Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 255743 |
|---|---|
| ensemblid | ENSG00000168743.13 |
| hgncid | 27405 |
| symbol | NPNT |
| name | nephronectin |
| refseq_nuc | NM_001033047.3 |
| refseq_prot | NP_001028219.1 |
| ensembl_nuc | ENST00000379987.7 |
| ensembl_prot | ENSP00000369323.2 |
| mane_status | MANE Select |
| chr | chr4 |
| start | 105895471 |
| end | 105971671 |
| strand | + |
| ver | v1.2 |
| region | chr4:105895471-105971671 |
| region5000 | chr4:105890471-105976671 |
| regionname0 | NPNT_chr4_105895471_105971671 |
| regionname5000 | NPNT_chr4_105890471_105976671 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 565 | 103 | 28 | 27 | 27 | 6 | 15 | 19 | NPNT_chr4_105890471_105976671 | NPNT | copy fasta | chr4 | 105890471 | 105976671 |
| a0002 | 0/1 | 565 | 84 | 21 | 11 | 31 | 6 | 14 | 23 | NPNT_chr4_105890471_105976671 | NPNT | copy fasta | chr4 | 105890471 | 105976671 |
| a0003 | 1/0 | 565 | 27 | 17 | 6 | 0 | 2 | 1 | 0 | NPNT_chr4_105890471_105976671 | NPNT | copy fasta | chr4 | 105890471 | 105976671 |
| a0004 | 0/0 | 565 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | copy fasta | chr4 | 105890471 | 105976671 |
| a0005 | 0/0 | 565 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | copy fasta | chr4 | 105890471 | 105976671 |
| a0006 | 0/0 | 565 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | copy fasta | chr4 | 105890471 | 105976671 |
| a0007 | 0/0 | 565 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | copy fasta | chr4 | 105890471 | 105976671 |
| a0008 | 0/0 | 565 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | copy fasta | chr4 | 105890471 | 105976671 |
| a0009 | 0/0 | 565 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | NPNT_chr4_105890471_105976671 | NPNT | copy fasta | chr4 | 105890471 | 105976671 |
| a0010 | 0/0 | 565 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | copy fasta | chr4 | 105890471 | 105976671 |
| a0011 | 0/0 | 565 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | copy fasta | chr4 | 105890471 | 105976671 |
| a0012 | 0/0 | 565 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | copy fasta | chr4 | 105890471 | 105976671 |
| a0013 | 0/0 | 565 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | copy fasta | chr4 | 105890471 | 105976671 |
| chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/0 | 1698 | 103 | 28 | 27 | 27 | 6 | 15 | NPNT_chr4_105890471_105976671 | NPNT | copy fasta | chr4 | 105890471 | 105976671 |
| c0002 | 0/1 | 1698 | 84 | 21 | 11 | 31 | 6 | 14 | NPNT_chr4_105890471_105976671 | NPNT | copy fasta | chr4 | 105890471 | 105976671 |
| c0003 | 1/0 | 1698 | 26 | 17 | 5 | 0 | 2 | 1 | NPNT_chr4_105890471_105976671 | NPNT | copy fasta | chr4 | 105890471 | 105976671 |
| c0004 | 0/0 | 1698 | 6 | 6 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | copy fasta | chr4 | 105890471 | 105976671 |
| c0005 | 0/0 | 1698 | 4 | 4 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | copy fasta | chr4 | 105890471 | 105976671 |
| c0006 | 0/0 | 1698 | 2 | 2 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | copy fasta | chr4 | 105890471 | 105976671 |
| c0007 | 0/0 | 1698 | 2 | 2 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | copy fasta | chr4 | 105890471 | 105976671 |
| c0008 | 0/0 | 1698 | 2 | 1 | 1 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | copy fasta | chr4 | 105890471 | 105976671 |
| c0009 | 0/0 | 1698 | 2 | 0 | 0 | 2 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | copy fasta | chr4 | 105890471 | 105976671 |
| c0010 | 0/0 | 1698 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | copy fasta | chr4 | 105890471 | 105976671 |
| c0011 | 0/0 | 1698 | 1 | 0 | 1 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | copy fasta | chr4 | 105890471 | 105976671 |
| c0012 | 0/0 | 1698 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | copy fasta | chr4 | 105890471 | 105976671 |
| c0013 | 0/0 | 1698 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | copy fasta | chr4 | 105890471 | 105976671 |
| c0014 | 0/0 | 1698 | 1 | 0 | 1 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | copy fasta | chr4 | 105890471 | 105976671 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 2864 | 96 | 26 | 26 | 34 | 2 | 8 | NPNT_chr4_105890471_105976671 | NPNT | copy fasta | chr4 | 105890471 | 105976671 |
| t0002 | 0/0 | 2864 | 93 | 44 | 10 | 17 | 8 | 14 | NPNT_chr4_105890471_105976671 | NPNT | copy fasta | chr4 | 105890471 | 105976671 |
| t0003 | 0/1 | 2864 | 14 | 0 | 3 | 7 | 0 | 3 | NPNT_chr4_105890471_105976671 | NPNT | copy fasta | chr4 | 105890471 | 105976671 |
| t0004 | 1/0 | 2864 | 8 | 2 | 3 | 0 | 1 | 1 | NPNT_chr4_105890471_105976671 | NPNT | copy fasta | chr4 | 105890471 | 105976671 |
| t0005 | 0/0 | 2864 | 7 | 7 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | copy fasta | chr4 | 105890471 | 105976671 |
| t0006 | 0/0 | 2864 | 5 | 0 | 3 | 0 | 1 | 1 | NPNT_chr4_105890471_105976671 | NPNT | copy fasta | chr4 | 105890471 | 105976671 |
| t0007 | 0/0 | 2864 | 2 | 0 | 1 | 0 | 1 | 0 | NPNT_chr4_105890471_105976671 | NPNT | copy fasta | chr4 | 105890471 | 105976671 |
| t0008 | 0/0 | 2864 | 2 | 0 | 0 | 0 | 0 | 2 | NPNT_chr4_105890471_105976671 | NPNT | copy fasta | chr4 | 105890471 | 105976671 |
| t0009 | 0/0 | 2864 | 2 | 0 | 0 | 0 | 1 | 1 | NPNT_chr4_105890471_105976671 | NPNT | copy fasta | chr4 | 105890471 | 105976671 |
| t0010 | 0/0 | 2864 | 2 | 2 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | copy fasta | chr4 | 105890471 | 105976671 |
| t0011 | 0/0 | 2864 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | copy fasta | chr4 | 105890471 | 105976671 |
| t0012 | 0/0 | 2864 | 1 | 0 | 0 | 1 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | copy fasta | chr4 | 105890471 | 105976671 |
| t0013 | 0/0 | 2864 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | copy fasta | chr4 | 105890471 | 105976671 |
| t0014 | 0/0 | 2864 | 1 | 0 | 0 | 1 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | copy fasta | chr4 | 105890471 | 105976671 |
| t0015 | 0/0 | 2864 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | copy fasta | chr4 | 105890471 | 105976671 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0002 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0004 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0011 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0016 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0018 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0037 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0057 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0171 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0223 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 1698 | 103 | 28 | 27 | 27 | 6 | 15 | NPNT_chr4_105890471_105976671 | NPNT | copy fasta | chr4 | 105890471 | 105976671 |
| a0002c0002 | 0/1 | 1698 | 84 | 21 | 11 | 31 | 6 | 14 | NPNT_chr4_105890471_105976671 | NPNT | copy fasta | chr4 | 105890471 | 105976671 |
| a0003c0003 | 1/0 | 1698 | 26 | 17 | 5 | 0 | 2 | 1 | NPNT_chr4_105890471_105976671 | NPNT | copy fasta | chr4 | 105890471 | 105976671 |
| a0003c0014 | 0/0 | 1698 | 1 | 0 | 1 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | copy fasta | chr4 | 105890471 | 105976671 |
| a0004c0004 | 0/0 | 1698 | 6 | 6 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | copy fasta | chr4 | 105890471 | 105976671 |
| a0005c0005 | 0/0 | 1698 | 4 | 4 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | copy fasta | chr4 | 105890471 | 105976671 |
| a0006c0006 | 0/0 | 1698 | 2 | 2 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | copy fasta | chr4 | 105890471 | 105976671 |
| a0007c0007 | 0/0 | 1698 | 2 | 2 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | copy fasta | chr4 | 105890471 | 105976671 |
| a0008c0008 | 0/0 | 1698 | 2 | 1 | 1 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | copy fasta | chr4 | 105890471 | 105976671 |
| a0009c0009 | 0/0 | 1698 | 2 | 0 | 0 | 2 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | copy fasta | chr4 | 105890471 | 105976671 |
| a0010c0012 | 0/0 | 1698 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | copy fasta | chr4 | 105890471 | 105976671 |
| a0011c0011 | 0/0 | 1698 | 1 | 0 | 1 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | copy fasta | chr4 | 105890471 | 105976671 |
| a0012c0013 | 0/0 | 1698 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | copy fasta | chr4 | 105890471 | 105976671 |
| a0013c0010 | 0/0 | 1698 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | copy fasta | chr4 | 105890471 | 105976671 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 4561 | 66 | 12 | 22 | 24 | 1 | 7 | NPNT_chr4_105890471_105976671 | NPNT | copy fasta | chr4 | 105890471 | 105976671 |
| a0001c0001t0002 | 0/0 | 4561 | 26 | 13 | 3 | 1 | 4 | 5 | NPNT_chr4_105890471_105976671 | NPNT | copy fasta | chr4 | 105890471 | 105976671 |
| a0001c0001t0003 | 0/0 | 4561 | 1 | 0 | 1 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | copy fasta | chr4 | 105890471 | 105976671 |
| a0001c0001t0004 | 0/0 | 4561 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | copy fasta | chr4 | 105890471 | 105976671 |
| a0001c0001t0005 | 0/0 | 4561 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | copy fasta | chr4 | 105890471 | 105976671 |
| a0001c0001t0006 | 0/0 | 4561 | 3 | 0 | 1 | 0 | 1 | 1 | NPNT_chr4_105890471_105976671 | NPNT | copy fasta | chr4 | 105890471 | 105976671 |
| a0001c0001t0008 | 0/0 | 4561 | 2 | 0 | 0 | 0 | 0 | 2 | NPNT_chr4_105890471_105976671 | NPNT | copy fasta | chr4 | 105890471 | 105976671 |
| a0001c0001t0011 | 0/0 | 4561 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | copy fasta | chr4 | 105890471 | 105976671 |
| a0001c0001t0012 | 0/0 | 4561 | 1 | 0 | 0 | 1 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | copy fasta | chr4 | 105890471 | 105976671 |
| a0001c0001t0014 | 0/0 | 4561 | 1 | 0 | 0 | 1 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | copy fasta | chr4 | 105890471 | 105976671 |
| a0002c0002t0001 | 0/0 | 4561 | 20 | 7 | 3 | 8 | 1 | 1 | NPNT_chr4_105890471_105976671 | NPNT | copy fasta | chr4 | 105890471 | 105976671 |
| a0002c0002t0002 | 0/0 | 4561 | 46 | 13 | 4 | 16 | 4 | 9 | NPNT_chr4_105890471_105976671 | NPNT | copy fasta | chr4 | 105890471 | 105976671 |
| a0002c0002t0003 | 0/1 | 4561 | 13 | 0 | 2 | 7 | 0 | 3 | NPNT_chr4_105890471_105976671 | NPNT | copy fasta | chr4 | 105890471 | 105976671 |
| a0002c0002t0006 | 0/0 | 4561 | 2 | 0 | 2 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | copy fasta | chr4 | 105890471 | 105976671 |
| a0002c0002t0009 | 0/0 | 4561 | 2 | 0 | 0 | 0 | 1 | 1 | NPNT_chr4_105890471_105976671 | NPNT | copy fasta | chr4 | 105890471 | 105976671 |
| a0002c0002t0013 | 0/0 | 4561 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | copy fasta | chr4 | 105890471 | 105976671 |
| a0003c0003t0001 | 0/0 | 4561 | 4 | 4 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | copy fasta | chr4 | 105890471 | 105976671 |
| a0003c0003t0002 | 0/0 | 4561 | 6 | 5 | 1 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | copy fasta | chr4 | 105890471 | 105976671 |
| a0003c0003t0004 | 1/0 | 4561 | 7 | 1 | 3 | 0 | 1 | 1 | NPNT_chr4_105890471_105976671 | NPNT | copy fasta | chr4 | 105890471 | 105976671 |
| a0003c0003t0005 | 0/0 | 4561 | 6 | 6 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | copy fasta | chr4 | 105890471 | 105976671 |
| a0003c0003t0007 | 0/0 | 4561 | 2 | 0 | 1 | 0 | 1 | 0 | NPNT_chr4_105890471_105976671 | NPNT | copy fasta | chr4 | 105890471 | 105976671 |
| a0003c0003t0015 | 0/0 | 4561 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | copy fasta | chr4 | 105890471 | 105976671 |
| a0003c0014t0001 | 0/0 | 4561 | 1 | 0 | 1 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | copy fasta | chr4 | 105890471 | 105976671 |
| a0004c0004t0002 | 0/0 | 4561 | 6 | 6 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | copy fasta | chr4 | 105890471 | 105976671 |
| a0005c0005t0001 | 0/0 | 4561 | 3 | 3 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | copy fasta | chr4 | 105890471 | 105976671 |
| a0005c0005t0002 | 0/0 | 4561 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | copy fasta | chr4 | 105890471 | 105976671 |
| a0006c0006t0002 | 0/0 | 4561 | 2 | 2 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | copy fasta | chr4 | 105890471 | 105976671 |
| a0007c0007t0002 | 0/0 | 4561 | 2 | 2 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | copy fasta | chr4 | 105890471 | 105976671 |
| a0008c0008t0002 | 0/0 | 4561 | 2 | 1 | 1 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | copy fasta | chr4 | 105890471 | 105976671 |
| a0009c0009t0001 | 0/0 | 4561 | 2 | 0 | 0 | 2 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | copy fasta | chr4 | 105890471 | 105976671 |
| a0010c0012t0010 | 0/0 | 4561 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | copy fasta | chr4 | 105890471 | 105976671 |
| a0011c0011t0002 | 0/0 | 4561 | 1 | 0 | 1 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | copy fasta | chr4 | 105890471 | 105976671 |
| a0012c0013t0010 | 0/0 | 4561 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | copy fasta | chr4 | 105890471 | 105976671 |
| a0013c0010t0002 | 0/0 | 4561 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | copy fasta | chr4 | 105890471 | 105976671 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0002g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0002g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0002g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0002g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0002g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0002g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0002g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0002g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0002g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0002g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0002g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0002g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0003g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0004g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0005g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0006g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0006g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0006g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0008g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0008g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0011g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0012g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0001c0001t0014g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0002c0002t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0002c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0002c0002t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0002c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0002c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0002c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0002c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0002c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0002c0002t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0002c0002t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0002c0002t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0002c0002t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0002c0002t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0002c0002t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0002c0002t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0002c0002t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0002c0002t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0002c0002t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0002c0002t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0002c0002t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0002c0002t0002g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0002c0002t0002g0004 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0002c0002t0002g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0002c0002t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0002c0002t0002g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0002c0002t0002g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0002c0002t0002g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0002c0002t0002g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0002c0002t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0002c0002t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0002c0002t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0002c0002t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0002c0002t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0002c0002t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0002c0002t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0002c0002t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0002c0002t0002g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0002c0002t0002g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0002c0002t0002g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0002c0002t0002g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0002c0002t0002g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0002c0002t0002g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0002c0002t0002g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0002c0002t0002g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0002c0002t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0002c0002t0002g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0002c0002t0002g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0002c0002t0002g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0002c0002t0002g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0002c0002t0002g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0002c0002t0002g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0002c0002t0002g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0002c0002t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0002c0002t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0002c0002t0002g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0002c0002t0002g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0002c0002t0002g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0002c0002t0002g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0002c0002t0002g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0002c0002t0002g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0002c0002t0002g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0002c0002t0002g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0002c0002t0002g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0002c0002t0002g0223 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0002c0002t0003g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0002c0002t0003g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0002c0002t0003g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0002c0002t0003g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0002c0002t0003g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0002c0002t0003g0171 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0002c0002t0003g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0002c0002t0003g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0002c0002t0003g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0002c0002t0003g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0002c0002t0003g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0002c0002t0003g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0002c0002t0003g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0002c0002t0006g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0002c0002t0006g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0002c0002t0009g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0002c0002t0009g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0002c0002t0013g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0003c0003t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0003c0003t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0003c0003t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0003c0003t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0003c0003t0002g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0003c0003t0002g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0003c0003t0002g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0003c0003t0002g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0003c0003t0002g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0003c0003t0002g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0003c0003t0004g0011 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0003c0003t0004g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0003c0003t0004g0057 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0003c0003t0004g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0003c0003t0004g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0003c0003t0004g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0003c0003t0004g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0003c0003t0005g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0003c0003t0005g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0003c0003t0005g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0003c0003t0005g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0003c0003t0005g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0003c0003t0005g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0003c0003t0007g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0003c0003t0007g0016 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0003c0003t0015g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0003c0014t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0004c0004t0002g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0004c0004t0002g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0004c0004t0002g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0004c0004t0002g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0004c0004t0002g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0004c0004t0002g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0005c0005t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0005c0005t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0005c0005t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0005c0005t0002g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0006c0006t0002g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0006c0006t0002g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0007c0007t0002g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0007c0007t0002g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0008c0008t0002g0001 