| geneid | 50507 |
|---|---|
| ensemblid | ENSG00000086991.13 |
| hgncid | 7891 |
| symbol | NOX4 |
| name | NADPH oxidase 4 |
| refseq_nuc | NM_016931.5 |
| refseq_prot | NP_058627.2 |
| ensembl_nuc | ENST00000263317.9 |
| ensembl_prot | ENSP00000263317.4 |
| mane_status | MANE Select |
| chr | chr11 |
| start | 89324353 |
| end | 89491375 |
| strand | - |
| ver | v1.2 |
| region | chr11:89324353-89491375 |
| region5000 | chr11:89319353-89496375 |
| regionname0 | NOX4_chr11_89324353_89491375 |
| regionname5000 | NOX4_chr11_89319353_89496375 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 578 | 281 | 77 | 52 | 114 | 16 | 21 | 86 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| a0002 | 0/0 | 578 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| a0003 | 0/0 | 578 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| a0004 | 0/0 | 578 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| a0005 | 0/0 | 578 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| a0006 | 0/0 | 578 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| a0007 | 1/0 | 578 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/1 | 1737 | 192 | 54 | 39 | 72 | 11 | 15 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| c0002 | 0/0 | 1737 | 51 | 21 | 3 | 27 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| c0003 | 0/0 | 1737 | 32 | 0 | 10 | 12 | 5 | 5 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| c0004 | 0/0 | 1737 | 2 | 2 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| c0005 | 0/0 | 1737 | 2 | 0 | 0 | 1 | 0 | 1 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| c0006 | 0/0 | 1737 | 2 | 0 | 0 | 2 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| c0007 | 0/0 | 1737 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| c0008 | 0/0 | 1737 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| c0009 | 0/0 | 1737 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| c0010 | 0/0 | 1737 | 1 | 0 | 0 | 0 | 0 | 1 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| c0011 | 1/0 | 1737 | 1 | 0 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| c0012 | 0/0 | 1737 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| c0013 | 0/0 | 1737 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/1 | 2533 | 40 | 5 | 11 | 18 | 1 | 4 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| t0002 | 0/0 | 2533 | 25 | 9 | 6 | 8 | 0 | 2 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| t0003 | 1/0 | 2533 | 13 | 0 | 5 | 6 | 1 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| t0004 | 0/0 | 2534 | 10 | 0 | 4 | 3 | 2 | 1 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| t0005 | 0/0 | 2533 | 9 | 3 | 2 | 3 | 1 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| t0006 | 0/0 | 2540 | 8 | 1 | 1 | 6 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| t0007 | 0/0 | 2534 | 6 | 0 | 1 | 4 | 0 | 1 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| t0008 | 0/0 | 2533 | 6 | 0 | 2 | 2 | 0 | 2 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| t0009 | 0/0 | 2542 | 6 | 3 | 0 | 3 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| t0010 | 0/0 | 2524 | 5 | 0 | 2 | 0 | 2 | 1 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| t0011 | 0/0 | 2542 | 5 | 4 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| t0012 | 0/0 | 2528 | 5 | 1 | 1 | 3 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| t0013 | 0/0 | 2533 | 4 | 0 | 1 | 2 | 1 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| t0014 | 0/0 | 2531 | 4 | 0 | 0 | 3 | 0 | 1 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| t0015 | 0/0 | 2533 | 4 | 0 | 0 | 4 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| t0016 | 0/0 | 2528 | 4 | 0 | 0 | 2 | 1 | 1 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| t0017 | 0/0 | 2527 | 4 | 3 | 1 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| t0018 | 0/0 | 2528 | 4 | 2 | 1 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| t0019 | 0/0 | 2533 | 4 | 1 | 0 | 3 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| t0020 | 0/0 | 2527 | 3 | 0 | 1 | 1 | 0 | 1 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| t0021 | 0/0 | 2533 | 3 | 0 | 0 | 3 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| t0022 | 0/0 | 2535 | 3 | 1 | 1 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| t0023 | 0/0 | 2534 | 3 | 2 | 1 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| t0024 | 0/0 | 2535 | 3 | 1 | 0 | 2 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| t0025 | 0/0 | 2541 | 2 | 0 | 0 | 2 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| t0026 | 0/0 | 2541 | 2 | 2 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| t0027 | 0/0 | 2535 | 2 | 0 | 0 | 2 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| t0028 | 0/0 | 2524 | 2 | 0 | 0 | 0 | 1 | 1 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| t0029 | 0/0 | 2540 | 2 | 1 | 1 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| t0030 | 0/0 | 2540 | 2 | 2 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| t0031 | 0/0 | 2520 | 2 | 2 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| t0032 | 0/0 | 2527 | 2 | 2 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| t0033 | 0/0 | 2540 | 2 | 2 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| t0034 | 0/0 | 2541 | 2 | 1 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| t0035 | 0/0 | 2540 | 2 | 0 | 0 | 2 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| t0036 | 0/0 | 2543 | 2 | 0 | 0 | 2 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| t0037 | 0/0 | 2531 | 2 | 1 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| t0038 | 0/0 | 2526 | 2 | 0 | 0 | 1 | 0 | 1 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| t0039 | 0/0 | 2528 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| t0040 | 0/0 | 2539 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| t0041 | 0/0 | 2549 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| t0042 | 0/0 | 2543 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| t0043 | 0/0 | 2542 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| t0044 | 0/0 | 2545 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| t0045 | 0/0 | 2544 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| t0046 | 0/0 | 2543 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| t0047 | 0/0 | 2534 | 1 | 0 | 0 | 0 | 0 | 1 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| t0048 | 0/0 | 2535 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| t0049 | 0/0 | 2529 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| t0050 | 0/0 | 2533 | 1 | 0 | 0 | 0 | 0 | 1 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| t0051 | 0/0 | 2531 | 1 | 0 | 1 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| t0052 | 0/0 | 2527 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| t0053 | 0/0 | 2533 | 1 | 0 | 0 | 0 | 1 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| t0054 | 0/0 | 2533 | 1 | 0 | 0 | 0 | 0 | 1 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| t0055 | 0/0 | 2534 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| t0056 | 0/0 | 2533 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| t0057 | 0/0 | 2539 | 1 | 0 | 0 | 0 | 1 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| t0058 | 0/0 | 2533 | 1 | 0 | 1 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| t0059 | 0/0 | 2535 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| t0060 | 0/0 | 2522 | 1 | 0 | 0 | 0 | 0 | 1 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| t0061 | 0/0 | 2526 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| t0062 | 0/0 | 2525 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| t0063 | 0/0 | 2531 | 1 | 0 | 1 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| t0064 | 0/0 | 2531 | 1 | 0 | 0 | 0 | 1 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| t0065 | 0/0 | 2531 | 1 | 0 | 0 | 0 | 1 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| t0066 | 0/0 | 2527 | 1 | 0 | 1 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| t0067 | 0/0 | 2535 | 1 | 0 | 1 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| t0068 | 0/0 | 2536 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| t0069 | 0/0 | 2535 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| t0070 | 0/0 | 2528 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| t0071 | 0/0 | 2522 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| t0072 | 0/0 | 2525 | 1 | 0 | 0 | 0 | 1 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| t0073 | 0/0 | 2534 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| t0074 | 0/0 | 2538 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| t0075 | 0/0 | 2545 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| t0076 | 0/0 | 2543 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| t0077 | 0/0 | 2531 | 1 | 0 | 0 | 0 | 0 | 1 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| t0078 | 0/0 | 2533 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| t0079 | 0/0 | 2535 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| t0080 | 0/0 | 2533 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| t0081 | 0/0 | 2534 | 1 | 0 | 1 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| t0082 | 0/0 | 2529 | 1 | 0 | 1 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| t0083 | 0/0 | 2536 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| t0084 | 0/0 | 2525 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| t0085 | 0/0 | 2538 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| t0086 | 0/0 | 2514 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| t0087 | 0/0 | 2525 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| t0088 | 0/0 | 2531 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| t0089 | 0/0 | 2540 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| t0090 | 0/0 | 2540 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| t0091 | 0/0 | 2531 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| t0092 | 0/0 | 2528 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| t0093 | 0/0 | 2543 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| t0094 | 0/0 | 2527 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| t0095 | 0/0 | 2531 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| t0096 | 0/0 | 2528 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| t0097 | 0/0 | 2530 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| t0098 | 0/0 | 2539 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| t0099 | 0/0 | 2546 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| t0100 | 0/0 | 2545 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| t0101 | 0/0 | 2543 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| t0102 | 0/0 | 2545 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| t0103 | 0/0 | 2534 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| t0104 | 0/0 | 2536 | 1 | 0 | 0 | 0 | 0 | 1 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| t0105 | 0/0 | 2529 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| t0106 | 0/0 | 2532 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| t0107 | 0/0 | 2527 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| t0108 | 0/0 | 2534 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| t0109 | 0/0 | 2534 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| t0110 | 0/0 | 2534 | 1 | 0 | 1 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| t0111 | 0/0 | 2525 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| t0112 | 0/0 | 2514 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| t0113 | 0/0 | 2542 | 1 | 0 | 1 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| t0114 | 0/0 | 2524 | 1 | 0 | 1 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| t0115 | 0/0 | 2533 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| t0116 | 0/0 | 2534 | 1 | 0 | 0 | 0 | 1 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| t0117 | 0/0 | 2528 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0128 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0184 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0185 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0271 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 1737 | 192 | 54 | 39 | 72 | 11 | 15 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| a0001c0002 | 0/0 | 1737 | 51 | 21 | 3 | 27 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| a0001c0003 | 0/0 | 1737 | 32 | 0 | 10 | 12 | 5 | 5 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| a0001c0005 | 0/0 | 1737 | 2 | 0 | 0 | 1 | 0 | 1 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| a0001c0006 | 0/0 | 1737 | 2 | 0 | 0 | 2 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| a0001c0008 | 0/0 | 1737 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| a0001c0012 | 0/0 | 1737 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| a0002c0004 | 0/0 | 1737 | 2 | 2 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| a0003c0013 | 0/0 | 1737 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| a0004c0007 | 0/0 | 1737 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| a0005c0009 | 0/0 | 1737 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| a0006c0010 | 0/0 | 1737 | 1 | 0 | 0 | 0 | 0 | 1 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| a0007c0011 | 1/0 | 1737 | 1 | 0 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 4269 | 39 | 5 | 11 | 18 | 1 | 3 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| a0001c0001t0002 | 0/0 | 4269 | 23 | 7 | 6 | 8 | 0 | 2 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| a0001c0001t0003 | 0/0 | 4269 | 8 | 0 | 3 | 5 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| a0001c0001t0004 | 0/0 | 4270 | 3 | 0 | 0 | 3 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| a0001c0001t0005 | 0/0 | 4269 | 3 | 3 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| a0001c0001t0007 | 0/0 | 4270 | 5 | 0 | 1 | 4 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| a0001c0001t0008 | 0/0 | 4269 | 6 | 0 | 2 | 2 | 0 | 2 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| a0001c0001t0010 | 0/0 | 4260 | 5 | 0 | 2 | 0 | 2 | 1 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| a0001c0001t0012 | 0/0 | 4264 | 5 | 1 | 1 | 3 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| a0001c0001t0013 | 0/0 | 4269 | 1 | 0 | 1 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| a0001c0001t0014 | 0/0 | 4267 | 4 | 0 | 0 | 3 | 0 | 1 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| a0001c0001t0015 | 0/0 | 4269 | 3 | 0 | 0 | 3 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| a0001c0001t0016 | 0/0 | 4264 | 3 | 0 | 0 | 2 | 1 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| a0001c0001t0017 | 0/0 | 4263 | 4 | 3 | 1 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| a0001c0001t0018 | 0/0 | 4264 | 4 | 2 | 1 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| a0001c0001t0019 | 0/0 | 4269 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| a0001c0001t0020 | 0/0 | 4263 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| a0001c0001t0021 | 0/0 | 4269 | 3 | 0 | 0 | 3 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| a0001c0001t0022 | 0/0 | 4271 | 3 | 1 | 1 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| a0001c0001t0023 | 0/0 | 4270 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| a0001c0001t0024 | 0/0 | 4271 | 2 | 1 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| a0001c0001t0027 | 0/0 | 4271 | 2 | 0 | 0 | 2 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| a0001c0001t0028 | 0/0 | 4260 | 2 | 0 | 0 | 0 | 1 | 1 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| a0001c0001t0031 | 0/0 | 4256 | 2 | 2 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| a0001c0001t0037 | 0/0 | 4267 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| a0001c0001t0038 | 0/0 | 4262 | 2 | 0 | 0 | 1 | 0 | 1 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| a0001c0001t0039 | 0/0 | 4264 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| a0001c0001t0047 | 0/0 | 4270 | 1 | 0 | 0 | 0 | 0 | 1 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| a0001c0001t0048 | 0/0 | 4271 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| a0001c0001t0049 | 0/0 | 4265 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| a0001c0001t0050 | 0/0 | 4269 | 1 | 0 | 0 | 0 | 0 | 1 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| a0001c0001t0052 | 0/0 | 4263 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| a0001c0001t0053 | 0/0 | 4269 | 1 | 0 | 0 | 0 | 1 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| a0001c0001t0054 | 0/0 | 4269 | 1 | 0 | 0 | 0 | 0 | 1 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| a0001c0001t0055 | 0/0 | 4270 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| a0001c0001t0056 | 0/0 | 4269 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| a0001c0001t0057 | 0/0 | 4275 | 1 | 0 | 0 | 0 | 1 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| a0001c0001t0058 | 0/0 | 4269 | 1 | 0 | 1 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| a0001c0001t0059 | 0/0 | 4271 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| a0001c0001t0060 | 0/0 | 4258 | 1 | 0 | 0 | 0 | 0 | 1 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| a0001c0001t0061 | 0/0 | 4262 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| a0001c0001t0062 | 0/0 | 4261 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| a0001c0001t0063 | 0/0 | 4267 | 1 | 0 | 1 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| a0001c0001t0064 | 0/0 | 4267 | 1 | 0 | 0 | 0 | 1 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| a0001c0001t0065 | 0/0 | 4267 | 1 | 0 | 0 | 0 | 1 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| a0001c0001t0066 | 0/0 | 4263 | 1 | 0 | 1 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| a0001c0001t0067 | 0/0 | 4271 | 1 | 0 | 1 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| a0001c0001t0068 | 0/0 | 4272 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| a0001c0001t0069 | 0/0 | 4271 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| a0001c0001t0070 | 0/0 | 4264 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| a0001c0001t0071 | 0/0 | 4258 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| a0001c0001t0072 | 0/0 | 4261 | 1 | 0 | 0 | 0 | 1 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| a0001c0001t0073 | 0/0 | 4270 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| a0001c0001t0078 | 0/0 | 4269 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| a0001c0001t0079 | 0/0 | 4271 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| a0001c0001t0080 | 0/0 | 4269 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| a0001c0001t0081 | 0/0 | 4270 | 1 | 0 | 1 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| a0001c0001t0082 | 0/0 | 4265 | 1 | 0 | 1 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| a0001c0001t0083 | 0/0 | 4272 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| a0001c0001t0084 | 0/0 | 4261 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| a0001c0001t0085 | 0/0 | 4274 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| a0001c0001t0086 | 0/0 | 4250 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| a0001c0001t0088 | 0/0 | 4267 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| a0001c0001t0091 | 0/0 | 4267 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| a0001c0001t0094 | 0/0 | 4263 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| a0001c0001t0095 | 0/0 | 4267 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| a0001c0001t0096 | 0/0 | 4264 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| a0001c0001t0097 | 0/0 | 4266 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| a0001c0001t0103 | 0/0 | 4270 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| a0001c0001t0105 | 0/0 | 4265 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| a0001c0001t0106 | 0/0 | 4268 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| a0001c0001t0107 | 0/0 | 4263 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| a0001c0001t0108 | 0/0 | 4270 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| a0001c0001t0109 | 0/0 | 4270 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| a0001c0001t0110 | 0/0 | 4270 | 1 | 0 | 1 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| a0001c0001t0111 | 0/0 | 4261 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| a0001c0001t0112 | 0/0 | 4250 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| a0001c0001t0113 | 0/0 | 4278 | 1 | 0 | 1 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| a0001c0001t0114 | 0/0 | 4260 | 1 | 0 | 1 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| a0001c0001t0115 | 0/0 | 4269 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| a0001c0001t0116 | 0/0 | 4270 | 1 | 0 | 0 | 0 | 1 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| a0001c0001t0117 | 0/0 | 4264 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| a0001c0002t0006 | 0/0 | 4276 | 8 | 1 | 1 | 6 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| a0001c0002t0009 | 0/0 | 4278 | 6 | 3 | 0 | 3 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| a0001c0002t0011 | 0/0 | 4278 | 5 | 4 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| a0001c0002t0025 | 0/0 | 4277 | 2 | 0 | 0 | 2 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| a0001c0002t0026 | 0/0 | 4277 | 2 | 2 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| a0001c0002t0029 | 0/0 | 4276 | 2 | 1 | 1 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| a0001c0002t0030 | 0/0 | 4276 | 2 | 2 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| a0001c0002t0033 | 0/0 | 4276 | 2 | 2 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| a0001c0002t0034 | 0/0 | 4277 | 2 | 1 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| a0001c0002t0035 | 0/0 | 4276 | 2 | 0 | 0 | 2 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| a0001c0002t0036 | 0/0 | 4279 | 2 | 0 | 0 | 2 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| a0001c0002t0041 | 0/0 | 4285 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| a0001c0002t0042 | 0/0 | 4279 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| a0001c0002t0043 | 0/0 | 4278 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| a0001c0002t0044 | 0/0 | 4281 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| a0001c0002t0045 | 0/0 | 4280 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| a0001c0002t0046 | 0/0 | 4279 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| a0001c0002t0051 | 0/0 | 4267 | 1 | 0 | 1 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| a0001c0002t0074 | 0/0 | 4274 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| a0001c0002t0075 | 0/0 | 4281 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| a0001c0002t0076 | 0/0 | 4279 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| a0001c0002t0093 | 0/0 | 4279 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| a0001c0002t0098 | 0/0 | 4275 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| a0001c0002t0099 | 0/0 | 4282 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| a0001c0002t0100 | 0/0 | 4281 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| a0001c0002t0101 | 0/0 | 4279 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| a0001c0002t0102 | 0/0 | 4281 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| a0001c0003t0001 | 0/0 | 4269 | 1 | 0 | 0 | 0 | 0 | 1 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| a0001c0003t0003 | 0/0 | 4269 | 4 | 0 | 2 | 1 | 1 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| a0001c0003t0004 | 0/0 | 4270 | 7 | 0 | 4 | 0 | 2 | 1 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| a0001c0003t0005 | 0/0 | 4269 | 6 | 0 | 2 | 3 | 1 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| a0001c0003t0007 | 0/0 | 4270 | 1 | 0 | 0 | 0 | 0 | 1 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| a0001c0003t0013 | 0/0 | 4269 | 2 | 0 | 0 | 1 | 1 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| a0001c0003t0019 | 0/0 | 4269 | 3 | 0 | 0 | 3 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| a0001c0003t0020 | 0/0 | 4263 | 2 | 0 | 1 | 0 | 0 | 1 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| a0001c0003t0023 | 0/0 | 4270 | 1 | 0 | 1 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| a0001c0003t0037 | 0/0 | 4267 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| a0001c0003t0089 | 0/0 | 4276 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| a0001c0003t0090 | 0/0 | 4276 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| a0001c0003t0092 | 0/0 | 4264 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| a0001c0003t0104 | 0/0 | 4272 | 1 | 0 | 0 | 0 | 0 | 1 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| a0001c0005t0040 | 0/0 | 4275 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| a0001c0005t0077 | 0/0 | 4267 | 1 | 0 | 0 | 0 | 0 | 1 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| a0001c0006t0024 | 0/0 | 4271 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| a0001c0006t0087 | 0/0 | 4261 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| a0001c0008t0002 | 0/0 | 4269 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| a0001c0012t0023 | 0/0 | 4270 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| a0002c0004t0032 | 0/0 | 4263 | 2 | 2 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| a0003c0013t0002 | 0/0 | 4269 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| a0004c0007t0013 | 0/0 | 4269 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| a0005c0009t0015 | 0/0 | 4269 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| a0006c0010t0016 | 0/0 | 4264 | 1 | 0 | 0 | 0 | 0 | 1 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| a0007c0011t0003 | 1/0 | 4269 | 1 | 0 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | copy fasta | chr11 | 89319353 | 89496375 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0001g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0001g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0001g0128 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0002g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0002g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0002g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0002g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0002g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0002g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0002g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0002g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0002g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0002g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0002g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0002g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0002g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0002g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0003g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0003g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0003g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0003g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0003g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0003g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0003g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0003g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0004g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0004g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0004g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0005g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0005g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0005g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0007g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0007g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0007g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0007g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0007g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0008g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0008g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0008g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0008g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0008g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0008g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0010g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0010g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0010g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0010g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0010g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0012g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0012g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0012g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0012g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0012g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0013g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0014g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0014g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0014g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0014g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0015g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0015g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0015g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0016g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0016g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0016g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0017g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0017g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0017g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0017g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0018g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0018g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0018g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0018g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0019g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0020g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0021g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0021g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0021g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0022g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0022g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0022g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0023g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0024g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0024g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0027g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0027g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0028g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0028g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0031g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0031g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0037g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0038g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0038g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0039g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0047g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0048g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0049g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0050g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0052g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0053g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0054g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0055g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0056g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0057g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0058g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0059g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0060g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0061g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0062g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0063g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0064g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0065g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0066g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0067g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0068g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0069g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0070g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0071g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0072g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0073g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0078g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0079g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0080g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0081g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0082g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0083g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0084g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0085g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0086g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0088g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0091g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0094g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0095g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0096g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0097g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0103g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0105g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0106g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0107g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0108g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0109g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0110g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0111g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0112g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0113g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0114g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0115g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0116g0271 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0001t0117g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0002t0006g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0002t0006g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0002t0006g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0002t0006g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0002t0006g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0002t0006g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0002t0006g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0002t0006g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0002t0009g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0002t0009g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0002t0009g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0002t0009g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0002t0009g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0002t0009g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0002t0011g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0002t0011g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0002t0011g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0002t0011g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0002t0011g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0002t0025g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0002t0025g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0002t0026g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0002t0026g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0002t0029g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0002t0029g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0002t0030g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0002t0030g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0002t0033g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0002t0033g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0002t0034g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0002t0034g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0002t0035g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0002t0035g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0002t0036g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0002t0036g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0002t0041g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0002t0042g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0002t0043g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0002t0044g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0002t0045g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0002t0046g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0002t0051g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0002t0074g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0002t0075g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0002t0076g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0002t0093g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0002t0098g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0002t0099g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0002t0100g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0002t0101g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0002t0102g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0003t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0003t0003g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0003t0003g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0003t0003g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0003t0003g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0003t0004g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0003t0004g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0003t0004g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0003t0004g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0003t0004g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0003t0004g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0003t0004g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0003t0005g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0003t0005g0184 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0003t0005g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0003t0005g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0003t0005g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0003t0005g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0003t0007g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0003t0013g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0003t0013g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0003t0019g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0003t0019g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0003t0019g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0003t0020g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0003t0020g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0003t0023g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0003t0037g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0003t0089g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0003t0090g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0003t0092g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0003t0104g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0005t0040g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0005t0077g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0006t0024g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0006t0087g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0008t0002g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0001c0012t0023g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0002c0004t0032g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0002c0004t0032g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0003c0013t0002g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0004c0007t0013g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0005c0009t0015g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0006c0010t0016g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| a0007c0011t0003g0185 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0116 | g0271 | EUR | GBR | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| HG00099 | hp2 | a0001 | c0001 | t0016 | g0047 | EUR | GBR | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| HG00140 | hp1 | a0001 | c0001 | t0010 | g0133 | EUR | GBR | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| HG00140 | hp2 | a0001 | c0003 | t0005 | g0184 | EUR | GBR | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| HG00323 | hp1 | a0001 | c0001 | t0053 | g0101 | EUR | FIN | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| HG00323 | hp2 | a0001 | c0001 | t0010 | g0087 | EUR | FIN | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| HG00408 | hp1 | a0001 | c0001 | t0022 | g0099 | EAS | CHS | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| HG00408 | hp2 | a0001 | c0006 | t0024 | g0199 | EAS | CHS | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| HG00544 | hp1 | a0001 | c0001 | t0016 | g0012 | EAS | CHS | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | CHS | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| HG00558 | hp1 | a0001 | c0001 | t0008 | g0002 | EAS | CHS | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| HG00558 | hp2 | a0001 | c0001 | t0062 | g0114 | EAS | CHS | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| HG00621 | hp1 | a0001 | c0002 | t0011 | g0198 | EAS | CHS | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| HG00621 | hp2 | a0001 | c0001 | t0007 | g0126 | EAS | CHS | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| HG00639 | hp1 | a0001 | c0001 | t0007 | g0049 | AMR | PUR | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| HG00639 | hp2 | a0001 | c0003 | t0004 | g0066 | AMR | PUR | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| HG00642 | hp1 | a0001 | c0001 | t0110 | g0274 | AMR | PUR | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| HG00642 | hp2 | a0001 | c0003 | t0004 | g0119 | AMR | PUR | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| HG00673 | hp1 | a0001 | c0001 | t0003 | g0207 | EAS | CHS | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| HG00673 | hp2 | a0001 | c0001 | t0056 | g0055 | EAS | CHS | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| HG00735 | hp1 | a0001 | c0001 | t0010 | g0065 | AMR | PUR | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0269 | AMR | PUR | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| HG00741 | hp1 | a0001 | c0001 | t0003 | g0170 | AMR | PUR | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0270 | AMR | PUR | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0131 | AMR | PUR | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0268 | AMR | PUR | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| HG01074 | hp1 | a0001 | c0003 | t0003 | g0193 | AMR | PUR | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| HG01074 | hp2 | a0001 | c0001 | t0017 | g0171 | AMR | PUR | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| HG01081 | hp1 | a0001 | c0001 | t0022 | g0140 | AMR | PUR | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| HG01099 | hp1 | a0001 | c0001 | t0082 | g0174 | AMR | PUR | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0045 | AMR | PUR | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| HG01106 | hp1 | a0001 | c0001 | t0063 | g0067 | AMR | PUR | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| HG01106 | hp2 | a0001 | c0003 | t0020 | g0118 | AMR | PUR | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| HG01109 | hp1 | a0001 | c0002 | t0029 | g0154 | AMR | PUR | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| HG01109 | hp2 | a0001 | c0001 | t0012 | g0247 | AMR | PUR | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0266 | AMR | PUR | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| HG01167 | hp2 | a0001 | c0001 | t0010 | g0071 | AMR | PUR | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| HG01243 | hp1 | a0001 | c0001 | t0113 | g0227 | AMR | PUR | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| HG01243 | hp2 | a0001 | c0001 | t0081 | g0163 | AMR | PUR | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| HG01255 | hp1 | a0001 | c0003 | t0004 | g0116 | AMR | CLM | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0130 | AMR | CLM | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0129 | AMR | CLM | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| HG01256 | hp2 | a0001 | c0001 | t0013 | g0082 | AMR | CLM | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| HG01257 | hp1 | a0001 | c0001 | t0066 | g0096 | AMR | CLM | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| HG01257 | hp2 | a0001 | c0003 | t0003 | g0189 | AMR | CLM | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| HG01346 | hp1 | a0001 | c0002 | t0051 | g0009 | AMR | CLM | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| HG01346 | hp2 | a0001 | c0003 | t0004 | g0037 | AMR | CLM | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| HG01358 | hp1 | a0001 | c0001 | t0067 | g0111 | AMR | CLM | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| HG01358 | hp2 | a0001 | c0003 | t0005 | g0194 | AMR | CLM | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| HG01515 | hp1 | a0001 | c0001 | t0028 | g0075 | EUR | IBS | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| HG01515 | hp2 | a0001 | c0001 | t0064 | g0104 | EUR | IBS | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| HG01516 | hp1 | a0001 | c0001 | t0057 | g0127 | EUR | IBS | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| HG01516 | hp2 | a0001 | c0003 | t0004 | g0117 | EUR | IBS | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| HG01517 | hp1 | a0001 | c0001 | t0065 | g0105 | EUR | IBS | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| HG01517 | hp2 | a0001 | c0003 | t0004 | g0120 | EUR | IBS | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| HG01884 | hp1 | a0001 | c0002 | t0030 | g0159 | AFR | ACB | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| HG01884 | hp2 | a0001 | c0001 | t0068 | g0064 | AFR | ACB | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | ACB | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| HG01891 | hp2 | a0001 | c0002 | t0009 | g0249 | AFR | ACB | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0238 | AMR | PEL | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| HG01928 | hp2 | a0001 | c0001 | t0003 | g0188 | AMR | PEL | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0060 | AMR | PEL | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| HG01934 | hp2 | a0001 | c0001 | t0018 | g0187 | AMR | PEL | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| HG01952 | hp1 | a0001 | c0001 | t0058 | g0005 | AMR | PEL | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| HG01952 | hp2 | a0001 | c0001 | t0008 | g0051 | AMR | PEL | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| HG01978 | hp1 | a0001 | c0002 | t0006 | g0034 | AMR | PEL | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| HG01978 | hp2 | a0001 | c0001 | t0008 | g0112 | AMR | PEL | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0231 | AMR | PEL | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| HG01981 | hp2 | a0001 | c0003 | t0023 | g0202 | AMR | PEL | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| HG02004 | hp1 | a0001 | c0001 | t0114 | g0241 | AMR | PEL | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0103 | AMR | PEL | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0260 | EAS | KHV | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| HG02015 | hp2 | a0001 | c0001 | t0012 | g0257 | EAS | KHV | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| HG02055 | hp1 | a0001 | c0001 | t0095 | g0215 | AFR | ACB | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| HG02055 | hp2 | a0001 | c0002 | t0026 | g0046 | AFR | ACB | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| HG02056 | hp1 | a0001 | c0003 | t0037 | g0251 | EAS | KHV | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0261 | EAS | KHV | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| HG02074 | hp1 | a0001 | c0001 | t0007 | g0141 | EAS | KHV | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | KHV | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | KHV | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| HG02080 | hp2 | a0001 | c0001 | t0007 | g0125 | EAS | KHV | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| HG02083 | hp1 | a0001 | c0003 | t0092 | g0196 | EAS | KHV | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| HG02083 | hp2 | a0001 | c0001 | t0014 | g0068 | EAS | KHV | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0259 | EAS | KHV | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| HG02132 | hp2 | a0001 | c0002 | t0045 | g0095 | EAS | KHV | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| HG02145 | hp1 | a0001 | c0001 | t0022 | g0040 | AFR | ACB | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| HG02145 | hp2 | a0001 | c0001 | t0052 | g0122 | AFR | ACB | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| HG02148 | hp1 | a0001 | c0001 | t0003 | g0182 | AMR | PEL | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | PEL | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| HG02155 | hp1 | a0001 | c0001 | t0070 | g0094 | EAS | CDX | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| HG02155 | hp2 | a0001 | c0001 | t0003 | g0186 | EAS | CDX | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | ACB | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| HG02257 | hp2 | a0001 | c0002 | t0093 | g0219 | AFR | ACB | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0279 | AFR | ACB | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | ACB | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0081 | AMR | PEL | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| HG02280 | hp1 | a0001 | c0001 | t0078 | g0143 | AFR | ACB | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| HG02280 | hp2 | a0001 | c0001 | t0091 | g0151 | AFR | ACB | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| HG02300 | hp1 | a0001 | c0003 | t0005 | g0190 | AMR | PEL | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0123 | AMR | PEL | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| HG02451 | hp1 | a0001 | c0001 | t0002 | g0224 | AFR | ACB | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| HG02451 | hp2 | a0001 | c0001 | t0088 | g0158 | AFR | ACB | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| HG02572 | hp1 | a0001 | c0001 | t0094 | g0218 | AFR | GWD | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| HG02572 | hp2 | a0001 | c0001 | t0005 | g0178 | AFR | GWD | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| HG02615 | hp1 | a0002 | c0004 | t0032 | g0144 | AFR | GWD | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| HG02615 | hp2 | a0001 | c0001 | t0107 | g0225 | AFR | GWD | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| HG02622 | hp1 | a0001 | c0001 | t0002 | g0252 | AFR | GWD | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| HG02622 | hp2 | a0001 | c0001 | t0086 | g0152 | AFR | GWD | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| HG02630 | hp1 | a0001 | c0001 | t0109 | g0281 | AFR | GWD | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| HG02630 | hp2 | a0001 | c0002 | t0011 | g0157 | AFR | GWD | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| HG02647 | hp1 | a0001 | c0002 | t0009 | g0278 | AFR | GWD | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| HG02647 | hp2 | a0001 | c0002 | t0011 | g0156 | AFR | GWD | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| HG02698 | hp1 | a0001 | c0001 | t0038 | g0230 | SAS | PJL | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| HG02698 | hp2 | a0001 | c0001 | t0014 | g0109 | SAS | PJL | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| HG02717 | hp1 | a0001 | c0001 | t0017 | g0160 | AFR | GWD | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| HG02717 | hp2 | a0001 | c0008 | t0002 | g0275 | AFR | GWD | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0245 | AFR | GWD | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| HG02723 | hp2 | a0001 | c0001 | t0017 | g0172 | AFR | GWD | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| HG02738 | hp1 | a0001 | c0001 | t0047 | g0139 | SAS | PJL | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0276 | SAS | PJL | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| HG02809 | hp1 | a0001 | c0001 | t0019 | g0166 | AFR | GWD | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| HG02809 | hp2 | a0001 | c0001 | t0017 | g0165 | AFR | GWD | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| HG02895 | hp1 | a0001 | c0001 | t0002 | g0283 | AFR | GWD | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| HG02895 | hp2 | a0001 | c0001 | t0048 | g0044 | AFR | GWD | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| HG02896 | hp1 | a0001 | c0001 | t0005 | g0150 | AFR | GWD | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| HG02896 | hp2 | a0001 | c0001 | t0069 | g0015 | AFR | GWD | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| HG02897 | hp1 | a0001 | c0001 | t0049 | g0043 | AFR | GWD | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| HG02897 | hp2 | a0001 | c0001 | t0005 | g0149 | AFR | GWD | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| HG02922 | hp1 | a0001 | c0001 | t0112 | g0282 | AFR | ESN | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| HG02922 | hp2 | a0001 | c0001 | t0111 | g0277 | AFR | ESN | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| HG02965 | hp1 | a0001 | c0002 | t0100 | g0258 | AFR | ESN | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| HG02965 | hp2 | a0001 | c0001 | t0079 | g0169 | AFR | ESN | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| HG02976 | hp1 | a0001 | c0002 | t0099 | g0286 | AFR | ESN | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| HG02976 | hp2 | a0001 | c0001 | t0085 | g0179 | AFR | ESN | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| HG03098 | hp1 | a0001 | c0002 | t0029 | g0168 | AFR | MSL | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| HG03098 | hp2 | a0001 | c0002 | t0074 | g0146 | AFR | MSL | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| HG03130 | hp1 | a0001 | c0001 | t0024 | g0155 | AFR | ESN | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| HG03130 | hp2 | a0001 | c0002 | t0030 | g0145 | AFR | ESN | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| HG03139 | hp1 | a0001 | c0002 | t0011 | g0173 | AFR | ESN | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| HG03139 | hp2 | a0001 | c0001 | t0106 | g0228 | AFR | ESN | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| HG03195 | hp1 | a0001 | c0002 | t0033 | g0285 | AFR | ESN | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| HG03195 | hp2 | a0001 | c0002 | t0034 | g0250 | AFR | ESN | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| HG03209 | hp1 | a0001 | c0001 | t0031 | g0177 | AFR | MSL | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| HG03209 | hp2 | a0001 | c0001 | t0115 | g0253 | AFR | MSL | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| HG03225 | hp1 | a0001 | c0001 | t0117 | g0287 | AFR | MSL | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| HG03225 | hp2 | a0001 | c0002 | t0011 | g0153 | AFR | MSL | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| HG03490 | hp1 | a0006 | c0010 | t0016 | g0027 | SAS | PJL | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| HG03490 | hp2 | a0001 | c0003 | t0104 | g0267 | SAS | PJL | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| HG03579 | hp1 | a0001 | c0002 | t0033 | g0262 | AFR | MSL | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0063 | AFR | MSL | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| HG03654 | hp1 | a0001 | c0001 | t0010 | g0102 | SAS | PJL | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0050 | SAS | PJL | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| HG03669 | hp1 | a0001 | c0001 | t0060 | g0106 | SAS | PJL | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| HG03669 | hp2 | a0001 | c0003 | t0007 | g0053 | SAS | PJL | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0221 | SAS | STU | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| HG03688 | hp2 | a0001 | c0001 | t0050 | g0080 | SAS | STU | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| HG03834 | hp1 | a0001 | c0003 | t0020 | g0121 | SAS | BEB | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| HG03834 | hp2 | a0001 | c0003 | t0001 | g0058 | SAS | BEB | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| HG03927 | hp1 | a0001 | c0001 | t0028 | g0108 | SAS | BEB | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0059 | SAS | BEB | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0023 | SAS | STU | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| HG04115 | hp2 | a0001 | c0001 | t0054 | g0048 | SAS | STU | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| HG04199 | hp1 | a0001 | c0005 | t0077 | g0214 | SAS | STU | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| HG04199 | hp2 | a0001 | c0001 | t0008 | g0086 | SAS | STU | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| HG04228 | hp1 | a0001 | c0003 | t0004 | g0076 | SAS | STU | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| HG04228 | hp2 | a0001 | c0001 | t0008 | g0072 | SAS | STU | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| NA18522 | hp1 | a0001 | c0001 | t0031 | g0176 | AFR | YRI | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| NA18522 | hp2 | a0001 | c0001 | t0084 | g0148 | AFR | YRI | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| NA18612 | hp1 | a0001 | c0002 | t0035 | g0248 | EAS | CHB | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| NA18612 | hp2 | a0001 | c0001 | t0021 | g0010 | EAS | CHB | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0265 | EAS | CHB | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| NA18747 | hp2 | a0001 | c0002 | t0006 | g0021 | EAS | CHB | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| NA18906 | hp1 | a0001 | c0001 | t0103 | g0272 | AFR | YRI | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| NA18906 | hp2 | a0002 | c0004 | t0032 | g0162 | AFR | YRI | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| NA18939 | hp2 | a0001 | c0001 | t0105 | g0233 | EAS | JPT | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| NA18941 | hp1 | a0001 | c0001 | t0015 | g0019 | EAS | JPT | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| NA18941 | hp2 | a0001 | c0003 | t0019 | g0213 | EAS | JPT | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| NA18942 | hp1 | a0001 | c0003 | t0005 | g0180 | EAS | JPT | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| NA18942 | hp2 | a0001 | c0002 | t0006 | g0091 | EAS | JPT | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| NA18944 | hp2 | a0001 | c0002 | t0075 | g0183 | EAS | JPT | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| NA18946 | hp1 | a0001 | c0001 | t0018 | g0192 | EAS | JPT | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| NA18947 | hp1 | a0001 | c0001 | t0008 | g0107 | EAS | JPT | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| NA18950 | hp2 | a0001 | c0001 | t0003 | g0205 | EAS | JPT | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| NA18951 | hp1 | a0001 | c0001 | t0059 | g0054 | EAS | JPT | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| NA18951 | hp2 | a0001 | c0001 | t0003 | g0191 | EAS | JPT | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| NA18954 | hp1 | a0001 | c0002 | t0041 | g0022 | EAS | JPT | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| NA18954 | hp2 | a0001 | c0001 | t0014 | g0038 | EAS | JPT | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| NA18957 | hp1 | a0001 | c0002 | t0034 | g0237 | EAS | JPT | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| NA18957 | hp2 | a0001 | c0001 | t0007 | g0007 | EAS | JPT | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| NA18959 | hp1 | a0001 | c0003 | t0005 | g0208 | EAS | JPT | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| NA18959 | hp2 | a0001 | c0001 | t0012 | g0222 | EAS | JPT | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| NA18961 | hp1 | a0001 | c0002 | t0036 | g0234 | EAS | JPT | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| NA18962 | hp1 | a0001 | c0002 | t0076 | g0209 | EAS | JPT | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| NA18962 | hp2 | a0001 | c0001 | t0015 | g0078 | EAS | JPT | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| NA18963 | hp2 | a0001 | c0001 | t0080 | g0203 | EAS | JPT | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| NA18965 | hp1 | a0001 | c0002 | t0006 | g0083 | EAS | JPT | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| NA18965 | hp2 | a0001 | c0002 | t0035 | g0229 | EAS | JPT | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| NA18966 | hp1 | a0001 | c0003 | t0019 | g0204 | EAS | JPT | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| NA18966 | hp2 | a0001 | c0001 | t0020 | g0056 | EAS | JPT | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| NA18968 | hp1 | a0001 | c0001 | t0027 | g0020 | EAS | JPT | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| NA18968 | hp2 | a0001 | c0003 | t0090 | g0211 | EAS | JPT | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| NA18971 | hp1 | a0001 | c0001 | t0083 | g0147 | EAS | JPT | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| NA18971 | hp2 | a0001 | c0002 | t0046 | g0115 | EAS | JPT | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| NA18977 | hp1 | a0001 | c0002 | t0006 | g0085 | EAS | JPT | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| NA18977 | hp2 | a0001 | c0001 | t0061 | g0042 | EAS | JPT | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| NA18984 | hp1 | a0001 | c0002 | t0042 | g0136 | EAS | JPT | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| NA18984 | hp2 | a0005 | c0009 | t0015 | g0077 | EAS | JPT | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| NA18985 | hp1 | a0001 | c0001 | t0002 | g0256 | EAS | JPT | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| NA18985 | hp2 | a0001 | c0002 | t0025 | g0039 | EAS | JPT | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| NA18986 | hp1 | a0001 | c0003 | t0003 | g0201 | EAS | JPT | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| NA18986 | hp2 | a0001 | c0002 | t0009 | g0232 | EAS | JPT | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| NA18988 | hp1 | a0001 | c0001 | t0015 | g0057 | EAS | JPT | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| NA18988 | hp2 | a0001 | c0005 | t0040 | g0137 | EAS | JPT | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| NA18990 | hp1 | a0001 | c0003 | t0005 | g0206 | EAS | JPT | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| NA18993 | hp1 | a0001 | c0001 | t0027 | g0018 | EAS | JPT | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| NA18993 | hp2 | a0001 | c0001 | t0021 | g0124 | EAS | JPT | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| NA18994 | hp1 | a0001 | c0001 | t0012 | g0244 | EAS | JPT | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| NA18994 | hp2 | a0001 | c0001 | t0016 | g0100 | EAS | JPT | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| NA18995 | hp1 | a0001 | c0001 | t0055 | g0097 | EAS | JPT | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| NA18995 | hp2 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| NA18998 | hp1 | a0001 | c0001 | t0108 | g0223 | EAS | JPT | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| NA18998 | hp2 | a0001 | c0002 | t0043 | g0024 | EAS | JPT | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| NA19001 | hp1 | a0001 | c0002 | t0044 | g0017 | EAS | JPT | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| NA19001 | hp2 | a0001 | c0001 | t0003 | g0164 | EAS | JPT | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| NA19003 | hp1 | a0001 | c0002 | t0009 | g0236 | EAS | JPT | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| NA19003 | hp2 | a0001 | c0003 | t0019 | g0197 | EAS | JPT | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0264 | EAS | JPT | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| NA19004 | hp2 | a0001 | c0001 | t0038 | g0243 | EAS | JPT | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| NA19005 | hp1 | a0001 | c0001 | t0024 | g0210 | EAS | JPT | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| NA19005 | hp2 | a0001 | c0001 | t0039 | g0092 | EAS | JPT | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| NA19007 | hp2 | a0001 | c0002 | t0006 | g0084 | EAS | JPT | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| NA19030 | hp1 | a0001 | c0001 | t0071 | g0090 | AFR | LWK | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| NA19030 | hp2 | a0001 | c0002 | t0026 | g0074 | AFR | LWK | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| NA19043 | hp1 | a0001 | c0002 | t0006 | g0025 | AFR | LWK | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| NA19043 | hp2 | a0001 | c0002 | t0098 | g0284 | AFR | LWK | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| NA19054 | hp1 | a0001 | c0001 | t0004 | g0052 | EAS | JPT | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| NA19054 | hp2 | a0001 | c0002 | t0009 | g0240 | EAS | JPT | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| NA19057 | hp1 | a0001 | c0002 | t0006 | g0079 | EAS | JPT | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| NA19064 | hp1 | a0001 | c0002 | t0025 | g0016 | EAS | JPT | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| NA19064 | hp2 | a0001 | c0002 | t0102 | g0226 | EAS | JPT | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| NA19066 | hp1 | a0001 | c0001 | t0004 | g0011 | EAS | JPT | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| NA19066 | hp2 | a0001 | c0002 | t0101 | g0239 | EAS | JPT | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| NA19070 | hp1 | a0001 | c0003 | t0013 | g0135 | EAS | JPT | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| NA19070 | hp2 | a0001 | c0002 | t0036 | g0235 | EAS | JPT | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| NA19076 | hp2 | a0001 | c0006 | t0087 | g0200 | EAS | JPT | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| NA19077 | hp2 | a0004 | c0007 | t0013 | g0089 | EAS | JPT | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| NA19083 | hp1 | a0001 | c0001 | t0002 | g0246 | EAS | JPT | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| NA19083 | hp2 | a0001 | c0001 | t0014 | g0036 | EAS | JPT | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0242 | EAS | JPT | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| NA19088 | hp1 | a0001 | c0001 | t0021 | g0113 | EAS | JPT | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| NA19088 | hp2 | a0001 | c0003 | t0089 | g0195 | EAS | JPT | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| NA19240 | hp1 | a0001 | c0001 | t0018 | g0142 | AFR | YRI | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| NA19240 | hp2 | a0001 | c0001 | t0097 | g0216 | AFR | YRI | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| NA20129 | hp1 | a0001 | c0001 | t0012 | g0273 | AFR | ASW | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0073 | AFR | ASW | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| NA20752 | hp2 | a0001 | c0003 | t0003 | g0212 | EUR | TSI | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| NA20805 | hp1 | a0001 | c0003 | t0013 | g0041 | EUR | TSI | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| NA20805 | hp2 | a0001 | c0001 | t0072 | g0093 | EUR | TSI | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| HG02486 | hp1 | a0001 | c0001 | t0073 | g0167 | AFR | ACB | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| HG02486 | hp2 | a0001 | c0001 | t0023 | g0161 | AFR | ACB | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| HG02559 | hp1 | a0001 | c0001 | t0096 | g0217 | AFR | ACB | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| HG02559 | hp2 | a0003 | c0013 | t0002 | g0220 | AFR | ACB | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| HG03471 | hp1 | a0001 | c0001 | t0002 | g0255 | AFR | MSL | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| HG03471 | hp2 | a0001 | c0002 | t0009 | g0263 | AFR | MSL | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0254 | AFR | USA | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| NA20300 | hp2 | a0001 | c0001 | t0037 | g0280 | AFR | USA | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| NA21309 | hp1 | a0001 | c0001 | t0018 | g0175 | AFR | LWK | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| NA21309 | hp2 | a0001 | c0012 | t0023 | g0181 | AFR | LWK | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0128 | REF | REF | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| homoSapiens_grch38 | hp1 | a0007 | c0011 | t0003 | g0185 | REF | REF | NOX4_chr11_89319353_89496375 | NOX4 | chr11 | 89319353 | 89496375 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:89326839
|
G | C | 1 | a0005 | 1 | NA18984.hp2 | missense_variant | MODERATE | c.1654C>G | p.Leu552Val | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 18/18 | 1783/4269 | 1654/1737 | 552/578 | chr11 | 89326839 | ||
| chr11:89340101
|
G | A | 1 | a0002 | 2 | HG02615.hp1 NA18906.hp2 |
missense_variant | MODERATE | c.1408C>T | p.Arg470Cys | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 15/18 | 1537/4269 | 1408/1737 | 470/578 | chr11 | 89340101 | ||
| chr11:89355017
|
G | A | 1 | a0006 | 1 | HG03490.hp1 | missense_variant | MODERATE | c.1162C>T | p.Pro388Ser | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 13/18 | 1291/4269 | 1162/1737 | 388/578 | chr11 | 89355017 | ||
| chr11:89400252
|
C | T | 1 | a0004 | 1 | NA19077.hp2 | missense_variant | MODERATE | c.974G>A | p.Arg325Gln | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 10/18 | 1103/4269 | 974/1737 | 325/578 | chr11 | 89400252 | ||
| chr11:89400281
|
C | T | 6 | a0001a0002a0003others(3): Show | 287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
missense_variant | MODERATE | c.945G>A | p.Met315Ile | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 10/18 | 1074/4269 | 945/1737 | 315/578 | chr11 | 89400281 | ||
| chr11:89449498
|
C | A | 1 | a0003 | 1 | HG02559.hp2 | missense_variant | MODERATE | c.291G>T | p.Leu97Phe | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 4/18 | 420/4269 | 291/1737 | 97/578 | chr11 | 89449498 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:89326818
|
G | A | 1 | a0001c0008 | 1 | HG02717.hp2 | synonymous_variant | LOW | c.1675C>T | p.Leu559Leu | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 18/18 | 1804/4269 | 1675/1737 | 559/578 | chr11 | 89326818 | ||
| chr11:89326834
|
G | A | 2 | a0001c0002a0001c0005 | 53 | HG00621.hp1 HG01109.hp1 HG01346.hp1 others(50): Show |
synonymous_variant | LOW | c.1659C>T | p.Ser553Ser | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 18/18 | 1788/4269 | 1659/1737 | 553/578 | chr11 | 89326834 | ||
| chr11:89355000
|
G | A | 3 | a0001c0003a0001c0005a0004c0007 | 35 | HG00140.hp2 HG00639.hp2 HG00642.hp2 others(32): Show |
synonymous_variant | LOW | c.1179C>T | p.Ser393Ser | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 13/18 | 1308/4269 | 1179/1737 | 393/578 | chr11 | 89355000 | ||
| chr11:89400338
|
G | C | 1 | a0001c0012 | 1 | NA21309.hp2 | synonymous_variant | LOW | c.888C>G | p.Ala296Ala | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 10/18 | 1017/4269 | 888/1737 | 296/578 | chr11 | 89400338 | ||
| chr11:89444216
|
G | C | 1 | a0001c0006 | 2 | HG00408.hp2 NA19076.hp2 |
synonymous_variant | LOW | c.366C>G | p.Ala122Ala | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 5/18 | 495/4269 | 366/1737 | 122/578 | chr11 | 89444216 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:89324366
|
A | G | 2 | a0001c0001t0056a0001c0001t0059 | 2 | HG00673.hp2 NA18951.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2390T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 18/18 | 2390 | chr11 | 89324366 | |||||
| chr11:89324374
|
C | A | 1 | a0001c0001t0086 | 1 | HG02622.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2382G>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 18/18 | 2382 | chr11 | 89324374 | |||||
| chr11:89324463
|
G | A | 1 | a0001c0003t0090 | 1 | NA18968.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2293C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 18/18 | 2293 | chr11 | 89324463 | |||||
| chr11:89324566
|
G | T | 2 | a0001c0001t0084a0001c0001t0111 | 2 | HG02922.hp2 NA18522.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2190C>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 18/18 | 2190 | chr11 | 89324566 | |||||
| chr11:89324639
|
G | A | 2 | a0001c0001t0031a0001c0001t0071 | 3 | HG03209.hp1 NA18522.hp1 NA19030.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2117C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 18/18 | 2117 | chr11 | 89324639 | |||||
| chr11:89324674
|
G | C | 1 | a0001c0002t0051 | 1 | HG01346.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2082C>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 18/18 | 2082 | chr11 | 89324674 | |||||
| chr11:89324693
|
G | T | 1 | a0001c0002t0051 | 1 | HG01346.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2063C>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 18/18 | 2063 | chr11 | 89324693 | |||||
| chr11:89324762
|
A | G | 1 | a0001c0001t0086 | 1 | HG02622.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1994T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 18/18 | 1994 | chr11 | 89324762 | |||||
| chr11:89324797
|
G | A | 2 | a0001c0001t0085a0001c0001t0112 | 2 | HG02922.hp1 HG02976.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1959C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 18/18 | 1959 | chr11 | 89324797 | |||||
| chr11:89324933
|
T | C | 33 | a0001c0001t0010a0001c0001t0012a0001c0001t0016others(30): Show | 51 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(48): Show |
3_prime_UTR_variant | MODIFIER | c.*1823A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 18/18 | 1823 | chr11 | 89324933 | |||||
| chr11:89324935
|
C | T | 1 | a0001c0001t0086 | 1 | HG02622.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1821G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 18/18 | 1821 | chr11 | 89324935 | |||||
| chr11:89325009
|
A | T | 4 | a0001c0001t0015a0001c0001t0027a0001c0001t0108others(1): Show | 7 | NA18941.hp1 NA18962.hp2 NA18968.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1747T>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 18/18 | 1747 | chr11 | 89325009 | |||||
| chr11:89325090
|
A | G | 3 | a0001c0001t0084a0001c0001t0086a0001c0001t0111 | 3 | HG02622.hp2 HG02922.hp2 NA18522.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1666T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 18/18 | 1666 | chr11 | 89325090 | |||||
| chr11:89325108
|
TTTAATTC | T | 2 | a0001c0001t0010a0001c0001t0114 | 6 | HG00140.hp1 HG00323.hp2 HG00735.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1641_*1647delGAAT others(3): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 18/18 | 1641 | chr11 | 89325108 | |||||
