Show |
2 | a0001c0001t0001g0238a0001c0001t0001g0240 | 2 | HG02257.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.341-2564_341-2563i others(30): Show |
NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 4/13 | chr6 | 155445981 | ||||||
| chr6:155445981
|
C | CTATATAT others(29): Show |
1 | a0001c0001t0001g0108 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.341-2564_341-2563i others(38): Show |
NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 4/13 | chr6 | 155445981 | ||||||
| chr6:155445981
|
C | CTATATAT others(15): Show |
1 | a0010c0018t0001g0275 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.341-2564_341-2563i others(24): Show |
NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 4/13 | chr6 | 155445981 | ||||||
| chr6:155445981
|
C | CTATATAT others(24): Show |
1 | a0001c0003t0001g0144 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.341-2564_341-2563i others(33): Show |
NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 4/13 | chr6 | 155445981 | ||||||
| chr6:155445996
|
T | A | 7 | a0001c0001t0001g0080a0001c0001t0001g0165a0001c0001t0001g0166others(4): Show | 7 | HG00280.hp2 HG00639.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.341-2578A>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 4/13 | chr6 | 155445996 | ||||||
| chr6:155445996
|
T | TAA | 8 | a0001c0001t0001g0229a0001c0001t0001g0230a0001c0001t0001g0232others(5): Show | 8 | HG00642.hp2 HG01168.hp2 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.341-2580_341-2579d others(4): Show |
NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 4/13 | chr6 | 155445996 | ||||||
| chr6:155445996
|
T | TATATAA | 41 | a0001c0001t0001g0018a0001c0001t0001g0028a0001c0001t0001g0082others(38): Show | 41 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(38): Show |
intron_variant | MODIFIER | c.341-2579_341-2578i others(8): Show |
NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 4/13 | chr6 | 155445996 | ||||||
| chr6:155445996
|
T | TATATATA others(1): Show |
5 | a0001c0001t0001g0284a0001c0003t0001g0160a0001c0003t0001g0161others(2): Show | 5 | HG01069.hp2 HG01071.hp2 HG01243.hp2 others(2): Show |
intron_variant | MODIFIER | c.341-2579_341-2578i others(10): Show |
NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 4/13 | chr6 | 155445996 | ||||||
| chr6:155446104
|
C | T | 6 | a0002c0002t0001g0178a0002c0002t0001g0186a0002c0002t0001g0187others(3): Show | 6 | HG00609.hp1 HG03490.hp1 HG03492.hp1 others(3): Show |
intron_variant | MODIFIER | c.341-2686G>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 4/13 | chr6 | 155446104 | ||||||
| chr6:155446146
|
T | G | 13 | a0001c0001t0001g0016a0001c0001t0002g0046a0001c0003t0001g0048others(10): Show | 13 | HG01109.hp2 HG01243.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.341-2728A>C | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 4/13 | chr6 | 155446146 | ||||||
| chr6:155446201
|
C | T | 1 | a0001c0004t0001g0344 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.341-2783G>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 4/13 | chr6 | 155446201 | ||||||
| chr6:155446229
|
G | A | 3 | a0001c0001t0002g0069a0003c0012t0001g0070a0003c0012t0001g0138 | 3 | HG03490.hp2 NA18939.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.341-2811C>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 4/13 | chr6 | 155446229 | ||||||
| chr6:155446372
|
G | A | 1 | a0001c0004t0001g0346 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.341-2954C>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 4/13 | chr6 | 155446372 | ||||||
| chr6:155446408
|
A | T | 1 | a0001c0003t0001g0073 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.341-2990T>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 4/13 | chr6 | 155446408 | ||||||
| chr6:155446428
|
A | C | 1 | a0001c0003t0001g0239 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.341-3010T>G | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 4/13 | chr6 | 155446428 | ||||||
| chr6:155446472
|
C | T | 2 | a0001c0001t0001g0238a0001c0001t0001g0240 | 2 | HG02257.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.341-3054G>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 4/13 | chr6 | 155446472 | ||||||
| chr6:155446752
|
C | T | 1 | a0002c0002t0002g0228 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.341-3334G>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 4/13 | chr6 | 155446752 | ||||||