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0009c0009t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0009c0009t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0010c0012t0010g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0011c0011t0002g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0012c0013t0010g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| a0013c0010t0002g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0002 | t0009 | g0227 | EUR | GBR | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG00099 | hp2 | a0003 | c0003 | t0004 | g0011 | EUR | GBR | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG00140 | hp1 | a0003 | c0003 | t0007 | g0016 | EUR | GBR | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0037 | EUR | GBR | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0148 | EUR | FIN | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG00280 | hp2 | a0002 | c0002 | t0002 | g0223 | EUR | FIN | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG00408 | hp1 | a0002 | c0002 | t0003 | g0184 | EAS | CHS | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | CHS | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG00438 | hp1 | a0002 | c0002 | t0003 | g0176 | EAS | CHS | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | CHS | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | CHS | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG00597 | hp2 | a0002 | c0002 | t0003 | g0225 | EAS | CHS | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG00639 | hp2 | a0002 | c0002 | t0002 | g0158 | AMR | PUR | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0065 | AMR | PUR | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG00642 | hp2 | a0003 | c0003 | t0004 | g0226 | AMR | PUR | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG00735 | hp1 | a0008 | c0008 | t0002 | g0001 | AMR | PUR | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG00735 | hp2 | a0001 | c0001 | t0006 | g0010 | AMR | PUR | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG00741 | hp1 | a0002 | c0002 | t0006 | g0149 | AMR | PUR | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG00741 | hp2 | a0003 | c0003 | t0007 | g0015 | AMR | PUR | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0102 | AMR | PUR | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0059 | AMR | PUR | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG01070 | hp2 | a0011 | c0011 | t0002 | g0130 | AMR | PUR | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0046 | AMR | PUR | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG01081 | hp1 | a0003 | c0003 | t0004 | g0224 | AMR | PUR | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0055 | AMR | PUR | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0189 | AMR | PUR | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG01109 | hp2 | a0002 | c0002 | t0002 | g0117 | AMR | PUR | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG01167 | hp1 | a0002 | c0002 | t0002 | g0167 | AMR | PUR | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0187 | AMR | PUR | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG01175 | hp2 | a0002 | c0002 | t0002 | g0182 | AMR | PUR | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG01192 | hp2 | a0003 | c0014 | t0001 | g0131 | AMR | PUR | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0174 | AMR | PUR | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG01243 | hp2 | a0003 | c0003 | t0002 | g0001 | AMR | PUR | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG01255 | hp1 | a0002 | c0002 | t0001 | g0062 | AMR | CLM | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0094 | AMR | CLM | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0137 | AMR | CLM | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0068 | AMR | CLM | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG01261 | hp1 | a0002 | c0002 | t0003 | g0047 | AMR | CLM | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG01261 | hp2 | a0001 | c0001 | t0003 | g0012 | AMR | CLM | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0101 | AMR | CLM | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG01346 | hp2 | a0002 | c0002 | t0006 | g0150 | AMR | CLM | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG01361 | hp1 | a0002 | c0002 | t0001 | g0042 | AMR | CLM | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG01361 | hp2 | a0002 | c0002 | t0001 | g0165 | AMR | CLM | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | CLM | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0229 | AMR | CLM | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG01516 | hp1 | a0001 | c0001 | t0006 | g0096 | EUR | IBS | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG01516 | hp2 | a0002 | c0002 | t0002 | g0004 | EUR | IBS | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG01517 | hp1 | a0002 | c0002 | t0001 | g0175 | EUR | IBS | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG01517 | hp2 | a0002 | c0002 | t0002 | g0004 | EUR | IBS | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG01884 | hp1 | a0003 | c0003 | t0001 | g0210 | AFR | ACB | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG01884 | hp2 | a0005 | c0005 | t0001 | g0132 | AFR | ACB | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0056 | AMR | PEL | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0202 | AMR | PEL | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG01993 | hp1 | a0002 | c0002 | t0003 | g0039 | AMR | PEL | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0052 | AMR | PEL | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0103 | AMR | PEL | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG02004 | hp2 | a0003 | c0003 | t0004 | g0208 | AMR | PEL | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG02040 | hp1 | a0002 | c0002 | t0002 | g0091 | EAS | KHV | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | KHV | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG02055 | hp1 | a0003 | c0003 | t0005 | g0121 | AFR | ACB | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG02055 | hp2 | a0002 | c0002 | t0001 | g0173 | AFR | ACB | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG02080 | hp1 | a0002 | c0002 | t0003 | g0179 | EAS | KHV | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | KHV | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG02083 | hp1 | a0002 | c0002 | t0002 | g0026 | EAS | KHV | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | KHV | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG02129 | hp1 | a0002 | c0002 | t0002 | g0040 | EAS | KHV | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | KHV | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG02145 | hp1 | a0002 | c0002 | t0002 | g0160 | AFR | ACB | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG02145 | hp2 | a0003 | c0003 | t0001 | g0114 | AFR | ACB | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG02257 | hp1 | a0001 | c0001 | t0002 | g0213 | AFR | ACB | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG02280 | hp1 | a0001 | c0001 | t0011 | g0115 | AFR | ACB | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG02280 | hp2 | a0012 | c0013 | t0010 | g0136 | AFR | ACB | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG02451 | hp1 | a0001 | c0001 | t0005 | g0112 | AFR | ACB | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG02451 | hp2 | a0007 | c0007 | t0002 | g0186 | AFR | ACB | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG02523 | hp1 | a0002 | c0002 | t0001 | g0161 | EAS | KHV | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | KHV | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0106 | SAS | PJL | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG02602 | hp2 | a0002 | c0002 | t0002 | g0152 | SAS | PJL | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG02615 | hp1 | a0001 | c0001 | t0002 | g0122 | AFR | GWD | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG02615 | hp2 | a0002 | c0002 | t0001 | g0118 | AFR | GWD | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG02622 | hp1 | a0003 | c0003 | t0004 | g0200 | AFR | GWD | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG02622 | hp2 | a0002 | c0002 | t0013 | g0107 | AFR | GWD | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG02630 | hp1 | a0001 | c0001 | t0002 | g0078 | AFR | GWD | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG02630 | hp2 | a0003 | c0003 | t0005 | g0127 | AFR | GWD | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG02647 | hp1 | a0002 | c0002 | t0002 | g0110 | AFR | GWD | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG02647 | hp2 | a0002 | c0002 | t0002 | g0157 | AFR | GWD | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0105 | SAS | PJL | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0024 | SAS | PJL | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG02723 | hp1 | a0004 | c0004 | t0002 | g0146 | AFR | GWD | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG02723 | hp2 | a0005 | c0005 | t0002 | g0133 | AFR | GWD | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0097 | SAS | PJL | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG02738 | hp2 | a0003 | c0003 | t0004 | g0017 | SAS | PJL | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG02809 | hp1 | a0001 | c0001 | t0002 | g0005 | AFR | GWD | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG02809 | hp2 | a0003 | c0003 | t0005 | g0197 | AFR | GWD | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG02818 | hp1 | a0003 | c0003 | t0005 | g0113 | AFR | GWD | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0198 | AFR | GWD | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG02886 | hp1 | a0003 | c0003 | t0002 | g0190 | AFR | GWD | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG02886 | hp2 | a0002 | c0002 | t0002 | g0212 | AFR | GWD | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG02895 | hp1 | a0003 | c0003 | t0005 | g0126 | AFR | GWD | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG02895 | hp2 | a0002 | c0002 | t0002 | g0003 | AFR | GWD | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG02896 | hp1 | a0006 | c0006 | t0002 | g0193 | AFR | GWD | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG02896 | hp2 | a0004 | c0004 | t0002 | g0147 | AFR | GWD | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG02897 | hp1 | a0006 | c0006 | t0002 | g0195 | AFR | GWD | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG02897 | hp2 | a0002 | c0002 | t0002 | g0003 | AFR | GWD | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | ESN | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG02922 | hp2 | a0002 | c0002 | t0002 | g0108 | AFR | ESN | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG02965 | hp1 | a0001 | c0001 | t0002 | g0203 | AFR | ESN | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG02965 | hp2 | a0013 | c0010 | t0002 | g0191 | AFR | ESN | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0206 | AFR | ESN | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG02970 | hp2 | a0001 | c0001 | t0002 | g0030 | AFR | ESN | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG02976 | hp1 | a0001 | c0001 | t0002 | g0005 | AFR | ESN | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG02976 | hp2 | a0002 | c0002 | t0002 | g0109 | AFR | ESN | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0041 | SAS | PJL | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0222 | SAS | PJL | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG03098 | hp1 | a0008 | c0008 | t0002 | g0001 | AFR | MSL | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | MSL | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG03130 | hp1 | a0002 | c0002 | t0001 | g0144 | AFR | ESN | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG03130 | hp2 | a0002 | c0002 | t0002 | g0104 | AFR | ESN | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG03139 | hp1 | a0004 | c0004 | t0002 | g0153 | AFR | ESN | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG03139 | hp2 | a0002 | c0002 | t0002 | g0192 | AFR | ESN | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG03195 | hp1 | a0004 | c0004 | t0002 | g0145 | AFR | ESN | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0124 | AFR | ESN | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0215 | AFR | MSL | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0199 | AFR | MSL | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG03225 | hp1 | a0004 | c0004 | t0002 | g0141 | AFR | MSL | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG03225 | hp2 | a0001 | c0001 | t0004 | g0214 | AFR | MSL | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG03453 | hp1 | a0002 | c0002 | t0001 | g0119 | AFR | MSL | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG03453 | hp2 | a0003 | c0003 | t0002 | g0217 | AFR | MSL | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG03486 | hp1 | a0002 | c0002 | t0001 | g0116 | AFR | MSL | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG03486 | hp2 | a0002 | c0002 | t0001 | g0180 | AFR | MSL | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG03490 | hp1 | a0002 | c0002 | t0003 | g0166 | SAS | PJL | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0220 | SAS | PJL | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG03492 | hp1 | a0001 | c0001 | t0008 | g0045 | SAS | PJL | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG03492 | hp2 | a0002 | c0002 | t0003 | g0172 | SAS | PJL | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG03516 | hp1 | a0002 | c0002 | t0001 | g0125 | AFR | ESN | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG03516 | hp2 | a0003 | c0003 | t0001 | g0120 | AFR | ESN | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0021 | SAS | PJL | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG03654 | hp2 | a0002 | c0002 | t0002 | g0139 | SAS | PJL | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG03688 | hp1 | a0002 | c0002 | t0002 | g0196 | SAS | STU | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG03688 | hp2 | a0001 | c0001 | t0008 | g0058 | SAS | STU | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG03710 | hp1 | a0002 | c0002 | t0001 | g0164 | SAS | PJL | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0221 | SAS | PJL | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG03927 | hp1 | a0002 | c0002 | t0002 | g0140 | SAS | BEB | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0185 | SAS | BEB | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG03942 | hp2 | a0002 | c0002 | t0009 | g0228 | SAS | BEB | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG04115 | hp1 | a0002 | c0002 | t0002 | g0034 | SAS | STU | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG04115 | hp2 | a0002 | c0002 | t0002 | g0154 | SAS | STU | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0072 | SAS | BEB | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG04184 | hp2 | a0002 | c0002 | t0002 | g0159 | SAS | BEB | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG04199 | hp1 | a0002 | c0002 | t0003 | g0023 | SAS | STU | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG04199 | hp2 | a0002 | c0002 | t0002 | g0169 | SAS | STU | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG04204 | hp1 | a0002 | c0002 | t0002 | g0168 | SAS | STU | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG04204 | hp2 | a0001 | c0001 | t0006 | g0098 | SAS | STU | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| NA18522 | hp1 | a0005 | c0005 | t0001 | g0135 | AFR | YRI | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0201 | AFR | YRI | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | YRI | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| NA18906 | hp2 | a0007 | c0007 | t0002 | g0183 | AFR | YRI | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| NA18942 | hp1 | a0002 | c0002 | t0002 | g0063 | EAS | JPT | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| NA18950 | hp1 | a0002 | c0002 | t0001 | g0061 | EAS | JPT | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| NA18950 | hp2 | a0001 | c0001 | t0002 | g0099 | EAS | JPT | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| NA18953 | hp2 | a0002 | c0002 | t0002 | g0143 | EAS | JPT | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| NA18956 | hp1 | a0001 | c0001 | t0014 | g0076 | EAS | JPT | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| NA18956 | hp2 | a0002 | c0002 | t0002 | g0081 | EAS | JPT | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| NA18963 | hp1 | a0002 | c0002 | t0003 | g0181 | EAS | JPT | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| NA18974 | hp1 | a0002 | c0002 | t0002 | g0007 | EAS | JPT | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| NA18979 | hp1 | a0002 | c0002 | t0002 | g0066 | EAS | JPT | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| NA18979 | hp2 | a0002 | c0002 | t0001 | g0092 | EAS | JPT | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| NA18982 | hp1 | a0009 | c0009 | t0001 | g0156 | EAS | JPT | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| NA18994 | hp1 | a0002 | c0002 | t0002 | g0163 | EAS | JPT | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| NA18998 | hp2 | a0002 | c0002 | t0002 | g0043 | EAS | JPT | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| NA19002 | hp1 | a0002 | c0002 | t0001 | g0088 | EAS | JPT | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| NA19002 | hp2 | a0001 | c0001 | t0012 | g0080 | EAS | JPT | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| NA19004 | hp1 | a0002 | c0002 | t0002 | g0162 | EAS | JPT | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| NA19005 | hp2 | a0002 | c0002 | t0001 | g0070 | EAS | JPT | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| NA19009 | hp1 | a0002 | c0002 | t0002 | g0028 | EAS | JPT | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| NA19030 | hp1 | a0003 | c0003 | t0002 | g0218 | AFR | LWK | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | LWK | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0204 | AFR | LWK | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| NA19043 | hp2 | a0003 | c0003 | t0015 | g0129 | AFR | LWK | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| NA19060 | hp2 | a0002 | c0002 | t0002 | g0085 | EAS | JPT | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| NA19064 | hp2 | a0002 | c0002 | t0001 | g0089 | EAS | JPT | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| NA19072 | hp1 | a0002 | c0002 | t0003 | g0048 | EAS | JPT | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| NA19072 | hp2 | a0002 | c0002 | t0001 | g0177 | EAS | JPT | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| NA19074 | hp1 | a0009 | c0009 | t0001 | g0049 | EAS | JPT | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| NA19074 | hp2 | a0002 | c0002 | t0001 | g0093 | EAS | JPT | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| NA19077 | hp1 | a0002 | c0002 | t0002 | g0082 | EAS | JPT | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| NA19079 | hp2 | a0002 | c0002 | t0002 | g0029 | EAS | JPT | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| NA19086 | hp1 | a0002 | c0002 | t0002 | g0027 | EAS | JPT | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| NA19086 | hp2 | a0002 | c0002 | t0003 | g0178 | EAS | JPT | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| NA19240 | hp1 | a0003 | c0003 | t0005 | g0128 | AFR | YRI | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| NA19240 | hp2 | a0001 | c0001 | t0002 | g0050 | AFR | YRI | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| NA20129 | hp1 | a0010 | c0012 | t0010 | g0123 | AFR | ASW | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0207 | AFR | ASW | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| NA20752 | hp1 | a0002 | c0002 | t0002 | g0151 | EUR | TSI | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0053 | EUR | TSI | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0018 | EUR | TSI | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0069 | EUR | TSI | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG02486 | hp1 | a0002 | c0002 | t0002 | g0111 | AFR | ACB | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG02486 | hp2 | a0001 | c0001 | t0002 | g0025 | AFR | ACB | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG02559 | hp1 | a0004 | c0004 | t0002 | g0142 | AFR | ACB | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG02559 | hp2 | a0005 | c0005 | t0001 | g0134 | AFR | ACB | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG03471 | hp1 | a0003 | c0003 | t0002 | g0209 | AFR | MSL | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG03471 | hp2 | a0003 | c0003 | t0002 | g0216 | AFR | MSL | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | USA | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| HG06807 | hp2 | a0002 | c0002 | t0002 | g0211 | AFR | USA | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0205 | AFR | USA | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | USA | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| NA21309 | hp1 | a0003 | c0003 | t0001 | g0219 | AFR | LWK | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| NA21309 | hp2 | a0002 | c0002 | t0002 | g0188 | AFR | LWK | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| homoSapiens_chm13v2 | hp1 | a0002 | c0002 | t0003 | g0171 | REF | REF | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| homoSapiens_grch38 | hp1 | a0003 | c0003 | t0004 | g0057 | REF | REF | NPNT_chr4_105890471_105976671 | NPNT | chr4 | 105890471 | 105976671 |
| chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:105897987
|
G | C | 1 | a0006 | 2 | HG02896.hp1 HG02897.hp1 |
missense_variant | MODERATE | c.158G>C | p.Trp53Ser | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/12 | 340/4561 | 158/1698 | 53/565 | chr4 | 105897987 | ||
| chr4:105938382
|
C | T | 1 | a0005 | 4 | HG01884.hp2 HG02559.hp2 HG02723.hp2 others(1): Show |
missense_variant | MODERATE | c.467C>T | p.Pro156Leu | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 5/12 | 649/4561 | 467/1698 | 156/565 | chr4 | 105938382 | ||
| chr4:105938392
|
G | C | 4 | a0002a0004a0006others(1): Show | 94 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(91): Show |