| chr11:89325115
|
C | CT | 12 | a0001c0001t0007a0001c0001t0055a0001c0001t0068others(9): Show | 16 | HG00099.hp1 HG00621.hp2 HG00639.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*1640dupA | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 18/18 | 1640 | chr11 | 89325115 | |||||
| chr11:89325115
|
C | CTTTTTT | 8 | a0001c0001t0005a0001c0001t0013a0001c0001t0048others(5): Show | 16 | HG00140.hp2 HG01256.hp2 HG01358.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*1635_*1640dupAAAA others(2): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 18/18 | 1640 | chr11 | 89325115 | |||||
| chr11:89325115
|
C | CTTTTTTT | 10 | a0001c0001t0004a0001c0001t0023a0001c0001t0047others(7): Show | 18 | HG00639.hp2 HG00642.hp2 HG01255.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*1634_*1640dupAAAA others(3): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 18/18 | 1640 | chr11 | 89325115 | |||||
| chr11:89325115
|
C | CTTTTTTT others(2): Show |
4 | a0001c0002t0006a0001c0002t0030a0001c0002t0035others(1): Show | 13 | HG01884.hp1 HG01978.hp1 HG03098.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1632_*1640dupAAAA others(5): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 18/18 | 1640 | chr11 | 89325115 | |||||
| chr11:89325115
|
C | CTTTTTTT others(3): Show |
6 | a0001c0002t0026a0001c0002t0034a0001c0002t0036others(3): Show | 9 | HG02055.hp2 HG03195.hp2 NA18957.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1631_*1640dupAAAA others(6): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 18/18 | 1640 | chr11 | 89325115 | |||||
| chr11:89325115
|
C | CTTTTTTT others(4): Show |
8 | a0001c0001t0085a0001c0001t0113a0001c0002t0009others(5): Show | 19 | HG00621.hp1 HG01109.hp1 HG01243.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*1630_*1640dupAAAA others(7): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 18/18 | 1640 | chr11 | 89325115 | |||||
| chr11:89325115
|
C | CTTTTTTT others(5): Show |
7 | a0001c0002t0025a0001c0002t0042a0001c0002t0044others(4): Show | 8 | HG02257.hp2 NA18962.hp1 NA18984.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1629_*1640dupAAAA others(8): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 18/18 | 1640 | chr11 | 89325115 | |||||
| chr11:89325115
|
C | CTTTTTTT others(7): Show |
1 | a0001c0002t0075 | 1 | NA18944.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1627_*1640dupAAAA others(10): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 18/18 | 1640 | chr11 | 89325115 | |||||
| chr11:89325115
|
C | CTTTTTTT others(9): Show |
1 | a0001c0002t0100 | 1 | HG02965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1625_*1640dupAAAA others(12): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 18/18 | 1640 | chr11 | 89325115 | |||||
| chr11:89325115
|
C | CTTTTTTT others(10): Show |
1 | a0001c0002t0099 | 1 | HG02976.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1624_*1640dupAAAA others(13): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 18/18 | 1640 | chr11 | 89325115 | |||||
| chr11:89325115
|
C | CTTTTTTT others(11): Show |
1 | a0001c0002t0041 | 1 | NA18954.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1623_*1640dupAAAA others(14): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 18/18 | 1640 | chr11 | 89325115 | |||||
| chr11:89325115
|
CTTT | C | 14 | a0001c0001t0012a0001c0001t0016a0001c0001t0018others(11): Show | 25 | HG00099.hp2 HG00544.hp1 HG01109.hp2 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*1638_*1640delAAA | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 18/18 | 1638 | chr11 | 89325115 | |||||
| chr11:89325115
|
CTTTT | C | 8 | a0001c0001t0017a0001c0001t0052a0001c0001t0062others(5): Show | 11 | HG00558.hp2 HG01074.hp2 HG01099.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1637_*1640delAAAA | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 18/18 | 1637 | chr11 | 89325115 | |||||
| chr11:89325115
|
CTTTTTTT others(4): Show |
C | 3 | a0001c0001t0031a0001c0001t0071a0001c0001t0112 | 4 | HG02922.hp1 HG03209.hp1 NA18522.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1630_*1640delAAAA others(7): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 18/18 | 1630 | chr11 | 89325115 | |||||
| chr11:89325115
|
CTTTTTTT others(6): Show |
C | 1 | a0001c0001t0086 | 1 | HG02622.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1628_*1640delAAAA others(9): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 18/18 | 1628 | chr11 | 89325115 | |||||
| chr11:89325117
|
T | C | 1 | a0001c0001t0063 | 1 | HG01106.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1639A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 18/18 | 1639 | chr11 | 89325117 | |||||
| chr11:89325118
|
T | C | 3 | a0001c0001t0010a0001c0001t0064a0001c0001t0114 | 7 | HG00140.hp1 HG00323.hp2 HG00735.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1638A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 18/18 | 1638 | chr11 | 89325118 | |||||
| chr11:89325119
|
T | C | 1 | a0001c0001t0065 | 1 | HG01517.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1637A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 18/18 | 1637 | chr11 | 89325119 | |||||
| chr11:89325145
|
G | A | 2 | a0001c0001t0068a0001c0001t0115 | 2 | HG01884.hp2 HG03209.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1611C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 18/18 | 1611 | chr11 | 89325145 | |||||
| chr11:89325146
|
A | G | 28 | a0001c0002t0006a0001c0002t0009a0001c0002t0011others(25): Show | 52 | HG00621.hp1 HG01109.hp1 HG01884.hp1 others(49): Show |
3_prime_UTR_variant | MODIFIER | c.*1610T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 18/18 | 1610 | chr11 | 89325146 | |||||
| chr11:89325159
|
C | T | 5 | a0001c0001t0021a0001c0001t0055a0001c0001t0056others(2): Show | 7 | HG00673.hp2 NA18612.hp2 NA18951.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1597G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 18/18 | 1597 | chr11 | 89325159 | |||||
| chr11:89325263
|
A | T | 3 | a0001c0001t0048a0001c0001t0049a0001c0001t0079 | 3 | HG02895.hp2 HG02897.hp1 HG02965.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1493T>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 18/18 | 1493 | chr11 | 89325263 | |||||
| chr11:89325272
|
C | T | 1 | a0001c0001t0054 | 1 | HG04115.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1484G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 18/18 | 1484 | chr11 | 89325272 | |||||
| chr11:89325273
|
G | A | 2 | a0001c0001t0058a0001c0001t0110 | 2 | HG00642.hp1 HG01952.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1483C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 18/18 | 1483 | chr11 | 89325273 | |||||
| chr11:89325297
|
T | C | 1 | a0001c0001t0071 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1459A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 18/18 | 1459 | chr11 | 89325297 | |||||
| chr11:89325499
|
A | G | 1 | a0001c0001t0053 | 1 | HG00323.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1257T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 18/18 | 1257 | chr11 | 89325499 | |||||
| chr11:89325885
|
G | GTA | 9 | a0001c0001t0022a0001c0001t0024a0001c0001t0027others(6): Show | 13 | HG00408.hp1 HG00408.hp2 HG01081.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*869_*870dupTA | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 18/18 | 870 | chr11 | 89325885 | |||||
| chr11:89325885
|
GTA | G | 25 | a0001c0001t0014a0001c0001t0017a0001c0001t0031others(22): Show | 52 | HG00621.hp1 HG01074.hp2 HG01346.hp1 others(49): Show |
3_prime_UTR_variant | MODIFIER | c.*869_*870delTA | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 18/18 | 869 | chr11 | 89325885 | |||||
| chr11:89325885
|
GTATA | G | 13 | a0001c0001t0048a0001c0001t0049a0001c0001t0079others(10): Show | 16 | HG01109.hp1 HG02895.hp2 HG02897.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*867_*870delTATA | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 18/18 | 867 | chr11 | 89325885 | |||||
| chr11:89325885
|
GTATATA | G | 14 | a0001c0001t0004a0001c0001t0005a0001c0001t0013others(11): Show | 31 | HG00140.hp2 HG00639.hp2 HG00642.hp2 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*865_*870delTATATA | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 18/18 | 865 | chr11 | 89325885 | |||||
| chr11:89325887
|
A | G | 3 | a0001c0001t0050a0001c0001t0084a0001c0001t0111 | 3 | HG02922.hp2 HG03688.hp2 NA18522.hp2 |
3_prime_UTR_variant | MODIFIER | c.*869T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 18/18 | 869 | chr11 | 89325887 | |||||
| chr11:89325893
|
A | G | 1 | a0001c0001t0047 | 1 | HG02738.hp1 | 3_prime_UTR_variant | MODIFIER | c.*863T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 18/18 | 863 | chr11 | 89325893 | |||||
| chr11:89325903
|
ATATATAT others(1): Show |
A | 5 | a0001c0001t0060a0001c0001t0072a0001c0001t0084others(2): Show | 5 | HG02922.hp1 HG02922.hp2 HG03669.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*845_*852delCATATA others(2): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 18/18 | 845 | chr11 | 89325903 | |||||
| chr11:89325905
|
ATATATG | A | 4 | a0001c0001t0028a0001c0001t0085a0001c0001t0086others(1): Show | 6 | HG01515.hp1 HG02615.hp1 HG02622.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*845_*850delCATATA | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 18/18 | 845 | chr11 | 89325905 | |||||
| chr11:89325907
|
A | G | 1 | a0001c0002t0098 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*849T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 18/18 | 849 | chr11 | 89325907 | |||||
| chr11:89325907
|
ATATG | A | 4 | a0001c0001t0038a0001c0001t0061a0001c0001t0062others(1): Show | 5 | HG00558.hp2 HG02698.hp1 NA18977.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*845_*848delCATA | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 18/18 | 845 | chr11 | 89325907 | |||||
| chr11:89325909
|
A | G | 30 | a0001c0001t0031a0001c0001t0078a0001c0002t0006others(27): Show | 55 | HG00621.hp1 HG01109.hp1 HG01884.hp1 others(52): Show |
3_prime_UTR_variant | MODIFIER | c.*847T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 18/18 | 847 | chr11 | 89325909 | |||||
| chr11:89325909
|
ATG | A | 19 | a0001c0001t0010a0001c0001t0012a0001c0001t0016others(16): Show | 32 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*845_*846delCA | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 18/18 | 845 | chr11 | 89325909 | |||||
| chr11:89325911
|
G | A | 11 | a0001c0001t0008a0001c0001t0019a0001c0001t0067others(8): Show | 18 | HG00099.hp1 HG00558.hp1 HG01358.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*845C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 18/18 | 845 | chr11 | 89325911 | |||||
| chr11:89325913
|
G | A | 1 | a0001c0001t0069 | 1 | HG02896.hp2 | 3_prime_UTR_variant | MODIFIER | c.*843C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 18/18 | 843 | chr11 | 89325913 | |||||
| chr11:89325925
|
A | G | 1 | a0001c0001t0073 | 1 | HG02486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*831T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 18/18 | 831 | chr11 | 89325925 | |||||
| chr11:89326042
|
C | T | 1 | a0001c0001t0071 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*714G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 18/18 | 714 | chr11 | 89326042 | |||||
| chr11:89326117
|
T | C | 1 | a0001c0001t0091 | 1 | HG02280.hp2 | 3_prime_UTR_variant | MODIFIER | c.*639A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 18/18 | 639 | chr11 | 89326117 | |||||
| chr11:89326121
|
T | C | 1 | a0001c0001t0116 | 1 | HG00099.hp1 | 3_prime_UTR_variant | MODIFIER | c.*635A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 18/18 | 635 | chr11 | 89326121 | |||||
| chr11:89326311
|
C | T | 1 | a0001c0001t0039 | 1 | NA19005.hp2 | 3_prime_UTR_variant | MODIFIER | c.*445G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 18/18 | 445 | chr11 | 89326311 | |||||
| chr11:89326444
|
T | G | 2 | a0001c0001t0070a0001c0003t0092 | 2 | HG02083.hp1 HG02155.hp1 |
3_prime_UTR_variant | MODIFIER | c.*312A>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 18/18 | 312 | chr11 | 89326444 | |||||
| chr11:89326466
|
T | G | 4 | a0001c0001t0031a0001c0001t0071a0001c0001t0072others(1): Show | 6 | HG02615.hp1 HG03209.hp1 NA18522.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*290A>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 18/18 | 290 | chr11 | 89326466 | |||||
| chr11:89491285
|
A | C | 64 | a0001c0001t0001a0001c0001t0004a0001c0001t0007others(61): Show | 147 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(144): Show |
5_prime_UTR_variant | MODIFIER | c.-39T>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 1/18 | 39 | chr11 | 89491285 | |||||
| chr11:89491298
|
G | A | 5 | a0001c0001t0094a0001c0001t0095a0001c0001t0096others(2): Show | 5 | HG02055.hp1 HG02257.hp2 HG02559.hp1 others(2): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-52C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 1/18 | chr11 | 89491298 | ||||||
| chr11:89491309
|
G | A | 31 | a0001c0001t0002a0001c0001t0012a0001c0001t0037others(28): Show | 67 | HG00099.hp1 HG00642.hp1 HG00735.hp2 others(64): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-63C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 1/18 | chr11 | 89491309 | ||||||
| chr11:89491341
|
G | A | 1 | a0001c0001t0117 | 1 | HG03225.hp1 | 5_prime_UTR_variant | MODIFIER | c.-95C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 1/18 | 95 | chr11 | 89491341 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:89327212
|
G | C | 3 | a0001c0001t0095g0215a0001c0001t0096g0217a0001c0001t0097g0216 | 3 | HG02055.hp1 HG02559.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1617-336C>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 17/17 | chr11 | 89327212 | ||||||
| chr11:89327306
|
A | T | 1 | a0001c0001t0113g0227 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1617-430T>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 17/17 | chr11 | 89327306 | ||||||
| chr11:89327327
|
G | A | 3 | a0001c0001t0048g0044a0001c0001t0049g0043a0001c0001t0079g0169 | 3 | HG02895.hp2 HG02897.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1617-451C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 17/17 | chr11 | 89327327 | ||||||
| chr11:89327432
|
CAT | C | 3 | a0001c0001t0002g0231a0001c0001t0002g0238a0001c0001t0003g0182 | 3 | HG01928.hp1 HG01981.hp1 HG02148.hp1 |
intron_variant | MODIFIER | c.1617-558_1617-557d others(4): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 17/17 | chr11 | 89327432 | ||||||
| chr11:89327453
|
T | C | 1 | a0001c0002t0051g0009 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1617-577A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 17/17 | chr11 | 89327453 | ||||||
| chr11:89327467
|
A | T | 44 | a0001c0002t0006g0021a0001c0002t0006g0025a0001c0002t0006g0034others(41): Show | 44 | HG00621.hp1 HG01884.hp1 HG01891.hp2 others(41): Show |
intron_variant | MODIFIER | c.1617-591T>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 17/17 | chr11 | 89327467 | ||||||
| chr11:89327694
|
T | C | 1 | a0001c0003t0019g0213 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1617-818A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 17/17 | chr11 | 89327694 | ||||||
| chr11:89327763
|
A | G | 4 | a0001c0001t0068g0064a0001c0001t0085g0179a0001c0001t0112g0282others(1): Show | 4 | HG01884.hp2 HG02922.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1617-887T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 17/17 | chr11 | 89327763 | ||||||
| chr11:89327814
|
T | C | 1 | a0001c0001t0001g0098 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1617-938A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 17/17 | chr11 | 89327814 | ||||||
| chr11:89328080
|
A | G | 1 | a0001c0001t0072g0093 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1617-1204T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 17/17 | chr11 | 89328080 | ||||||
| chr11:89328163
|
A | T | 1 | a0001c0002t0009g0232 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1617-1287T>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 17/17 | chr11 | 89328163 | ||||||
| chr11:89328213
|
A | C | 1 | a0001c0001t0001g0035 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1617-1337T>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 17/17 | chr11 | 89328213 | ||||||
| chr11:89328454
|
C | T | 97 | a0001c0001t0004g0003a0001c0001t0004g0011a0001c0001t0005g0149others(94): Show | 97 | HG00140.hp2 HG00621.hp1 HG00639.hp2 others(94): Show |
intron_variant | MODIFIER | c.1617-1578G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 17/17 | chr11 | 89328454 | ||||||
| chr11:89328479
|
G | A | 35 | a0001c0001t0004g0003a0001c0001t0004g0011a0001c0001t0005g0149others(32): Show | 35 | HG00140.hp2 HG00639.hp2 HG00642.hp2 others(32): Show |
intron_variant | MODIFIER | c.1617-1603C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 17/17 | chr11 | 89328479 | ||||||
| chr11:89328570
|
C | T | 1 | a0001c0001t0052g0122 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1617-1694G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 17/17 | chr11 | 89328570 | ||||||
| chr11:89328604
|
C | T | 2 | a0001c0001t0031g0176a0001c0001t0031g0177 | 2 | HG03209.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1617-1728G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 17/17 | chr11 | 89328604 | ||||||
| chr11:89328664
|
G | A | 1 | a0001c0001t0001g0131 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.1617-1788C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 17/17 | chr11 | 89328664 | ||||||
| chr11:89328690
|
G | A | 42 | a0001c0001t0004g0003a0001c0001t0004g0011a0001c0001t0005g0149others(39): Show | 42 | HG00140.hp2 HG00639.hp2 HG00642.hp2 others(39): Show |
intron_variant | MODIFIER | c.1617-1814C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 17/17 | chr11 | 89328690 | ||||||
| chr11:89328710
|
T | C | 52 | a0001c0002t0006g0021a0001c0002t0006g0025a0001c0002t0006g0034others(49): Show | 52 | HG00621.hp1 HG01109.hp1 HG01884.hp1 others(49): Show |
intron_variant | MODIFIER | c.1617-1834A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 17/17 | chr11 | 89328710 | ||||||
| chr11:89328820
|
T | C | 45 | a0001c0002t0006g0021a0001c0002t0006g0025a0001c0002t0006g0034others(42): Show | 45 | HG00621.hp1 HG01884.hp1 HG01891.hp2 others(42): Show |
intron_variant | MODIFIER | c.1617-1944A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 17/17 | chr11 | 89328820 | ||||||
| chr11:89329043
|
C | A | 2 | a0001c0001t0084g0148a0001c0001t0111g0277 | 2 | HG02922.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1617-2167G>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 17/17 | chr11 | 89329043 | ||||||
| chr11:89329113
|
G | A | 3 | a0001c0001t0017g0160a0001c0001t0017g0165a0001c0001t0107g0225 | 3 | HG02615.hp2 HG02717.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.1617-2237C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 17/17 | chr11 | 89329113 | ||||||
| chr11:89329142
|
G | A | 1 | a0001c0001t0071g0090 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1617-2266C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 17/17 | chr11 | 89329142 | ||||||
| chr11:89329249
|
A | C | 1 | a0001c0001t0063g0067 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1617-2373T>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 17/17 | chr11 | 89329249 | ||||||
| chr11:89329276
|
C | T | 97 | a0001c0001t0004g0003a0001c0001t0004g0011a0001c0001t0005g0149others(94): Show | 97 | HG00140.hp2 HG00621.hp1 HG00639.hp2 others(94): Show |
intron_variant | MODIFIER | c.1617-2400G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 17/17 | chr11 | 89329276 | ||||||
| chr11:89329356
|
G | GA | 6 | a0001c0001t0001g0035a0001c0001t0002g0259a0001c0001t0052g0122others(3): Show | 6 | HG01243.hp2 HG02055.hp1 HG02074.hp2 others(3): Show |
intron_variant | MODIFIER | c.1617-2481dupT | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 17/17 | chr11 | 89329356 | ||||||
| chr11:89329373
|
A | AAAAAG | 6 | a0001c0001t0031g0176a0001c0001t0031g0177a0001c0001t0072g0093others(3): Show | 6 | HG01346.hp1 HG02615.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.1617-2498_1617-249 others(9): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 17/17 | chr11 | 89329373 | ||||||
| chr11:89329373
|
A | AAG | 53 | a0001c0001t0048g0044a0001c0001t0049g0043a0001c0001t0079g0169others(50): Show | 53 | HG00621.hp1 HG01109.hp1 HG01884.hp1 others(50): Show |
intron_variant | MODIFIER | c.1617-2498_1617-249 others(6): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 17/17 | chr11 | 89329373 | ||||||
| chr11:89329373
|
A | AG | 33 | a0001c0001t0004g0003a0001c0001t0004g0011a0001c0001t0005g0149others(30): Show | 33 | HG00140.hp2 HG00639.hp2 HG00642.hp2 others(30): Show |
intron_variant | MODIFIER | c.1617-2498_1617-249 others(5): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 17/17 | chr11 | 89329373 | ||||||
| chr11:89329376
|
G | C | 92 | a0001c0001t0004g0003a0001c0001t0004g0011a0001c0001t0005g0149others(89): Show | 92 | HG00140.hp2 HG00621.hp1 HG00639.hp2 others(89): Show |
intron_variant | MODIFIER | c.1617-2500C>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 17/17 | chr11 | 89329376 | ||||||
| chr11:89329376
|
G | GAAC | 5 | a0001c0001t0071g0090a0001c0002t0006g0034a0001c0002t0006g0085others(2): Show | 5 | HG01978.hp1 NA18977.hp1 NA19001.hp1 others(2): Show |
intron_variant | MODIFIER | c.1617-2503_1617-250 others(7): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 17/17 | chr11 | 89329376 | ||||||
| chr11:89329384
|
C | T | 2 | a0001c0001t0058g0005a0001c0001t0110g0274 | 2 | HG00642.hp1 HG01952.hp1 |
intron_variant | MODIFIER | c.1617-2508G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 17/17 | chr11 | 89329384 | ||||||
| chr11:89329450
|
T | C | 3 | a0001c0001t0001g0063a0001c0001t0024g0155a0001c0001t0081g0163 | 3 | HG01243.hp2 HG03130.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1617-2574A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 17/17 | chr11 | 89329450 | ||||||
| chr11:89329478
|
GA | G | 283 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(280): Show | 284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.1617-2603delT | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 17/17 | chr11 | 89329478 | ||||||
| chr11:89329570
|
C | T | 1 | a0001c0001t0086g0152 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1617-2694G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 17/17 | chr11 | 89329570 | ||||||
| chr11:89329581
|
A | G | 3 | a0001c0001t0072g0093a0001c0001t0085g0179a0001c0001t0112g0282 | 3 | HG02922.hp1 HG02976.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.1617-2705T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 17/17 | chr11 | 89329581 | ||||||
| chr11:89329611
|
G | A | 7 | a0001c0002t0029g0154a0001c0002t0029g0168a0001c0002t0033g0262others(4): Show | 7 | HG01109.hp1 HG02965.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.1617-2735C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 17/17 | chr11 | 89329611 | ||||||
| chr11:89329832
|
C | T | 1 | a0001c0002t0051g0009 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1617-2956G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 17/17 | chr11 | 89329832 | ||||||
| chr11:89330080
|
T | C | 1 | a0001c0001t0050g0080 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1617-3204A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 17/17 | chr11 | 89330080 | ||||||
| chr11:89330101
|
G | A | 1 | a0001c0002t0074g0146 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1617-3225C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 17/17 | chr11 | 89330101 | ||||||
| chr11:89330103
|
A | G | 2 | a0001c0001t0031g0176a0001c0001t0031g0177 | 2 | HG03209.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1617-3227T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 17/17 | chr11 | 89330103 | ||||||
| chr11:89330135
|
A | G | 1 | a0001c0003t0007g0053 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1617-3259T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 17/17 | chr11 | 89330135 | ||||||
| chr11:89330227
|
T | C | 1 | a0001c0001t0071g0090 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1617-3351A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 17/17 | chr11 | 89330227 | ||||||
| chr11:89330255
|
G | A | 2 | a0001c0001t0005g0149a0001c0001t0005g0150 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1617-3379C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 17/17 | chr11 | 89330255 | ||||||
| chr11:89330424
|
G | C | 2 | a0001c0001t0031g0176a0001c0001t0031g0177 | 2 | HG03209.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1617-3548C>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 17/17 | chr11 | 89330424 | ||||||
| chr11:89330450
|
C | T | 8 | a0001c0001t0017g0160a0001c0001t0017g0165a0001c0001t0017g0171others(5): Show | 8 | HG01074.hp2 HG01099.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.1617-3574G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 17/17 | chr11 | 89330450 | ||||||
| chr11:89330480
|
C | T | 1 | a0001c0003t0001g0058 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1617-3604G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 17/17 | chr11 | 89330480 | ||||||
| chr11:89330547
|
T | A | 1 | a0001c0003t0005g0194 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1617-3671A>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 17/17 | chr11 | 89330547 | ||||||
| chr11:89330628
|
GA | G | 40 | a0001c0001t0004g0003a0001c0001t0004g0011a0001c0001t0005g0149others(37): Show | 40 | HG00140.hp2 HG00639.hp2 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.1617-3753delT | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 17/17 | chr11 | 89330628 | ||||||
| chr11:89330745
|
A | G | 44 | a0001c0002t0006g0021a0001c0002t0006g0025a0001c0002t0006g0034others(41): Show | 44 | HG00621.hp1 HG01884.hp1 HG01891.hp2 others(41): Show |
intron_variant | MODIFIER | c.1617-3869T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 17/17 | chr11 | 89330745 | ||||||
| chr11:89330746
|
G | C | 1 | a0001c0001t0001g0060 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1617-3870C>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 17/17 | chr11 | 89330746 | ||||||
| chr11:89330797
|
C | T | 44 | a0001c0002t0006g0021a0001c0002t0006g0025a0001c0002t0006g0034others(41): Show | 44 | HG00621.hp1 HG01884.hp1 HG01891.hp2 others(41): Show |
intron_variant | MODIFIER | c.1617-3921G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 17/17 | chr11 | 89330797 | ||||||
| chr11:89330881
|
T | C | 2 | a0001c0001t0085g0179a0001c0001t0112g0282 | 2 | HG02922.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1617-4005A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 17/17 | chr11 | 89330881 | ||||||
| chr11:89331015
|
T | C | 1 | a0001c0001t0019g0166 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1617-4139A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 17/17 | chr11 | 89331015 | ||||||
| chr11:89331069
|
A | G | 2 | a0001c0001t0084g0148a0001c0001t0111g0277 | 2 | HG02922.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1617-4193T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 17/17 | chr11 | 89331069 | ||||||
| chr11:89331173
|
T | G | 1 | a0001c0002t0035g0229 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1617-4297A>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 17/17 | chr11 | 89331173 | ||||||
| chr11:89331345
|
T | C | 2 | a0001c0001t0056g0055a0001c0001t0059g0054 | 2 | HG00673.hp2 NA18951.hp1 |
intron_variant | MODIFIER | c.1617-4469A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 17/17 | chr11 | 89331345 | ||||||
| chr11:89331365
|
T | C | 1 | a0001c0001t0008g0051 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1616+4480A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 17/17 | chr11 | 89331365 | ||||||
| chr11:89331480
|
A | T | 1 | a0001c0001t0012g0257 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1616+4365T>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 17/17 | chr11 | 89331480 | ||||||
| chr11:89331635
|
G | T | 1 | a0001c0001t0002g0260 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1616+4210C>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 17/17 | chr11 | 89331635 | ||||||
| chr11:89331849
|
C | T | 83 | a0001c0001t0002g0224a0001c0001t0002g0245a0001c0001t0002g0252others(80): Show | 83 | HG00621.hp1 HG00741.hp1 HG01074.hp2 others(80): Show |
intron_variant | MODIFIER | c.1616+3996G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 17/17 | chr11 | 89331849 | ||||||
| chr11:89331857
|
T | C | 2 | a0001c0001t0023g0161a0001c0012t0023g0181 | 2 | HG02486.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1616+3988A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 17/17 | chr11 | 89331857 | ||||||
| chr11:89332092
|
T | A | 1 | a0001c0001t0001g0031 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1616+3753A>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 17/17 | chr11 | 89332092 | ||||||
| chr11:89332148
|
A | G | 4 | a0001c0001t0005g0178a0001c0001t0084g0148a0001c0001t0088g0158others(1): Show | 4 | HG02280.hp2 HG02451.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.1616+3697T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 17/17 | chr11 | 89332148 | ||||||
| chr11:89332208
|
A | AACTG | 101 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0063others(98): Show | 101 | HG00408.hp1 HG00741.hp1 HG01074.hp2 others(98): Show |
intron_variant | MODIFIER | c.1616+3636_1616+363 others(8): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 17/17 | chr11 | 89332208 | ||||||
| chr11:89332223
|
G | C | 1 | a0001c0001t0060g0106 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1616+3622C>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 17/17 | chr11 | 89332223 | ||||||
| chr11:89332242
|
G | A | 29 | a0001c0001t0002g0246a0001c0001t0003g0170a0001c0001t0005g0149others(26): Show | 29 | HG00408.hp1 HG00741.hp1 HG01891.hp2 others(26): Show |
intron_variant | MODIFIER | c.1616+3603C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 17/17 | chr11 | 89332242 | ||||||
| chr11:89332363
|
C | T | 1 | a0001c0001t0001g0059 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1616+3482G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 17/17 | chr11 | 89332363 | ||||||
| chr11:89332497
|
T | C | 1 | a0001c0003t0020g0121 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1616+3348A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 17/17 | chr11 | 89332497 | ||||||
| chr11:89332546
|
T | C | 46 | a0001c0001t0002g0242a0001c0001t0002g0246a0001c0001t0002g0264others(43): Show | 46 | HG00408.hp1 HG00741.hp1 HG01243.hp1 others(43): Show |
intron_variant | MODIFIER | c.1616+3299A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 17/17 | chr11 | 89332546 | ||||||
| chr11:89332649
|
T | C | 2 | a0001c0001t0031g0176a0001c0001t0031g0177 | 2 | HG03209.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1616+3196A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 17/17 | chr11 | 89332649 | ||||||
| chr11:89332651
|
T | C | 1 | a0001c0001t0052g0122 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1616+3194A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 17/17 | chr11 | 89332651 | ||||||
| chr11:89332699
|
C | T | 1 | a0001c0001t0016g0047 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1616+3146G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 17/17 | chr11 | 89332699 | ||||||
| chr11:89333171
|
T | G | 7 | a0001c0001t0002g0224a0001c0001t0002g0252a0001c0001t0002g0254others(4): Show | 7 | HG02451.hp1 HG02622.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.1616+2674A>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 17/17 | chr11 | 89333171 | ||||||
| chr11:89333180
|
C | A | 7 | a0001c0001t0002g0224a0001c0001t0002g0252a0001c0001t0002g0254others(4): Show | 7 | HG02451.hp1 HG02622.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.1616+2665G>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 17/17 | chr11 | 89333180 | ||||||
| chr11:89333462
|
G | GT | 6 | a0001c0001t0002g0224a0001c0001t0002g0252a0001c0001t0002g0254others(3): Show | 6 | HG02451.hp1 HG02622.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.1616+2382dupA | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 17/17 | chr11 | 89333462 | ||||||
| chr11:89333639
|
T | C | 3 | a0001c0001t0023g0161a0001c0001t0071g0090a0001c0012t0023g0181 | 3 | HG02486.hp2 NA19030.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1616+2206A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 17/17 | chr11 | 89333639 | ||||||
| chr11:89333905
|
C | T | 2 | a0001c0002t0029g0154a0001c0002t0029g0168 | 2 | HG01109.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1616+1940G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 17/17 | chr11 | 89333905 | ||||||
| chr11:89334156
|
T | A | 33 | a0001c0003t0001g0058a0001c0003t0003g0193a0001c0003t0003g0201others(30): Show | 33 | HG00140.hp2 HG00639.hp2 HG00642.hp2 others(30): Show |
intron_variant | MODIFIER | c.1616+1689A>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 17/17 | chr11 | 89334156 | ||||||
| chr11:89334186
|
A | G | 60 | a0001c0001t0001g0035a0001c0001t0001g0061a0001c0001t0001g0062others(57): Show | 60 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(57): Show |
intron_variant | MODIFIER | c.1616+1659T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 17/17 | chr11 | 89334186 | ||||||
| chr11:89334256
|
G | A | 1 | a0001c0001t0073g0167 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1616+1589C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 17/17 | chr11 | 89334256 | ||||||
| chr11:89334270
|
A | T | 2 | a0001c0002t0029g0154a0001c0002t0029g0168 | 2 | HG01109.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1616+1575T>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 17/17 | chr11 | 89334270 | ||||||
| chr11:89334271
|
T | C | 42 | a0001c0001t0002g0242a0001c0001t0002g0245a0001c0001t0002g0246others(39): Show | 42 | HG00408.hp1 HG00741.hp1 HG01891.hp2 others(39): Show |
intron_variant | MODIFIER | c.1616+1574A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 17/17 | chr11 | 89334271 | ||||||
| chr11:89334319
|
T | C | 3 | a0001c0001t0001g0063a0001c0001t0022g0140a0001c0002t0100g0258 | 3 | HG01081.hp1 HG02965.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1616+1526A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 17/17 | chr11 | 89334319 | ||||||
| chr11:89334335
|
T | C | 42 | a0001c0001t0002g0242a0001c0001t0002g0245a0001c0001t0002g0246others(39): Show | 42 | HG00408.hp1 HG00741.hp1 HG01891.hp2 others(39): Show |
intron_variant | MODIFIER | c.1616+1510A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 17/17 | chr11 | 89334335 | ||||||
| chr11:89334602
|
A | T | 1 | a0001c0001t0111g0277 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1616+1243T>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 17/17 | chr11 | 89334602 | ||||||
| chr11:89334973
|
A | T | 1 | a0001c0001t0019g0166 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1616+872T>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 17/17 | chr11 | 89334973 | ||||||
| chr11:89335009
|
G | A | 7 | a0001c0001t0052g0122a0001c0001t0069g0015a0001c0001t0071g0090others(4): Show | 7 | HG01099.hp1 HG01109.hp1 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.1616+836C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 17/17 | chr11 | 89335009 | ||||||
| chr11:89335025
|
G | A | 1 | a0001c0005t0040g0137 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.1616+820C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 17/17 | chr11 | 89335025 | ||||||
| chr11:89335074
|
T | C | 1 | a0001c0001t0117g0287 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1616+771A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 17/17 | chr11 | 89335074 | ||||||
| chr11:89335091
|
C | A | 1 | a0001c0003t0001g0058 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1616+754G>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 17/17 | chr11 | 89335091 | ||||||
| chr11:89335137
|
C | G | 33 | a0001c0003t0001g0058a0001c0003t0003g0193a0001c0003t0003g0201others(30): Show | 33 | HG00140.hp2 HG00639.hp2 HG00642.hp2 others(30): Show |
intron_variant | MODIFIER | c.1616+708G>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 17/17 | chr11 | 89335137 | ||||||
| chr11:89335220
|
C | T | 33 | a0001c0003t0001g0058a0001c0003t0003g0193a0001c0003t0003g0201others(30): Show | 33 | HG00140.hp2 HG00639.hp2 HG00642.hp2 others(30): Show |
intron_variant | MODIFIER | c.1616+625G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 17/17 | chr11 | 89335220 | ||||||
| chr11:89335333
|
T | C | 3 | a0001c0001t0052g0122a0001c0001t0069g0015a0001c0001t0082g0174 | 3 | HG01099.hp1 HG02145.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.1616+512A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 17/17 | chr11 | 89335333 | ||||||
| chr11:89335367
|
G | A | 1 | a0001c0001t0001g0045 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1616+478C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 17/17 | chr11 | 89335367 | ||||||
| chr11:89336138
|
C | T | 33 | a0001c0003t0001g0058a0001c0003t0003g0193a0001c0003t0003g0201others(30): Show | 33 | HG00140.hp2 HG00639.hp2 HG00642.hp2 others(30): Show |
intron_variant | MODIFIER | c.1516-193G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 16/17 | chr11 | 89336138 | ||||||
| chr11:89336265
|
A | C | 2 | a0001c0001t0031g0176a0001c0001t0031g0177 | 2 | HG03209.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1516-320T>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 16/17 | chr11 | 89336265 | ||||||
| chr11:89336341
|
A | G | 2 | a0001c0002t0029g0154a0001c0002t0029g0168 | 2 | HG01109.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1516-396T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 16/17 | chr11 | 89336341 | ||||||
| chr11:89336370
|
T | C | 1 | a0001c0001t0016g0012 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1516-425A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 16/17 | chr11 | 89336370 | ||||||
| chr11:89336397
|
A | G | 31 | a0001c0003t0001g0058a0001c0003t0003g0193a0001c0003t0003g0201others(28): Show | 31 | HG00140.hp2 HG00639.hp2 HG00642.hp2 others(28): Show |
intron_variant | MODIFIER | c.1516-452T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 16/17 | chr11 | 89336397 | ||||||
| chr11:89336566
|
G | A | 41 | a0001c0001t0002g0242a0001c0001t0002g0245a0001c0001t0002g0246others(38): Show | 41 | HG00408.hp1 HG00741.hp1 HG01891.hp2 others(38): Show |
intron_variant | MODIFIER | c.1516-621C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 16/17 | chr11 | 89336566 | ||||||
| chr11:89336845
|
T | C | 1 | a0001c0001t0116g0271 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1515+602A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 16/17 | chr11 | 89336845 | ||||||
| chr11:89336954
|
C | T | 34 | a0001c0001t0002g0242a0001c0001t0002g0246a0001c0001t0002g0264others(31): Show | 34 | HG00408.hp1 HG00741.hp1 HG01891.hp2 others(31): Show |
intron_variant | MODIFIER | c.1515+493G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 16/17 | chr11 | 89336954 | ||||||
| chr11:89336959
|
A | C | 1 | a0001c0001t0003g0191 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1515+488T>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 16/17 | chr11 | 89336959 | ||||||
| chr11:89337075
|
T | G | 1 | a0001c0012t0023g0181 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1515+372A>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 16/17 | chr11 | 89337075 | ||||||
| chr11:89337329
|
G | A | 33 | a0001c0003t0001g0058a0001c0003t0003g0193a0001c0003t0003g0201others(30): Show | 33 | HG00140.hp2 HG00639.hp2 HG00642.hp2 others(30): Show |
intron_variant | MODIFIER | c.1515+118C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 16/17 | chr11 | 89337329 | ||||||
| chr11:89337537
|
T | C | 33 | a0001c0003t0001g0058a0001c0003t0003g0193a0001c0003t0003g0201others(30): Show | 33 | HG00140.hp2 HG00639.hp2 HG00642.hp2 others(30): Show |
intron_variant | MODIFIER | c.1447-22A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 15/17 | chr11 | 89337537 | ||||||
| chr11:89337618
|
C | G | 8 | a0001c0001t0017g0160a0001c0001t0017g0165a0001c0001t0048g0044others(5): Show | 8 | HG01884.hp1 HG02615.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1447-103G>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 15/17 | chr11 | 89337618 | ||||||
| chr11:89337857
|
T | C | 3 | a0001c0001t0005g0149a0001c0001t0005g0150a0001c0001t0115g0253 | 3 | HG02896.hp1 HG02897.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1447-342A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 15/17 | chr11 | 89337857 | ||||||
| chr11:89338026
|
G | A | 1 | a0001c0001t0085g0179 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1447-511C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 15/17 | chr11 | 89338026 | ||||||
| chr11:89338061
|
GA | G | 5 | a0001c0001t0001g0131a0001c0001t0002g0266a0001c0001t0002g0268others(2): Show | 5 | HG00735.hp2 HG00741.hp2 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.1447-547delT | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 15/17 | chr11 | 89338061 | ||||||
| chr11:89338159
|
A | G | 7 | a0001c0001t0002g0224a0001c0001t0002g0252a0001c0001t0002g0254others(4): Show | 7 | HG02451.hp1 HG02622.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.1447-644T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 15/17 | chr11 | 89338159 | ||||||
| chr11:89338311
|
A | G | 1 | a0001c0001t0054g0048 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1447-796T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 15/17 | chr11 | 89338311 | ||||||
| chr11:89338813
|
C | T | 1 | a0001c0001t0001g0031 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1446+1250G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 15/17 | chr11 | 89338813 | ||||||
| chr11:89338824
|
A | G | 1 | a0001c0001t0081g0163 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1446+1239T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 15/17 | chr11 | 89338824 | ||||||
| chr11:89339111
|
T | C | 14 | a0001c0001t0017g0160a0001c0001t0017g0165a0001c0001t0024g0155others(11): Show | 14 | HG01099.hp1 HG01109.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.1446+952A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 15/17 | chr11 | 89339111 | ||||||
| chr11:89339151
|
T | C | 1 | a0001c0001t0001g0033 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1446+912A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 15/17 | chr11 | 89339151 | ||||||
| chr11:89339175
|
T | C | 33 | a0001c0003t0001g0058a0001c0003t0003g0193a0001c0003t0003g0201others(30): Show | 33 | HG00140.hp2 HG00639.hp2 HG00642.hp2 others(30): Show |
intron_variant | MODIFIER | c.1446+888A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 15/17 | chr11 | 89339175 | ||||||
| chr11:89339242
|
T | A | 217 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0008others(214): Show | 217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
intron_variant | MODIFIER | c.1446+821A>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 15/17 | chr11 | 89339242 | ||||||
| chr11:89339269
|
G | A | 3 | a0001c0001t0017g0171a0001c0001t0017g0172a0001c0001t0024g0155 | 3 | HG01074.hp2 HG02723.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1446+794C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 15/17 | chr11 | 89339269 | ||||||
| chr11:89339547
|
T | G | 2 | a0001c0001t0002g0245a0001c0001t0002g0279 | 2 | HG02258.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1446+516A>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 15/17 | chr11 | 89339547 | ||||||
| chr11:89339883
|
A | T | 2 | a0001c0002t0029g0154a0001c0002t0029g0168 | 2 | HG01109.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1446+180T>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 15/17 | chr11 | 89339883 | ||||||
| chr11:89340246
|
G | C | 33 | a0001c0003t0001g0058a0001c0003t0003g0193a0001c0003t0003g0201others(30): Show | 33 | HG00140.hp2 HG00639.hp2 HG00642.hp2 others(30): Show |
intron_variant | MODIFIER | c.1338-75C>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 14/17 | chr11 | 89340246 | ||||||
| chr11:89340363
|
A | T | 2 | a0001c0001t0024g0210a0001c0002t0076g0209 | 2 | NA18962.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.1338-192T>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 14/17 | chr11 | 89340363 | ||||||
| chr11:89340409
|
GTGTTAAA | G | 170 | a0001c0001t0001g0035a0001c0001t0001g0061a0001c0001t0001g0062others(167): Show | 170 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.1338-245_1338-239d others(9): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 14/17 | chr11 | 89340409 | ||||||
| chr11:89340742
|
C | T | 2 | a0001c0002t0044g0017a0001c0002t0102g0226 | 2 | NA19001.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.1338-571G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 14/17 | chr11 | 89340742 | ||||||
| chr11:89340807
|
A | G | 6 | a0001c0001t0001g0098a0001c0001t0012g0222a0001c0001t0056g0055others(3): Show | 6 | HG00673.hp2 NA18942.hp2 NA18951.hp1 others(3): Show |
intron_variant | MODIFIER | c.1338-636T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 14/17 | chr11 | 89340807 | ||||||
| chr11:89341124
|
C | CT | 58 | a0001c0001t0002g0242a0001c0001t0002g0245a0001c0001t0002g0246others(55): Show | 58 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(55): Show |
intron_variant | MODIFIER | c.1337+949dupA | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 14/17 | chr11 | 89341124 | ||||||
| chr11:89341124
|
CT | C | 31 | a0001c0001t0018g0142a0001c0001t0018g0175a0001c0003t0001g0058others(28): Show | 31 | HG00140.hp2 HG00639.hp2 HG00642.hp2 others(28): Show |
intron_variant | MODIFIER | c.1337+949delA | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 14/17 | chr11 | 89341124 | ||||||
| chr11:89341214
|
C | T | 2 | a0001c0001t0031g0176a0001c0001t0031g0177 | 2 | HG03209.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1337+860G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 14/17 | chr11 | 89341214 | ||||||
| chr11:89341400
|
G | T | 7 | a0001c0001t0002g0245a0001c0001t0002g0279a0001c0001t0002g0283others(4): Show | 7 | HG02258.hp1 HG02280.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1337+674C>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 14/17 | chr11 | 89341400 | ||||||
| chr11:89341508
|
C | T | 1 | a0001c0003t0007g0053 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1337+566G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 14/17 | chr11 | 89341508 | ||||||
| chr11:89341818
|
G | A | 6 | a0001c0001t0081g0163a0001c0001t0086g0152a0001c0002t0033g0262others(3): Show | 6 | HG01243.hp2 HG02622.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.1337+256C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 14/17 | chr11 | 89341818 | ||||||
| chr11:89341906
|
C | A | 1 | a0001c0001t0001g0029 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1337+168G>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 14/17 | chr11 | 89341906 | ||||||
| chr11:89341924
|
T | A | 1 | a0001c0001t0066g0096 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1337+150A>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 14/17 | chr11 | 89341924 | ||||||
| chr11:89341934
|
C | T | 34 | a0001c0001t0002g0242a0001c0001t0002g0246a0001c0001t0002g0264others(31): Show | 34 | HG00408.hp1 HG00741.hp1 HG01891.hp2 others(31): Show |
intron_variant | MODIFIER | c.1337+140G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 14/17 | chr11 | 89341934 | ||||||
| chr11:89342041
|
T | C | 8 | a0001c0001t0001g0063a0001c0001t0002g0252a0001c0001t0005g0178others(5): Show | 8 | HG01081.hp1 HG01884.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1337+33A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 14/17 | chr11 | 89342041 | ||||||
| chr11:89342199
|
G | A | 5 | a0001c0001t0002g0224a0001c0001t0002g0254a0001c0001t0106g0228others(2): Show | 5 | HG02451.hp1 HG02922.hp1 HG03098.hp2 others(2): Show |
splice_region_variant&intron_variant | LOW | c.1218-6C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 13/17 | chr11 | 89342199 | ||||||
| chr11:89342236
|
G | T | 34 | a0001c0001t0002g0242a0001c0001t0002g0246a0001c0001t0002g0264others(31): Show | 34 | HG00408.hp1 HG00741.hp1 HG01891.hp2 others(31): Show |
intron_variant | MODIFIER | c.1218-43C>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 13/17 | chr11 | 89342236 | ||||||
| chr11:89342276
|
T | A | 4 | a0001c0001t0002g0255a0001c0001t0111g0277a0001c0002t0026g0046others(1): Show | 4 | HG02055.hp2 HG02922.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1218-83A>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 13/17 | chr11 | 89342276 | ||||||
| chr11:89342387
|
C | T | 4 | a0001c0001t0052g0122a0001c0001t0082g0174a0001c0002t0029g0154others(1): Show | 4 | HG01099.hp1 HG01109.hp1 HG02145.hp2 others(1): Show |
intron_variant | MODIFIER | c.1218-194G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 13/17 | chr11 | 89342387 | ||||||
| chr11:89342586
|
A | G | 34 | a0001c0001t0021g0124a0001c0003t0001g0058a0001c0003t0003g0193others(31): Show | 34 | HG00140.hp2 HG00639.hp2 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.1218-393T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 13/17 | chr11 | 89342586 | ||||||
| chr11:89342596
|
T | C | 1 | a0001c0001t0001g0110 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1218-403A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 13/17 | chr11 | 89342596 | ||||||
| chr11:89342670
|
G | T | 8 | a0001c0001t0001g0063a0001c0001t0002g0252a0001c0001t0005g0178others(5): Show | 8 | HG01081.hp1 HG01884.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1218-477C>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 13/17 | chr11 | 89342670 | ||||||
| chr11:89342871
|
A | G | 8 | a0001c0001t0001g0063a0001c0001t0002g0252a0001c0001t0005g0178others(5): Show | 8 | HG01081.hp1 HG01884.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1218-678T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 13/17 | chr11 | 89342871 | ||||||
| chr11:89343092
|
C | T | 1 | a0001c0001t0014g0036 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1218-899G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 13/17 | chr11 | 89343092 | ||||||
| chr11:89343156
|
G | A | 2 | a0001c0001t0052g0122a0001c0001t0082g0174 | 2 | HG01099.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.1218-963C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 13/17 | chr11 | 89343156 | ||||||
| chr11:89343198
|
C | T | 7 | a0001c0001t0001g0063a0001c0001t0002g0252a0001c0001t0005g0178others(4): Show | 7 | HG01081.hp1 HG02280.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.1218-1005G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 13/17 | chr11 | 89343198 | ||||||
| chr11:89343313
|
C | T | 40 | a0001c0001t0002g0242a0001c0001t0002g0245a0001c0001t0002g0246others(37): Show | 40 | HG00408.hp1 HG00741.hp1 HG01891.hp2 others(37): Show |
intron_variant | MODIFIER | c.1218-1120G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 13/17 | chr11 | 89343313 | ||||||
| chr11:89343461
|
A | AT | 21 | a0001c0001t0002g0224a0001c0001t0002g0254a0001c0001t0002g0256others(18): Show | 21 | HG01074.hp2 HG01884.hp1 HG02451.hp1 others(18): Show |
intron_variant | MODIFIER | c.1218-1269dupA | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 13/17 | chr11 | 89343461 | ||||||
| chr11:89343477
|
A | G | 1 | a0001c0001t0007g0141 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1218-1284T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 13/17 | chr11 | 89343477 | ||||||
| chr11:89343656
|
G | A | 2 | a0002c0004t0032g0144a0002c0004t0032g0162 | 2 | HG02615.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1218-1463C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 13/17 | chr11 | 89343656 | ||||||
| chr11:89343763
|
G | T | 7 | a0001c0001t0002g0255a0001c0001t0072g0093a0001c0002t0009g0278others(4): Show | 7 | HG02055.hp2 HG02257.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.1218-1570C>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 13/17 | chr11 | 89343763 | ||||||
| chr11:89343896
|
T | C | 1 | a0001c0001t0111g0277 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1218-1703A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 13/17 | chr11 | 89343896 | ||||||
| chr11:89343936
|
G | C | 2 | a0001c0001t0012g0222a0001c0002t0042g0136 | 2 | NA18959.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.1218-1743C>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 13/17 | chr11 | 89343936 | ||||||
| chr11:89344176
|
A | T | 5 | a0001c0001t0002g0224a0001c0001t0002g0254a0001c0001t0106g0228others(2): Show | 5 | HG02451.hp1 HG02922.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1218-1983T>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 13/17 | chr11 | 89344176 | ||||||
| chr11:89344360
|
G | C | 1 | a0001c0001t0002g0266 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1218-2167C>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 13/17 | chr11 | 89344360 | ||||||
| chr11:89344977
|
T | C | 1 | a0001c0001t0068g0064 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1218-2784A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 13/17 | chr11 | 89344977 | ||||||
| chr11:89345219
|
T | C | 27 | a0001c0001t0002g0242a0001c0001t0002g0246a0001c0001t0002g0264others(24): Show | 27 | HG00408.hp1 HG02145.hp2 HG02559.hp2 others(24): Show |
intron_variant | MODIFIER | c.1218-3026A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 13/17 | chr11 | 89345219 | ||||||
| chr11:89345386
|
T | C | 1 | a0001c0001t0003g0191 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1218-3193A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 13/17 | chr11 | 89345386 | ||||||
| chr11:89345431
|
AG | A | 34 | a0001c0003t0001g0058a0001c0003t0003g0189a0001c0003t0003g0193others(31): Show | 34 | HG00140.hp2 HG00639.hp2 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.1218-3239delC | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 13/17 | chr11 | 89345431 | ||||||
| chr11:89345579
|
C | A | 2 | a0001c0001t0012g0222a0001c0002t0042g0136 | 2 | NA18959.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.1218-3386G>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 13/17 | chr11 | 89345579 | ||||||
| chr11:89345638
|
C | T | 1 | a0001c0001t0068g0064 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1218-3445G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 13/17 | chr11 | 89345638 | ||||||
| chr11:89345827
|
C | A | 1 | a0001c0001t0071g0090 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1218-3634G>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 13/17 | chr11 | 89345827 | ||||||
| chr11:89345853
|
A | G | 1 | a0001c0001t0002g0270 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1218-3660T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 13/17 | chr11 | 89345853 | ||||||
| chr11:89346153
|
G | C | 96 | a0001c0001t0001g0063a0001c0001t0002g0242a0001c0001t0002g0245others(93): Show | 96 | HG00140.hp2 HG00408.hp1 HG00639.hp2 others(93): Show |
intron_variant | MODIFIER | c.1218-3960C>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 13/17 | chr11 | 89346153 | ||||||
| chr11:89346226
|
T | C | 1 | a0001c0002t0011g0156 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1218-4033A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 13/17 | chr11 | 89346226 | ||||||
| chr11:89346380
|
A | G | 19 | a0001c0001t0003g0170a0001c0001t0005g0149a0001c0001t0005g0150others(16): Show | 19 | HG00741.hp1 HG01074.hp2 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.1218-4187T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 13/17 | chr11 | 89346380 | ||||||
| chr11:89346471
|
A | T | 1 | a0001c0001t0018g0142 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1218-4278T>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 13/17 | chr11 | 89346471 | ||||||
| chr11:89346472
|
T | TA | 9 | a0001c0001t0017g0160a0001c0001t0017g0165a0001c0001t0048g0044others(6): Show | 9 | HG01884.hp1 HG02615.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.1218-4280dupT | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 13/17 | chr11 | 89346472 | ||||||
| chr11:89346472
|
TA | T | 7 | a0001c0001t0002g0245a0001c0001t0002g0279a0001c0001t0002g0283others(4): Show | 7 | HG02258.hp1 HG02280.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1218-4280delT | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 13/17 | chr11 | 89346472 | ||||||
| chr11:89346484
|
C | A | 13 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0017g0160others(10): Show | 13 | HG01081.hp2 HG01884.hp1 HG01952.hp1 others(10): Show |
intron_variant | MODIFIER | c.1218-4291G>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 13/17 | chr11 | 89346484 | ||||||
| chr11:89346579
|
A | AAATGGCT others(12): Show |
193 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0031others(190): Show | 193 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(190): Show |
intron_variant | MODIFIER | c.1218-4387_1218-438 others(23): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 13/17 | chr11 | 89346579 | ||||||
| chr11:89346579
|
A | AAATGGCT others(9): Show |
1 | a0001c0001t0028g0108 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1218-4387_1218-438 others(20): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 13/17 | chr11 | 89346579 | ||||||
| chr11:89346579
|
A | AAATGGCT others(10): Show |
1 | a0001c0001t0016g0012 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1218-4387_1218-438 others(21): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 13/17 | chr11 | 89346579 | ||||||
| chr11:89346684
|
C | T | 3 | a0001c0001t0002g0255a0001c0002t0026g0046a0001c0002t0030g0145 | 3 | HG02055.hp2 HG03130.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1218-4491G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 13/17 | chr11 | 89346684 | ||||||
| chr11:89346808
|
G | A | 8 | a0001c0001t0017g0160a0001c0001t0017g0165a0001c0001t0048g0044others(5): Show | 8 | HG01884.hp1 HG02615.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1218-4615C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 13/17 | chr11 | 89346808 | ||||||
| chr11:89346980
|
T | C | 3 | a0001c0002t0011g0153a0001c0002t0029g0154a0001c0002t0029g0168 | 3 | HG01109.hp1 HG03098.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1218-4787A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 13/17 | chr11 | 89346980 | ||||||
| chr11:89347012
|
C | A | 1 | a0001c0001t0010g0071 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1218-4819G>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 13/17 | chr11 | 89347012 | ||||||
| chr11:89347238
|
G | A | 1 | a0001c0001t0106g0228 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1218-5045C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 13/17 | chr11 | 89347238 | ||||||
| chr11:89347402
|
C | G | 3 | a0001c0002t0011g0153a0001c0002t0029g0154a0001c0002t0029g0168 | 3 | HG01109.hp1 HG03098.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1218-5209G>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 13/17 | chr11 | 89347402 | ||||||
| chr11:89347402
|
C | T | 1 | a0001c0001t0001g0134 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1218-5209G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 13/17 | chr11 | 89347402 | ||||||
| chr11:89347448
|
T | C | 63 | a0001c0001t0001g0063a0001c0001t0002g0242a0001c0001t0002g0245others(60): Show | 63 | HG00408.hp1 HG00741.hp1 HG01074.hp2 others(60): Show |
intron_variant | MODIFIER | c.1218-5255A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 13/17 | chr11 | 89347448 | ||||||
| chr11:89347461
|
T | G | 4 | a0001c0001t0001g0081a0001c0001t0001g0103a0001c0001t0003g0188others(1): Show | 4 | HG01256.hp2 HG01928.hp2 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.1218-5268A>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 13/17 | chr11 | 89347461 | ||||||
| chr11:89347477
|
T | G | 3 | a0001c0001t0002g0252a0001c0001t0023g0161a0001c0012t0023g0181 | 3 | HG02486.hp2 HG02622.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1218-5284A>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 13/17 | chr11 | 89347477 | ||||||
| chr11:89347482
|
A | G | 2 | a0001c0001t0062g0114a0001c0006t0087g0200 | 2 | HG00558.hp2 NA19076.hp2 |
intron_variant | MODIFIER | c.1218-5289T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 13/17 | chr11 | 89347482 | ||||||
| chr11:89347597
|
C | T | 22 | a0001c0001t0002g0242a0001c0001t0002g0246a0001c0001t0002g0264others(19): Show | 22 | HG00408.hp1 HG02559.hp2 HG02698.hp1 others(19): Show |
intron_variant | MODIFIER | c.1218-5404G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 13/17 | chr11 | 89347597 | ||||||
| chr11:89347771
|
A | T | 1 | a0001c0001t0084g0148 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1218-5578T>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 13/17 | chr11 | 89347771 | ||||||
| chr11:89348134
|
C | G | 7 | a0001c0001t0038g0230a0001c0001t0038g0243a0001c0001t0061g0042others(4): Show | 7 | HG02698.hp1 NA18939.hp2 NA18961.hp1 others(4): Show |
intron_variant | MODIFIER | c.1218-5941G>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 13/17 | chr11 | 89348134 | ||||||
| chr11:89348164
|
T | C | 1 | a0001c0001t0018g0175 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1218-5971A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 13/17 | chr11 | 89348164 | ||||||
| chr11:89348273
|
G | A | 1 | a0001c0003t0089g0195 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1218-6080C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 13/17 | chr11 | 89348273 | ||||||
| chr11:89348306
|
T | C | 1 | a0001c0001t0001g0035 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1218-6113A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 13/17 | chr11 | 89348306 | ||||||
| chr11:89348422
|
C | CA | 34 | a0001c0003t0001g0058a0001c0003t0003g0189a0001c0003t0003g0193others(31): Show | 34 | HG00140.hp2 HG00639.hp2 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.1218-6230dupT | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 13/17 | chr11 | 89348422 | ||||||
| chr11:89348431
|
A | C | 10 | a0001c0001t0003g0170a0001c0001t0005g0149a0001c0001t0005g0150others(7): Show | 10 | HG00741.hp1 HG01891.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.1218-6238T>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 13/17 | chr11 | 89348431 | ||||||
| chr11:89348453
|
C | CTA | 10 | a0001c0001t0002g0255a0001c0001t0018g0175a0001c0001t0085g0179others(7): Show | 10 | HG01109.hp1 HG02055.hp2 HG02922.hp2 others(7): Show |
intron_variant | MODIFIER | c.1218-6262_1218-626 others(6): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 13/17 | chr11 | 89348453 | ||||||
| chr11:89348675
|
T | G | 1 | a0001c0001t0021g0010 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1217+6287A>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 13/17 | chr11 | 89348675 | ||||||
| chr11:89348838
|
T | C | 1 | a0001c0002t0074g0146 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1217+6124A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 13/17 | chr11 | 89348838 | ||||||
| chr11:89348894
|
T | C | 60 | a0001c0001t0001g0063a0001c0001t0002g0242a0001c0001t0002g0245others(57): Show | 60 | HG00408.hp1 HG00741.hp1 HG01074.hp2 others(57): Show |
intron_variant | MODIFIER | c.1217+6068A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 13/17 | chr11 | 89348894 | ||||||
| chr11:89349060
|
G | A | 3 | a0001c0001t0095g0215a0001c0001t0096g0217a0001c0001t0097g0216 | 3 | HG02055.hp1 HG02559.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1217+5902C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 13/17 | chr11 | 89349060 | ||||||
| chr11:89349115
|
T | C | 3 | a0001c0001t0005g0178a0001c0001t0088g0158a0001c0001t0091g0151 | 3 | HG02280.hp2 HG02451.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.1217+5847A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 13/17 | chr11 | 89349115 | ||||||
| chr11:89349125
|
A | G | 8 | a0001c0001t0017g0160a0001c0001t0017g0165a0001c0001t0048g0044others(5): Show | 8 | HG01884.hp1 HG02615.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1217+5837T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 13/17 | chr11 | 89349125 | ||||||
| chr11:89349212
|
G | A | 8 | a0001c0001t0017g0160a0001c0001t0017g0165a0001c0001t0048g0044others(5): Show | 8 | HG01884.hp1 HG02615.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1217+5750C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 13/17 | chr11 | 89349212 | ||||||
| chr11:89349244
|
A | G | 2 | a0001c0001t0062g0114a0001c0006t0087g0200 | 2 | HG00558.hp2 NA19076.hp2 |
intron_variant | MODIFIER | c.1217+5718T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 13/17 | chr11 | 89349244 | ||||||
| chr11:89349265
|
C | T | 1 | a0001c0002t0101g0239 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1217+5697G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 13/17 | chr11 | 89349265 | ||||||
| chr11:89349287
|
A | AAAAAT | 3 | a0001c0001t0001g0006a0001c0001t0002g0269a0001c0006t0024g0199 | 3 | HG00408.hp2 HG00735.hp2 HG01081.hp2 |
intron_variant | MODIFIER | c.1217+5670_1217+567 others(9): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 13/17 | chr11 | 89349287 | ||||||
| chr11:89349287
|
AAAAAT | A | 20 | a0001c0001t0002g0245a0001c0001t0002g0252a0001c0001t0002g0279others(17): Show | 20 | HG01099.hp1 HG01243.hp1 HG01243.hp2 others(17): Show |
intron_variant | MODIFIER | c.1217+5670_1217+567 others(9): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 13/17 | chr11 | 89349287 | ||||||
| chr11:89349287
|
AAAAATAA others(3): Show |
A | 101 | a0001c0001t0001g0063a0001c0001t0002g0224a0001c0001t0002g0242others(98): Show | 101 | HG00140.hp2 HG00408.hp1 HG00639.hp2 others(98): Show |
intron_variant | MODIFIER | c.1217+5665_1217+567 others(14): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 13/17 | chr11 | 89349287 | ||||||
| chr11:89349287
|
AAAAATAA others(13): Show |
A | 4 | a0001c0001t0001g0098a0001c0001t0056g0055a0001c0001t0059g0054others(1): Show | 4 | HG00673.hp2 NA18942.hp2 NA18951.hp1 others(1): Show |
intron_variant | MODIFIER | c.1217+5655_1217+567 others(24): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 13/17 | chr11 | 89349287 | ||||||
| chr11:89349294
|
A | G | 1 | a0001c0001t0002g0276 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1217+5668T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 13/17 | chr11 | 89349294 | ||||||
| chr11:89349334
|
G | A | 34 | a0001c0003t0001g0058a0001c0003t0003g0189a0001c0003t0003g0193others(31): Show | 34 | HG00140.hp2 HG00639.hp2 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.1217+5628C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 13/17 | chr11 | 89349334 | ||||||
| chr11:89349404
|
C | A | 4 | a0001c0001t0002g0224a0001c0001t0002g0254a0001c0001t0106g0228others(1): Show | 4 | HG02451.hp1 HG03098.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1217+5558G>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 13/17 | chr11 | 89349404 | ||||||
| chr11:89349428
|
C | T | 1 | a0001c0001t0050g0080 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1217+5534G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 13/17 | chr11 | 89349428 | ||||||
| chr11:89349626
|
A | G | 1 | a0001c0001t0010g0102 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1217+5336T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 13/17 | chr11 | 89349626 | ||||||
| chr11:89349628
|
A | G | 1 | a0001c0001t0103g0272 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1217+5334T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 13/17 | chr11 | 89349628 | ||||||
| chr11:89349693
|
A | G | 4 | a0001c0001t0071g0090a0001c0002t0033g0285a0001c0002t0098g0284others(1): Show | 4 | HG02976.hp1 HG03195.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.1217+5269T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 13/17 | chr11 | 89349693 | ||||||
| chr11:89349828
|
C | T | 3 | a0001c0002t0011g0153a0001c0002t0029g0154a0001c0002t0029g0168 | 3 | HG01109.hp1 HG03098.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1217+5134G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 13/17 | chr11 | 89349828 | ||||||
| chr11:89349853
|
C | A | 49 | a0001c0001t0001g0063a0001c0001t0002g0242a0001c0001t0002g0245others(46): Show | 49 | HG00408.hp1 HG00741.hp1 HG01074.hp2 others(46): Show |
intron_variant | MODIFIER | c.1217+5109G>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 13/17 | chr11 | 89349853 | ||||||
| chr11:89349870
|
T | A | 2 | a0001c0002t0044g0017a0001c0002t0102g0226 | 2 | NA19001.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.1217+5092A>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 13/17 | chr11 | 89349870 | ||||||
| chr11:89349910
|
T | C | 1 | a0001c0001t0053g0101 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1217+5052A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 13/17 | chr11 | 89349910 | ||||||
| chr11:89350102
|
A | T | 4 | a0001c0001t0002g0224a0001c0001t0002g0254a0001c0001t0106g0228others(1): Show | 4 | HG02451.hp1 HG03098.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1217+4860T>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 13/17 | chr11 | 89350102 | ||||||
| chr11:89350126
|
A | C | 12 | a0001c0001t0002g0252a0001c0001t0005g0178a0001c0001t0018g0175others(9): Show | 12 | HG01099.hp1 HG01243.hp1 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.1217+4836T>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 13/17 | chr11 | 89350126 | ||||||
| chr11:89350206
|
T | A | 1 | a0001c0001t0086g0152 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1217+4756A>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 13/17 | chr11 | 89350206 | ||||||
| chr11:89350219
|
A | T | 54 | a0001c0001t0001g0063a0001c0001t0002g0242a0001c0001t0002g0245others(51): Show | 54 | HG00408.hp1 HG00741.hp1 HG01074.hp2 others(51): Show |
intron_variant | MODIFIER | c.1217+4743T>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 13/17 | chr11 | 89350219 | ||||||
| chr11:89350381
|
T | C | 22 | a0001c0001t0002g0242a0001c0001t0002g0246a0001c0001t0002g0264others(19): Show | 22 | HG00408.hp1 HG02559.hp2 HG02698.hp1 others(19): Show |
intron_variant | MODIFIER | c.1217+4581A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 13/17 | chr11 | 89350381 | ||||||
| chr11:89350657
|
A | C | 61 | a0001c0001t0001g0063a0001c0001t0002g0242a0001c0001t0002g0245others(58): Show | 61 | HG00408.hp1 HG00741.hp1 HG01074.hp2 others(58): Show |
intron_variant | MODIFIER | c.1217+4305T>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 13/17 | chr11 | 89350657 | ||||||
| chr11:89350672
|
T | C | 1 | a0001c0001t0023g0161 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1217+4290A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 13/17 | chr11 | 89350672 | ||||||
| chr11:89350676
|
G | A | 115 | a0001c0001t0001g0063a0001c0001t0002g0224a0001c0001t0002g0242others(112): Show | 115 | HG00140.hp2 HG00408.hp1 HG00639.hp2 others(112): Show |
intron_variant | MODIFIER | c.1217+4286C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 13/17 | chr11 | 89350676 | ||||||
| chr11:89350732
|
GA | G | 3 | a0001c0001t0002g0255a0001c0002t0026g0046a0001c0002t0030g0145 | 3 | HG02055.hp2 HG03130.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1217+4229delT | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 13/17 | chr11 | 89350732 | ||||||
| chr11:89350977
|
G | A | 9 | a0001c0001t0005g0178a0001c0001t0018g0175a0001c0001t0081g0163others(6): Show | 9 | HG01099.hp1 HG01243.hp1 HG01243.hp2 others(6): Show |
intron_variant | MODIFIER | c.1217+3985C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 13/17 | chr11 | 89350977 | ||||||
| chr11:89351038
|
C | T | 1 | a0001c0003t0089g0195 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1217+3924G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 13/17 | chr11 | 89351038 | ||||||
| chr11:89351039
|
G | A | 23 | a0001c0001t0002g0242a0001c0001t0002g0246a0001c0001t0002g0264others(20): Show | 23 | HG00408.hp1 HG02559.hp2 HG02698.hp1 others(20): Show |
intron_variant | MODIFIER | c.1217+3923C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 13/17 | chr11 | 89351039 | ||||||
| chr11:89351065
|
G | T | 5 | a0001c0001t0017g0160a0001c0001t0017g0165a0001c0001t0107g0225others(2): Show | 5 | HG01884.hp1 HG02615.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1217+3897C>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 13/17 | chr11 | 89351065 | ||||||
| chr11:89351213
|
C | T | 1 | a0001c0002t0006g0021 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1217+3749G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 13/17 | chr11 | 89351213 | ||||||
| chr11:89351379
|
C | T | 6 | a0001c0001t0012g0244a0001c0001t0015g0019a0001c0001t0015g0078others(3): Show | 6 | NA18941.hp1 NA18962.hp2 NA18968.hp1 others(3): Show |
intron_variant | MODIFIER | c.1217+3583G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 13/17 | chr11 | 89351379 | ||||||
| chr11:89351398
|
A | C | 4 | a0001c0001t0002g0224a0001c0001t0002g0254a0001c0001t0073g0167others(1): Show | 4 | HG02451.hp1 HG02486.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1217+3564T>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 13/17 | chr11 | 89351398 | ||||||
| chr11:89351502
|
C | T | 11 | a0001c0001t0001g0063a0001c0001t0002g0245a0001c0001t0002g0279others(8): Show | 11 | HG01081.hp1 HG02258.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.1217+3460G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 13/17 | chr11 | 89351502 | ||||||
| chr11:89351645
|
G | A | 1 | a0001c0001t0001g0073 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1217+3317C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 13/17 | chr11 | 89351645 | ||||||
| chr11:89351739
|
C | T | 1 | a0001c0002t0034g0250 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1217+3223G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 13/17 | chr11 | 89351739 | ||||||
| chr11:89351869
|
A | T | 22 | a0001c0001t0002g0242a0001c0001t0002g0246a0001c0001t0002g0264others(19): Show | 22 | HG00408.hp1 HG02559.hp2 HG02698.hp1 others(19): Show |
intron_variant | MODIFIER | c.1217+3093T>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 13/17 | chr11 | 89351869 | ||||||
| chr11:89351898
|
T | A | 1 | a0001c0001t0091g0151 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1217+3064A>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 13/17 | chr11 | 89351898 | ||||||
| chr11:89351977
|
A | G | 34 | a0001c0003t0001g0058a0001c0003t0003g0189a0001c0003t0003g0193others(31): Show | 34 | HG00140.hp2 HG00639.hp2 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.1217+2985T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 13/17 | chr11 | 89351977 | ||||||
| chr11:89352221
|
A | G | 1 | a0001c0003t0013g0041 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1217+2741T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 13/17 | chr11 | 89352221 | ||||||
| chr11:89352239
|
C | T | 5 | a0001c0001t0081g0163a0001c0001t0082g0174a0001c0001t0086g0152others(2): Show | 5 | HG01099.hp1 HG01243.hp1 HG01243.hp2 others(2): Show |
intron_variant | MODIFIER | c.1217+2723G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 13/17 | chr11 | 89352239 | ||||||
| chr11:89352313