| chr6:155446876
|
C | A | 1 | a0002c0002t0001g0029 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.341-3458G>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 4/13 | chr6 | 155446876 | ||||||
| chr6:155447048
|
C | CT | 8 | a0001c0001t0001g0145a0001c0001t0002g0004a0001c0001t0002g0146others(5): Show | 9 | HG00639.hp1 HG01099.hp2 HG01106.hp2 others(6): Show |
intron_variant | MODIFIER | c.341-3631dupA | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 4/13 | chr6 | 155447048 | ||||||
| chr6:155447173
|
T | C | 1 | a0001c0001t0002g0019 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.341-3755A>G | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 4/13 | chr6 | 155447173 | ||||||
| chr6:155447180
|
G | T | 88 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(85): Show | 91 | HG00423.hp2 HG00558.hp1 HG00609.hp1 others(88): Show |
intron_variant | MODIFIER | c.341-3762C>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 4/13 | chr6 | 155447180 | ||||||
| chr6:155447192
|
A | G | 324 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(321): Show | 332 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(329): Show |
intron_variant | MODIFIER | c.341-3774T>C | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 4/13 | chr6 | 155447192 | ||||||
| chr6:155447205
|
C | A | 3 | a0001c0001t0001g0145a0001c0001t0002g0004a0001c0001t0002g0146 | 4 | HG02258.hp1 HG02922.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.341-3787G>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 4/13 | chr6 | 155447205 | ||||||
| chr6:155447283
|
C | T | 1 | a0001c0003t0002g0147 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.341-3865G>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 4/13 | chr6 | 155447283 | ||||||
| chr6:155447317
|
G | A | 1 | a0001c0006t0002g0059 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.341-3899C>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 4/13 | chr6 | 155447317 | ||||||
| chr6:155447341
|
A | G | 1 | a0001c0001t0002g0231 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.341-3923T>C | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 4/13 | chr6 | 155447341 | ||||||
| chr6:155447350
|
C | T | 1 | a0001c0003t0001g0142 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.341-3932G>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 4/13 | chr6 | 155447350 | ||||||
| chr6:155447397
|
T | G | 1 | a0001c0001t0001g0106 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.341-3979A>C | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 4/13 | chr6 | 155447397 | ||||||
| chr6:155447499
|
G | A | 2 | a0001c0001t0002g0272a0001c0005t0002g0036 | 2 | HG00280.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.341-4081C>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 4/13 | chr6 | 155447499 | ||||||
| chr6:155447612
|
C | T | 1 | a0001c0003t0001g0073 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.341-4194G>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 4/13 | chr6 | 155447612 | ||||||
| chr6:155447986
|
G | T | 1 | a0001c0003t0001g0045 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.341-4568C>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 4/13 | chr6 | 155447986 | ||||||
| chr6:155447996
|
G | C | 3 | a0001c0001t0001g0145a0001c0001t0002g0004a0001c0001t0002g0146 | 4 | HG02258.hp1 HG02922.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.341-4578C>G | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 4/13 | chr6 | 155447996 | ||||||
| chr6:155448183
|
A | T | 2 | a0002c0002t0001g0020a0002c0002t0001g0021 | 2 | HG02723.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.341-4765T>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 4/13 | chr6 | 155448183 | ||||||
| chr6:155448201
|
C | G | 1 | a0001c0003t0001g0037 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.341-4783G>C | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 4/13 | chr6 | 155448201 | ||||||
| chr6:155448250
|
C | T | 1 | a0001c0001t0001g0044 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.341-4832G>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 4/13 | chr6 | 155448250 | ||||||
| chr6:155448255
|
A | G | 65 | a0001c0001t0001g0018a0001c0001t0001g0028a0001c0001t0001g0044others(62): Show | 65 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(62): Show |