missense_variant | MODERATE | c.477G>C | p.Gln159His | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 5/12 | 659/4561 | 477/1698 | 159/565 | chr4 | 105938392 | ||
| chr4:105940089
|
G | A | 1 | a0013 | 1 | HG02965.hp2 | missense_variant | MODERATE | c.520G>A | p.Ala174Thr | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 6/12 | 702/4561 | 520/1698 | 174/565 | chr4 | 105940089 | ||
| chr4:105940573
|
A | G | 7 | a0001a0002a0004others(4): Show | 200 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(197): Show |
missense_variant | MODERATE | c.700A>G | p.Ile234Val | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 7/12 | 882/4561 | 700/1698 | 234/565 | chr4 | 105940573 | ||
| chr4:105942325
|
T | C | 1 | a0011 | 1 | HG01070.hp2 | missense_variant | MODERATE | c.782T>C | p.Ile261Thr | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/12 | 964/4561 | 782/1698 | 261/565 | chr4 | 105942325 | ||
| chr4:105942469
|
G | A | 1 | a0007 | 2 | HG02451.hp2 NA18906.hp2 |
missense_variant | MODERATE | c.926G>A | p.Arg309Lys | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/12 | 1108/4561 | 926/1698 | 309/565 | chr4 | 105942469 | ||
| chr4:105967259
|
G | A | 2 | a0004a0008 | 8 | HG00735.hp1 HG02559.hp1 HG02723.hp1 others(5): Show |
missense_variant | MODERATE | c.1417G>A | p.Gly473Ser | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 11/12 | 1599/4561 | 1417/1698 | 473/565 | chr4 | 105967259 | ||
| chr4:105967269
|
T | C | 2 | a0010a0012 | 2 | HG02280.hp2 NA20129.hp1 |
missense_variant | MODERATE | c.1427T>C | p.Met476Thr | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 11/12 | 1609/4561 | 1427/1698 | 476/565 | chr4 | 105967269 | ||
| chr4:105968920
|
G | A | 1 | a0009 | 2 | NA18982.hp1 NA19074.hp1 |
missense_variant | MODERATE | c.1628G>A | p.Arg543His | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 12/12 | 1810/4561 | 1628/1698 | 543/565 | chr4 | 105968920 |
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:105927367
|
A | G | 1 | a0003c0014 | 1 | HG01192.hp2 | synonymous_variant | LOW | c.204A>G | p.Glu68Glu | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/12 | 386/4561 | 204/1698 | 68/565 | chr4 | 105927367 |
| chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:105969030
|
C | A | 1 | a0003c0003t0007 | 2 | HG00140.hp1 HG00741.hp2 |
3_prime_UTR_variant | MODIFIER | c.*40C>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 12/12 | 40 | chr4 | 105969030 | |||||
| chr4:105969035
|
T | G | 1 | a0001c0001t0011 | 1 | HG02280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*45T>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 12/12 | 45 | chr4 | 105969035 | |||||
| chr4:105969193
|
G | A | 2 | a0001c0001t0006a0002c0002t0006 | 5 | HG00735.hp2 HG00741.hp1 HG01346.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*203G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 12/12 | 203 | chr4 | 105969193 | |||||
| chr4:105969197
|
C | G | 2 | a0010c0012t0010a0012c0013t0010 | 2 | HG02280.hp2 NA20129.hp1 |
3_prime_UTR_variant | MODIFIER | c.*207C>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 12/12 | 207 | chr4 | 105969197 | |||||
| chr4:105969213
|
C | T | 5 | a0001c0001t0005a0003c0003t0005a0003c0003t0015others(2): Show | 10 | HG02055.hp1 HG02280.hp2 HG02451.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*223C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 12/12 | 223 | chr4 | 105969213 | |||||
| chr4:105969702
|
G | A | 3 | a0001c0001t0005a0003c0003t0005a0003c0003t0015 | 8 | HG02055.hp1 HG02451.hp1 HG02630.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*712G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 12/12 | 712 | chr4 | 105969702 | |||||
| chr4:105970196
|
C | T | 1 | a0001c0001t0014 | 1 | NA18956.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1206C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 12/12 | 1206 | chr4 | 105970196 | |||||
| chr4:105970260
|
G | A | 1 | a0001c0001t0008 | 2 | HG03492.hp1 HG03688.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1270G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 12/12 | 1270 | chr4 | 105970260 | |||||
| chr4:105970374
|
A | G | 17 | a0001c0001t0001a0001c0001t0005a0001c0001t0006others(14): Show | 116 | HG00408.hp2 HG00438.hp2 HG00597.hp1 others(113): Show |
3_prime_UTR_variant | MODIFIER | c.*1384A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 12/12 | 1384 | chr4 | 105970374 | |||||
| chr4:105970688
|
T | A | 5 | a0001c0001t0005a0003c0003t0005a0003c0003t0015others(2): Show | 10 | HG02055.hp1 HG02280.hp2 HG02451.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1698T>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 12/12 | 1698 | chr4 | 105970688 | |||||
| chr4:105970737
|
G | A | 5 | a0001c0001t0005a0003c0003t0005a0003c0003t0015others(2): Show | 10 | HG02055.hp1 HG02280.hp2 HG02451.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1747G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 12/12 | 1747 | chr4 | 105970737 | |||||
| chr4:105970781
|
C | G | 1 | a0002c0002t0013 | 1 | HG02622.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1791C>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 12/12 | 1791 | chr4 | 105970781 | |||||
| chr4:105971038
|
C | A | 5 | a0001c0001t0005a0003c0003t0005a0003c0003t0015others(2): Show | 10 | HG02055.hp1 HG02280.hp2 HG02451.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*2048C>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 12/12 | 2048 | chr4 | 105971038 | |||||
| chr4:105971053
|
T | G | 31 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(28): Show | 226 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(223): Show |
3_prime_UTR_variant | MODIFIER | c.*2063T>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 12/12 | 2063 | chr4 | 105971053 | |||||
| chr4:105971151
|
C | T | 1 | a0002c0002t0009 | 2 | HG00099.hp1 HG03942.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2161C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 12/12 | 2161 | chr4 | 105971151 | |||||
| chr4:105971180
|
C | T | 2 | a0001c0001t0005a0003c0003t0005 | 7 | HG02055.hp1 HG02451.hp1 HG02630.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2190C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 12/12 | 2190 | chr4 | 105971180 | |||||
| chr4:105971393
|
T | C | 5 | a0001c0001t0005a0003c0003t0005a0003c0003t0015others(2): Show | 10 | HG02055.hp1 HG02280.hp2 HG02451.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*2403T>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 12/12 | 2403 | chr4 | 105971393 | |||||
| chr4:105971401
|
C | T | 1 | a0001c0001t0012 | 1 | NA19002.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2411C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 12/12 | 2411 | chr4 | 105971401 | |||||
| chr4:105971418
|
G | A | 2 | a0001c0001t0003a0002c0002t0003 | 14 | HG00408.hp1 HG00438.hp1 HG00597.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*2428G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 12/12 | 2428 | chr4 | 105971418 | |||||
| chr4:105971489
|
T | C | 5 | a0001c0001t0005a0003c0003t0005a0003c0003t0015others(2): Show | 10 | HG02055.hp1 HG02280.hp2 HG02451.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*2499T>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 12/12 | 2499 | chr4 | 105971489 |
| chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:105895757
|
C | A | 1 | a0002c0002t0002g0007 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.71+34C>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 1/11 | chr4 | 105895757 | ||||||
| chr4:105895947
|
C | T | 1 | a0001c0001t0001g0229 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.71+224C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 1/11 | chr4 | 105895947 | ||||||
| chr4:105896018
|
C | T | 3 | a0002c0002t0009g0227a0002c0002t0009g0228a0003c0003t0004g0226 | 3 | HG00099.hp1 HG00642.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.71+295C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 1/11 | chr4 | 105896018 | ||||||
| chr4:105896035
|
T | C | 1 | a0001c0001t0001g0008 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.71+312T>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 1/11 | chr4 | 105896035 | ||||||
| chr4:105896064
|
A | G | 129 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0137others(126): Show | 134 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(131): Show |
intron_variant | MODIFIER | c.71+341A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 1/11 | chr4 | 105896064 | ||||||
| chr4:105896077
|
C | T | 1 | a0002c0002t0003g0225 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.71+354C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 1/11 | chr4 | 105896077 | ||||||
| chr4:105896105
|
G | C | 1 | a0001c0001t0001g0009 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.71+382G>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 1/11 | chr4 | 105896105 | ||||||
| chr4:105896258
|
G | T | 1 | a0003c0003t0004g0224 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.71+535G>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 1/11 | chr4 | 105896258 | ||||||
| chr4:105896335
|
A | C | 8 | a0001c0001t0001g0105a0001c0001t0002g0106a0001c0001t0002g0220others(5): Show | 8 | HG00280.hp2 HG01081.hp1 HG02602.hp1 others(5): Show |
intron_variant | MODIFIER | c.71+612A>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 1/11 | chr4 | 105896335 | ||||||
| chr4:105896376
|
G | C | 1 | a0002c0002t0013g0107 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.71+653G>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 1/11 | chr4 | 105896376 | ||||||
| chr4:105896589
|
T | C | 19 | a0001c0001t0002g0122a0001c0001t0005g0112a0001c0001t0011g0115others(16): Show | 20 | HG00735.hp1 HG01109.hp2 HG01243.hp2 others(17): Show |
intron_variant | MODIFIER | c.71+866T>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 1/11 | chr4 | 105896589 | ||||||
| chr4:105896699
|
T | C | 4 | a0002c0002t0002g0108a0002c0002t0002g0109a0002c0002t0002g0110others(1): Show | 4 | HG02486.hp1 HG02647.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.71+976T>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 1/11 | chr4 | 105896699 | ||||||
| chr4:105896939
|
T | C | 16 | a0001c0001t0002g0124a0001c0001t0005g0112a0002c0002t0001g0125others(13): Show | 16 | HG01070.hp2 HG01192.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.72-962T>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 1/11 | chr4 | 105896939 | ||||||
| chr4:105897099
|
A | G | 9 | a0001c0001t0002g0122a0001c0001t0002g0215a0001c0001t0004g0214others(6): Show | 10 | HG00735.hp1 HG01243.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.72-802A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 1/11 | chr4 | 105897099 | ||||||
| chr4:105897435
|
C | G | 37 | a0001c0001t0001g0006a0001c0001t0001g0198a0001c0001t0001g0199others(34): Show | 39 | HG00735.hp1 HG01069.hp1 HG01070.hp2 others(36): Show |
intron_variant | MODIFIER | c.72-466C>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 1/11 | chr4 | 105897435 | ||||||
| chr4:105897691
|
G | A | 3 | a0001c0001t0002g0124a0001c0001t0005g0112a0002c0002t0013g0107 | 3 | HG02451.hp1 HG02622.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.72-210G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 1/11 | chr4 | 105897691 | ||||||
| chr4:105897712
|
A | C | 1 | a0003c0003t0015g0129 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.72-189A>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 1/11 | chr4 | 105897712 | ||||||
| chr4:105897742
|
T | A | 1 | a0012c0013t0010g0136 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.72-159T>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 1/11 | chr4 | 105897742 | ||||||
| chr4:105897754
|
G | A | 2 | a0003c0014t0001g0131a0011c0011t0002g0130 | 2 | HG01070.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.72-147G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 1/11 | chr4 | 105897754 | ||||||
| chr4:105897826
|
G | A | 34 | a0001c0001t0001g0006a0001c0001t0001g0198a0001c0001t0001g0199others(31): Show | 36 | HG00735.hp1 HG00735.hp2 HG01069.hp1 others(33): Show |
intron_variant | MODIFIER | c.72-75G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 1/11 | chr4 | 105897826 | ||||||
| chr4:105897896
|
G | A | 13 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0018others(10): Show | 13 | HG00099.hp2 HG00140.hp1 HG00639.hp1 others(10): Show |
splice_region_variant&intron_variant | LOW | c.72-5G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 1/11 | chr4 | 105897896 | ||||||
| chr4:105898245
|
T | C | 1 | a0001c0001t0001g0138 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.172+244T>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105898245 | ||||||
| chr4:105898289
|
TTTCTCTC others(30): Show |
T | 1 | a0001c0001t0005g0112 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.172+290_172+326del others(37): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 105898289 | |||||
| chr4:105898290
|
TTCTCTCT others(31): Show |
T | 1 | a0003c0003t0015g0129 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.172+311_172+348del others(38): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 105898290 | |||||
| chr4:105898290
|
TTCTCTCT others(33): Show |
T | 6 | a0003c0003t0001g0114a0003c0003t0001g0219a0005c0005t0001g0132others(3): Show | 6 | HG01884.hp2 HG02145.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.172+311_172+350del others(40): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 105898290 | |||||
| chr4:105898294
|
CTCTCTCT others(27): Show |
C | 10 | a0001c0001t0002g0215a0003c0003t0001g0210a0003c0003t0002g0001others(7): Show | 11 | HG00735.hp1 HG01081.hp1 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.172+311_172+344del others(34): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 105898294 | |||||
| chr4:105898296
|
CTCTCTCT others(25): Show |
C | 2 | a0001c0001t0002g0124a0010c0012t0010g0123 | 2 | HG03195.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.172+311_172+342del others(32): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 105898296 | |||||
| chr4:105898298
|
CTCTCTCT others(23): Show |
C | 2 | a0001c0001t0002g0207a0001c0001t0004g0214 | 2 | HG03225.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.172+311_172+340del others(30): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 105898298 | |||||
| chr4:105898300
|
CTCTCTCT others(21): Show |
C | 1 | a0002c0002t0013g0107 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.172+311_172+338del others(28): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 105898300 | |||||
| chr4:105898308
|
CTCTGTCT others(13): Show |
C | 1 | a0001c0001t0002g0122 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.172+311_172+330del others(20): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 105898308 | |||||
| chr4:105898312
|
GTCTCTCT others(11): Show |
G | 1 | a0003c0003t0004g0011 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.172+327_172+344del others(18): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 105898312 | |||||
| chr4:105898312
|
GTCTCTCT others(17): Show |
G | 2 | a0001c0001t0001g0198a0003c0003t0005g0197 | 2 | HG02809.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.172+327_172+350del others(24): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 105898312 | |||||
| chr4:105898312
|
GTCTCTCT others(19): Show |
G | 1 | a0001c0001t0001g0199 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.172+327_172+352del others(26): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 105898312 | |||||
| chr4:105898312
|
GTCTCTCT others(21): Show |
G | 2 | a0001c0001t0001g0006a0003c0003t0004g0200 | 3 | HG01069.hp1 HG01192.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.172+327_172+354del others(28): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 105898312 | |||||
| chr4:105898312
|
GTCTCTCT others(23): Show |
G | 1 | a0011c0011t0002g0130 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.172+327_172+356del others(30): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 105898312 | |||||
| chr4:105898312
|
GTCTCTCT others(25): Show |
G | 6 | a0001c0001t0001g0201a0001c0001t0001g0205a0001c0001t0001g0206others(3): Show | 6 | HG01975.hp2 HG02965.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.172+327_172+358del others(32): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 105898312 | |||||
| chr4:105898318
|
CTCTCTCT others(3): Show |
C | 1 | a0001c0001t0011g0115 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.172+327_172+336del others(10): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 105898318 | |||||
| chr4:105898320
|
C | CTCTCCTC others(4): Show |
2 | a0002c0002t0002g0139a0002c0002t0002g0140 | 2 | HG03654.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.172+323_172+324ins others(11): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 105898320 | |||||
| chr4:105898324
|
C | G | 1 | a0003c0014t0001g0131 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.172+323C>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105898324 | ||||||
| chr4:105898326
|
CTG | C | 3 | a0001c0001t0001g0022a0003c0014t0001g0131a0004c0004t0002g0141 | 3 | HG01106.hp2 HG01192.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.172+327_172+328del others(2): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 105898326 | |||||
| chr4:105898328
|
G | C | 4 | a0001c0001t0002g0220a0001c0001t0005g0112a0002c0002t0002g0139others(1): Show | 4 | HG02451.hp1 HG03490.hp2 HG03654.hp2 others(1): Show |
intron_variant | MODIFIER | c.172+327G>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105898328 | ||||||
| chr4:105898328
|
G | GTC | 18 | a0001c0001t0001g0060a0001c0001t0001g0064a0001c0001t0001g0067others(15): Show | 18 | HG00408.hp2 HG00438.hp2 HG00639.hp2 others(15): Show |
intron_variant | MODIFIER | c.172+378_172+379dup others(2): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 105898328 | |||||
| chr4:105898328
|
G | GTCTC | 23 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0071others(20): Show | 24 | HG00280.hp2 HG00639.hp1 HG00735.hp2 others(21): Show |
intron_variant | MODIFIER | c.172+376_172+379dup others(4): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 105898328 | |||||
| chr4:105898328
|
G | GTCTCCCT others(11): Show |
1 | a0002c0002t0003g0023 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.172+331_172+332ins others(18): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 105898328 | |||||
| chr4:105898328
|
G | GTCTCTC | 14 | a0001c0001t0001g0021a0001c0001t0001g0079a0001c0001t0001g0083others(11): Show | 14 | HG01167.hp1 HG01361.hp2 HG02080.hp2 others(11): Show |
intron_variant | MODIFIER | c.172+374_172+379dup others(6): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 105898328 | |||||
| chr4:105898328
|
G | GTCTCTCT others(1): Show |
11 | a0001c0001t0001g0002a0001c0001t0001g0090a0001c0001t0001g0170others(8): Show | 12 | HG02055.hp2 HG02886.hp2 HG03492.hp2 others(9): Show |
intron_variant | MODIFIER | c.172+372_172+379dup others(8): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 105898328 | |||||
| chr4:105898328
|
G | GTCTCTCT others(3): Show |
11 | a0001c0001t0001g0094a0001c0001t0001g0174a0001c0001t0001g0229others(8): Show | 11 | HG00438.hp1 HG01243.hp1 HG01255.hp2 others(8): Show |
intron_variant | MODIFIER | c.172+370_172+379dup others(10): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 105898328 | |||||
| chr4:105898328
|
G | GTCTCTCT others(5): Show |
10 | a0001c0001t0001g0095a0001c0001t0001g0097a0001c0001t0006g0096others(7): Show | 10 | HG00597.hp2 HG01175.hp2 HG01516.hp1 others(7): Show |
intron_variant | MODIFIER | c.172+368_172+379dup others(12): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 105898328 | |||||
| chr4:105898328
|
G | GTCTCTCT others(7): Show |
4 | a0001c0001t0002g0099a0001c0001t0002g0185a0002c0002t0003g0184others(1): Show | 4 | HG00408.hp1 HG03927.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.172+366_172+379dup others(14): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 105898328 | |||||
| chr4:105898328
|
G | GTCTCTCT others(9): Show |
1 | a0007c0007t0002g0186 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.172+364_172+379dup others(16): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 105898328 | |||||
| chr4:105898328
|
G | GTCTCTCT others(13): Show |
3 | a0001c0001t0001g0187a0002c0002t0001g0118a0002c0002t0001g0119 | 3 | HG01175.hp1 HG02615.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.172+360_172+379dup others(20): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 105898328 | |||||
| chr4:105898328
|
G | GTCTCTCT others(15): Show |
1 | a0002c0002t0002g0188 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.172+358_172+379dup others(22): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 105898328 | |||||
| chr4:105898328
|
G | GTCTCTCT others(19): Show |
1 | a0001c0001t0001g0189 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.172+354_172+379dup others(26): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 105898328 | |||||
| chr4:105898328
|
G | GTCTGTCT others(7): Show |
1 | a0002c0002t0002g0196 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.172+330_172+331ins others(14): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 105898328 | |||||
| chr4:105898328
|
GTC | G | 17 | a0001c0001t0001g0041a0001c0001t0001g0044a0001c0001t0001g0046others(14): Show | 17 | HG00280.hp1 HG00741.hp1 HG00741.hp2 others(14): Show |
intron_variant | MODIFIER | c.172+378_172+379del others(2): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 105898328 | |||||
| chr4:105898328
|
GTCTC | G | 10 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0038others(7): Show | 10 | HG00140.hp2 HG00597.hp1 HG02602.hp1 others(7): Show |
intron_variant | MODIFIER | c.172+376_172+379del others(4): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 105898328 | |||||
| chr4:105898328
|
GTCTCTC | G | 9 | a0001c0001t0001g0014a0001c0001t0001g0031a0001c0001t0001g0032others(6): Show | 9 | HG01074.hp2 HG02083.hp1 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.172+374_172+379del others(6): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 105898328 | |||||
| chr4:105898328
|
GTCTCTCT others(1): Show |
G | 6 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0138others(3): Show | 7 | HG02257.hp2 HG02486.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.172+372_172+379del others(8): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 105898328 | |||||
| chr4:105898328
|