|
C | A | 4 | a0001c0001t0002g0224a0001c0001t0002g0254a0001c0001t0106g0228others(1): Show | 4 | HG02451.hp1 HG03098.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1217+2649G>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 13/17 | chr11 | 89352313 | ||||||
| chr11:89352325
|
A | G | 1 | a0001c0001t0071g0090 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1217+2637T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 13/17 | chr11 | 89352325 | ||||||
| chr11:89352472
|
C | T | 2 | a0001c0001t0024g0210a0001c0002t0076g0209 | 2 | NA18962.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.1217+2490G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 13/17 | chr11 | 89352472 | ||||||
| chr11:89352633
|
C | G | 146 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0063others(143): Show | 146 | HG00140.hp2 HG00408.hp1 HG00621.hp2 others(143): Show |
intron_variant | MODIFIER | c.1217+2329G>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 13/17 | chr11 | 89352633 | ||||||
| chr11:89352792
|
T | C | 37 | a0001c0003t0001g0058a0001c0003t0003g0189a0001c0003t0003g0193others(34): Show | 37 | HG00140.hp2 HG00639.hp2 HG00642.hp2 others(34): Show |
intron_variant | MODIFIER | c.1217+2170A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 13/17 | chr11 | 89352792 | ||||||
| chr11:89353002
|
T | C | 1 | a0001c0001t0001g0023 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1217+1960A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 13/17 | chr11 | 89353002 | ||||||
| chr11:89353004
|
G | A | 9 | a0001c0001t0017g0160a0001c0001t0017g0165a0001c0001t0048g0044others(6): Show | 9 | HG01884.hp1 HG02615.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.1217+1958C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 13/17 | chr11 | 89353004 | ||||||
| chr11:89353056
|
C | T | 1 | a0001c0001t0071g0090 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1217+1906G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 13/17 | chr11 | 89353056 | ||||||
| chr11:89353071
|
G | A | 37 | a0001c0003t0001g0058a0001c0003t0003g0189a0001c0003t0003g0193others(34): Show | 37 | HG00140.hp2 HG00639.hp2 HG00642.hp2 others(34): Show |
intron_variant | MODIFIER | c.1217+1891C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 13/17 | chr11 | 89353071 | ||||||
| chr11:89353420
|
G | C | 5 | a0001c0001t0081g0163a0001c0001t0082g0174a0001c0001t0086g0152others(2): Show | 5 | HG01099.hp1 HG01243.hp1 HG01243.hp2 others(2): Show |
intron_variant | MODIFIER | c.1217+1542C>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 13/17 | chr11 | 89353420 | ||||||
| chr11:89353582
|
T | A | 1 | a0006c0010t0016g0027 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1217+1380A>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 13/17 | chr11 | 89353582 | ||||||
| chr11:89353655
|
C | A | 2 | a0001c0001t0014g0036a0001c0001t0014g0068 | 2 | HG02083.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.1217+1307G>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 13/17 | chr11 | 89353655 | ||||||
| chr11:89353664
|
T | G | 3 | a0001c0001t0017g0171a0001c0001t0017g0172a0001c0001t0024g0155 | 3 | HG01074.hp2 HG02723.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1217+1298A>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 13/17 | chr11 | 89353664 | ||||||
| chr11:89353812
|
G | A | 1 | a0001c0002t0006g0091 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1217+1150C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 13/17 | chr11 | 89353812 | ||||||
| chr11:89354295
|
T | C | 1 | a0001c0001t0003g0205 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1217+667A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 13/17 | chr11 | 89354295 | ||||||
| chr11:89354314
|
G | A | 2 | a0001c0002t0026g0046a0001c0002t0030g0145 | 2 | HG02055.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1217+648C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 13/17 | chr11 | 89354314 | ||||||
| chr11:89354350
|
G | A | 1 | a0001c0001t0052g0122 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1217+612C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 13/17 | chr11 | 89354350 | ||||||
| chr11:89354369
|
C | T | 1 | a0001c0001t0002g0260 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1217+593G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 13/17 | chr11 | 89354369 | ||||||
| chr11:89354468
|
T | C | 144 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0063others(141): Show | 144 | HG00140.hp2 HG00408.hp1 HG00621.hp2 others(141): Show |
intron_variant | MODIFIER | c.1217+494A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 13/17 | chr11 | 89354468 | ||||||
| chr11:89354475
|
T | A | 103 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0063others(100): Show | 103 | HG00408.hp1 HG00741.hp1 HG01074.hp2 others(100): Show |
intron_variant | MODIFIER | c.1217+487A>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 13/17 | chr11 | 89354475 | ||||||
| chr11:89354617
|
C | A | 1 | a0001c0001t0018g0175 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1217+345G>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 13/17 | chr11 | 89354617 | ||||||
| chr11:89354659
|
G | T | 1 | a0001c0001t0007g0126 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1217+303C>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 13/17 | chr11 | 89354659 | ||||||
| chr11:89354661
|
C | T | 1 | a0001c0001t0001g0073 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1217+301G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 13/17 | chr11 | 89354661 | ||||||
| chr11:89354729
|
C | T | 7 | a0001c0001t0018g0142a0001c0001t0052g0122a0001c0001t0081g0163others(4): Show | 7 | HG01099.hp1 HG01243.hp1 HG01243.hp2 others(4): Show |
intron_variant | MODIFIER | c.1217+233G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 13/17 | chr11 | 89354729 | ||||||
| chr11:89354735
|
C | T | 2 | a0002c0004t0032g0144a0002c0004t0032g0162 | 2 | HG02615.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1217+227G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 13/17 | chr11 | 89354735 | ||||||
| chr11:89355206
|
C | T | 60 | a0001c0001t0002g0242a0001c0001t0002g0246a0001c0001t0002g0264others(57): Show | 60 | HG00140.hp2 HG00408.hp1 HG00639.hp2 others(57): Show |
intron_variant | MODIFIER | c.1136-163G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89355206 | ||||||
| chr11:89355230
|
G | GTA | 4 | a0001c0001t0008g0051a0001c0001t0008g0112a0001c0001t0067g0111others(1): Show | 4 | HG01358.hp1 HG01952.hp2 HG01978.hp1 others(1): Show |
intron_variant | MODIFIER | c.1136-189_1136-188d others(4): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89355230 | ||||||
| chr11:89355312
|
A | G | 3 | a0001c0002t0011g0153a0001c0002t0029g0154a0001c0002t0029g0168 | 3 | HG01109.hp1 HG03098.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1136-269T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89355312 | ||||||
| chr11:89355313
|
T | A | 1 | a0001c0001t0117g0287 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1136-270A>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89355313 | ||||||
| chr11:89355331
|
A | ATATT | 23 | a0001c0001t0002g0242a0001c0001t0002g0246a0001c0001t0002g0264others(20): Show | 23 | HG00408.hp1 HG02559.hp2 HG02698.hp1 others(20): Show |
intron_variant | MODIFIER | c.1136-292_1136-289d others(6): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89355331 | ||||||
| chr11:89355354
|
G | A | 1 | a0001c0001t0060g0106 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1136-311C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89355354 | ||||||
| chr11:89355462
|
TC | T | 35 | a0001c0003t0001g0058a0001c0003t0003g0189a0001c0003t0003g0193others(32): Show | 35 | HG00140.hp2 HG00639.hp2 HG00642.hp2 others(32): Show |
intron_variant | MODIFIER | c.1136-420delG | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89355462 | ||||||
| chr11:89355503
|
T | C | 1 | a0001c0001t0111g0277 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1136-460A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89355503 | ||||||
| chr11:89355619
|
T | C | 1 | a0001c0001t0002g0224 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1136-576A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89355619 | ||||||
| chr11:89355773
|
A | G | 35 | a0001c0003t0001g0058a0001c0003t0003g0189a0001c0003t0003g0193others(32): Show | 35 | HG00140.hp2 HG00639.hp2 HG00642.hp2 others(32): Show |
intron_variant | MODIFIER | c.1136-730T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89355773 | ||||||
| chr11:89356049
|
G | A | 23 | a0001c0001t0002g0242a0001c0001t0002g0246a0001c0001t0002g0264others(20): Show | 23 | HG00408.hp1 HG02559.hp2 HG02698.hp1 others(20): Show |
intron_variant | MODIFIER | c.1136-1006C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89356049 | ||||||
| chr11:89356190
|
G | A | 7 | a0001c0003t0003g0193a0001c0003t0003g0201a0001c0003t0004g0037others(4): Show | 7 | HG01074.hp1 HG01346.hp2 HG01358.hp2 others(4): Show |
intron_variant | MODIFIER | c.1136-1147C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89356190 | ||||||
| chr11:89356320
|
A | G | 38 | a0001c0001t0001g0063a0001c0001t0002g0242a0001c0001t0002g0245others(35): Show | 38 | HG00408.hp1 HG01081.hp1 HG02055.hp2 others(35): Show |
intron_variant | MODIFIER | c.1136-1277T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89356320 | ||||||
| chr11:89356338
|
G | C | 7 | a0001c0003t0003g0193a0001c0003t0003g0201a0001c0003t0004g0037others(4): Show | 7 | HG01074.hp1 HG01346.hp2 HG01358.hp2 others(4): Show |
intron_variant | MODIFIER | c.1136-1295C>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89356338 | ||||||
| chr11:89356346
|
A | G | 17 | a0001c0001t0001g0063a0001c0001t0002g0245a0001c0001t0002g0279others(14): Show | 17 | HG01081.hp1 HG02055.hp2 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.1136-1303T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89356346 | ||||||
| chr11:89356381
|
T | A | 9 | a0001c0001t0017g0160a0001c0001t0017g0165a0001c0001t0024g0155others(6): Show | 9 | HG01884.hp1 HG02615.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.1136-1338A>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89356381 | ||||||
| chr11:89356436
|
A | AAAG | 205 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0014others(202): Show | 205 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(202): Show |
intron_variant | MODIFIER | c.1136-1396_1136-139 others(7): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89356436 | ||||||
| chr11:89356508
|
A | T | 1 | a0001c0001t0014g0036 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1136-1465T>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89356508 | ||||||
| chr11:89356659
|
T | C | 9 | a0001c0001t0017g0160a0001c0001t0017g0165a0001c0001t0024g0155others(6): Show | 9 | HG01884.hp1 HG02615.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.1136-1616A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89356659 | ||||||
| chr11:89356709
|
A | C | 9 | a0001c0001t0017g0160a0001c0001t0017g0165a0001c0001t0018g0175others(6): Show | 9 | HG01243.hp1 HG01884.hp1 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.1136-1666T>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89356709 | ||||||
| chr11:89357076
|
G | T | 1 | a0001c0001t0113g0227 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1136-2033C>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89357076 | ||||||
| chr11:89357122
|
A | G | 1 | a0001c0003t0005g0184 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1136-2079T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89357122 | ||||||
| chr11:89357200
|
A | G | 2 | a0001c0001t0048g0044a0001c0001t0049g0043 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1136-2157T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89357200 | ||||||
| chr11:89357216
|
G | GT | 107 | a0001c0001t0001g0014a0001c0001t0001g0063a0001c0001t0002g0245others(104): Show | 107 | HG00408.hp2 HG00621.hp1 HG00639.hp2 others(104): Show |
intron_variant | MODIFIER | c.1136-2174dupA | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89357216 | ||||||
| chr11:89357225
|
T | C | 1 | a0001c0001t0008g0072 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1136-2182A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89357225 | ||||||
| chr11:89357413
|
G | A | 4 | a0001c0001t0001g0131a0001c0001t0002g0266a0001c0001t0002g0269others(1): Show | 4 | HG00735.hp2 HG00741.hp2 HG01071.hp1 others(1): Show |
intron_variant | MODIFIER | c.1136-2370C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89357413 | ||||||
| chr11:89357648
|
C | T | 102 | a0001c0001t0001g0063a0001c0001t0002g0245a0001c0001t0002g0252others(99): Show | 102 | HG00408.hp2 HG00621.hp1 HG00639.hp2 others(99): Show |
intron_variant | MODIFIER | c.1136-2605G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89357648 | ||||||
| chr11:89358023
|
C | T | 8 | a0001c0001t0017g0160a0001c0001t0017g0165a0001c0001t0048g0044others(5): Show | 8 | HG01884.hp1 HG02615.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1136-2980G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89358023 | ||||||
| chr11:89358235
|
A | C | 1 | a0001c0001t0085g0179 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1136-3192T>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89358235 | ||||||
| chr11:89358386
|
CA | C | 190 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(187): Show | 191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.1136-3344delT | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89358386 | ||||||
| chr11:89358386
|
CAA | C | 69 | a0001c0001t0001g0060a0001c0001t0001g0063a0001c0001t0001g0103others(66): Show | 69 | HG00408.hp2 HG00621.hp1 HG00639.hp2 others(66): Show |
intron_variant | MODIFIER | c.1136-3345_1136-334 others(6): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89358386 | ||||||
| chr11:89358386
|
CAAA | C | 18 | a0001c0001t0002g0252a0001c0001t0002g0279a0001c0001t0002g0283others(15): Show | 18 | HG01074.hp1 HG01074.hp2 HG01346.hp2 others(15): Show |
intron_variant | MODIFIER | c.1136-3346_1136-334 others(7): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89358386 | ||||||
| chr11:89358396
|
A | T | 1 | a0001c0003t0023g0202 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1136-3353T>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89358396 | ||||||
| chr11:89358594
|
T | G | 1 | a0001c0003t0090g0211 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1136-3551A>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89358594 | ||||||
| chr11:89358917
|
T | C | 1 | a0001c0002t0009g0278 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1136-3874A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89358917 | ||||||
| chr11:89359004
|
C | T | 1 | a0001c0002t0011g0156 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1136-3961G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89359004 | ||||||
| chr11:89359230
|
A | C | 1 | a0001c0001t0068g0064 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1136-4187T>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89359230 | ||||||
| chr11:89359315
|
C | T | 3 | a0001c0002t0011g0153a0001c0002t0029g0154a0001c0002t0029g0168 | 3 | HG01109.hp1 HG03098.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1136-4272G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89359315 | ||||||
| chr11:89359379
|
A | AT | 16 | a0001c0001t0002g0260a0001c0001t0002g0261a0001c0001t0002g0266others(13): Show | 16 | HG00099.hp1 HG00642.hp1 HG01167.hp1 others(13): Show |
intron_variant | MODIFIER | c.1136-4337dupA | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89359379 | ||||||
| chr11:89359379
|
AT | A | 66 | a0001c0001t0001g0063a0001c0001t0002g0256a0001c0001t0003g0191others(63): Show | 66 | HG00408.hp2 HG00621.hp1 HG00621.hp2 others(63): Show |
intron_variant | MODIFIER | c.1136-4337delA | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89359379 | ||||||
| chr11:89359379
|
ATT | A | 6 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0003g0182others(3): Show | 6 | HG01081.hp2 HG01952.hp1 HG02132.hp2 others(3): Show |
intron_variant | MODIFIER | c.1136-4338_1136-433 others(6): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89359379 | ||||||
| chr11:89359488
|
G | A | 8 | a0001c0001t0017g0160a0001c0001t0017g0165a0001c0001t0048g0044others(5): Show | 8 | HG01884.hp1 HG02615.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1136-4445C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89359488 | ||||||
| chr11:89359506
|
A | G | 5 | a0001c0001t0002g0252a0001c0001t0017g0171a0001c0001t0017g0172others(2): Show | 5 | HG01074.hp2 HG02622.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.1136-4463T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89359506 | ||||||
| chr11:89359574
|
T | C | 4 | a0001c0002t0009g0236a0001c0002t0034g0237a0001c0002t0035g0229others(1): Show | 4 | NA18957.hp1 NA18965.hp2 NA18998.hp2 others(1): Show |
intron_variant | MODIFIER | c.1136-4531A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89359574 | ||||||
| chr11:89359687
|
C | T | 1 | a0001c0001t0057g0127 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1136-4644G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89359687 | ||||||
| chr11:89359866
|
A | C | 8 | a0001c0001t0017g0160a0001c0001t0017g0165a0001c0001t0048g0044others(5): Show | 8 | HG01884.hp1 HG02615.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1136-4823T>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89359866 | ||||||
| chr11:89359995
|
G | A | 51 | a0001c0001t0001g0035a0001c0001t0001g0061a0001c0001t0001g0062others(48): Show | 51 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(48): Show |
intron_variant | MODIFIER | c.1136-4952C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89359995 | ||||||
| chr11:89360016
|
CTA | C | 3 | a0001c0001t0095g0215a0001c0001t0096g0217a0001c0001t0097g0216 | 3 | HG02055.hp1 HG02559.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1136-4975_1136-497 others(6): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89360016 | ||||||
| chr11:89360202
|
A | T | 1 | a0001c0001t0004g0052 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.1136-5159T>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89360202 | ||||||
| chr11:89360244
|
T | A | 18 | a0001c0001t0001g0063a0001c0001t0002g0245a0001c0001t0002g0279others(15): Show | 18 | HG01081.hp1 HG02055.hp2 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.1136-5201A>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89360244 | ||||||
| chr11:89360260
|
T | C | 1 | a0001c0001t0052g0122 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1136-5217A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89360260 | ||||||
| chr11:89360359
|
A | G | 3 | a0001c0002t0033g0285a0001c0002t0098g0284a0001c0002t0099g0286 | 3 | HG02976.hp1 HG03195.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1136-5316T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89360359 | ||||||
| chr11:89360803
|
A | G | 3 | a0001c0001t0048g0044a0001c0001t0049g0043a0001c0001t0079g0169 | 3 | HG02895.hp2 HG02897.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1136-5760T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89360803 | ||||||
| chr11:89360963
|
G | A | 3 | a0001c0001t0001g0008a0001c0001t0004g0003a0001c0001t0008g0002 | 3 | HG00558.hp1 NA18995.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.1136-5920C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89360963 | ||||||
| chr11:89361246
|
A | G | 3 | a0001c0001t0003g0191a0001c0001t0018g0192a0001c0001t0080g0203 | 3 | NA18946.hp1 NA18951.hp2 NA18963.hp2 |
intron_variant | MODIFIER | c.1136-6203T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89361246 | ||||||
| chr11:89361438
|
T | C | 1 | a0001c0002t0009g0278 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1136-6395A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89361438 | ||||||
| chr11:89361461
|
T | C | 1 | a0001c0001t0068g0064 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1136-6418A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89361461 | ||||||
| chr11:89361493
|
A | G | 1 | a0001c0003t0003g0201 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1136-6450T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89361493 | ||||||
| chr11:89361497
|
T | G | 1 | a0001c0001t0017g0165 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1136-6454A>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89361497 | ||||||
| chr11:89361504
|
A | C | 1 | a0001c0003t0092g0196 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1136-6461T>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89361504 | ||||||
| chr11:89361552
|
A | G | 1 | a0001c0003t0003g0212 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1136-6509T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89361552 | ||||||
| chr11:89361654
|
C | A | 1 | a0001c0001t0018g0142 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1136-6611G>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89361654 | ||||||
| chr11:89361654
|
C | T | 1 | a0001c0002t0009g0278 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1136-6611G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89361654 | ||||||
| chr11:89361722
|
T | G | 171 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0035others(168): Show | 171 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(168): Show |
intron_variant | MODIFIER | c.1136-6679A>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89361722 | ||||||
| chr11:89361731
|
C | A | 1 | a0001c0002t0009g0278 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1136-6688G>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89361731 | ||||||
| chr11:89361852
|
T | C | 1 | a0001c0001t0024g0155 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1136-6809A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89361852 | ||||||
| chr11:89361881
|
C | T | 1 | a0001c0001t0003g0188 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1136-6838G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89361881 | ||||||
| chr11:89362114
|
T | C | 2 | a0001c0001t0018g0142a0001c0001t0068g0064 | 2 | HG01884.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1136-7071A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89362114 | ||||||
| chr11:89362118
|
T | C | 1 | a0001c0001t0117g0287 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1136-7075A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89362118 | ||||||
| chr11:89362173
|
G | GACACAGA others(17): Show |
1 | a0001c0002t0009g0278 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1136-7131_1136-713 others(28): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89362173 | ||||||
| chr11:89362173
|
GAC | G | 94 | a0001c0001t0001g0063a0001c0001t0002g0245a0001c0001t0002g0252others(91): Show | 94 | HG00408.hp2 HG00621.hp1 HG00639.hp2 others(91): Show |
intron_variant | MODIFIER | c.1136-7132_1136-713 others(6): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89362173 | ||||||
| chr11:89362276
|
G | A | 1 | a0001c0001t0066g0096 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1136-7233C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89362276 | ||||||
| chr11:89362553
|
A | G | 16 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0002g0256others(13): Show | 16 | HG01081.hp2 HG01952.hp1 HG02132.hp2 others(13): Show |
intron_variant | MODIFIER | c.1136-7510T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89362553 | ||||||
| chr11:89362565
|
G | A | 54 | a0001c0001t0003g0191a0001c0001t0003g0205a0001c0001t0008g0107others(51): Show | 54 | HG00408.hp2 HG00621.hp1 HG00639.hp2 others(51): Show |
intron_variant | MODIFIER | c.1136-7522C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89362565 | ||||||
| chr11:89362605
|
A | G | 201 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0035others(198): Show | 201 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(198): Show |
intron_variant | MODIFIER | c.1136-7562T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89362605 | ||||||
| chr11:89362790
|
C | T | 1 | a0001c0001t0022g0140 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1136-7747G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89362790 | ||||||
| chr11:89362826
|
A | T | 89 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0035others(86): Show | 89 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(86): Show |
intron_variant | MODIFIER | c.1136-7783T>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89362826 | ||||||
| chr11:89363272
|
G | A | 2 | a0002c0004t0032g0144a0002c0004t0032g0162 | 2 | HG02615.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1136-8229C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89363272 | ||||||
| chr11:89363494
|
A | G | 2 | a0001c0001t0109g0281a0001c0001t0116g0271 | 2 | HG00099.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.1136-8451T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89363494 | ||||||
| chr11:89363589
|
T | C | 99 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0035others(96): Show | 99 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(96): Show |
intron_variant | MODIFIER | c.1136-8546A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89363589 | ||||||
| chr11:89363629
|
G | C | 67 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0035others(64): Show | 67 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(64): Show |
intron_variant | MODIFIER | c.1136-8586C>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89363629 | ||||||
| chr11:89363718
|
T | C | 3 | a0001c0002t0006g0083a0001c0002t0006g0084a0001c0002t0006g0085 | 3 | NA18965.hp1 NA18977.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.1136-8675A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89363718 | ||||||
| chr11:89363777
|
C | T | 8 | a0001c0001t0017g0160a0001c0001t0017g0165a0001c0001t0048g0044others(5): Show | 8 | HG01884.hp1 HG02615.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1136-8734G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89363777 | ||||||
| chr11:89363821
|
T | C | 4 | a0001c0001t0001g0131a0001c0001t0002g0266a0001c0001t0002g0269others(1): Show | 4 | HG00735.hp2 HG00741.hp2 HG01071.hp1 others(1): Show |
intron_variant | MODIFIER | c.1136-8778A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89363821 | ||||||
| chr11:89363826
|
A | G | 1 | a0001c0001t0002g0221 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1136-8783T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89363826 | ||||||
| chr11:89363880
|
C | T | 1 | a0001c0001t0068g0064 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1136-8837G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89363880 | ||||||
| chr11:89364536
|
T | C | 1 | a0002c0004t0032g0144 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1135+8896A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89364536 | ||||||
| chr11:89364540
|
T | A | 1 | a0001c0001t0001g0070 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1135+8892A>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89364540 | ||||||
| chr11:89364635
|
A | C | 1 | a0001c0001t0003g0164 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1135+8797T>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89364635 | ||||||
| chr11:89365227
|
G | T | 31 | a0001c0001t0002g0224a0001c0001t0002g0242a0001c0001t0002g0246others(28): Show | 31 | HG00408.hp1 HG00621.hp2 HG02145.hp2 others(28): Show |
intron_variant | MODIFIER | c.1135+8205C>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89365227 | ||||||
| chr11:89365392
|
A | G | 1 | a0001c0001t0068g0064 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1135+8040T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89365392 | ||||||
| chr11:89365455
|
GA | G | 162 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0035others(159): Show | 162 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(159): Show |
intron_variant | MODIFIER | c.1135+7976delT | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89365455 | ||||||
| chr11:89365455
|
GAA | G | 37 | a0001c0001t0001g0063a0001c0001t0002g0245a0001c0001t0002g0279others(34): Show | 37 | HG00741.hp1 HG01081.hp1 HG01099.hp1 others(34): Show |
intron_variant | MODIFIER | c.1135+7975_1135+797 others(6): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89365455 | ||||||
| chr11:89365630
|
T | C | 3 | a0001c0002t0033g0285a0001c0002t0098g0284a0001c0002t0099g0286 | 3 | HG02976.hp1 HG03195.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1135+7802A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89365630 | ||||||
| chr11:89365748
|
G | C | 199 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0035others(196): Show | 199 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(196): Show |
intron_variant | MODIFIER | c.1135+7684C>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89365748 | ||||||
| chr11:89365753
|
C | CA | 79 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0061others(76): Show | 79 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(76): Show |
intron_variant | MODIFIER | c.1135+7678dupT | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89365753 | ||||||
| chr11:89365753
|
C | CAA | 31 | a0001c0001t0001g0032a0001c0001t0002g0279a0001c0001t0014g0036others(28): Show | 31 | HG00408.hp1 HG01106.hp1 HG01243.hp1 others(28): Show |
intron_variant | MODIFIER | c.1135+7677_1135+767 others(6): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89365753 | ||||||
| chr11:89365753
|
C | CAAA | 10 | a0001c0001t0002g0231a0001c0001t0002g0238a0001c0001t0002g0252others(7): Show | 10 | HG00544.hp1 HG01928.hp1 HG01981.hp1 others(7): Show |
intron_variant | MODIFIER | c.1135+7676_1135+767 others(7): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89365753 | ||||||
| chr11:89365753
|
C | CAAAA | 38 | a0001c0001t0001g0035a0001c0001t0001g0070a0001c0001t0001g0088others(35): Show | 38 | HG00408.hp2 HG00621.hp1 HG00639.hp2 others(35): Show |
intron_variant | MODIFIER | c.1135+7675_1135+767 others(8): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89365753 | ||||||
| chr11:89365753
|
C | CAAAAA | 12 | a0001c0001t0003g0191a0001c0001t0071g0090a0001c0002t0006g0084others(9): Show | 12 | HG00642.hp2 HG01346.hp2 HG02300.hp1 others(9): Show |
intron_variant | MODIFIER | c.1135+7674_1135+767 others(9): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89365753 | ||||||
| chr11:89365753
|
C | CAAAAAA | 6 | a0001c0001t0039g0092a0001c0001t0080g0203a0001c0002t0006g0083others(3): Show | 6 | HG01358.hp2 HG01981.hp2 NA18963.hp2 others(3): Show |
intron_variant | MODIFIER | c.1135+7673_1135+767 others(10): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89365753 | ||||||
| chr11:89365753
|
CA | C | 18 | a0001c0001t0001g0026a0001c0001t0001g0029a0001c0001t0001g0030others(15): Show | 18 | HG00741.hp1 HG01109.hp1 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.1135+7678delT | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89365753 | ||||||
| chr11:89365768
|
A | C | 2 | a0001c0001t0008g0112a0001c0001t0067g0111 | 2 | HG01358.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.1135+7664T>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89365768 | ||||||
| chr11:89365776
|
A | C | 1 | a0001c0002t0025g0039 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.1135+7656T>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89365776 | ||||||
| chr11:89365823
|
G | A | 3 | a0001c0001t0048g0044a0001c0001t0049g0043a0001c0001t0079g0169 | 3 | HG02895.hp2 HG02897.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1135+7609C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89365823 | ||||||
| chr11:89366087
|
G | A | 1 | a0001c0001t0019g0166 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1135+7345C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89366087 | ||||||
| chr11:89366095
|
C | T | 46 | a0001c0001t0003g0191a0001c0001t0003g0205a0001c0001t0008g0107others(43): Show | 46 | HG00408.hp2 HG00621.hp1 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.1135+7337G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89366095 | ||||||
| chr11:89366106
|
C | G | 5 | a0001c0001t0002g0252a0001c0001t0017g0171a0001c0001t0017g0172others(2): Show | 5 | HG01074.hp2 HG02622.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.1135+7326G>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89366106 | ||||||
| chr11:89366144
|
G | A | 2 | a0001c0001t0031g0176a0001c0001t0031g0177 | 2 | HG03209.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1135+7288C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89366144 | ||||||
| chr11:89366201
|
T | A | 1 | a0001c0002t0026g0074 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1135+7231A>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89366201 | ||||||
| chr11:89366700
|
GA | G | 183 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0035others(180): Show | 183 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(180): Show |
intron_variant | MODIFIER | c.1135+6731delT | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89366700 | ||||||
| chr11:89366700
|
GAA | G | 15 | a0001c0001t0005g0149a0001c0001t0005g0150a0001c0001t0017g0160others(12): Show | 15 | HG01884.hp1 HG02615.hp1 HG02615.hp2 others(12): Show |
intron_variant | MODIFIER | c.1135+6730_1135+673 others(6): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89366700 | ||||||
| chr11:89366747
|
A | G | 2 | a0001c0001t0018g0142a0001c0001t0068g0064 | 2 | HG01884.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1135+6685T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89366747 | ||||||
| chr11:89366848
|
C | T | 5 | a0001c0001t0002g0224a0001c0001t0002g0254a0001c0001t0002g0255others(2): Show | 5 | HG00621.hp2 HG02451.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.1135+6584G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89366848 | ||||||
| chr11:89366982
|
A | G | 1 | a0001c0001t0068g0064 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1135+6450T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89366982 | ||||||
| chr11:89366996
|
T | A | 5 | a0001c0001t0001g0033a0001c0001t0003g0186a0001c0001t0003g0207others(2): Show | 5 | HG00673.hp1 HG02080.hp1 HG02155.hp2 others(2): Show |
intron_variant | MODIFIER | c.1135+6436A>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89366996 | ||||||
| chr11:89367052
|
C | G | 1 | a0001c0002t0074g0146 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1135+6380G>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89367052 | ||||||
| chr11:89367082
|
T | C | 1 | a0001c0001t0016g0100 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.1135+6350A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89367082 | ||||||
| chr11:89367138
|
T | C | 11 | a0001c0001t0002g0245a0001c0001t0002g0279a0001c0001t0002g0283others(8): Show | 11 | HG02055.hp2 HG02258.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.1135+6294A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89367138 | ||||||
| chr11:89367161
|
A | G | 107 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0035others(104): Show | 107 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(104): Show |
intron_variant | MODIFIER | c.1135+6271T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89367161 | ||||||
| chr11:89367203
|
T | C | 8 | a0001c0003t0004g0066a0001c0003t0004g0076a0001c0003t0004g0116others(5): Show | 8 | HG00639.hp2 HG00642.hp2 HG01106.hp2 others(5): Show |
intron_variant | MODIFIER | c.1135+6229A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89367203 | ||||||
| chr11:89367774
|
C | T | 2 | a0001c0001t0018g0142a0001c0002t0051g0009 | 2 | HG01346.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1135+5658G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89367774 | ||||||
| chr11:89367918
|
C | T | 1 | a0001c0002t0006g0025 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1135+5514G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89367918 | ||||||
| chr11:89367925
|
T | C | 5 | a0001c0001t0002g0252a0001c0001t0017g0171a0001c0001t0017g0172others(2): Show | 5 | HG01074.hp2 HG02622.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.1135+5507A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89367925 | ||||||
| chr11:89367958
|
C | G | 5 | a0001c0001t0002g0252a0001c0001t0017g0171a0001c0001t0017g0172others(2): Show | 5 | HG01074.hp2 HG02622.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.1135+5474G>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89367958 | ||||||
| chr11:89367983
|
C | A | 1 | a0001c0001t0083g0147 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1135+5449G>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89367983 | ||||||
| chr11:89368026
|
C | T | 2 | a0001c0001t0031g0176a0001c0001t0031g0177 | 2 | HG03209.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1135+5406G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89368026 | ||||||
| chr11:89368072
|
G | A | 4 | a0001c0001t0005g0149a0001c0001t0005g0150a0001c0001t0103g0272others(1): Show | 4 | HG02896.hp1 HG02897.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1135+5360C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89368072 | ||||||
| chr11:89368208
|
G | A | 2 | a0001c0001t0031g0176a0001c0001t0031g0177 | 2 | HG03209.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1135+5224C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89368208 | ||||||
| chr11:89368390
|
G | T | 1 | a0001c0001t0002g0256 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1135+5042C>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89368390 | ||||||
| chr11:89368580
|
T | C | 26 | a0001c0001t0003g0170a0001c0001t0005g0149a0001c0001t0005g0150others(23): Show | 26 | HG00741.hp1 HG01099.hp1 HG01109.hp1 others(23): Show |
intron_variant | MODIFIER | c.1135+4852A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89368580 | ||||||
| chr11:89368959
|
A | G | 1 | a0001c0001t0001g0031 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1135+4473T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89368959 | ||||||
| chr11:89368964
|
C | A | 3 | a0001c0001t0005g0178a0001c0001t0088g0158a0001c0001t0091g0151 | 3 | HG02280.hp2 HG02451.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.1135+4468G>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89368964 | ||||||
| chr11:89369016
|
T | C | 102 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0035others(99): Show | 102 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(99): Show |
intron_variant | MODIFIER | c.1135+4416A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89369016 | ||||||
| chr11:89369108
|
G | A | 20 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0014others(17): Show | 20 | HG00099.hp1 HG00558.hp1 HG01256.hp2 others(17): Show |
intron_variant | MODIFIER | c.1135+4324C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89369108 | ||||||
| chr11:89369167
|
A | G | 1 | a0001c0001t0068g0064 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1135+4265T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89369167 | ||||||
| chr11:89369323
|
C | T | 1 | a0001c0002t0035g0248 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1135+4109G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89369323 | ||||||
| chr11:89369430
|
C | T | 2 | a0001c0001t0001g0123a0001c0001t0028g0075 | 2 | HG01515.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.1135+4002G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89369430 | ||||||
| chr11:89369495
|
T | G | 201 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0035others(198): Show | 201 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(198): Show |
intron_variant | MODIFIER | c.1135+3937A>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89369495 | ||||||
| chr11:89369629
|
G | C | 1 | a0001c0001t0012g0222 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1135+3803C>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89369629 | ||||||
| chr11:89369701
|
A | C | 1 | a0001c0001t0117g0287 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1135+3731T>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89369701 | ||||||
| chr11:89369713
|
T | C | 55 | a0001c0001t0003g0191a0001c0001t0003g0205a0001c0001t0008g0107others(52): Show | 55 | HG00408.hp2 HG00621.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.1135+3719A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89369713 | ||||||
| chr11:89369740
|
ATTTATTT others(1): Show |
A | 3 | a0001c0001t0003g0205a0001c0003t0013g0135a0004c0007t0013g0089 | 3 | NA18950.hp2 NA19070.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.1135+3684_1135+369 others(12): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89369740 | ||||||
| chr11:89369744
|
A | ATTTG | 86 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0013others(83): Show | 87 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(84): Show |
intron_variant | MODIFIER | c.1135+3684_1135+368 others(8): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89369744 | ||||||
| chr11:89369744
|
ATTTG | A | 195 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0035others(192): Show | 195 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(192): Show |
intron_variant | MODIFIER | c.1135+3684_1135+368 others(8): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89369744 | ||||||
| chr11:89369764
|
G | A | 199 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0035others(196): Show | 199 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(196): Show |
intron_variant | MODIFIER | c.1135+3668C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89369764 | ||||||
| chr11:89369796
|
A | C | 1 | a0001c0001t0003g0186 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1135+3636T>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89369796 | ||||||
| chr11:89369826
|
G | A | 55 | a0001c0001t0003g0191a0001c0001t0003g0205a0001c0001t0008g0107others(52): Show | 55 | HG00408.hp2 HG00621.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.1135+3606C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89369826 | ||||||
| chr11:89369830
|
G | A | 1 | a0001c0002t0006g0079 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1135+3602C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89369830 | ||||||
| chr11:89369841
|
T | C | 4 | a0001c0001t0005g0149a0001c0001t0005g0150a0001c0001t0103g0272others(1): Show | 4 | HG02896.hp1 HG02897.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1135+3591A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89369841 | ||||||
| chr11:89369929
|
G | GA | 25 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0014others(22): Show | 25 | HG00099.hp1 HG00558.hp1 HG01256.hp2 others(22): Show |
intron_variant | MODIFIER | c.1135+3502dupT | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89369929 | ||||||
| chr11:89370014
|
G | C | 4 | a0001c0001t0017g0171a0001c0001t0017g0172a0001c0001t0117g0287others(1): Show | 4 | HG01074.hp2 HG02723.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1135+3418C>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89370014 | ||||||
| chr11:89370059
|
T | C | 1 | a0001c0001t0001g0028 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1135+3373A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89370059 | ||||||
| chr11:89370110
|
G | T | 3 | a0001c0001t0048g0044a0001c0001t0049g0043a0001c0001t0079g0169 | 3 | HG02895.hp2 HG02897.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1135+3322C>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89370110 | ||||||
| chr11:89370155
|
G | A | 30 | a0001c0001t0002g0224a0001c0001t0002g0242a0001c0001t0002g0246others(27): Show | 30 | HG00408.hp1 HG00621.hp2 HG02451.hp1 others(27): Show |
intron_variant | MODIFIER | c.1135+3277C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89370155 | ||||||
| chr11:89370371
|
G | A | 1 | a0001c0001t0113g0227 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1135+3061C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89370371 | ||||||
| chr11:89370512
|
A | C | 1 | a0001c0001t0002g0252 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1135+2920T>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89370512 | ||||||
| chr11:89370517
|
T | C | 1 | a0001c0002t0075g0183 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1135+2915A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89370517 | ||||||
| chr11:89370565
|
G | A | 8 | a0001c0001t0017g0160a0001c0001t0017g0165a0001c0001t0048g0044others(5): Show | 8 | HG01884.hp1 HG02615.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1135+2867C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89370565 | ||||||
| chr11:89371000
|
A | T | 1 | a0001c0001t0012g0247 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1135+2432T>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89371000 | ||||||
| chr11:89371109
|
G | A | 2 | a0001c0001t0069g0015a0001c0001t0112g0282 | 2 | HG02896.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1135+2323C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89371109 | ||||||
| chr11:89371328
|
C | T | 1 | a0001c0002t0009g0278 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1135+2104G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89371328 | ||||||
| chr11:89371405
|
T | A | 55 | a0001c0001t0003g0191a0001c0001t0003g0205a0001c0001t0008g0107others(52): Show | 55 | HG00408.hp2 HG00621.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.1135+2027A>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89371405 | ||||||
| chr11:89371459
|
G | T | 1 | a0001c0001t0117g0287 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1135+1973C>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89371459 | ||||||
| chr11:89371470
|
A | T | 55 | a0001c0001t0003g0191a0001c0001t0003g0205a0001c0001t0008g0107others(52): Show | 55 | HG00408.hp2 HG00621.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.1135+1962T>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89371470 | ||||||
| chr11:89371521
|
G | A | 4 | a0001c0001t0001g0063a0001c0001t0019g0166a0001c0001t0022g0140others(1): Show | 4 | HG01081.hp1 HG02809.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1135+1911C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89371521 | ||||||
| chr11:89371750
|
C | T | 1 | a0001c0001t0001g0103 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1135+1682G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89371750 | ||||||
| chr11:89371774
|
C | T | 22 | a0001c0001t0002g0242a0001c0001t0002g0246a0001c0001t0002g0264others(19): Show | 22 | HG00408.hp1 HG02698.hp1 HG03139.hp1 others(19): Show |
intron_variant | MODIFIER | c.1135+1658G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89371774 | ||||||
| chr11:89371775
|
G | A | 2 | a0001c0001t0031g0176a0001c0001t0031g0177 | 2 | HG03209.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1135+1657C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89371775 | ||||||
| chr11:89371800
|
C | T | 1 | a0001c0002t0009g0278 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1135+1632G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89371800 | ||||||
| chr11:89371817
|
T | C | 1 | a0001c0001t0010g0102 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1135+1615A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89371817 | ||||||
| chr11:89371997
|
T | A | 1 | a0001c0001t0012g0222 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1135+1435A>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89371997 | ||||||
| chr11:89372025
|
A | G | 1 | a0001c0001t0018g0142 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1135+1407T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89372025 | ||||||
| chr11:89372106
|
T | C | 1 | a0001c0001t0002g0252 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1135+1326A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89372106 | ||||||
| chr11:89372143
|
A | T | 1 | a0001c0001t0016g0047 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1135+1289T>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89372143 | ||||||
| chr11:89372208
|
T | C | 5 | a0001c0001t0002g0224a0001c0001t0002g0254a0001c0001t0002g0255others(2): Show | 5 | HG00621.hp2 HG02451.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.1135+1224A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89372208 | ||||||
| chr11:89372214
|
C | A | 1 | a0001c0001t0010g0133 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1135+1218G>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89372214 | ||||||
| chr11:89372214
|
C | G | 1 | a0001c0002t0006g0091 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1135+1218G>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89372214 | ||||||
| chr11:89372558
|
A | G | 5 | a0001c0001t0002g0252a0001c0001t0017g0171a0001c0001t0017g0172others(2): Show | 5 | HG01074.hp2 HG02622.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.1135+874T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89372558 | ||||||
| chr11:89372579
|
T | C | 1 | a0001c0001t0017g0172 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1135+853A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89372579 | ||||||
| chr11:89372686
|
A | C | 1 | a0001c0001t0018g0142 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1135+746T>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89372686 | ||||||
| chr11:89372812
|
T | A | 1 | a0001c0001t0068g0064 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1135+620A>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89372812 | ||||||
| chr11:89372865
|
G | A | 1 | a0001c0001t0023g0161 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1135+567C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89372865 | ||||||
| chr11:89372958
|
C | T | 1 | a0001c0002t0009g0278 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1135+474G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89372958 | ||||||
| chr11:89373096
|
T | C | 1 | a0001c0001t0038g0230 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1135+336A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89373096 | ||||||
| chr11:89373277
|
C | CA | 23 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0031others(20): Show | 23 | HG00642.hp1 HG00673.hp2 HG00735.hp2 others(20): Show |
intron_variant | MODIFIER | c.1135+154dupT | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89373277 | ||||||
| chr11:89373277
|
CA | C | 51 | a0001c0001t0001g0006a0001c0001t0001g0070a0001c0001t0003g0170others(48): Show | 51 | HG00408.hp2 HG00621.hp1 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.1135+154delT | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89373277 | ||||||
| chr11:89373277
|
CAA | C | 44 | a0001c0001t0001g0063a0001c0001t0002g0245a0001c0001t0002g0252others(41): Show | 44 | HG01074.hp2 HG01081.hp1 HG01099.hp1 others(41): Show |
intron_variant | MODIFIER | c.1135+153_1135+154d others(4): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89373277 | ||||||
| chr11:89373287
|
A | C | 1 | a0001c0001t0004g0011 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1135+145T>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89373287 | ||||||
| chr11:89373294
|
A | C | 1 | a0001c0001t0052g0122 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1135+138T>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89373294 | ||||||
| chr11:89373297
|
A | C | 2 | a0001c0002t0026g0046a0001c0008t0002g0275 | 2 | HG02055.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1135+135T>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89373297 | ||||||
| chr11:89373299
|
C | A | 1 | a0001c0001t0012g0247 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1135+133G>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89373299 | ||||||
| chr11:89373300
|
A | C | 1 | a0001c0001t0012g0247 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1135+132T>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89373300 | ||||||
| chr11:89373320
|
T | C | 1 | a0003c0013t0002g0220 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1135+112A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89373320 | ||||||
| chr11:89373383
|
A | G | 1 | a0001c0002t0026g0046 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1135+49T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 12/17 | chr11 | 89373383 | ||||||
| chr11:89373656
|
C | A | 7 | a0001c0001t0017g0160a0001c0001t0048g0044a0001c0001t0049g0043others(4): Show | 7 | HG01884.hp1 HG02615.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1075-164G>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89373656 | ||||||
| chr11:89373723
|
A | C | 5 | a0001c0001t0002g0245a0001c0001t0002g0279a0001c0001t0002g0283others(2): Show | 5 | HG02258.hp1 HG02717.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.1075-231T>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89373723 | ||||||
| chr11:89373831
|
G | A | 2 | a0001c0001t0048g0044a0001c0001t0049g0043 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1075-339C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89373831 | ||||||
| chr11:89373977
|
T | G | 2 | a0001c0001t0018g0142a0001c0001t0078g0143 | 2 | HG02280.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1075-485A>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89373977 | ||||||
| chr11:89374077
|
T | C | 20 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0014others(17): Show | 20 | HG00099.hp1 HG00558.hp1 HG01256.hp2 others(17): Show |
intron_variant | MODIFIER | c.1075-585A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89374077 | ||||||
| chr11:89374178
|
A | T | 4 | a0001c0001t0018g0175a0001c0002t0033g0285a0001c0002t0098g0284others(1): Show | 4 | HG02976.hp1 HG03195.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.1075-686T>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89374178 | ||||||
| chr11:89374369
|
G | A | 1 | a0001c0002t0030g0159 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1075-877C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89374369 | ||||||
| chr11:89374440
|
T | C | 4 | a0001c0001t0001g0134a0001c0001t0008g0051a0001c0001t0008g0112others(1): Show | 4 | HG01358.hp1 HG01952.hp2 HG01978.hp2 others(1): Show |
intron_variant | MODIFIER | c.1075-948A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89374440 | ||||||
| chr11:89374468
|
C | T | 1 | a0001c0001t0012g0222 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1075-976G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89374468 | ||||||
| chr11:89374507
|
A | G | 2 | a0001c0001t0001g0026a0001c0001t0007g0007 | 2 | NA18944.hp1 NA18957.hp2 |
intron_variant | MODIFIER | c.1075-1015T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89374507 | ||||||
| chr11:89374553
|
T | C | 12 | a0001c0001t0017g0160a0001c0001t0024g0155a0001c0001t0048g0044others(9): Show | 12 | HG01884.hp1 HG02615.hp1 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.1075-1061A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89374553 | ||||||
| chr11:89374554
|
T | C | 3 | a0001c0001t0052g0122a0001c0001t0069g0015a0001c0001t0112g0282 | 3 | HG02145.hp2 HG02896.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1075-1062A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89374554 | ||||||
| chr11:89374719
|
C | T | 22 | a0001c0001t0002g0242a0001c0001t0002g0246a0001c0001t0002g0264others(19): Show | 22 | HG00408.hp1 HG02698.hp1 HG03139.hp1 others(19): Show |
intron_variant | MODIFIER | c.1075-1227G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89374719 | ||||||
| chr11:89374737
|
G | A | 2 | a0001c0001t0018g0142a0001c0001t0078g0143 | 2 | HG02280.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1075-1245C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89374737 | ||||||
| chr11:89374820
|
A | G | 2 | a0001c0001t0017g0171a0001c0001t0017g0172 | 2 | HG01074.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1075-1328T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89374820 | ||||||
| chr11:89374826
|
T | C | 222 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0008others(219): Show | 222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.1075-1334A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89374826 | ||||||
| chr11:89375305
|
T | TTTG | 12 | a0001c0001t0017g0160a0001c0001t0024g0155a0001c0001t0048g0044others(9): Show | 12 | HG01884.hp1 HG02615.hp1 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.1075-1816_1075-181 others(7): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89375305 | ||||||
| chr11:89375470
|
T | C | 1 | a0001c0001t0019g0166 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1075-1978A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89375470 | ||||||
| chr11:89375478
|
T | C | 4 | a0001c0001t0023g0161a0001c0001t0031g0176a0001c0001t0031g0177others(1): Show | 4 | HG02486.hp2 HG03209.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.1075-1986A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89375478 | ||||||
| chr11:89375520
|
C | A | 22 | a0001c0001t0002g0242a0001c0001t0002g0246a0001c0001t0002g0264others(19): Show | 22 | HG00408.hp1 HG02698.hp1 HG03139.hp1 others(19): Show |
intron_variant | MODIFIER | c.1075-2028G>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89375520 | ||||||
| chr11:89375763
|
G | A | 1 | a0001c0001t0072g0093 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1075-2271C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89375763 | ||||||
| chr11:89375797
|
C | T | 2 | a0001c0001t0072g0093a0001c0002t0093g0219 | 2 | HG02257.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.1075-2305G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89375797 | ||||||
| chr11:89375883
|
A | C | 1 | a0001c0003t0003g0193 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1075-2391T>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89375883 | ||||||
| chr11:89375904
|
G | T | 1 | a0001c0002t0034g0250 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1075-2412C>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89375904 | ||||||
| chr11:89376035
|
C | T | 1 | a0001c0001t0023g0161 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1075-2543G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89376035 | ||||||
| chr11:89376043
|
G | A | 2 | a0001c0001t0017g0171a0001c0001t0017g0172 | 2 | HG01074.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1075-2551C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89376043 | ||||||
| chr11:89376145
|
G | A | 4 | a0001c0001t0081g0163a0001c0001t0082g0174a0001c0001t0086g0152others(1): Show | 4 | HG01099.hp1 HG01243.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.1075-2653C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89376145 | ||||||
| chr11:89376216
|
A | G | 1 | a0001c0001t0022g0140 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1075-2724T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89376216 | ||||||
| chr11:89376508
|
G | A | 1 | a0001c0001t0084g0148 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1075-3016C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89376508 | ||||||
| chr11:89376520
|
A | G | 51 | a0001c0001t0003g0170a0001c0001t0003g0191a0001c0001t0003g0205others(48): Show | 51 | HG00408.hp2 HG00621.hp1 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.1075-3028T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89376520 | ||||||
| chr11:89376708
|
C | G | 3 | a0001c0001t0052g0122a0001c0001t0069g0015a0001c0001t0112g0282 | 3 | HG02145.hp2 HG02896.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1075-3216G>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89376708 | ||||||
| chr11:89376743
|
A | G | 28 | a0001c0001t0002g0242a0001c0001t0002g0246a0001c0001t0002g0264others(25): Show | 28 | HG00408.hp1 HG02145.hp2 HG02698.hp1 others(25): Show |
intron_variant | MODIFIER | c.1075-3251T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89376743 | ||||||
| chr11:89376838
|
C | T | 2 | a0001c0001t0018g0142a0001c0001t0078g0143 | 2 | HG02280.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1075-3346G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89376838 | ||||||
| chr11:89376973
|
A | G | 204 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0008others(201): Show | 204 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(201): Show |
intron_variant | MODIFIER | c.1075-3481T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89376973 | ||||||
| chr11:89376978
|
A | T | 1 | a0001c0001t0068g0064 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1075-3486T>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89376978 | ||||||
| chr11:89376989
|
C | T | 4 | a0001c0001t0001g0131a0001c0001t0002g0266a0001c0001t0002g0269others(1): Show | 4 | HG00735.hp2 HG00741.hp2 HG01071.hp1 others(1): Show |
intron_variant | MODIFIER | c.1075-3497G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89376989 | ||||||
| chr11:89377019
|
C | A | 1 | a0001c0002t0034g0250 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1075-3527G>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89377019 | ||||||
| chr11:89377078
|
C | T | 1 | a0001c0012t0023g0181 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1075-3586G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89377078 | ||||||
| chr11:89377182
|
G | A | 22 | a0001c0001t0002g0242a0001c0001t0002g0246a0001c0001t0002g0264others(19): Show | 22 | HG00408.hp1 HG02698.hp1 HG03139.hp1 others(19): Show |
intron_variant | MODIFIER | c.1075-3690C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89377182 | ||||||
| chr11:89377266
|
A | G | 6 | a0001c0001t0052g0122a0001c0001t0069g0015a0001c0001t0112g0282others(3): Show | 6 | HG02145.hp2 HG02896.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.1075-3774T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89377266 | ||||||
| chr11:89377351
|
C | T | 2 | a0001c0001t0117g0287a0001c0002t0074g0146 | 2 | HG03098.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1075-3859G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89377351 | ||||||
| chr11:89377383
|
A | G | 11 | a0001c0001t0017g0160a0001c0001t0024g0155a0001c0001t0048g0044others(8): Show | 11 | HG01884.hp1 HG02615.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.1075-3891T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89377383 | ||||||
| chr11:89377417
|
C | T | 3 | a0001c0002t0033g0285a0001c0002t0098g0284a0001c0002t0099g0286 | 3 | HG02976.hp1 HG03195.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1075-3925G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89377417 | ||||||
| chr11:89377736
|
A | C | 1 | a0001c0001t0001g0006 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1075-4244T>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89377736 | ||||||
| chr11:89378139
|
C | A | 203 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0008others(200): Show | 203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
intron_variant | MODIFIER | c.1075-4647G>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89378139 | ||||||
| chr11:89378214
|
T | G | 51 | a0001c0001t0003g0170a0001c0001t0003g0191a0001c0001t0003g0205others(48): Show | 51 | HG00408.hp2 HG00621.hp1 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.1075-4722A>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89378214 | ||||||
| chr11:89378218
|
T | C | 3 | a0001c0001t0024g0155a0001c0002t0011g0156a0001c0002t0029g0168 | 3 | HG02647.hp2 HG03098.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1075-4726A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89378218 | ||||||
| chr11:89378262
|
C | T | 216 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0008others(213): Show | 216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
intron_variant | MODIFIER | c.1075-4770G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89378262 | ||||||
| chr11:89378276
|
G | A | 8 | a0001c0001t0017g0171a0001c0001t0017g0172a0001c0001t0052g0122others(5): Show | 8 | HG01074.hp2 HG02145.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.1075-4784C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89378276 | ||||||
| chr11:89378719
|
A | G | 1 | a0003c0013t0002g0220 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1075-5227T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89378719 | ||||||
| chr11:89378898
|
T | C | 11 | a0001c0001t0017g0160a0001c0001t0024g0155a0001c0001t0048g0044others(8): Show | 11 | HG01884.hp1 HG02615.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.1075-5406A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89378898 | ||||||
| chr11:89379002
|
A | G | 3 | a0001c0002t0033g0285a0001c0002t0098g0284a0001c0002t0099g0286 | 3 | HG02976.hp1 HG03195.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1075-5510T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89379002 | ||||||
| chr11:89379372
|
T | TA | 22 | a0001c0001t0002g0242a0001c0001t0002g0246a0001c0001t0002g0264others(19): Show | 22 | HG00408.hp1 HG02698.hp1 HG03139.hp1 others(19): Show |
intron_variant | MODIFIER | c.1075-5881dupT | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89379372 | ||||||
| chr11:89379456
|
T | G | 1 | a0001c0001t0001g0060 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1075-5964A>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89379456 | ||||||
| chr11:89379482
|
G | A | 51 | a0001c0001t0003g0170a0001c0001t0003g0191a0001c0001t0003g0205others(48): Show | 51 | HG00408.hp2 HG00621.hp1 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.1075-5990C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89379482 | ||||||
| chr11:89379653
|
C | A | 2 | a0001c0001t0002g0265a0001c0001t0007g0141 | 2 | HG02074.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.1075-6161G>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89379653 | ||||||
| chr11:89379693
|
T | C | 1 | a0001c0001t0002g0261 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1075-6201A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89379693 | ||||||
| chr11:89379733
|
T | C | 118 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0008others(115): Show | 118 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(115): Show |
intron_variant | MODIFIER | c.1075-6241A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89379733 | ||||||
| chr11:89379799
|
T | C | 11 | a0001c0001t0017g0160a0001c0001t0024g0155a0001c0001t0048g0044others(8): Show | 11 | HG01884.hp1 HG02615.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.1075-6307A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89379799 | ||||||
| chr11:89379878
|
C | T | 1 | a0001c0002t0029g0168 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1075-6386G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89379878 | ||||||
| chr11:89380180
|
G | C | 1 | a0001c0002t0098g0284 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1075-6688C>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89380180 | ||||||
| chr11:89380223
|
T | C | 1 | a0001c0001t0085g0179 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1075-6731A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89380223 | ||||||
| chr11:89380537
|
T | C | 3 | a0001c0001t0002g0252a0001c0001t0117g0287a0001c0002t0074g0146 | 3 | HG02622.hp1 HG03098.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1075-7045A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89380537 | ||||||
| chr11:89380538
|
T | C | 2 | a0001c0001t0005g0178a0001c0001t0091g0151 | 2 | HG02280.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.1075-7046A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89380538 | ||||||
| chr11:89380829
|
T | C | 1 | a0001c0001t0017g0172 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1075-7337A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89380829 | ||||||
| chr11:89380893
|
G | A | 4 | a0001c0001t0052g0122a0001c0002t0033g0285a0001c0002t0098g0284others(1): Show | 4 | HG02145.hp2 HG02976.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1075-7401C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89380893 | ||||||
| chr11:89380900
|
T | C | 1 | a0001c0001t0001g0081 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1075-7408A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89380900 | ||||||
| chr11:89380903
|
A | G | 4 | a0001c0001t0005g0149a0001c0001t0005g0150a0001c0001t0103g0272others(1): Show | 4 | HG02896.hp1 HG02897.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1075-7411T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89380903 | ||||||
| chr11:89381018
|
G | C | 4 | a0001c0001t0001g0128a0001c0001t0010g0133a0001c0001t0047g0139others(1): Show | 4 | HG00140.hp1 HG01516.hp1 HG02738.hp1 others(1): Show |
intron_variant | MODIFIER | c.1075-7526C>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89381018 | ||||||
| chr11:89381111
|
T | C | 1 | a0001c0001t0052g0122 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1075-7619A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89381111 | ||||||
| chr11:89381316
|
G | T | 4 | a0001c0001t0052g0122a0001c0002t0033g0285a0001c0002t0098g0284others(1): Show | 4 | HG02145.hp2 HG02976.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1075-7824C>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89381316 | ||||||
| chr11:89381365
|
G | A | 1 | a0001c0002t0029g0168 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1075-7873C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89381365 | ||||||
| chr11:89381407
|
C | T | 22 | a0001c0001t0002g0242a0001c0001t0002g0246a0001c0001t0002g0264others(19): Show | 22 | HG00408.hp1 HG02698.hp1 HG03139.hp1 others(19): Show |
intron_variant | MODIFIER | c.1075-7915G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89381407 | ||||||
| chr11:89381448
|
C | G | 1 | a0001c0001t0068g0064 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1075-7956G>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89381448 | ||||||
| chr11:89381454
|
A | G | 4 | a0001c0001t0012g0247a0001c0001t0015g0057a0001c0001t0072g0093others(1): Show | 4 | HG01109.hp2 HG02257.hp2 NA18988.hp1 others(1): Show |
intron_variant | MODIFIER | c.1075-7962T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89381454 | ||||||
| chr11:89381479
|
C | G | 1 | a0001c0001t0113g0227 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1075-7987G>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89381479 | ||||||
| chr11:89381566
|
G | A | 29 | a0001c0001t0002g0242a0001c0001t0002g0246a0001c0001t0002g0252others(26): Show | 29 | HG00408.hp1 HG02145.hp2 HG02622.hp1 others(26): Show |
intron_variant | MODIFIER | c.1075-8074C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89381566 | ||||||
| chr11:89381656
|
C | A | 1 | a0001c0001t0018g0175 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1075-8164G>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89381656 | ||||||
| chr11:89381656
|
C | T | 1 | a0001c0001t0113g0227 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1075-8164G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89381656 | ||||||
| chr11:89381657
|
G | A | 2 | a0001c0001t0014g0036a0001c0001t0014g0068 | 2 | HG02083.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.1075-8165C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89381657 | ||||||
| chr11:89381683
|
T | C | 2 | a0001c0001t0031g0176a0001c0001t0031g0177 | 2 | HG03209.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1075-8191A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89381683 | ||||||
| chr11:89381693
|
C | CG | 157 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0008others(154): Show | 157 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(154): Show |
intron_variant | MODIFIER | c.1075-8202dupC | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89381693 | ||||||
| chr11:89381754
|
A | T | 22 | a0001c0001t0002g0242a0001c0001t0002g0246a0001c0001t0002g0264others(19): Show | 22 | HG00408.hp1 HG02698.hp1 HG03139.hp1 others(19): Show |
intron_variant | MODIFIER | c.1075-8262T>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89381754 | ||||||
| chr11:89381879
|
T | A | 3 | a0001c0001t0081g0163a0001c0001t0082g0174a0001c0001t0086g0152 | 3 | HG01099.hp1 HG01243.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.1075-8387A>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89381879 | ||||||
| chr11:89381985
|
C | T | 5 | a0001c0001t0005g0149a0001c0001t0005g0150a0001c0001t0017g0165others(2): Show | 5 | HG02809.hp2 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1075-8493G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89381985 | ||||||
| chr11:89381997
|
C | G | 1 | a0001c0001t0001g0070 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1075-8505G>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89381997 | ||||||
| chr11:89382050
|
T | C | 218 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0008others(215): Show | 218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.1075-8558A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89382050 | ||||||
| chr11:89382096
|
C | T | 25 | a0001c0001t0002g0242a0001c0001t0002g0246a0001c0001t0002g0252others(22): Show | 25 | HG00408.hp1 HG02622.hp1 HG02698.hp1 others(22): Show |
intron_variant | MODIFIER | c.1075-8604G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89382096 | ||||||
| chr11:89382185
|
A | C | 1 | a0001c0001t0068g0064 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1075-8693T>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89382185 | ||||||
| chr11:89382208
|
C | T | 4 | a0001c0001t0005g0149a0001c0001t0005g0150a0001c0001t0103g0272others(1): Show | 4 | HG02896.hp1 HG02897.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1075-8716G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89382208 | ||||||
| chr11:89382227
|
C | A | 106 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0008others(103): Show | 106 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(103): Show |
intron_variant | MODIFIER | c.1075-8735G>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89382227 | ||||||
| chr11:89382265
|
G | C | 3 | a0001c0001t0002g0252a0001c0001t0117g0287a0001c0002t0074g0146 | 3 | HG02622.hp1 HG03098.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1075-8773C>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89382265 | ||||||
| chr11:89382347
|
C | A | 51 | a0001c0001t0003g0170a0001c0001t0003g0191a0001c0001t0003g0205others(48): Show | 51 | HG00408.hp2 HG00621.hp1 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.1075-8855G>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89382347 | ||||||
| chr11:89382362
|
G | T | 1 | a0001c0002t0009g0263 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1075-8870C>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89382362 | ||||||
| chr11:89382421
|
T | A | 1 | a0001c0001t0001g0128 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1075-8929A>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89382421 | ||||||
| chr11:89382433
|
TAA | T | 25 | a0001c0001t0002g0242a0001c0001t0002g0246a0001c0001t0002g0252others(22): Show | 25 | HG00408.hp1 HG02622.hp1 HG02698.hp1 others(22): Show |
intron_variant | MODIFIER | c.1075-8943_1075-894 others(6): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89382433 | ||||||
| chr11:89382496
|
C | T | 51 | a0001c0001t0003g0170a0001c0001t0003g0191a0001c0001t0003g0205others(48): Show | 51 | HG00408.hp2 HG00621.hp1 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.1075-9004G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89382496 | ||||||
| chr11:89382512
|
A | T | 22 | a0001c0001t0002g0242a0001c0001t0002g0246a0001c0001t0002g0264others(19): Show | 22 | HG00408.hp1 HG02698.hp1 HG03139.hp1 others(19): Show |
intron_variant | MODIFIER | c.1075-9020T>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89382512 | ||||||
| chr11:89382698
|