intron_variant | MODIFIER | c.341-4837T>C | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 4/13 | chr6 | 155448255 | ||||||
| chr6:155448298
|
G | A | 1 | a0001c0001t0001g0089 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.341-4880C>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 4/13 | chr6 | 155448298 | ||||||
| chr6:155448404
|
C | G | 8 | a0001c0001t0001g0017a0001c0001t0001g0089a0001c0001t0001g0179others(5): Show | 9 | HG01891.hp1 HG02572.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.341-4986G>C | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 4/13 | chr6 | 155448404 | ||||||
| chr6:155448444
|
G | A | 1 | a0008c0019t0001g0033 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.340+4960C>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 4/13 | chr6 | 155448444 | ||||||
| chr6:155448494
|
G | C | 1 | a0001c0001t0001g0280 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.340+4910C>G | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 4/13 | chr6 | 155448494 | ||||||
| chr6:155448580
|
G | A | 1 | a0001c0003t0001g0045 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.340+4824C>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 4/13 | chr6 | 155448580 | ||||||
| chr6:155448641
|
C | CA | 76 | a0001c0001t0001g0018a0001c0001t0001g0028a0001c0001t0001g0042others(73): Show | 76 | HG00280.hp1 HG00280.hp2 HG00642.hp2 others(73): Show |
intron_variant | MODIFIER | c.340+4762dupT | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 4/13 | chr6 | 155448641 | ||||||
| chr6:155448641
|
C | CAA | 7 | a0001c0001t0001g0083a0001c0001t0001g0175a0001c0001t0002g0289others(4): Show | 7 | HG00423.hp1 HG00639.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.340+4761_340+4762d others(4): Show |
NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 4/13 | chr6 | 155448641 | ||||||
| chr6:155448641
|
CA | C | 81 | a0001c0001t0001g0075a0001c0001t0001g0081a0001c0001t0001g0089others(78): Show | 84 | HG00438.hp2 HG00558.hp2 HG00673.hp1 others(81): Show |
intron_variant | MODIFIER | c.340+4762delT | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 4/13 | chr6 | 155448641 | ||||||
| chr6:155448641
|
CAA | C | 14 | a0001c0001t0001g0016a0001c0001t0001g0268a0001c0001t0002g0046others(11): Show | 14 | HG01243.hp1 HG02055.hp2 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.340+4761_340+4762d others(4): Show |
NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 4/13 | chr6 | 155448641 | ||||||
| chr6:155448662
|
T | A | 1 | a0008c0019t0001g0033 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.340+4742A>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 4/13 | chr6 | 155448662 | ||||||
| chr6:155448839
|
C | T | 5 | a0001c0001t0001g0145a0001c0001t0002g0004a0001c0001t0002g0146others(2): Show | 6 | HG02145.hp1 HG02258.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.340+4565G>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 4/13 | chr6 | 155448839 | ||||||
| chr6:155448889
|
C | T | 1 | a0001c0003t0001g0160 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.340+4515G>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 4/13 | chr6 | 155448889 | ||||||
| chr6:155448978
|
G | T | 90 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(87): Show | 93 | HG00423.hp2 HG00558.hp1 HG00609.hp1 others(90): Show |
intron_variant | MODIFIER | c.340+4426C>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 4/13 | chr6 | 155448978 | ||||||
| chr6:155449059
|
G | A | 44 | a0001c0001t0001g0075a0001c0001t0001g0081a0001c0001t0001g0108others(41): Show | 44 | HG00438.hp2 HG00558.hp2 HG00673.hp1 others(41): Show |
intron_variant | MODIFIER | c.340+4345C>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 4/13 | chr6 | 155449059 | ||||||
| chr6:155449108
|
T | G | 1 | a0002c0002t0002g0158 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.340+4296A>C | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 4/13 | chr6 | 155449108 | ||||||
| chr6:155449215
|
T | C | 1 | a0001c0001t0001g0017 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.340+4189A>G | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 4/13 | chr6 | 155449215 | ||||||
| chr6:155449259
|
T | C | 1 | a0001c0001t0001g0057 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.340+4145A>G | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 4/13 | chr6 | 155449259 | ||||||