GTCTCTCT others(3): Show |
G | 5 | a0001c0001t0001g0024a0001c0001t0002g0005a0002c0002t0001g0144others(2): Show | 6 | HG02559.hp1 HG02698.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.172+370_172+379del others(10): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 105898328 | |||||
| chr4:105898328
|
GTCTCTCT others(5): Show |
G | 1 | a0001c0001t0003g0012 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.172+368_172+379del others(12): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 105898328 | |||||
| chr4:105898330
|
C | CTCTCTCT others(7): Show |
1 | a0006c0006t0002g0195 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.172+342_172+343ins others(14): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 105898330 | |||||
| chr4:105898330
|
C | G | 1 | a0001c0001t0002g0122 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.172+329C>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105898330 | ||||||
| chr4:105898332
|
C | CTCTCTCT others(5): Show |
2 | a0001c0001t0001g0194a0006c0006t0002g0193 | 2 | HG02896.hp1 NA18957.hp2 |
intron_variant | MODIFIER | c.172+342_172+343ins others(12): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 105898332 | |||||
| chr4:105898332
|
C | G | 1 | a0004c0004t0002g0141 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.172+331C>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105898332 | ||||||
| chr4:105898334
|
C | CTCTCTCT others(3): Show |
1 | a0002c0002t0002g0192 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.172+342_172+343ins others(10): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 105898334 | |||||
| chr4:105898334
|
C | G | 1 | a0001c0001t0001g0022 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.172+333C>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105898334 | ||||||
| chr4:105898340
|
C | G | 2 | a0001c0001t0002g0207a0001c0001t0004g0214 | 2 | HG03225.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.172+339C>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105898340 | ||||||
| chr4:105898342
|
C | G | 1 | a0010c0012t0010g0123 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.172+341C>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105898342 | ||||||
| chr4:105898344
|
C | G | 10 | a0001c0001t0002g0215a0003c0003t0001g0210a0003c0003t0002g0001others(7): Show | 11 | HG00735.hp1 HG01081.hp1 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.172+343C>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105898344 | ||||||
| chr4:105898350
|
C | G | 6 | a0003c0003t0001g0114a0003c0003t0001g0219a0005c0005t0001g0132others(3): Show | 6 | HG01884.hp2 HG02145.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.172+349C>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105898350 | ||||||
| chr4:105898352
|
C | G | 1 | a0001c0001t0001g0008 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.172+351C>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105898352 | ||||||
| chr4:105898354
|
C | G | 1 | a0001c0001t0002g0005 | 2 | HG02809.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.172+353C>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105898354 | ||||||
| chr4:105898362
|
C | G | 4 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102others(1): Show | 4 | HG01069.hp2 HG01346.hp1 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.172+361C>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105898362 | ||||||
| chr4:105898380
|
C | CTCTCTCT others(7): Show |
5 | a0001c0001t0002g0213a0002c0002t0001g0125a0003c0003t0001g0120others(2): Show | 5 | HG02055.hp1 HG02257.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.172+379_172+380ins others(14): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105898380 | ||||||
| chr4:105898380
|
C | CTCTCTCT others(5): Show |
4 | a0003c0003t0002g0190a0003c0003t0005g0126a0003c0003t0005g0127others(1): Show | 4 | HG02630.hp2 HG02886.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.172+379_172+380ins others(12): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105898380 | ||||||
| chr4:105898380
|
C | T | 37 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0138others(34): Show | 40 | HG00735.hp1 HG01069.hp1 HG01070.hp2 others(37): Show |
intron_variant | MODIFIER | c.172+379C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105898380 | ||||||
| chr4:105898408
|
ATGGGGAT others(29): Show |
A | 3 | a0001c0001t0001g0060a0001c0001t0001g0079a0001c0001t0012g0080 | 3 | HG02080.hp2 HG02083.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.172+444_172+479del others(36): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 105898408 | |||||
| chr4:105898456
|
T | C | 5 | a0003c0003t0004g0011a0003c0003t0004g0017a0003c0003t0004g0226others(2): Show | 5 | HG00099.hp2 HG00140.hp1 HG00642.hp2 others(2): Show |
intron_variant | MODIFIER | c.172+455T>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105898456 | ||||||
| chr4:105898633
|
C | T | 27 | a0001c0001t0002g0185a0002c0002t0001g0165a0002c0002t0001g0173others(24): Show | 27 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(24): Show |
intron_variant | MODIFIER | c.172+632C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105898633 | ||||||
| chr4:105898667
|
T | C | 1 | a0002c0002t0001g0165 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.172+666T>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105898667 | ||||||
| chr4:105898723
|
A | G | 11 | a0001c0001t0001g0006a0001c0001t0001g0198a0001c0001t0001g0199others(8): Show | 12 | HG01069.hp1 HG01192.hp1 HG01975.hp2 others(9): Show |
intron_variant | MODIFIER | c.172+722A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105898723 | ||||||
| chr4:105898732
|
T | C | 87 | a0001c0001t0001g0041a0001c0001t0002g0185a0001c0001t0011g0115others(84): Show | 89 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(86): Show |
intron_variant | MODIFIER | c.172+731T>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105898732 | ||||||
| chr4:105898979
|
T | C | 5 | a0001c0001t0001g0006a0001c0001t0001g0198a0001c0001t0001g0199others(2): Show | 6 | HG01069.hp1 HG01192.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.172+978T>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105898979 | ||||||
| chr4:105899104
|
G | A | 7 | a0001c0001t0002g0122a0001c0001t0002g0124a0001c0001t0002g0215others(4): Show | 7 | HG02451.hp1 HG02615.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.172+1103G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105899104 | ||||||
| chr4:105899187
|
T | G | 30 | a0001c0001t0001g0006a0001c0001t0001g0198a0001c0001t0001g0199others(27): Show | 32 | HG00735.hp1 HG01069.hp1 HG01070.hp2 others(29): Show |
intron_variant | MODIFIER | c.172+1186T>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105899187 | ||||||
| chr4:105899390
|
A | G | 17 | a0001c0001t0002g0207a0003c0003t0001g0114a0003c0003t0001g0210others(14): Show | 18 | HG00735.hp1 HG01081.hp1 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.172+1389A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105899390 | ||||||
| chr4:105899468
|
A | G | 3 | a0002c0002t0002g0007a0002c0002t0002g0081a0002c0002t0002g0082 | 3 | NA18956.hp2 NA18974.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.172+1467A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105899468 | ||||||
| chr4:105899545
|
C | T | 17 | a0001c0001t0002g0207a0003c0003t0001g0114a0003c0003t0001g0210others(14): Show | 18 | HG00735.hp1 HG01081.hp1 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.172+1544C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105899545 | ||||||
| chr4:105899575
|
G | A | 11 | a0001c0001t0001g0006a0001c0001t0001g0198a0001c0001t0001g0199others(8): Show | 12 | HG01069.hp1 HG01192.hp1 HG01975.hp2 others(9): Show |
intron_variant | MODIFIER | c.172+1574G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105899575 | ||||||
| chr4:105899626
|
G | A | 1 | a0013c0010t0002g0191 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.172+1625G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105899626 | ||||||
| chr4:105899679
|
T | C | 51 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0138others(48): Show | 54 | HG00735.hp1 HG01069.hp1 HG01070.hp2 others(51): Show |
intron_variant | MODIFIER | c.172+1678T>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105899679 | ||||||
| chr4:105900228
|
A | G | 1 | a0001c0001t0002g0078 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.172+2227A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105900228 | ||||||
| chr4:105900276
|
G | A | 1 | a0002c0002t0003g0048 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.172+2275G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105900276 | ||||||
| chr4:105900277
|
A | G | 1 | a0002c0002t0003g0048 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.172+2276A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105900277 | ||||||
| chr4:105900304
|
T | C | 1 | a0002c0002t0003g0048 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.172+2303T>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105900304 | ||||||
| chr4:105900305
|
C | T | 1 | a0002c0002t0003g0048 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.172+2304C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105900305 | ||||||
| chr4:105900331
|
T | C | 1 | a0011c0011t0002g0130 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.172+2330T>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105900331 | ||||||
| chr4:105900421
|
C | T | 30 | a0001c0001t0001g0006a0001c0001t0001g0198a0001c0001t0001g0199others(27): Show | 32 | HG00735.hp1 HG01069.hp1 HG01070.hp2 others(29): Show |
intron_variant | MODIFIER | c.172+2420C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105900421 | ||||||
| chr4:105900487
|
C | G | 1 | a0003c0003t0015g0129 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.172+2486C>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105900487 | ||||||
| chr4:105900569
|
C | T | 4 | a0003c0003t0002g0001a0003c0003t0002g0217a0003c0003t0002g0218others(1): Show | 5 | HG00735.hp1 HG01243.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.172+2568C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105900569 | ||||||
| chr4:105900595
|
G | T | 1 | a0001c0001t0002g0124 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.172+2594G>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105900595 | ||||||
| chr4:105900831
|
GTTGT | G | 6 | a0001c0001t0002g0122a0001c0001t0002g0124a0001c0001t0002g0215others(3): Show | 6 | HG02451.hp1 HG02615.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.172+2833_172+2836d others(6): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 105900831 | |||||
| chr4:105900831
|
GTTGTT | G | 12 | a0001c0001t0002g0005a0001c0001t0002g0213a0002c0002t0001g0125others(9): Show | 13 | HG02055.hp1 HG02257.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.172+2833_172+2837d others(7): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 105900831 | |||||
| chr4:105900834
|
G | GT | 29 | a0001c0001t0001g0059a0001c0001t0001g0077a0001c0001t0001g0087others(26): Show | 30 | HG00735.hp1 HG01069.hp2 HG01070.hp1 others(27): Show |
intron_variant | MODIFIER | c.172+2853dupT | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 105900834 | |||||
| chr4:105900834
|
GT | G | 14 | a0001c0001t0001g0024a0001c0001t0001g0094a0001c0001t0006g0010others(11): Show | 14 | HG00408.hp1 HG00438.hp1 HG00597.hp2 others(11): Show |
intron_variant | MODIFIER | c.172+2853delT | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 105900834 | |||||
| chr4:105900840
|
T | TTTG | 5 | a0001c0001t0001g0006a0001c0001t0001g0198a0001c0001t0001g0199others(2): Show | 6 | HG01069.hp1 HG01192.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.172+2841_172+2842i others(5): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 105900840 | |||||
| chr4:105900841
|
T | TTG | 6 | a0001c0001t0001g0201a0001c0001t0001g0205a0001c0001t0001g0206others(3): Show | 6 | HG01975.hp2 HG02965.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.172+2841_172+2842i others(4): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 105900841 | |||||
| chr4:105900964
|
G | T | 1 | a0013c0010t0002g0191 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.172+2963G>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105900964 | ||||||
| chr4:105901099
|
T | C | 19 | a0001c0001t0002g0005a0001c0001t0002g0122a0001c0001t0002g0124others(16): Show | 20 | HG02055.hp1 HG02257.hp1 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.172+3098T>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105901099 | ||||||
| chr4:105901144
|
A | G | 1 | a0003c0003t0001g0114 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.172+3143A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105901144 | ||||||
| chr4:105901162
|
C | T | 19 | a0001c0001t0002g0005a0001c0001t0002g0122a0001c0001t0002g0124others(16): Show | 20 | HG02055.hp1 HG02257.hp1 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.172+3161C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105901162 | ||||||
| chr4:105901357
|
A | G | 5 | a0002c0002t0002g0027a0002c0002t0002g0028a0002c0002t0002g0029others(2): Show | 5 | NA18942.hp1 NA18998.hp2 NA19009.hp1 others(2): Show |
intron_variant | MODIFIER | c.172+3356A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105901357 | ||||||
| chr4:105901542
|
G | T | 19 | a0001c0001t0002g0005a0001c0001t0002g0122a0001c0001t0002g0124others(16): Show | 20 | HG02055.hp1 HG02257.hp1 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.172+3541G>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105901542 | ||||||
| chr4:105901703
|
A | T | 1 | a0011c0011t0002g0130 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.172+3702A>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105901703 | ||||||
| chr4:105901796
|
C | T | 11 | a0001c0001t0001g0006a0001c0001t0001g0198a0001c0001t0001g0199others(8): Show | 12 | HG01069.hp1 HG01192.hp1 HG01975.hp2 others(9): Show |
intron_variant | MODIFIER | c.172+3795C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105901796 | ||||||
| chr4:105901807
|
A | G | 1 | a0001c0001t0004g0214 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.172+3806A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105901807 | ||||||
| chr4:105902114
|
G | T | 1 | a0003c0003t0015g0129 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.172+4113G>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105902114 | ||||||
| chr4:105902143
|
A | C | 2 | a0002c0002t0002g0162a0002c0002t0002g0163 | 2 | NA18994.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.172+4142A>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105902143 | ||||||
| chr4:105902299
|
C | T | 1 | a0002c0002t0001g0177 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.172+4298C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105902299 | ||||||
| chr4:105902328
|
C | G | 1 | a0003c0014t0001g0131 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.172+4327C>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105902328 | ||||||
| chr4:105902356
|
G | A | 11 | a0001c0001t0002g0005a0001c0001t0002g0122a0001c0001t0002g0124others(8): Show | 12 | HG02257.hp1 HG02280.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.172+4355G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105902356 | ||||||
| chr4:105902428
|
T | C | 1 | a0003c0003t0005g0126 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.172+4427T>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105902428 | ||||||
| chr4:105902550
|
G | A | 11 | a0001c0001t0002g0005a0001c0001t0002g0122a0001c0001t0002g0124others(8): Show | 12 | HG02257.hp1 HG02280.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.172+4549G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105902550 | ||||||
| chr4:105902886
|
A | C | 1 | a0003c0003t0005g0121 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.172+4885A>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105902886 | ||||||
| chr4:105903220
|
C | T | 1 | a0001c0001t0002g0213 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.172+5219C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105903220 | ||||||
| chr4:105903232
|
C | A | 1 | a0012c0013t0010g0136 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.172+5231C>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105903232 | ||||||
| chr4:105903410
|
G | T | 1 | a0002c0002t0003g0023 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.172+5409G>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105903410 | ||||||
| chr4:105903481
|
G | C | 47 | a0001c0001t0001g0006a0001c0001t0001g0198a0001c0001t0001g0199others(44): Show | 50 | HG00735.hp1 HG01069.hp1 HG01070.hp2 others(47): Show |
intron_variant | MODIFIER | c.172+5480G>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105903481 | ||||||
| chr4:105903582
|
C | T | 11 | a0001c0001t0002g0005a0001c0001t0002g0122a0001c0001t0002g0124others(8): Show | 12 | HG02257.hp1 HG02280.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.172+5581C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105903582 | ||||||
| chr4:105903783
|
C | CT | 23 | a0001c0001t0008g0058a0002c0002t0001g0062a0002c0002t0002g0028others(20): Show | 23 | HG01070.hp2 HG01081.hp1 HG01255.hp1 others(20): Show |
intron_variant | MODIFIER | c.172+5801dupT | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 105903783 | |||||
| chr4:105903783
|
C | CTT | 14 | a0001c0001t0001g0006a0001c0001t0001g0198a0001c0001t0001g0199others(11): Show | 15 | HG01069.hp1 HG01192.hp1 HG01975.hp2 others(12): Show |
intron_variant | MODIFIER | c.172+5800_172+5801d others(4): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 105903783 | |||||
| chr4:105903783
|
C | CTTT | 7 | a0001c0001t0002g0122a0001c0001t0002g0213a0001c0001t0002g0215others(4): Show | 7 | HG01192.hp2 HG02257.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.172+5799_172+5801d others(5): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 105903783 | |||||
| chr4:105903802
|
T | G | 1 | a0002c0002t0002g0139 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.172+5801T>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105903802 | ||||||
| chr4:105903824
|
G | A | 1 | a0010c0012t0010g0123 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.172+5823G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105903824 | ||||||
| chr4:105903883
|
C | T | 2 | a0001c0001t0001g0205a0001c0001t0001g0206 | 2 | HG02970.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.172+5882C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105903883 | ||||||
| chr4:105903929
|
T | C | 11 | a0001c0001t0002g0005a0001c0001t0002g0122a0001c0001t0002g0124others(8): Show | 12 | HG02257.hp1 HG02280.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.172+5928T>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105903929 | ||||||
| chr4:105903970
|
T | C | 11 | a0001c0001t0002g0005a0001c0001t0002g0122a0001c0001t0002g0124others(8): Show | 12 | HG02257.hp1 HG02280.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.172+5969T>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105903970 | ||||||
| chr4:105904064
|
G | A | 5 | a0001c0001t0002g0122a0001c0001t0002g0124a0001c0001t0002g0215others(2): Show | 5 | HG02451.hp1 HG02615.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.172+6063G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105904064 | ||||||
| chr4:105904083
|
T | C | 11 | a0001c0001t0002g0005a0001c0001t0002g0122a0001c0001t0002g0124others(8): Show | 12 | HG02257.hp1 HG02280.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.172+6082T>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105904083 | ||||||
| chr4:105904100
|
A | G | 1 | a0004c0004t0002g0146 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.172+6099A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105904100 | ||||||
| chr4:105904112
|
T | C | 11 | a0001c0001t0002g0005a0001c0001t0002g0122a0001c0001t0002g0124others(8): Show | 12 | HG02257.hp1 HG02280.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.172+6111T>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105904112 | ||||||
| chr4:105904182
|
T | C | 11 | a0001c0001t0002g0005a0001c0001t0002g0122a0001c0001t0002g0124others(8): Show | 12 | HG02257.hp1 HG02280.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.172+6181T>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105904182 | ||||||
| chr4:105904230
|
G | A | 11 | a0001c0001t0002g0005a0001c0001t0002g0122a0001c0001t0002g0124others(8): Show | 12 | HG02257.hp1 HG02280.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.172+6229G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105904230 | ||||||
| chr4:105904252
|
G | C | 2 | a0001c0001t0002g0207a0012c0013t0010g0136 | 2 | HG02280.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.172+6251G>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105904252 | ||||||
| chr4:105904323
|
A | G | 1 | a0013c0010t0002g0191 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.172+6322A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105904323 | ||||||
| chr4:105904374
|
G | A | 47 | a0001c0001t0001g0006a0001c0001t0001g0198a0001c0001t0001g0199others(44): Show | 50 | HG00735.hp1 HG01069.hp1 HG01070.hp2 others(47): Show |
intron_variant | MODIFIER | c.172+6373G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105904374 | ||||||
| chr4:105904578
|
G | A | 2 | a0002c0002t0002g0162a0002c0002t0002g0163 | 2 | NA18994.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.172+6577G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105904578 | ||||||
| chr4:105904603
|
A | G | 11 | a0001c0001t0002g0005a0001c0001t0002g0122a0001c0001t0002g0124others(8): Show | 12 | HG02257.hp1 HG02280.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.172+6602A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105904603 | ||||||
| chr4:105904619
|
G | A | 11 | a0001c0001t0002g0005a0001c0001t0002g0122a0001c0001t0002g0124others(8): Show | 12 | HG02257.hp1 HG02280.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.172+6618G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105904619 | ||||||
| chr4:105904626
|
G | A | 11 | a0001c0001t0002g0005a0001c0001t0002g0122a0001c0001t0002g0124others(8): Show | 12 | HG02257.hp1 HG02280.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.172+6625G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105904626 | ||||||
| chr4:105904686
|
AT | A | 13 | a0003c0003t0001g0210a0003c0003t0002g0001a0003c0003t0002g0209others(10): Show | 14 | HG00735.hp1 HG01081.hp1 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.172+6695delT | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 105904686 | |||||