C | T | 2 | a0001c0001t0072g0093a0001c0002t0093g0219 | 2 | HG02257.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.1075-9206G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89382698 | ||||||
| chr11:89382706
|
C | G | 5 | a0001c0001t0002g0279a0001c0001t0002g0283a0001c0001t0037g0280others(2): Show | 5 | HG02258.hp1 HG02717.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1075-9214G>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89382706 | ||||||
| chr11:89382736
|
T | C | 202 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0008others(199): Show | 202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.1075-9244A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89382736 | ||||||
| chr11:89382762
|
T | C | 202 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0008others(199): Show | 202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.1075-9270A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89382762 | ||||||
| chr11:89382763
|
G | A | 4 | a0001c0002t0009g0236a0001c0002t0034g0237a0001c0002t0035g0229others(1): Show | 4 | NA18957.hp1 NA18965.hp2 NA18998.hp2 others(1): Show |
intron_variant | MODIFIER | c.1075-9271C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89382763 | ||||||
| chr11:89382780
|
C | T | 25 | a0001c0001t0002g0242a0001c0001t0002g0246a0001c0001t0002g0252others(22): Show | 25 | HG00408.hp1 HG02622.hp1 HG02698.hp1 others(22): Show |
intron_variant | MODIFIER | c.1075-9288G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89382780 | ||||||
| chr11:89382784
|
C | T | 5 | a0001c0001t0024g0155a0001c0001t0048g0044a0001c0001t0049g0043others(2): Show | 5 | HG02647.hp2 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1075-9292G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89382784 | ||||||
| chr11:89382846
|
G | A | 3 | a0001c0001t0002g0252a0001c0001t0117g0287a0001c0002t0074g0146 | 3 | HG02622.hp1 HG03098.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1075-9354C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89382846 | ||||||
| chr11:89382964
|
C | T | 2 | a0001c0001t0017g0171a0001c0001t0017g0172 | 2 | HG01074.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1075-9472G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89382964 | ||||||
| chr11:89382983
|
C | T | 1 | a0001c0001t0007g0049 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1075-9491G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89382983 | ||||||
| chr11:89383065
|
C | T | 1 | a0001c0002t0074g0146 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1075-9573G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89383065 | ||||||
| chr11:89383085
|
C | A | 11 | a0001c0001t0017g0160a0001c0001t0024g0155a0001c0001t0048g0044others(8): Show | 11 | HG01884.hp1 HG02615.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.1075-9593G>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89383085 | ||||||
| chr11:89383119
|
A | G | 1 | a0001c0001t0012g0247 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1075-9627T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89383119 | ||||||
| chr11:89383172
|
A | G | 1 | a0001c0001t0022g0140 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1075-9680T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89383172 | ||||||
| chr11:89383220
|
G | C | 217 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0008others(214): Show | 217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
intron_variant | MODIFIER | c.1075-9728C>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89383220 | ||||||
| chr11:89383341
|
C | T | 22 | a0001c0001t0002g0242a0001c0001t0002g0246a0001c0001t0002g0264others(19): Show | 22 | HG00408.hp1 HG02698.hp1 HG03139.hp1 others(19): Show |
intron_variant | MODIFIER | c.1075-9849G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89383341 | ||||||
| chr11:89383343
|
T | C | 1 | a0001c0001t0008g0002 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1075-9851A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89383343 | ||||||
| chr11:89383370
|
A | G | 25 | a0001c0001t0002g0242a0001c0001t0002g0246a0001c0001t0002g0252others(22): Show | 25 | HG00408.hp1 HG02622.hp1 HG02698.hp1 others(22): Show |
intron_variant | MODIFIER | c.1075-9878T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89383370 | ||||||
| chr11:89383381
|
C | T | 1 | a0001c0001t0017g0165 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1075-9889G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89383381 | ||||||
| chr11:89383473
|
G | A | 2 | a0001c0001t0068g0064a0001c0002t0006g0091 | 2 | HG01884.hp2 NA18942.hp2 |
intron_variant | MODIFIER | c.1075-9981C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89383473 | ||||||
| chr11:89383593
|
G | A | 2 | a0001c0001t0017g0171a0001c0001t0017g0172 | 2 | HG01074.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1075-10101C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89383593 | ||||||
| chr11:89383742
|
G | T | 2 | a0001c0001t0023g0161a0001c0001t0071g0090 | 2 | HG02486.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1075-10250C>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89383742 | ||||||
| chr11:89383873
|
C | T | 3 | a0001c0001t0002g0252a0001c0001t0117g0287a0001c0002t0074g0146 | 3 | HG02622.hp1 HG03098.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1075-10381G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89383873 | ||||||
| chr11:89384034
|
C | T | 1 | a0001c0001t0068g0064 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1075-10542G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89384034 | ||||||
| chr11:89384096
|
G | C | 20 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0014others(17): Show | 20 | HG00099.hp1 HG00558.hp1 HG01256.hp2 others(17): Show |
intron_variant | MODIFIER | c.1075-10604C>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89384096 | ||||||
| chr11:89384154
|
C | T | 2 | a0001c0001t0012g0247a0001c0001t0015g0057 | 2 | HG01109.hp2 NA18988.hp1 |
intron_variant | MODIFIER | c.1075-10662G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89384154 | ||||||
| chr11:89384155
|
C | T | 22 | a0001c0001t0002g0242a0001c0001t0002g0246a0001c0001t0002g0264others(19): Show | 22 | HG00408.hp1 HG02698.hp1 HG03139.hp1 others(19): Show |
intron_variant | MODIFIER | c.1075-10663G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89384155 | ||||||
| chr11:89384225
|
T | C | 1 | a0003c0013t0002g0220 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1075-10733A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89384225 | ||||||
| chr11:89384384
|
C | T | 6 | a0001c0001t0003g0191a0001c0001t0018g0192a0001c0001t0080g0203others(3): Show | 6 | NA18946.hp1 NA18951.hp2 NA18959.hp1 others(3): Show |
intron_variant | MODIFIER | c.1075-10892G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89384384 | ||||||
| chr11:89384425
|
C | G | 2 | a0001c0001t0031g0176a0001c0001t0031g0177 | 2 | HG03209.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1075-10933G>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89384425 | ||||||
| chr11:89384453
|
C | T | 1 | a0001c0001t0085g0179 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1075-10961G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89384453 | ||||||
| chr11:89384454
|
T | G | 1 | a0001c0003t0007g0053 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1075-10962A>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89384454 | ||||||
| chr11:89384486
|
A | G | 2 | a0001c0001t0031g0176a0001c0001t0031g0177 | 2 | HG03209.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1075-10994T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89384486 | ||||||
| chr11:89384840
|
G | A | 22 | a0001c0001t0002g0242a0001c0001t0002g0246a0001c0001t0002g0264others(19): Show | 22 | HG00408.hp1 HG02698.hp1 HG03139.hp1 others(19): Show |
intron_variant | MODIFIER | c.1075-11348C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89384840 | ||||||
| chr11:89384878
|
A | G | 2 | a0001c0002t0006g0021a0001c0002t0041g0022 | 2 | NA18747.hp2 NA18954.hp1 |
intron_variant | MODIFIER | c.1075-11386T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89384878 | ||||||
| chr11:89384949
|
C | T | 1 | a0001c0012t0023g0181 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1075-11457G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89384949 | ||||||
| chr11:89384955
|
G | C | 2 | a0001c0002t0006g0021a0001c0002t0041g0022 | 2 | NA18747.hp2 NA18954.hp1 |
intron_variant | MODIFIER | c.1075-11463C>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89384955 | ||||||
| chr11:89384965
|
G | C | 22 | a0001c0001t0002g0242a0001c0001t0002g0246a0001c0001t0002g0264others(19): Show | 22 | HG00408.hp1 HG02698.hp1 HG03139.hp1 others(19): Show |
intron_variant | MODIFIER | c.1075-11473C>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89384965 | ||||||
| chr11:89385373
|
C | A | 1 | a0002c0004t0032g0144 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1075-11881G>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89385373 | ||||||
| chr11:89385424
|
A | G | 1 | a0001c0001t0113g0227 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1075-11932T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89385424 | ||||||
| chr11:89385479
|
C | G | 1 | a0001c0001t0002g0279 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1075-11987G>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89385479 | ||||||
| chr11:89385515
|
A | G | 2 | a0001c0003t0013g0135a0004c0007t0013g0089 | 2 | NA19070.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.1075-12023T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89385515 | ||||||
| chr11:89385534
|
A | C | 25 | a0001c0001t0002g0242a0001c0001t0002g0246a0001c0001t0002g0252others(22): Show | 25 | HG00408.hp1 HG02622.hp1 HG02698.hp1 others(22): Show |
intron_variant | MODIFIER | c.1075-12042T>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89385534 | ||||||
| chr11:89385721
|
G | A | 2 | a0001c0001t0021g0010a0001c0001t0113g0227 | 2 | HG01243.hp1 NA18612.hp2 |
intron_variant | MODIFIER | c.1075-12229C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89385721 | ||||||
| chr11:89385919
|
C | T | 215 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0008others(212): Show | 215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
intron_variant | MODIFIER | c.1075-12427G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89385919 | ||||||
| chr11:89385929
|
T | C | 1 | a0001c0001t0002g0224 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1075-12437A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89385929 | ||||||
| chr11:89386101
|
A | G | 2 | a0001c0002t0011g0153a0001c0002t0029g0154 | 2 | HG01109.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1075-12609T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89386101 | ||||||
| chr11:89386241
|
C | T | 6 | a0001c0001t0017g0171a0001c0001t0017g0172a0001c0001t0081g0163others(3): Show | 6 | HG01074.hp2 HG01099.hp1 HG01243.hp2 others(3): Show |
intron_variant | MODIFIER | c.1075-12749G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89386241 | ||||||
| chr11:89386242
|
A | G | 217 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0008others(214): Show | 217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
intron_variant | MODIFIER | c.1075-12750T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89386242 | ||||||
| chr11:89386254
|
T | C | 210 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0008others(207): Show | 210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.1075-12762A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89386254 | ||||||
| chr11:89386399
|
T | C | 29 | a0001c0001t0002g0242a0001c0001t0002g0246a0001c0001t0002g0252others(26): Show | 29 | HG00408.hp1 HG02145.hp2 HG02622.hp1 others(26): Show |
intron_variant | MODIFIER | c.1075-12907A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89386399 | ||||||
| chr11:89386400
|
G | T | 3 | a0001c0002t0033g0285a0001c0002t0098g0284a0001c0002t0099g0286 | 3 | HG02976.hp1 HG03195.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1075-12908C>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89386400 | ||||||
| chr11:89386404
|
C | G | 1 | a0001c0001t0005g0178 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1075-12912G>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89386404 | ||||||
| chr11:89386560
|
C | T | 2 | a0001c0001t0031g0176a0001c0001t0031g0177 | 2 | HG03209.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1075-13068G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89386560 | ||||||
| chr11:89386737
|
C | T | 1 | a0001c0001t0003g0164 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1075-13245G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89386737 | ||||||
| chr11:89386787
|
A | G | 1 | a0001c0001t0018g0142 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1074+13230T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89386787 | ||||||
| chr11:89386843
|
GTC | G | 9 | a0001c0001t0017g0160a0001c0001t0048g0044a0001c0001t0049g0043others(6): Show | 9 | HG01884.hp1 HG02615.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.1074+13172_1074+13 others(8): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89386843 | ||||||
| chr11:89386874
|
T | C | 9 | a0001c0001t0017g0160a0001c0001t0048g0044a0001c0001t0049g0043others(6): Show | 9 | HG01884.hp1 HG02615.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.1074+13143A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89386874 | ||||||
| chr11:89386995
|
A | G | 6 | a0001c0001t0052g0122a0001c0001t0069g0015a0001c0001t0112g0282others(3): Show | 6 | HG02145.hp2 HG02896.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.1074+13022T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89386995 | ||||||
| chr11:89387051
|
C | T | 1 | a0001c0001t0091g0151 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1074+12966G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89387051 | ||||||
| chr11:89387061
|
C | A | 25 | a0001c0001t0002g0242a0001c0001t0002g0246a0001c0001t0002g0252others(22): Show | 25 | HG00408.hp1 HG02622.hp1 HG02698.hp1 others(22): Show |
intron_variant | MODIFIER | c.1074+12956G>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89387061 | ||||||
| chr11:89387116
|
C | T | 1 | a0001c0001t0021g0010 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1074+12901G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89387116 | ||||||
| chr11:89387323
|
C | T | 51 | a0001c0001t0003g0170a0001c0001t0003g0191a0001c0001t0003g0205others(48): Show | 51 | HG00408.hp2 HG00621.hp1 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.1074+12694G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89387323 | ||||||
| chr11:89387364
|
T | C | 217 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0008others(214): Show | 217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
intron_variant | MODIFIER | c.1074+12653A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89387364 | ||||||
| chr11:89387439
|
T | C | 203 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0008others(200): Show | 203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
intron_variant | MODIFIER | c.1074+12578A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89387439 | ||||||
| chr11:89387569
|
T | C | 3 | a0001c0001t0002g0246a0001c0002t0009g0240a0001c0002t0075g0183 | 3 | NA18944.hp2 NA19054.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.1074+12448A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89387569 | ||||||
| chr11:89387655
|
T | C | 1 | a0001c0003t0003g0189 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1074+12362A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89387655 | ||||||
| chr11:89387724
|
C | T | 1 | a0001c0001t0001g0028 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1074+12293G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89387724 | ||||||
| chr11:89387757
|
C | G | 2 | a0001c0001t0031g0176a0001c0001t0031g0177 | 2 | HG03209.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1074+12260G>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89387757 | ||||||
| chr11:89387760
|
T | C | 1 | a0001c0001t0001g0013 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1074+12257A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89387760 | ||||||
| chr11:89387763
|
C | T | 1 | a0001c0001t0110g0274 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1074+12254G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89387763 | ||||||
| chr11:89387905
|
C | T | 15 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0061others(12): Show | 15 | HG01081.hp2 HG01952.hp1 HG02132.hp1 others(12): Show |
intron_variant | MODIFIER | c.1074+12112G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89387905 | ||||||
| chr11:89387992
|
A | G | 3 | a0001c0001t0002g0252a0001c0001t0117g0287a0001c0002t0074g0146 | 3 | HG02622.hp1 HG03098.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1074+12025T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89387992 | ||||||
| chr11:89387997
|
T | C | 1 | a0001c0001t0108g0223 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1074+12020A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89387997 | ||||||
| chr11:89388002
|
T | G | 1 | a0001c0001t0068g0064 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1074+12015A>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89388002 | ||||||
| chr11:89388033
|
C | G | 1 | a0001c0003t0003g0201 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1074+11984G>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89388033 | ||||||
| chr11:89388151
|
T | C | 1 | a0001c0002t0006g0034 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1074+11866A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89388151 | ||||||
| chr11:89388180
|
G | C | 1 | a0001c0001t0071g0090 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1074+11837C>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89388180 | ||||||
| chr11:89388386
|
A | G | 1 | a0001c0001t0085g0179 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1074+11631T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89388386 | ||||||
| chr11:89388428
|
T | C | 1 | a0001c0001t0113g0227 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1074+11589A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89388428 | ||||||
| chr11:89388435
|
G | A | 1 | a0001c0003t0092g0196 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1074+11582C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89388435 | ||||||
| chr11:89388592
|
C | T | 22 | a0001c0001t0002g0242a0001c0001t0002g0246a0001c0001t0002g0264others(19): Show | 22 | HG00408.hp1 HG02698.hp1 HG03139.hp1 others(19): Show |
intron_variant | MODIFIER | c.1074+11425G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89388592 | ||||||
| chr11:89388652
|
C | T | 4 | a0001c0001t0052g0122a0001c0002t0033g0285a0001c0002t0098g0284others(1): Show | 4 | HG02145.hp2 HG02976.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1074+11365G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89388652 | ||||||
| chr11:89388659
|
C | T | 2 | a0001c0001t0017g0171a0001c0001t0017g0172 | 2 | HG01074.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1074+11358G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89388659 | ||||||
| chr11:89388796
|
A | T | 1 | a0001c0001t0001g0134 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1074+11221T>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89388796 | ||||||
| chr11:89388828
|
A | G | 9 | a0001c0001t0017g0160a0001c0001t0048g0044a0001c0001t0049g0043others(6): Show | 9 | HG01884.hp1 HG02615.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.1074+11189T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89388828 | ||||||
| chr11:89388927
|
T | G | 1 | a0001c0001t0047g0139 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1074+11090A>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89388927 | ||||||
| chr11:89389028
|
G | C | 1 | a0001c0001t0018g0175 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1074+10989C>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89389028 | ||||||
| chr11:89389085
|
C | T | 1 | a0001c0001t0001g0035 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1074+10932G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89389085 | ||||||
| chr11:89389090
|
G | T | 3 | a0001c0001t0018g0142a0001c0001t0018g0175a0001c0001t0078g0143 | 3 | HG02280.hp1 NA19240.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1074+10927C>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89389090 | ||||||
| chr11:89389243
|
G | C | 3 | a0001c0001t0052g0122a0001c0001t0069g0015a0001c0001t0112g0282 | 3 | HG02145.hp2 HG02896.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1074+10774C>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89389243 | ||||||
| chr11:89389303
|
A | ATTCGTGC others(18): Show |
1 | a0001c0001t0001g0029 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1074+10689_1074+10 others(31): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89389303 | ||||||
| chr11:89389309
|
G | A | 1 | a0001c0002t0006g0085 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1074+10708C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89389309 | ||||||
| chr11:89389339
|
T | C | 4 | a0001c0001t0005g0149a0001c0001t0005g0150a0001c0001t0103g0272others(1): Show | 4 | HG02896.hp1 HG02897.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1074+10678A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89389339 | ||||||
| chr11:89389375
|
T | G | 1 | a0001c0001t0031g0177 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1074+10642A>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89389375 | ||||||
| chr11:89389504
|
T | C | 4 | a0001c0001t0002g0224a0001c0001t0002g0254a0001c0001t0002g0255others(1): Show | 4 | HG02451.hp1 HG03139.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1074+10513A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89389504 | ||||||
| chr11:89389568
|
T | G | 119 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0008others(116): Show | 119 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(116): Show |
intron_variant | MODIFIER | c.1074+10449A>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89389568 | ||||||
| chr11:89389688
|
T | C | 4 | a0001c0001t0052g0122a0001c0002t0033g0285a0001c0002t0098g0284others(1): Show | 4 | HG02145.hp2 HG02976.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1074+10329A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89389688 | ||||||
| chr11:89389896
|
G | A | 22 | a0001c0001t0002g0242a0001c0001t0002g0246a0001c0001t0002g0264others(19): Show | 22 | HG00408.hp1 HG02698.hp1 HG03139.hp1 others(19): Show |
intron_variant | MODIFIER | c.1074+10121C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89389896 | ||||||
| chr11:89389974
|
T | G | 2 | a0001c0001t0005g0178a0001c0001t0091g0151 | 2 | HG02280.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.1074+10043A>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89389974 | ||||||
| chr11:89390156
|
A | T | 1 | a0001c0001t0013g0082 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1074+9861T>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89390156 | ||||||
| chr11:89390231
|
G | T | 9 | a0001c0001t0017g0160a0001c0001t0048g0044a0001c0001t0049g0043others(6): Show | 9 | HG01884.hp1 HG02615.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.1074+9786C>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89390231 | ||||||
| chr11:89390323
|
G | A | 1 | a0001c0001t0107g0225 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1074+9694C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89390323 | ||||||
| chr11:89390482
|
A | G | 1 | a0001c0001t0001g0134 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1074+9535T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89390482 | ||||||
| chr11:89390511
|
A | C | 2 | a0001c0001t0031g0176a0001c0001t0031g0177 | 2 | HG03209.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1074+9506T>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89390511 | ||||||
| chr11:89390580
|
C | A | 1 | a0001c0001t0113g0227 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1074+9437G>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89390580 | ||||||
| chr11:89390600
|
C | T | 83 | a0001c0001t0002g0242a0001c0001t0002g0246a0001c0001t0002g0252others(80): Show | 83 | HG00408.hp1 HG00408.hp2 HG00621.hp1 others(80): Show |
intron_variant | MODIFIER | c.1074+9417G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89390600 | ||||||
| chr11:89390749
|
T | A | 22 | a0001c0001t0002g0242a0001c0001t0002g0246a0001c0001t0002g0264others(19): Show | 22 | HG00408.hp1 HG02698.hp1 HG03139.hp1 others(19): Show |
intron_variant | MODIFIER | c.1074+9268A>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89390749 | ||||||
| chr11:89390764
|
G | A | 1 | a0001c0001t0113g0227 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1074+9253C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89390764 | ||||||
| chr11:89390911
|
G | C | 6 | a0001c0001t0052g0122a0001c0001t0069g0015a0001c0001t0112g0282others(3): Show | 6 | HG02145.hp2 HG02896.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.1074+9106C>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89390911 | ||||||
| chr11:89391052
|
G | A | 1 | a0001c0001t0066g0096 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1074+8965C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89391052 | ||||||
| chr11:89391074
|
G | C | 22 | a0001c0001t0002g0242a0001c0001t0002g0246a0001c0001t0002g0264others(19): Show | 22 | HG00408.hp1 HG02698.hp1 HG03139.hp1 others(19): Show |
intron_variant | MODIFIER | c.1074+8943C>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89391074 | ||||||
| chr11:89391211
|
G | A | 25 | a0001c0001t0002g0242a0001c0001t0002g0246a0001c0001t0002g0252others(22): Show | 25 | HG00408.hp1 HG02622.hp1 HG02698.hp1 others(22): Show |
intron_variant | MODIFIER | c.1074+8806C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89391211 | ||||||
| chr11:89391211
|
G | C | 52 | a0001c0001t0003g0170a0001c0001t0003g0191a0001c0001t0003g0205others(49): Show | 52 | HG00408.hp2 HG00621.hp1 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.1074+8806C>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89391211 | ||||||
| chr11:89391414
|
C | A | 4 | a0001c0001t0002g0245a0001c0001t0088g0158a0001c0001t0111g0277others(1): Show | 4 | HG02451.hp2 HG02723.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1074+8603G>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89391414 | ||||||
| chr11:89391484
|
G | T | 1 | a0001c0001t0002g0265 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1074+8533C>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89391484 | ||||||
| chr11:89391577
|
G | A | 51 | a0001c0001t0003g0170a0001c0001t0003g0191a0001c0001t0003g0205others(48): Show | 51 | HG00408.hp2 HG00621.hp1 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.1074+8440C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89391577 | ||||||
| chr11:89391662
|
A | G | 31 | a0001c0001t0002g0242a0001c0001t0002g0246a0001c0001t0002g0252others(28): Show | 31 | HG00408.hp1 HG02145.hp2 HG02622.hp1 others(28): Show |
intron_variant | MODIFIER | c.1074+8355T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89391662 | ||||||
| chr11:89391739
|
C | CA | 129 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0008others(126): Show | 129 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(126): Show |
intron_variant | MODIFIER | c.1074+8277dupT | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89391739 | ||||||
| chr11:89391739
|
CA | C | 30 | a0001c0001t0002g0242a0001c0001t0002g0246a0001c0001t0002g0264others(27): Show | 30 | HG00408.hp1 HG01074.hp2 HG02698.hp1 others(27): Show |
intron_variant | MODIFIER | c.1074+8277delT | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89391739 | ||||||
| chr11:89391753
|
A | AG | 3 | a0001c0001t0002g0252a0001c0001t0117g0287a0001c0002t0074g0146 | 3 | HG02622.hp1 HG03098.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1074+8263_1074+826 others(5): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89391753 | ||||||
| chr11:89391921
|
TCCCTTC | T | 9 | a0001c0001t0017g0160a0001c0001t0048g0044a0001c0001t0049g0043others(6): Show | 9 | HG01884.hp1 HG02615.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.1074+8090_1074+809 others(10): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89391921 | ||||||
| chr11:89391921
|
TCCCTTCC others(5): Show |
T | 1 | a0001c0001t0027g0018 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1074+8084_1074+809 others(16): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89391921 | ||||||
| chr11:89391952
|
T | C | 23 | a0001c0001t0002g0242a0001c0001t0002g0246a0001c0001t0002g0252others(20): Show | 23 | HG00408.hp1 HG02622.hp1 HG02698.hp1 others(20): Show |
intron_variant | MODIFIER | c.1074+8065A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89391952 | ||||||
| chr11:89391955
|
T | TTC | 23 | a0001c0001t0002g0242a0001c0001t0002g0246a0001c0001t0002g0252others(20): Show | 23 | HG00408.hp1 HG02622.hp1 HG02698.hp1 others(20): Show |
intron_variant | MODIFIER | c.1074+8060_1074+806 others(6): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89391955 | ||||||
| chr11:89391970
|
C | T | 1 | a0001c0001t0002g0279 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1074+8047G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89391970 | ||||||
| chr11:89392010
|
C | T | 2 | a0002c0004t0032g0144a0002c0004t0032g0162 | 2 | HG02615.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1074+8007G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89392010 | ||||||
| chr11:89392233
|
T | C | 3 | a0001c0001t0024g0155a0001c0002t0011g0156a0001c0002t0029g0168 | 3 | HG02647.hp2 HG03098.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1074+7784A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89392233 | ||||||
| chr11:89392339
|
G | A | 31 | a0001c0001t0002g0242a0001c0001t0002g0246a0001c0001t0002g0252others(28): Show | 31 | HG00408.hp1 HG02145.hp2 HG02622.hp1 others(28): Show |
intron_variant | MODIFIER | c.1074+7678C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89392339 | ||||||
| chr11:89392424
|
G | T | 2 | a0001c0001t0017g0171a0001c0001t0017g0172 | 2 | HG01074.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1074+7593C>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89392424 | ||||||
| chr11:89392517
|
T | C | 2 | a0001c0001t0017g0171a0001c0001t0017g0172 | 2 | HG01074.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1074+7500A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89392517 | ||||||
| chr11:89392588
|
A | T | 25 | a0001c0001t0002g0242a0001c0001t0002g0246a0001c0001t0002g0252others(22): Show | 25 | HG00408.hp1 HG02622.hp1 HG02698.hp1 others(22): Show |
intron_variant | MODIFIER | c.1074+7429T>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89392588 | ||||||
| chr11:89392685
|
G | C | 1 | a0001c0002t0075g0183 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1074+7332C>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89392685 | ||||||
| chr11:89392946
|
G | A | 4 | a0001c0001t0081g0163a0001c0001t0082g0174a0001c0001t0086g0152others(1): Show | 4 | HG01099.hp1 HG01243.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.1074+7071C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89392946 | ||||||
| chr11:89393194
|
G | A | 2 | a0001c0001t0017g0171a0001c0001t0017g0172 | 2 | HG01074.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1074+6823C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89393194 | ||||||
| chr11:89393256
|
C | G | 25 | a0001c0001t0002g0242a0001c0001t0002g0246a0001c0001t0002g0252others(22): Show | 25 | HG00408.hp1 HG02622.hp1 HG02698.hp1 others(22): Show |
intron_variant | MODIFIER | c.1074+6761G>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89393256 | ||||||
| chr11:89393282
|
G | A | 1 | a0001c0001t0018g0175 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1074+6735C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89393282 | ||||||
| chr11:89393438
|
G | GA | 6 | a0001c0001t0052g0122a0001c0001t0069g0015a0001c0001t0112g0282others(3): Show | 6 | HG02145.hp2 HG02896.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.1074+6578dupT | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89393438 | ||||||
| chr11:89393495
|
T | G | 25 | a0001c0001t0002g0242a0001c0001t0002g0246a0001c0001t0002g0252others(22): Show | 25 | HG00408.hp1 HG02622.hp1 HG02698.hp1 others(22): Show |
intron_variant | MODIFIER | c.1074+6522A>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89393495 | ||||||
| chr11:89393541
|
T | A | 6 | a0001c0001t0052g0122a0001c0001t0069g0015a0001c0001t0112g0282others(3): Show | 6 | HG02145.hp2 HG02896.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.1074+6476A>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89393541 | ||||||
| chr11:89393919
|
T | C | 213 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0008others(210): Show | 213 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(210): Show |
intron_variant | MODIFIER | c.1074+6098A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89393919 | ||||||
| chr11:89393920
|
C | T | 4 | a0001c0002t0009g0236a0001c0002t0034g0237a0001c0002t0035g0229others(1): Show | 4 | NA18957.hp1 NA18965.hp2 NA18998.hp2 others(1): Show |
intron_variant | MODIFIER | c.1074+6097G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89393920 | ||||||
| chr11:89394103
|
C | T | 1 | a0001c0001t0113g0227 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1074+5914G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89394103 | ||||||
| chr11:89394246
|
G | A | 51 | a0001c0001t0003g0170a0001c0001t0003g0191a0001c0001t0003g0205others(48): Show | 51 | HG00408.hp2 HG00621.hp1 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.1074+5771C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89394246 | ||||||
| chr11:89394291
|
G | A | 105 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0008others(102): Show | 105 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(102): Show |
intron_variant | MODIFIER | c.1074+5726C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89394291 | ||||||
| chr11:89394308
|
A | G | 3 | a0001c0002t0033g0285a0001c0002t0098g0284a0001c0002t0099g0286 | 3 | HG02976.hp1 HG03195.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1074+5709T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89394308 | ||||||
| chr11:89394324
|
TTTTG | T | 22 | a0001c0001t0002g0242a0001c0001t0002g0246a0001c0001t0002g0264others(19): Show | 22 | HG00408.hp1 HG02698.hp1 HG03139.hp1 others(19): Show |
intron_variant | MODIFIER | c.1074+5689_1074+569 others(8): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89394324 | ||||||
| chr11:89394358
|
CA | C | 213 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0008others(210): Show | 213 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(210): Show |
intron_variant | MODIFIER | c.1074+5658delT | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89394358 | ||||||
| chr11:89394361
|
A | C | 1 | a0001c0001t0007g0126 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1074+5656T>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89394361 | ||||||
| chr11:89394362
|
A | C | 31 | a0001c0001t0002g0242a0001c0001t0002g0246a0001c0001t0002g0252others(28): Show | 31 | HG00408.hp1 HG02145.hp2 HG02622.hp1 others(28): Show |
intron_variant | MODIFIER | c.1074+5655T>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89394362 | ||||||
| chr11:89394453
|
A | G | 51 | a0001c0001t0003g0170a0001c0001t0003g0191a0001c0001t0003g0205others(48): Show | 51 | HG00408.hp2 HG00621.hp1 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.1074+5564T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89394453 | ||||||
| chr11:89394480
|
G | C | 1 | a0001c0001t0001g0088 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1074+5537C>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89394480 | ||||||
| chr11:89394502
|
A | AT | 25 | a0001c0001t0002g0242a0001c0001t0002g0246a0001c0001t0002g0252others(22): Show | 25 | HG00408.hp1 HG02622.hp1 HG02698.hp1 others(22): Show |
intron_variant | MODIFIER | c.1074+5514dupA | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89394502 | ||||||
| chr11:89394512
|
T | C | 1 | a0001c0003t0004g0119 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1074+5505A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89394512 | ||||||
| chr11:89394659
|
C | T | 1 | a0001c0001t0058g0005 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1074+5358G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89394659 | ||||||
| chr11:89394788
|
T | A | 1 | a0001c0002t0006g0025 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1074+5229A>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89394788 | ||||||
| chr11:89394808
|
C | T | 1 | a0001c0001t0117g0287 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1074+5209G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89394808 | ||||||
| chr11:89394872
|
T | C | 1 | a0001c0002t0074g0146 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1074+5145A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89394872 | ||||||
| chr11:89394876
|
C | T | 22 | a0001c0001t0002g0242a0001c0001t0002g0246a0001c0001t0002g0264others(19): Show | 22 | HG00408.hp1 HG02698.hp1 HG03139.hp1 others(19): Show |
intron_variant | MODIFIER | c.1074+5141G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89394876 | ||||||
| chr11:89394898
|
A | G | 1 | a0001c0008t0002g0275 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1074+5119T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89394898 | ||||||
| chr11:89394950
|
C | G | 2 | a0001c0001t0023g0161a0001c0001t0071g0090 | 2 | HG02486.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1074+5067G>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89394950 | ||||||
| chr11:89395062
|
T | C | 203 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0008others(200): Show | 203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
intron_variant | MODIFIER | c.1074+4955A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89395062 | ||||||
| chr11:89395432
|
A | C | 4 | a0001c0001t0005g0149a0001c0001t0005g0150a0001c0001t0103g0272others(1): Show | 4 | HG02896.hp1 HG02897.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1074+4585T>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89395432 | ||||||
| chr11:89395709
|
G | A | 4 | a0001c0001t0002g0224a0001c0001t0002g0254a0001c0001t0002g0255others(1): Show | 4 | HG02451.hp1 HG03139.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1074+4308C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89395709 | ||||||
| chr11:89395746
|
T | A | 3 | a0001c0001t0018g0142a0001c0001t0018g0175a0001c0001t0078g0143 | 3 | HG02280.hp1 NA19240.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1074+4271A>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89395746 | ||||||
| chr11:89395775
|
G | T | 25 | a0001c0001t0002g0242a0001c0001t0002g0246a0001c0001t0002g0252others(22): Show | 25 | HG00408.hp1 HG02622.hp1 HG02698.hp1 others(22): Show |
intron_variant | MODIFIER | c.1074+4242C>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89395775 | ||||||
| chr11:89395810
|
T | C | 1 | a0001c0001t0068g0064 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1074+4207A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89395810 | ||||||
| chr11:89395821
|
C | T | 3 | a0001c0001t0002g0252a0001c0001t0117g0287a0001c0002t0074g0146 | 3 | HG02622.hp1 HG03098.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1074+4196G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89395821 | ||||||
| chr11:89395965
|
T | C | 46 | a0001c0001t0001g0035a0001c0001t0001g0062a0001c0001t0001g0070others(43): Show | 46 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(43): Show |
intron_variant | MODIFIER | c.1074+4052A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89395965 | ||||||
| chr11:89395985
|
A | G | 28 | a0001c0001t0002g0242a0001c0001t0002g0246a0001c0001t0002g0252others(25): Show | 28 | HG00408.hp1 HG02280.hp1 HG02622.hp1 others(25): Show |
intron_variant | MODIFIER | c.1074+4032T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89395985 | ||||||
| chr11:89396018
|
T | C | 2 | a0001c0001t0031g0176a0001c0001t0031g0177 | 2 | HG03209.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1074+3999A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89396018 | ||||||
| chr11:89396048
|
T | C | 4 | a0001c0001t0081g0163a0001c0001t0082g0174a0001c0001t0086g0152others(1): Show | 4 | HG01099.hp1 HG01243.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.1074+3969A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89396048 | ||||||
| chr11:89396049
|
A | T | 1 | a0001c0001t0113g0227 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1074+3968T>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89396049 | ||||||
| chr11:89396249
|
T | C | 2 | a0001c0001t0031g0176a0001c0001t0031g0177 | 2 | HG03209.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1074+3768A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89396249 | ||||||
| chr11:89396259
|
T | C | 4 | a0001c0001t0081g0163a0001c0001t0082g0174a0001c0001t0086g0152others(1): Show | 4 | HG01099.hp1 HG01243.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.1074+3758A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89396259 | ||||||
| chr11:89396369
|
C | T | 3 | a0001c0001t0002g0252a0001c0001t0117g0287a0001c0002t0074g0146 | 3 | HG02622.hp1 HG03098.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1074+3648G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89396369 | ||||||
| chr11:89396371
|
C | A | 1 | a0001c0001t0068g0064 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1074+3646G>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89396371 | ||||||
| chr11:89396372
|
T | A | 1 | a0001c0001t0068g0064 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1074+3645A>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89396372 | ||||||
| chr11:89396466
|
T | C | 1 | a0001c0001t0113g0227 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1074+3551A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89396466 | ||||||
| chr11:89396517
|
G | A | 9 | a0001c0001t0017g0160a0001c0001t0048g0044a0001c0001t0049g0043others(6): Show | 9 | HG01884.hp1 HG02615.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.1074+3500C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89396517 | ||||||
| chr11:89396561
|
A | T | 25 | a0001c0001t0002g0242a0001c0001t0002g0246a0001c0001t0002g0252others(22): Show | 25 | HG00408.hp1 HG02622.hp1 HG02698.hp1 others(22): Show |
intron_variant | MODIFIER | c.1074+3456T>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89396561 | ||||||
| chr11:89396616
|
G | A | 6 | a0001c0001t0012g0244a0001c0001t0015g0019a0001c0001t0015g0078others(3): Show | 6 | NA18941.hp1 NA18962.hp2 NA18968.hp1 others(3): Show |
intron_variant | MODIFIER | c.1074+3401C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89396616 | ||||||
| chr11:89396663
|
G | A | 1 | a0001c0001t0117g0287 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1074+3354C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89396663 | ||||||
| chr11:89396783
|
C | T | 1 | a0003c0013t0002g0220 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1074+3234G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89396783 | ||||||
| chr11:89396834
|
C | G | 22 | a0001c0001t0002g0242a0001c0001t0002g0246a0001c0001t0002g0264others(19): Show | 22 | HG00408.hp1 HG02698.hp1 HG03139.hp1 others(19): Show |
intron_variant | MODIFIER | c.1074+3183G>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89396834 | ||||||
| chr11:89396886
|
C | T | 1 | a0001c0002t0074g0146 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1074+3131G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89396886 | ||||||
| chr11:89396920
|
G | A | 1 | a0001c0001t0001g0031 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1074+3097C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89396920 | ||||||
| chr11:89396965
|
G | A | 25 | a0001c0001t0002g0242a0001c0001t0002g0246a0001c0001t0002g0252others(22): Show | 25 | HG00408.hp1 HG02622.hp1 HG02698.hp1 others(22): Show |
intron_variant | MODIFIER | c.1074+3052C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89396965 | ||||||
| chr11:89396973
|
T | C | 1 | a0001c0003t0013g0041 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1074+3044A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89396973 | ||||||
| chr11:89396983
|
C | CA | 217 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0008others(214): Show | 217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
intron_variant | MODIFIER | c.1074+3033_1074+303 others(5): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89396983 | ||||||
| chr11:89397062
|
C | T | 5 | a0001c0003t0019g0197a0001c0003t0019g0204a0001c0003t0019g0213others(2): Show | 5 | NA18941.hp2 NA18966.hp1 NA18968.hp2 others(2): Show |
intron_variant | MODIFIER | c.1074+2955G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89397062 | ||||||
| chr11:89397074
|
C | A | 6 | a0001c0001t0052g0122a0001c0001t0069g0015a0001c0001t0112g0282others(3): Show | 6 | HG02145.hp2 HG02896.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.1074+2943G>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89397074 | ||||||
| chr11:89397317
|
C | A | 4 | a0001c0001t0005g0149a0001c0001t0005g0150a0001c0001t0103g0272others(1): Show | 4 | HG02896.hp1 HG02897.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1074+2700G>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89397317 | ||||||
| chr11:89397428
|
C | T | 22 | a0001c0001t0002g0242a0001c0001t0002g0246a0001c0001t0002g0264others(19): Show | 22 | HG00408.hp1 HG02698.hp1 HG03139.hp1 others(19): Show |
intron_variant | MODIFIER | c.1074+2589G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89397428 | ||||||
| chr11:89397450
|
G | T | 4 | a0001c0001t0005g0149a0001c0001t0005g0150a0001c0001t0103g0272others(1): Show | 4 | HG02896.hp1 HG02897.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1074+2567C>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89397450 | ||||||
| chr11:89397712
|
T | C | 1 | a0001c0001t0018g0142 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1074+2305A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89397712 | ||||||
| chr11:89397914
|
T | C | 6 | a0001c0001t0002g0279a0001c0001t0002g0283a0001c0001t0017g0165others(3): Show | 6 | HG02258.hp1 HG02717.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1074+2103A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89397914 | ||||||
| chr11:89397969
|
G | C | 52 | a0001c0001t0003g0170a0001c0001t0003g0191a0001c0001t0003g0205others(49): Show | 52 | HG00408.hp2 HG00621.hp1 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.1074+2048C>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89397969 | ||||||
| chr11:89398236
|
T | C | 1 | a0001c0001t0113g0227 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1074+1781A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89398236 | ||||||
| chr11:89398324
|
A | G | 28 | a0001c0001t0002g0242a0001c0001t0002g0246a0001c0001t0002g0252others(25): Show | 28 | HG00408.hp1 HG02280.hp1 HG02622.hp1 others(25): Show |
intron_variant | MODIFIER | c.1074+1693T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89398324 | ||||||
| chr11:89398380
|
G | T | 51 | a0001c0001t0003g0170a0001c0001t0003g0191a0001c0001t0003g0205others(48): Show | 51 | HG00408.hp2 HG00621.hp1 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.1074+1637C>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89398380 | ||||||
| chr11:89398431
|
G | A | 1 | a0001c0001t0085g0179 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1074+1586C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89398431 | ||||||
| chr11:89398534
|
A | G | 2 | a0001c0001t0023g0161a0001c0001t0071g0090 | 2 | HG02486.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1074+1483T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89398534 | ||||||
| chr11:89398573
|
C | T | 1 | a0001c0001t0113g0227 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1074+1444G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89398573 | ||||||
| chr11:89398642
|
T | A | 1 | a0001c0001t0113g0227 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1074+1375A>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89398642 | ||||||
| chr11:89398793
|
C | T | 3 | a0001c0002t0033g0285a0001c0002t0098g0284a0001c0002t0099g0286 | 3 | HG02976.hp1 HG03195.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1074+1224G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89398793 | ||||||
| chr11:89398801
|
A | G | 2 | a0001c0001t0062g0114a0001c0006t0087g0200 | 2 | HG00558.hp2 NA19076.hp2 |
intron_variant | MODIFIER | c.1074+1216T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89398801 | ||||||
| chr11:89398886
|
G | A | 1 | a0001c0001t0109g0281 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1074+1131C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89398886 | ||||||
| chr11:89398923
|
C | T | 51 | a0001c0001t0003g0170a0001c0001t0003g0191a0001c0001t0003g0205others(48): Show | 51 | HG00408.hp2 HG00621.hp1 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.1074+1094G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89398923 | ||||||
| chr11:89399130
|
A | G | 2 | a0001c0001t0017g0171a0001c0001t0017g0172 | 2 | HG01074.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1074+887T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89399130 | ||||||
| chr11:89399285
|
T | C | 3 | a0001c0001t0048g0044a0001c0001t0049g0043a0001c0001t0079g0169 | 3 | HG02895.hp2 HG02897.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1074+732A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89399285 | ||||||
| chr11:89399303
|
T | C | 28 | a0001c0001t0002g0242a0001c0001t0002g0246a0001c0001t0002g0252others(25): Show | 28 | HG00408.hp1 HG02280.hp1 HG02622.hp1 others(25): Show |
intron_variant | MODIFIER | c.1074+714A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89399303 | ||||||
| chr11:89399335
|
C | T | 2 | a0001c0001t0018g0142a0001c0001t0078g0143 | 2 | HG02280.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1074+682G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89399335 | ||||||
| chr11:89399429
|
T | TTAAATAT others(5): Show |
1 | a0001c0001t0111g0277 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1074+576_1074+587d others(14): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89399429 | ||||||
| chr11:89399432
|
A | AAT | 26 | a0001c0001t0001g0001a0001c0001t0001g0026a0001c0001t0001g0050others(23): Show | 27 | HG00140.hp1 HG00621.hp1 HG00621.hp2 others(24): Show |
intron_variant | MODIFIER | c.1074+583_1074+584d others(4): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89399432 | ||||||
| chr11:89399432
|
A | AATAT | 20 | a0001c0001t0001g0132a0001c0001t0002g0270a0001c0001t0002g0276others(17): Show | 20 | HG00642.hp2 HG00741.hp2 HG01106.hp2 others(17): Show |
intron_variant | MODIFIER | c.1074+581_1074+584d others(6): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89399432 | ||||||
| chr11:89399432
|
A | AATATAT | 14 | a0001c0001t0001g0129a0001c0001t0003g0170a0001c0001t0007g0007others(11): Show | 14 | HG00741.hp1 HG01256.hp1 HG01257.hp2 others(11): Show |
intron_variant | MODIFIER | c.1074+579_1074+584d others(8): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89399432 | ||||||
| chr11:89399432
|
A | AATATATA others(1): Show |
20 | a0001c0001t0001g0023a0001c0001t0001g0029a0001c0001t0002g0266others(17): Show | 20 | HG00140.hp2 HG00735.hp2 HG01167.hp1 others(17): Show |
intron_variant | MODIFIER | c.1074+577_1074+584d others(10): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89399432 | ||||||
| chr11:89399432
|
A | AATATATA others(3): Show |
11 | a0001c0001t0001g0030a0001c0001t0091g0151a0001c0001t0115g0253others(8): Show | 11 | HG01074.hp1 HG02280.hp2 HG02300.hp1 others(8): Show |
intron_variant | MODIFIER | c.1074+575_1074+584d others(12): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89399432 | ||||||
| chr11:89399432
|
A | AATATATA others(9): Show |
2 | a0001c0002t0011g0153a0001c0002t0029g0154 | 2 | HG01109.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1074+584_1074+585i others(18): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89399432 | ||||||
| chr11:89399432
|
A | AATATATA others(5): Show |
1 | a0001c0003t0037g0251 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1074+573_1074+584d others(14): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89399432 | ||||||
| chr11:89399432
|
A | AATATATA others(7): Show |
1 | a0001c0003t0007g0053 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1074+571_1074+584d others(16): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89399432 | ||||||
| chr11:89399432
|
A | AATATATA others(9): Show |
1 | a0001c0006t0024g0199 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1074+569_1074+584d others(18): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89399432 | ||||||
| chr11:89399432
|
A | AATATATA others(11): Show |
1 | a0001c0002t0029g0168 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1074+567_1074+584d others(20): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89399432 | ||||||
| chr11:89399432
|
A | ATATATAT others(12): Show |
1 | a0001c0001t0001g0131 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.1074+584_1074+585i others(21): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89399432 | ||||||
| chr11:89399432
|
AAT | A | 17 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0003g0164others(14): Show | 17 | HG00639.hp1 HG00673.hp1 HG01109.hp2 others(14): Show |
intron_variant | MODIFIER | c.1074+583_1074+584d others(4): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89399432 | ||||||
| chr11:89399432
|
AATAT | A | 14 | a0001c0001t0002g0224a0001c0001t0002g0252a0001c0001t0003g0191others(11): Show | 14 | HG01978.hp1 HG02451.hp1 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.1074+581_1074+584d others(6): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89399432 | ||||||
| chr11:89399432
|
AATATATA others(1): Show |
A | 3 | a0001c0001t0002g0254a0001c0001t0002g0255a0001c0001t0106g0228 | 3 | HG03139.hp2 HG03471.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1074+577_1074+584d others(10): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89399432 | ||||||
| chr11:89399432
|
AATATATA others(5): Show |
A | 4 | a0001c0001t0085g0179a0001c0001t0094g0218a0001c0002t0011g0173others(1): Show | 4 | HG02572.hp1 HG02976.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1074+573_1074+584d others(14): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89399432 | ||||||
| chr11:89399432
|
AATATATA others(7): Show |
A | 19 | a0001c0001t0002g0242a0001c0001t0002g0246a0001c0001t0002g0264others(16): Show | 19 | HG00408.hp1 HG02698.hp1 HG02896.hp2 others(16): Show |
intron_variant | MODIFIER | c.1074+571_1074+584d others(16): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89399432 | ||||||
| chr11:89399432
|
AATATATA others(9): Show |
A | 3 | a0001c0001t0024g0210a0001c0002t0009g0240a0001c0002t0075g0183 | 3 | NA18944.hp2 NA19005.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.1074+569_1074+584d others(18): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89399432 | ||||||
| chr11:89399434
|
T | TATATATA others(3): Show |
3 | a0001c0001t0002g0245a0001c0001t0017g0165a0001c0001t0109g0281 | 3 | HG02630.hp1 HG02723.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.1074+582_1074+583i others(12): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89399434 | ||||||
| chr11:89399436
|
T | TATATATA others(1): Show |
4 | a0001c0001t0001g0004a0001c0001t0001g0061a0001c0001t0022g0140others(1): Show | 4 | HG00673.hp2 HG01081.hp1 NA19065.hp1 others(1): Show |
intron_variant | MODIFIER | c.1074+580_1074+581i others(10): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89399436 | ||||||
| chr11:89399438
|
T | TATATAA | 6 | a0001c0001t0001g0006a0001c0001t0003g0182a0001c0001t0058g0005others(3): Show | 6 | HG01081.hp2 HG01257.hp1 HG01952.hp1 others(3): Show |
intron_variant | MODIFIER | c.1074+578_1074+579i others(8): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89399438 | ||||||
| chr11:89399440
|
T | TATAA | 30 | a0001c0001t0001g0014a0001c0001t0001g0059a0001c0001t0001g0063others(27): Show | 30 | HG00099.hp1 HG00323.hp2 HG00735.hp1 others(27): Show |
intron_variant | MODIFIER | c.1074+576_1074+577i others(6): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89399440 | ||||||
| chr11:89399442
|
T | TAA | 55 | a0001c0001t0001g0008a0001c0001t0001g0035a0001c0001t0001g0062others(52): Show | 55 | HG00099.hp2 HG00544.hp1 HG00558.hp1 others(52): Show |
intron_variant | MODIFIER | c.1074+574_1074+575i others(4): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89399442 | ||||||
| chr11:89399442
|
T | TAAATATA others(7): Show |
1 | a0001c0001t0082g0174 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1074+574_1074+575i others(16): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89399442 | ||||||
| chr11:89399444
|
T | A | 2 | a0001c0001t0001g0013a0001c0001t0001g0103 | 2 | HG02004.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.1074+573A>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89399444 | ||||||
| chr11:89399456
|
T | C | 1 | a0001c0001t0052g0122 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1074+561A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89399456 | ||||||
| chr11:89399472
|
T | TATATATA others(14): Show |
1 | a0001c0001t0002g0268 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.1074+544_1074+545i others(23): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89399472 | ||||||
| chr11:89399535
|
C | T | 15 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0061others(12): Show | 15 | HG01081.hp2 HG01952.hp1 HG02132.hp1 others(12): Show |
intron_variant | MODIFIER | c.1074+482G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89399535 | ||||||
| chr11:89399544
|
A | T | 1 | a0001c0001t0113g0227 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1074+473T>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89399544 | ||||||
| chr11:89399843
|
G | A | 1 | a0001c0001t0007g0125 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1074+174C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89399843 | ||||||
| chr11:89399911
|
G | A | 28 | a0001c0001t0002g0242a0001c0001t0002g0246a0001c0001t0002g0252others(25): Show | 28 | HG00408.hp1 HG02280.hp1 HG02622.hp1 others(25): Show |
intron_variant | MODIFIER | c.1074+106C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89399911 | ||||||
| chr11:89400002
|
A | C | 2 | a0001c0001t0018g0142a0001c0001t0078g0143 | 2 | HG02280.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1074+15T>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89400002 | ||||||
| chr11:89400005
|
T | G | 1 | a0001c0001t0021g0010 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1074+12A>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 11/17 | chr11 | 89400005 | ||||||
| chr11:89400404
|
C | T | 1 | a0001c0001t0113g0227 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.847-25G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 9/17 | chr11 | 89400404 | ||||||
| chr11:89400509
|
C | T | 1 | a0001c0001t0002g0261 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.847-130G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 9/17 | chr11 | 89400509 | ||||||
| chr11:89400516
|
G | A | 51 | a0001c0001t0003g0170a0001c0001t0003g0191a0001c0001t0003g0205others(48): Show | 51 | HG00408.hp2 HG00621.hp1 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.847-137C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 9/17 | chr11 | 89400516 | ||||||
| chr11:89400609
|
C | T | 83 | a0001c0001t0002g0242a0001c0001t0002g0246a0001c0001t0002g0252others(80): Show | 83 | HG00408.hp1 HG00408.hp2 HG00621.hp1 others(80): Show |
intron_variant | MODIFIER | c.847-230G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 9/17 | chr11 | 89400609 | ||||||
| chr11:89400630
|
G | A | 83 | a0001c0001t0002g0242a0001c0001t0002g0246a0001c0001t0002g0252others(80): Show | 83 | HG00408.hp1 HG00408.hp2 HG00621.hp1 others(80): Show |
intron_variant | MODIFIER | c.847-251C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 9/17 | chr11 | 89400630 | ||||||
| chr11:89400718
|
G | A | 1 | a0001c0001t0052g0122 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.847-339C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 9/17 | chr11 | 89400718 | ||||||
| chr11:89400733
|
C | T | 1 | a0001c0001t0107g0225 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.847-354G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 9/17 | chr11 | 89400733 | ||||||
| chr11:89400746
|
G | A | 25 | a0001c0001t0002g0242a0001c0001t0002g0246a0001c0001t0002g0252others(22): Show | 25 | HG00408.hp1 HG02622.hp1 HG02698.hp1 others(22): Show |
intron_variant | MODIFIER | c.847-367C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 9/17 | chr11 | 89400746 | ||||||
| chr11:89400849
|
G | GTA | 8 | a0001c0001t0017g0160a0001c0001t0107g0225a0001c0002t0011g0157others(5): Show | 8 | HG01884.hp1 HG02615.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.847-472_847-471dup others(2): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 9/17 | chr11 | 89400849 | ||||||
| chr11:89400849
|
GTA | G | 142 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0008others(139): Show | 142 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(139): Show |
intron_variant | MODIFIER | c.847-472_847-471del others(2): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 9/17 | chr11 | 89400849 | ||||||
| chr11:89400902
|
G | C | 1 | a0001c0003t0004g0037 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.847-523C>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 9/17 | chr11 | 89400902 | ||||||
| chr11:89401035
|
T | C | 2 | a0001c0001t0002g0245a0001c0012t0023g0181 | 2 | HG02723.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.847-656A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 9/17 | chr11 | 89401035 | ||||||
| chr11:89401058
|
G | T | 2 | a0001c0001t0017g0171a0001c0001t0017g0172 | 2 | HG01074.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.847-679C>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 9/17 | chr11 | 89401058 | ||||||
| chr11:89401062
|
T | A | 1 | a0001c0001t0001g0134 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.847-683A>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 9/17 | chr11 | 89401062 | ||||||
| chr11:89401117
|
C | T | 3 | a0001c0001t0095g0215a0001c0001t0096g0217a0001c0001t0097g0216 | 3 | HG02055.hp1 HG02559.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.847-738G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 9/17 | chr11 | 89401117 | ||||||
| chr11:89401126
|
G | T | 9 | a0001c0001t0017g0160a0001c0001t0048g0044a0001c0001t0049g0043others(6): Show | 9 | HG01884.hp1 HG02615.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.847-747C>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 9/17 | chr11 | 89401126 | ||||||
| chr11:89401194
|
C | T | 86 | a0001c0001t0002g0242a0001c0001t0002g0246a0001c0001t0002g0252others(83): Show | 86 | HG00408.hp1 HG00408.hp2 HG00621.hp1 others(83): Show |
intron_variant | MODIFIER | c.847-815G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 9/17 | chr11 | 89401194 | ||||||
| chr11:89401251
|
A | G | 36 | a0001c0001t0002g0242a0001c0001t0002g0246a0001c0001t0002g0252others(33): Show | 36 | HG00408.hp1 HG01074.hp2 HG02145.hp2 others(33): Show |
intron_variant | MODIFIER | c.847-872T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 9/17 | chr11 | 89401251 | ||||||
| chr11:89401268
|
A | T | 3 | a0001c0001t0002g0252a0001c0001t0117g0287a0001c0002t0074g0146 | 3 | HG02622.hp1 HG03098.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.847-889T>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 9/17 | chr11 | 89401268 | ||||||
| chr11:89401409
|
C | T | 3 | a0001c0001t0002g0252a0001c0001t0117g0287a0001c0002t0074g0146 | 3 | HG02622.hp1 HG03098.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.846+917G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 9/17 | chr11 | 89401409 | ||||||
| chr11:89401605
|
A | T | 22 | a0001c0001t0002g0242a0001c0001t0002g0246a0001c0001t0002g0264others(19): Show | 22 | HG00408.hp1 HG02698.hp1 HG03139.hp1 others(19): Show |
intron_variant | MODIFIER | c.846+721T>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 9/17 | chr11 | 89401605 | ||||||
| chr11:89401708
|
T | G | 1 | a0001c0002t0042g0136 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.846+618A>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 9/17 | chr11 | 89401708 | ||||||
| chr11:89401828
|
T | C | 1 | a0001c0001t0015g0057 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.846+498A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 9/17 | chr11 | 89401828 | ||||||
| chr11:89401833
|
G | A | 4 | a0001c0001t0023g0161a0001c0001t0031g0176a0001c0001t0031g0177others(1): Show | 4 | HG02486.hp2 HG03209.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.846+493C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 9/17 | chr11 | 89401833 | ||||||
| chr11:89401903
|
T | C | 1 | a0001c0001t0113g0227 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.846+423A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 9/17 | chr11 | 89401903 | ||||||
| chr11:89401920
|
C | T | 1 | a0001c0001t0079g0169 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.846+406G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 9/17 | chr11 | 89401920 | ||||||
| chr11:89401938
|
A | G | 4 | a0001c0001t0002g0224a0001c0001t0002g0254a0001c0001t0002g0255others(1): Show | 4 | HG02451.hp1 HG03139.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.846+388T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 9/17 | chr11 | 89401938 | ||||||
| chr11:89402000
|
A | T | 215 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0008others(212): Show | 215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
intron_variant | MODIFIER | c.846+326T>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 9/17 | chr11 | 89402000 | ||||||
| chr11:89402004
|
A | G | 1 | a0001c0002t0009g0278 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.846+322T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 9/17 | chr11 | 89402004 | ||||||
| chr11:89402084
|
G | A | 1 | a0001c0002t0029g0168 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.846+242C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 9/17 | chr11 | 89402084 | ||||||
| chr11:89402085
|
T | C | 1 | a0001c0001t0068g0064 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.846+241A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 9/17 | chr11 | 89402085 | ||||||
| chr11:89402186
|
T | C | 3 | a0001c0001t0018g0142a0001c0001t0018g0175a0001c0001t0078g0143 | 3 | HG02280.hp1 NA19240.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.846+140A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 9/17 | chr11 | 89402186 | ||||||
| chr11:89402257
|
T | A | 1 | a0001c0001t0071g0090 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.846+69A>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 9/17 | chr11 | 89402257 | ||||||
| chr11:89402602
|
C | T | 3 | a0001c0002t0033g0285a0001c0002t0098g0284a0001c0002t0099g0286 | 3 | HG02976.hp1 HG03195.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.630-60G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89402602 | ||||||
| chr11:89402823
|
A | G | 2 | a0001c0001t0031g0176a0001c0001t0031g0177 | 2 | HG03209.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.630-281T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89402823 | ||||||
| chr11:89403413
|
C | T | 4 | a0001c0001t0005g0149a0001c0001t0005g0150a0001c0001t0103g0272others(1): Show | 4 | HG02896.hp1 HG02897.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.630-871G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89403413 | ||||||
| chr11:89403467
|
G | A | 1 | a0001c0001t0003g0164 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.630-925C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89403467 | ||||||
| chr11:89403499
|
C | T | 4 | a0001c0001t0002g0224a0001c0001t0002g0254a0001c0001t0002g0255others(1): Show | 4 | HG02451.hp1 HG03139.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.630-957G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89403499 | ||||||
| chr11:89403547
|
C | T | 1 | a0001c0001t0088g0158 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.630-1005G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89403547 | ||||||
| chr11:89403557
|
G | C | 216 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0008others(213): Show | 216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
intron_variant | MODIFIER | c.630-1015C>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89403557 | ||||||
| chr11:89403557
|
G | T | 1 | a0001c0001t0023g0161 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.630-1015C>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89403557 | ||||||
| chr11:89403571
|
C | T | 4 | a0001c0002t0009g0236a0001c0002t0034g0237a0001c0002t0035g0229others(1): Show | 4 | NA18957.hp1 NA18965.hp2 NA18998.hp2 others(1): Show |
intron_variant | MODIFIER | c.630-1029G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89403571 | ||||||
| chr11:89404048
|
CA | C | 51 | a0001c0001t0003g0170a0001c0001t0003g0191a0001c0001t0003g0205others(48): Show | 51 | HG00408.hp2 HG00621.hp1 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.630-1507delT | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89404048 | ||||||
| chr11:89404268
|
GA | G | 22 | a0001c0001t0002g0242a0001c0001t0002g0246a0001c0001t0002g0264others(19): Show | 22 | HG00408.hp1 HG02698.hp1 HG03139.hp1 others(19): Show |
intron_variant | MODIFIER | c.630-1727delT | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89404268 | ||||||
| chr11:89404340
|
G | A | 3 | a0001c0001t0018g0142a0001c0001t0018g0175a0001c0001t0078g0143 | 3 | HG02280.hp1 NA19240.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.630-1798C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89404340 | ||||||
| chr11:89404369
|
G | A | 1 | a0001c0001t0017g0165 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.630-1827C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89404369 | ||||||
| chr11:89404539
|
C | A | 4 | a0001c0001t0052g0122a0001c0002t0033g0285a0001c0002t0098g0284others(1): Show | 4 | HG02145.hp2 HG02976.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.630-1997G>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89404539 | ||||||
| chr11:89404557
|
T | C | 2 | a0001c0001t0005g0178a0001c0001t0091g0151 | 2 | HG02280.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.630-2015A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89404557 | ||||||
| chr11:89404708
|
A | G | 2 | a0001c0001t0018g0142a0001c0001t0078g0143 | 2 | HG02280.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.630-2166T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89404708 | ||||||
| chr11:89404742
|
C | T | 4 | a0001c0001t0023g0161a0001c0001t0031g0176a0001c0001t0031g0177others(1): Show | 4 | HG02486.hp2 HG03209.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.630-2200G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89404742 | ||||||
| chr11:89404897
|
A | G | 2 | a0001c0001t0005g0178a0001c0001t0091g0151 | 2 | HG02280.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.630-2355T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89404897 | ||||||
| chr11:89404954
|
G | A | 51 | a0001c0001t0003g0170a0001c0001t0003g0191a0001c0001t0003g0205others(48): Show | 51 | HG00408.hp2 HG00621.hp1 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.630-2412C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89404954 | ||||||
| chr11:89404982
|
C | T | 42 | a0001c0001t0003g0191a0001c0001t0003g0205a0001c0001t0008g0107others(39): Show | 42 | HG00408.hp2 HG00621.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.630-2440G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89404982 | ||||||
| chr11:89405080
|
T | TTG | 7 | a0001c0001t0002g0224a0001c0001t0002g0254a0001c0001t0002g0255others(4): Show | 7 | HG00639.hp1 HG00642.hp1 HG01346.hp1 others(4): Show |
intron_variant | MODIFIER | c.630-2540_630-2539d others(4): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89405080 | ||||||
| chr11:89405080
|
T | TTGTG | 5 | a0001c0001t0018g0142a0001c0001t0018g0175a0001c0001t0078g0143others(2): Show | 5 | HG02280.hp1 HG02976.hp2 NA18612.hp1 others(2): Show |
intron_variant | MODIFIER | c.630-2542_630-2539d others(6): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89405080 | ||||||
| chr11:89405080
|
T | TTGTGTG | 6 | a0001c0001t0002g0266a0001c0001t0002g0268a0001c0001t0002g0269others(3): Show | 6 | HG00735.hp2 HG00741.hp2 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.630-2544_630-2539d others(8): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89405080 | ||||||
| chr11:89405080
|
T | TTGTGTGT others(1): Show |
4 | a0001c0001t0052g0122a0001c0002t0033g0285a0001c0002t0098g0284others(1): Show | 4 | HG02145.hp2 HG02976.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.630-2546_630-2539d others(10): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89405080 | ||||||
| chr11:89405080
|
T | TTGTGTGT others(3): Show |
14 | a0001c0001t0017g0160a0001c0001t0023g0161a0001c0001t0024g0155others(11): Show | 14 | HG01884.hp1 HG02486.hp2 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.630-2548_630-2539d others(12): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89405080 | ||||||
| chr11:89405080
|
T | TTGTGTGT others(5): Show |
10 | a0001c0001t0001g0062a0001c0001t0001g0088a0001c0001t0001g0138others(7): Show | 10 | HG01243.hp1 HG03139.hp1 HG03209.hp1 others(7): Show |
intron_variant | MODIFIER | c.630-2550_630-2539d others(14): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89405080 | ||||||
| chr11:89405080
|
T | TTGTGTGT others(7): Show |
24 | a0001c0001t0001g0098a0001c0001t0002g0283a0001c0001t0005g0149others(21): Show | 24 | HG00558.hp1 HG00673.hp2 HG01109.hp1 others(21): Show |
intron_variant | MODIFIER | c.630-2552_630-2539d others(16): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89405080 | ||||||
| chr11:89405080
|
T | TTGTGTGT others(9): Show |
51 | a0001c0001t0001g0008a0001c0001t0001g0081a0001c0001t0001g0110others(48): Show | 51 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(48): Show |
intron_variant | MODIFIER | c.630-2554_630-2539d others(18): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89405080 | ||||||
| chr11:89405080
|
T | TTGTGTGT others(11): Show |
70 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0013others(67): Show | 70 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(67): Show |
intron_variant | MODIFIER | c.630-2556_630-2539d others(20): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89405080 | ||||||
| chr11:89405080
|
T | TTGTGTGT others(13): Show |
20 | a0001c0001t0001g0014a0001c0001t0001g0134a0001c0001t0002g0256others(17): Show | 20 | HG01243.hp2 HG01255.hp1 HG01346.hp2 others(17): Show |
intron_variant | MODIFIER | c.630-2558_630-2539d others(22): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89405080 | ||||||
| chr11:89405080
|
T | TTGTGTGT others(15): Show |
4 | a0001c0001t0002g0260a0001c0002t0100g0258a0001c0003t0003g0193others(1): Show | 4 | HG01074.hp1 HG01981.hp2 HG02015.hp1 others(1): Show |
intron_variant | MODIFIER | c.630-2560_630-2539d others(24): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89405080 | ||||||