| chr6:155449298
|
T | C | 115 | a0001c0001t0001g0057a0001c0001t0001g0064a0001c0001t0001g0075others(112): Show | 118 | HG00438.hp2 HG00558.hp2 HG00621.hp2 others(115): Show |
intron_variant | MODIFIER | c.340+4106A>G | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 4/13 | chr6 | 155449298 | ||||||
| chr6:155449308
|
A | G | 1 | a0001c0003t0001g0236 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.340+4096T>C | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 4/13 | chr6 | 155449308 | ||||||
| chr6:155449649
|
G | C | 1 | a0001c0001t0001g0173 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.340+3755C>G | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 4/13 | chr6 | 155449649 | ||||||
| chr6:155449768
|
C | T | 1 | a0002c0002t0001g0185 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.340+3636G>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 4/13 | chr6 | 155449768 | ||||||
| chr6:155449852
|
C | T | 1 | a0001c0001t0001g0280 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.340+3552G>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 4/13 | chr6 | 155449852 | ||||||
| chr6:155449874
|
C | T | 119 | a0001c0001t0001g0018a0001c0001t0001g0028a0001c0001t0001g0082others(116): Show | 122 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(119): Show |
intron_variant | MODIFIER | c.340+3530G>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 4/13 | chr6 | 155449874 | ||||||
| chr6:155449924
|
A | G | 1 | a0001c0001t0001g0292 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.340+3480T>C | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 4/13 | chr6 | 155449924 | ||||||
| chr6:155449976
|
G | A | 1 | a0001c0001t0001g0016 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.340+3428C>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 4/13 | chr6 | 155449976 | ||||||
| chr6:155450008
|
G | T | 26 | a0001c0001t0001g0018a0001c0001t0001g0028a0001c0001t0001g0082others(23): Show | 26 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(23): Show |
intron_variant | MODIFIER | c.340+3396C>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 4/13 | chr6 | 155450008 | ||||||
| chr6:155450095
|
G | A | 4 | a0001c0001t0001g0145a0001c0001t0001g0153a0001c0001t0002g0004others(1): Show | 5 | HG02258.hp1 HG02717.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.340+3309C>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 4/13 | chr6 | 155450095 | ||||||
| chr6:155450116
|
G | C | 41 | a0001c0001t0001g0060a0001c0001t0001g0063a0001c0001t0001g0071others(38): Show | 42 | HG00738.hp2 HG00741.hp2 HG01069.hp2 others(39): Show |
intron_variant | MODIFIER | c.340+3288C>G | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 4/13 | chr6 | 155450116 | ||||||
| chr6:155450179
|
C | T | 1 | a0001c0001t0001g0081 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.340+3225G>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 4/13 | chr6 | 155450179 | ||||||
| chr6:155450240
|
G | T | 1 | a0001c0001t0001g0285 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.340+3164C>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 4/13 | chr6 | 155450240 | ||||||
| chr6:155450389
|
G | A | 1 | a0001c0003t0001g0263 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.340+3015C>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 4/13 | chr6 | 155450389 | ||||||
| chr6:155450463
|
C | T | 19 | a0001c0001t0001g0057a0001c0001t0001g0060a0001c0001t0001g0063others(16): Show | 19 | HG00738.hp2 HG01069.hp2 HG01071.hp2 others(16): Show |
intron_variant | MODIFIER | c.340+2941G>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 4/13 | chr6 | 155450463 | ||||||
| chr6:155450504
|
G | A | 1 | a0002c0002t0002g0264 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.340+2900C>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 4/13 | chr6 | 155450504 | ||||||
| chr6:155450795
|
A | G | 234 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(231): Show | 239 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(236): Show |
intron_variant | MODIFIER | c.340+2609T>C | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 4/13 | chr6 | 155450795 | ||||||
| chr6:155450905
|
G | A | 71 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0023others(68): Show | 73 | HG00280.hp1 HG00438.hp1 HG01069.hp2 others(70): Show |