| chr4:105904797
|
A | G | 1 | a0003c0003t0015g0129 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.172+6796A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105904797 | ||||||
| chr4:105904849
|
T | G | 1 | a0003c0014t0001g0131 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.172+6848T>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105904849 | ||||||
| chr4:105904891
|
A | G | 1 | a0001c0001t0001g0086 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.172+6890A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105904891 | ||||||
| chr4:105904892
|
C | T | 1 | a0001c0001t0014g0076 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.172+6891C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105904892 | ||||||
| chr4:105904951
|
G | A | 1 | a0003c0003t0015g0129 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.172+6950G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105904951 | ||||||
| chr4:105904977
|
C | T | 1 | a0010c0012t0010g0123 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.172+6976C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105904977 | ||||||
| chr4:105905026
|
G | A | 4 | a0003c0003t0002g0001a0003c0003t0002g0217a0003c0003t0002g0218others(1): Show | 5 | HG00735.hp1 HG01243.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.172+7025G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105905026 | ||||||
| chr4:105905054
|
A | G | 18 | a0003c0003t0001g0114a0003c0003t0001g0210a0003c0003t0001g0219others(15): Show | 19 | HG00735.hp1 HG01081.hp1 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.172+7053A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105905054 | ||||||
| chr4:105905074
|
C | A | 1 | a0011c0011t0002g0130 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.172+7073C>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105905074 | ||||||
| chr4:105905074
|
CT | C | 11 | a0001c0001t0002g0005a0001c0001t0002g0122a0001c0001t0002g0124others(8): Show | 12 | HG02257.hp1 HG02280.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.172+7084delT | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 105905074 | |||||
| chr4:105905153
|
C | T | 1 | a0001c0001t0001g0075 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.172+7152C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105905153 | ||||||
| chr4:105905159
|
T | C | 18 | a0003c0003t0001g0114a0003c0003t0001g0210a0003c0003t0001g0219others(15): Show | 19 | HG00735.hp1 HG01081.hp1 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.172+7158T>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105905159 | ||||||
| chr4:105905204
|
A | G | 2 | a0001c0001t0002g0069a0013c0010t0002g0191 | 2 | HG02965.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.172+7203A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105905204 | ||||||
| chr4:105905315
|
G | A | 11 | a0001c0001t0002g0005a0001c0001t0002g0122a0001c0001t0002g0124others(8): Show | 12 | HG02257.hp1 HG02280.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.172+7314G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105905315 | ||||||
| chr4:105905436
|
T | A | 11 | a0001c0001t0002g0005a0001c0001t0002g0122a0001c0001t0002g0124others(8): Show | 12 | HG02257.hp1 HG02280.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.172+7435T>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105905436 | ||||||
| chr4:105905550
|
G | A | 1 | a0013c0010t0002g0191 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.172+7549G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105905550 | ||||||
| chr4:105905816
|
G | C | 48 | a0001c0001t0001g0006a0001c0001t0001g0138a0001c0001t0001g0198others(45): Show | 51 | HG00735.hp1 HG01069.hp1 HG01070.hp2 others(48): Show |
intron_variant | MODIFIER | c.172+7815G>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105905816 | ||||||
| chr4:105906176
|
G | A | 1 | a0011c0011t0002g0130 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.172+8175G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105906176 | ||||||
| chr4:105906268
|
A | C | 11 | a0001c0001t0002g0005a0001c0001t0002g0122a0001c0001t0002g0124others(8): Show | 12 | HG02257.hp1 HG02280.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.172+8267A>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105906268 | ||||||
| chr4:105906286
|
C | G | 11 | a0001c0001t0002g0005a0001c0001t0002g0122a0001c0001t0002g0124others(8): Show | 12 | HG02257.hp1 HG02280.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.172+8285C>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105906286 | ||||||
| chr4:105906311
|
G | A | 5 | a0002c0002t0002g0027a0002c0002t0002g0028a0002c0002t0002g0029others(2): Show | 5 | NA18942.hp1 NA18998.hp2 NA19009.hp1 others(2): Show |
intron_variant | MODIFIER | c.172+8310G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105906311 | ||||||
| chr4:105906331
|
G | A | 47 | a0001c0001t0001g0006a0001c0001t0001g0198a0001c0001t0001g0199others(44): Show | 50 | HG00735.hp1 HG01069.hp1 HG01070.hp2 others(47): Show |
intron_variant | MODIFIER | c.172+8330G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105906331 | ||||||
| chr4:105906343
|
C | A | 1 | a0001c0001t0001g0194 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.172+8342C>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105906343 | ||||||
| chr4:105906486
|
G | A | 29 | a0001c0001t0001g0006a0001c0001t0001g0198a0001c0001t0001g0199others(26): Show | 31 | HG01069.hp1 HG01070.hp2 HG01192.hp1 others(28): Show |
intron_variant | MODIFIER | c.172+8485G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105906486 | ||||||
| chr4:105906500
|
C | CA | 48 | a0001c0001t0001g0006a0001c0001t0001g0138a0001c0001t0001g0198others(45): Show | 51 | HG00735.hp1 HG01069.hp1 HG01070.hp2 others(48): Show |
intron_variant | MODIFIER | c.172+8499_172+8500i others(3): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105906500 | ||||||
| chr4:105906513
|
A | C | 11 | a0001c0001t0002g0005a0001c0001t0002g0122a0001c0001t0002g0124others(8): Show | 12 | HG02257.hp1 HG02280.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.172+8512A>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105906513 | ||||||
| chr4:105906708
|
A | G | 11 | a0001c0001t0002g0005a0001c0001t0002g0122a0001c0001t0002g0124others(8): Show | 12 | HG02257.hp1 HG02280.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.172+8707A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105906708 | ||||||
| chr4:105906773
|
A | T | 11 | a0001c0001t0002g0005a0001c0001t0002g0122a0001c0001t0002g0124others(8): Show | 12 | HG02257.hp1 HG02280.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.172+8772A>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105906773 | ||||||
| chr4:105906866
|
A | T | 16 | a0001c0001t0001g0006a0001c0001t0001g0198a0001c0001t0001g0199others(13): Show | 17 | HG01069.hp1 HG01192.hp1 HG01975.hp2 others(14): Show |
intron_variant | MODIFIER | c.172+8865A>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105906866 | ||||||
| chr4:105906872
|
A | G | 11 | a0001c0001t0002g0005a0001c0001t0002g0122a0001c0001t0002g0124others(8): Show | 12 | HG02257.hp1 HG02280.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.172+8871A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105906872 | ||||||
| chr4:105907269
|
C | T | 2 | a0002c0002t0002g0004a0002c0002t0002g0154 | 3 | HG01516.hp2 HG01517.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.172+9268C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105907269 | ||||||
| chr4:105907273
|
A | G | 18 | a0001c0001t0001g0006a0001c0001t0001g0198a0001c0001t0001g0199others(15): Show | 19 | HG01069.hp1 HG01070.hp2 HG01192.hp1 others(16): Show |
intron_variant | MODIFIER | c.172+9272A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105907273 | ||||||
| chr4:105907343
|
A | G | 5 | a0003c0003t0002g0001a0003c0003t0002g0216a0003c0003t0002g0217others(2): Show | 6 | HG00735.hp1 HG01243.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.172+9342A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105907343 | ||||||
| chr4:105907376
|
T | G | 11 | a0001c0001t0002g0005a0001c0001t0002g0122a0001c0001t0002g0124others(8): Show | 12 | HG02257.hp1 HG02280.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.172+9375T>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105907376 | ||||||
| chr4:105907471
|
C | A | 1 | a0001c0001t0002g0213 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.172+9470C>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105907471 | ||||||
| chr4:105907630
|
T | G | 5 | a0001c0001t0001g0071a0001c0001t0001g0083a0001c0001t0001g0087others(2): Show | 5 | NA18942.hp2 NA18957.hp1 NA19060.hp1 others(2): Show |
intron_variant | MODIFIER | c.172+9629T>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105907630 | ||||||
| chr4:105907638
|
T | C | 17 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0018others(14): Show | 17 | HG00099.hp2 HG00140.hp1 HG00639.hp1 others(14): Show |
intron_variant | MODIFIER | c.172+9637T>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105907638 | ||||||
| chr4:105907946
|
G | A | 1 | a0002c0002t0002g0151 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.172+9945G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105907946 | ||||||
| chr4:105908323
|
C | A | 3 | a0001c0001t0002g0030a0001c0001t0002g0050a0001c0001t0002g0078 | 3 | HG02630.hp1 HG02970.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.172+10322C>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105908323 | ||||||
| chr4:105908488
|
T | C | 144 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0041others(141): Show | 149 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(146): Show |
intron_variant | MODIFIER | c.172+10487T>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105908488 | ||||||
| chr4:105908569
|
C | CT | 20 | a0001c0001t0001g0006a0001c0001t0001g0086a0001c0001t0001g0198others(17): Show | 21 | HG01069.hp1 HG01192.hp1 HG01192.hp2 others(18): Show |
intron_variant | MODIFIER | c.172+10580dupT | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 105908569 | |||||
| chr4:105908569
|
CTT | C | 11 | a0001c0001t0002g0005a0001c0001t0002g0122a0001c0001t0002g0124others(8): Show | 12 | HG02257.hp1 HG02280.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.172+10579_172+1058 others(6): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 105908569 | |||||
| chr4:105908586
|
C | T | 16 | a0001c0001t0001g0006a0001c0001t0001g0198a0001c0001t0001g0199others(13): Show | 17 | HG01069.hp1 HG01192.hp1 HG01975.hp2 others(14): Show |
intron_variant | MODIFIER | c.172+10585C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105908586 | ||||||
| chr4:105908632
|
C | T | 1 | a0001c0001t0001g0008 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.172+10631C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105908632 | ||||||
| chr4:105908656
|
T | C | 1 | a0011c0011t0002g0130 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.172+10655T>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105908656 | ||||||
| chr4:105908756
|
G | C | 1 | a0011c0011t0002g0130 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.172+10755G>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105908756 | ||||||
| chr4:105908829
|
C | T | 1 | a0001c0001t0002g0222 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.172+10828C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105908829 | ||||||
| chr4:105909075
|
G | A | 139 | a0001c0001t0001g0006a0001c0001t0001g0041a0001c0001t0001g0138others(136): Show | 144 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(141): Show |
intron_variant | MODIFIER | c.172+11074G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105909075 | ||||||
| chr4:105909187
|
T | C | 1 | a0012c0013t0010g0136 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.172+11186T>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105909187 | ||||||
| chr4:105909426
|
T | A | 229 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0008others(226): Show | 235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): Show |
intron_variant | MODIFIER | c.172+11425T>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105909426 | ||||||
| chr4:105909648
|
T | C | 11 | a0001c0001t0002g0005a0001c0001t0002g0122a0001c0001t0002g0124others(8): Show | 12 | HG02257.hp1 HG02280.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.172+11647T>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105909648 | ||||||
| chr4:105909834
|
G | T | 18 | a0003c0003t0001g0114a0003c0003t0001g0210a0003c0003t0001g0219others(15): Show | 19 | HG00735.hp1 HG01081.hp1 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.172+11833G>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105909834 | ||||||
| chr4:105910030
|
A | T | 1 | a0011c0011t0002g0130 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.172+12029A>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105910030 | ||||||
| chr4:105910065
|
TA | T | 11 | a0001c0001t0002g0005a0001c0001t0002g0122a0001c0001t0002g0207others(8): Show | 12 | HG01361.hp1 HG02257.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.172+12076delA | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 105910065 | |||||
| chr4:105910121
|
G | A | 1 | a0011c0011t0002g0130 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.172+12120G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105910121 | ||||||
| chr4:105910143
|
C | T | 18 | a0003c0003t0001g0114a0003c0003t0001g0210a0003c0003t0001g0219others(15): Show | 19 | HG00735.hp1 HG01081.hp1 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.172+12142C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105910143 | ||||||
| chr4:105910189
|
G | A | 11 | a0001c0001t0002g0005a0001c0001t0002g0122a0001c0001t0002g0124others(8): Show | 12 | HG02257.hp1 HG02280.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.172+12188G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105910189 | ||||||
| chr4:105910256
|
A | G | 11 | a0001c0001t0002g0005a0001c0001t0002g0122a0001c0001t0002g0124others(8): Show | 12 | HG02257.hp1 HG02280.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.172+12255A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105910256 | ||||||
| chr4:105910261
|
G | T | 1 | a0001c0001t0002g0213 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.172+12260G>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105910261 | ||||||
| chr4:105910443
|
T | A | 11 | a0001c0001t0002g0005a0001c0001t0002g0122a0001c0001t0002g0124others(8): Show | 12 | HG02257.hp1 HG02280.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.172+12442T>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105910443 | ||||||
| chr4:105910502
|
CA | C | 37 | a0001c0001t0001g0006a0001c0001t0001g0138a0001c0001t0001g0198others(34): Show | 39 | HG00735.hp1 HG01069.hp1 HG01070.hp2 others(36): Show |
intron_variant | MODIFIER | c.172+12513delA | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 105910502 | |||||
| chr4:105910513
|
AATTGT | A | 10 | a0001c0001t0002g0005a0001c0001t0002g0122a0001c0001t0002g0124others(7): Show | 11 | HG02257.hp1 HG02280.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.172+12515_172+1251 others(9): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 105910513 | |||||
| chr4:105910519
|
A | T | 10 | a0001c0001t0002g0005a0001c0001t0002g0122a0001c0001t0002g0124others(7): Show | 11 | HG02257.hp1 HG02280.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.172+12518A>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105910519 | ||||||
| chr4:105910526
|
G | T | 10 | a0001c0001t0002g0005a0001c0001t0002g0122a0001c0001t0002g0124others(7): Show | 11 | HG02257.hp1 HG02280.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.172+12525G>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105910526 | ||||||
| chr4:105910605
|
G | T | 1 | a0003c0014t0001g0131 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.172+12604G>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105910605 | ||||||
| chr4:105910888
|
A | C | 3 | a0002c0002t0002g0108a0002c0002t0002g0109a0002c0002t0002g0110 | 3 | HG02647.hp1 HG02922.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.172+12887A>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105910888 | ||||||
| chr4:105910935
|
C | T | 16 | a0001c0001t0001g0006a0001c0001t0001g0198a0001c0001t0001g0199others(13): Show | 17 | HG01069.hp1 HG01192.hp1 HG01975.hp2 others(14): Show |
intron_variant | MODIFIER | c.172+12934C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105910935 | ||||||
| chr4:105911047
|
A | G | 1 | a0001c0001t0001g0041 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.172+13046A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105911047 | ||||||
| chr4:105911355
|
G | A | 1 | a0011c0011t0002g0130 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.172+13354G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105911355 | ||||||
| chr4:105911452
|
C | A | 11 | a0001c0001t0002g0005a0001c0001t0002g0122a0001c0001t0002g0124others(8): Show | 12 | HG02257.hp1 HG02280.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.172+13451C>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105911452 | ||||||
| chr4:105911563
|
G | T | 1 | a0001c0001t0002g0005 | 2 | HG02809.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.172+13562G>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105911563 | ||||||
| chr4:105911596
|
G | T | 11 | a0001c0001t0002g0005a0001c0001t0002g0122a0001c0001t0002g0124others(8): Show | 12 | HG02257.hp1 HG02280.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.172+13595G>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105911596 | ||||||
| chr4:105911602
|
A | G | 6 | a0003c0003t0002g0001a0003c0003t0002g0216a0003c0003t0002g0217others(3): Show | 7 | HG00735.hp1 HG01243.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.172+13601A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105911602 | ||||||
| chr4:105911792
|
T | C | 1 | a0002c0002t0002g0182 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.172+13791T>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105911792 | ||||||
| chr4:105911983
|
T | G | 1 | a0002c0002t0003g0184 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.172+13982T>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105911983 | ||||||
| chr4:105912011
|
T | A | 1 | a0001c0001t0001g0138 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.172+14010T>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105912011 | ||||||
| chr4:105912368
|
C | T | 11 | a0001c0001t0002g0005a0001c0001t0002g0122a0001c0001t0002g0124others(8): Show | 12 | HG02257.hp1 HG02280.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.172+14367C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105912368 | ||||||
| chr4:105912449
|
G | A | 11 | a0001c0001t0002g0005a0001c0001t0002g0122a0001c0001t0002g0124others(8): Show | 12 | HG02257.hp1 HG02280.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.172+14448G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105912449 | ||||||
| chr4:105912690
|
TATA | T | 16 | a0001c0001t0001g0006a0001c0001t0001g0198a0001c0001t0001g0199others(13): Show | 17 | HG01069.hp1 HG01192.hp1 HG01975.hp2 others(14): Show |
intron_variant | MODIFIER | c.173-14642_173-1464 others(7): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 105912690 | |||||
| chr4:105912753
|
A | G | 1 | a0002c0002t0002g0004 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.173-14583A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105912753 | ||||||
| chr4:105912763
|
C | T | 1 | a0007c0007t0002g0183 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.173-14573C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105912763 | ||||||
| chr4:105912798
|
T | C | 1 | a0013c0010t0002g0191 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.173-14538T>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105912798 | ||||||
| chr4:105912809
|
G | A | 1 | a0003c0003t0002g0209 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.173-14527G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105912809 | ||||||
| chr4:105912956
|
C | T | 1 | a0003c0014t0001g0131 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.173-14380C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105912956 | ||||||
| chr4:105913004
|
A | T | 2 | a0001c0001t0002g0122a0001c0001t0002g0215 | 2 | HG02615.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.173-14332A>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105913004 | ||||||
| chr4:105913143
|
A | G | 11 | a0001c0001t0002g0005a0001c0001t0002g0122a0001c0001t0002g0124others(8): Show | 12 | HG02257.hp1 HG02280.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.173-14193A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105913143 | ||||||
| chr4:105913207
|
T | C | 11 | a0001c0001t0002g0005a0001c0001t0002g0122a0001c0001t0002g0124others(8): Show | 12 | HG02257.hp1 HG02280.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.173-14129T>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105913207 | ||||||
| chr4:105913284
|
G | T | 11 | a0001c0001t0002g0005a0001c0001t0002g0122a0001c0001t0002g0124others(8): Show | 12 | HG02257.hp1 HG02280.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.173-14052G>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105913284 | ||||||
| chr4:105913381
|
G | A | 1 | a0001c0001t0001g0138 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.173-13955G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105913381 | ||||||
| chr4:105913466
|
A | G | 11 | a0001c0001t0002g0005a0001c0001t0002g0122a0001c0001t0002g0124others(8): Show | 12 | HG02257.hp1 HG02280.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.173-13870A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105913466 | ||||||
| chr4:105913467
|
A | G | 1 | a0001c0001t0001g0138 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.173-13869A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105913467 | ||||||
| chr4:105913500
|
A | G | 1 | a0001c0001t0002g0207 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.173-13836A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105913500 | ||||||
| chr4:105913825
|
T | G | 16 | a0001c0001t0001g0006a0001c0001t0001g0198a0001c0001t0001g0199others(13): Show | 17 | HG01069.hp1 HG01192.hp1 HG01975.hp2 others(14): Show |
intron_variant | MODIFIER | c.173-13511T>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105913825 | ||||||
| chr4:105914177
|