| chr11:89405080
|
T | TTGTGTGT others(17): Show |
8 | a0001c0001t0001g0059a0001c0001t0001g0063a0001c0001t0019g0166others(5): Show | 8 | HG01081.hp1 HG02809.hp1 HG03579.hp2 others(5): Show |
intron_variant | MODIFIER | c.630-2562_630-2539d others(26): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89405080 | ||||||
| chr11:89405080
|
TTGTG | T | 3 | a0001c0001t0002g0252a0001c0001t0117g0287a0001c0002t0074g0146 | 3 | HG02622.hp1 HG03098.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.630-2542_630-2539d others(6): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89405080 | ||||||
| chr11:89405103
|
T | TGTGTGTG others(7): Show |
2 | a0001c0001t0017g0171a0001c0001t0017g0172 | 2 | HG01074.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.630-2562_630-2561i others(16): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89405103 | ||||||
| chr11:89405204
|
A | C | 28 | a0001c0001t0002g0242a0001c0001t0002g0246a0001c0001t0002g0252others(25): Show | 28 | HG00408.hp1 HG02280.hp1 HG02622.hp1 others(25): Show |
intron_variant | MODIFIER | c.630-2662T>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89405204 | ||||||
| chr11:89405271
|
C | T | 1 | a0001c0003t0003g0189 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.630-2729G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89405271 | ||||||
| chr11:89405317
|
C | T | 1 | a0001c0001t0007g0126 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.630-2775G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89405317 | ||||||
| chr11:89405323
|
A | C | 1 | a0001c0002t0006g0034 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.630-2781T>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89405323 | ||||||
| chr11:89405552
|
T | A | 3 | a0001c0001t0001g0008a0001c0001t0004g0003a0001c0001t0008g0002 | 3 | HG00558.hp1 NA18995.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.630-3010A>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89405552 | ||||||
| chr11:89405570
|
C | A | 1 | a0001c0003t0020g0121 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.630-3028G>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89405570 | ||||||
| chr11:89405624
|
C | CA | 89 | a0001c0001t0001g0026a0001c0001t0002g0242a0001c0001t0002g0246others(86): Show | 89 | HG00408.hp1 HG00408.hp2 HG00621.hp1 others(86): Show |
intron_variant | MODIFIER | c.630-3083dupT | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89405624 | ||||||
| chr11:89405643
|
G | A | 3 | a0001c0001t0001g0063a0001c0001t0022g0140a0001c0002t0100g0258 | 3 | HG01081.hp1 HG02965.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.630-3101C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89405643 | ||||||
| chr11:89405694
|
G | A | 9 | a0001c0001t0017g0160a0001c0001t0048g0044a0001c0001t0049g0043others(6): Show | 9 | HG01884.hp1 HG02615.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.630-3152C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89405694 | ||||||
| chr11:89405745
|
T | TA | 11 | a0001c0001t0003g0205a0001c0001t0017g0160a0001c0001t0068g0064others(8): Show | 11 | HG01884.hp1 HG01884.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.630-3204dupT | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89405745 | ||||||
| chr11:89405749
|
AAAG | A | 25 | a0001c0001t0002g0242a0001c0001t0002g0246a0001c0001t0002g0264others(22): Show | 25 | HG00408.hp1 HG01074.hp2 HG02698.hp1 others(22): Show |
intron_variant | MODIFIER | c.630-3210_630-3208d others(5): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89405749 | ||||||
| chr11:89405750
|
AAG | A | 7 | a0001c0001t0001g0110a0001c0001t0002g0224a0001c0001t0002g0254others(4): Show | 7 | HG01515.hp2 HG02451.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.630-3210_630-3209d others(4): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89405750 | ||||||
| chr11:89405751
|
AG | A | 93 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0013others(90): Show | 93 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(90): Show |
intron_variant | MODIFIER | c.630-3210delC | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89405751 | ||||||
| chr11:89405752
|
G | A | 94 | a0001c0001t0001g0008a0001c0001t0001g0035a0001c0001t0001g0070others(91): Show | 94 | HG00408.hp2 HG00544.hp1 HG00621.hp1 others(91): Show |
intron_variant | MODIFIER | c.630-3210C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89405752 | ||||||
| chr11:89405757
|
A | C | 2 | a0001c0002t0101g0239a0001c0003t0005g0194 | 2 | HG01358.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.630-3215T>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89405757 | ||||||
| chr11:89405761
|
A | C | 9 | a0001c0001t0005g0149a0001c0001t0005g0150a0001c0001t0005g0178others(6): Show | 9 | HG02280.hp2 HG02572.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.630-3219T>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89405761 | ||||||
| chr11:89405797
|
T | C | 1 | a0001c0001t0023g0161 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.630-3255A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89405797 | ||||||
| chr11:89405826
|
A | G | 51 | a0001c0001t0003g0170a0001c0001t0003g0191a0001c0001t0003g0205others(48): Show | 51 | HG00408.hp2 HG00621.hp1 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.630-3284T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89405826 | ||||||
| chr11:89405869
|
T | C | 4 | a0001c0001t0002g0224a0001c0001t0002g0254a0001c0001t0002g0255others(1): Show | 4 | HG02451.hp1 HG03139.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.630-3327A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89405869 | ||||||
| chr11:89406045
|
C | A | 24 | a0001c0001t0002g0242a0001c0001t0002g0246a0001c0001t0002g0264others(21): Show | 24 | HG00408.hp1 HG02698.hp1 HG03098.hp2 others(21): Show |
intron_variant | MODIFIER | c.630-3503G>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89406045 | ||||||
| chr11:89406191
|
T | C | 1 | a0001c0001t0081g0163 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.630-3649A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89406191 | ||||||
| chr11:89406196
|
A | G | 1 | a0001c0001t0017g0165 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.630-3654T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89406196 | ||||||
| chr11:89406296
|
A | T | 1 | a0001c0002t0035g0248 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.630-3754T>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89406296 | ||||||
| chr11:89406313
|
G | A | 1 | a0001c0001t0113g0227 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.630-3771C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89406313 | ||||||
| chr11:89406356
|
A | G | 1 | a0001c0001t0068g0064 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.630-3814T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89406356 | ||||||
| chr11:89406360
|
T | C | 1 | a0001c0001t0003g0205 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.630-3818A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89406360 | ||||||
| chr11:89406423
|
C | T | 2 | a0002c0004t0032g0144a0002c0004t0032g0162 | 2 | HG02615.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.630-3881G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89406423 | ||||||
| chr11:89406796
|
T | C | 22 | a0001c0001t0002g0242a0001c0001t0002g0246a0001c0001t0002g0264others(19): Show | 22 | HG00408.hp1 HG02698.hp1 HG03139.hp1 others(19): Show |
intron_variant | MODIFIER | c.630-4254A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89406796 | ||||||
| chr11:89407046
|
T | C | 1 | a0001c0003t0005g0206 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.630-4504A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89407046 | ||||||
| chr11:89407055
|
T | C | 3 | a0001c0001t0052g0122a0001c0001t0069g0015a0001c0001t0112g0282 | 3 | HG02145.hp2 HG02896.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.630-4513A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89407055 | ||||||
| chr11:89407064
|
T | C | 2 | a0001c0001t0017g0171a0001c0001t0017g0172 | 2 | HG01074.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.630-4522A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89407064 | ||||||
| chr11:89407120
|
A | G | 1 | a0001c0001t0068g0064 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.630-4578T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89407120 | ||||||
| chr11:89407200
|
T | C | 51 | a0001c0001t0003g0170a0001c0001t0003g0191a0001c0001t0003g0205others(48): Show | 51 | HG00408.hp2 HG00621.hp1 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.630-4658A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89407200 | ||||||
| chr11:89407322
|
T | A | 1 | a0001c0001t0113g0227 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.630-4780A>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89407322 | ||||||
| chr11:89407338
|
T | C | 2 | a0001c0001t0017g0171a0001c0001t0017g0172 | 2 | HG01074.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.630-4796A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89407338 | ||||||
| chr11:89407405
|
G | T | 3 | a0001c0001t0002g0252a0001c0001t0117g0287a0001c0002t0074g0146 | 3 | HG02622.hp1 HG03098.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.630-4863C>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89407405 | ||||||
| chr11:89407554
|
T | A | 6 | a0001c0001t0017g0160a0001c0001t0107g0225a0001c0002t0011g0157others(3): Show | 6 | HG01884.hp1 HG02615.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.630-5012A>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89407554 | ||||||
| chr11:89407635
|
G | T | 2 | a0001c0001t0085g0179a0001c0001t0113g0227 | 2 | HG01243.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.630-5093C>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89407635 | ||||||
| chr11:89407657
|
T | C | 1 | a0001c0001t0085g0179 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.630-5115A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89407657 | ||||||
| chr11:89407660
|
G | C | 1 | a0001c0001t0085g0179 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.630-5118C>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89407660 | ||||||
| chr11:89407662
|
T | C | 10 | a0001c0001t0001g0063a0001c0001t0002g0252a0001c0001t0019g0166others(7): Show | 10 | HG01081.hp1 HG01109.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.630-5120A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89407662 | ||||||
| chr11:89407814
|
A | G | 3 | a0001c0001t0001g0032a0001c0001t0007g0049a0001c0001t0022g0040 | 3 | HG00639.hp1 HG02145.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.630-5272T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89407814 | ||||||
| chr11:89407825
|
GC | G | 50 | a0001c0001t0003g0170a0001c0001t0003g0191a0001c0001t0003g0205others(47): Show | 50 | HG00408.hp2 HG00621.hp1 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.630-5284delG | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89407825 | ||||||
| chr11:89407986
|
A | AT | 211 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0008others(208): Show | 211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.630-5445dupA | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89407986 | ||||||
| chr11:89407999
|
A | G | 2 | a0001c0001t0023g0161a0001c0001t0071g0090 | 2 | HG02486.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.630-5457T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89407999 | ||||||
| chr11:89408010
|
A | T | 2 | a0001c0001t0017g0171a0001c0001t0017g0172 | 2 | HG01074.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.630-5468T>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89408010 | ||||||
| chr11:89408211
|
A | G | 50 | a0001c0001t0003g0170a0001c0001t0003g0191a0001c0001t0003g0205others(47): Show | 50 | HG00408.hp2 HG00621.hp1 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.630-5669T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89408211 | ||||||
| chr11:89408338
|
C | T | 214 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0008others(211): Show | 214 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(211): Show |
intron_variant | MODIFIER | c.630-5796G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89408338 | ||||||
| chr11:89408436
|
C | T | 76 | a0001c0001t0002g0242a0001c0001t0002g0246a0001c0001t0002g0264others(73): Show | 76 | HG00408.hp1 HG00408.hp2 HG00621.hp1 others(73): Show |
intron_variant | MODIFIER | c.630-5894G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89408436 | ||||||
| chr11:89408446
|
T | C | 3 | a0001c0001t0048g0044a0001c0001t0049g0043a0001c0001t0079g0169 | 3 | HG02895.hp2 HG02897.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.630-5904A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89408446 | ||||||
| chr11:89408669
|
A | G | 22 | a0001c0001t0002g0242a0001c0001t0002g0246a0001c0001t0002g0264others(19): Show | 22 | HG00408.hp1 HG02698.hp1 HG03139.hp1 others(19): Show |
intron_variant | MODIFIER | c.630-6127T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89408669 | ||||||
| chr11:89408718
|
T | C | 1 | a0001c0002t0009g0278 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.630-6176A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89408718 | ||||||
| chr11:89408750
|
T | A | 128 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0008others(125): Show | 128 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(125): Show |
intron_variant | MODIFIER | c.630-6208A>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89408750 | ||||||
| chr11:89408828
|
C | T | 53 | a0001c0001t0003g0170a0001c0001t0003g0191a0001c0001t0003g0205others(50): Show | 53 | HG00408.hp2 HG00621.hp1 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.630-6286G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89408828 | ||||||
| chr11:89408829
|
G | A | 2 | a0001c0002t0011g0153a0001c0002t0029g0154 | 2 | HG01109.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.630-6287C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89408829 | ||||||
| chr11:89408838
|
T | C | 7 | a0001c0001t0017g0160a0001c0001t0048g0044a0001c0001t0049g0043others(4): Show | 7 | HG01884.hp1 HG02615.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.630-6296A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89408838 | ||||||
| chr11:89408882
|
G | A | 2 | a0001c0001t0017g0171a0001c0001t0017g0172 | 2 | HG01074.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.630-6340C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89408882 | ||||||
| chr11:89408934
|
A | T | 128 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0008others(125): Show | 128 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(125): Show |
intron_variant | MODIFIER | c.630-6392T>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89408934 | ||||||
| chr11:89409097
|
GA | G | 50 | a0001c0001t0003g0170a0001c0001t0003g0191a0001c0001t0003g0205others(47): Show | 50 | HG00408.hp2 HG00621.hp1 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.630-6556delT | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89409097 | ||||||
| chr11:89409234
|
G | C | 1 | a0001c0001t0016g0012 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.630-6692C>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89409234 | ||||||
| chr11:89409403
|
T | A | 3 | a0001c0001t0048g0044a0001c0001t0049g0043a0001c0001t0079g0169 | 3 | HG02895.hp2 HG02897.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.630-6861A>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89409403 | ||||||
| chr11:89409490
|
A | G | 5 | a0001c0001t0001g0063a0001c0001t0019g0166a0001c0001t0022g0140others(2): Show | 5 | HG01081.hp1 HG01884.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.630-6948T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89409490 | ||||||
| chr11:89409529
|
G | A | 1 | a0001c0001t0001g0030 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.630-6987C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89409529 | ||||||
| chr11:89409593
|
CA | C | 9 | a0001c0001t0017g0160a0001c0001t0031g0176a0001c0001t0031g0177others(6): Show | 9 | HG01884.hp1 HG02615.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.630-7052delT | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89409593 | ||||||
| chr11:89409658
|
A | G | 3 | a0001c0002t0009g0236a0001c0002t0034g0237a0001c0002t0035g0229 | 3 | NA18957.hp1 NA18965.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.630-7116T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89409658 | ||||||
| chr11:89409739
|
A | T | 17 | a0001c0001t0002g0224a0001c0001t0002g0254a0001c0001t0002g0255others(14): Show | 17 | HG02258.hp1 HG02451.hp1 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.630-7197T>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89409739 | ||||||
| chr11:89409740
|
A | T | 17 | a0001c0001t0002g0224a0001c0001t0002g0254a0001c0001t0002g0255others(14): Show | 17 | HG02258.hp1 HG02451.hp1 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.630-7198T>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89409740 | ||||||
| chr11:89409741
|
A | T | 17 | a0001c0001t0002g0224a0001c0001t0002g0254a0001c0001t0002g0255others(14): Show | 17 | HG02258.hp1 HG02451.hp1 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.630-7199T>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89409741 | ||||||
| chr11:89409742
|
A | T | 17 | a0001c0001t0002g0224a0001c0001t0002g0254a0001c0001t0002g0255others(14): Show | 17 | HG02258.hp1 HG02451.hp1 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.630-7200T>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89409742 | ||||||
| chr11:89409743
|
A | T | 17 | a0001c0001t0002g0224a0001c0001t0002g0254a0001c0001t0002g0255others(14): Show | 17 | HG02258.hp1 HG02451.hp1 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.630-7201T>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89409743 | ||||||
| chr11:89409867
|
A | G | 2 | a0001c0003t0013g0135a0004c0007t0013g0089 | 2 | NA19070.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.630-7325T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89409867 | ||||||
| chr11:89410034
|
C | A | 140 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0008others(137): Show | 140 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(137): Show |
intron_variant | MODIFIER | c.630-7492G>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89410034 | ||||||
| chr11:89410057
|
AAAAAT | A | 151 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0008others(148): Show | 151 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(148): Show |
intron_variant | MODIFIER | c.630-7520_630-7516d others(7): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89410057 | ||||||
| chr11:89410079
|
A | C | 1 | a0001c0001t0001g0073 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.630-7537T>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89410079 | ||||||
| chr11:89410087
|
G | C | 3 | a0001c0002t0033g0285a0001c0002t0098g0284a0001c0002t0099g0286 | 3 | HG02976.hp1 HG03195.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.630-7545C>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89410087 | ||||||
| chr11:89410138
|
A | G | 140 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0008others(137): Show | 140 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(137): Show |
intron_variant | MODIFIER | c.630-7596T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89410138 | ||||||
| chr11:89410195
|
C | T | 3 | a0001c0002t0033g0285a0001c0002t0098g0284a0001c0002t0099g0286 | 3 | HG02976.hp1 HG03195.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.630-7653G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89410195 | ||||||
| chr11:89410209
|
G | A | 2 | a0001c0003t0005g0184a0001c0008t0002g0275 | 2 | HG00140.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.630-7667C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89410209 | ||||||
| chr11:89410245
|
T | C | 1 | a0001c0002t0074g0146 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.630-7703A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89410245 | ||||||
| chr11:89410362
|
T | C | 2 | a0001c0001t0031g0176a0001c0001t0031g0177 | 2 | HG03209.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.630-7820A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89410362 | ||||||
| chr11:89410456
|
G | A | 2 | a0001c0001t0081g0163a0001c0001t0086g0152 | 2 | HG01243.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.630-7914C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89410456 | ||||||
| chr11:89410503
|
C | T | 3 | a0001c0001t0081g0163a0001c0001t0082g0174a0001c0001t0086g0152 | 3 | HG01099.hp1 HG01243.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.630-7961G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89410503 | ||||||
| chr11:89410629
|
C | G | 5 | a0001c0001t0002g0252a0001c0001t0024g0155a0001c0002t0011g0156others(2): Show | 5 | HG02622.hp1 HG02647.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.630-8087G>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89410629 | ||||||
| chr11:89410643
|
A | G | 4 | a0001c0001t0002g0252a0001c0001t0024g0155a0001c0002t0011g0156others(1): Show | 4 | HG02622.hp1 HG02647.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.630-8101T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89410643 | ||||||
| chr11:89410860
|
T | G | 155 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0008others(152): Show | 155 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(152): Show |
intron_variant | MODIFIER | c.630-8318A>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89410860 | ||||||
| chr11:89410867
|
C | A | 140 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0008others(137): Show | 140 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(137): Show |
intron_variant | MODIFIER | c.630-8325G>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89410867 | ||||||
| chr11:89410957
|
G | C | 8 | a0001c0001t0003g0170a0001c0001t0073g0167a0001c0001t0094g0218others(5): Show | 8 | HG00741.hp1 HG01891.hp2 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.630-8415C>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89410957 | ||||||
| chr11:89411001
|
G | T | 1 | a0001c0002t0043g0024 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.630-8459C>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89411001 | ||||||
| chr11:89411017
|
C | T | 8 | a0001c0001t0001g0063a0001c0001t0019g0166a0001c0001t0022g0140others(5): Show | 8 | HG01081.hp1 HG01884.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.630-8475G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89411017 | ||||||
| chr11:89411080
|
C | T | 10 | a0001c0001t0017g0160a0001c0001t0031g0176a0001c0001t0031g0177others(7): Show | 10 | HG01884.hp1 HG02615.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.630-8538G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89411080 | ||||||
| chr11:89411081
|
C | T | 10 | a0001c0001t0017g0160a0001c0001t0031g0176a0001c0001t0031g0177others(7): Show | 10 | HG01884.hp1 HG02615.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.630-8539G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89411081 | ||||||
| chr11:89411096
|
A | G | 140 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0008others(137): Show | 140 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(137): Show |
intron_variant | MODIFIER | c.630-8554T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89411096 | ||||||
| chr11:89411230
|
G | A | 18 | a0001c0001t0002g0224a0001c0001t0002g0254a0001c0001t0002g0255others(15): Show | 18 | HG02083.hp1 HG02258.hp1 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.630-8688C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89411230 | ||||||
| chr11:89411263
|
G | A | 1 | a0001c0003t0020g0121 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.630-8721C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89411263 | ||||||
| chr11:89411270
|
A | T | 220 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0008others(217): Show | 220 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(217): Show |
intron_variant | MODIFIER | c.630-8728T>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89411270 | ||||||
| chr11:89411327
|
C | G | 5 | a0001c0001t0002g0252a0001c0001t0024g0155a0001c0002t0011g0156others(2): Show | 5 | HG02622.hp1 HG02647.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.630-8785G>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89411327 | ||||||
| chr11:89411335
|
G | A | 1 | a0001c0001t0007g0126 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.630-8793C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89411335 | ||||||
| chr11:89411363
|
G | A | 140 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0008others(137): Show | 140 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(137): Show |
intron_variant | MODIFIER | c.630-8821C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89411363 | ||||||
| chr11:89411634
|
T | C | 1 | a0001c0001t0016g0012 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.630-9092A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89411634 | ||||||
| chr11:89411677
|
T | C | 1 | a0002c0004t0032g0162 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.630-9135A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89411677 | ||||||
| chr11:89411797
|
G | C | 51 | a0001c0001t0002g0260a0001c0001t0003g0170a0001c0001t0003g0191others(48): Show | 51 | HG00408.hp2 HG00621.hp1 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.630-9255C>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89411797 | ||||||
| chr11:89411798
|
G | A | 3 | a0001c0001t0005g0178a0001c0001t0091g0151a0001c0001t0111g0277 | 3 | HG02280.hp2 HG02572.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.630-9256C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89411798 | ||||||
| chr11:89411934
|
C | T | 1 | a0001c0001t0007g0126 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.630-9392G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89411934 | ||||||
| chr11:89411949
|
C | T | 220 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0008others(217): Show | 220 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(217): Show |
intron_variant | MODIFIER | c.630-9407G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89411949 | ||||||
| chr11:89412150
|
C | T | 1 | a0001c0003t0004g0116 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.630-9608G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89412150 | ||||||
| chr11:89412254
|
C | T | 137 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0008others(134): Show | 137 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(134): Show |
intron_variant | MODIFIER | c.629+9648G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89412254 | ||||||
| chr11:89412472
|
C | A | 51 | a0001c0001t0002g0260a0001c0001t0003g0170a0001c0001t0003g0191others(48): Show | 51 | HG00408.hp2 HG00621.hp1 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.629+9430G>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89412472 | ||||||
| chr11:89412530
|
C | T | 3 | a0001c0002t0033g0285a0001c0002t0098g0284a0001c0002t0099g0286 | 3 | HG02976.hp1 HG03195.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.629+9372G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89412530 | ||||||
| chr11:89412868
|
A | G | 3 | a0001c0001t0018g0142a0001c0001t0018g0175a0001c0001t0078g0143 | 3 | HG02280.hp1 NA19240.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.629+9034T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89412868 | ||||||
| chr11:89412935
|
A | T | 2 | a0001c0001t0024g0210a0001c0002t0076g0209 | 2 | NA18962.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.629+8967T>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89412935 | ||||||
| chr11:89412982
|
GA | G | 10 | a0001c0001t0017g0160a0001c0001t0031g0176a0001c0001t0031g0177others(7): Show | 10 | HG01884.hp1 HG02615.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.629+8919delT | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89412982 | ||||||
| chr11:89413076
|
G | T | 3 | a0001c0001t0018g0142a0001c0001t0018g0175a0001c0001t0078g0143 | 3 | HG02280.hp1 NA19240.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.629+8826C>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89413076 | ||||||
| chr11:89413124
|
G | A | 1 | a0001c0001t0001g0131 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.629+8778C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89413124 | ||||||
| chr11:89413294
|
G | C | 10 | a0001c0001t0017g0160a0001c0001t0031g0176a0001c0001t0031g0177others(7): Show | 10 | HG01884.hp1 HG02615.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.629+8608C>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89413294 | ||||||
| chr11:89413481
|
G | A | 139 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0008others(136): Show | 139 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(136): Show |
intron_variant | MODIFIER | c.629+8421C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89413481 | ||||||
| chr11:89413495
|
C | T | 1 | a0001c0003t0089g0195 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.629+8407G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89413495 | ||||||
| chr11:89413515
|
C | G | 140 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0008others(137): Show | 140 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(137): Show |
intron_variant | MODIFIER | c.629+8387G>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89413515 | ||||||
| chr11:89413657
|
C | T | 15 | a0001c0001t0002g0252a0001c0001t0017g0160a0001c0001t0024g0155others(12): Show | 15 | HG01884.hp1 HG02615.hp1 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.629+8245G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89413657 | ||||||
| chr11:89413674
|
G | A | 140 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0008others(137): Show | 140 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(137): Show |
intron_variant | MODIFIER | c.629+8228C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89413674 | ||||||
| chr11:89413804
|
A | G | 1 | a0001c0003t0089g0195 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.629+8098T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89413804 | ||||||
| chr11:89413826
|
C | T | 140 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0008others(137): Show | 140 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(137): Show |
intron_variant | MODIFIER | c.629+8076G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89413826 | ||||||
| chr11:89413838
|
T | C | 1 | a0001c0002t0074g0146 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.629+8064A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89413838 | ||||||
| chr11:89413860
|
C | T | 15 | a0001c0001t0002g0252a0001c0001t0017g0160a0001c0001t0024g0155others(12): Show | 15 | HG01884.hp1 HG02615.hp1 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.629+8042G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89413860 | ||||||
| chr11:89413893
|
A | G | 1 | a0001c0001t0003g0205 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.629+8009T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89413893 | ||||||
| chr11:89413959
|
T | G | 2 | a0001c0001t0005g0178a0001c0001t0091g0151 | 2 | HG02280.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.629+7943A>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89413959 | ||||||
| chr11:89414140
|
T | C | 15 | a0001c0001t0002g0252a0001c0001t0017g0160a0001c0001t0024g0155others(12): Show | 15 | HG01884.hp1 HG02615.hp1 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.629+7762A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89414140 | ||||||
| chr11:89414148
|
C | G | 155 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0008others(152): Show | 155 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(152): Show |
intron_variant | MODIFIER | c.629+7754G>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89414148 | ||||||
| chr11:89414230
|
T | C | 1 | a0001c0002t0035g0248 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.629+7672A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89414230 | ||||||
| chr11:89414343
|
T | G | 3 | a0001c0001t0018g0142a0001c0001t0018g0175a0001c0001t0078g0143 | 3 | HG02280.hp1 NA19240.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.629+7559A>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89414343 | ||||||
| chr11:89414361
|
A | C | 6 | a0001c0001t0003g0191a0001c0001t0018g0192a0001c0001t0080g0203others(3): Show | 6 | NA18946.hp1 NA18951.hp2 NA18959.hp1 others(3): Show |
intron_variant | MODIFIER | c.629+7541T>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89414361 | ||||||
| chr11:89414613
|
T | A | 139 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0008others(136): Show | 139 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(136): Show |
intron_variant | MODIFIER | c.629+7289A>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89414613 | ||||||
| chr11:89414614
|
T | A | 139 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0008others(136): Show | 139 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(136): Show |
intron_variant | MODIFIER | c.629+7288A>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89414614 | ||||||
| chr11:89414615
|
T | A | 139 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0008others(136): Show | 139 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(136): Show |
intron_variant | MODIFIER | c.629+7287A>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89414615 | ||||||
| chr11:89414617
|
T | A | 139 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0008others(136): Show | 139 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(136): Show |
intron_variant | MODIFIER | c.629+7285A>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89414617 | ||||||
| chr11:89414619
|
T | A | 154 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0008others(151): Show | 154 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(151): Show |
intron_variant | MODIFIER | c.629+7283A>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89414619 | ||||||
| chr11:89414881
|
G | A | 139 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0008others(136): Show | 139 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(136): Show |
intron_variant | MODIFIER | c.629+7021C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89414881 | ||||||
| chr11:89414884
|
G | A | 154 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0008others(151): Show | 154 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(151): Show |
intron_variant | MODIFIER | c.629+7018C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89414884 | ||||||
| chr11:89414919
|
T | C | 10 | a0001c0001t0017g0160a0001c0001t0031g0176a0001c0001t0031g0177others(7): Show | 10 | HG01884.hp1 HG02615.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.629+6983A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89414919 | ||||||
| chr11:89415029
|
A | T | 5 | a0001c0001t0002g0252a0001c0001t0024g0155a0001c0002t0011g0156others(2): Show | 5 | HG02622.hp1 HG02647.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.629+6873T>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89415029 | ||||||
| chr11:89415065
|
G | C | 1 | a0001c0002t0011g0157 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.629+6837C>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89415065 | ||||||
| chr11:89415204
|
C | T | 55 | a0001c0001t0002g0260a0001c0001t0003g0170a0001c0001t0003g0191others(52): Show | 55 | HG00408.hp2 HG00621.hp1 HG00621.hp2 others(52): Show |
intron_variant | MODIFIER | c.629+6698G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89415204 | ||||||
| chr11:89415300
|
T | C | 116 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0008others(113): Show | 116 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(113): Show |
intron_variant | MODIFIER | c.629+6602A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89415300 | ||||||
| chr11:89415483
|
C | T | 1 | a0001c0002t0033g0262 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.629+6419G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89415483 | ||||||
| chr11:89415508
|
T | C | 1 | a0001c0001t0115g0253 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.629+6394A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89415508 | ||||||
| chr11:89415518
|
A | C | 2 | a0001c0002t0011g0153a0001c0002t0029g0154 | 2 | HG01109.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.629+6384T>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89415518 | ||||||
| chr11:89415579
|
T | C | 139 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0008others(136): Show | 139 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(136): Show |
intron_variant | MODIFIER | c.629+6323A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89415579 | ||||||
| chr11:89415614
|
C | T | 154 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0008others(151): Show | 154 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(151): Show |
intron_variant | MODIFIER | c.629+6288G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89415614 | ||||||
| chr11:89415787
|
C | A | 15 | a0001c0001t0002g0252a0001c0001t0017g0160a0001c0001t0024g0155others(12): Show | 15 | HG01884.hp1 HG02615.hp1 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.629+6115G>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89415787 | ||||||
| chr11:89415803
|
G | C | 5 | a0001c0001t0001g0110a0001c0001t0014g0036a0001c0001t0014g0068others(2): Show | 5 | HG02083.hp2 NA18612.hp2 NA18939.hp1 others(2): Show |
intron_variant | MODIFIER | c.629+6099C>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89415803 | ||||||
| chr11:89415975
|
C | G | 119 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0008others(116): Show | 119 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(116): Show |
intron_variant | MODIFIER | c.629+5927G>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89415975 | ||||||
| chr11:89416110
|
T | A | 52 | a0001c0001t0002g0260a0001c0001t0003g0170a0001c0001t0003g0191others(49): Show | 52 | HG00408.hp2 HG00621.hp1 HG00621.hp2 others(49): Show |
intron_variant | MODIFIER | c.629+5792A>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89416110 | ||||||
| chr11:89416244
|
T | C | 2 | a0002c0004t0032g0144a0002c0004t0032g0162 | 2 | HG02615.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.629+5658A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89416244 | ||||||
| chr11:89416273
|
T | C | 3 | a0001c0001t0001g0088a0001c0001t0001g0138a0001c0001t0055g0097 | 3 | NA18990.hp2 NA18995.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.629+5629A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89416273 | ||||||
| chr11:89416442
|
G | A | 285 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(282): Show | 286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.629+5460C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89416442 | ||||||
| chr11:89416505
|
C | CT | 3 | a0001c0001t0001g0008a0001c0002t0044g0017a0001c0002t0102g0226 | 3 | NA19001.hp1 NA19064.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.629+5396dupA | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89416505 | ||||||
| chr11:89416639
|
T | C | 1 | a0001c0001t0053g0101 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.629+5263A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89416639 | ||||||
| chr11:89416813
|
T | C | 12 | a0001c0001t0001g0001a0001c0001t0001g0060a0001c0001t0001g0069others(9): Show | 13 | HG01071.hp1 HG01167.hp2 HG01255.hp2 others(10): Show |
intron_variant | MODIFIER | c.629+5089A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89416813 | ||||||
| chr11:89416904
|
A | G | 4 | a0001c0001t0008g0107a0001c0001t0024g0210a0001c0002t0011g0198others(1): Show | 4 | HG00621.hp1 NA18947.hp1 NA18962.hp1 others(1): Show |
intron_variant | MODIFIER | c.629+4998T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89416904 | ||||||
| chr11:89417204
|
G | A | 80 | a0001c0001t0001g0063a0001c0001t0002g0252a0001c0001t0002g0260others(77): Show | 80 | HG00408.hp2 HG00621.hp1 HG00639.hp2 others(77): Show |
intron_variant | MODIFIER | c.629+4698C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89417204 | ||||||
| chr11:89417255
|
T | C | 15 | a0001c0001t0002g0252a0001c0001t0017g0160a0001c0001t0024g0155others(12): Show | 15 | HG01884.hp1 HG02615.hp1 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.629+4647A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89417255 | ||||||
| chr11:89417475
|
T | A | 8 | a0001c0001t0003g0170a0001c0001t0073g0167a0001c0001t0094g0218others(5): Show | 8 | HG00741.hp1 HG01891.hp2 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.629+4427A>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89417475 | ||||||
| chr11:89417477
|
C | T | 51 | a0001c0001t0002g0260a0001c0001t0003g0170a0001c0001t0003g0191others(48): Show | 51 | HG00408.hp2 HG00621.hp1 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.629+4425G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89417477 | ||||||
| chr11:89417500
|
C | T | 1 | a0001c0001t0018g0175 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.629+4402G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89417500 | ||||||
| chr11:89417573
|
A | C | 3 | a0001c0001t0052g0122a0001c0001t0069g0015a0001c0001t0112g0282 | 3 | HG02145.hp2 HG02896.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.629+4329T>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89417573 | ||||||
| chr11:89417591
|
C | A | 1 | a0001c0001t0012g0257 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.629+4311G>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89417591 | ||||||
| chr11:89417748
|
T | C | 2 | a0001c0001t0088g0158a0001c0002t0011g0157 | 2 | HG02451.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.629+4154A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89417748 | ||||||
| chr11:89418075
|
A | G | 8 | a0001c0001t0001g0063a0001c0001t0019g0166a0001c0001t0022g0140others(5): Show | 8 | HG01081.hp1 HG01884.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.629+3827T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89418075 | ||||||
| chr11:89418078
|
G | A | 1 | a0001c0001t0012g0222 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.629+3824C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89418078 | ||||||
| chr11:89418160
|
A | G | 1 | a0001c0002t0025g0016 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.629+3742T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89418160 | ||||||
| chr11:89418240
|
G | A | 15 | a0001c0001t0002g0252a0001c0001t0017g0160a0001c0001t0024g0155others(12): Show | 15 | HG01884.hp1 HG02615.hp1 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.629+3662C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89418240 | ||||||
| chr11:89418262
|
G | A | 112 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0008others(109): Show | 112 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(109): Show |
intron_variant | MODIFIER | c.629+3640C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89418262 | ||||||
| chr11:89418290
|
C | A | 2 | a0001c0002t0009g0232a0001c0002t0101g0239 | 2 | NA18986.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.629+3612G>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89418290 | ||||||
| chr11:89418304
|
T | C | 15 | a0001c0001t0002g0252a0001c0001t0017g0160a0001c0001t0024g0155others(12): Show | 15 | HG01884.hp1 HG02615.hp1 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.629+3598A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89418304 | ||||||
| chr11:89418422
|
G | GAAT | 119 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0023others(116): Show | 120 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(117): Show |
intron_variant | MODIFIER | c.629+3477_629+3479d others(5): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89418422 | ||||||
| chr11:89418422
|
G | GAATAAT | 23 | a0001c0001t0001g0070a0001c0001t0001g0103a0001c0001t0001g0110others(20): Show | 23 | HG00323.hp2 HG00735.hp1 HG01167.hp2 others(20): Show |
intron_variant | MODIFIER | c.629+3474_629+3479d others(8): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89418422 | ||||||
| chr11:89418422
|
G | GAATAATA others(2): Show |
3 | a0001c0001t0001g0033a0001c0001t0002g0256a0001c0001t0114g0241 | 3 | HG02004.hp1 HG02080.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.629+3471_629+3479d others(11): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89418422 | ||||||
| chr11:89418422
|
G | GAATAATA others(5): Show |
1 | a0001c0001t0021g0113 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.629+3468_629+3479d others(14): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89418422 | ||||||
| chr11:89418422
|
GAAT | G | 14 | a0001c0001t0001g0031a0001c0001t0018g0175a0001c0001t0050g0080others(11): Show | 14 | HG01109.hp1 HG01243.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.629+3477_629+3479d others(5): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89418422 | ||||||
| chr11:89418422
|
GAATAAT | G | 5 | a0001c0001t0002g0224a0001c0001t0002g0252a0001c0001t0002g0265others(2): Show | 5 | HG02155.hp2 HG02451.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.629+3474_629+3479d others(8): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89418422 | ||||||
| chr11:89418422
|
GAATAATA others(2): Show |
G | 3 | a0001c0001t0113g0227a0001c0002t0026g0074a0001c0002t0074g0146 | 3 | HG01243.hp1 HG03098.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.629+3471_629+3479d others(11): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89418422 | ||||||
| chr11:89418422
|
GAATAATA others(5): Show |
G | 55 | a0001c0001t0002g0260a0001c0001t0003g0170a0001c0001t0003g0191others(52): Show | 55 | HG00408.hp2 HG00621.hp1 HG00621.hp2 others(52): Show |
intron_variant | MODIFIER | c.629+3468_629+3479d others(14): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89418422 | ||||||
| chr11:89418422
|
GAATAATA others(8): Show |
G | 10 | a0001c0001t0017g0160a0001c0001t0031g0176a0001c0001t0031g0177others(7): Show | 10 | HG01884.hp1 HG02615.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.629+3465_629+3479d others(17): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89418422 | ||||||
| chr11:89419020
|
A | G | 4 | a0001c0001t0002g0279a0001c0001t0002g0283a0001c0001t0037g0280others(1): Show | 4 | HG02258.hp1 HG02717.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.629+2882T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89419020 | ||||||
| chr11:89419060
|
A | G | 1 | a0001c0008t0002g0275 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.629+2842T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89419060 | ||||||
| chr11:89419240
|
T | C | 3 | a0001c0001t0008g0051a0001c0001t0008g0112a0001c0001t0067g0111 | 3 | HG01358.hp1 HG01952.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.629+2662A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89419240 | ||||||
| chr11:89419242
|
C | T | 1 | a0001c0002t0045g0095 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.629+2660G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89419242 | ||||||
| chr11:89419403
|
C | T | 1 | a0006c0010t0016g0027 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.629+2499G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89419403 | ||||||
| chr11:89419476
|
A | T | 1 | a0001c0001t0059g0054 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.629+2426T>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89419476 | ||||||
| chr11:89419551
|
G | T | 11 | a0001c0001t0001g0063a0001c0001t0018g0142a0001c0001t0018g0175others(8): Show | 11 | HG01081.hp1 HG01884.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.629+2351C>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89419551 | ||||||
| chr11:89419604
|
G | A | 15 | a0001c0001t0002g0252a0001c0001t0017g0160a0001c0001t0024g0155others(12): Show | 15 | HG01884.hp1 HG02615.hp1 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.629+2298C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89419604 | ||||||
| chr11:89419639
|
T | A | 3 | a0001c0001t0018g0142a0001c0001t0018g0175a0001c0001t0078g0143 | 3 | HG02280.hp1 NA19240.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.629+2263A>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89419639 | ||||||
| chr11:89419672
|
T | TATTTCTC others(27): Show |
1 | a0001c0001t0001g0059 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.629+2196_629+2229d others(36): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89419672 | ||||||
| chr11:89419750
|
C | T | 5 | a0001c0001t0002g0266a0001c0001t0002g0268a0001c0001t0002g0269others(2): Show | 5 | HG00735.hp2 HG00741.hp2 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.629+2152G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89419750 | ||||||
| chr11:89420151
|
G | A | 10 | a0001c0001t0017g0160a0001c0001t0031g0176a0001c0001t0031g0177others(7): Show | 10 | HG01884.hp1 HG02615.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.629+1751C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89420151 | ||||||
| chr11:89420219
|
T | C | 5 | a0001c0001t0002g0252a0001c0001t0024g0155a0001c0002t0011g0156others(2): Show | 5 | HG02622.hp1 HG02647.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.629+1683A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89420219 | ||||||
| chr11:89420237
|
C | T | 4 | a0001c0001t0001g0063a0001c0001t0022g0140a0001c0001t0068g0064others(1): Show | 4 | HG01081.hp1 HG01884.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.629+1665G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89420237 | ||||||
| chr11:89420536
|
C | T | 4 | a0001c0001t0002g0252a0001c0001t0024g0155a0001c0002t0011g0156others(1): Show | 4 | HG02622.hp1 HG02647.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.629+1366G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89420536 | ||||||
| chr11:89420597
|
T | C | 15 | a0001c0001t0002g0252a0001c0001t0017g0160a0001c0001t0024g0155others(12): Show | 15 | HG01884.hp1 HG02615.hp1 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.629+1305A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89420597 | ||||||
| chr11:89420607
|
T | G | 220 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0008others(217): Show | 220 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(217): Show |
intron_variant | MODIFIER | c.629+1295A>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89420607 | ||||||
| chr11:89420752
|
T | A | 5 | a0001c0001t0002g0252a0001c0001t0024g0155a0001c0002t0011g0156others(2): Show | 5 | HG02622.hp1 HG02647.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.629+1150A>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89420752 | ||||||
| chr11:89420782
|
T | C | 1 | a0001c0002t0074g0146 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.629+1120A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89420782 | ||||||
| chr11:89420824
|
G | A | 1 | a0001c0002t0042g0136 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.629+1078C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89420824 | ||||||
| chr11:89420976
|
G | A | 1 | a0001c0001t0002g0252 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.629+926C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89420976 | ||||||
| chr11:89421069
|
A | G | 1 | a0001c0001t0001g0023 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.629+833T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89421069 | ||||||
| chr11:89421092
|
T | C | 15 | a0001c0001t0002g0252a0001c0001t0017g0160a0001c0001t0024g0155others(12): Show | 15 | HG01884.hp1 HG02615.hp1 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.629+810A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89421092 | ||||||
| chr11:89421094
|
T | C | 15 | a0001c0001t0002g0252a0001c0001t0017g0160a0001c0001t0024g0155others(12): Show | 15 | HG01884.hp1 HG02615.hp1 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.629+808A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89421094 | ||||||
| chr11:89421186
|
T | C | 10 | a0001c0001t0017g0160a0001c0001t0031g0176a0001c0001t0031g0177others(7): Show | 10 | HG01884.hp1 HG02615.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.629+716A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89421186 | ||||||
| chr11:89421410
|
T | C | 1 | a0001c0001t0001g0050 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.629+492A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89421410 | ||||||
| chr11:89421424
|
G | A | 1 | a0001c0001t0002g0252 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.629+478C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89421424 | ||||||
| chr11:89421553
|
T | C | 116 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0008others(113): Show | 116 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(113): Show |
intron_variant | MODIFIER | c.629+349A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89421553 | ||||||
| chr11:89421656
|
G | A | 15 | a0001c0001t0002g0252a0001c0001t0017g0160a0001c0001t0024g0155others(12): Show | 15 | HG01884.hp1 HG02615.hp1 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.629+246C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89421656 | ||||||
| chr11:89421763
|
G | A | 15 | a0001c0001t0002g0252a0001c0001t0017g0160a0001c0001t0024g0155others(12): Show | 15 | HG01884.hp1 HG02615.hp1 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.629+139C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89421763 | ||||||
| chr11:89421895
|
A | G | 1 | a0001c0001t0023g0161 | 1 | HG02486.hp2 | splice_region_variant&intron_variant | LOW | c.629+7T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 8/17 | chr11 | 89421895 | ||||||
| chr11:89422181
|
A | G | 1 | a0001c0001t0062g0114 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.549-199T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 7/17 | chr11 | 89422181 | ||||||
| chr11:89422183
|
T | G | 15 | a0001c0001t0002g0252a0001c0001t0017g0160a0001c0001t0024g0155others(12): Show | 15 | HG01884.hp1 HG02615.hp1 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.549-201A>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 7/17 | chr11 | 89422183 | ||||||
| chr11:89422278
|
ATAG | A | 15 | a0001c0001t0002g0252a0001c0001t0017g0160a0001c0001t0024g0155others(12): Show | 15 | HG01884.hp1 HG02615.hp1 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.549-299_549-297del others(3): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 7/17 | chr11 | 89422278 | ||||||
| chr11:89422295
|
T | C | 1 | a0001c0001t0001g0110 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.549-313A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 7/17 | chr11 | 89422295 | ||||||
| chr11:89422441
|
T | C | 2 | a0001c0001t0017g0171a0001c0001t0017g0172 | 2 | HG01074.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.549-459A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 7/17 | chr11 | 89422441 | ||||||
| chr11:89422521
|
A | G | 15 | a0001c0001t0002g0252a0001c0001t0017g0160a0001c0001t0024g0155others(12): Show | 15 | HG01884.hp1 HG02615.hp1 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.549-539T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 7/17 | chr11 | 89422521 | ||||||
| chr11:89422593
|
T | A | 15 | a0001c0001t0002g0252a0001c0001t0017g0160a0001c0001t0024g0155others(12): Show | 15 | HG01884.hp1 HG02615.hp1 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.549-611A>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 7/17 | chr11 | 89422593 | ||||||
| chr11:89422795
|
A | AT | 20 | a0001c0001t0001g0063a0001c0001t0001g0128a0001c0001t0002g0231others(17): Show | 20 | HG00140.hp1 HG00621.hp2 HG01074.hp2 others(17): Show |
intron_variant | MODIFIER | c.549-814dupA | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 7/17 | chr11 | 89422795 | ||||||
| chr11:89422795
|
A | ATT | 7 | a0001c0001t0024g0155a0001c0002t0011g0156a0001c0002t0029g0168others(4): Show | 7 | HG01884.hp1 HG02615.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.549-815_549-814dup others(2): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 7/17 | chr11 | 89422795 | ||||||
| chr11:89422795
|
AT | A | 92 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0013others(89): Show | 93 | HG00140.hp2 HG00323.hp1 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.549-814delA | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 7/17 | chr11 | 89422795 | ||||||
| chr11:89422795
|
ATT | A | 9 | a0001c0001t0001g0031a0001c0001t0003g0170a0001c0001t0018g0192others(6): Show | 9 | HG00741.hp1 HG01074.hp1 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.549-815_549-814del others(2): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 7/17 | chr11 | 89422795 | ||||||
| chr11:89422849
|
G | C | 14 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0002g0256others(11): Show | 14 | HG01081.hp2 HG01952.hp1 HG02132.hp1 others(11): Show |
intron_variant | MODIFIER | c.549-867C>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 7/17 | chr11 | 89422849 | ||||||
| chr11:89423002
|
G | A | 1 | a0001c0003t0104g0267 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.549-1020C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 7/17 | chr11 | 89423002 | ||||||
| chr11:89423179
|
C | T | 3 | a0001c0002t0033g0285a0001c0002t0098g0284a0001c0002t0099g0286 | 3 | HG02976.hp1 HG03195.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.549-1197G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 7/17 | chr11 | 89423179 | ||||||
| chr11:89423203
|
G | A | 220 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0008others(217): Show | 220 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(217): Show |
intron_variant | MODIFIER | c.549-1221C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 7/17 | chr11 | 89423203 | ||||||
| chr11:89423261
|
G | A | 7 | a0001c0001t0001g0103a0001c0001t0010g0065a0001c0001t0010g0087others(4): Show | 7 | HG00323.hp2 HG00735.hp1 HG01106.hp1 others(4): Show |
intron_variant | MODIFIER | c.549-1279C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 7/17 | chr11 | 89423261 | ||||||
| chr11:89423376
|
ATAGAG | A | 11 | a0001c0001t0001g0063a0001c0001t0018g0142a0001c0001t0018g0175others(8): Show | 11 | HG01081.hp1 HG01884.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.549-1399_549-1395d others(7): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 7/17 | chr11 | 89423376 | ||||||
| chr11:89423446
|
A | T | 1 | a0001c0003t0005g0180 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.549-1464T>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 7/17 | chr11 | 89423446 | ||||||
| chr11:89423457
|
C | T | 11 | a0001c0001t0002g0224a0001c0001t0002g0254a0001c0001t0002g0255others(8): Show | 11 | HG02451.hp1 HG02486.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.549-1475G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 7/17 | chr11 | 89423457 | ||||||
| chr11:89423530
|
G | A | 54 | a0001c0001t0002g0260a0001c0001t0003g0170a0001c0001t0003g0191others(51): Show | 54 | HG00408.hp2 HG00621.hp1 HG00639.hp2 others(51): Show |
intron_variant | MODIFIER | c.549-1548C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 7/17 | chr11 | 89423530 | ||||||
| chr11:89423532
|
T | C | 1 | a0001c0001t0022g0140 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.549-1550A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 7/17 | chr11 | 89423532 | ||||||
| chr11:89423627
|
T | G | 1 | a0001c0003t0090g0211 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.549-1645A>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 7/17 | chr11 | 89423627 | ||||||
| chr11:89423725
|
C | G | 1 | a0001c0003t0003g0189 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.549-1743G>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 7/17 | chr11 | 89423725 | ||||||
| chr11:89423753
|
A | AATAT | 5 | a0001c0001t0002g0266a0001c0001t0002g0268a0001c0001t0002g0269others(2): Show | 5 | HG00735.hp2 HG00741.hp2 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.549-1775_549-1772d others(6): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 7/17 | chr11 | 89423753 | ||||||
| chr11:89423764
|
A | G | 1 | a0001c0001t0002g0252 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.549-1782T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 7/17 | chr11 | 89423764 | ||||||
| chr11:89423777
|
A | C | 15 | a0001c0001t0002g0252a0001c0001t0017g0160a0001c0001t0024g0155others(12): Show | 15 | HG01884.hp1 HG02615.hp1 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.549-1795T>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 7/17 | chr11 | 89423777 | ||||||
| chr11:89423866
|
A | C | 220 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0008others(217): Show | 220 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(217): Show |
intron_variant | MODIFIER | c.549-1884T>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 7/17 | chr11 | 89423866 | ||||||
| chr11:89423890
|
C | T | 1 | a0001c0002t0042g0136 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.549-1908G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 7/17 | chr11 | 89423890 | ||||||
| chr11:89424098
|
G | C | 4 | a0001c0001t0002g0252a0001c0001t0024g0155a0001c0002t0011g0156others(1): Show | 4 | HG02622.hp1 HG02647.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.549-2116C>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 7/17 | chr11 | 89424098 | ||||||
| chr11:89424165
|
A | G | 17 | a0001c0001t0002g0224a0001c0001t0002g0254a0001c0001t0002g0255others(14): Show | 17 | HG02258.hp1 HG02451.hp1 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.549-2183T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 7/17 | chr11 | 89424165 | ||||||
| chr11:89424375
|
A | ATTATTTC others(44): Show |
2 | a0001c0002t0011g0153a0001c0002t0029g0154 | 2 | HG01109.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.549-2444_549-2394d others(53): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 7/17 | chr11 | 89424375 | ||||||
| chr11:89424413
|
G | T | 8 | a0001c0001t0001g0063a0001c0001t0019g0166a0001c0001t0022g0140others(5): Show | 8 | HG01081.hp1 HG01884.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.549-2431C>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 7/17 | chr11 | 89424413 | ||||||
| chr11:89424427
|
T | G | 5 | a0001c0001t0015g0019a0001c0001t0015g0078a0001c0001t0027g0018others(2): Show | 5 | NA18941.hp1 NA18962.hp2 NA18968.hp1 others(2): Show |
intron_variant | MODIFIER | c.549-2445A>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 7/17 | chr11 | 89424427 | ||||||
| chr11:89424488
|
A | G | 223 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0008others(220): Show | 223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.549-2506T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 7/17 | chr11 | 89424488 | ||||||
| chr11:89424712
|
C | T | 1 | a0001c0001t0001g0110 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.549-2730G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 7/17 | chr11 | 89424712 | ||||||
| chr11:89424722
|
C | T | 2 | a0001c0002t0011g0153a0001c0002t0029g0154 | 2 | HG01109.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.549-2740G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 7/17 | chr11 | 89424722 | ||||||
| chr11:89424744
|
C | T | 15 | a0001c0001t0002g0252a0001c0001t0017g0160a0001c0001t0024g0155others(12): Show | 15 | HG01884.hp1 HG02615.hp1 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.549-2762G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 7/17 | chr11 | 89424744 | ||||||
| chr11:89424809
|
C | T | 15 | a0001c0001t0002g0252a0001c0001t0017g0160a0001c0001t0024g0155others(12): Show | 15 | HG01884.hp1 HG02615.hp1 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.549-2827G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 7/17 | chr11 | 89424809 | ||||||
| chr11:89424989
|
C | G | 3 | a0001c0001t0052g0122a0001c0001t0069g0015a0001c0001t0112g0282 | 3 | HG02145.hp2 HG02896.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.549-3007G>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 7/17 | chr11 | 89424989 | ||||||
| chr11:89425011
|
G | A | 1 | a0001c0002t0006g0025 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.549-3029C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 7/17 | chr11 | 89425011 | ||||||
| chr11:89425167
|
G | GT | 11 | a0001c0001t0001g0063a0001c0001t0018g0142a0001c0001t0018g0175others(8): Show | 11 | HG01081.hp1 HG01884.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.549-3186dupA | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 7/17 | chr11 | 89425167 | ||||||
| chr11:89425353
|
T | C | 1 | a0001c0002t0006g0079 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.549-3371A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 7/17 | chr11 | 89425353 | ||||||
| chr11:89425365
|
G | A | 1 | a0001c0001t0002g0254 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.549-3383C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 7/17 | chr11 | 89425365 | ||||||
| chr11:89425409
|
C | CA | 15 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0063others(12): Show | 15 | HG00639.hp2 HG01081.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.549-3428dupT | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 7/17 | chr11 | 89425409 | ||||||
| chr11:89425424
|
AC | A | 10 | a0001c0001t0017g0160a0001c0001t0031g0176a0001c0001t0031g0177others(7): Show | 10 | HG01884.hp1 HG02615.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.549-3443delG | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 7/17 | chr11 | 89425424 | ||||||
| chr11:89425425
|
C | A | 1 | a0002c0004t0032g0162 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.549-3443G>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 7/17 | chr11 | 89425425 | ||||||
| chr11:89425624
|
C | T | 1 | a0001c0001t0001g0098 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.549-3642G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 7/17 | chr11 | 89425624 | ||||||
| chr11:89425747
|
G | A | 1 | a0001c0001t0068g0064 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.549-3765C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 7/17 | chr11 | 89425747 | ||||||
| chr11:89425805
|
T | C | 1 | a0001c0001t0113g0227 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.549-3823A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 7/17 | chr11 | 89425805 | ||||||
| chr11:89425861
|
A | G | 1 | a0001c0001t0057g0127 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.549-3879T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 7/17 | chr11 | 89425861 | ||||||
| chr11:89425924
|
T | C | 1 | a0001c0003t0019g0213 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.549-3942A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 7/17 | chr11 | 89425924 | ||||||
| chr11:89425961
|
T | C | 5 | a0001c0001t0002g0252a0001c0001t0024g0155a0001c0002t0011g0156others(2): Show | 5 | HG02622.hp1 HG02647.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.549-3979A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 7/17 | chr11 | 89425961 | ||||||
| chr11:89426000
|
C | T | 1 | a0003c0013t0002g0220 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.549-4018G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 7/17 | chr11 | 89426000 | ||||||
| chr11:89426044
|
C | G | 1 | a0001c0001t0001g0134 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.549-4062G>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 7/17 | chr11 | 89426044 | ||||||
| chr11:89426142
|
T | A | 2 | a0001c0001t0005g0149a0001c0001t0005g0150 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.549-4160A>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 7/17 | chr11 | 89426142 | ||||||
| chr11:89426259
|
A | G | 26 | a0001c0001t0001g0063a0001c0001t0002g0252a0001c0001t0017g0160others(23): Show | 26 | HG01081.hp1 HG01884.hp1 HG01884.hp2 others(23): Show |
intron_variant | MODIFIER | c.549-4277T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 7/17 | chr11 | 89426259 | ||||||
| chr11:89426300
|
C | T | 1 | a0001c0001t0004g0003 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.549-4318G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 7/17 | chr11 | 89426300 | ||||||
| chr11:89426451
|
G | A | 1 | a0001c0001t0007g0126 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.549-4469C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 7/17 | chr11 | 89426451 | ||||||
| chr11:89426646
|
G | A | 51 | a0001c0001t0002g0260a0001c0001t0003g0170a0001c0001t0003g0191others(48): Show | 51 | HG00408.hp2 HG00621.hp1 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.549-4664C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 7/17 | chr11 | 89426646 | ||||||
| chr11:89426650
|
T | C | 3 | a0001c0002t0033g0285a0001c0002t0098g0284a0001c0002t0099g0286 | 3 | HG02976.hp1 HG03195.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.549-4668A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 7/17 | chr11 | 89426650 | ||||||
| chr11:89426655
|
G | A | 1 | a0001c0001t0054g0048 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.549-4673C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 7/17 | chr11 | 89426655 | ||||||
| chr11:89426676
|
G | A | 3 | a0001c0001t0008g0051a0001c0001t0008g0112a0001c0001t0067g0111 | 3 | HG01358.hp1 HG01952.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.549-4694C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 7/17 | chr11 | 89426676 | ||||||
| chr11:89426698
|
C | A | 51 | a0001c0001t0002g0260a0001c0001t0003g0170a0001c0001t0003g0191others(48): Show | 51 | HG00408.hp2 HG00621.hp1 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.549-4716G>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 7/17 | chr11 | 89426698 | ||||||
| chr11:89426701
|
G | C | 1 | a0001c0002t0009g0240 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.549-4719C>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 7/17 | chr11 | 89426701 | ||||||
| chr11:89426742
|
A | G | 11 | a0001c0001t0001g0063a0001c0001t0018g0142a0001c0001t0018g0175others(8): Show | 11 | HG01081.hp1 HG01884.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.549-4760T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 7/17 | chr11 | 89426742 | ||||||
| chr11:89426808
|
C | T | 1 | a0001c0001t0052g0122 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.549-4826G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 7/17 | chr11 | 89426808 | ||||||
| chr11:89426909
|
C | T | 1 | a0001c0002t0035g0248 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.549-4927G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 7/17 | chr11 | 89426909 | ||||||
| chr11:89426941
|
C | A | 1 | a0001c0001t0004g0052 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.549-4959G>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 7/17 | chr11 | 89426941 | ||||||
| chr11:89427072
|
A | G | 2 | a0001c0001t0001g0061a0001c0001t0001g0062 | 2 | NA18950.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.549-5090T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 7/17 | chr11 | 89427072 | ||||||
| chr11:89427094
|
T | G | 3 | a0001c0002t0033g0285a0001c0002t0098g0284a0001c0002t0099g0286 | 3 | HG02976.hp1 HG03195.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.549-5112A>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 7/17 | chr11 | 89427094 | ||||||
| chr11:89427158
|
G | A | 1 | a0001c0001t0109g0281 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.549-5176C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 7/17 | chr11 | 89427158 | ||||||
| chr11:89427199
|
A | G | 3 | a0001c0001t0018g0142a0001c0001t0018g0175a0001c0001t0078g0143 | 3 | HG02280.hp1 NA19240.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.549-5217T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 7/17 | chr11 | 89427199 | ||||||
| chr11:89427219
|
C | T | 15 | a0001c0001t0002g0252a0001c0001t0017g0160a0001c0001t0024g0155others(12): Show | 15 | HG01884.hp1 HG02615.hp1 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.549-5237G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 7/17 | chr11 | 89427219 | ||||||
| chr11:89427248
|
C | T | 220 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0008others(217): Show | 220 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(217): Show |
intron_variant | MODIFIER | c.549-5266G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 7/17 | chr11 | 89427248 | ||||||
| chr11:89427276
|
A | C | 1 | a0001c0001t0113g0227 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.549-5294T>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 7/17 | chr11 | 89427276 | ||||||
| chr11:89427314
|
G | A | 2 | a0001c0001t0001g0061a0001c0001t0001g0062 | 2 | NA18950.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.549-5332C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 7/17 | chr11 | 89427314 | ||||||
| chr11:89427443
|
C | T | 4 | a0001c0001t0005g0149a0001c0001t0005g0150a0001c0001t0103g0272others(1): Show | 4 | HG02896.hp1 HG02897.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.548+5341G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 7/17 | chr11 | 89427443 | ||||||
| chr11:89427487
|
C | T | 1 | a0001c0001t0068g0064 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.548+5297G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 7/17 | chr11 | 89427487 | ||||||
| chr11:89427567
|
G | A | 1 | a0001c0002t0009g0232 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.548+5217C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 7/17 | chr11 | 89427567 | ||||||
| chr11:89427572
|
G | A | 3 | a0001c0001t0007g0126a0001c0001t0018g0142a0001c0001t0078g0143 | 3 | HG00621.hp2 HG02280.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.548+5212C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 7/17 | chr11 | 89427572 | ||||||
| chr11:89427648
|
G | T | 1 | a0001c0002t0006g0079 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.548+5136C>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 7/17 | chr11 | 89427648 | ||||||
| chr11:89427669
|
G | C | 14 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0002g0256others(11): Show | 14 | HG01081.hp2 HG01952.hp1 HG02132.hp1 others(11): Show |
intron_variant | MODIFIER | c.548+5115C>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 7/17 | chr11 | 89427669 | ||||||
| chr11:89427798
|
A | G | 220 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0008others(217): Show | 220 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(217): Show |
intron_variant | MODIFIER | c.548+4986T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 7/17 | chr11 | 89427798 | ||||||
| chr11:89427851
|
T | C | 3 | a0001c0001t0082g0174a0001c0002t0011g0153a0001c0002t0029g0154 | 3 | HG01099.hp1 HG01109.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.548+4933A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 7/17 | chr11 | 89427851 | ||||||
| chr11:89427869
|
C | T | 51 | a0001c0001t0002g0260a0001c0001t0003g0170a0001c0001t0003g0191others(48): Show | 51 | HG00408.hp2 HG00621.hp1 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.548+4915G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 7/17 | chr11 | 89427869 | ||||||
| chr11:89427887
|
C | T | 5 | a0001c0001t0002g0252a0001c0001t0024g0155a0001c0002t0011g0156others(2): Show | 5 | HG02622.hp1 HG02647.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.548+4897G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 7/17 | chr11 | 89427887 | ||||||
| chr11:89427907
|