intron_variant | MODIFIER | c.340+2499C>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 4/13 | chr6 | 155450905 | ||||||
| chr6:155450982
|
A | T | 1 | a0001c0004t0004g0014 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.340+2422T>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 4/13 | chr6 | 155450982 | ||||||
| chr6:155450983
|
T | A | 50 | a0001c0001t0001g0280a0001c0001t0001g0281a0001c0001t0001g0282others(47): Show | 53 | HG00621.hp2 HG00642.hp1 HG01081.hp1 others(50): Show |
intron_variant | MODIFIER | c.340+2421A>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 4/13 | chr6 | 155450983 | ||||||
| chr6:155450984
|
T | A | 4 | a0001c0001t0001g0280a0001c0001t0001g0281a0001c0001t0001g0282others(1): Show | 4 | HG02145.hp2 HG02886.hp1 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.340+2420A>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 4/13 | chr6 | 155450984 | ||||||
| chr6:155451139
|
T | C | 156 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0023others(153): Show | 158 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(155): Show |
intron_variant | MODIFIER | c.340+2265A>G | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 4/13 | chr6 | 155451139 | ||||||
| chr6:155451231
|
G | A | 1 | a0001c0001t0001g0268 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.340+2173C>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 4/13 | chr6 | 155451231 | ||||||
| chr6:155451248
|
G | C | 10 | a0001c0001t0001g0165a0001c0001t0001g0166a0001c0001t0001g0167others(7): Show | 10 | HG01069.hp2 HG01071.hp2 HG01243.hp2 others(7): Show |
intron_variant | MODIFIER | c.340+2156C>G | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 4/13 | chr6 | 155451248 | ||||||
| chr6:155451259
|
G | A | 1 | a0001c0001t0002g0143 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.340+2145C>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 4/13 | chr6 | 155451259 | ||||||
| chr6:155451270
|
C | T | 58 | a0001c0001t0001g0071a0001c0001t0002g0069a0001c0003t0001g0067others(55): Show | 62 | HG00621.hp2 HG00642.hp1 HG01081.hp1 others(59): Show |
intron_variant | MODIFIER | c.340+2134G>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 4/13 | chr6 | 155451270 | ||||||
| chr6:155451271
|
G | A | 1 | a0001c0001t0001g0044 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.340+2133C>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 4/13 | chr6 | 155451271 | ||||||
| chr6:155451274
|
C | T | 49 | a0001c0001t0001g0054a0001c0001t0001g0057a0001c0001t0001g0060others(46): Show | 49 | HG00280.hp1 HG00438.hp1 HG01069.hp2 others(46): Show |
intron_variant | MODIFIER | c.340+2130G>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 4/13 | chr6 | 155451274 | ||||||
| chr6:155451282
|
A | G | 1 | a0001c0001t0001g0284 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.340+2122T>C | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 4/13 | chr6 | 155451282 | ||||||
| chr6:155451310
|
A | C | 1 | a0001c0003t0001g0159 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.340+2094T>G | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 4/13 | chr6 | 155451310 | ||||||
| chr6:155451496
|
C | T | 5 | a0001c0001t0001g0145a0001c0001t0002g0004a0001c0001t0002g0146others(2): Show | 6 | HG01109.hp2 HG02258.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.340+1908G>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 4/13 | chr6 | 155451496 | ||||||
| chr6:155451498
|
T | C | 2 | a0002c0002t0001g0269a0002c0002t0001g0270 | 2 | NA19011.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.340+1906A>G | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 4/13 | chr6 | 155451498 | ||||||
| chr6:155451533
|
C | T | 61 | a0001c0001t0001g0016a0001c0001t0002g0046a0001c0003t0001g0048others(58): Show | 65 | HG00621.hp2 HG00642.hp1 HG01081.hp1 others(62): Show |
intron_variant | MODIFIER | c.340+1871G>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 4/13 | chr6 | 155451533 | ||||||
| chr6:155451780
|
A | C | 1 | a0002c0002t0002g0158 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.340+1624T>G | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 4/13 | chr6 | 155451780 | ||||||
| chr6:155451838
|
G | A | 1 | a0001c0004t0001g0346 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.340+1566C>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 4/13 | chr6 | 155451838 | ||||||