A | G | 11 | a0001c0001t0002g0005a0001c0001t0002g0122a0001c0001t0002g0124others(8): Show | 12 | HG02257.hp1 HG02280.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.173-13159A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105914177 | ||||||
| chr4:105914367
|
C | CTA | 6 | a0001c0001t0002g0005a0003c0003t0001g0114a0003c0003t0001g0219others(3): Show | 7 | HG01884.hp2 HG02145.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.173-12968_173-1296 others(6): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 105914367 | |||||
| chr4:105914369
|
C | A | 16 | a0001c0001t0001g0138a0001c0001t0002g0005a0001c0001t0002g0122others(13): Show | 17 | HG01192.hp2 HG01884.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.173-12967C>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105914369 | ||||||
| chr4:105914371
|
C | A | 54 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0079others(51): Show | 58 | HG00735.hp1 HG01069.hp1 HG01081.hp1 others(55): Show |
intron_variant | MODIFIER | c.173-12965C>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105914371 | ||||||
| chr4:105914373
|
C | A | 103 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0013others(100): Show | 107 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(104): Show |
intron_variant | MODIFIER | c.173-12963C>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105914373 | ||||||
| chr4:105914375
|
A | C | 9 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0038others(6): Show | 9 | HG00735.hp2 HG02280.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.173-12961A>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105914375 | ||||||
| chr4:105914382
|
T | A | 2 | a0001c0001t0002g0207a0012c0013t0010g0136 | 2 | HG02280.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.173-12954T>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105914382 | ||||||
| chr4:105914383
|
A | T | 2 | a0001c0001t0002g0207a0012c0013t0010g0136 | 2 | HG02280.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.173-12953A>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105914383 | ||||||
| chr4:105914480
|
T | G | 11 | a0001c0001t0001g0071a0001c0001t0001g0083a0001c0001t0001g0087others(8): Show | 11 | HG01255.hp2 HG02004.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.173-12856T>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105914480 | ||||||
| chr4:105914480
|
TAGAGAGA others(6): Show |
T | 1 | a0001c0001t0002g0122 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.173-12854_173-1284 others(17): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 105914480 | |||||
| chr4:105914482
|
G | T | 29 | a0001c0001t0001g0006a0001c0001t0001g0018a0001c0001t0001g0020others(26): Show | 30 | HG00140.hp2 HG01069.hp1 HG01106.hp1 others(27): Show |
intron_variant | MODIFIER | c.173-12854G>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105914482 | ||||||
| chr4:105914483
|
AGAGAGAG others(6): Show |
A | 2 | a0001c0001t0002g0215a0001c0001t0004g0214 | 2 | HG03209.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.173-12844_173-1283 others(17): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 105914483 | |||||
| chr4:105914484
|
G | T | 4 | a0003c0003t0005g0113a0003c0003t0005g0126a0003c0003t0005g0127others(1): Show | 4 | HG02630.hp2 HG02818.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.173-12852G>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105914484 | ||||||
| chr4:105914496
|
G | A | 1 | a0001c0001t0002g0122 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.173-12840G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105914496 | ||||||
| chr4:105914502
|
A | G | 2 | a0003c0003t0004g0200a0003c0003t0005g0197 | 2 | HG02622.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.173-12834A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105914502 | ||||||
| chr4:105914522
|
C | G | 16 | a0001c0001t0001g0006a0001c0001t0001g0198a0001c0001t0001g0199others(13): Show | 17 | HG01069.hp1 HG01192.hp1 HG01975.hp2 others(14): Show |
intron_variant | MODIFIER | c.173-12814C>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105914522 | ||||||
| chr4:105914816
|
C | T | 1 | a0003c0003t0005g0121 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.173-12520C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105914816 | ||||||
| chr4:105914850
|
G | A | 11 | a0001c0001t0002g0005a0001c0001t0002g0122a0001c0001t0002g0124others(8): Show | 12 | HG02257.hp1 HG02280.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.173-12486G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105914850 | ||||||
| chr4:105914881
|
G | C | 11 | a0001c0001t0002g0005a0001c0001t0002g0122a0001c0001t0002g0124others(8): Show | 12 | HG02257.hp1 HG02280.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.173-12455G>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105914881 | ||||||
| chr4:105915031
|
A | G | 19 | a0003c0003t0001g0114a0003c0003t0001g0210a0003c0003t0001g0219others(16): Show | 20 | HG00735.hp1 HG01070.hp2 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.173-12305A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105915031 | ||||||
| chr4:105915100
|
C | T | 48 | a0001c0001t0001g0006a0001c0001t0001g0138a0001c0001t0001g0198others(45): Show | 51 | HG00735.hp1 HG01069.hp1 HG01070.hp2 others(48): Show |
intron_variant | MODIFIER | c.173-12236C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105915100 | ||||||
| chr4:105915144
|
C | T | 18 | a0003c0003t0001g0114a0003c0003t0001g0210a0003c0003t0001g0219others(15): Show | 19 | HG00735.hp1 HG01081.hp1 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.173-12192C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105915144 | ||||||
| chr4:105915171
|
A | C | 1 | a0013c0010t0002g0191 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.173-12165A>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105915171 | ||||||
| chr4:105915620
|
G | T | 1 | a0002c0002t0001g0161 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.173-11716G>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105915620 | ||||||
| chr4:105915722
|
T | C | 1 | a0001c0001t0001g0077 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.173-11614T>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105915722 | ||||||
| chr4:105915737
|
G | A | 30 | a0001c0001t0001g0138a0001c0001t0002g0005a0001c0001t0002g0122others(27): Show | 32 | HG00735.hp1 HG01070.hp2 HG01081.hp1 others(29): Show |
intron_variant | MODIFIER | c.173-11599G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105915737 | ||||||
| chr4:105915780
|
T | G | 1 | a0001c0001t0001g0138 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.173-11556T>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105915780 | ||||||
| chr4:105915881
|
T | C | 1 | a0002c0002t0001g0118 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.173-11455T>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105915881 | ||||||
| chr4:105915902
|
T | A | 16 | a0001c0001t0001g0006a0001c0001t0001g0198a0001c0001t0001g0199others(13): Show | 17 | HG01069.hp1 HG01192.hp1 HG01975.hp2 others(14): Show |
intron_variant | MODIFIER | c.173-11434T>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105915902 | ||||||
| chr4:105915905
|
A | C | 2 | a0001c0001t0002g0207a0012c0013t0010g0136 | 2 | HG02280.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.173-11431A>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105915905 | ||||||
| chr4:105915925
|
A | G | 1 | a0001c0001t0001g0199 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.173-11411A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105915925 | ||||||
| chr4:105916132
|
G | T | 1 | a0013c0010t0002g0191 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.173-11204G>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105916132 | ||||||
| chr4:105916196
|
A | T | 8 | a0001c0001t0002g0005a0001c0001t0002g0122a0001c0001t0002g0124others(5): Show | 9 | HG02257.hp1 HG02451.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.173-11140A>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105916196 | ||||||
| chr4:105916217
|
C | T | 1 | a0001c0001t0001g0021 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.173-11119C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105916217 | ||||||
| chr4:105916221
|
C | CT | 19 | a0003c0003t0001g0114a0003c0003t0001g0210a0003c0003t0001g0219others(16): Show | 20 | HG00735.hp1 HG01070.hp2 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.173-11103dupT | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 105916221 | |||||
| chr4:105916221
|
CT | C | 5 | a0001c0001t0002g0122a0001c0001t0002g0124a0001c0001t0002g0215others(2): Show | 5 | HG02451.hp1 HG02615.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.173-11103delT | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 105916221 | |||||
| chr4:105916248
|
C | T | 1 | a0001c0001t0002g0124 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.173-11088C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105916248 | ||||||
| chr4:105916269
|
G | C | 1 | a0002c0002t0002g0026 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.173-11067G>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105916269 | ||||||
| chr4:105916386
|
AT | A | 4 | a0001c0001t0001g0008a0001c0001t0001g0201a0001c0001t0002g0005others(1): Show | 5 | HG00741.hp1 HG02809.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.173-10934delT | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 105916386 | |||||
| chr4:105916461
|
A | G | 1 | a0001c0001t0001g0100 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.173-10875A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105916461 | ||||||
| chr4:105916691
|
T | A | 1 | a0002c0002t0001g0042 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.173-10645T>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105916691 | ||||||
| chr4:105916769
|
G | A | 36 | a0001c0001t0001g0006a0001c0001t0001g0198a0001c0001t0001g0199others(33): Show | 38 | HG00735.hp1 HG01069.hp1 HG01070.hp2 others(35): Show |
intron_variant | MODIFIER | c.173-10567G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105916769 | ||||||
| chr4:105916779
|
A | G | 36 | a0001c0001t0001g0006a0001c0001t0001g0198a0001c0001t0001g0199others(33): Show | 38 | HG00735.hp1 HG01069.hp1 HG01070.hp2 others(35): Show |
intron_variant | MODIFIER | c.173-10557A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105916779 | ||||||
| chr4:105916790
|
C | T | 1 | a0001c0001t0003g0012 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.173-10546C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105916790 | ||||||
| chr4:105916962
|
G | T | 3 | a0001c0001t0002g0122a0001c0001t0002g0215a0001c0001t0004g0214 | 3 | HG02615.hp1 HG03209.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.173-10374G>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105916962 | ||||||
| chr4:105916987
|
G | GACCTTAT others(1): Show |
19 | a0003c0003t0001g0114a0003c0003t0001g0210a0003c0003t0001g0219others(16): Show | 20 | HG00735.hp1 HG01070.hp2 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.173-10346_173-1033 others(12): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 105916987 | |||||
| chr4:105917047
|
A | G | 1 | a0013c0010t0002g0191 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.173-10289A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105917047 | ||||||
| chr4:105917177
|
A | T | 47 | a0001c0001t0001g0006a0001c0001t0001g0138a0001c0001t0001g0198others(44): Show | 50 | HG00735.hp1 HG01069.hp1 HG01070.hp2 others(47): Show |
intron_variant | MODIFIER | c.173-10159A>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105917177 | ||||||
| chr4:105917270
|
T | C | 7 | a0002c0002t0002g0003a0004c0004t0002g0141a0004c0004t0002g0142others(4): Show | 8 | HG02559.hp1 HG02723.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.173-10066T>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105917270 | ||||||
| chr4:105917572
|
A | C | 2 | a0002c0002t0002g0004a0002c0002t0002g0154 | 3 | HG01516.hp2 HG01517.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.173-9764A>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105917572 | ||||||
| chr4:105917685
|
T | G | 1 | a0004c0004t0002g0153 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.173-9651T>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105917685 | ||||||
| chr4:105917861
|
T | C | 36 | a0001c0001t0001g0006a0001c0001t0001g0198a0001c0001t0001g0199others(33): Show | 38 | HG00735.hp1 HG01069.hp1 HG01070.hp2 others(35): Show |
intron_variant | MODIFIER | c.173-9475T>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105917861 | ||||||
| chr4:105917873
|
T | C | 6 | a0001c0001t0002g0122a0001c0001t0002g0124a0001c0001t0002g0215others(3): Show | 6 | HG02451.hp1 HG02615.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.173-9463T>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105917873 | ||||||
| chr4:105917874
|
G | T | 1 | a0003c0003t0001g0210 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.173-9462G>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105917874 | ||||||
| chr4:105917953
|
A | G | 1 | a0002c0002t0001g0144 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.173-9383A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105917953 | ||||||
| chr4:105917981
|
G | A | 36 | a0001c0001t0001g0006a0001c0001t0001g0198a0001c0001t0001g0199others(33): Show | 38 | HG00735.hp1 HG01069.hp1 HG01070.hp2 others(35): Show |
intron_variant | MODIFIER | c.173-9355G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105917981 | ||||||
| chr4:105918027
|
C | T | 1 | a0013c0010t0002g0191 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.173-9309C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105918027 | ||||||
| chr4:105918694
|
G | A | 1 | a0001c0001t0002g0005 | 2 | HG02809.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.173-8642G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105918694 | ||||||
| chr4:105918732
|
A | C | 19 | a0003c0003t0001g0114a0003c0003t0001g0210a0003c0003t0001g0219others(16): Show | 20 | HG00735.hp1 HG01070.hp2 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.173-8604A>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105918732 | ||||||
| chr4:105918740
|
T | C | 3 | a0002c0002t0001g0116a0002c0002t0001g0118a0002c0002t0001g0125 | 3 | HG02615.hp2 HG03486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.173-8596T>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105918740 | ||||||
| chr4:105918924
|
G | T | 36 | a0001c0001t0001g0006a0001c0001t0001g0198a0001c0001t0001g0199others(33): Show | 38 | HG00735.hp1 HG01069.hp1 HG01070.hp2 others(35): Show |
intron_variant | MODIFIER | c.173-8412G>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105918924 | ||||||
| chr4:105919007
|
G | T | 18 | a0003c0003t0001g0114a0003c0003t0001g0210a0003c0003t0001g0219others(15): Show | 19 | HG00735.hp1 HG01081.hp1 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.173-8329G>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105919007 | ||||||
| chr4:105919240
|
A | C | 35 | a0001c0001t0001g0006a0001c0001t0001g0198a0001c0001t0001g0199others(32): Show | 37 | HG00735.hp1 HG01069.hp1 HG01070.hp2 others(34): Show |
intron_variant | MODIFIER | c.173-8096A>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105919240 | ||||||
| chr4:105919241
|
T | C | 1 | a0013c0010t0002g0191 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.173-8095T>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105919241 | ||||||
| chr4:105919302
|
G | C | 91 | a0001c0001t0001g0041a0001c0001t0002g0185a0001c0001t0011g0115others(88): Show | 93 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(90): Show |
intron_variant | MODIFIER | c.173-8034G>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105919302 | ||||||
| chr4:105919468
|
G | C | 1 | a0002c0002t0002g0212 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.173-7868G>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105919468 | ||||||
| chr4:105919474
|
A | G | 1 | a0013c0010t0002g0191 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.173-7862A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105919474 | ||||||
| chr4:105919794
|
TAA | T | 18 | a0003c0003t0001g0114a0003c0003t0001g0210a0003c0003t0001g0219others(15): Show | 19 | HG00735.hp1 HG01081.hp1 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.173-7541_173-7540d others(4): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105919794 | ||||||
| chr4:105919976
|
AATT | A | 2 | a0002c0002t0009g0227a0002c0002t0009g0228 | 2 | HG00099.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.173-7356_173-7354d others(5): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 105919976 | |||||
| chr4:105920093
|
C | T | 3 | a0002c0002t0002g0157a0002c0002t0002g0160a0002c0002t0002g0182 | 3 | HG01175.hp2 HG02145.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.173-7243C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105920093 | ||||||
| chr4:105920395
|
T | TA | 7 | a0001c0001t0001g0032a0001c0001t0002g0005a0001c0001t0002g0124others(4): Show | 8 | HG01175.hp2 HG02257.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.173-6917dupA | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 105920395 | |||||
| chr4:105920395
|
T | TAAAA | 10 | a0003c0003t0001g0114a0003c0003t0001g0210a0003c0003t0001g0219others(7): Show | 10 | HG01081.hp1 HG01884.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.173-6920_173-6917d others(6): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 105920395 | |||||
| chr4:105920395
|
T | TAAAAA | 6 | a0001c0001t0002g0204a0003c0003t0002g0001a0003c0003t0002g0209others(3): Show | 7 | HG00735.hp1 HG01243.hp2 HG02004.hp2 others(4): Show |
intron_variant | MODIFIER | c.173-6921_173-6917d others(7): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 105920395 | |||||
| chr4:105920395
|
T | TAAAAAAA others(8): Show |
1 | a0001c0001t0001g0198 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.173-6931_173-6917d others(17): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 105920395 | |||||
| chr4:105920395
|
T | TAAAAAAA others(9): Show |
4 | a0001c0001t0001g0006a0001c0001t0001g0199a0001c0001t0001g0206others(1): Show | 5 | HG01069.hp1 HG01192.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.173-6932_173-6917d others(18): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 105920395 | |||||
| chr4:105920395
|
T | TAAAAAAA others(10): Show |
2 | a0001c0001t0001g0205a0001c0001t0002g0202 | 2 | HG01975.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.173-6933_173-6917d others(19): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 105920395 | |||||
| chr4:105920395
|
T | TAAAAAAA others(18): Show |
1 | a0003c0014t0001g0131 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.173-6917_173-6916i others(27): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 105920395 | |||||
| chr4:105920395
|
T | TAAAAAAA others(21): Show |
4 | a0003c0003t0002g0190a0003c0003t0005g0113a0003c0003t0005g0127others(1): Show | 4 | HG02630.hp2 HG02818.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.173-6917_173-6916i others(30): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 105920395 | |||||
| chr4:105920395
|
T | TAAAAAAA others(23): Show |
2 | a0003c0003t0001g0120a0003c0003t0005g0126 | 2 | HG02895.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.173-6917_173-6916i others(32): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 105920395 | |||||
| chr4:105920395
|
T | TAAAAAAA others(29): Show |
1 | a0003c0003t0005g0121 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.173-6917_173-6916i others(38): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 105920395 | |||||
| chr4:105920395
|
TA | T | 157 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(154): Show | 160 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(157): Show |
intron_variant | MODIFIER | c.173-6917delA | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 105920395 | |||||
| chr4:105920465
|
A | G | 2 | a0006c0006t0002g0193a0006c0006t0002g0195 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.173-6871A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105920465 | ||||||
| chr4:105920560
|
C | G | 35 | a0001c0001t0001g0006a0001c0001t0001g0198a0001c0001t0001g0199others(32): Show | 37 | HG00735.hp1 HG01069.hp1 HG01070.hp2 others(34): Show |
intron_variant | MODIFIER | c.173-6776C>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105920560 | ||||||
| chr4:105920590
|
A | G | 3 | a0002c0002t0001g0116a0002c0002t0001g0118a0002c0002t0001g0125 | 3 | HG02615.hp2 HG03486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.173-6746A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105920590 | ||||||
| chr4:105920660
|
C | T | 2 | a0002c0002t0002g0004a0002c0002t0002g0154 | 3 | HG01516.hp2 HG01517.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.173-6676C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105920660 | ||||||
| chr4:105920721
|
G | C | 1 | a0012c0013t0010g0136 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.173-6615G>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105920721 | ||||||
| chr4:105920758
|
T | G | 15 | a0001c0001t0001g0006a0001c0001t0001g0198a0001c0001t0001g0199others(12): Show | 16 | HG01069.hp1 HG01192.hp1 HG01975.hp2 others(13): Show |
intron_variant | MODIFIER | c.173-6578T>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105920758 | ||||||
| chr4:105920805
|
G | T | 157 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0032others(154): Show | 162 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(159): Show |
intron_variant | MODIFIER | c.173-6531G>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105920805 | ||||||
| chr4:105921235
|
C | G | 2 | a0003c0003t0001g0210a0003c0003t0002g0209 | 2 | HG01884.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.173-6101C>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105921235 | ||||||
| chr4:105921276
|
G | A | 2 | a0003c0003t0001g0210a0003c0003t0002g0209 | 2 | HG01884.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.173-6060G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105921276 | ||||||
| chr4:105921360
|
A | G | 15 | a0001c0001t0001g0006a0001c0001t0001g0198a0001c0001t0001g0199others(12): Show | 16 | HG01069.hp1 HG01192.hp1 HG01975.hp2 others(13): Show |
intron_variant | MODIFIER | c.173-5976A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105921360 | ||||||
| chr4:105921408
|
G | C | 19 | a0003c0003t0001g0114a0003c0003t0001g0210a0003c0003t0001g0219others(16): Show | 20 | HG00735.hp1 HG01070.hp2 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.173-5928G>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105921408 | ||||||