C | T | 51 | a0001c0001t0002g0260a0001c0001t0003g0170a0001c0001t0003g0191others(48): Show | 51 | HG00408.hp2 HG00621.hp1 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.548+4877G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 7/17 | chr11 | 89427907 | ||||||
| chr11:89428050
|
G | A | 1 | a0001c0001t0020g0056 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.548+4734C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 7/17 | chr11 | 89428050 | ||||||
| chr11:89428053
|
A | G | 223 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0008others(220): Show | 223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.548+4731T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 7/17 | chr11 | 89428053 | ||||||
| chr11:89428123
|
T | C | 1 | a0001c0001t0113g0227 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.548+4661A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 7/17 | chr11 | 89428123 | ||||||
| chr11:89428293
|
A | AG | 80 | a0001c0001t0001g0063a0001c0001t0002g0252a0001c0001t0002g0260others(77): Show | 80 | HG00408.hp2 HG00621.hp1 HG00639.hp2 others(77): Show |
intron_variant | MODIFIER | c.548+4490dupC | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 7/17 | chr11 | 89428293 | ||||||
| chr11:89428315
|
G | A | 15 | a0001c0001t0002g0252a0001c0001t0017g0160a0001c0001t0024g0155others(12): Show | 15 | HG01884.hp1 HG02615.hp1 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.548+4469C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 7/17 | chr11 | 89428315 | ||||||
| chr11:89428324
|
A | C | 3 | a0001c0001t0018g0142a0001c0001t0018g0175a0001c0001t0078g0143 | 3 | HG02280.hp1 NA19240.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.548+4460T>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 7/17 | chr11 | 89428324 | ||||||
| chr11:89428332
|
A | C | 1 | a0001c0001t0113g0227 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.548+4452T>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 7/17 | chr11 | 89428332 | ||||||
| chr11:89428340
|
A | G | 1 | a0001c0001t0007g0125 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.548+4444T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 7/17 | chr11 | 89428340 | ||||||
| chr11:89428376
|
C | T | 2 | a0001c0001t0001g0063a0001c0001t0068g0064 | 2 | HG01884.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.548+4408G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 7/17 | chr11 | 89428376 | ||||||
| chr11:89428482
|
C | CAG | 220 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0008others(217): Show | 220 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(217): Show |
intron_variant | MODIFIER | c.548+4300_548+4301d others(4): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 7/17 | chr11 | 89428482 | ||||||
| chr11:89428507
|
G | A | 1 | a0001c0002t0074g0146 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.548+4277C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 7/17 | chr11 | 89428507 | ||||||
| chr11:89428643
|
T | A | 3 | a0001c0001t0088g0158a0001c0001t0117g0287a0001c0002t0011g0157 | 3 | HG02451.hp2 HG02630.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.548+4141A>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 7/17 | chr11 | 89428643 | ||||||
| chr11:89428816
|
A | G | 3 | a0001c0001t0002g0242a0001c0001t0012g0244a0001c0001t0038g0243 | 3 | NA18994.hp1 NA19004.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.548+3968T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 7/17 | chr11 | 89428816 | ||||||
| chr11:89428817
|
G | A | 50 | a0001c0001t0001g0023a0001c0001t0001g0035a0001c0001t0001g0061others(47): Show | 50 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(47): Show |
intron_variant | MODIFIER | c.548+3967C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 7/17 | chr11 | 89428817 | ||||||
| chr11:89428965
|
C | T | 220 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0008others(217): Show | 220 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(217): Show |
intron_variant | MODIFIER | c.548+3819G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 7/17 | chr11 | 89428965 | ||||||
| chr11:89428974
|
C | T | 2 | a0001c0001t0081g0163a0001c0001t0086g0152 | 2 | HG01243.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.548+3810G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 7/17 | chr11 | 89428974 | ||||||
| chr11:89429007
|
T | C | 52 | a0001c0001t0001g0023a0001c0001t0001g0035a0001c0001t0001g0061others(49): Show | 52 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(49): Show |
intron_variant | MODIFIER | c.548+3777A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 7/17 | chr11 | 89429007 | ||||||
| chr11:89429048
|
T | G | 1 | a0001c0002t0009g0278 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.548+3736A>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 7/17 | chr11 | 89429048 | ||||||
| chr11:89429067
|
G | A | 2 | a0001c0001t0003g0207a0001c0001t0014g0038 | 2 | HG00673.hp1 NA18954.hp2 |
intron_variant | MODIFIER | c.548+3717C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 7/17 | chr11 | 89429067 | ||||||
| chr11:89429268
|
A | C | 1 | a0001c0001t0001g0035 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.548+3516T>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 7/17 | chr11 | 89429268 | ||||||
| chr11:89429285
|
T | C | 140 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0008others(137): Show | 140 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(137): Show |
intron_variant | MODIFIER | c.548+3499A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 7/17 | chr11 | 89429285 | ||||||
| chr11:89429387
|
C | T | 10 | a0001c0001t0017g0160a0001c0001t0031g0176a0001c0001t0031g0177others(7): Show | 10 | HG01884.hp1 HG02615.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.548+3397G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 7/17 | chr11 | 89429387 | ||||||
| chr11:89429416
|
C | G | 3 | a0001c0001t0005g0178a0001c0001t0091g0151a0001c0001t0111g0277 | 3 | HG02280.hp2 HG02572.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.548+3368G>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 7/17 | chr11 | 89429416 | ||||||
| chr11:89429458
|
G | A | 14 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0002g0256others(11): Show | 14 | HG01081.hp2 HG01952.hp1 HG02132.hp1 others(11): Show |
intron_variant | MODIFIER | c.548+3326C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 7/17 | chr11 | 89429458 | ||||||
| chr11:89429493
|
A | G | 1 | a0001c0001t0001g0073 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.548+3291T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 7/17 | chr11 | 89429493 | ||||||
| chr11:89429536
|
C | T | 15 | a0001c0001t0002g0252a0001c0001t0017g0160a0001c0001t0024g0155others(12): Show | 15 | HG01884.hp1 HG02615.hp1 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.548+3248G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 7/17 | chr11 | 89429536 | ||||||
| chr11:89429587
|
C | T | 4 | a0001c0001t0002g0252a0001c0001t0024g0155a0001c0002t0011g0156others(1): Show | 4 | HG02622.hp1 HG02647.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.548+3197G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 7/17 | chr11 | 89429587 | ||||||
| chr11:89429688
|
T | C | 3 | a0001c0002t0033g0285a0001c0002t0098g0284a0001c0002t0099g0286 | 3 | HG02976.hp1 HG03195.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.548+3096A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 7/17 | chr11 | 89429688 | ||||||
| chr11:89429712
|
TAATTAAT others(25): Show |
T | 2 | a0001c0001t0005g0178a0001c0001t0091g0151 | 2 | HG02280.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.548+3040_548+3071d others(34): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 7/17 | chr11 | 89429712 | ||||||
| chr11:89429753
|
A | C | 15 | a0001c0001t0002g0252a0001c0001t0017g0160a0001c0001t0024g0155others(12): Show | 15 | HG01884.hp1 HG02615.hp1 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.548+3031T>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 7/17 | chr11 | 89429753 | ||||||
| chr11:89429881
|
G | A | 1 | a0001c0002t0006g0034 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.548+2903C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 7/17 | chr11 | 89429881 | ||||||
| chr11:89429939
|
G | A | 2 | a0001c0001t0048g0044a0001c0001t0049g0043 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.548+2845C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 7/17 | chr11 | 89429939 | ||||||
| chr11:89429967
|
C | A | 3 | a0001c0002t0033g0285a0001c0002t0098g0284a0001c0002t0099g0286 | 3 | HG02976.hp1 HG03195.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.548+2817G>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 7/17 | chr11 | 89429967 | ||||||
| chr11:89430015
|
T | C | 26 | a0001c0001t0001g0063a0001c0001t0002g0252a0001c0001t0017g0160others(23): Show | 26 | HG01081.hp1 HG01884.hp1 HG01884.hp2 others(23): Show |
intron_variant | MODIFIER | c.548+2769A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 7/17 | chr11 | 89430015 | ||||||
| chr11:89430039
|
G | T | 10 | a0001c0001t0017g0160a0001c0001t0031g0176a0001c0001t0031g0177others(7): Show | 10 | HG01884.hp1 HG02615.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.548+2745C>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 7/17 | chr11 | 89430039 | ||||||
| chr11:89430155
|
C | A | 2 | a0001c0002t0011g0153a0001c0002t0029g0154 | 2 | HG01109.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.548+2629G>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 7/17 | chr11 | 89430155 | ||||||
| chr11:89430494
|
A | G | 1 | a0001c0002t0035g0248 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.548+2290T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 7/17 | chr11 | 89430494 | ||||||
| chr11:89430582
|
C | T | 1 | a0001c0001t0001g0023 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.548+2202G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 7/17 | chr11 | 89430582 | ||||||
| chr11:89430626
|
A | G | 141 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0008others(138): Show | 141 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(138): Show |
intron_variant | MODIFIER | c.548+2158T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 7/17 | chr11 | 89430626 | ||||||
| chr11:89430673
|
A | G | 1 | a0001c0003t0003g0193 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.548+2111T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 7/17 | chr11 | 89430673 | ||||||
| chr11:89430686
|
T | C | 12 | a0001c0001t0001g0001a0001c0001t0001g0060a0001c0001t0001g0069others(9): Show | 13 | HG01071.hp1 HG01167.hp2 HG01255.hp2 others(10): Show |
intron_variant | MODIFIER | c.548+2098A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 7/17 | chr11 | 89430686 | ||||||
| chr11:89430698
|
TAA | T | 5 | a0001c0001t0002g0252a0001c0001t0024g0155a0001c0002t0011g0156others(2): Show | 5 | HG02622.hp1 HG02647.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.548+2084_548+2085d others(4): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 7/17 | chr11 | 89430698 | ||||||
| chr11:89430705
|
G | A | 1 | a0001c0002t0046g0115 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.548+2079C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 7/17 | chr11 | 89430705 | ||||||
| chr11:89430740
|
G | T | 3 | a0001c0001t0024g0155a0001c0002t0011g0156a0001c0002t0029g0168 | 3 | HG02647.hp2 HG03098.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.548+2044C>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 7/17 | chr11 | 89430740 | ||||||
| chr11:89430755
|
A | G | 42 | a0001c0001t0002g0260a0001c0001t0003g0191a0001c0001t0003g0205others(39): Show | 42 | HG00408.hp2 HG00621.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.548+2029T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 7/17 | chr11 | 89430755 | ||||||
| chr11:89430838
|
G | T | 1 | a0001c0001t0018g0142 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.548+1946C>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 7/17 | chr11 | 89430838 | ||||||
| chr11:89430861
|
G | A | 1 | a0001c0001t0001g0110 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.548+1923C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 7/17 | chr11 | 89430861 | ||||||
| chr11:89431131
|
C | A | 3 | a0001c0002t0033g0285a0001c0002t0098g0284a0001c0002t0099g0286 | 3 | HG02976.hp1 HG03195.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.548+1653G>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 7/17 | chr11 | 89431131 | ||||||
| chr11:89431277
|
T | C | 10 | a0001c0001t0017g0160a0001c0001t0031g0176a0001c0001t0031g0177others(7): Show | 10 | HG01884.hp1 HG02615.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.548+1507A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 7/17 | chr11 | 89431277 | ||||||
| chr11:89431343
|
A | C | 3 | a0001c0001t0002g0245a0001c0002t0011g0173a0001c0012t0023g0181 | 3 | HG02723.hp1 HG03139.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.548+1441T>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 7/17 | chr11 | 89431343 | ||||||
| chr11:89431349
|
A | AC | 3 | a0001c0001t0002g0245a0001c0002t0011g0173a0001c0012t0023g0181 | 3 | HG02723.hp1 HG03139.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.548+1434_548+1435i others(3): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 7/17 | chr11 | 89431349 | ||||||
| chr11:89431396
|
C | G | 15 | a0001c0001t0002g0252a0001c0001t0017g0160a0001c0001t0024g0155others(12): Show | 15 | HG01884.hp1 HG02615.hp1 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.548+1388G>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 7/17 | chr11 | 89431396 | ||||||
| chr11:89431621
|
C | T | 1 | a0001c0001t0018g0187 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.548+1163G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 7/17 | chr11 | 89431621 | ||||||
| chr11:89431744
|
C | G | 1 | a0001c0002t0074g0146 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.548+1040G>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 7/17 | chr11 | 89431744 | ||||||
| chr11:89431745
|
T | C | 17 | a0001c0001t0002g0224a0001c0001t0002g0254a0001c0001t0002g0255others(14): Show | 17 | HG02258.hp1 HG02451.hp1 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.548+1039A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 7/17 | chr11 | 89431745 | ||||||
| chr11:89431803
|
G | A | 15 | a0001c0001t0002g0252a0001c0001t0017g0160a0001c0001t0024g0155others(12): Show | 15 | HG01884.hp1 HG02615.hp1 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.548+981C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 7/17 | chr11 | 89431803 | ||||||
| chr11:89431853
|
A | G | 3 | a0001c0001t0018g0142a0001c0001t0018g0175a0001c0001t0078g0143 | 3 | HG02280.hp1 NA19240.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.548+931T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 7/17 | chr11 | 89431853 | ||||||
| chr11:89431901
|
C | T | 3 | a0001c0001t0002g0245a0001c0002t0011g0173a0001c0012t0023g0181 | 3 | HG02723.hp1 HG03139.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.548+883G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 7/17 | chr11 | 89431901 | ||||||
| chr11:89431946
|
C | A | 10 | a0001c0001t0017g0160a0001c0001t0031g0176a0001c0001t0031g0177others(7): Show | 10 | HG01884.hp1 HG02615.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.548+838G>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 7/17 | chr11 | 89431946 | ||||||
| chr11:89431958
|
C | A | 2 | a0001c0001t0088g0158a0001c0002t0011g0157 | 2 | HG02451.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.548+826G>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 7/17 | chr11 | 89431958 | ||||||
| chr11:89432030
|
G | A | 1 | a0001c0001t0001g0013 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.548+754C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 7/17 | chr11 | 89432030 | ||||||
| chr11:89432100
|
GACAAAAA | G | 15 | a0001c0001t0002g0252a0001c0001t0017g0160a0001c0001t0024g0155others(12): Show | 15 | HG01884.hp1 HG02615.hp1 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.548+677_548+683del others(7): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 7/17 | chr11 | 89432100 | ||||||
| chr11:89432112
|
T | A | 15 | a0001c0001t0002g0252a0001c0001t0017g0160a0001c0001t0024g0155others(12): Show | 15 | HG01884.hp1 HG02615.hp1 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.548+672A>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 7/17 | chr11 | 89432112 | ||||||
| chr11:89432190
|
G | A | 1 | a0001c0001t0083g0147 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.548+594C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 7/17 | chr11 | 89432190 | ||||||
| chr11:89432214
|
G | C | 1 | a0001c0002t0074g0146 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.548+570C>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 7/17 | chr11 | 89432214 | ||||||
| chr11:89432240
|
A | G | 1 | a0001c0001t0038g0230 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.548+544T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 7/17 | chr11 | 89432240 | ||||||
| chr11:89432246
|
T | C | 1 | a0001c0001t0002g0246 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.548+538A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 7/17 | chr11 | 89432246 | ||||||
| chr11:89432269
|
C | T | 51 | a0001c0001t0002g0260a0001c0001t0003g0170a0001c0001t0003g0191others(48): Show | 51 | HG00408.hp2 HG00621.hp1 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.548+515G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 7/17 | chr11 | 89432269 | ||||||
| chr11:89432289
|
T | C | 8 | a0001c0001t0001g0063a0001c0001t0019g0166a0001c0001t0022g0140others(5): Show | 8 | HG01081.hp1 HG01884.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.548+495A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 7/17 | chr11 | 89432289 | ||||||
| chr11:89432318
|
A | T | 15 | a0001c0001t0002g0252a0001c0001t0017g0160a0001c0001t0024g0155others(12): Show | 15 | HG01884.hp1 HG02615.hp1 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.548+466T>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 7/17 | chr11 | 89432318 | ||||||
| chr11:89432488
|
G | A | 11 | a0001c0001t0001g0063a0001c0001t0018g0142a0001c0001t0018g0175others(8): Show | 11 | HG01081.hp1 HG01884.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.548+296C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 7/17 | chr11 | 89432488 | ||||||
| chr11:89432493
|
C | G | 15 | a0001c0001t0002g0252a0001c0001t0017g0160a0001c0001t0024g0155others(12): Show | 15 | HG01884.hp1 HG02615.hp1 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.548+291G>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 7/17 | chr11 | 89432493 | ||||||
| chr11:89432531
|
C | T | 1 | a0001c0001t0072g0093 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.548+253G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 7/17 | chr11 | 89432531 | ||||||
| chr11:89432612
|
A | G | 1 | a0001c0001t0007g0126 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.548+172T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 7/17 | chr11 | 89432612 | ||||||
| chr11:89432656
|
C | G | 1 | a0001c0001t0002g0255 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.548+128G>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 7/17 | chr11 | 89432656 | ||||||
| chr11:89432769
|
G | C | 1 | a0001c0001t0002g0252 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.548+15C>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 7/17 | chr11 | 89432769 | ||||||
| chr11:89432935
|
G | A | 8 | a0001c0001t0001g0063a0001c0001t0019g0166a0001c0001t0022g0140others(5): Show | 8 | HG01081.hp1 HG01884.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.476-79C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89432935 | ||||||
| chr11:89433028
|
A | T | 15 | a0001c0001t0002g0252a0001c0001t0017g0160a0001c0001t0024g0155others(12): Show | 15 | HG01884.hp1 HG02615.hp1 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.476-172T>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89433028 | ||||||
| chr11:89433139
|
C | G | 51 | a0001c0001t0002g0260a0001c0001t0003g0170a0001c0001t0003g0191others(48): Show | 51 | HG00408.hp2 HG00621.hp1 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.476-283G>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89433139 | ||||||
| chr11:89433169
|
T | A | 1 | a0001c0001t0117g0287 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.476-313A>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89433169 | ||||||
| chr11:89433219
|
C | T | 2 | a0001c0001t0017g0171a0001c0001t0017g0172 | 2 | HG01074.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.476-363G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89433219 | ||||||
| chr11:89433354
|
C | T | 8 | a0001c0001t0001g0063a0001c0001t0019g0166a0001c0001t0022g0140others(5): Show | 8 | HG01081.hp1 HG01884.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.476-498G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89433354 | ||||||
| chr11:89433358
|
T | C | 1 | a0001c0002t0074g0146 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.476-502A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89433358 | ||||||
| chr11:89433443
|
T | A | 3 | a0001c0003t0019g0197a0001c0003t0019g0204a0001c0003t0019g0213 | 3 | NA18941.hp2 NA18966.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.476-587A>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89433443 | ||||||
| chr11:89433497
|
T | G | 17 | a0001c0001t0002g0224a0001c0001t0002g0254a0001c0001t0002g0255others(14): Show | 17 | HG02258.hp1 HG02451.hp1 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.476-641A>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89433497 | ||||||
| chr11:89433527
|
T | C | 1 | a0001c0001t0001g0050 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.476-671A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89433527 | ||||||
| chr11:89433528
|
G | A | 1 | a0001c0001t0001g0035 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.476-672C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89433528 | ||||||
| chr11:89433574
|
A | G | 1 | a0001c0002t0074g0146 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.476-718T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89433574 | ||||||
| chr11:89433595
|
T | C | 15 | a0001c0001t0002g0252a0001c0001t0017g0160a0001c0001t0024g0155others(12): Show | 15 | HG01884.hp1 HG02615.hp1 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.476-739A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89433595 | ||||||
| chr11:89433788
|
T | C | 1 | a0001c0002t0006g0025 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.476-932A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89433788 | ||||||
| chr11:89433800
|
T | C | 5 | a0001c0001t0001g0063a0001c0001t0019g0166a0001c0001t0022g0140others(2): Show | 5 | HG01081.hp1 HG01884.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.476-944A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89433800 | ||||||
| chr11:89433860
|
T | G | 4 | a0001c0001t0002g0252a0001c0001t0024g0155a0001c0002t0011g0156others(1): Show | 4 | HG02622.hp1 HG02647.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.476-1004A>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89433860 | ||||||
| chr11:89433941
|
C | T | 1 | a0001c0001t0053g0101 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.476-1085G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89433941 | ||||||
| chr11:89433942
|
C | T | 7 | a0001c0001t0001g0035a0001c0001t0001g0088a0001c0001t0001g0138others(4): Show | 7 | HG01928.hp1 HG01934.hp2 HG01981.hp1 others(4): Show |
intron_variant | MODIFIER | c.476-1086G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89433942 | ||||||
| chr11:89433975
|
G | A | 1 | a0001c0001t0001g0014 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.476-1119C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89433975 | ||||||
| chr11:89434225
|
G | A | 15 | a0001c0001t0002g0252a0001c0001t0017g0160a0001c0001t0024g0155others(12): Show | 15 | HG01884.hp1 HG02615.hp1 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.476-1369C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89434225 | ||||||
| chr11:89434301
|
G | A | 1 | a0001c0003t0005g0184 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.476-1445C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89434301 | ||||||
| chr11:89434317
|
A | T | 9 | a0001c0001t0002g0224a0001c0001t0002g0254a0001c0001t0002g0255others(6): Show | 9 | HG02451.hp1 HG02615.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.476-1461T>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89434317 | ||||||
| chr11:89434324
|
G | A | 5 | a0001c0001t0048g0044a0001c0001t0049g0043a0001c0001t0079g0169others(2): Show | 5 | HG02615.hp1 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.476-1468C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89434324 | ||||||
| chr11:89434335
|
C | T | 15 | a0001c0001t0002g0252a0001c0001t0017g0160a0001c0001t0024g0155others(12): Show | 15 | HG01884.hp1 HG02615.hp1 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.476-1479G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89434335 | ||||||
| chr11:89434501
|
G | A | 218 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0008others(215): Show | 218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.476-1645C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89434501 | ||||||
| chr11:89434564
|
A | G | 2 | a0001c0001t0017g0160a0001c0002t0030g0159 | 2 | HG01884.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.476-1708T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89434564 | ||||||
| chr11:89434568
|
T | C | 3 | a0001c0001t0001g0088a0001c0001t0001g0138a0001c0001t0055g0097 | 3 | NA18990.hp2 NA18995.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.476-1712A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89434568 | ||||||
| chr11:89434595
|
T | C | 1 | a0001c0002t0051g0009 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.476-1739A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89434595 | ||||||
| chr11:89434607
|
G | C | 1 | a0001c0001t0015g0057 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.476-1751C>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89434607 | ||||||
| chr11:89434699
|
C | T | 1 | a0001c0001t0002g0259 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.476-1843G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89434699 | ||||||
| chr11:89434700
|
G | A | 1 | a0001c0002t0074g0146 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.476-1844C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89434700 | ||||||
| chr11:89434775
|
TA | T | 52 | a0001c0001t0002g0260a0001c0001t0003g0170a0001c0001t0003g0191others(49): Show | 52 | HG00408.hp2 HG00621.hp1 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.476-1920delT | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89434775 | ||||||
| chr11:89434887
|
T | G | 2 | a0001c0001t0048g0044a0001c0001t0049g0043 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.476-2031A>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89434887 | ||||||
| chr11:89435098
|
T | G | 1 | a0001c0001t0022g0040 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.476-2242A>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89435098 | ||||||
| chr11:89435196
|
A | G | 1 | a0001c0001t0002g0252 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.476-2340T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89435196 | ||||||
| chr11:89435347
|
A | T | 1 | a0001c0001t0085g0179 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.476-2491T>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89435347 | ||||||
| chr11:89435374
|
C | T | 1 | a0001c0002t0098g0284 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.476-2518G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89435374 | ||||||
| chr11:89435414
|
G | C | 1 | a0001c0001t0001g0059 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.476-2558C>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89435414 | ||||||
| chr11:89435506
|
C | G | 1 | a0001c0002t0006g0079 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.476-2650G>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89435506 | ||||||
| chr11:89435588
|
A | G | 51 | a0001c0001t0002g0260a0001c0001t0003g0170a0001c0001t0003g0191others(48): Show | 51 | HG00408.hp2 HG00621.hp1 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.476-2732T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89435588 | ||||||
| chr11:89435635
|
C | T | 1 | a0001c0003t0005g0184 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.476-2779G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89435635 | ||||||
| chr11:89435677
|
T | TA | 5 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0002g0259others(2): Show | 5 | HG01081.hp2 HG01952.hp1 HG02132.hp1 others(2): Show |
intron_variant | MODIFIER | c.476-2822dupT | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89435677 | ||||||
| chr11:89435717
|
C | T | 1 | a0001c0001t0002g0252 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.476-2861G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89435717 | ||||||
| chr11:89435789
|
G | A | 1 | a0001c0002t0006g0079 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.476-2933C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89435789 | ||||||
| chr11:89435970
|
T | C | 15 | a0001c0001t0002g0252a0001c0001t0017g0160a0001c0001t0024g0155others(12): Show | 15 | HG01884.hp1 HG02615.hp1 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.476-3114A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89435970 | ||||||
| chr11:89436372
|
G | A | 10 | a0001c0001t0017g0160a0001c0001t0031g0176a0001c0001t0031g0177others(7): Show | 10 | HG01884.hp1 HG02615.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.476-3516C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89436372 | ||||||
| chr11:89436625
|
G | A | 15 | a0001c0001t0002g0252a0001c0001t0017g0160a0001c0001t0024g0155others(12): Show | 15 | HG01884.hp1 HG02615.hp1 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.476-3769C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89436625 | ||||||
| chr11:89436638
|
C | A | 5 | a0001c0001t0001g0063a0001c0001t0019g0166a0001c0001t0022g0140others(2): Show | 5 | HG01081.hp1 HG01884.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.476-3782G>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89436638 | ||||||
| chr11:89436750
|
T | C | 1 | a0001c0001t0113g0227 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.476-3894A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89436750 | ||||||
| chr11:89436779
|
C | A | 1 | a0001c0002t0074g0146 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.475+3909G>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89436779 | ||||||
| chr11:89436797
|
T | C | 1 | a0002c0004t0032g0162 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.475+3891A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89436797 | ||||||
| chr11:89437138
|
A | G | 15 | a0001c0001t0002g0252a0001c0001t0017g0160a0001c0001t0024g0155others(12): Show | 15 | HG01884.hp1 HG02615.hp1 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.475+3550T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89437138 | ||||||
| chr11:89437224
|
C | T | 3 | a0001c0002t0009g0236a0001c0002t0034g0237a0001c0002t0035g0229 | 3 | NA18957.hp1 NA18965.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.475+3464G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89437224 | ||||||
| chr11:89437339
|
T | C | 10 | a0001c0001t0017g0160a0001c0001t0031g0176a0001c0001t0031g0177others(7): Show | 10 | HG01884.hp1 HG02615.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.475+3349A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89437339 | ||||||
| chr11:89437347
|
T | C | 220 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0008others(217): Show | 220 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(217): Show |
intron_variant | MODIFIER | c.475+3341A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89437347 | ||||||
| chr11:89437369
|
A | G | 1 | a0001c0001t0115g0253 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.475+3319T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89437369 | ||||||
| chr11:89437475
|
C | T | 1 | a0001c0001t0002g0254 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.475+3213G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89437475 | ||||||
| chr11:89437554
|
G | A | 15 | a0001c0001t0002g0252a0001c0001t0017g0160a0001c0001t0024g0155others(12): Show | 15 | HG01884.hp1 HG02615.hp1 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.475+3134C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89437554 | ||||||
| chr11:89437557
|
C | T | 15 | a0001c0001t0002g0252a0001c0001t0017g0160a0001c0001t0024g0155others(12): Show | 15 | HG01884.hp1 HG02615.hp1 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.475+3131G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89437557 | ||||||
| chr11:89437610
|
T | G | 1 | a0001c0001t0016g0047 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.475+3078A>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89437610 | ||||||
| chr11:89437677
|
A | G | 5 | a0001c0001t0002g0279a0001c0001t0002g0283a0001c0001t0037g0280others(2): Show | 5 | HG02258.hp1 HG02717.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.475+3011T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89437677 | ||||||
| chr11:89437739
|
C | T | 15 | a0001c0001t0002g0252a0001c0001t0017g0160a0001c0001t0024g0155others(12): Show | 15 | HG01884.hp1 HG02615.hp1 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.475+2949G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89437739 | ||||||
| chr11:89437804
|
T | C | 5 | a0001c0001t0002g0252a0001c0001t0024g0155a0001c0002t0011g0156others(2): Show | 5 | HG02622.hp1 HG02647.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.475+2884A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89437804 | ||||||
| chr11:89437980
|
T | C | 1 | a0001c0001t0003g0186 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.475+2708A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89437980 | ||||||
| chr11:89438016
|
G | A | 1 | a0001c0001t0002g0238 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.475+2672C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89438016 | ||||||
| chr11:89438070
|
G | A | 5 | a0001c0001t0002g0252a0001c0001t0024g0155a0001c0002t0011g0156others(2): Show | 5 | HG02622.hp1 HG02647.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.475+2618C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89438070 | ||||||
| chr11:89438163
|
T | C | 3 | a0001c0001t0024g0155a0001c0002t0011g0156a0001c0002t0029g0168 | 3 | HG02647.hp2 HG03098.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.475+2525A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89438163 | ||||||
| chr11:89438323
|
T | C | 1 | a0001c0002t0033g0262 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.475+2365A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89438323 | ||||||
| chr11:89438337
|
TTATATAC others(2): Show |
T | 9 | a0001c0003t0003g0193a0001c0003t0003g0201a0001c0003t0004g0037others(6): Show | 9 | HG00408.hp2 HG01074.hp1 HG01346.hp2 others(6): Show |
intron_variant | MODIFIER | c.475+2342_475+2350d others(11): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89438337 | ||||||
| chr11:89438353
|
C | T | 1 | a0001c0001t0069g0015 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.475+2335G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89438353 | ||||||
| chr11:89438368
|
TATATATA | T | 51 | a0001c0001t0002g0260a0001c0001t0003g0170a0001c0001t0003g0191others(48): Show | 51 | HG00408.hp2 HG00621.hp1 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.475+2313_475+2319d others(9): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89438368 | ||||||
| chr11:89438374
|
T | G | 3 | a0001c0001t0082g0174a0001c0002t0011g0153a0001c0002t0029g0154 | 3 | HG01099.hp1 HG01109.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.475+2314A>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89438374 | ||||||
| chr11:89438375
|
A | T | 3 | a0001c0001t0082g0174a0001c0002t0011g0153a0001c0002t0029g0154 | 3 | HG01099.hp1 HG01109.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.475+2313T>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89438375 | ||||||
| chr11:89438394
|
T | C | 6 | a0001c0001t0002g0279a0001c0001t0002g0283a0001c0001t0017g0165others(3): Show | 6 | HG02258.hp1 HG02717.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.475+2294A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89438394 | ||||||
| chr11:89438445
|
A | G | 3 | a0001c0001t0024g0155a0001c0002t0011g0156a0001c0002t0029g0168 | 3 | HG02647.hp2 HG03098.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.475+2243T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89438445 | ||||||
| chr11:89438446
|
TTATATAA others(32): Show |
T | 65 | a0001c0001t0001g0063a0001c0001t0002g0260a0001c0001t0003g0170others(62): Show | 65 | HG00408.hp2 HG00621.hp1 HG00639.hp2 others(62): Show |
intron_variant | MODIFIER | c.475+2203_475+2241d others(41): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89438446 | ||||||
| chr11:89438476
|
C | T | 15 | a0001c0001t0002g0252a0001c0001t0017g0160a0001c0001t0024g0155others(12): Show | 15 | HG01884.hp1 HG02615.hp1 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.475+2212G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89438476 | ||||||
| chr11:89438492
|
A | T | 15 | a0001c0001t0002g0252a0001c0001t0017g0160a0001c0001t0024g0155others(12): Show | 15 | HG01884.hp1 HG02615.hp1 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.475+2196T>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89438492 | ||||||
| chr11:89438495
|
T | C | 15 | a0001c0001t0002g0252a0001c0001t0017g0160a0001c0001t0024g0155others(12): Show | 15 | HG01884.hp1 HG02615.hp1 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.475+2193A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89438495 | ||||||
| chr11:89438499
|
G | C | 15 | a0001c0001t0002g0252a0001c0001t0017g0160a0001c0001t0024g0155others(12): Show | 15 | HG01884.hp1 HG02615.hp1 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.475+2189C>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89438499 | ||||||
| chr11:89438500
|
C | T | 15 | a0001c0001t0002g0252a0001c0001t0017g0160a0001c0001t0024g0155others(12): Show | 15 | HG01884.hp1 HG02615.hp1 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.475+2188G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89438500 | ||||||
| chr11:89438506
|
T | TA | 15 | a0001c0001t0002g0252a0001c0001t0017g0160a0001c0001t0024g0155others(12): Show | 15 | HG01884.hp1 HG02615.hp1 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.475+2181dupT | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89438506 | ||||||
| chr11:89438509
|
T | A | 15 | a0001c0001t0002g0252a0001c0001t0017g0160a0001c0001t0024g0155others(12): Show | 15 | HG01884.hp1 HG02615.hp1 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.475+2179A>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89438509 | ||||||
| chr11:89438515
|
C | T | 1 | a0006c0010t0016g0027 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.475+2173G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89438515 | ||||||
| chr11:89438516
|
T | TATATATA others(5): Show |
4 | a0001c0001t0002g0252a0001c0001t0024g0155a0001c0002t0011g0156others(1): Show | 4 | HG02622.hp1 HG02647.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.475+2171_475+2172i others(14): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89438516 | ||||||
| chr11:89438523
|
ACT | A | 11 | a0001c0001t0017g0160a0001c0001t0031g0176a0001c0001t0031g0177others(8): Show | 11 | HG01884.hp1 HG02615.hp1 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.475+2163_475+2164d others(4): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89438523 | ||||||
| chr11:89438531
|
T | A | 11 | a0001c0001t0017g0160a0001c0001t0031g0176a0001c0001t0031g0177others(8): Show | 11 | HG01884.hp1 HG02615.hp1 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.475+2157A>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89438531 | ||||||
| chr11:89438534
|
C | T | 15 | a0001c0001t0002g0252a0001c0001t0017g0160a0001c0001t0024g0155others(12): Show | 15 | HG01884.hp1 HG02615.hp1 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.475+2154G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89438534 | ||||||
| chr11:89438536
|
C | T | 15 | a0001c0001t0002g0252a0001c0001t0017g0160a0001c0001t0024g0155others(12): Show | 15 | HG01884.hp1 HG02615.hp1 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.475+2152G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89438536 | ||||||
| chr11:89438543
|
TATA | T | 10 | a0001c0001t0017g0160a0001c0001t0031g0176a0001c0001t0031g0177others(7): Show | 10 | HG01884.hp1 HG02615.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.475+2142_475+2144d others(5): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89438543 | ||||||
| chr11:89438546
|
A | T | 1 | a0001c0002t0074g0146 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.475+2142T>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89438546 | ||||||
| chr11:89438549
|
A | ATATAGTA others(36): Show |
3 | a0001c0001t0024g0155a0001c0002t0011g0156a0001c0002t0029g0168 | 3 | HG02647.hp2 HG03098.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.475+2138_475+2139i others(45): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89438549 | ||||||
| chr11:89438549
|
A | T | 10 | a0001c0001t0017g0160a0001c0001t0031g0176a0001c0001t0031g0177others(7): Show | 10 | HG01884.hp1 HG02615.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.475+2139T>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89438549 | ||||||
| chr11:89438555
|
C | A | 1 | a0001c0002t0074g0146 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.475+2133G>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89438555 | ||||||
| chr11:89438555
|
C | T | 1 | a0001c0001t0002g0252 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.475+2133G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89438555 | ||||||
| chr11:89438558
|
TATATA | T | 10 | a0001c0001t0017g0160a0001c0001t0031g0176a0001c0001t0031g0177others(7): Show | 10 | HG01884.hp1 HG02615.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.475+2125_475+2129d others(7): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89438558 | ||||||
| chr11:89438562
|
T | G | 1 | a0001c0002t0074g0146 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.475+2126A>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89438562 | ||||||
| chr11:89438563
|
A | AATACTAT | 3 | a0001c0001t0024g0155a0001c0002t0011g0156a0001c0002t0029g0168 | 3 | HG02647.hp2 HG03098.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.475+2124_475+2125i others(9): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89438563 | ||||||
| chr11:89438563
|
A | T | 1 | a0001c0002t0074g0146 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.475+2125T>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89438563 | ||||||
| chr11:89438569
|
A | T | 1 | a0001c0002t0074g0146 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.475+2119T>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89438569 | ||||||
| chr11:89438576
|
C | G | 25 | a0001c0001t0001g0063a0001c0001t0002g0252a0001c0001t0017g0160others(22): Show | 25 | HG01081.hp1 HG01884.hp1 HG01884.hp2 others(22): Show |
intron_variant | MODIFIER | c.475+2112G>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89438576 | ||||||
| chr11:89438586
|
TATACTAT others(5): Show |
T | 53 | a0001c0001t0002g0260a0001c0001t0003g0170a0001c0001t0003g0191others(50): Show | 53 | HG00408.hp2 HG00621.hp1 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.475+2090_475+2101d others(14): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89438586 | ||||||
| chr11:89438590
|
C | G | 1 | a0001c0002t0074g0146 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.475+2098G>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89438590 | ||||||
| chr11:89438592
|
A | G | 76 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0014others(73): Show | 76 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(73): Show |
intron_variant | MODIFIER | c.475+2096T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89438592 | ||||||
| chr11:89438595
|
T | C | 1 | a0001c0002t0045g0095 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.475+2093A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89438595 | ||||||
| chr11:89438598
|
A | T | 1 | a0001c0002t0074g0146 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.475+2090T>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89438598 | ||||||
| chr11:89438598
|
AATACTAT others(74): Show |
A | 1 | a0001c0003t0005g0180 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.475+2009_475+2089d others(83): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89438598 | ||||||
| chr11:89438644
|
C | T | 1 | a0001c0002t0074g0146 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.475+2044G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89438644 | ||||||
| chr11:89438645
|
T | A | 1 | a0001c0002t0074g0146 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.475+2043A>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89438645 | ||||||
| chr11:89438646
|
C | G | 1 | a0001c0002t0074g0146 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.475+2042G>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89438646 | ||||||
| chr11:89438653
|
A | T | 1 | a0001c0002t0074g0146 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.475+2035T>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89438653 | ||||||
| chr11:89438668
|
T | A | 1 | a0001c0002t0074g0146 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.475+2020A>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89438668 | ||||||
| chr11:89438674
|
C | T | 1 | a0001c0002t0074g0146 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.475+2014G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89438674 | ||||||
| chr11:89438675
|
T | A | 1 | a0001c0002t0074g0146 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.475+2013A>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89438675 | ||||||
| chr11:89438676
|
A | G | 1 | a0001c0002t0074g0146 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.475+2012T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89438676 | ||||||
| chr11:89438679
|
T | TATA | 212 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0008others(209): Show | 212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): Show |
intron_variant | MODIFIER | c.475+2006_475+2008d others(5): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89438679 | ||||||
| chr11:89438683
|
C | A | 1 | a0001c0002t0029g0168 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.475+2005G>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89438683 | ||||||
| chr11:89438683
|
C | T | 1 | a0001c0002t0074g0146 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.475+2005G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89438683 | ||||||
| chr11:89438686
|
T | C | 1 | a0001c0002t0029g0168 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.475+2002A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89438686 | ||||||
| chr11:89438687
|
A | T | 1 | a0001c0002t0029g0168 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.475+2001T>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89438687 | ||||||
| chr11:89438689
|
A | T | 1 | a0001c0002t0029g0168 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.475+1999T>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89438689 | ||||||
| chr11:89438690
|
T | A | 1 | a0001c0002t0029g0168 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.475+1998A>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89438690 | ||||||
| chr11:89438692
|
A | C | 1 | a0001c0002t0074g0146 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.475+1996T>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89438692 | ||||||
| chr11:89438699
|
A | T | 1 | a0001c0002t0074g0146 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.475+1989T>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89438699 | ||||||
| chr11:89438700
|
T | A | 1 | a0001c0002t0074g0146 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.475+1988A>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89438700 | ||||||
| chr11:89438714
|
T | A | 1 | a0001c0002t0074g0146 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.475+1974A>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89438714 | ||||||
| chr11:89438722
|
T | G | 1 | a0001c0002t0074g0146 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.475+1966A>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89438722 | ||||||
| chr11:89438728
|
C | A | 1 | a0001c0002t0074g0146 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.475+1960G>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89438728 | ||||||
| chr11:89438729
|
A | T | 1 | a0001c0002t0074g0146 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.475+1959T>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89438729 | ||||||
| chr11:89438750
|
A | C | 1 | a0001c0002t0074g0146 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.475+1938T>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89438750 | ||||||
| chr11:89438751
|
TATATA | T | 20 | a0001c0001t0002g0252a0001c0001t0002g0279a0001c0001t0002g0283others(17): Show | 20 | HG01884.hp1 HG02258.hp1 HG02615.hp1 others(17): Show |
intron_variant | MODIFIER | c.475+1932_475+1936d others(7): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89438751 | ||||||
| chr11:89438766
|
A | T | 1 | a0001c0002t0074g0146 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.475+1922T>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89438766 | ||||||
| chr11:89438768
|
TATA | T | 8 | a0001c0001t0001g0063a0001c0001t0019g0166a0001c0001t0022g0140others(5): Show | 8 | HG01081.hp1 HG01884.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.475+1917_475+1919d others(5): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89438768 | ||||||
| chr11:89438772
|
A | C | 1 | a0001c0002t0074g0146 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.475+1916T>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89438772 | ||||||
| chr11:89438786
|
T | A | 1 | a0001c0002t0074g0146 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.475+1902A>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89438786 | ||||||
| chr11:89438790
|
G | A | 1 | a0001c0002t0074g0146 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.475+1898C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89438790 | ||||||
| chr11:89438792
|
G | A | 1 | a0001c0002t0074g0146 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.475+1896C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89438792 | ||||||
| chr11:89438792
|
G | GTATAATA | 6 | a0001c0001t0002g0256a0001c0001t0021g0113a0001c0001t0021g0124others(3): Show | 6 | HG02145.hp2 HG03669.hp1 HG03927.hp1 others(3): Show |
intron_variant | MODIFIER | c.475+1889_475+1895d others(9): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89438792 | ||||||
| chr11:89438792
|
G | GTATAATA others(28): Show |
4 | a0001c0001t0001g0081a0001c0001t0003g0188a0001c0001t0013g0082others(1): Show | 4 | HG01256.hp2 HG01928.hp2 HG02004.hp1 others(1): Show |
intron_variant | MODIFIER | c.475+1895_475+1896i others(37): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89438792 | ||||||
| chr11:89438792
|
GTATAATA others(72): Show |
G | 14 | a0001c0001t0002g0252a0001c0001t0017g0160a0001c0001t0024g0155others(11): Show | 14 | HG01884.hp1 HG02615.hp1 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.475+1817_475+1895d others(81): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89438792 | ||||||
| chr11:89438797
|
ATATATTA others(14): Show |
A | 110 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0008others(107): Show | 110 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(107): Show |
intron_variant | MODIFIER | c.475+1870_475+1890d others(23): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89438797 | ||||||
| chr11:89438801
|
A | ATTATATA others(21): Show |
1 | a0001c0001t0027g0018 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.475+1859_475+1886d others(30): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89438801 | ||||||
| chr11:89438802
|
T | C | 1 | a0001c0002t0074g0146 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.475+1886A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89438802 | ||||||
| chr11:89438803
|
T | A | 81 | a0001c0001t0001g0063a0001c0001t0002g0224a0001c0001t0002g0254others(78): Show | 81 | HG00408.hp2 HG00621.hp1 HG00639.hp2 others(78): Show |
intron_variant | MODIFIER | c.475+1885A>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89438803 | ||||||
| chr11:89438809
|
TTATATAT others(81): Show |
T | 3 | a0001c0001t0018g0142a0001c0001t0018g0175a0001c0001t0078g0143 | 3 | HG02280.hp1 NA19240.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.475+1791_475+1878d others(90): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89438809 | ||||||
| chr11:89438812
|
TATATATT others(48): Show |
T | 1 | a0001c0002t0009g0278 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.475+1821_475+1875d others(57): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89438812 | ||||||
| chr11:89438815
|
A | ATTATATA others(22): Show |
1 | a0001c0002t0101g0239 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.475+1872_475+1873i others(31): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89438815 | ||||||
| chr11:89438816
|
TATTATAT others(11): Show |
T | 1 | a0001c0001t0113g0227 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.475+1854_475+1871d others(20): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89438816 | ||||||
| chr11:89438816
|
TATTATAT others(44): Show |
T | 54 | a0001c0001t0002g0260a0001c0001t0003g0170a0001c0001t0003g0191others(51): Show | 54 | HG00408.hp2 HG00621.hp1 HG00639.hp2 others(51): Show |
intron_variant | MODIFIER | c.475+1821_475+1871d others(53): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89438816 | ||||||
| chr11:89438816
|
TATTATAT others(74): Show |
T | 16 | a0001c0001t0002g0224a0001c0001t0002g0254a0001c0001t0002g0255others(13): Show | 16 | HG02258.hp1 HG02451.hp1 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.475+1791_475+1871d others(83): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89438816 | ||||||
| chr11:89438817
|
A | T | 2 | a0001c0001t0017g0171a0001c0001t0017g0172 | 2 | HG01074.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.475+1871T>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89438817 | ||||||
| chr11:89438818
|
T | A | 11 | a0001c0001t0001g0081a0001c0001t0002g0256a0001c0001t0003g0188others(8): Show | 11 | HG01074.hp2 HG01256.hp2 HG01928.hp2 others(8): Show |
intron_variant | MODIFIER | c.475+1870A>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89438818 | ||||||
| chr11:89438824
|
A | AT | 3 | a0001c0001t0001g0063a0001c0001t0068g0064a0001c0002t0100g0258 | 3 | HG01884.hp2 HG02965.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.475+1863_475+1864i others(3): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89438824 | ||||||
| chr11:89438824
|
A | C | 1 | a0001c0002t0074g0146 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.475+1864T>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89438824 | ||||||
| chr11:89438825
|
ATATCTTA others(12): Show |
A | 2 | a0001c0001t0017g0171a0001c0001t0017g0172 | 2 | HG01074.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.475+1844_475+1862d others(21): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89438825 | ||||||
| chr11:89438825
|
ATATCTTA others(14): Show |
A | 1 | a0001c0003t0013g0041 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.475+1842_475+1862d others(23): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89438825 | ||||||
| chr11:89438829
|
C | A | 124 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0008others(121): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.475+1859G>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89438829 | ||||||
| chr11:89438831
|
T | A | 4 | a0001c0001t0001g0063a0001c0001t0068g0064a0001c0001t0111g0277others(1): Show | 4 | HG01884.hp2 HG02922.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.475+1857A>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89438831 | ||||||
| chr11:89438832
|
A | G | 3 | a0001c0001t0001g0063a0001c0001t0068g0064a0001c0002t0100g0258 | 3 | HG01884.hp2 HG02965.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.475+1856T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89438832 | ||||||
| chr11:89438836
|
ATT | A | 3 | a0001c0001t0001g0063a0001c0001t0068g0064a0001c0002t0100g0258 | 3 | HG01884.hp2 HG02965.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.475+1850_475+1851d others(4): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89438836 | ||||||
| chr11:89438837
|
T | A | 1 | a0001c0002t0074g0146 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.475+1851A>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89438837 | ||||||
| chr11:89438846
|
T | A | 122 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0008others(119): Show | 122 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(119): Show |
intron_variant | MODIFIER | c.475+1842A>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89438846 | ||||||
| chr11:89438846
|
T | TAA | 4 | a0001c0001t0001g0081a0001c0001t0003g0188a0001c0001t0013g0082others(1): Show | 4 | HG01256.hp2 HG01928.hp2 HG02004.hp1 others(1): Show |
intron_variant | MODIFIER | c.475+1841_475+1842i others(4): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89438846 | ||||||
| chr11:89438846
|
T | TTATATAA others(23): Show |
7 | a0001c0001t0001g0001a0001c0001t0001g0069a0001c0001t0001g0129others(4): Show | 8 | HG01071.hp1 HG01255.hp2 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.475+1812_475+1841d others(32): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89438846 | ||||||
| chr11:89438846
|
TTATATAA others(23): Show |
T | 1 | a0001c0001t0003g0164 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.475+1812_475+1841d others(32): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89438846 | ||||||
| chr11:89438847
|
T | A | 1 | a0001c0002t0074g0146 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.475+1841A>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89438847 | ||||||
| chr11:89438853
|
A | C | 1 | a0001c0001t0020g0056 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.475+1835T>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89438853 | ||||||
| chr11:89438858
|
T | A | 1 | a0001c0002t0074g0146 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.475+1830A>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89438858 | ||||||
| chr11:89438859
|
T | A | 2 | a0001c0002t0035g0248a0001c0002t0093g0219 | 2 | HG02257.hp2 NA18612.hp1 |
intron_variant | MODIFIER | c.475+1829A>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89438859 | ||||||
| chr11:89438861
|
T | A | 1 | a0001c0002t0074g0146 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.475+1827A>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89438861 | ||||||
| chr11:89438863
|
T | C | 1 | a0001c0001t0113g0227 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.475+1825A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89438863 | ||||||
| chr11:89438865
|
T | A | 1 | a0001c0002t0074g0146 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.475+1823A>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89438865 | ||||||
| chr11:89438884
|
T | TATAAA | 3 | a0001c0001t0001g0063a0001c0001t0068g0064a0001c0002t0100g0258 | 3 | HG01884.hp2 HG02965.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.475+1803_475+1804i others(7): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89438884 | ||||||
| chr11:89438889
|
T | A | 1 | a0001c0002t0006g0025 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.475+1799A>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89438889 | ||||||
| chr11:89438890
|
A | G | 10 | a0001c0001t0017g0160a0001c0001t0031g0176a0001c0001t0031g0177others(7): Show | 10 | HG01884.hp1 HG02615.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.475+1798T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89438890 | ||||||
| chr11:89438895
|
TTA | T | 4 | a0001c0001t0005g0178a0001c0001t0071g0090a0001c0001t0091g0151others(1): Show | 4 | HG02280.hp2 HG02572.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.475+1791_475+1792d others(4): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89438895 | ||||||
| chr11:89438896
|
T | A | 6 | a0001c0001t0001g0063a0001c0001t0002g0245a0001c0001t0068g0064others(3): Show | 6 | HG01884.hp2 HG02723.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.475+1792A>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89438896 | ||||||
| chr11:89438897
|
A | T | 3 | a0001c0001t0002g0245a0001c0002t0011g0173a0001c0012t0023g0181 | 3 | HG02723.hp1 HG03139.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.475+1791T>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89438897 | ||||||
| chr11:89438898
|
T | A | 3 | a0001c0001t0002g0245a0001c0002t0011g0173a0001c0012t0023g0181 | 3 | HG02723.hp1 HG03139.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.475+1790A>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89438898 | ||||||
| chr11:89438900
|
T | TAATATAT others(6): Show |
3 | a0001c0001t0001g0063a0001c0001t0068g0064a0001c0002t0100g0258 | 3 | HG01884.hp2 HG02965.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.475+1787_475+1788i others(15): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89438900 | ||||||
| chr11:89438905
|
A | T | 3 | a0001c0001t0018g0142a0001c0001t0018g0175a0001c0001t0078g0143 | 3 | HG02280.hp1 NA19240.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.475+1783T>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89438905 | ||||||
| chr11:89438919
|
AAT | A | 51 | a0001c0001t0002g0260a0001c0001t0003g0170a0001c0001t0003g0191others(48): Show | 51 | HG00408.hp2 HG00621.hp1 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.475+1767_475+1768d others(4): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89438919 | ||||||
| chr11:89438926
|
A | G | 1 | a0001c0001t0094g0218 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.475+1762T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89438926 | ||||||
| chr11:89438947
|
T | C | 3 | a0001c0001t0018g0142a0001c0001t0018g0175a0001c0001t0078g0143 | 3 | HG02280.hp1 NA19240.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.475+1741A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89438947 | ||||||
| chr11:89438952
|
T | TATATA | 14 | a0001c0001t0002g0252a0001c0001t0017g0160a0001c0001t0024g0155others(11): Show | 14 | HG01884.hp1 HG02615.hp1 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.475+1731_475+1735d others(7): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89438952 | ||||||
| chr11:89438972
|
A | G | 15 | a0001c0001t0002g0252a0001c0001t0017g0160a0001c0001t0024g0155others(12): Show | 15 | HG01884.hp1 HG02615.hp1 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.475+1716T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89438972 | ||||||
| chr11:89439055
|
A | C | 1 | a0001c0001t0008g0086 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.475+1633T>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89439055 | ||||||
| chr11:89439227
|
C | T | 1 | a0001c0001t0111g0277 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.475+1461G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89439227 | ||||||
| chr11:89439284
|
T | C | 6 | a0001c0001t0002g0252a0001c0001t0007g0126a0001c0001t0024g0155others(3): Show | 6 | HG00621.hp2 HG02622.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.475+1404A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89439284 | ||||||
| chr11:89439561
|
G | A | 4 | a0001c0001t0001g0081a0001c0001t0003g0188a0001c0001t0013g0082others(1): Show | 4 | HG01256.hp2 HG01928.hp2 HG02004.hp1 others(1): Show |
intron_variant | MODIFIER | c.475+1127C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89439561 | ||||||
| chr11:89439796
|
A | G | 1 | a0001c0003t0003g0212 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.475+892T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89439796 | ||||||
| chr11:89439938
|
G | A | 1 | a0001c0001t0023g0161 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.475+750C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89439938 | ||||||
| chr11:89440024
|
G | GT | 4 | a0001c0001t0002g0252a0001c0001t0024g0155a0001c0002t0011g0156others(1): Show | 4 | HG02622.hp1 HG02647.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.475+663dupA | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89440024 | ||||||
| chr11:89440085
|
A | G | 1 | a0001c0001t0002g0252 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.475+603T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89440085 | ||||||
| chr11:89440099
|
G | A | 14 | a0001c0001t0002g0252a0001c0001t0017g0160a0001c0001t0024g0155others(11): Show | 14 | HG01884.hp1 HG02615.hp1 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.475+589C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89440099 | ||||||
| chr11:89440282
|
T | C | 5 | a0001c0001t0002g0266a0001c0001t0002g0268a0001c0001t0002g0269others(2): Show | 5 | HG00735.hp2 HG00741.hp2 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.475+406A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89440282 | ||||||
| chr11:89440319
|
T | G | 14 | a0001c0001t0002g0252a0001c0001t0017g0160a0001c0001t0024g0155others(11): Show | 14 | HG01884.hp1 HG02615.hp1 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.475+369A>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89440319 | ||||||
| chr11:89440400
|
A | G | 1 | a0001c0001t0054g0048 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.475+288T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89440400 | ||||||
| chr11:89440469
|
G | T | 134 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0008others(131): Show | 134 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(131): Show |
intron_variant | MODIFIER | c.475+219C>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89440469 | ||||||
| chr11:89440523
|
T | C | 1 | a0001c0001t0002g0255 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.475+165A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89440523 | ||||||
| chr11:89440616
|
C | T | 1 | a0001c0002t0009g0278 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.475+72G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 6/17 | chr11 | 89440616 | ||||||
| chr11:89440767
|
T | C | 10 | a0001c0001t0017g0160a0001c0001t0031g0176a0001c0001t0031g0177others(7): Show | 10 | HG01884.hp1 HG02615.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.448-52A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 5/17 | chr11 | 89440767 | ||||||
| chr11:89440914
|
T | C | 1 | a0001c0003t0007g0053 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.448-199A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 5/17 | chr11 | 89440914 | ||||||
| chr11:89441046
|
T | C | 51 | a0001c0001t0002g0260a0001c0001t0003g0170a0001c0001t0003g0191others(48): Show | 51 | HG00408.hp2 HG00621.hp1 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.448-331A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 5/17 | chr11 | 89441046 | ||||||
| chr11:89441110
|
A | T | 10 | a0001c0001t0017g0160a0001c0001t0031g0176a0001c0001t0031g0177others(7): Show | 10 | HG01884.hp1 HG02615.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.448-395T>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 5/17 | chr11 | 89441110 | ||||||
| chr11:89441155
|
C | T | 17 | a0001c0001t0002g0224a0001c0001t0002g0254a0001c0001t0002g0255others(14): Show | 17 | HG02258.hp1 HG02451.hp1 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.448-440G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 5/17 | chr11 | 89441155 | ||||||
| chr11:89441225
|
G | A | 8 | a0001c0001t0001g0063a0001c0001t0019g0166a0001c0001t0022g0140others(5): Show | 8 | HG01081.hp1 HG01884.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.448-510C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 5/17 | chr11 | 89441225 | ||||||
| chr11:89441371
|
G | A | 3 | a0001c0002t0033g0285a0001c0002t0098g0284a0001c0002t0099g0286 | 3 | HG02976.hp1 HG03195.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.448-656C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 5/17 | chr11 | 89441371 | ||||||
| chr11:89441738
|
A | G | 2 | a0001c0001t0007g0126a0001c0002t0074g0146 | 2 | HG00621.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.448-1023T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 5/17 | chr11 | 89441738 | ||||||
| chr11:89441939
|
T | A | 8 | a0001c0001t0001g0063a0001c0001t0019g0166a0001c0001t0022g0140others(5): Show | 8 | HG01081.hp1 HG01884.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.448-1224A>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 5/17 | chr11 | 89441939 | ||||||
| chr11:89441947
|
C | CTA | 8 | a0001c0001t0001g0050a0001c0001t0002g0221a0001c0001t0062g0114others(5): Show | 8 | HG00558.hp2 HG00621.hp1 HG01243.hp2 others(5): Show |
intron_variant | MODIFIER | c.448-1234_448-1233d others(4): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 5/17 | chr11 | 89441947 | ||||||
| chr11:89441947
|
C | CTATA | 6 | a0001c0001t0001g0063a0001c0001t0019g0166a0001c0001t0022g0140others(3): Show | 6 | HG01081.hp1 HG01884.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.448-1236_448-1233d others(6): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 5/17 | chr11 | 89441947 | ||||||
| chr11:89441947
|
C | CTATATA | 3 | a0001c0001t0088g0158a0001c0001t0117g0287a0001c0002t0011g0157 | 3 | HG02451.hp2 HG02630.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.448-1238_448-1233d others(8): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 5/17 | chr11 | 89441947 | ||||||
| chr11:89441947
|
CTA | C | 120 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0008others(117): Show | 120 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(117): Show |
intron_variant | MODIFIER | c.448-1234_448-1233d others(4): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 5/17 | chr11 | 89441947 | ||||||
| chr11:89441947
|
CTATA | C | 22 | a0001c0001t0002g0252a0001c0001t0002g0256a0001c0001t0005g0178others(19): Show | 22 | HG01109.hp1 HG01884.hp1 HG02280.hp1 others(19): Show |
intron_variant | MODIFIER | c.448-1236_448-1233d others(6): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 5/17 | chr11 | 89441947 | ||||||
| chr11:89442057
|
A | G | 51 | a0001c0001t0002g0260a0001c0001t0003g0170a0001c0001t0003g0191others(48): Show | 51 | HG00408.hp2 HG00621.hp1 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.448-1342T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 5/17 | chr11 | 89442057 | ||||||
| chr11:89442066
|
T | C | 1 | a0001c0001t0012g0222 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.448-1351A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 5/17 | chr11 | 89442066 | ||||||
| chr11:89442167
|
G | A | 1 | a0001c0002t0098g0284 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.448-1452C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 5/17 | chr11 | 89442167 | ||||||
| chr11:89442219
|
G | A | 215 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0008others(212): Show | 215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
intron_variant | MODIFIER | c.448-1504C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 5/17 | chr11 | 89442219 | ||||||
| chr11:89442272
|
G | T | 1 | a0001c0003t0005g0206 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.448-1557C>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 5/17 | chr11 | 89442272 | ||||||
| chr11:89442724
|
G | A | 1 | a0001c0001t0110g0274 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.447+1411C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 5/17 | chr11 | 89442724 | ||||||
| chr11:89442772
|
T | G | 14 | a0001c0001t0002g0246a0001c0001t0002g0264a0001c0001t0022g0099others(11): Show | 14 | HG00408.hp1 HG02698.hp1 NA18939.hp2 others(11): Show |
intron_variant | MODIFIER | c.447+1363A>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 5/17 | chr11 | 89442772 | ||||||
| chr11:89442998
|
G | C | 2 | a0001c0001t0088g0158a0001c0002t0011g0157 | 2 | HG02451.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.447+1137C>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 5/17 | chr11 | 89442998 | ||||||
| chr11:89443082
|
A | G | 1 | a0001c0001t0002g0259 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.447+1053T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 5/17 | chr11 | 89443082 | ||||||
| chr11:89443290
|
G | A | 1 | a0001c0001t0023g0161 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.447+845C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 5/17 | chr11 | 89443290 | ||||||
| chr11:89443347
|
G | A | 1 | a0001c0001t0022g0099 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.447+788C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 5/17 | chr11 | 89443347 | ||||||
| chr11:89443350
|
G | A | 29 | a0001c0001t0001g0063a0001c0001t0002g0252a0001c0001t0017g0160others(26): Show | 29 | HG01081.hp1 HG01884.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.447+785C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 5/17 | chr11 | 89443350 | ||||||
| chr11:89443400
|
A | G | 15 | a0001c0001t0002g0252a0001c0001t0017g0160a0001c0001t0024g0155others(12): Show | 15 | HG01884.hp1 HG02615.hp1 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.447+735T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 5/17 | chr11 | 89443400 | ||||||
| chr11:89443551
|
G | C | 221 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0008others(218): Show | 221 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(218): Show |
intron_variant | MODIFIER | c.447+584C>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 5/17 | chr11 | 89443551 | ||||||
| chr11:89443866
|
G | A | 1 | a0001c0001t0117g0287 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.447+269C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 5/17 | chr11 | 89443866 | ||||||
| chr11:89443904
|
T | A | 4 | a0001c0001t0002g0252a0001c0001t0024g0155a0001c0002t0011g0156others(1): Show | 4 | HG02622.hp1 HG02647.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.447+231A>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 5/17 | chr11 | 89443904 | ||||||
| chr11:89443968
|
A | G | 14 | a0001c0001t0002g0252a0001c0001t0017g0160a0001c0001t0024g0155others(11): Show | 14 | HG01884.hp1 HG02615.hp1 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.447+167T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 5/17 | chr11 | 89443968 | ||||||
| chr11:89444262
|
G | A | 2 | a0001c0001t0017g0171a0001c0001t0017g0172 | 2 | HG01074.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.350-30C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 4/17 | chr11 | 89444262 | ||||||
| chr11:89444466
|
A | AACACACA others(3): Show |
5 | a0001c0001t0002g0252a0001c0001t0024g0155a0001c0001t0079g0169others(2): Show | 5 | HG02622.hp1 HG02647.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.350-244_350-235dup others(10): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 4/17 | chr11 | 89444466 | ||||||
| chr11:89444466
|
A | AACACACA others(5): Show |