| chr6:155451847
|
C | T | 66 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(63): Show | 66 | HG00280.hp1 HG00438.hp1 HG01070.hp2 others(63): Show |
intron_variant | MODIFIER | c.340+1557G>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 4/13 | chr6 | 155451847 | ||||||
| chr6:155451891
|
G | C | 5 | a0001c0001t0001g0016a0001c0001t0001g0276a0001c0003t0001g0277others(2): Show | 5 | HG02055.hp2 HG02976.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.340+1513C>G | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 4/13 | chr6 | 155451891 | ||||||
| chr6:155451921
|
C | T | 3 | a0001c0001t0001g0280a0001c0001t0001g0281a0001c0001t0001g0282 | 3 | HG02145.hp2 HG02886.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.340+1483G>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 4/13 | chr6 | 155451921 | ||||||
| chr6:155451923
|
C | T | 3 | a0001c0004t0003g0015a0001c0004t0004g0014a0001c0005t0003g0003 | 4 | HG02145.hp1 HG03098.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.340+1481G>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 4/13 | chr6 | 155451923 | ||||||
| chr6:155451992
|
C | T | 3 | a0001c0004t0004g0011a0002c0009t0003g0012a0002c0009t0003g0013 | 3 | HG01243.hp1 HG02622.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.340+1412G>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 4/13 | chr6 | 155451992 | ||||||
| chr6:155452033
|
G | A | 53 | a0001c0004t0001g0002a0001c0004t0001g0010a0001c0004t0001g0309others(50): Show | 57 | HG00621.hp2 HG00642.hp1 HG01081.hp1 others(54): Show |
intron_variant | MODIFIER | c.340+1371C>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 4/13 | chr6 | 155452033 | ||||||
| chr6:155452201
|
G | A | 5 | a0001c0001t0001g0280a0001c0001t0001g0281a0001c0001t0001g0282others(2): Show | 5 | HG01884.hp1 HG02145.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.340+1203C>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 4/13 | chr6 | 155452201 | ||||||
| chr6:155452220
|
T | A | 1 | a0001c0001t0001g0028 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.340+1184A>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 4/13 | chr6 | 155452220 | ||||||
| chr6:155452270
|
C | T | 1 | a0001c0001t0001g0283 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.340+1134G>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 4/13 | chr6 | 155452270 | ||||||
| chr6:155452312
|
G | A | 2 | a0001c0001t0001g0281a0001c0001t0001g0282 | 2 | HG02145.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.340+1092C>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 4/13 | chr6 | 155452312 | ||||||
| chr6:155452383
|
C | T | 5 | a0001c0001t0001g0280a0001c0001t0001g0281a0001c0001t0001g0282others(2): Show | 5 | HG01884.hp1 HG02145.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.340+1021G>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 4/13 | chr6 | 155452383 | ||||||
| chr6:155452384
|
T | A | 2 | a0001c0001t0001g0042a0001c0001t0001g0043 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.340+1020A>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 4/13 | chr6 | 155452384 | ||||||
| chr6:155452432
|
C | T | 1 | a0001c0014t0002g0035 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.340+972G>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 4/13 | chr6 | 155452432 | ||||||
| chr6:155452498
|
T | C | 5 | a0001c0001t0001g0280a0001c0001t0001g0281a0001c0001t0001g0282others(2): Show | 5 | HG01884.hp1 HG02145.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.340+906A>G | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 4/13 | chr6 | 155452498 | ||||||
| chr6:155452507
|
G | A | 58 | a0001c0001t0001g0280a0001c0001t0001g0281a0001c0001t0001g0282others(55): Show | 62 | HG00621.hp2 HG00642.hp1 HG01081.hp1 others(59): Show |
intron_variant | MODIFIER | c.340+897C>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 4/13 | chr6 | 155452507 | ||||||
| chr6:155452522
|
T | C | 1 | a0002c0002t0002g0271 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.340+882A>G | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 4/13 | chr6 | 155452522 | ||||||
| chr6:155452544
|
C | A | 5 | a0001c0001t0001g0280a0001c0001t0001g0281a0001c0001t0001g0282others(2): Show | 5 | HG01884.hp1 HG02145.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.340+860G>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 4/13 | chr6 | 155452544 | ||||||