| chr4:105921660
|
T | A | 18 | a0003c0003t0001g0114a0003c0003t0001g0210a0003c0003t0001g0219others(15): Show | 19 | HG00735.hp1 HG01081.hp1 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.173-5676T>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105921660 | ||||||
| chr4:105921687
|
C | T | 1 | a0003c0003t0005g0113 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.173-5649C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105921687 | ||||||
| chr4:105921826
|
C | T | 1 | a0001c0001t0001g0022 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.173-5510C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105921826 | ||||||
| chr4:105922311
|
T | C | 1 | a0001c0001t0001g0138 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.173-5025T>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105922311 | ||||||
| chr4:105922335
|
G | C | 18 | a0003c0003t0001g0114a0003c0003t0001g0210a0003c0003t0001g0219others(15): Show | 19 | HG00735.hp1 HG01081.hp1 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.173-5001G>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105922335 | ||||||
| chr4:105922388
|
TA | T | 3 | a0002c0002t0003g0166a0002c0002t0003g0171a0002c0002t0003g0172 | 3 | HG03490.hp1 HG03492.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.173-4947delA | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105922388 | ||||||
| chr4:105922389
|
AT | A | 68 | a0001c0001t0001g0041a0001c0001t0001g0138a0001c0001t0002g0005others(65): Show | 71 | HG01109.hp2 HG01255.hp1 HG01361.hp1 others(68): Show |
intron_variant | MODIFIER | c.173-4931delT | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 105922389 | |||||
| chr4:105922389
|
ATTTT | A | 35 | a0001c0001t0001g0006a0001c0001t0001g0198a0001c0001t0001g0199others(32): Show | 37 | HG00735.hp1 HG01069.hp1 HG01070.hp2 others(34): Show |
intron_variant | MODIFIER | c.173-4934_173-4931d others(6): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 105922389 | |||||
| chr4:105922557
|
T | A | 1 | a0003c0014t0001g0131 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.173-4779T>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105922557 | ||||||
| chr4:105922798
|
A | T | 36 | a0001c0001t0001g0006a0001c0001t0001g0198a0001c0001t0001g0199others(33): Show | 38 | HG00735.hp1 HG01069.hp1 HG01070.hp2 others(35): Show |
intron_variant | MODIFIER | c.173-4538A>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105922798 | ||||||
| chr4:105922801
|
G | C | 5 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0020others(2): Show | 5 | HG00639.hp1 HG01106.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.173-4535G>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105922801 | ||||||
| chr4:105922852
|
A | G | 36 | a0001c0001t0001g0006a0001c0001t0001g0198a0001c0001t0001g0199others(33): Show | 38 | HG00735.hp1 HG01069.hp1 HG01070.hp2 others(35): Show |
intron_variant | MODIFIER | c.173-4484A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105922852 | ||||||
| chr4:105922859
|
G | A | 1 | a0001c0001t0005g0112 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.173-4477G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105922859 | ||||||
| chr4:105922891
|
C | T | 36 | a0001c0001t0001g0006a0001c0001t0001g0198a0001c0001t0001g0199others(33): Show | 38 | HG00735.hp1 HG01069.hp1 HG01070.hp2 others(35): Show |
intron_variant | MODIFIER | c.173-4445C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105922891 | ||||||
| chr4:105922944
|
A | G | 2 | a0002c0002t0002g0029a0002c0002t0002g0043 | 2 | NA18998.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.173-4392A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105922944 | ||||||
| chr4:105922996
|
A | C | 18 | a0003c0003t0001g0114a0003c0003t0001g0210a0003c0003t0001g0219others(15): Show | 19 | HG00735.hp1 HG01081.hp1 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.173-4340A>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105922996 | ||||||
| chr4:105923060
|
T | C | 4 | a0003c0003t0002g0001a0003c0003t0002g0217a0003c0003t0002g0218others(1): Show | 5 | HG00735.hp1 HG01243.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.173-4276T>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105923060 | ||||||
| chr4:105923315
|
G | GT | 26 | a0001c0001t0001g0041a0002c0002t0001g0042a0002c0002t0001g0061others(23): Show | 27 | HG01361.hp1 HG01516.hp2 HG01517.hp2 others(24): Show |
intron_variant | MODIFIER | c.173-4011dupT | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 105923315 | |||||
| chr4:105923827
|
C | G | 8 | a0001c0001t0001g0006a0001c0001t0001g0198a0001c0001t0001g0199others(5): Show | 9 | HG01069.hp1 HG01192.hp1 HG01975.hp2 others(6): Show |
intron_variant | MODIFIER | c.173-3509C>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105923827 | ||||||
| chr4:105923996
|
C | T | 2 | a0001c0001t0008g0058a0003c0003t0002g0216 | 2 | HG03471.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.173-3340C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105923996 | ||||||
| chr4:105924039
|
G | GC | 28 | a0001c0001t0001g0008a0001c0001t0001g0019a0001c0001t0001g0020others(25): Show | 28 | HG00639.hp1 HG00735.hp2 HG01106.hp1 others(25): Show |
intron_variant | MODIFIER | c.173-3287dupC | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 105924039 | |||||
| chr4:105924039
|
GC | G | 20 | a0001c0001t0001g0054a0001c0001t0002g0005a0001c0001t0002g0122others(17): Show | 22 | HG00735.hp1 HG01070.hp2 HG01243.hp2 others(19): Show |
intron_variant | MODIFIER | c.173-3287delC | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 105924039 | |||||
| chr4:105924041
|
C | A | 1 | a0002c0002t0002g0168 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.173-3295C>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105924041 | ||||||
| chr4:105924041
|
C | T | 1 | a0001c0001t0002g0148 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.173-3295C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105924041 | ||||||
| chr4:105924042
|
C | T | 10 | a0001c0001t0002g0005a0001c0001t0002g0122a0001c0001t0002g0124others(7): Show | 11 | HG01070.hp2 HG02280.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.173-3294C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105924042 | ||||||
| chr4:105924049
|
C | A | 1 | a0010c0012t0010g0123 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.173-3287C>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105924049 | ||||||
| chr4:105924061
|
TA | T | 1 | a0001c0001t0002g0005 | 2 | HG02809.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.173-3274delA | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105924061 | ||||||
| chr4:105924101
|
A | G | 11 | a0003c0003t0001g0210a0003c0003t0002g0209a0003c0003t0004g0011others(8): Show | 11 | HG00099.hp2 HG00140.hp1 HG00642.hp2 others(8): Show |
intron_variant | MODIFIER | c.173-3235A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105924101 | ||||||
| chr4:105924232
|
T | C | 3 | a0002c0002t0002g0192a0006c0006t0002g0193a0006c0006t0002g0195 | 3 | HG02896.hp1 HG02897.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.173-3104T>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105924232 | ||||||
| chr4:105924351
|
A | G | 1 | a0003c0014t0001g0131 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.173-2985A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105924351 | ||||||
| chr4:105924455
|
C | G | 1 | a0001c0001t0001g0014 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.173-2881C>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105924455 | ||||||
| chr4:105924462
|
A | G | 1 | a0001c0001t0011g0115 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.173-2874A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105924462 | ||||||
| chr4:105924525
|
G | A | 206 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0008others(203): Show | 211 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.173-2811G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105924525 | ||||||
| chr4:105924656
|
A | G | 9 | a0003c0003t0001g0120a0003c0003t0002g0190a0003c0003t0005g0113others(6): Show | 9 | HG02055.hp1 HG02630.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.173-2680A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105924656 | ||||||
| chr4:105924750
|
GCTACAGC others(8): Show |
G | 1 | a0011c0011t0002g0130 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.173-2583_173-2569d others(17): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 105924750 | |||||
| chr4:105924803
|
T | A | 195 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0008others(192): Show | 200 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.173-2533T>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105924803 | ||||||
| chr4:105924989
|
A | G | 3 | a0001c0001t0002g0122a0001c0001t0002g0215a0001c0001t0004g0214 | 3 | HG02615.hp1 HG03209.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.173-2347A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105924989 | ||||||
| chr4:105925132
|
G | A | 8 | a0003c0003t0001g0120a0003c0003t0002g0190a0003c0003t0005g0113others(5): Show | 8 | HG01192.hp2 HG02055.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.173-2204G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105925132 | ||||||
| chr4:105925384
|
T | C | 1 | a0001c0001t0001g0137 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.173-1952T>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105925384 | ||||||
| chr4:105925403
|
G | T | 1 | a0003c0003t0001g0120 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.173-1933G>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105925403 | ||||||
| chr4:105925762
|
G | A | 1 | a0001c0001t0001g0138 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.173-1574G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105925762 | ||||||
| chr4:105925834
|
A | C | 195 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0008others(192): Show | 200 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.173-1502A>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105925834 | ||||||
| chr4:105925846
|
G | A | 1 | a0002c0002t0002g0151 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.173-1490G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105925846 | ||||||
| chr4:105925846
|
G | T | 1 | a0001c0001t0002g0050 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.173-1490G>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105925846 | ||||||
| chr4:105926175
|
C | T | 3 | a0002c0002t0002g0192a0006c0006t0002g0193a0006c0006t0002g0195 | 3 | HG02896.hp1 HG02897.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.173-1161C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105926175 | ||||||
| chr4:105926280
|
A | G | 195 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0008others(192): Show | 200 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.173-1056A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105926280 | ||||||
| chr4:105926308
|
T | G | 5 | a0001c0001t0001g0071a0001c0001t0001g0083a0001c0001t0001g0087others(2): Show | 5 | NA18942.hp2 NA18957.hp1 NA19060.hp1 others(2): Show |
intron_variant | MODIFIER | c.173-1028T>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105926308 | ||||||
| chr4:105926334
|
A | T | 5 | a0001c0001t0002g0122a0001c0001t0002g0124a0001c0001t0002g0215others(2): Show | 5 | HG02451.hp1 HG02615.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.173-1002A>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105926334 | ||||||
| chr4:105926346
|
A | T | 7 | a0003c0003t0001g0120a0003c0003t0002g0190a0003c0003t0005g0113others(4): Show | 7 | HG02055.hp1 HG02630.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.173-990A>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105926346 | ||||||
| chr4:105926522
|
A | G | 1 | a0001c0001t0001g0074 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.173-814A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105926522 | ||||||
| chr4:105926597
|
C | T | 1 | a0003c0003t0002g0216 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.173-739C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105926597 | ||||||
| chr4:105926809
|
CTTGAA | C | 2 | a0003c0003t0015g0129a0013c0010t0002g0191 | 2 | HG02965.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.173-521_173-517del others(5): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 105926809 | |||||
| chr4:105927044
|
A | T | 195 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0008others(192): Show | 200 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.173-292A>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105927044 | ||||||
| chr4:105927157
|
C | T | 185 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0008others(182): Show | 189 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(186): Show |
intron_variant | MODIFIER | c.173-179C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 2/11 | chr4 | 105927157 | ||||||
| chr4:105927479
|
C | T | 3 | a0002c0002t0001g0088a0002c0002t0001g0092a0002c0002t0001g0093 | 3 | NA18979.hp2 NA19002.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.265+51C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | chr4 | 105927479 | ||||||
| chr4:105927546
|
C | T | 195 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0008others(192): Show | 200 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.265+118C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | chr4 | 105927546 | ||||||
| chr4:105927702
|
G | A | 1 | a0005c0005t0002g0133 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.265+274G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | chr4 | 105927702 | ||||||
| chr4:105927905
|
T | C | 1 | a0002c0002t0002g0140 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.265+477T>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | chr4 | 105927905 | ||||||
| chr4:105928051
|
G | A | 1 | a0003c0014t0001g0131 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.265+623G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | chr4 | 105928051 | ||||||
| chr4:105928052
|
C | T | 1 | a0011c0011t0002g0130 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.265+624C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | chr4 | 105928052 | ||||||
| chr4:105928095
|
C | T | 195 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0008others(192): Show | 200 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.265+667C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | chr4 | 105928095 | ||||||
| chr4:105928176
|
G | A | 1 | a0012c0013t0010g0136 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.265+748G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | chr4 | 105928176 | ||||||
| chr4:105928178
|
C | T | 1 | a0012c0013t0010g0136 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.265+750C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | chr4 | 105928178 | ||||||
| chr4:105928181
|
C | T | 1 | a0012c0013t0010g0136 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.265+753C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | chr4 | 105928181 | ||||||
| chr4:105928182
|
T | C | 1 | a0012c0013t0010g0136 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.265+754T>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | chr4 | 105928182 | ||||||
| chr4:105928183
|
T | C | 1 | a0012c0013t0010g0136 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.265+755T>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | chr4 | 105928183 | ||||||
| chr4:105928185
|
G | T | 1 | a0012c0013t0010g0136 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.265+757G>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | chr4 | 105928185 | ||||||
| chr4:105928187
|
G | T | 1 | a0012c0013t0010g0136 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.265+759G>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | chr4 | 105928187 | ||||||
| chr4:105928188
|
C | T | 1 | a0012c0013t0010g0136 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.265+760C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | chr4 | 105928188 | ||||||
| chr4:105928352
|
A | G | 220 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0008others(217): Show | 226 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.265+924A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | chr4 | 105928352 | ||||||
| chr4:105928384
|
C | T | 1 | a0001c0001t0001g0024 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.265+956C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | chr4 | 105928384 | ||||||
| chr4:105928408
|
G | A | 8 | a0001c0001t0001g0006a0001c0001t0001g0198a0001c0001t0001g0199others(5): Show | 9 | HG01069.hp1 HG01192.hp1 HG01975.hp2 others(6): Show |
intron_variant | MODIFIER | c.265+980G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | chr4 | 105928408 | ||||||
| chr4:105928471
|
C | T | 5 | a0001c0001t0002g0122a0001c0001t0002g0124a0001c0001t0002g0215others(2): Show | 5 | HG02451.hp1 HG02615.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.265+1043C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | chr4 | 105928471 | ||||||
| chr4:105928485
|
T | C | 1 | a0003c0014t0001g0131 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.265+1057T>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | chr4 | 105928485 | ||||||
| chr4:105928506
|
A | G | 6 | a0003c0003t0001g0114a0003c0003t0001g0219a0005c0005t0001g0132others(3): Show | 6 | HG01884.hp2 HG02145.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.265+1078A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | chr4 | 105928506 | ||||||
| chr4:105928523
|
G | C | 1 | a0001c0001t0011g0115 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.265+1095G>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | chr4 | 105928523 | ||||||
| chr4:105928613
|
C | CA | 13 | a0003c0003t0001g0114a0003c0003t0001g0120a0003c0003t0001g0219others(10): Show | 13 | HG01884.hp2 HG02055.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.265+1202dupA | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 105928613 | |||||
| chr4:105928613
|
CA | C | 107 | a0001c0001t0001g0006a0001c0001t0001g0041a0001c0001t0001g0138others(104): Show | 110 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(107): Show |
intron_variant | MODIFIER | c.265+1202delA | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 105928613 | |||||
| chr4:105928613
|
CAA | C | 7 | a0001c0001t0002g0122a0001c0001t0002g0124a0001c0001t0002g0215others(4): Show | 7 | HG02451.hp1 HG02615.hp1 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.265+1201_265+1202d others(4): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 105928613 | |||||
| chr4:105928630
|
A | G | 1 | a0001c0001t0002g0215 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.265+1202A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | chr4 | 105928630 | ||||||
| chr4:105928632
|
A | G | 1 | a0002c0002t0002g0003 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.265+1204A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | chr4 | 105928632 | ||||||
| chr4:105928736
|
T | G | 1 | a0003c0003t0015g0129 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.265+1308T>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | chr4 | 105928736 | ||||||
| chr4:105928782
|
CAT | C | 177 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(174): Show | 180 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(177): Show |
intron_variant | MODIFIER | c.265+1357_265+1358d others(4): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 105928782 | |||||
| chr4:105928929
|
AC | A | 2 | a0001c0001t0002g0207a0012c0013t0010g0136 | 2 | HG02280.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.265+1502delC | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | chr4 | 105928929 | ||||||
| chr4:105928931
|
A | G | 2 | a0001c0001t0002g0207a0012c0013t0010g0136 | 2 | HG02280.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.265+1503A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | chr4 | 105928931 | ||||||
| chr4:105928932
|
G | GT | 203 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0008others(200): Show | 208 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(205): Show |
intron_variant | MODIFIER | c.265+1512dupT | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 105928932 | |||||
| chr4:105928932
|
G | T | 2 | a0001c0001t0002g0207a0012c0013t0010g0136 | 2 | HG02280.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.265+1504G>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | chr4 | 105928932 | ||||||
| chr4:105929055
|
A | C | 206 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0008others(203): Show | 211 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.265+1627A>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | chr4 | 105929055 | ||||||
| chr4:105929088
|
A | G | 195 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0008others(192): Show | 200 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.265+1660A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | chr4 | 105929088 | ||||||
| chr4:105929205
|
A | T | 7 | a0003c0003t0001g0120a0003c0003t0002g0190a0003c0003t0005g0113others(4): Show | 7 | HG02055.hp1 HG02630.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.265+1777A>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | chr4 | 105929205 | ||||||
| chr4:105929231
|
C | T | 6 | a0003c0003t0001g0114a0003c0003t0001g0219a0005c0005t0001g0132others(3): Show | 6 | HG01884.hp2 HG02145.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.265+1803C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | chr4 | 105929231 | ||||||
| chr4:105929343
|
A | G | 92 | a0002c0002t0001g0042a0002c0002t0001g0061a0002c0002t0001g0062others(89): Show | 94 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(91): Show |
intron_variant | MODIFIER | c.265+1915A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | chr4 | 105929343 | ||||||
| chr4:105929622
|
AGTATACT others(101): Show |
A | 1 | a0001c0001t0002g0213 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.265+2196_265+2303d others(2): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 105929622 | |||||
| chr4:105929710
|
G | A | 3 | a0001c0001t0001g0174a0001c0001t0001g0187a0001c0001t0001g0189 | 3 | HG01109.hp1 HG01175.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.265+2282G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | chr4 | 105929710 | ||||||
| chr4:105929738
|