5 | a0001c0001t0017g0160a0001c0001t0031g0176a0001c0001t0031g0177others(2): Show | 5 | HG01884.hp1 HG02717.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.350-246_350-235dup others(12): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 4/17 | chr11 | 89444466 | ||||||
| chr11:89444466
|
A | AACACACA others(7): Show |
2 | a0002c0004t0032g0144a0002c0004t0032g0162 | 2 | HG02615.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.350-248_350-235dup others(14): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 4/17 | chr11 | 89444466 | ||||||
| chr11:89444466
|
AAC | A | 184 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0013others(181): Show | 184 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(181): Show |
intron_variant | MODIFIER | c.350-236_350-235del others(2): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 4/17 | chr11 | 89444466 | ||||||
| chr11:89444466
|
AACAC | A | 11 | a0001c0001t0001g0103a0001c0001t0010g0065a0001c0001t0010g0087others(8): Show | 11 | HG00323.hp2 HG00735.hp1 HG01106.hp1 others(8): Show |
intron_variant | MODIFIER | c.350-238_350-235del others(4): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 4/17 | chr11 | 89444466 | ||||||
| chr11:89444492
|
C | T | 1 | a0001c0002t0043g0024 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.350-260G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 4/17 | chr11 | 89444492 | ||||||
| chr11:89444494
|
T | C | 2 | a0001c0001t0081g0163a0001c0001t0086g0152 | 2 | HG01243.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.350-262A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 4/17 | chr11 | 89444494 | ||||||
| chr11:89444524
|
TAC | T | 188 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0008others(185): Show | 188 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(185): Show |
intron_variant | MODIFIER | c.350-294_350-293del others(2): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 4/17 | chr11 | 89444524 | ||||||
| chr11:89444524
|
TACAC | T | 19 | a0001c0001t0001g0134a0001c0001t0002g0231a0001c0001t0002g0252others(16): Show | 19 | HG01074.hp2 HG01884.hp1 HG01981.hp1 others(16): Show |
intron_variant | MODIFIER | c.350-296_350-293del others(4): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 4/17 | chr11 | 89444524 | ||||||
| chr11:89444524
|
TACACACA others(1): Show |
T | 3 | a0001c0002t0033g0285a0001c0002t0098g0284a0001c0002t0099g0286 | 3 | HG02976.hp1 HG03195.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.350-300_350-293del others(8): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 4/17 | chr11 | 89444524 | ||||||
| chr11:89444547
|
A | G | 4 | a0001c0001t0002g0252a0001c0001t0024g0155a0001c0002t0011g0156others(1): Show | 4 | HG02622.hp1 HG02647.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.350-315T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 4/17 | chr11 | 89444547 | ||||||
| chr11:89444713
|
C | T | 1 | a0001c0001t0002g0261 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.350-481G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 4/17 | chr11 | 89444713 | ||||||
| chr11:89445261
|
T | G | 4 | a0001c0001t0002g0252a0001c0001t0024g0155a0001c0002t0011g0156others(1): Show | 4 | HG02622.hp1 HG02647.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.350-1029A>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 4/17 | chr11 | 89445261 | ||||||
| chr11:89445320
|
G | A | 1 | a0001c0001t0002g0252 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.350-1088C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 4/17 | chr11 | 89445320 | ||||||
| chr11:89445354
|
C | A | 21 | a0001c0001t0001g0063a0001c0001t0002g0252a0001c0001t0017g0160others(18): Show | 21 | HG01884.hp1 HG01884.hp2 HG02280.hp1 others(18): Show |
intron_variant | MODIFIER | c.350-1122G>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 4/17 | chr11 | 89445354 | ||||||
| chr11:89445356
|
C | A | 78 | a0001c0001t0001g0063a0001c0001t0002g0252a0001c0001t0002g0260others(75): Show | 78 | HG00408.hp2 HG00621.hp1 HG00639.hp2 others(75): Show |
intron_variant | MODIFIER | c.350-1124G>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 4/17 | chr11 | 89445356 | ||||||
| chr11:89445366
|
GA | G | 14 | a0001c0001t0001g0063a0001c0001t0018g0142a0001c0001t0018g0175others(11): Show | 14 | HG01081.hp1 HG01884.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.350-1135delT | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 4/17 | chr11 | 89445366 | ||||||
| chr11:89445496
|
G | A | 14 | a0001c0001t0001g0063a0001c0001t0018g0142a0001c0001t0018g0175others(11): Show | 14 | HG01081.hp1 HG01884.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.350-1264C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 4/17 | chr11 | 89445496 | ||||||
| chr11:89445559
|
C | T | 1 | a0001c0001t0002g0245 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.350-1327G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 4/17 | chr11 | 89445559 | ||||||
| chr11:89445572
|
A | T | 17 | a0001c0001t0002g0252a0001c0001t0017g0160a0001c0001t0017g0171others(14): Show | 17 | HG01074.hp2 HG01884.hp1 HG02615.hp1 others(14): Show |
intron_variant | MODIFIER | c.350-1340T>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 4/17 | chr11 | 89445572 | ||||||
| chr11:89445727
|
A | C | 3 | a0001c0001t0017g0171a0001c0001t0017g0172a0001c0002t0074g0146 | 3 | HG01074.hp2 HG02723.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.350-1495T>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 4/17 | chr11 | 89445727 | ||||||
| chr11:89445909
|
T | G | 227 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0008others(224): Show | 227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.350-1677A>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 4/17 | chr11 | 89445909 | ||||||
| chr11:89445967
|
C | T | 4 | a0001c0001t0002g0252a0001c0001t0024g0155a0001c0002t0011g0156others(1): Show | 4 | HG02622.hp1 HG02647.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.350-1735G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 4/17 | chr11 | 89445967 | ||||||
| chr11:89445979
|
A | G | 17 | a0001c0001t0002g0252a0001c0001t0017g0160a0001c0001t0017g0171others(14): Show | 17 | HG01074.hp2 HG01884.hp1 HG02615.hp1 others(14): Show |
intron_variant | MODIFIER | c.350-1747T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 4/17 | chr11 | 89445979 | ||||||
| chr11:89446066
|
A | C | 1 | a0001c0002t0006g0091 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.350-1834T>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 4/17 | chr11 | 89446066 | ||||||
| chr11:89446094
|
G | A | 3 | a0001c0001t0081g0163a0001c0001t0086g0152a0001c0001t0113g0227 | 3 | HG01243.hp1 HG01243.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.350-1862C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 4/17 | chr11 | 89446094 | ||||||
| chr11:89446120
|
C | G | 14 | a0001c0001t0001g0063a0001c0001t0018g0142a0001c0001t0018g0175others(11): Show | 14 | HG01081.hp1 HG01884.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.350-1888G>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 4/17 | chr11 | 89446120 | ||||||
| chr11:89446158
|
A | T | 1 | a0001c0002t0009g0278 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.350-1926T>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 4/17 | chr11 | 89446158 | ||||||
| chr11:89446167
|
T | C | 5 | a0001c0001t0048g0044a0001c0001t0049g0043a0001c0001t0079g0169others(2): Show | 5 | HG02615.hp1 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.350-1935A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 4/17 | chr11 | 89446167 | ||||||
| chr11:89446178
|
T | C | 3 | a0001c0002t0009g0236a0001c0002t0034g0237a0001c0002t0035g0229 | 3 | NA18957.hp1 NA18965.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.350-1946A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 4/17 | chr11 | 89446178 | ||||||
| chr11:89446445
|
G | A | 1 | a0001c0002t0075g0183 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.350-2213C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 4/17 | chr11 | 89446445 | ||||||
| chr11:89446484
|
T | C | 1 | a0001c0012t0023g0181 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.350-2252A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 4/17 | chr11 | 89446484 | ||||||
| chr11:89446488
|
T | TA | 51 | a0001c0001t0002g0260a0001c0001t0003g0170a0001c0001t0003g0191others(48): Show | 51 | HG00408.hp2 HG00621.hp1 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.350-2257dupT | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 4/17 | chr11 | 89446488 | ||||||
| chr11:89446708
|
C | T | 2 | a0001c0001t0081g0163a0001c0001t0086g0152 | 2 | HG01243.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.350-2476G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 4/17 | chr11 | 89446708 | ||||||
| chr11:89446778
|
G | T | 115 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0008others(112): Show | 115 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(112): Show |
intron_variant | MODIFIER | c.350-2546C>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 4/17 | chr11 | 89446778 | ||||||
| chr11:89447077
|
A | G | 1 | a0001c0001t0003g0188 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.349+2363T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 4/17 | chr11 | 89447077 | ||||||
| chr11:89447101
|
G | A | 31 | a0001c0001t0001g0063a0001c0001t0002g0252a0001c0001t0017g0160others(28): Show | 31 | HG01074.hp2 HG01081.hp1 HG01884.hp1 others(28): Show |
intron_variant | MODIFIER | c.349+2339C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 4/17 | chr11 | 89447101 | ||||||
| chr11:89447173
|
A | C | 8 | a0001c0001t0002g0252a0001c0001t0007g0126a0001c0001t0017g0171others(5): Show | 8 | HG00621.hp2 HG01074.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.349+2267T>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 4/17 | chr11 | 89447173 | ||||||
| chr11:89447262
|
A | C | 10 | a0001c0001t0017g0160a0001c0001t0031g0176a0001c0001t0031g0177others(7): Show | 10 | HG01884.hp1 HG02615.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.349+2178T>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 4/17 | chr11 | 89447262 | ||||||
| chr11:89447494
|
T | C | 2 | a0001c0003t0013g0135a0004c0007t0013g0089 | 2 | NA19070.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.349+1946A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 4/17 | chr11 | 89447494 | ||||||
| chr11:89447527
|
A | G | 1 | a0001c0002t0006g0025 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.349+1913T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 4/17 | chr11 | 89447527 | ||||||
| chr11:89447715
|
A | G | 4 | a0001c0001t0007g0126a0001c0001t0017g0171a0001c0001t0017g0172others(1): Show | 4 | HG00621.hp2 HG01074.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.349+1725T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 4/17 | chr11 | 89447715 | ||||||
| chr11:89447716
|
C | A | 51 | a0001c0001t0002g0260a0001c0001t0003g0170a0001c0001t0003g0191others(48): Show | 51 | HG00408.hp2 HG00621.hp1 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.349+1724G>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 4/17 | chr11 | 89447716 | ||||||
| chr11:89447773
|
T | G | 4 | a0001c0001t0002g0279a0001c0001t0002g0283a0001c0001t0037g0280others(1): Show | 4 | HG02258.hp1 HG02717.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.349+1667A>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 4/17 | chr11 | 89447773 | ||||||
| chr11:89447940
|
A | G | 225 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0008others(222): Show | 225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.349+1500T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 4/17 | chr11 | 89447940 | ||||||
| chr11:89448061
|
G | T | 7 | a0001c0001t0002g0252a0001c0001t0017g0171a0001c0001t0017g0172others(4): Show | 7 | HG01074.hp2 HG02622.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.349+1379C>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 4/17 | chr11 | 89448061 | ||||||
| chr11:89448136
|
A | G | 10 | a0001c0001t0017g0160a0001c0001t0031g0176a0001c0001t0031g0177others(7): Show | 10 | HG01884.hp1 HG02615.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.349+1304T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 4/17 | chr11 | 89448136 | ||||||
| chr11:89448169
|
G | A | 1 | a0001c0001t0001g0031 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.349+1271C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 4/17 | chr11 | 89448169 | ||||||
| chr11:89448247
|
G | A | 1 | a0001c0001t0015g0078 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.349+1193C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 4/17 | chr11 | 89448247 | ||||||
| chr11:89448318
|
G | A | 1 | a0001c0001t0001g0128 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.349+1122C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 4/17 | chr11 | 89448318 | ||||||
| chr11:89448465
|
C | T | 1 | a0001c0002t0102g0226 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.349+975G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 4/17 | chr11 | 89448465 | ||||||
| chr11:89448514
|
A | G | 3 | a0001c0001t0001g0008a0001c0002t0025g0016a0001c0002t0044g0017 | 3 | NA19001.hp1 NA19064.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.349+926T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 4/17 | chr11 | 89448514 | ||||||
| chr11:89448685
|
C | T | 2 | a0002c0004t0032g0144a0002c0004t0032g0162 | 2 | HG02615.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.349+755G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 4/17 | chr11 | 89448685 | ||||||
| chr11:89448800
|
T | C | 1 | a0001c0001t0001g0131 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.349+640A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 4/17 | chr11 | 89448800 | ||||||
| chr11:89448843
|
G | A | 1 | a0001c0001t0001g0088 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.349+597C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 4/17 | chr11 | 89448843 | ||||||
| chr11:89448877
|
T | C | 2 | a0001c0001t0047g0139a0001c0001t0057g0127 | 2 | HG01516.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.349+563A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 4/17 | chr11 | 89448877 | ||||||
| chr11:89449107
|
C | T | 10 | a0001c0001t0017g0160a0001c0001t0031g0176a0001c0001t0031g0177others(7): Show | 10 | HG01884.hp1 HG02615.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.349+333G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 4/17 | chr11 | 89449107 | ||||||
| chr11:89449125
|
C | A | 1 | a0001c0001t0014g0109 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.349+315G>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 4/17 | chr11 | 89449125 | ||||||
| chr11:89449151
|
C | T | 10 | a0001c0001t0017g0160a0001c0001t0031g0176a0001c0001t0031g0177others(7): Show | 10 | HG01884.hp1 HG02615.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.349+289G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 4/17 | chr11 | 89449151 | ||||||
| chr11:89449216
|
C | T | 3 | a0001c0002t0033g0285a0001c0002t0098g0284a0001c0002t0099g0286 | 3 | HG02976.hp1 HG03195.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.349+224G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 4/17 | chr11 | 89449216 | ||||||
| chr11:89449217
|
G | A | 10 | a0001c0001t0017g0160a0001c0001t0031g0176a0001c0001t0031g0177others(7): Show | 10 | HG01884.hp1 HG02615.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.349+223C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 4/17 | chr11 | 89449217 | ||||||
| chr11:89449357
|
C | T | 1 | a0001c0001t0117g0287 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.349+83G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 4/17 | chr11 | 89449357 | ||||||
| chr11:89449811
|
T | C | 10 | a0001c0001t0017g0160a0001c0001t0031g0176a0001c0001t0031g0177others(7): Show | 10 | HG01884.hp1 HG02615.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.265-287A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 3/17 | chr11 | 89449811 | ||||||
| chr11:89449826
|
T | C | 1 | a0001c0001t0050g0080 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.265-302A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 3/17 | chr11 | 89449826 | ||||||
| chr11:89449900
|
T | C | 8 | a0001c0001t0001g0063a0001c0001t0019g0166a0001c0001t0022g0140others(5): Show | 8 | HG01081.hp1 HG01884.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.265-376A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 3/17 | chr11 | 89449900 | ||||||
| chr11:89450287
|
A | G | 11 | a0001c0001t0001g0063a0001c0001t0018g0142a0001c0001t0018g0175others(8): Show | 11 | HG01081.hp1 HG01884.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.265-763T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 3/17 | chr11 | 89450287 | ||||||
| chr11:89450368
|
C | T | 1 | a0001c0001t0039g0092 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.265-844G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 3/17 | chr11 | 89450368 | ||||||
| chr11:89450395
|
G | A | 10 | a0001c0001t0017g0160a0001c0001t0031g0176a0001c0001t0031g0177others(7): Show | 10 | HG01884.hp1 HG02615.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.265-871C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 3/17 | chr11 | 89450395 | ||||||
| chr11:89450480
|
A | C | 8 | a0001c0001t0001g0063a0001c0001t0019g0166a0001c0001t0022g0140others(5): Show | 8 | HG01081.hp1 HG01884.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.265-956T>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 3/17 | chr11 | 89450480 | ||||||
| chr11:89450563
|
A | T | 11 | a0001c0001t0001g0063a0001c0001t0018g0142a0001c0001t0018g0175others(8): Show | 11 | HG01081.hp1 HG01884.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.265-1039T>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 3/17 | chr11 | 89450563 | ||||||
| chr11:89450676
|
C | T | 1 | a0001c0001t0110g0274 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.264+1109G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 3/17 | chr11 | 89450676 | ||||||
| chr11:89450768
|
G | A | 6 | a0001c0001t0002g0279a0001c0001t0002g0283a0001c0001t0017g0165others(3): Show | 6 | HG02258.hp1 HG02717.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.264+1017C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 3/17 | chr11 | 89450768 | ||||||
| chr11:89450875
|
T | C | 3 | a0001c0002t0033g0285a0001c0002t0098g0284a0001c0002t0099g0286 | 3 | HG02976.hp1 HG03195.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.264+910A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 3/17 | chr11 | 89450875 | ||||||
| chr11:89450962
|
G | A | 1 | a0001c0001t0007g0126 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.264+823C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 3/17 | chr11 | 89450962 | ||||||
| chr11:89451074
|
G | A | 10 | a0001c0001t0017g0160a0001c0001t0031g0176a0001c0001t0031g0177others(7): Show | 10 | HG01884.hp1 HG02615.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.264+711C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 3/17 | chr11 | 89451074 | ||||||
| chr11:89451140
|
C | T | 10 | a0001c0001t0017g0160a0001c0001t0031g0176a0001c0001t0031g0177others(7): Show | 10 | HG01884.hp1 HG02615.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.264+645G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 3/17 | chr11 | 89451140 | ||||||
| chr11:89451171
|
G | A | 78 | a0001c0001t0001g0063a0001c0001t0002g0252a0001c0001t0002g0260others(75): Show | 78 | HG00408.hp2 HG00621.hp1 HG00639.hp2 others(75): Show |
intron_variant | MODIFIER | c.264+614C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 3/17 | chr11 | 89451171 | ||||||
| chr11:89451204
|
A | C | 14 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0002g0256others(11): Show | 14 | HG01081.hp2 HG01952.hp1 HG02132.hp1 others(11): Show |
intron_variant | MODIFIER | c.264+581T>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 3/17 | chr11 | 89451204 | ||||||
| chr11:89451360
|
A | C | 10 | a0001c0001t0017g0160a0001c0001t0031g0176a0001c0001t0031g0177others(7): Show | 10 | HG01884.hp1 HG02615.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.264+425T>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 3/17 | chr11 | 89451360 | ||||||
| chr11:89451578
|
G | A | 2 | a0001c0001t0004g0003a0001c0001t0008g0002 | 2 | HG00558.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.264+207C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 3/17 | chr11 | 89451578 | ||||||
| chr11:89451690
|
T | C | 21 | a0001c0001t0001g0063a0001c0001t0017g0160a0001c0001t0018g0142others(18): Show | 21 | HG01081.hp1 HG01884.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.264+95A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 3/17 | chr11 | 89451690 | ||||||
| chr11:89451728
|
C | T | 11 | a0001c0001t0001g0063a0001c0001t0018g0142a0001c0001t0018g0175others(8): Show | 11 | HG01081.hp1 HG01884.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.264+57G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 3/17 | chr11 | 89451728 | ||||||
| chr11:89452060
|
C | T | 1 | a0001c0002t0011g0173 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.154-165G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89452060 | ||||||
| chr11:89452075
|
C | A | 1 | a0001c0001t0019g0166 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.154-180G>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89452075 | ||||||
| chr11:89452314
|
C | T | 11 | a0001c0001t0001g0063a0001c0001t0018g0142a0001c0001t0018g0175others(8): Show | 11 | HG01081.hp1 HG01884.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.154-419G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89452314 | ||||||
| chr11:89452322
|
G | A | 2 | a0001c0001t0017g0171a0001c0001t0017g0172 | 2 | HG01074.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.154-427C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89452322 | ||||||
| chr11:89452395
|
ACT | A | 4 | a0001c0001t0002g0252a0001c0001t0024g0155a0001c0002t0011g0156others(1): Show | 4 | HG02622.hp1 HG02647.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.154-502_154-501del others(2): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89452395 | ||||||
| chr11:89452429
|
G | T | 1 | a0001c0003t0003g0189 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.154-534C>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89452429 | ||||||
| chr11:89452466
|
G | C | 11 | a0001c0001t0001g0063a0001c0001t0018g0142a0001c0001t0018g0175others(8): Show | 11 | HG01081.hp1 HG01884.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.154-571C>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89452466 | ||||||
| chr11:89452585
|
G | A | 2 | a0001c0001t0017g0160a0001c0002t0030g0159 | 2 | HG01884.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.154-690C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89452585 | ||||||
| chr11:89452817
|
C | G | 3 | a0001c0002t0033g0285a0001c0002t0098g0284a0001c0002t0099g0286 | 3 | HG02976.hp1 HG03195.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.154-922G>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89452817 | ||||||
| chr11:89452872
|
G | A | 8 | a0001c0001t0001g0063a0001c0001t0019g0166a0001c0001t0022g0140others(5): Show | 8 | HG01081.hp1 HG01884.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.154-977C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89452872 | ||||||
| chr11:89452996
|
T | C | 8 | a0001c0001t0001g0063a0001c0001t0019g0166a0001c0001t0022g0140others(5): Show | 8 | HG01081.hp1 HG01884.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.154-1101A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89452996 | ||||||
| chr11:89453000
|
T | C | 1 | a0001c0001t0018g0175 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.154-1105A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89453000 | ||||||
| chr11:89453030
|
C | T | 11 | a0001c0001t0002g0224a0001c0001t0002g0254a0001c0001t0002g0255others(8): Show | 11 | HG02451.hp1 HG02486.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.154-1135G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89453030 | ||||||
| chr11:89453034
|
ACT | A | 116 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0008others(113): Show | 116 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(113): Show |
intron_variant | MODIFIER | c.154-1141_154-1140d others(4): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89453034 | ||||||
| chr11:89453153
|
G | A | 11 | a0001c0001t0002g0224a0001c0001t0002g0254a0001c0001t0002g0255others(8): Show | 11 | HG02451.hp1 HG02486.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.154-1258C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89453153 | ||||||
| chr11:89453228
|
CCAG | C | 21 | a0001c0001t0001g0063a0001c0001t0017g0160a0001c0001t0018g0142others(18): Show | 21 | HG01081.hp1 HG01884.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.154-1336_154-1334d others(5): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89453228 | ||||||
| chr11:89453254
|
A | G | 1 | a0001c0001t0117g0287 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.154-1359T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89453254 | ||||||
| chr11:89453311
|
C | A | 2 | a0001c0001t0064g0104a0001c0001t0065g0105 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.154-1416G>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89453311 | ||||||
| chr11:89453548
|
G | A | 1 | a0001c0001t0110g0274 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.154-1653C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89453548 | ||||||
| chr11:89453557
|
G | A | 8 | a0001c0001t0001g0063a0001c0001t0019g0166a0001c0001t0022g0140others(5): Show | 8 | HG01081.hp1 HG01884.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.154-1662C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89453557 | ||||||
| chr11:89453759
|
C | A | 1 | a0001c0003t0003g0189 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.154-1864G>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89453759 | ||||||
| chr11:89453803
|
C | T | 10 | a0001c0001t0017g0160a0001c0001t0031g0176a0001c0001t0031g0177others(7): Show | 10 | HG01884.hp1 HG02615.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.154-1908G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89453803 | ||||||
| chr11:89453822
|
C | T | 1 | a0001c0001t0020g0056 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.154-1927G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89453822 | ||||||
| chr11:89453834
|
A | G | 21 | a0001c0001t0001g0063a0001c0001t0017g0160a0001c0001t0018g0142others(18): Show | 21 | HG01081.hp1 HG01884.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.154-1939T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89453834 | ||||||
| chr11:89453888
|
T | C | 3 | a0001c0001t0081g0163a0001c0001t0082g0174a0001c0001t0086g0152 | 3 | HG01099.hp1 HG01243.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.154-1993A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89453888 | ||||||
| chr11:89453888
|
T | G | 4 | a0001c0001t0007g0126a0001c0001t0017g0171a0001c0001t0017g0172others(1): Show | 4 | HG00621.hp2 HG01074.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.154-1993A>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89453888 | ||||||
| chr11:89453974
|
T | C | 3 | a0001c0001t0081g0163a0001c0001t0082g0174a0001c0001t0086g0152 | 3 | HG01099.hp1 HG01243.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.154-2079A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89453974 | ||||||
| chr11:89454291
|
CA | C | 11 | a0001c0001t0001g0063a0001c0001t0018g0142a0001c0001t0018g0175others(8): Show | 11 | HG01081.hp1 HG01884.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.154-2397delT | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89454291 | ||||||
| chr11:89454456
|
G | A | 24 | a0001c0001t0001g0063a0001c0001t0017g0160a0001c0001t0018g0142others(21): Show | 24 | HG01081.hp1 HG01884.hp1 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.154-2561C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89454456 | ||||||
| chr11:89454529
|
C | T | 3 | a0001c0002t0033g0285a0001c0002t0098g0284a0001c0002t0099g0286 | 3 | HG02976.hp1 HG03195.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.154-2634G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89454529 | ||||||
| chr11:89454575
|
A | C | 3 | a0001c0002t0033g0285a0001c0002t0098g0284a0001c0002t0099g0286 | 3 | HG02976.hp1 HG03195.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.154-2680T>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89454575 | ||||||
| chr11:89454687
|
G | C | 7 | a0001c0001t0002g0264a0001c0001t0038g0230a0001c0001t0061g0042others(4): Show | 7 | HG02698.hp1 NA18939.hp2 NA18961.hp1 others(4): Show |
intron_variant | MODIFIER | c.154-2792C>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89454687 | ||||||
| chr11:89454702
|
C | T | 21 | a0001c0001t0001g0063a0001c0001t0017g0160a0001c0001t0018g0142others(18): Show | 21 | HG01081.hp1 HG01884.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.154-2807G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89454702 | ||||||
| chr11:89454714
|
C | T | 3 | a0001c0001t0048g0044a0001c0001t0049g0043a0001c0001t0079g0169 | 3 | HG02895.hp2 HG02897.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.154-2819G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89454714 | ||||||
| chr11:89454786
|
G | A | 4 | a0001c0001t0081g0163a0001c0001t0082g0174a0001c0001t0086g0152others(1): Show | 4 | HG01099.hp1 HG01243.hp1 HG01243.hp2 others(1): Show |
intron_variant | MODIFIER | c.154-2891C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89454786 | ||||||
| chr11:89454855
|
A | G | 1 | a0001c0001t0080g0203 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.154-2960T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89454855 | ||||||
| chr11:89455004
|
C | T | 10 | a0001c0001t0017g0160a0001c0001t0031g0176a0001c0001t0031g0177others(7): Show | 10 | HG01884.hp1 HG02615.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.154-3109G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89455004 | ||||||
| chr11:89455107
|
A | C | 51 | a0001c0001t0002g0260a0001c0001t0003g0170a0001c0001t0003g0191others(48): Show | 51 | HG00408.hp2 HG00621.hp1 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.154-3212T>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89455107 | ||||||
| chr11:89455238
|
C | CTT | 21 | a0001c0001t0001g0063a0001c0001t0017g0160a0001c0001t0018g0142others(18): Show | 21 | HG01081.hp1 HG01884.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.154-3344_154-3343i others(4): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89455238 | ||||||
| chr11:89455312
|
G | T | 1 | a0001c0001t0024g0155 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.154-3417C>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89455312 | ||||||
| chr11:89455323
|
G | A | 21 | a0001c0001t0001g0063a0001c0001t0017g0160a0001c0001t0018g0142others(18): Show | 21 | HG01081.hp1 HG01884.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.154-3428C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89455323 | ||||||
| chr11:89455353
|
C | G | 21 | a0001c0001t0001g0063a0001c0001t0017g0160a0001c0001t0018g0142others(18): Show | 21 | HG01081.hp1 HG01884.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.154-3458G>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89455353 | ||||||
| chr11:89455572
|
T | G | 1 | a0001c0001t0113g0227 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.154-3677A>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89455572 | ||||||
| chr11:89455587
|
A | C | 2 | a0001c0001t0017g0160a0001c0002t0030g0159 | 2 | HG01884.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.154-3692T>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89455587 | ||||||
| chr11:89455719
|
C | CAT | 24 | a0001c0001t0001g0001a0001c0001t0001g0026a0001c0001t0001g0029others(21): Show | 25 | HG00621.hp2 HG00673.hp1 HG01071.hp1 others(22): Show |
intron_variant | MODIFIER | c.154-3826_154-3825d others(4): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89455719 | ||||||
| chr11:89455719
|
C | CATAT | 8 | a0001c0001t0010g0071a0001c0001t0054g0048a0001c0001t0069g0015others(5): Show | 8 | HG01099.hp1 HG01167.hp2 HG01243.hp2 others(5): Show |
intron_variant | MODIFIER | c.154-3828_154-3825d others(6): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89455719 | ||||||
| chr11:89455719
|
C | CATATATA others(3): Show |
1 | a0001c0002t0074g0146 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.154-3834_154-3825d others(12): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89455719 | ||||||
| chr11:89455719
|
C | CATATATA others(13): Show |
2 | a0001c0001t0017g0171a0001c0001t0017g0172 | 2 | HG01074.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.154-3844_154-3825d others(22): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89455719 | ||||||
| chr11:89455719
|
CAT | C | 23 | a0001c0001t0002g0224a0001c0001t0002g0254a0001c0001t0002g0255others(20): Show | 23 | HG00099.hp1 HG01243.hp1 HG02056.hp1 others(20): Show |
intron_variant | MODIFIER | c.154-3826_154-3825d others(4): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89455719 | ||||||
| chr11:89455719
|
CATAT | C | 162 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0008others(159): Show | 162 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(159): Show |
intron_variant | MODIFIER | c.154-3828_154-3825d others(6): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89455719 | ||||||
| chr11:89455719
|
CATATAT | C | 4 | a0001c0001t0024g0155a0001c0002t0011g0156a0001c0002t0029g0168others(1): Show | 4 | HG02647.hp2 HG03098.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.154-3830_154-3825d others(8): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89455719 | ||||||
| chr11:89455719
|
CATATATA others(1): Show |
C | 10 | a0001c0001t0017g0160a0001c0001t0031g0176a0001c0001t0031g0177others(7): Show | 10 | HG01884.hp1 HG02615.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.154-3832_154-3825d others(10): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89455719 | ||||||
| chr11:89455744
|
A | ATATATAT others(25): Show |
2 | a0001c0001t0022g0140a0001c0001t0068g0064 | 2 | HG01081.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.154-3850_154-3849i others(34): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89455744 | ||||||
| chr11:89455744
|
A | ATATATAT others(23): Show |
1 | a0001c0001t0001g0063 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.154-3850_154-3849i others(32): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89455744 | ||||||
| chr11:89455744
|
A | ATATATAT others(21): Show |
1 | a0001c0001t0117g0287 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.154-3850_154-3849i others(30): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89455744 | ||||||
| chr11:89455744
|
A | ATATATAT others(19): Show |
3 | a0001c0001t0078g0143a0001c0002t0011g0157a0001c0002t0100g0258 | 3 | HG02280.hp1 HG02630.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.154-3850_154-3849i others(28): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89455744 | ||||||
| chr11:89455744
|
A | ATATATAT others(15): Show |
3 | a0001c0001t0018g0175a0001c0001t0019g0166a0001c0001t0088g0158 | 3 | HG02451.hp2 HG02809.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.154-3850_154-3849i others(24): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89455744 | ||||||
| chr11:89455744
|
A | ATATATAT others(13): Show |
1 | a0001c0001t0018g0142 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.154-3850_154-3849i others(22): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89455744 | ||||||
| chr11:89455803
|
A | G | 10 | a0001c0001t0017g0160a0001c0001t0031g0176a0001c0001t0031g0177others(7): Show | 10 | HG01884.hp1 HG02615.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.154-3908T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89455803 | ||||||
| chr11:89455826
|
A | G | 8 | a0001c0001t0002g0252a0001c0001t0007g0126a0001c0001t0017g0171others(5): Show | 8 | HG00621.hp2 HG01074.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.154-3931T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89455826 | ||||||
| chr11:89455851
|
G | T | 1 | a0001c0001t0012g0257 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.154-3956C>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89455851 | ||||||
| chr11:89455953
|
T | C | 10 | a0001c0001t0017g0160a0001c0001t0031g0176a0001c0001t0031g0177others(7): Show | 10 | HG01884.hp1 HG02615.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.154-4058A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89455953 | ||||||
| chr11:89456091
|
T | C | 10 | a0001c0001t0017g0160a0001c0001t0031g0176a0001c0001t0031g0177others(7): Show | 10 | HG01884.hp1 HG02615.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.154-4196A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89456091 | ||||||
| chr11:89456260
|
C | A | 21 | a0001c0001t0001g0063a0001c0001t0017g0160a0001c0001t0018g0142others(18): Show | 21 | HG01081.hp1 HG01884.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.154-4365G>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89456260 | ||||||
| chr11:89456271
|
AAATG | A | 3 | a0001c0002t0033g0285a0001c0002t0098g0284a0001c0002t0099g0286 | 3 | HG02976.hp1 HG03195.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.154-4380_154-4377d others(6): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89456271 | ||||||
| chr11:89456520
|
G | T | 1 | a0001c0002t0098g0284 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.154-4625C>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89456520 | ||||||
| chr11:89456642
|
A | T | 10 | a0001c0001t0017g0160a0001c0001t0031g0176a0001c0001t0031g0177others(7): Show | 10 | HG01884.hp1 HG02615.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.154-4747T>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89456642 | ||||||
| chr11:89456665
|
C | T | 10 | a0001c0001t0017g0160a0001c0001t0031g0176a0001c0001t0031g0177others(7): Show | 10 | HG01884.hp1 HG02615.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.154-4770G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89456665 | ||||||
| chr11:89456706
|
C | T | 2 | a0001c0001t0027g0018a0001c0001t0027g0020 | 2 | NA18968.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.154-4811G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89456706 | ||||||
| chr11:89456805
|
G | A | 10 | a0001c0001t0017g0160a0001c0001t0031g0176a0001c0001t0031g0177others(7): Show | 10 | HG01884.hp1 HG02615.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.154-4910C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89456805 | ||||||
| chr11:89456813
|
G | A | 1 | a0001c0001t0062g0114 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.154-4918C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89456813 | ||||||
| chr11:89456859
|
G | A | 2 | a0001c0002t0011g0153a0001c0002t0029g0154 | 2 | HG01109.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.154-4964C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89456859 | ||||||
| chr11:89456866
|
C | G | 1 | a0001c0001t0113g0227 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.154-4971G>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89456866 | ||||||
| chr11:89457026
|
C | T | 2 | a0001c0001t0069g0015a0001c0001t0112g0282 | 2 | HG02896.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.154-5131G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89457026 | ||||||
| chr11:89457055
|
C | T | 3 | a0001c0001t0024g0155a0001c0002t0011g0156a0001c0002t0029g0168 | 3 | HG02647.hp2 HG03098.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.154-5160G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89457055 | ||||||
| chr11:89457124
|
C | A | 10 | a0001c0001t0017g0160a0001c0001t0031g0176a0001c0001t0031g0177others(7): Show | 10 | HG01884.hp1 HG02615.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.154-5229G>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89457124 | ||||||
| chr11:89457321
|
G | A | 51 | a0001c0001t0002g0260a0001c0001t0003g0170a0001c0001t0003g0191others(48): Show | 51 | HG00408.hp2 HG00621.hp1 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.154-5426C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89457321 | ||||||
| chr11:89457357
|
C | T | 3 | a0001c0001t0002g0268a0001c0001t0002g0269a0001c0001t0002g0270 | 3 | HG00735.hp2 HG00741.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.154-5462G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89457357 | ||||||
| chr11:89457395
|
C | G | 1 | a0001c0001t0111g0277 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.154-5500G>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89457395 | ||||||
| chr11:89457397
|
A | G | 10 | a0001c0001t0017g0160a0001c0001t0031g0176a0001c0001t0031g0177others(7): Show | 10 | HG01884.hp1 HG02615.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.154-5502T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89457397 | ||||||
| chr11:89457413
|
C | T | 1 | a0001c0002t0033g0262 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.154-5518G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89457413 | ||||||
| chr11:89457448
|
C | A | 4 | a0001c0001t0002g0252a0001c0001t0024g0155a0001c0002t0011g0156others(1): Show | 4 | HG02622.hp1 HG02647.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.154-5553G>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89457448 | ||||||
| chr11:89457542
|
T | C | 21 | a0001c0001t0001g0063a0001c0001t0017g0160a0001c0001t0018g0142others(18): Show | 21 | HG01081.hp1 HG01884.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.154-5647A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89457542 | ||||||
| chr11:89457561
|
C | G | 1 | a0001c0001t0004g0011 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.154-5666G>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89457561 | ||||||
| chr11:89457781
|
AAATCCAG others(3): Show |
A | 11 | a0001c0001t0001g0063a0001c0001t0018g0142a0001c0001t0018g0175others(8): Show | 11 | HG01081.hp1 HG01884.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.154-5896_154-5887d others(12): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89457781 | ||||||
| chr11:89457794
|
A | C | 11 | a0001c0001t0001g0063a0001c0001t0018g0142a0001c0001t0018g0175others(8): Show | 11 | HG01081.hp1 HG01884.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.154-5899T>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89457794 | ||||||
| chr11:89457855
|
A | G | 24 | a0001c0001t0001g0063a0001c0001t0017g0160a0001c0001t0018g0142others(21): Show | 24 | HG01081.hp1 HG01884.hp1 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.154-5960T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89457855 | ||||||
| chr11:89457861
|
C | G | 83 | a0001c0001t0001g0063a0001c0001t0002g0252a0001c0001t0002g0260others(80): Show | 83 | HG00408.hp2 HG00621.hp1 HG00621.hp2 others(80): Show |
intron_variant | MODIFIER | c.154-5966G>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89457861 | ||||||
| chr11:89457931
|
T | A | 11 | a0001c0001t0001g0063a0001c0001t0018g0142a0001c0001t0018g0175others(8): Show | 11 | HG01081.hp1 HG01884.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.154-6036A>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89457931 | ||||||
| chr11:89458033
|
T | G | 1 | a0001c0001t0024g0210 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.154-6138A>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89458033 | ||||||
| chr11:89458047
|
GA | G | 21 | a0001c0001t0001g0063a0001c0001t0017g0160a0001c0001t0018g0142others(18): Show | 21 | HG01081.hp1 HG01884.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.154-6153delT | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89458047 | ||||||
| chr11:89458153
|
G | A | 1 | a0001c0001t0007g0126 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.154-6258C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89458153 | ||||||
| chr11:89458206
|
T | C | 3 | a0001c0001t0017g0171a0001c0001t0017g0172a0001c0002t0074g0146 | 3 | HG01074.hp2 HG02723.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.154-6311A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89458206 | ||||||
| chr11:89458378
|
A | C | 4 | a0001c0001t0081g0163a0001c0001t0082g0174a0001c0001t0086g0152others(1): Show | 4 | HG01099.hp1 HG01243.hp1 HG01243.hp2 others(1): Show |
intron_variant | MODIFIER | c.154-6483T>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89458378 | ||||||
| chr11:89458397
|
C | T | 11 | a0001c0001t0001g0063a0001c0001t0018g0142a0001c0001t0018g0175others(8): Show | 11 | HG01081.hp1 HG01884.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.154-6502G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89458397 | ||||||
| chr11:89458546
|
C | A | 1 | a0001c0001t0010g0065 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.154-6651G>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89458546 | ||||||
| chr11:89458749
|
A | G | 1 | a0001c0001t0110g0274 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.154-6854T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89458749 | ||||||
| chr11:89458888
|
T | C | 3 | a0001c0001t0018g0142a0001c0001t0018g0175a0001c0001t0078g0143 | 3 | HG02280.hp1 NA19240.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.154-6993A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89458888 | ||||||
| chr11:89458907
|
C | T | 1 | a0001c0001t0001g0006 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.154-7012G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89458907 | ||||||
| chr11:89458911
|
A | C | 83 | a0001c0001t0001g0063a0001c0001t0002g0252a0001c0001t0002g0260others(80): Show | 83 | HG00408.hp2 HG00621.hp1 HG00621.hp2 others(80): Show |
intron_variant | MODIFIER | c.154-7016T>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89458911 | ||||||
| chr11:89458950
|
T | C | 3 | a0001c0002t0033g0285a0001c0002t0098g0284a0001c0002t0099g0286 | 3 | HG02976.hp1 HG03195.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.154-7055A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89458950 | ||||||
| chr11:89458952
|
G | T | 8 | a0001c0001t0001g0063a0001c0001t0019g0166a0001c0001t0022g0140others(5): Show | 8 | HG01081.hp1 HG01884.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.154-7057C>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89458952 | ||||||
| chr11:89459191
|
A | G | 10 | a0001c0001t0017g0160a0001c0001t0031g0176a0001c0001t0031g0177others(7): Show | 10 | HG01884.hp1 HG02615.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.154-7296T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89459191 | ||||||
| chr11:89459204
|
T | C | 1 | a0001c0001t0017g0165 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.154-7309A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89459204 | ||||||
| chr11:89459285
|
G | A | 1 | a0001c0002t0029g0168 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.154-7390C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89459285 | ||||||
| chr11:89459318
|
G | A | 2 | a0001c0001t0031g0176a0001c0001t0031g0177 | 2 | HG03209.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.154-7423C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89459318 | ||||||
| chr11:89459387
|
C | A | 1 | a0001c0001t0002g0252 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.154-7492G>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89459387 | ||||||
| chr11:89459454
|
T | TA | 11 | a0001c0001t0001g0063a0001c0001t0018g0142a0001c0001t0018g0175others(8): Show | 11 | HG01081.hp1 HG01884.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.154-7560dupT | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89459454 | ||||||
| chr11:89459455
|
A | T | 11 | a0001c0001t0001g0059a0001c0001t0017g0160a0001c0001t0031g0176others(8): Show | 11 | HG01884.hp1 HG02615.hp1 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.154-7560T>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89459455 | ||||||
| chr11:89459517
|
C | T | 6 | a0001c0001t0001g0001a0001c0001t0001g0129a0001c0001t0001g0130others(3): Show | 7 | HG01071.hp1 HG01255.hp2 HG01256.hp1 others(4): Show |
intron_variant | MODIFIER | c.154-7622G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89459517 | ||||||
| chr11:89459557
|
C | T | 4 | a0001c0001t0002g0252a0001c0001t0024g0155a0001c0002t0011g0156others(1): Show | 4 | HG02622.hp1 HG02647.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.154-7662G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89459557 | ||||||
| chr11:89459647
|
A | G | 1 | a0001c0001t0004g0011 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.154-7752T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89459647 | ||||||
| chr11:89459648
|
T | G | 10 | a0001c0001t0017g0160a0001c0001t0031g0176a0001c0001t0031g0177others(7): Show | 10 | HG01884.hp1 HG02615.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.154-7753A>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89459648 | ||||||
| chr11:89459694
|
T | G | 21 | a0001c0001t0001g0063a0001c0001t0017g0160a0001c0001t0018g0142others(18): Show | 21 | HG01081.hp1 HG01884.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.154-7799A>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89459694 | ||||||
| chr11:89459697
|
G | A | 21 | a0001c0001t0001g0063a0001c0001t0017g0160a0001c0001t0018g0142others(18): Show | 21 | HG01081.hp1 HG01884.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.154-7802C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89459697 | ||||||
| chr11:89459715
|
G | A | 11 | a0001c0001t0001g0063a0001c0001t0018g0142a0001c0001t0018g0175others(8): Show | 11 | HG01081.hp1 HG01884.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.154-7820C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89459715 | ||||||
| chr11:89459799
|
GA | G | 10 | a0001c0001t0017g0160a0001c0001t0031g0176a0001c0001t0031g0177others(7): Show | 10 | HG01884.hp1 HG02615.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.154-7905delT | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89459799 | ||||||
| chr11:89459812
|
T | G | 7 | a0001c0001t0001g0035a0001c0001t0001g0088a0001c0001t0001g0138others(4): Show | 7 | HG01928.hp1 HG01934.hp2 HG01981.hp1 others(4): Show |
intron_variant | MODIFIER | c.154-7917A>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89459812 | ||||||
| chr11:89459848
|
T | G | 21 | a0001c0001t0001g0063a0001c0001t0017g0160a0001c0001t0018g0142others(18): Show | 21 | HG01081.hp1 HG01884.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.154-7953A>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89459848 | ||||||
| chr11:89459895
|
A | G | 2 | a0001c0001t0088g0158a0001c0002t0011g0157 | 2 | HG02451.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.154-8000T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89459895 | ||||||
| chr11:89459929
|
A | C | 1 | a0001c0003t0023g0202 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.154-8034T>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89459929 | ||||||
| chr11:89459985
|
A | G | 11 | a0001c0001t0001g0063a0001c0001t0018g0142a0001c0001t0018g0175others(8): Show | 11 | HG01081.hp1 HG01884.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.154-8090T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89459985 | ||||||
| chr11:89460082
|
T | C | 1 | a0001c0001t0002g0238 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.154-8187A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89460082 | ||||||
| chr11:89460091
|
G | C | 2 | a0001c0001t0048g0044a0001c0001t0049g0043 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.154-8196C>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89460091 | ||||||
| chr11:89460149
|
C | T | 3 | a0001c0001t0081g0163a0001c0001t0086g0152a0001c0001t0113g0227 | 3 | HG01243.hp1 HG01243.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.154-8254G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89460149 | ||||||
| chr11:89460199
|
A | G | 1 | a0001c0002t0099g0286 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.154-8304T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89460199 | ||||||
| chr11:89460256
|
G | C | 1 | a0001c0001t0117g0287 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.154-8361C>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89460256 | ||||||
| chr11:89460280
|
G | A | 11 | a0001c0001t0001g0063a0001c0001t0018g0142a0001c0001t0018g0175others(8): Show | 11 | HG01081.hp1 HG01884.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.154-8385C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89460280 | ||||||
| chr11:89460299
|
C | A | 1 | a0001c0003t0007g0053 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.154-8404G>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89460299 | ||||||
| chr11:89460316
|
C | G | 11 | a0001c0001t0001g0063a0001c0001t0018g0142a0001c0001t0018g0175others(8): Show | 11 | HG01081.hp1 HG01884.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.154-8421G>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89460316 | ||||||
| chr11:89460381
|
G | A | 5 | a0001c0001t0071g0090a0001c0002t0009g0236a0001c0002t0034g0237others(2): Show | 5 | NA18957.hp1 NA18965.hp2 NA18986.hp1 others(2): Show |
intron_variant | MODIFIER | c.154-8486C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89460381 | ||||||
| chr11:89460381
|
G | T | 8 | a0001c0001t0001g0063a0001c0001t0019g0166a0001c0001t0022g0140others(5): Show | 8 | HG01081.hp1 HG01884.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.154-8486C>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89460381 | ||||||
| chr11:89460382
|
G | A | 3 | a0001c0002t0009g0236a0001c0002t0034g0237a0001c0002t0035g0229 | 3 | NA18957.hp1 NA18965.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.154-8487C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89460382 | ||||||
| chr11:89460403
|
T | G | 1 | a0001c0003t0003g0201 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.154-8508A>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89460403 | ||||||
| chr11:89460431
|
C | T | 3 | a0001c0002t0033g0285a0001c0002t0098g0284a0001c0002t0099g0286 | 3 | HG02976.hp1 HG03195.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.154-8536G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89460431 | ||||||
| chr11:89460442
|
G | A | 82 | a0001c0001t0001g0063a0001c0001t0002g0252a0001c0001t0002g0260others(79): Show | 82 | HG00408.hp2 HG00621.hp1 HG00639.hp2 others(79): Show |
intron_variant | MODIFIER | c.154-8547C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89460442 | ||||||
| chr11:89460493
|
C | T | 4 | a0001c0001t0002g0252a0001c0001t0024g0155a0001c0002t0011g0156others(1): Show | 4 | HG02622.hp1 HG02647.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.154-8598G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89460493 | ||||||
| chr11:89460573
|
G | A | 1 | a0001c0001t0003g0205 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.154-8678C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89460573 | ||||||
| chr11:89460608
|
A | T | 5 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0002g0259others(2): Show | 5 | HG01081.hp2 HG01952.hp1 HG02132.hp1 others(2): Show |
intron_variant | MODIFIER | c.154-8713T>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89460608 | ||||||
| chr11:89460611
|
C | T | 8 | a0001c0001t0001g0063a0001c0001t0019g0166a0001c0001t0022g0140others(5): Show | 8 | HG01081.hp1 HG01884.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.154-8716G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89460611 | ||||||
| chr11:89460622
|
C | T | 10 | a0001c0001t0017g0160a0001c0001t0031g0176a0001c0001t0031g0177others(7): Show | 10 | HG01884.hp1 HG02615.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.154-8727G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89460622 | ||||||
| chr11:89460734
|
G | A | 14 | a0001c0001t0001g0063a0001c0001t0018g0142a0001c0001t0018g0175others(11): Show | 14 | HG01081.hp1 HG01884.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.154-8839C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89460734 | ||||||
| chr11:89460852
|
T | G | 10 | a0001c0001t0017g0160a0001c0001t0031g0176a0001c0001t0031g0177others(7): Show | 10 | HG01884.hp1 HG02615.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.154-8957A>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89460852 | ||||||
| chr11:89460999
|
T | C | 1 | a0001c0002t0051g0009 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.154-9104A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89460999 | ||||||
| chr11:89461017
|
G | A | 220 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0008others(217): Show | 220 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(217): Show |
intron_variant | MODIFIER | c.154-9122C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89461017 | ||||||
| chr11:89461100
|
T | A | 1 | a0001c0001t0001g0098 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.154-9205A>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89461100 | ||||||
| chr11:89461199
|
C | T | 51 | a0001c0001t0002g0260a0001c0001t0003g0170a0001c0001t0003g0191others(48): Show | 51 | HG00408.hp2 HG00621.hp1 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.154-9304G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89461199 | ||||||
| chr11:89461248
|
T | G | 2 | a0002c0004t0032g0144a0002c0004t0032g0162 | 2 | HG02615.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.154-9353A>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89461248 | ||||||
| chr11:89461280
|
T | C | 10 | a0001c0001t0017g0160a0001c0001t0031g0176a0001c0001t0031g0177others(7): Show | 10 | HG01884.hp1 HG02615.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.154-9385A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89461280 | ||||||
| chr11:89461303
|
T | C | 11 | a0001c0001t0001g0063a0001c0001t0018g0142a0001c0001t0018g0175others(8): Show | 11 | HG01081.hp1 HG01884.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.154-9408A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89461303 | ||||||
| chr11:89461331
|
A | G | 3 | a0001c0001t0018g0142a0001c0001t0018g0175a0001c0001t0078g0143 | 3 | HG02280.hp1 NA19240.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.154-9436T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89461331 | ||||||
| chr11:89461383
|
G | A | 3 | a0001c0002t0033g0285a0001c0002t0098g0284a0001c0002t0099g0286 | 3 | HG02976.hp1 HG03195.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.154-9488C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89461383 | ||||||
| chr11:89461420
|
G | A | 51 | a0001c0001t0002g0260a0001c0001t0003g0170a0001c0001t0003g0191others(48): Show | 51 | HG00408.hp2 HG00621.hp1 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.154-9525C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89461420 | ||||||
| chr11:89461426
|
T | C | 21 | a0001c0001t0001g0063a0001c0001t0017g0160a0001c0001t0018g0142others(18): Show | 21 | HG01081.hp1 HG01884.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.154-9531A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89461426 | ||||||
| chr11:89461429
|
G | T | 3 | a0001c0002t0033g0285a0001c0002t0098g0284a0001c0002t0099g0286 | 3 | HG02976.hp1 HG03195.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.154-9534C>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89461429 | ||||||
| chr11:89461430
|
G | T | 3 | a0001c0002t0033g0285a0001c0002t0098g0284a0001c0002t0099g0286 | 3 | HG02976.hp1 HG03195.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.154-9535C>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89461430 | ||||||
| chr11:89461502
|
G | A | 1 | a0001c0001t0007g0126 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.154-9607C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89461502 | ||||||
| chr11:89461616
|
A | G | 24 | a0001c0001t0001g0063a0001c0001t0017g0160a0001c0001t0018g0142others(21): Show | 24 | HG01081.hp1 HG01884.hp1 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.154-9721T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89461616 | ||||||
| chr11:89461647
|
A | AAAATAAA others(1): Show |
9 | a0001c0001t0031g0176a0001c0001t0031g0177a0001c0001t0048g0044others(6): Show | 9 | HG01243.hp1 HG02615.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.154-9760_154-9753d others(10): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89461647 | ||||||
| chr11:89461647
|
A | AAAATAAA others(5): Show |
4 | a0001c0001t0017g0160a0001c0001t0081g0163a0001c0001t0086g0152others(1): Show | 4 | HG01243.hp2 HG01884.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.154-9764_154-9753d others(14): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89461647 | ||||||
| chr11:89461647
|
A | AAAATAAA others(9): Show |
38 | a0001c0001t0001g0063a0001c0001t0002g0245a0001c0001t0002g0256others(35): Show | 38 | HG00408.hp1 HG00741.hp1 HG01099.hp1 others(35): Show |
intron_variant | MODIFIER | c.154-9768_154-9753d others(18): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89461647 | ||||||
| chr11:89461647
|
A | AAAATAAA others(13): Show |
155 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0023others(152): Show | 155 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(152): Show |
intron_variant | MODIFIER | c.154-9772_154-9753d others(22): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89461647 | ||||||
| chr11:89461647
|
A | AAAATAAA others(17): Show |
13 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0014others(10): Show | 13 | HG01081.hp2 HG01952.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.154-9753_154-9752i others(26): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89461647 | ||||||
| chr11:89461661
|
A | AATAAATA others(13): Show |
1 | a0001c0003t0005g0190 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.154-9767_154-9766i others(22): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89461661 | ||||||
| chr11:89461670
|
G | A | 3 | a0001c0001t0048g0044a0001c0001t0049g0043a0001c0001t0079g0169 | 3 | HG02895.hp2 HG02897.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.154-9775C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89461670 | ||||||
| chr11:89461706
|
C | G | 24 | a0001c0001t0001g0063a0001c0001t0017g0160a0001c0001t0018g0142others(21): Show | 24 | HG01081.hp1 HG01884.hp1 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.154-9811G>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89461706 | ||||||
| chr11:89461735
|
A | G | 1 | a0001c0002t0046g0115 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.154-9840T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89461735 | ||||||
| chr11:89462000
|
G | A | 1 | a0001c0002t0009g0278 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.154-10105C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89462000 | ||||||
| chr11:89462003
|
G | GA | 11 | a0001c0001t0001g0063a0001c0001t0018g0142a0001c0001t0018g0175others(8): Show | 11 | HG01081.hp1 HG01884.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.154-10109dupT | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89462003 | ||||||
| chr11:89462026
|
G | T | 1 | a0001c0001t0002g0252 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.154-10131C>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89462026 | ||||||
| chr11:89462083
|
C | A | 7 | a0001c0001t0002g0252a0001c0001t0017g0171a0001c0001t0017g0172others(4): Show | 7 | HG01074.hp2 HG02622.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.154-10188G>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89462083 | ||||||
| chr11:89462134
|
TA | T | 3 | a0001c0002t0033g0285a0001c0002t0098g0284a0001c0002t0099g0286 | 3 | HG02976.hp1 HG03195.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.154-10240delT | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89462134 | ||||||
| chr11:89462189
|
C | T | 2 | a0001c0001t0081g0163a0001c0001t0086g0152 | 2 | HG01243.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.154-10294G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89462189 | ||||||
| chr11:89462379
|
G | A | 24 | a0001c0001t0001g0063a0001c0001t0017g0160a0001c0001t0018g0142others(21): Show | 24 | HG01081.hp1 HG01884.hp1 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.154-10484C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89462379 | ||||||
| chr11:89462567
|
A | T | 10 | a0001c0001t0017g0160a0001c0001t0031g0176a0001c0001t0031g0177others(7): Show | 10 | HG01884.hp1 HG02615.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.154-10672T>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89462567 | ||||||
| chr11:89462624
|
A | G | 24 | a0001c0001t0001g0063a0001c0001t0017g0160a0001c0001t0018g0142others(21): Show | 24 | HG01081.hp1 HG01884.hp1 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.154-10729T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89462624 | ||||||
| chr11:89462657
|
C | T | 3 | a0001c0002t0033g0285a0001c0002t0098g0284a0001c0002t0099g0286 | 3 | HG02976.hp1 HG03195.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.154-10762G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89462657 | ||||||
| chr11:89462677
|
C | G | 2 | a0001c0001t0005g0178a0001c0001t0091g0151 | 2 | HG02280.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.154-10782G>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89462677 | ||||||
| chr11:89462754
|
A | C | 1 | a0001c0001t0001g0031 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.154-10859T>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89462754 | ||||||
| chr11:89462780
|
G | A | 3 | a0001c0002t0033g0285a0001c0002t0098g0284a0001c0002t0099g0286 | 3 | HG02976.hp1 HG03195.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.154-10885C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89462780 | ||||||
| chr11:89462985
|
T | C | 7 | a0001c0001t0001g0103a0001c0001t0010g0065a0001c0001t0010g0087others(4): Show | 7 | HG00323.hp2 HG00735.hp1 HG01106.hp1 others(4): Show |
intron_variant | MODIFIER | c.154-11090A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89462985 | ||||||
| chr11:89463161
|
G | A | 21 | a0001c0001t0002g0224a0001c0001t0002g0252a0001c0001t0002g0254others(18): Show | 21 | HG02055.hp1 HG02258.hp1 HG02451.hp1 others(18): Show |
intron_variant | MODIFIER | c.154-11266C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89463161 | ||||||
| chr11:89463204
|
A | G | 3 | a0001c0001t0024g0155a0001c0002t0011g0156a0001c0002t0029g0168 | 3 | HG02647.hp2 HG03098.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.154-11309T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89463204 | ||||||
| chr11:89463267
|
T | C | 1 | a0001c0001t0007g0126 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.154-11372A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89463267 | ||||||
| chr11:89463426
|
A | G | 4 | a0001c0001t0002g0279a0001c0001t0002g0283a0001c0001t0037g0280others(1): Show | 4 | HG02258.hp1 HG02717.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.154-11531T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89463426 | ||||||
| chr11:89463526
|
C | T | 3 | a0001c0002t0033g0285a0001c0002t0098g0284a0001c0002t0099g0286 | 3 | HG02976.hp1 HG03195.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.154-11631G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89463526 | ||||||
| chr11:89463549
|
A | G | 2 | a0001c0001t0001g0061a0001c0001t0001g0062 | 2 | NA18950.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.154-11654T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89463549 | ||||||
| chr11:89463708
|
C | CCAGTTAG others(253): Show |
1 | a0001c0001t0022g0140 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.154-11814_154-1181 others(264): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89463708 | ||||||
| chr11:89463708
|
C | CCAGTTAG others(259): Show |
1 | a0001c0001t0018g0175 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.154-11814_154-1181 others(270): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89463708 | ||||||
| chr11:89463708
|
C | CCAGTTAG others(260): Show |
1 | a0001c0001t0018g0142 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.154-11814_154-1181 others(271): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89463708 | ||||||
| chr11:89463708
|
C | CCAGTTAG others(261): Show |
3 | a0001c0001t0078g0143a0001c0001t0088g0158a0001c0002t0011g0157 | 3 | HG02280.hp1 HG02451.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.154-11814_154-1181 others(272): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89463708 | ||||||
| chr11:89463708
|
C | CCAGTTAG others(267): Show |
1 | a0001c0001t0068g0064 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.154-11814_154-1181 others(278): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89463708 | ||||||
| chr11:89463708
|
C | CCAGTTAG others(269): Show |
2 | a0001c0001t0001g0063a0001c0002t0100g0258 | 2 | HG02965.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.154-11814_154-1181 others(280): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89463708 | ||||||
| chr11:89463708
|
C | CCAGTTAG others(274): Show |
1 | a0001c0001t0117g0287 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.154-11814_154-1181 others(285): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89463708 | ||||||
| chr11:89463708
|
C | CCAGTTAG others(276): Show |
1 | a0001c0001t0019g0166 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.154-11814_154-1181 others(287): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89463708 | ||||||
| chr11:89463944
|
G | A | 1 | a0001c0001t0002g0252 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.154-12049C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89463944 | ||||||
| chr11:89464047
|
T | C | 1 | a0001c0002t0099g0286 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.154-12152A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89464047 | ||||||
| chr11:89464233
|
G | A | 1 | a0001c0002t0102g0226 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.154-12338C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89464233 | ||||||
| chr11:89464306
|
C | T | 3 | a0001c0002t0033g0285a0001c0002t0098g0284a0001c0002t0099g0286 | 3 | HG02976.hp1 HG03195.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.154-12411G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89464306 | ||||||
| chr11:89464315
|
C | T | 117 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0008others(114): Show | 117 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(114): Show |
intron_variant | MODIFIER | c.154-12420G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89464315 | ||||||
| chr11:89464376
|
G | A | 3 | a0001c0001t0018g0142a0001c0001t0018g0175a0001c0001t0078g0143 | 3 | HG02280.hp1 NA19240.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.154-12481C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89464376 | ||||||
| chr11:89464394
|
G | T | 11 | a0001c0001t0001g0063a0001c0001t0018g0142a0001c0001t0018g0175others(8): Show | 11 | HG01081.hp1 HG01884.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.154-12499C>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89464394 | ||||||
| chr11:89464446
|
A | G | 1 | a0001c0001t0022g0140 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.154-12551T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89464446 | ||||||
| chr11:89464511
|
A | G | 2 | a0001c0002t0006g0021a0001c0002t0041g0022 | 2 | NA18747.hp2 NA18954.hp1 |
intron_variant | MODIFIER | c.154-12616T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89464511 | ||||||
| chr11:89464544
|
G | C | 117 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0008others(114): Show | 117 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(114): Show |
intron_variant | MODIFIER | c.154-12649C>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89464544 | ||||||
| chr11:89464545
|
C | T | 1 | a0001c0001t0001g0129 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.154-12650G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89464545 | ||||||
| chr11:89464591
|
T | C | 51 | a0001c0001t0002g0260a0001c0001t0003g0170a0001c0001t0003g0191others(48): Show | 51 | HG00408.hp2 HG00621.hp1 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.154-12696A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89464591 | ||||||
| chr11:89464606
|
G | A | 3 | a0001c0001t0088g0158a0001c0001t0117g0287a0001c0002t0011g0157 | 3 | HG02451.hp2 HG02630.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.154-12711C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89464606 | ||||||
| chr11:89464742
|
A | C | 10 | a0001c0001t0017g0160a0001c0001t0031g0176a0001c0001t0031g0177others(7): Show | 10 | HG01884.hp1 HG02615.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.154-12847T>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89464742 | ||||||
| chr11:89464806
|
A | T | 24 | a0001c0001t0001g0063a0001c0001t0017g0160a0001c0001t0018g0142others(21): Show | 24 | HG01081.hp1 HG01884.hp1 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.154-12911T>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89464806 | ||||||
| chr11:89464979
|
C | T | 13 | a0001c0001t0017g0160a0001c0001t0031g0176a0001c0001t0031g0177others(10): Show | 13 | HG01884.hp1 HG02615.hp1 HG02717.hp1 others(10): Show |
intron_variant | MODIFIER | c.154-13084G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89464979 | ||||||
| chr11:89465087
|
C | T | 14 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0002g0256others(11): Show | 14 | HG01081.hp2 HG01952.hp1 HG02132.hp1 others(11): Show |
intron_variant | MODIFIER | c.154-13192G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89465087 | ||||||
| chr11:89465096
|
C | G | 11 | a0001c0001t0001g0063a0001c0001t0018g0142a0001c0001t0018g0175others(8): Show | 11 | HG01081.hp1 HG01884.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.154-13201G>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89465096 | ||||||
| chr11:89465284
|
G | A | 1 | a0001c0001t0004g0003 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.154-13389C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89465284 | ||||||
| chr11:89465319
|
CT | C | 13 | a0001c0001t0017g0160a0001c0001t0031g0176a0001c0001t0031g0177others(10): Show | 13 | HG01884.hp1 HG02615.hp1 HG02717.hp1 others(10): Show |
intron_variant | MODIFIER | c.154-13425delA | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89465319 | ||||||
| chr11:89465331
|
T | C | 11 | a0001c0001t0001g0063a0001c0001t0018g0142a0001c0001t0018g0175others(8): Show | 11 | HG01081.hp1 HG01884.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.154-13436A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89465331 | ||||||
| chr11:89465349
|
G | A | 1 | a0001c0001t0005g0178 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.154-13454C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89465349 | ||||||
| chr11:89465372
|
C | T | 13 | a0001c0001t0017g0160a0001c0001t0031g0176a0001c0001t0031g0177others(10): Show | 13 | HG01884.hp1 HG02615.hp1 HG02717.hp1 others(10): Show |
intron_variant | MODIFIER | c.154-13477G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89465372 | ||||||
| chr11:89465388
|
T | C | 1 | a0001c0001t0028g0075 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.154-13493A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89465388 | ||||||
| chr11:89465479
|
C | T | 3 | a0001c0002t0033g0285a0001c0002t0098g0284a0001c0002t0099g0286 | 3 | HG02976.hp1 HG03195.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.154-13584G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89465479 | ||||||
| chr11:89465507
|
T | C | 19 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0014others(16): Show | 19 | HG00099.hp2 HG00558.hp1 HG01256.hp2 others(16): Show |