| chr6:155452576
|
C | T | 1 | a0002c0002t0001g0157 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.340+828G>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 4/13 | chr6 | 155452576 | ||||||
| chr6:155452625
|
T | C | 3 | a0001c0001t0001g0030a0001c0001t0001g0031a0002c0002t0001g0029 | 3 | HG02818.hp2 HG02976.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.340+779A>G | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 4/13 | chr6 | 155452625 | ||||||
| chr6:155452638
|
C | CT | 185 | a0001c0001t0001g0016a0001c0001t0001g0044a0001c0001t0001g0054others(182): Show | 189 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(186): Show |
intron_variant | MODIFIER | c.340+765dupA | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 4/13 | chr6 | 155452638 | ||||||
| chr6:155452672
|
T | C | 1 | a0008c0019t0001g0033 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.340+732A>G | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 4/13 | chr6 | 155452672 | ||||||
| chr6:155452818
|
C | A | 1 | a0001c0001t0001g0044 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.340+586G>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 4/13 | chr6 | 155452818 | ||||||
| chr6:155452910
|
C | G | 1 | a0001c0001t0001g0017 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.340+494G>C | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 4/13 | chr6 | 155452910 | ||||||
| chr6:155452995
|
C | G | 1 | a0002c0002t0002g0053 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.340+409G>C | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 4/13 | chr6 | 155452995 | ||||||
| chr6:155453112
|
T | C | 1 | a0001c0001t0002g0272 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.340+292A>G | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 4/13 | chr6 | 155453112 | ||||||
| chr6:155453126
|
G | T | 1 | a0002c0002t0002g0053 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.340+278C>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 4/13 | chr6 | 155453126 | ||||||
| chr6:155453166
|
C | A | 1 | a0001c0001t0001g0273 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.340+238G>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 4/13 | chr6 | 155453166 | ||||||
| chr6:155453167
|
G | A | 2 | a0001c0006t0001g0154a0001c0006t0001g0155 | 2 | HG01884.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.340+237C>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 4/13 | chr6 | 155453167 | ||||||
| chr6:155453200
|
A | G | 15 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0044others(12): Show | 15 | HG01891.hp2 HG02258.hp2 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.340+204T>C | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 4/13 | chr6 | 155453200 | ||||||
| chr6:155453212
|
G | T | 7 | a0001c0001t0002g0046a0001c0003t0001g0048a0001c0003t0001g0050others(4): Show | 7 | HG02258.hp2 HG02559.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.340+192C>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 4/13 | chr6 | 155453212 | ||||||
| chr6:155453214
|
AG | A | 5 | a0001c0001t0001g0280a0001c0001t0001g0281a0001c0001t0001g0282others(2): Show | 5 | HG01884.hp1 HG02145.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.340+189delC | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 4/13 | chr6 | 155453214 | ||||||
| chr6:155453639
|
G | C | 1 | a0002c0002t0001g0034 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.256-151C>G | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 3/13 | chr6 | 155453639 | ||||||
| chr6:155453672
|
C | T | 7 | a0001c0001t0002g0046a0001c0003t0001g0048a0001c0003t0001g0050others(4): Show | 7 | HG02258.hp2 HG02559.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.256-184G>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 3/13 | chr6 | 155453672 | ||||||
| chr6:155453691
|
T | A | 1 | a0001c0001t0002g0032 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.256-203A>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 3/13 | chr6 | 155453691 | ||||||
| chr6:155453824
|
A | C | 225 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(222): Show | 231 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(228): Show |
intron_variant | MODIFIER | c.256-336T>G | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 3/13 | chr6 | 155453824 | ||||||
| chr6:155453859
|
T | G | 1 | a0010c0018t0001g0275 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.256-371A>C | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 3/13 | chr6 | 155453859 | ||||||
| chr6:155453865
|
T | C | 5 | a0001c0001t0001g0016a0001c0001t0001g0276a0001c0003t0001g0277others(2): Show | 5 | HG02055.hp2 HG02976.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.256-377A>G | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 3/13 | chr6 | 155453865 | ||||||
| chr6:155453911
|
G | A | 3 | a0001c0001t0001g0280a0001c0001t0001g0281a0001c0001t0001g0282 | 3 | HG02145.hp2 HG02886.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.256-423C>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 3/13 | chr6 | 155453911 | ||||||
| chr6:155453932
|
T | A | 1 | a0001c0004t0002g0349 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.256-444A>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 3/13 | chr6 | 155453932 | ||||||
| chr6:155454034
|
A | G | 2 | a0001c0005t0002g0036a0001c0014t0002g0035 | 2 | HG04184.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.256-546T>C | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 3/13 | chr6 | 155454034 | ||||||
| chr6:155454149
|
C | T | 1 | a0001c0003t0001g0045 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.256-661G>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 3/13 | chr6 | 155454149 | ||||||
| chr6:155454165
|
C | A | 1 | a0001c0005t0001g0350 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.255+646G>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 3/13 | chr6 | 155454165 | ||||||
| chr6:155454334
|
A | C | 8 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0044others(5): Show | 8 | HG01891.hp2 HG02280.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.255+477T>G | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 3/13 | chr6 | 155454334 | ||||||
| chr6:155454472
|
G | T | 53 | a0001c0004t0001g0002a0001c0004t0001g0010a0001c0004t0001g0309others(50): Show | 57 | HG00621.hp2 HG00642.hp1 HG01081.hp1 others(54): Show |
intron_variant | MODIFIER | c.255+339C>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 3/13 | chr6 | 155454472 | ||||||
| chr6:155454554
|
A | T | 5 | a0001c0003t0001g0037a0001c0003t0001g0039a0001c0003t0001g0040others(2): Show | 5 | HG01891.hp2 HG02280.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.255+257T>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 3/13 | chr6 | 155454554 | ||||||
| chr6:155454743
|
T | C | 16 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0023others(13): Show | 16 | HG01257.hp1 HG01433.hp1 HG02056.hp1 others(13): Show |
intron_variant | MODIFIER | c.255+68A>G | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 3/13 | chr6 | 155454743 | ||||||
| chr6:155455152
|
C | T | 1 | a0002c0002t0001g0034 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.49-23G>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 1/13 | chr6 | 155455152 | ||||||
| chr6:155455255
|
C | G | 1 | a0008c0019t0001g0033 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.49-126G>C | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 1/13 | chr6 | 155455255 | ||||||
| chr6:155455352
|
A | G | 16 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0023others(13): Show | 16 | HG01257.hp1 HG01433.hp1 HG02056.hp1 others(13): Show |
intron_variant | MODIFIER | c.49-223T>C | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 1/13 | chr6 | 155455352 | ||||||
| chr6:155455438
|
C | T | 1 | a0001c0001t0001g0016 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.49-309G>A | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 1/13 | chr6 | 155455438 | ||||||
| chr6:155455580
|
G | A | 25 | a0001c0001t0001g0283a0001c0001t0001g0284a0001c0001t0001g0285others(22): Show | 25 | HG00280.hp1 HG00438.hp1 HG01070.hp2 others(22): Show |
intron_variant | MODIFIER | c.48+173C>T | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 1/13 | chr6 | 155455580 | ||||||
| chr6:155455720
|
T | G | 45 | a0001c0004t0001g0002a0001c0004t0001g0010a0001c0004t0001g0309others(42): Show | 48 | HG00621.hp2 HG00642.hp1 HG01081.hp1 others(45): Show |
intron_variant | MODIFIER | c.48+33A>C | NOX3 | ENSG00000074771.4 | transcript | ENST00000159060.3 | protein_coding | 1/13 | chr6 | 155455720 |