intron_variant | MODIFIER | c.154-13612A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89465507 | ||||||
| chr11:89465558
|
T | C | 2 | a0001c0001t0001g0029a0001c0001t0001g0030 | 2 | NA18961.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.154-13663A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89465558 | ||||||
| chr11:89465559
|
G | C | 13 | a0001c0001t0017g0160a0001c0001t0031g0176a0001c0001t0031g0177others(10): Show | 13 | HG01884.hp1 HG02615.hp1 HG02717.hp1 others(10): Show |
intron_variant | MODIFIER | c.154-13664C>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89465559 | ||||||
| chr11:89465597
|
A | G | 1 | a0001c0001t0018g0175 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.154-13702T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89465597 | ||||||
| chr11:89465605
|
A | G | 4 | a0001c0001t0007g0126a0001c0001t0017g0171a0001c0001t0017g0172others(1): Show | 4 | HG00621.hp2 HG01074.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.154-13710T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89465605 | ||||||
| chr11:89465622
|
C | G | 24 | a0001c0001t0001g0063a0001c0001t0017g0160a0001c0001t0018g0142others(21): Show | 24 | HG01081.hp1 HG01884.hp1 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.154-13727G>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89465622 | ||||||
| chr11:89465628
|
T | C | 225 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0008others(222): Show | 225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.154-13733A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89465628 | ||||||
| chr11:89465667
|
A | C | 223 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0008others(220): Show | 223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.154-13772T>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89465667 | ||||||
| chr11:89465681
|
G | A | 2 | a0001c0001t0017g0171a0001c0001t0017g0172 | 2 | HG01074.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.154-13786C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89465681 | ||||||
| chr11:89465732
|
A | G | 79 | a0001c0001t0001g0063a0001c0001t0002g0252a0001c0001t0002g0260others(76): Show | 79 | HG00408.hp2 HG00621.hp1 HG00639.hp2 others(76): Show |
intron_variant | MODIFIER | c.154-13837T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89465732 | ||||||
| chr11:89465809
|
T | C | 10 | a0001c0001t0017g0160a0001c0001t0031g0176a0001c0001t0031g0177others(7): Show | 10 | HG01884.hp1 HG02615.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.154-13914A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89465809 | ||||||
| chr11:89465816
|
A | T | 10 | a0001c0001t0017g0160a0001c0001t0031g0176a0001c0001t0031g0177others(7): Show | 10 | HG01884.hp1 HG02615.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.154-13921T>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89465816 | ||||||
| chr11:89465824
|
G | GTTGT | 10 | a0001c0001t0017g0160a0001c0001t0031g0176a0001c0001t0031g0177others(7): Show | 10 | HG01884.hp1 HG02615.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.154-13930_154-1392 others(8): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89465824 | ||||||
| chr11:89465824
|
G | T | 4 | a0001c0001t0024g0155a0001c0001t0084g0148a0001c0002t0011g0156others(1): Show | 4 | HG02647.hp2 HG03098.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.154-13929C>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89465824 | ||||||
| chr11:89465824
|
GT | G | 11 | a0001c0001t0001g0063a0001c0001t0018g0142a0001c0001t0018g0175others(8): Show | 11 | HG01081.hp1 HG01243.hp1 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.154-13930delA | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89465824 | ||||||
| chr11:89465827
|
T | G | 10 | a0001c0001t0017g0160a0001c0001t0031g0176a0001c0001t0031g0177others(7): Show | 10 | HG01884.hp1 HG02615.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.154-13932A>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89465827 | ||||||
| chr11:89465891
|
G | A | 1 | a0001c0002t0102g0226 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.154-13996C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89465891 | ||||||
| chr11:89465946
|
A | G | 1 | a0001c0001t0073g0167 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.154-14051T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89465946 | ||||||
| chr11:89466020
|
C | T | 51 | a0001c0001t0002g0260a0001c0001t0003g0170a0001c0001t0003g0191others(48): Show | 51 | HG00408.hp2 HG00621.hp1 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.154-14125G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89466020 | ||||||
| chr11:89466046
|
G | T | 8 | a0001c0001t0001g0063a0001c0001t0019g0166a0001c0001t0022g0140others(5): Show | 8 | HG01081.hp1 HG01884.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.154-14151C>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89466046 | ||||||
| chr11:89466575
|
G | A | 22 | a0001c0001t0001g0063a0001c0001t0017g0160a0001c0001t0018g0142others(19): Show | 22 | HG01081.hp1 HG01884.hp1 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.154-14680C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89466575 | ||||||
| chr11:89466724
|
G | A | 1 | a0001c0001t0111g0277 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.154-14829C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89466724 | ||||||
| chr11:89466795
|
C | A | 3 | a0001c0001t0017g0171a0001c0001t0017g0172a0001c0002t0074g0146 | 3 | HG01074.hp2 HG02723.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.154-14900G>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89466795 | ||||||
| chr11:89466944
|
A | G | 3 | a0001c0002t0033g0285a0001c0002t0098g0284a0001c0002t0099g0286 | 3 | HG02976.hp1 HG03195.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.154-15049T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89466944 | ||||||
| chr11:89467029
|
C | T | 22 | a0001c0001t0001g0063a0001c0001t0017g0160a0001c0001t0018g0142others(19): Show | 22 | HG01081.hp1 HG01884.hp1 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.154-15134G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89467029 | ||||||
| chr11:89467149
|
C | G | 1 | a0001c0002t0041g0022 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.154-15254G>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89467149 | ||||||
| chr11:89467165
|
A | G | 79 | a0001c0001t0001g0063a0001c0001t0002g0252a0001c0001t0002g0260others(76): Show | 79 | HG00408.hp2 HG00621.hp1 HG00639.hp2 others(76): Show |
intron_variant | MODIFIER | c.154-15270T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89467165 | ||||||
| chr11:89467220
|
G | A | 11 | a0001c0001t0017g0160a0001c0001t0048g0044a0001c0001t0049g0043others(8): Show | 11 | HG01884.hp1 HG02615.hp1 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.154-15325C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89467220 | ||||||
| chr11:89467223
|
C | T | 8 | a0001c0001t0017g0160a0001c0001t0048g0044a0001c0001t0049g0043others(5): Show | 8 | HG01884.hp1 HG02615.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.154-15328G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89467223 | ||||||
| chr11:89467340
|
A | G | 24 | a0001c0001t0001g0063a0001c0001t0017g0160a0001c0001t0018g0142others(21): Show | 24 | HG01081.hp1 HG01884.hp1 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.154-15445T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89467340 | ||||||
| chr11:89467349
|
C | CA | 31 | a0001c0001t0001g0031a0001c0001t0001g0033a0001c0001t0001g0132others(28): Show | 31 | HG00639.hp1 HG00642.hp1 HG00673.hp1 others(28): Show |
intron_variant | MODIFIER | c.154-15455dupT | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89467349 | ||||||
| chr11:89467349
|
C | CAA | 6 | a0001c0001t0001g0032a0001c0001t0002g0279a0001c0001t0007g0126others(3): Show | 6 | HG00621.hp2 HG02145.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.154-15456_154-1545 others(6): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89467349 | ||||||
| chr11:89467349
|
C | CAAA | 7 | a0001c0001t0001g0069a0001c0001t0068g0064a0001c0001t0088g0158others(4): Show | 7 | HG01884.hp2 HG01978.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.154-15457_154-1545 others(7): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89467349 | ||||||
| chr11:89467349
|
C | CAAAAAAA others(3): Show |
2 | a0001c0002t0033g0285a0001c0002t0099g0286 | 2 | HG02976.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.154-15464_154-1545 others(14): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89467349 | ||||||
| chr11:89467349
|
C | CAAAAAAA others(4): Show |
1 | a0001c0002t0098g0284 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.154-15465_154-1545 others(15): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89467349 | ||||||
| chr11:89467349
|
CA | C | 102 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0008others(99): Show | 102 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(99): Show |
intron_variant | MODIFIER | c.154-15455delT | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89467349 | ||||||
| chr11:89467349
|
CAA | C | 10 | a0001c0001t0001g0061a0001c0001t0005g0149a0001c0001t0024g0155others(7): Show | 10 | HG02486.hp1 HG02647.hp2 HG02698.hp1 others(7): Show |
intron_variant | MODIFIER | c.154-15456_154-1545 others(6): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89467349 | ||||||
| chr11:89467349
|
CAAAAAAA others(3): Show |
C | 8 | a0001c0001t0017g0160a0001c0001t0048g0044a0001c0001t0049g0043others(5): Show | 8 | HG01884.hp1 HG02615.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.154-15464_154-1545 others(14): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89467349 | ||||||
| chr11:89467349
|
CAAAAAAA others(5): Show |
C | 1 | a0001c0003t0003g0212 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.154-15466_154-1545 others(16): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89467349 | ||||||
| chr11:89467378
|
T | A | 2 | a0001c0001t0095g0215a0001c0001t0096g0217 | 2 | HG02055.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.154-15483A>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89467378 | ||||||
| chr11:89467411
|
G | T | 1 | a0001c0002t0006g0025 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.154-15516C>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89467411 | ||||||
| chr11:89467423
|
T | C | 1 | a0001c0001t0002g0255 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.154-15528A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89467423 | ||||||
| chr11:89467582
|
A | G | 24 | a0001c0001t0001g0063a0001c0001t0017g0160a0001c0001t0018g0142others(21): Show | 24 | HG01081.hp1 HG01884.hp1 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.154-15687T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89467582 | ||||||
| chr11:89467705
|
C | T | 221 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0008others(218): Show | 221 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(218): Show |
intron_variant | MODIFIER | c.154-15810G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89467705 | ||||||
| chr11:89467725
|
G | A | 4 | a0001c0001t0001g0081a0001c0001t0003g0188a0001c0001t0013g0082others(1): Show | 4 | HG01256.hp2 HG01928.hp2 HG02004.hp1 others(1): Show |
intron_variant | MODIFIER | c.154-15830C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89467725 | ||||||
| chr11:89467737
|
A | T | 2 | a0001c0001t0017g0160a0001c0002t0030g0159 | 2 | HG01884.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.154-15842T>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89467737 | ||||||
| chr11:89467828
|
G | A | 1 | a0001c0001t0019g0166 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.154-15933C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89467828 | ||||||
| chr11:89467993
|
C | G | 1 | a0001c0001t0023g0161 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.154-16098G>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89467993 | ||||||
| chr11:89468315
|
A | C | 75 | a0001c0001t0001g0063a0001c0001t0002g0260a0001c0001t0003g0170others(72): Show | 75 | HG00408.hp2 HG00621.hp1 HG00639.hp2 others(72): Show |
intron_variant | MODIFIER | c.154-16420T>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89468315 | ||||||
| chr11:89468428
|
G | A | 1 | a0001c0001t0022g0140 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.154-16533C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89468428 | ||||||
| chr11:89468459
|
G | A | 116 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0008others(113): Show | 116 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(113): Show |
intron_variant | MODIFIER | c.154-16564C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89468459 | ||||||
| chr11:89468642
|
G | T | 3 | a0001c0002t0033g0285a0001c0002t0098g0284a0001c0002t0099g0286 | 3 | HG02976.hp1 HG03195.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.154-16747C>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89468642 | ||||||
| chr11:89468656
|
G | A | 1 | a0001c0001t0001g0033 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.154-16761C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89468656 | ||||||
| chr11:89468798
|
C | T | 2 | a0001c0001t0088g0158a0001c0002t0011g0157 | 2 | HG02451.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.154-16903G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89468798 | ||||||
| chr11:89468801
|
A | G | 1 | a0001c0003t0005g0180 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.154-16906T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89468801 | ||||||
| chr11:89468846
|
C | G | 5 | a0001c0001t0001g0110a0001c0001t0002g0246a0001c0001t0014g0068others(2): Show | 5 | HG02083.hp2 NA18612.hp2 NA18939.hp1 others(2): Show |
intron_variant | MODIFIER | c.154-16951G>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89468846 | ||||||
| chr11:89468892
|
A | C | 11 | a0001c0001t0001g0063a0001c0001t0018g0142a0001c0001t0018g0175others(8): Show | 11 | HG01081.hp1 HG01884.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.154-16997T>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89468892 | ||||||
| chr11:89469116
|
ACT | A | 3 | a0001c0002t0033g0285a0001c0002t0098g0284a0001c0002t0099g0286 | 3 | HG02976.hp1 HG03195.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.154-17223_154-1722 others(6): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89469116 | ||||||
| chr11:89469280
|
G | C | 1 | a0001c0003t0005g0206 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.154-17385C>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89469280 | ||||||
| chr11:89469366
|
A | C | 73 | a0001c0001t0001g0063a0001c0001t0002g0260a0001c0001t0003g0170others(70): Show | 73 | HG00408.hp2 HG00621.hp1 HG00639.hp2 others(70): Show |
intron_variant | MODIFIER | c.154-17471T>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89469366 | ||||||
| chr11:89469401
|
G | A | 59 | a0001c0001t0002g0260a0001c0001t0003g0170a0001c0001t0003g0191others(56): Show | 59 | HG00408.hp2 HG00621.hp1 HG00639.hp2 others(56): Show |
intron_variant | MODIFIER | c.154-17506C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89469401 | ||||||
| chr11:89469431
|
T | C | 8 | a0001c0001t0001g0063a0001c0001t0019g0166a0001c0001t0022g0140others(5): Show | 8 | HG01081.hp1 HG01884.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.154-17536A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89469431 | ||||||
| chr11:89469569
|
A | T | 17 | a0001c0001t0002g0224a0001c0001t0002g0254a0001c0001t0002g0255others(14): Show | 17 | HG02258.hp1 HG02451.hp1 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.154-17674T>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89469569 | ||||||
| chr11:89469774
|
G | A | 3 | a0001c0002t0033g0285a0001c0002t0098g0284a0001c0002t0099g0286 | 3 | HG02976.hp1 HG03195.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.154-17879C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89469774 | ||||||
| chr11:89469975
|
G | A | 4 | a0001c0001t0002g0256a0001c0001t0021g0113a0001c0001t0021g0124others(1): Show | 4 | NA18985.hp1 NA18993.hp2 NA18998.hp1 others(1): Show |
intron_variant | MODIFIER | c.154-18080C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89469975 | ||||||
| chr11:89470001
|
C | T | 11 | a0001c0001t0001g0063a0001c0001t0018g0142a0001c0001t0018g0175others(8): Show | 11 | HG01081.hp1 HG01884.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.154-18106G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89470001 | ||||||
| chr11:89470064
|
T | C | 1 | a0001c0001t0022g0140 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.154-18169A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89470064 | ||||||
| chr11:89470076
|
A | AAAT | 3 | a0001c0001t0003g0207a0001c0001t0014g0038a0001c0002t0033g0262 | 3 | HG00673.hp1 HG03579.hp1 NA18954.hp2 |
intron_variant | MODIFIER | c.154-18184_154-1818 others(7): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89470076 | ||||||
| chr11:89470076
|
AAAT | A | 171 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0008others(168): Show | 171 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(168): Show |
intron_variant | MODIFIER | c.154-18184_154-1818 others(7): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89470076 | ||||||
| chr11:89470076
|
AAATAATA others(2): Show |
A | 11 | a0001c0001t0001g0063a0001c0001t0018g0142a0001c0001t0018g0175others(8): Show | 11 | HG01081.hp1 HG01884.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.154-18190_154-1818 others(13): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89470076 | ||||||
| chr11:89470089
|
A | AATG | 6 | a0001c0001t0002g0252a0001c0001t0024g0155a0001c0001t0031g0176others(3): Show | 6 | HG02622.hp1 HG02647.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.154-18195_154-1819 others(7): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89470089 | ||||||
| chr11:89470128
|
A | G | 2 | a0001c0001t0002g0245a0001c0012t0023g0181 | 2 | HG02723.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.154-18233T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89470128 | ||||||
| chr11:89470272
|
C | T | 8 | a0001c0001t0017g0160a0001c0001t0048g0044a0001c0001t0049g0043others(5): Show | 8 | HG01884.hp1 HG02615.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.154-18377G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89470272 | ||||||
| chr11:89470278
|
A | G | 136 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0008others(133): Show | 136 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(133): Show |
intron_variant | MODIFIER | c.154-18383T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89470278 | ||||||
| chr11:89470407
|
T | G | 16 | a0001c0001t0001g0063a0001c0001t0017g0160a0001c0001t0019g0166others(13): Show | 16 | HG01081.hp1 HG01884.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.154-18512A>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89470407 | ||||||
| chr11:89470575
|
G | A | 1 | a0001c0003t0005g0206 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.154-18680C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89470575 | ||||||
| chr11:89470788
|
G | T | 3 | a0001c0001t0018g0142a0001c0001t0018g0175a0001c0001t0078g0143 | 3 | HG02280.hp1 NA19240.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.154-18893C>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89470788 | ||||||
| chr11:89470810
|
T | C | 3 | a0001c0001t0018g0142a0001c0001t0018g0175a0001c0001t0078g0143 | 3 | HG02280.hp1 NA19240.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.154-18915A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89470810 | ||||||
| chr11:89470819
|
T | C | 51 | a0001c0001t0002g0260a0001c0001t0003g0170a0001c0001t0003g0191others(48): Show | 51 | HG00408.hp2 HG00621.hp1 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.154-18924A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89470819 | ||||||
| chr11:89471026
|
G | C | 28 | a0001c0001t0001g0063a0001c0001t0007g0126a0001c0001t0017g0160others(25): Show | 28 | HG00621.hp2 HG01074.hp2 HG01081.hp1 others(25): Show |
intron_variant | MODIFIER | c.154-19131C>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89471026 | ||||||
| chr11:89471037
|
T | G | 3 | a0001c0001t0017g0171a0001c0001t0017g0172a0001c0002t0074g0146 | 3 | HG01074.hp2 HG02723.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.154-19142A>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89471037 | ||||||
| chr11:89471052
|
G | C | 5 | a0001c0001t0002g0266a0001c0001t0002g0268a0001c0001t0002g0269others(2): Show | 5 | HG00735.hp2 HG00741.hp2 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.154-19157C>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89471052 | ||||||
| chr11:89471075
|
C | T | 3 | a0001c0001t0017g0171a0001c0001t0017g0172a0001c0002t0074g0146 | 3 | HG01074.hp2 HG02723.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.154-19180G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89471075 | ||||||
| chr11:89471181
|
G | C | 10 | a0001c0001t0001g0063a0001c0001t0019g0166a0001c0001t0022g0140others(7): Show | 10 | HG01081.hp1 HG01884.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.153+19277C>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89471181 | ||||||
| chr11:89471257
|
C | T | 1 | a0001c0001t0057g0127 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.153+19201G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89471257 | ||||||
| chr11:89471268
|
A | C | 16 | a0001c0001t0001g0063a0001c0001t0017g0171a0001c0001t0017g0172others(13): Show | 16 | HG01074.hp2 HG01081.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.153+19190T>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89471268 | ||||||
| chr11:89471385
|
C | CA | 4 | a0001c0001t0007g0126a0001c0001t0017g0171a0001c0001t0017g0172others(1): Show | 4 | HG00621.hp2 HG01074.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.153+19072dupT | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89471385 | ||||||
| chr11:89471602
|
T | C | 2 | a0001c0001t0069g0015a0001c0001t0112g0282 | 2 | HG02896.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.153+18856A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89471602 | ||||||
| chr11:89471672
|
G | C | 1 | a0001c0001t0007g0126 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.153+18786C>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89471672 | ||||||
| chr11:89471726
|
TTTTG | T | 6 | a0001c0001t0014g0068a0001c0001t0015g0019a0001c0001t0015g0078others(3): Show | 6 | HG02083.hp2 NA18941.hp1 NA18962.hp2 others(3): Show |
intron_variant | MODIFIER | c.153+18728_153+1873 others(8): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89471726 | ||||||
| chr11:89471743
|
T | C | 9 | a0001c0001t0001g0103a0001c0001t0010g0065a0001c0001t0010g0087others(6): Show | 9 | HG00323.hp2 HG00735.hp1 HG01106.hp1 others(6): Show |
intron_variant | MODIFIER | c.153+18715A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89471743 | ||||||
| chr11:89471827
|
C | T | 2 | a0002c0004t0032g0144a0002c0004t0032g0162 | 2 | HG02615.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.153+18631G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89471827 | ||||||
| chr11:89471828
|
G | A | 3 | a0001c0001t0017g0171a0001c0001t0017g0172a0001c0001t0018g0175 | 3 | HG01074.hp2 HG02723.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.153+18630C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89471828 | ||||||
| chr11:89471958
|
C | T | 10 | a0001c0001t0001g0063a0001c0001t0017g0171a0001c0001t0017g0172others(7): Show | 10 | HG01074.hp2 HG01081.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.153+18500G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89471958 | ||||||
| chr11:89471959
|
C | G | 3 | a0001c0001t0017g0171a0001c0001t0017g0172a0001c0001t0018g0175 | 3 | HG01074.hp2 HG02723.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.153+18499G>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89471959 | ||||||
| chr11:89471985
|
T | G | 12 | a0001c0001t0001g0063a0001c0001t0017g0171a0001c0001t0017g0172others(9): Show | 12 | HG01074.hp2 HG01081.hp1 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.153+18473A>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89471985 | ||||||
| chr11:89472148
|
G | A | 1 | a0001c0001t0017g0165 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.153+18310C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89472148 | ||||||
| chr11:89472245
|
T | C | 3 | a0001c0001t0017g0171a0001c0001t0017g0172a0001c0001t0018g0175 | 3 | HG01074.hp2 HG02723.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.153+18213A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89472245 | ||||||
| chr11:89472250
|
C | T | 61 | a0001c0001t0001g0063a0001c0001t0002g0260a0001c0001t0003g0170others(58): Show | 61 | HG00408.hp2 HG00621.hp1 HG00639.hp2 others(58): Show |
intron_variant | MODIFIER | c.153+18208G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89472250 | ||||||
| chr11:89472275
|
C | T | 13 | a0001c0001t0017g0160a0001c0001t0024g0155a0001c0001t0031g0176others(10): Show | 13 | HG01884.hp1 HG02615.hp1 HG02647.hp2 others(10): Show |
intron_variant | MODIFIER | c.153+18183G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89472275 | ||||||
| chr11:89472342
|
T | G | 3 | a0001c0001t0017g0171a0001c0001t0017g0172a0001c0001t0018g0175 | 3 | HG01074.hp2 HG02723.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.153+18116A>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89472342 | ||||||
| chr11:89472512
|
T | C | 1 | a0003c0013t0002g0220 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.153+17946A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89472512 | ||||||
| chr11:89472544
|
T | A | 7 | a0001c0001t0001g0063a0001c0001t0019g0166a0001c0001t0022g0140others(4): Show | 7 | HG01081.hp1 HG01884.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.153+17914A>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89472544 | ||||||
| chr11:89472550
|
C | T | 2 | a0001c0001t0007g0126a0001c0002t0074g0146 | 2 | HG00621.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.153+17908G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89472550 | ||||||
| chr11:89472565
|
A | G | 1 | a0001c0002t0009g0278 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.153+17893T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89472565 | ||||||
| chr11:89472668
|
A | C | 5 | a0001c0001t0001g0008a0001c0001t0004g0003a0001c0001t0008g0002others(2): Show | 5 | HG00558.hp1 NA18995.hp2 NA19001.hp1 others(2): Show |
intron_variant | MODIFIER | c.153+17790T>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89472668 | ||||||
| chr11:89472757
|
G | A | 51 | a0001c0001t0002g0260a0001c0001t0003g0170a0001c0001t0003g0191others(48): Show | 51 | HG00408.hp2 HG00621.hp1 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.153+17701C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89472757 | ||||||
| chr11:89473282
|
A | G | 87 | a0001c0001t0001g0063a0001c0001t0002g0252a0001c0001t0002g0260others(84): Show | 87 | HG00408.hp2 HG00621.hp1 HG00621.hp2 others(84): Show |
intron_variant | MODIFIER | c.153+17176T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89473282 | ||||||
| chr11:89473283
|
T | C | 8 | a0001c0001t0001g0001a0001c0001t0001g0060a0001c0001t0001g0069others(5): Show | 9 | HG01071.hp1 HG01255.hp2 HG01256.hp1 others(6): Show |
intron_variant | MODIFIER | c.153+17175A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89473283 | ||||||
| chr11:89473343
|
T | C | 61 | a0001c0001t0001g0063a0001c0001t0002g0260a0001c0001t0003g0170others(58): Show | 61 | HG00408.hp2 HG00621.hp1 HG00639.hp2 others(58): Show |
intron_variant | MODIFIER | c.153+17115A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89473343 | ||||||
| chr11:89473349
|
A | G | 22 | a0001c0001t0002g0252a0001c0001t0017g0160a0001c0001t0018g0142others(19): Show | 22 | HG01109.hp1 HG01884.hp1 HG02280.hp1 others(19): Show |
intron_variant | MODIFIER | c.153+17109T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89473349 | ||||||
| chr11:89473433
|
G | T | 1 | a0001c0002t0025g0039 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.153+17025C>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89473433 | ||||||
| chr11:89473439
|
A | AC | 63 | a0001c0001t0001g0063a0001c0001t0002g0260a0001c0001t0003g0170others(60): Show | 63 | HG00408.hp2 HG00621.hp1 HG00621.hp2 others(60): Show |
intron_variant | MODIFIER | c.153+17018_153+1701 others(5): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89473439 | ||||||
| chr11:89473464
|
C | CA | 45 | a0001c0001t0002g0260a0001c0001t0003g0191a0001c0001t0003g0205others(42): Show | 45 | HG00408.hp2 HG00621.hp1 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.153+16993dupT | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89473464 | ||||||
| chr11:89473464
|
CA | C | 30 | a0001c0001t0001g0063a0001c0001t0002g0252a0001c0001t0017g0160others(27): Show | 30 | HG01081.hp1 HG01109.hp1 HG01884.hp1 others(27): Show |
intron_variant | MODIFIER | c.153+16993delT | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89473464 | ||||||
| chr11:89473487
|
G | A | 2 | a0001c0001t0007g0126a0001c0002t0074g0146 | 2 | HG00621.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.153+16971C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89473487 | ||||||
| chr11:89473509
|
C | A | 58 | a0001c0001t0001g0063a0001c0001t0002g0260a0001c0001t0003g0170others(55): Show | 58 | HG00408.hp2 HG00621.hp1 HG00639.hp2 others(55): Show |
intron_variant | MODIFIER | c.153+16949G>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89473509 | ||||||
| chr11:89473687
|
T | C | 17 | a0001c0001t0002g0224a0001c0001t0002g0254a0001c0001t0002g0255others(14): Show | 17 | HG02258.hp1 HG02451.hp1 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.153+16771A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89473687 | ||||||
| chr11:89473755
|
G | A | 3 | a0001c0001t0017g0171a0001c0001t0017g0172a0001c0001t0018g0175 | 3 | HG01074.hp2 HG02723.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.153+16703C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89473755 | ||||||
| chr11:89473796
|
G | A | 51 | a0001c0001t0002g0260a0001c0001t0003g0170a0001c0001t0003g0191others(48): Show | 51 | HG00408.hp2 HG00621.hp1 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.153+16662C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89473796 | ||||||
| chr11:89473871
|
A | G | 1 | a0001c0001t0001g0050 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.153+16587T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89473871 | ||||||
| chr11:89474032
|
C | T | 64 | a0001c0001t0001g0063a0001c0001t0002g0260a0001c0001t0003g0170others(61): Show | 64 | HG00408.hp2 HG00621.hp1 HG00639.hp2 others(61): Show |
intron_variant | MODIFIER | c.153+16426G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89474032 | ||||||
| chr11:89474042
|
A | G | 64 | a0001c0001t0001g0063a0001c0001t0002g0260a0001c0001t0003g0170others(61): Show | 64 | HG00408.hp2 HG00621.hp1 HG00639.hp2 others(61): Show |
intron_variant | MODIFIER | c.153+16416T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89474042 | ||||||
| chr11:89474063
|
T | A | 1 | a0001c0001t0002g0252 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.153+16395A>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89474063 | ||||||
| chr11:89474064
|
G | T | 64 | a0001c0001t0001g0063a0001c0001t0002g0260a0001c0001t0003g0170others(61): Show | 64 | HG00408.hp2 HG00621.hp1 HG00639.hp2 others(61): Show |
intron_variant | MODIFIER | c.153+16394C>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89474064 | ||||||
| chr11:89474199
|
C | G | 64 | a0001c0001t0001g0063a0001c0001t0002g0260a0001c0001t0003g0170others(61): Show | 64 | HG00408.hp2 HG00621.hp1 HG00639.hp2 others(61): Show |
intron_variant | MODIFIER | c.153+16259G>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89474199 | ||||||
| chr11:89474234
|
A | C | 64 | a0001c0001t0001g0063a0001c0001t0002g0260a0001c0001t0003g0170others(61): Show | 64 | HG00408.hp2 HG00621.hp1 HG00639.hp2 others(61): Show |
intron_variant | MODIFIER | c.153+16224T>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89474234 | ||||||
| chr11:89474441
|
C | T | 3 | a0001c0001t0017g0171a0001c0001t0017g0172a0001c0001t0018g0175 | 3 | HG01074.hp2 HG02723.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.153+16017G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89474441 | ||||||
| chr11:89474450
|
T | A | 8 | a0001c0001t0003g0170a0001c0001t0073g0167a0001c0001t0094g0218others(5): Show | 8 | HG00741.hp1 HG01891.hp2 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.153+16008A>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89474450 | ||||||
| chr11:89474458
|
CA | C | 135 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0008others(132): Show | 135 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(132): Show |
intron_variant | MODIFIER | c.153+15999delT | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89474458 | ||||||
| chr11:89474458
|
CAA | C | 21 | a0001c0001t0001g0134a0001c0001t0002g0279a0001c0001t0002g0283others(18): Show | 21 | HG00323.hp2 HG01243.hp1 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.153+15998_153+1599 others(6): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89474458 | ||||||
| chr11:89474458
|
CAAA | C | 14 | a0001c0001t0002g0224a0001c0001t0002g0252a0001c0001t0002g0254others(11): Show | 14 | HG00621.hp2 HG02280.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.153+15997_153+1599 others(7): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89474458 | ||||||
| chr11:89474547
|
C | A | 1 | a0001c0001t0002g0252 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.153+15911G>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89474547 | ||||||
| chr11:89474735
|
T | C | 7 | a0001c0001t0082g0174a0001c0001t0117g0287a0001c0002t0011g0153others(4): Show | 7 | HG01099.hp1 HG01109.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.153+15723A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89474735 | ||||||
| chr11:89474784
|
A | G | 1 | a0001c0003t0003g0189 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.153+15674T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89474784 | ||||||
| chr11:89474847
|
C | T | 1 | a0001c0002t0074g0146 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.153+15611G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89474847 | ||||||
| chr11:89474877
|
G | A | 1 | a0001c0001t0001g0006 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.153+15581C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89474877 | ||||||
| chr11:89474958
|
T | C | 5 | a0001c0001t0001g0063a0001c0001t0019g0166a0001c0001t0022g0140others(2): Show | 5 | HG01081.hp1 HG01884.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.153+15500A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89474958 | ||||||
| chr11:89474979
|
T | TAAATAAC others(318): Show |
1 | a0001c0001t0002g0266 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.153+15478_153+1547 others(329): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89474979 | ||||||
| chr11:89474979
|
T | TAAATAAC others(320): Show |
1 | a0001c0003t0104g0267 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.153+15478_153+1547 others(331): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89474979 | ||||||
| chr11:89474979
|
T | TAAATAAC others(345): Show |
2 | a0001c0001t0002g0268a0001c0001t0002g0269 | 2 | HG00735.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.153+15478_153+1547 others(356): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89474979 | ||||||
| chr11:89474979
|
T | TAAATAAC others(346): Show |
1 | a0001c0001t0002g0270 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.153+15478_153+1547 others(357): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89474979 | ||||||
| chr11:89474984
|
A | G | 7 | a0001c0001t0001g0063a0001c0001t0019g0166a0001c0001t0022g0140others(4): Show | 7 | HG01081.hp1 HG01884.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.153+15474T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89474984 | ||||||
| chr11:89474996
|
C | T | 9 | a0001c0001t0001g0063a0001c0001t0007g0126a0001c0001t0019g0166others(6): Show | 9 | HG00621.hp2 HG01081.hp1 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.153+15462G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89474996 | ||||||
| chr11:89475084
|
T | A | 1 | a0001c0001t0113g0227 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.153+15374A>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89475084 | ||||||
| chr11:89475233
|
G | A | 1 | a0001c0001t0001g0110 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.153+15225C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89475233 | ||||||
| chr11:89475422
|
T | A | 71 | a0001c0001t0002g0252a0001c0001t0002g0260a0001c0001t0003g0191others(68): Show | 71 | HG00408.hp2 HG00621.hp1 HG00621.hp2 others(68): Show |
intron_variant | MODIFIER | c.153+15036A>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89475422 | ||||||
| chr11:89475493
|
T | C | 1 | a0001c0001t0001g0060 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.153+14965A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89475493 | ||||||
| chr11:89475507
|
A | G | 12 | a0001c0001t0007g0126a0001c0001t0024g0155a0001c0001t0031g0176others(9): Show | 12 | HG00621.hp2 HG02615.hp1 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.153+14951T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89475507 | ||||||
| chr11:89475621
|
C | T | 1 | a0001c0001t0001g0050 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.153+14837G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89475621 | ||||||
| chr11:89475656
|
C | T | 1 | a0004c0007t0013g0089 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.153+14802G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89475656 | ||||||
| chr11:89475686
|
T | C | 98 | a0001c0001t0001g0008a0001c0001t0001g0035a0001c0001t0001g0045others(95): Show | 98 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(95): Show |
intron_variant | MODIFIER | c.153+14772A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89475686 | ||||||
| chr11:89475925
|
T | C | 8 | a0001c0001t0001g0063a0001c0001t0017g0160a0001c0001t0018g0142others(5): Show | 8 | HG01884.hp1 HG01884.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.153+14533A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89475925 | ||||||
| chr11:89475945
|
T | C | 1 | a0001c0001t0008g0086 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.153+14513A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89475945 | ||||||
| chr11:89475986
|
C | T | 1 | a0001c0001t0017g0165 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.153+14472G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89475986 | ||||||
| chr11:89476197
|
T | C | 2 | a0001c0001t0002g0259a0001c0001t0002g0260 | 2 | HG02015.hp1 HG02132.hp1 |
intron_variant | MODIFIER | c.153+14261A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89476197 | ||||||
| chr11:89476306
|
A | G | 1 | a0001c0001t0005g0178 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.153+14152T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89476306 | ||||||
| chr11:89476469
|
T | A | 1 | a0001c0003t0005g0208 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.153+13989A>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89476469 | ||||||
| chr11:89476545
|
A | G | 1 | a0001c0001t0110g0274 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.153+13913T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89476545 | ||||||
| chr11:89476551
|
TA | T | 89 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0013others(86): Show | 89 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(86): Show |
intron_variant | MODIFIER | c.153+13906delT | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89476551 | ||||||
| chr11:89476817
|
G | A | 86 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0013others(83): Show | 86 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(83): Show |
intron_variant | MODIFIER | c.153+13641C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89476817 | ||||||
| chr11:89476862
|
T | C | 1 | a0001c0002t0025g0039 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.153+13596A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89476862 | ||||||
| chr11:89476882
|
T | C | 1 | a0001c0001t0002g0261 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.153+13576A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89476882 | ||||||
| chr11:89477029
|
T | C | 1 | a0001c0001t0085g0179 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.153+13429A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89477029 | ||||||
| chr11:89477063
|
G | A | 1 | a0001c0001t0001g0006 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.153+13395C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89477063 | ||||||
| chr11:89477198
|
G | C | 1 | a0001c0001t0002g0221 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.153+13260C>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89477198 | ||||||
| chr11:89477328
|
T | C | 252 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(249): Show | 253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.153+13130A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89477328 | ||||||
| chr11:89477415
|
T | A | 1 | a0001c0001t0052g0122 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.153+13043A>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89477415 | ||||||
| chr11:89477575
|
G | A | 2 | a0001c0001t0024g0210a0001c0002t0076g0209 | 2 | NA18962.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.153+12883C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89477575 | ||||||
| chr11:89477774
|
C | CA | 146 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0013others(143): Show | 146 | HG00099.hp1 HG00544.hp1 HG00544.hp2 others(143): Show |
intron_variant | MODIFIER | c.153+12683_153+1268 others(5): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89477774 | ||||||
| chr11:89477937
|
C | T | 3 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0016g0012 | 3 | HG00544.hp1 NA18947.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.153+12521G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89477937 | ||||||
| chr11:89478104
|
G | A | 2 | a0001c0001t0001g0063a0001c0001t0068g0064 | 2 | HG01884.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.153+12354C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89478104 | ||||||
| chr11:89478189
|
C | T | 1 | a0001c0001t0085g0179 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.153+12269G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89478189 | ||||||
| chr11:89478202
|
A | AC | 58 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0013others(55): Show | 58 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(55): Show |
intron_variant | MODIFIER | c.153+12255dupG | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89478202 | ||||||
| chr11:89478222
|
C | T | 84 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0023others(81): Show | 84 | HG00544.hp1 HG00544.hp2 HG00642.hp1 others(81): Show |
intron_variant | MODIFIER | c.153+12236G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89478222 | ||||||
| chr11:89478227
|
T | A | 1 | a0001c0002t0033g0262 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.153+12231A>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89478227 | ||||||
| chr11:89478582
|
G | A | 1 | a0001c0001t0113g0227 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.153+11876C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89478582 | ||||||
| chr11:89478764
|
C | A | 104 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0050others(101): Show | 105 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(102): Show |
intron_variant | MODIFIER | c.153+11694G>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89478764 | ||||||
| chr11:89478785
|
G | A | 2 | a0001c0001t0022g0040a0001c0005t0077g0214 | 2 | HG02145.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.153+11673C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89478785 | ||||||
| chr11:89478858
|
T | G | 1 | a0001c0001t0018g0175 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.153+11600A>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89478858 | ||||||
| chr11:89478894
|
G | A | 1 | a0001c0002t0030g0145 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.153+11564C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89478894 | ||||||
| chr11:89478967
|
T | C | 1 | a0001c0001t0047g0139 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.153+11491A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89478967 | ||||||
| chr11:89479005
|
A | G | 1 | a0001c0001t0010g0087 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.153+11453T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89479005 | ||||||
| chr11:89479009
|
T | TA | 82 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0014others(79): Show | 82 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.153+11448dupT | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89479009 | ||||||
| chr11:89479124
|
T | C | 1 | a0001c0001t0085g0179 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.153+11334A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89479124 | ||||||
| chr11:89479224
|
G | A | 1 | a0001c0001t0010g0133 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.153+11234C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89479224 | ||||||
| chr11:89479736
|
T | C | 1 | a0001c0002t0030g0145 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.153+10722A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89479736 | ||||||
| chr11:89479815
|
G | A | 1 | a0001c0001t0002g0283 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.153+10643C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89479815 | ||||||
| chr11:89479884
|
T | C | 8 | a0001c0001t0003g0170a0001c0001t0017g0171a0001c0001t0017g0172others(5): Show | 8 | HG00741.hp1 HG01074.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.153+10574A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89479884 | ||||||
| chr11:89479948
|
T | C | 1 | a0001c0001t0017g0165 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.153+10510A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89479948 | ||||||
| chr11:89480007
|
G | A | 3 | a0001c0001t0005g0149a0001c0001t0005g0150a0001c0001t0091g0151 | 3 | HG02280.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.153+10451C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89480007 | ||||||
| chr11:89480069
|
T | A | 63 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0062others(60): Show | 64 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(61): Show |
intron_variant | MODIFIER | c.153+10389A>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89480069 | ||||||
| chr11:89480076
|
C | A | 1 | a0001c0002t0030g0145 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.153+10382G>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89480076 | ||||||
| chr11:89480100
|
G | A | 104 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0050others(101): Show | 105 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(102): Show |
intron_variant | MODIFIER | c.153+10358C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89480100 | ||||||
| chr11:89480110
|
T | C | 2 | a0001c0001t0017g0171a0001c0001t0017g0172 | 2 | HG01074.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.153+10348A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89480110 | ||||||
| chr11:89480201
|
C | A | 3 | a0001c0001t0001g0063a0001c0001t0022g0140a0001c0001t0068g0064 | 3 | HG01081.hp1 HG01884.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.153+10257G>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89480201 | ||||||
| chr11:89480265
|
C | T | 1 | a0001c0001t0001g0069 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.153+10193G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89480265 | ||||||
| chr11:89480374
|
G | A | 1 | a0001c0001t0110g0274 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.153+10084C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89480374 | ||||||
| chr11:89480387
|
T | C | 1 | a0001c0002t0009g0263 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.153+10071A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89480387 | ||||||
| chr11:89480869
|
G | A | 1 | a0001c0001t0052g0122 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.153+9589C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89480869 | ||||||
| chr11:89480946
|
G | C | 251 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(248): Show | 252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
intron_variant | MODIFIER | c.153+9512C>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89480946 | ||||||
| chr11:89481067
|
C | A | 1 | a0001c0001t0085g0179 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.153+9391G>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89481067 | ||||||
| chr11:89481075
|
C | G | 111 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(108): Show | 112 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(109): Show |
intron_variant | MODIFIER | c.153+9383G>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89481075 | ||||||
| chr11:89481380
|
T | TGCTGAAT others(1): Show |
85 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0023others(82): Show | 85 | HG00544.hp1 HG00544.hp2 HG00642.hp1 others(82): Show |
intron_variant | MODIFIER | c.153+9070_153+9077d others(10): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89481380 | ||||||
| chr11:89481432
|
T | C | 140 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0023others(137): Show | 140 | HG00099.hp1 HG00544.hp1 HG00544.hp2 others(137): Show |
intron_variant | MODIFIER | c.153+9026A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89481432 | ||||||
| chr11:89481586
|
C | A | 1 | a0001c0002t0030g0145 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.153+8872G>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89481586 | ||||||
| chr11:89481658
|
T | C | 1 | a0001c0001t0001g0123 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.153+8800A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89481658 | ||||||
| chr11:89481716
|
T | G | 75 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0013others(72): Show | 75 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(72): Show |
intron_variant | MODIFIER | c.153+8742A>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89481716 | ||||||
| chr11:89481718
|
C | T | 2 | a0001c0001t0015g0057a0001c0001t0020g0056 | 2 | NA18966.hp2 NA18988.hp1 |
intron_variant | MODIFIER | c.153+8740G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89481718 | ||||||
| chr11:89481754
|
A | G | 1 | a0001c0002t0030g0145 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.153+8704T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89481754 | ||||||
| chr11:89482172
|
C | T | 11 | a0001c0001t0003g0170a0001c0001t0017g0171a0001c0001t0017g0172others(8): Show | 11 | HG00741.hp1 HG01074.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.153+8286G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89482172 | ||||||
| chr11:89482207
|
C | T | 1 | a0001c0001t0113g0227 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.153+8251G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89482207 | ||||||
| chr11:89482307
|
A | C | 1 | a0001c0001t0085g0179 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.153+8151T>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89482307 | ||||||
| chr11:89482460
|
C | T | 1 | a0001c0001t0085g0179 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.153+7998G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89482460 | ||||||
| chr11:89482568
|
C | A | 2 | a0001c0001t0002g0264a0001c0001t0002g0265 | 2 | NA18747.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.153+7890G>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89482568 | ||||||
| chr11:89482719
|
G | A | 1 | a0001c0001t0021g0124 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.153+7739C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89482719 | ||||||
| chr11:89483144
|
A | C | 1 | a0001c0005t0077g0214 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.153+7314T>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89483144 | ||||||
| chr11:89483228
|
A | G | 1 | a0001c0001t0002g0279 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.153+7230T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89483228 | ||||||
| chr11:89483257
|
T | A | 194 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(191): Show | 195 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(192): Show |
intron_variant | MODIFIER | c.153+7201A>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89483257 | ||||||
| chr11:89483279
|
A | G | 1 | a0001c0001t0086g0152 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.153+7179T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89483279 | ||||||
| chr11:89483312
|
A | G | 1 | a0001c0001t0014g0068 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.153+7146T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89483312 | ||||||
| chr11:89483491
|
C | T | 1 | a0001c0002t0102g0226 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.153+6967G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89483491 | ||||||
| chr11:89483617
|
G | A | 82 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0023others(79): Show | 82 | HG00544.hp1 HG00544.hp2 HG00642.hp1 others(79): Show |
intron_variant | MODIFIER | c.153+6841C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89483617 | ||||||
| chr11:89483655
|
TAGAC | T | 82 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0023others(79): Show | 82 | HG00544.hp1 HG00544.hp2 HG00642.hp1 others(79): Show |
intron_variant | MODIFIER | c.153+6799_153+6802d others(6): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89483655 | ||||||
| chr11:89483816
|
C | T | 1 | a0001c0001t0017g0165 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.153+6642G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89483816 | ||||||
| chr11:89483884
|
T | C | 1 | a0001c0001t0007g0125 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.153+6574A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89483884 | ||||||
| chr11:89484126
|
T | C | 8 | a0001c0001t0003g0170a0001c0001t0017g0171a0001c0001t0017g0172others(5): Show | 8 | HG00741.hp1 HG01074.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.153+6332A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89484126 | ||||||
| chr11:89484282
|
G | T | 1 | a0001c0003t0005g0180 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.153+6176C>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89484282 | ||||||
| chr11:89484328
|
G | T | 252 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(249): Show | 253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.153+6130C>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89484328 | ||||||
| chr11:89484540
|
T | C | 145 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0013others(142): Show | 145 | HG00099.hp1 HG00544.hp1 HG00544.hp2 others(142): Show |
intron_variant | MODIFIER | c.153+5918A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89484540 | ||||||
| chr11:89484567
|
T | C | 56 | a0001c0001t0002g0221a0001c0001t0002g0224a0001c0001t0002g0231others(53): Show | 56 | HG00099.hp1 HG00735.hp2 HG00741.hp2 others(53): Show |
intron_variant | MODIFIER | c.153+5891A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89484567 | ||||||
| chr11:89484634
|
T | C | 10 | a0001c0001t0001g0001a0001c0001t0001g0128a0001c0001t0001g0129others(7): Show | 11 | HG00140.hp1 HG00621.hp2 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.153+5824A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89484634 | ||||||
| chr11:89484698
|
A | G | 1 | a0001c0001t0014g0068 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.153+5760T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89484698 | ||||||
| chr11:89484699
|
T | C | 63 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0013others(60): Show | 63 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(60): Show |
intron_variant | MODIFIER | c.153+5759A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89484699 | ||||||
| chr11:89485306
|
A | G | 1 | a0001c0001t0018g0175 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.153+5152T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89485306 | ||||||
| chr11:89485309
|
A | G | 2 | a0001c0001t0004g0011a0001c0001t0021g0010 | 2 | NA18612.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.153+5149T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89485309 | ||||||
| chr11:89485519
|
C | T | 1 | a0001c0001t0001g0134 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.153+4939G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89485519 | ||||||
| chr11:89485671
|
A | T | 2 | a0001c0001t0012g0222a0001c0001t0108g0223 | 2 | NA18959.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.153+4787T>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89485671 | ||||||
| chr11:89485793
|
T | C | 1 | a0002c0004t0032g0144 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.153+4665A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89485793 | ||||||
| chr11:89485854
|
T | C | 6 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0134others(3): Show | 6 | NA18950.hp1 NA18963.hp1 NA18984.hp1 others(3): Show |
intron_variant | MODIFIER | c.153+4604A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89485854 | ||||||
| chr11:89485955
|
T | A | 6 | a0001c0001t0002g0279a0001c0001t0002g0283a0001c0001t0037g0280others(3): Show | 6 | HG02258.hp1 HG02630.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.153+4503A>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89485955 | ||||||
| chr11:89486225
|
A | T | 1 | a0001c0002t0030g0145 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.153+4233T>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89486225 | ||||||
| chr11:89486257
|
T | TTTTATTT others(27): Show |
7 | a0001c0001t0002g0266a0001c0001t0002g0268a0001c0001t0002g0269others(4): Show | 7 | HG00099.hp1 HG00735.hp2 HG00741.hp2 others(4): Show |
intron_variant | MODIFIER | c.153+4167_153+4200d others(36): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89486257 | ||||||
| chr11:89486293
|
T | A | 28 | a0001c0001t0003g0170a0001c0001t0017g0160a0001c0001t0017g0171others(25): Show | 28 | HG00741.hp1 HG01074.hp2 HG01099.hp1 others(25): Show |
intron_variant | MODIFIER | c.153+4165A>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89486293 | ||||||
| chr11:89486294
|
T | A | 28 | a0001c0001t0003g0170a0001c0001t0017g0160a0001c0001t0017g0171others(25): Show | 28 | HG00741.hp1 HG01074.hp2 HG01099.hp1 others(25): Show |
intron_variant | MODIFIER | c.153+4164A>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89486294 | ||||||
| chr11:89486451
|
G | A | 1 | a0001c0003t0090g0211 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.153+4007C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89486451 | ||||||
| chr11:89486452
|
C | T | 3 | a0001c0001t0002g0276a0001c0001t0012g0273a0001c0001t0110g0274 | 3 | HG00642.hp1 HG02738.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.153+4006G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89486452 | ||||||
| chr11:89486464
|
A | ATG | 75 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0023others(72): Show | 75 | HG00544.hp1 HG00544.hp2 HG00639.hp2 others(72): Show |
intron_variant | MODIFIER | c.153+3992_153+3993d others(4): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89486464 | ||||||
| chr11:89486464
|
A | G | 1 | a0001c0001t0063g0067 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.153+3994T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89486464 | ||||||
| chr11:89486464
|
ATG | A | 56 | a0001c0001t0002g0221a0001c0001t0002g0224a0001c0001t0002g0231others(53): Show | 56 | HG00099.hp1 HG00735.hp2 HG00741.hp2 others(53): Show |
intron_variant | MODIFIER | c.153+3992_153+3993d others(4): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89486464 | ||||||
| chr11:89486499
|
T | G | 11 | a0001c0001t0002g0276a0001c0001t0002g0279a0001c0001t0002g0283others(8): Show | 11 | HG00642.hp1 HG02258.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.153+3959A>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89486499 | ||||||
| chr11:89486520
|
A | ATATATAT others(23): Show |
3 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0058g0005 | 3 | HG01081.hp2 HG01952.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.153+3908_153+3937d others(32): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89486520 | ||||||
| chr11:89486539
|
C | CATATATG others(55): Show |
2 | a0001c0001t0001g0063a0001c0001t0068g0064 | 2 | HG01884.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.153+3918_153+3919i others(64): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89486539 | ||||||
| chr11:89486539
|
CATATATG others(25): Show |
C | 2 | a0001c0003t0003g0212a0001c0003t0019g0213 | 2 | NA18941.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.153+3887_153+3918d others(34): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89486539 | ||||||
| chr11:89486573
|
T | C | 1 | a0001c0002t0030g0145 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.153+3885A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89486573 | ||||||
| chr11:89486578
|
G | GTA | 83 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0023others(80): Show | 83 | HG00544.hp1 HG00544.hp2 HG00642.hp1 others(80): Show |
intron_variant | MODIFIER | c.153+3879_153+3880i others(4): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89486578 | ||||||
| chr11:89486578
|
GTGTGTAT others(1): Show |
G | 3 | a0001c0002t0033g0285a0001c0002t0098g0284a0001c0002t0099g0286 | 3 | HG02976.hp1 HG03195.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.153+3872_153+3879d others(10): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89486578 | ||||||
| chr11:89486598
|
ATACATAT others(69): Show |
A | 3 | a0001c0002t0033g0285a0001c0002t0098g0284a0001c0002t0099g0286 | 3 | HG02976.hp1 HG03195.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.153+3784_153+3859d others(78): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89486598 | ||||||
| chr11:89486601
|
CAT | C | 70 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0023others(67): Show | 70 | HG00544.hp1 HG00544.hp2 HG00741.hp1 others(67): Show |
intron_variant | MODIFIER | c.153+3855_153+3856d others(4): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89486601 | ||||||
| chr11:89486620
|
A | G | 2 | a0001c0001t0056g0055a0001c0001t0059g0054 | 2 | HG00673.hp2 NA18951.hp1 |
intron_variant | MODIFIER | c.153+3838T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89486620 | ||||||
| chr11:89486633
|
CAT | C | 6 | a0001c0001t0019g0166a0001c0001t0031g0176a0001c0001t0031g0177others(3): Show | 6 | HG02280.hp1 HG02486.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.153+3823_153+3824d others(4): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89486633 | ||||||
| chr11:89486635
|
TATATATG others(55): Show |
T | 20 | a0001c0001t0002g0276a0001c0001t0002g0279a0001c0001t0002g0283others(17): Show | 20 | HG00642.hp1 HG00741.hp1 HG01074.hp2 others(17): Show |
intron_variant | MODIFIER | c.153+3761_153+3822d others(64): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89486635 | ||||||
| chr11:89486640
|
A | G | 5 | a0001c0001t0001g0050a0001c0001t0004g0052a0001c0001t0007g0049others(2): Show | 5 | HG00639.hp1 HG01952.hp2 HG03654.hp2 others(2): Show |
intron_variant | MODIFIER | c.153+3818T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89486640 | ||||||
| chr11:89486667
|
TATATATG others(23): Show |
T | 115 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0023others(112): Show | 115 | HG00099.hp1 HG00544.hp1 HG00544.hp2 others(112): Show |
intron_variant | MODIFIER | c.153+3761_153+3790d others(32): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89486667 | ||||||
| chr11:89486672
|
A | G | 1 | a0001c0001t0002g0221 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.153+3786T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89486672 | ||||||
| chr11:89486697
|
C | CAT | 14 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0063others(11): Show | 14 | HG01081.hp2 HG01884.hp2 HG01952.hp1 others(11): Show |
intron_variant | MODIFIER | c.153+3759_153+3760d others(4): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89486697 | ||||||
| chr11:89486697
|
C | CATATATA others(27): Show |
1 | a0001c0001t0047g0139 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.153+3760_153+3761i others(36): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89486697 | ||||||
| chr11:89486697
|
C | CATATATA others(27): Show |
95 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0050others(92): Show | 96 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(93): Show |
intron_variant | MODIFIER | c.153+3760_153+3761i others(36): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89486697 | ||||||
| chr11:89486697
|
C | CATATATA others(59): Show |
6 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0061others(3): Show | 6 | HG01934.hp1 HG02055.hp1 HG03834.hp2 others(3): Show |
intron_variant | MODIFIER | c.153+3760_153+3761i others(68): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89486697 | ||||||
| chr11:89486697
|
C | CATATATA others(91): Show |
2 | a0001c0001t0015g0057a0001c0001t0020g0056 | 2 | NA18966.hp2 NA18988.hp1 |
intron_variant | MODIFIER | c.153+3760_153+3761i others(100): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89486697 | ||||||
| chr11:89487054
|
G | T | 56 | a0001c0001t0002g0221a0001c0001t0002g0224a0001c0001t0002g0231others(53): Show | 56 | HG00099.hp1 HG00735.hp2 HG00741.hp2 others(53): Show |
intron_variant | MODIFIER | c.153+3404C>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89487054 | ||||||
| chr11:89487164
|
C | T | 1 | a0001c0001t0085g0179 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.153+3294G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89487164 | ||||||
| chr11:89487220
|
C | T | 2 | a0001c0001t0018g0142a0001c0001t0078g0143 | 2 | HG02280.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.153+3238G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89487220 | ||||||
| chr11:89487223
|
C | T | 1 | a0001c0001t0017g0165 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.153+3235G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89487223 | ||||||
| chr11:89487243
|
G | A | 3 | a0001c0001t0005g0178a0001c0001t0117g0287a0001c0002t0074g0146 | 3 | HG02572.hp2 HG03098.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.153+3215C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89487243 | ||||||
| chr11:89487440
|
G | GCCTATAA | 143 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0023others(140): Show | 143 | HG00099.hp1 HG00544.hp1 HG00544.hp2 others(140): Show |
intron_variant | MODIFIER | c.153+3017_153+3018i others(9): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89487440 | ||||||
| chr11:89487635
|
T | C | 1 | a0001c0001t0018g0175 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.153+2823A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89487635 | ||||||
| chr11:89487921
|
C | T | 56 | a0001c0001t0002g0221a0001c0001t0002g0224a0001c0001t0002g0231others(53): Show | 56 | HG00099.hp1 HG00735.hp2 HG00741.hp2 others(53): Show |
intron_variant | MODIFIER | c.153+2537G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89487921 | ||||||
| chr11:89488088
|
A | C | 91 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0013others(88): Show | 91 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(88): Show |
intron_variant | MODIFIER | c.153+2370T>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89488088 | ||||||
| chr11:89488166
|
T | C | 1 | a0001c0001t0018g0175 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.153+2292A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89488166 | ||||||
| chr11:89488221
|
T | A | 1 | a0001c0001t0085g0179 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.153+2237A>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89488221 | ||||||
| chr11:89488404
|
A | G | 63 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0013others(60): Show | 63 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(60): Show |
intron_variant | MODIFIER | c.153+2054T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89488404 | ||||||
| chr11:89488431
|
T | C | 1 | a0001c0001t0116g0271 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.153+2027A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89488431 | ||||||
| chr11:89488504
|
C | A | 1 | a0001c0002t0030g0145 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.153+1954G>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89488504 | ||||||
| chr11:89488526
|
T | C | 91 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0013others(88): Show | 91 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(88): Show |
intron_variant | MODIFIER | c.153+1932A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89488526 | ||||||
| chr11:89488553
|
G | C | 1 | a0001c0002t0011g0173 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.153+1905C>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89488553 | ||||||
| chr11:89488644
|
G | A | 251 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(248): Show | 252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
intron_variant | MODIFIER | c.153+1814C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89488644 | ||||||
| chr11:89488688
|
C | A | 1 | a0001c0001t0082g0174 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.153+1770G>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89488688 | ||||||
| chr11:89488758
|
A | G | 1 | a0001c0001t0007g0049 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.153+1700T>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89488758 | ||||||
| chr11:89488790
|
G | C | 251 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(248): Show | 252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
intron_variant | MODIFIER | c.153+1668C>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89488790 | ||||||
| chr11:89488837
|
A | T | 1 | a0001c0001t0085g0179 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.153+1621T>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89488837 | ||||||
| chr11:89489073
|
C | A | 1 | a0001c0001t0103g0272 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.153+1385G>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89489073 | ||||||
| chr11:89489279
|
T | G | 1 | a0001c0001t0022g0140 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.153+1179A>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89489279 | ||||||
| chr11:89489385
|
G | A | 85 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0014others(82): Show | 85 | HG00544.hp1 HG00544.hp2 HG00642.hp1 others(82): Show |
intron_variant | MODIFIER | c.153+1073C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89489385 | ||||||
| chr11:89489415
|
T | G | 1 | a0001c0001t0007g0141 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.153+1043A>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89489415 | ||||||
| chr11:89489502
|
C | T | 2 | a0001c0001t0031g0176a0001c0001t0031g0177 | 2 | HG03209.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.153+956G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89489502 | ||||||
| chr11:89489722
|
T | C | 1 | a0001c0001t0018g0175 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.153+736A>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89489722 | ||||||
| chr11:89489727
|
C | CA | 154 | a0001c0001t0001g0001a0001c0001t0001g0050a0001c0001t0001g0059others(151): Show | 155 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.153+730dupT | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89489727 | ||||||
| chr11:89489727
|
CA | C | 6 | a0001c0001t0007g0007a0001c0001t0012g0273a0001c0001t0110g0274others(3): Show | 6 | HG00642.hp1 HG02615.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.153+730delT | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89489727 | ||||||
| chr11:89489741
|
G | A | 102 | a0001c0001t0001g0001a0001c0001t0001g0050a0001c0001t0001g0059others(99): Show | 103 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(100): Show |
intron_variant | MODIFIER | c.153+717C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89489741 | ||||||
| chr11:89489769
|
G | A | 1 | a0001c0001t0085g0179 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.153+689C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89489769 | ||||||
| chr11:89490350
|
A | C | 2 | a0001c0001t0018g0142a0001c0001t0078g0143 | 2 | HG02280.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.153+108T>G | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89490350 | ||||||
| chr11:89490448
|
C | G | 251 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(248): Show | 252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
intron_variant | MODIFIER | c.153+10G>C | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 2/17 | chr11 | 89490448 | ||||||
| chr11:89490763
|
G | A | 107 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(104): Show | 108 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(105): Show |
intron_variant | MODIFIER | c.58-210C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 1/17 | chr11 | 89490763 | ||||||
| chr11:89490885
|
C | T | 14 | a0001c0001t0002g0276a0001c0001t0002g0279a0001c0001t0002g0283others(11): Show | 14 | HG00642.hp1 HG02258.hp1 HG02630.hp1 others(11): Show |
intron_variant | MODIFIER | c.57+305G>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 1/17 | chr11 | 89490885 | ||||||
| chr11:89490890
|
G | A | 14 | a0001c0001t0002g0276a0001c0001t0002g0279a0001c0001t0002g0283others(11): Show | 14 | HG00642.hp1 HG02258.hp1 HG02630.hp1 others(11): Show |
intron_variant | MODIFIER | c.57+300C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 1/17 | chr11 | 89490890 | ||||||
| chr11:89490933
|
G | T | 108 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(105): Show | 109 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.57+257C>A | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 1/17 | chr11 | 89490933 | ||||||
| chr11:89490963
|
T | TCTC | 108 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(105): Show | 109 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.57+224_57+226dupGA others(1): Show |
NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 1/17 | chr11 | 89490963 | ||||||
| chr11:89490980
|
C | A | 2 | a0001c0002t0033g0285a0001c0002t0099g0286 | 2 | HG02976.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.57+210G>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 1/17 | chr11 | 89490980 | ||||||
| chr11:89491061
|
G | GT | 108 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(105): Show | 109 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.57+128dupA | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 1/17 | chr11 | 89491061 | ||||||
| chr11:89491158
|
G | A | 103 | a0001c0001t0001g0001a0001c0001t0001g0045a0001c0001t0001g0050others(100): Show | 104 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(101): Show |
intron_variant | MODIFIER | c.57+32C>T | NOX4 | ENSG00000086991.13 | transcript | ENST00000263317.9 | protein_coding | 1/17 | chr11 | 89491158 |