A | G | 1 | a0001c0001t0002g0005 | 2 | HG02809.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.265+2310A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | chr4 | 105929738 | ||||||
| chr4:105930101
|
T | C | 3 | a0002c0002t0002g0188a0007c0007t0002g0183a0007c0007t0002g0186 | 3 | HG02451.hp2 NA18906.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.265+2673T>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | chr4 | 105930101 | ||||||
| chr4:105930160
|
C | T | 2 | a0001c0001t0002g0207a0012c0013t0010g0136 | 2 | HG02280.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.265+2732C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | chr4 | 105930160 | ||||||
| chr4:105930250
|
C | T | 2 | a0001c0001t0002g0207a0012c0013t0010g0136 | 2 | HG02280.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.265+2822C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | chr4 | 105930250 | ||||||
| chr4:105930627
|
G | T | 1 | a0002c0002t0002g0167 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.265+3199G>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | chr4 | 105930627 | ||||||
| chr4:105930699
|
A | G | 183 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(180): Show | 186 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(183): Show |
intron_variant | MODIFIER | c.265+3271A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | chr4 | 105930699 | ||||||
| chr4:105931207
|
C | T | 1 | a0001c0001t0001g0094 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.265+3779C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | chr4 | 105931207 | ||||||
| chr4:105931423
|
T | G | 1 | a0011c0011t0002g0130 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.265+3995T>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | chr4 | 105931423 | ||||||
| chr4:105931668
|
CA | C | 181 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0008others(178): Show | 185 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.265+4262delA | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 105931668 | |||||
| chr4:105931668
|
CAA | C | 13 | a0001c0001t0001g0024a0001c0001t0002g0213a0001c0001t0002g0215others(10): Show | 14 | HG02257.hp1 HG02559.hp1 HG02698.hp2 others(11): Show |
intron_variant | MODIFIER | c.265+4261_265+4262d others(4): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 105931668 | |||||
| chr4:105931668
|
CAAA | C | 7 | a0001c0001t0002g0005a0003c0003t0001g0120a0003c0003t0002g0190others(4): Show | 8 | HG02630.hp2 HG02809.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.265+4260_265+4262d others(5): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 105931668 | |||||
| chr4:105931711
|
G | T | 195 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0008others(192): Show | 200 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.265+4283G>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | chr4 | 105931711 | ||||||
| chr4:105931901
|
T | A | 1 | a0011c0011t0002g0130 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.265+4473T>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | chr4 | 105931901 | ||||||
| chr4:105932089
|
C | T | 2 | a0001c0001t0001g0187a0001c0001t0001g0189 | 2 | HG01109.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.265+4661C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | chr4 | 105932089 | ||||||
| chr4:105932221
|
AC | A | 195 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0008others(192): Show | 200 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.266-4787delC | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | chr4 | 105932221 | ||||||
| chr4:105932360
|
A | G | 2 | a0001c0001t0001g0074a0001c0001t0001g0084 | 2 | HG02040.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.266-4649A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | chr4 | 105932360 | ||||||
| chr4:105932722
|
A | C | 1 | a0002c0002t0003g0178 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.266-4287A>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | chr4 | 105932722 | ||||||
| chr4:105932723
|
G | A | 1 | a0002c0002t0003g0178 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.266-4286G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | chr4 | 105932723 | ||||||
| chr4:105932777
|
A | G | 1 | a0010c0012t0010g0123 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.266-4232A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | chr4 | 105932777 | ||||||
| chr4:105932851
|
G | A | 2 | a0003c0003t0015g0129a0013c0010t0002g0191 | 2 | HG02965.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.266-4158G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | chr4 | 105932851 | ||||||
| chr4:105932964
|
A | G | 1 | a0013c0010t0002g0191 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.266-4045A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | chr4 | 105932964 | ||||||
| chr4:105933106
|
T | C | 1 | a0001c0001t0001g0071 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.266-3903T>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | chr4 | 105933106 | ||||||
| chr4:105933108
|
A | C | 7 | a0003c0003t0001g0120a0003c0003t0002g0190a0003c0003t0005g0113others(4): Show | 7 | HG02055.hp1 HG02630.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.266-3901A>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | chr4 | 105933108 | ||||||
| chr4:105933255
|
G | T | 2 | a0003c0003t0015g0129a0013c0010t0002g0191 | 2 | HG02965.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.266-3754G>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | chr4 | 105933255 | ||||||
| chr4:105933277
|
G | A | 2 | a0003c0003t0015g0129a0013c0010t0002g0191 | 2 | HG02965.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.266-3732G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | chr4 | 105933277 | ||||||
| chr4:105933362
|
C | A | 2 | a0002c0002t0001g0177a0002c0002t0003g0048 | 2 | NA19072.hp1 NA19072.hp2 |
intron_variant | MODIFIER | c.266-3647C>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | chr4 | 105933362 | ||||||
| chr4:105933482
|
T | C | 1 | a0001c0001t0003g0012 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.266-3527T>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | chr4 | 105933482 | ||||||
| chr4:105933629
|
T | C | 206 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0008others(203): Show | 211 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.266-3380T>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | chr4 | 105933629 | ||||||
| chr4:105933638
|
TA | T | 7 | a0003c0003t0001g0120a0003c0003t0002g0190a0003c0003t0005g0113others(4): Show | 7 | HG02055.hp1 HG02630.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.266-3367delA | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 105933638 | |||||
| chr4:105933946
|
T | G | 1 | a0002c0002t0002g0143 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.266-3063T>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | chr4 | 105933946 | ||||||
| chr4:105933951
|
A | G | 195 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0008others(192): Show | 200 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.266-3058A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | chr4 | 105933951 | ||||||
| chr4:105934020
|
A | G | 7 | a0003c0003t0001g0120a0003c0003t0002g0190a0003c0003t0005g0113others(4): Show | 7 | HG02055.hp1 HG02630.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.266-2989A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | chr4 | 105934020 | ||||||
| chr4:105934065
|
A | G | 1 | a0001c0001t0011g0115 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.266-2944A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | chr4 | 105934065 | ||||||
| chr4:105934068
|
A | G | 1 | a0001c0001t0001g0021 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.266-2941A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | chr4 | 105934068 | ||||||
| chr4:105934123
|
A | C | 7 | a0003c0003t0001g0120a0003c0003t0002g0190a0003c0003t0005g0113others(4): Show | 7 | HG02055.hp1 HG02630.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.266-2886A>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | chr4 | 105934123 | ||||||
| chr4:105934378
|
T | C | 195 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0008others(192): Show | 200 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.266-2631T>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | chr4 | 105934378 | ||||||
| chr4:105934379
|
G | A | 205 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0008others(202): Show | 210 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.266-2630G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | chr4 | 105934379 | ||||||
| chr4:105934566
|
G | T | 176 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(173): Show | 179 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(176): Show |
intron_variant | MODIFIER | c.266-2443G>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | chr4 | 105934566 | ||||||
| chr4:105934567
|
G | T | 3 | a0001c0001t0002g0122a0001c0001t0002g0215a0001c0001t0004g0214 | 3 | HG02615.hp1 HG03209.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.266-2442G>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | chr4 | 105934567 | ||||||
| chr4:105934817
|
A | G | 7 | a0003c0003t0001g0120a0003c0003t0002g0190a0003c0003t0005g0113others(4): Show | 7 | HG02055.hp1 HG02630.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.266-2192A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | chr4 | 105934817 | ||||||
| chr4:105934904
|
A | G | 1 | a0011c0011t0002g0130 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.266-2105A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | chr4 | 105934904 | ||||||
| chr4:105935071
|
T | C | 7 | a0003c0003t0001g0120a0003c0003t0002g0190a0003c0003t0005g0113others(4): Show | 7 | HG02055.hp1 HG02630.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.266-1938T>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | chr4 | 105935071 | ||||||
| chr4:105935102
|
A | G | 2 | a0001c0001t0001g0138a0001c0001t0011g0115 | 2 | HG02280.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.266-1907A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | chr4 | 105935102 | ||||||
| chr4:105935355
|
T | A | 1 | a0003c0014t0001g0131 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.266-1654T>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | chr4 | 105935355 | ||||||
| chr4:105935391
|
C | G | 1 | a0001c0001t0006g0098 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.266-1618C>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | chr4 | 105935391 | ||||||
| chr4:105935549
|
C | T | 24 | a0002c0002t0001g0062a0002c0002t0001g0164a0002c0002t0002g0007others(21): Show | 24 | HG01255.hp1 HG01261.hp1 HG01993.hp1 others(21): Show |
intron_variant | MODIFIER | c.266-1460C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | chr4 | 105935549 | ||||||
| chr4:105935644
|
A | G | 1 | a0002c0002t0003g0178 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.266-1365A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | chr4 | 105935644 | ||||||
| chr4:105935830
|
G | A | 176 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(173): Show | 179 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(176): Show |
intron_variant | MODIFIER | c.266-1179G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | chr4 | 105935830 | ||||||
| chr4:105935928
|
C | T | 1 | a0001c0001t0002g0124 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.266-1081C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | chr4 | 105935928 | ||||||
| chr4:105936074
|
G | T | 1 | a0001c0001t0001g0229 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.266-935G>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | chr4 | 105936074 | ||||||
| chr4:105936178
|
T | C | 1 | a0001c0001t0001g0060 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.266-831T>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | chr4 | 105936178 | ||||||
| chr4:105936247
|
G | A | 1 | a0012c0013t0010g0136 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.266-762G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | chr4 | 105936247 | ||||||
| chr4:105936300
|
A | G | 2 | a0001c0001t0001g0008a0001c0001t0001g0201 | 2 | HG03098.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.266-709A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | chr4 | 105936300 | ||||||
| chr4:105936448
|
T | TTGGGA | 195 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0008others(192): Show | 200 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.266-560_266-556dup others(5): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 105936448 | |||||
| chr4:105936500
|
G | A | 195 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0008others(192): Show | 200 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.266-509G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | chr4 | 105936500 | ||||||
| chr4:105936522
|
G | A | 1 | a0001c0001t0001g0138 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.266-487G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | chr4 | 105936522 | ||||||
| chr4:105936609
|
G | A | 1 | a0001c0001t0011g0115 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.266-400G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | chr4 | 105936609 | ||||||
| chr4:105936779
|
G | T | 2 | a0002c0002t0002g0104a0002c0002t0002g0212 | 2 | HG02886.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.266-230G>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | chr4 | 105936779 | ||||||
| chr4:105936808
|
A | T | 3 | a0002c0002t0001g0116a0002c0002t0001g0118a0002c0002t0001g0125 | 3 | HG02615.hp2 HG03486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.266-201A>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | chr4 | 105936808 | ||||||
| chr4:105936867
|
G | C | 7 | a0003c0003t0001g0120a0003c0003t0002g0190a0003c0003t0005g0113others(4): Show | 7 | HG02055.hp1 HG02630.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.266-142G>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | chr4 | 105936867 | ||||||
| chr4:105936894
|
AC | A | 7 | a0001c0001t0002g0005a0001c0001t0002g0122a0001c0001t0002g0124others(4): Show | 8 | HG02257.hp1 HG02451.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.266-114delC | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 3/11 | chr4 | 105936894 | ||||||
| chr4:105937165
|
G | T | 1 | a0004c0004t0002g0146 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.385+37G>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 4/11 | chr4 | 105937165 | ||||||
| chr4:105937320
|
C | T | 1 | a0001c0001t0001g0036 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.385+192C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 4/11 | chr4 | 105937320 | ||||||
| chr4:105937537
|
A | T | 1 | a0013c0010t0002g0191 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.385+409A>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 4/11 | chr4 | 105937537 | ||||||
| chr4:105937741
|
A | T | 177 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(174): Show | 180 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(177): Show |
intron_variant | MODIFIER | c.386-560A>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 4/11 | chr4 | 105937741 | ||||||
| chr4:105937880
|
C | T | 1 | a0011c0011t0002g0130 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.386-421C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 4/11 | chr4 | 105937880 | ||||||
| chr4:105938168
|
T | G | 1 | a0003c0014t0001g0131 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.386-133T>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 4/11 | chr4 | 105938168 | ||||||
| chr4:105938242
|
A | G | 1 | a0002c0002t0002g0040 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.386-59A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 4/11 | chr4 | 105938242 | ||||||
| chr4:105938441
|
T | G | 8 | a0001c0001t0001g0006a0001c0001t0001g0198a0001c0001t0001g0199others(5): Show | 9 | HG01069.hp1 HG01192.hp1 HG01975.hp2 others(6): Show |
intron_variant | MODIFIER | c.505+21T>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 5/11 | chr4 | 105938441 | ||||||
| chr4:105938535
|
A | G | 1 | a0011c0011t0002g0130 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.505+115A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 5/11 | chr4 | 105938535 | ||||||
| chr4:105938764
|
A | G | 1 | a0002c0002t0002g0140 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.505+344A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 5/11 | chr4 | 105938764 | ||||||
| chr4:105938785
|
A | G | 1 | a0013c0010t0002g0191 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.505+365A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 5/11 | chr4 | 105938785 | ||||||
| chr4:105938844
|
T | G | 5 | a0001c0001t0002g0122a0001c0001t0002g0124a0001c0001t0002g0215others(2): Show | 5 | HG02451.hp1 HG02615.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.505+424T>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 5/11 | chr4 | 105938844 | ||||||
| chr4:105939373
|
G | C | 7 | a0003c0003t0001g0120a0003c0003t0002g0190a0003c0003t0005g0113others(4): Show | 7 | HG02055.hp1 HG02630.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.506-702G>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 5/11 | chr4 | 105939373 | ||||||
| chr4:105939550
|
T | C | 211 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0008others(208): Show | 216 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.506-525T>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 5/11 | chr4 | 105939550 | ||||||
| chr4:105939824
|
C | G | 4 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0038others(1): Show | 4 | HG02486.hp2 HG02922.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.506-251C>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 5/11 | chr4 | 105939824 | ||||||
| chr4:105939879
|
T | A | 1 | a0002c0002t0001g0088 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.506-196T>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 5/11 | chr4 | 105939879 | ||||||
| chr4:105939995
|
A | T | 1 | a0001c0001t0002g0069 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.506-80A>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 5/11 | chr4 | 105939995 | ||||||
| chr4:105940286
|
G | C | 1 | a0001c0001t0002g0069 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.640+77G>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 6/11 | chr4 | 105940286 | ||||||
| chr4:105940400
|
A | T | 211 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0008others(208): Show | 216 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.641-114A>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 6/11 | chr4 | 105940400 | ||||||
| chr4:105940725
|
T | C | 1 | a0001c0001t0012g0080 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.763+89T>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 7/11 | chr4 | 105940725 | ||||||
| chr4:105940740
|
A | G | 1 | a0001c0001t0002g0037 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.763+104A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 7/11 | chr4 | 105940740 | ||||||
| chr4:105940860
|
T | G | 2 | a0001c0001t0001g0036a0001c0001t0001g0075 | 2 | HG00597.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.763+224T>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 7/11 | chr4 | 105940860 | ||||||
| chr4:105941003
|
AT | A | 7 | a0003c0003t0001g0114a0003c0003t0001g0219a0003c0014t0001g0131others(4): Show | 7 | HG01192.hp2 HG01884.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.763+374delT | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr4 | 105941003 | |||||
| chr4:105941024
|
T | G | 211 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0008others(208): Show | 216 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.763+388T>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 7/11 | chr4 | 105941024 | ||||||
| chr4:105941025
|
G | C | 211 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0008others(208): Show | 216 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.763+389G>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 7/11 | chr4 | 105941025 | ||||||
| chr4:105941056
|
C | T | 3 | a0002c0002t0002g0157a0002c0002t0002g0160a0002c0002t0002g0182 | 3 | HG01175.hp2 HG02145.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.763+420C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 7/11 | chr4 | 105941056 | ||||||
| chr4:105941151
|
C | A | 25 | a0002c0002t0001g0042a0002c0002t0001g0061a0002c0002t0001g0070others(22): Show | 26 | HG01361.hp1 HG01516.hp2 HG01517.hp2 others(23): Show |
intron_variant | MODIFIER | c.763+515C>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 7/11 | chr4 | 105941151 | ||||||
| chr4:105941210
|
G | A | 1 | a0002c0002t0001g0089 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.763+574G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 7/11 | chr4 | 105941210 | ||||||
| chr4:105941686
|
A | G | 1 | a0001c0001t0002g0050 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.764-621A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 7/11 | chr4 | 105941686 | ||||||
| chr4:105941921
|
T | C | 3 | a0002c0002t0001g0116a0002c0002t0001g0118a0002c0002t0001g0125 | 3 | HG02615.hp2 HG03486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.764-386T>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 7/11 | chr4 | 105941921 | ||||||
| chr4:105941925
|
A | AT | 6 | a0003c0003t0001g0114a0003c0003t0001g0219a0005c0005t0001g0132others(3): Show | 6 | HG01884.hp2 HG02145.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.764-380dupT | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr4 | 105941925 | |||||
| chr4:105942017
|
G | C | 1 | a0001c0001t0011g0115 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.764-290G>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 7/11 | chr4 | 105942017 | ||||||
| chr4:105942039
|
T | G | 195 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0008others(192): Show | 200 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.764-268T>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 7/11 | chr4 | 105942039 | ||||||
| chr4:105942077
|
A | C | 1 | a0013c0010t0002g0191 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.764-230A>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 7/11 | chr4 | 105942077 | ||||||
| chr4:105942105
|
CTG | C | 7 | a0001c0001t0001g0138a0001c0001t0002g0005a0001c0001t0002g0124others(4): Show | 8 | HG02257.hp1 HG02280.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.764-192_764-191del others(2): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr4 | 105942105 | |||||
| chr4:105942111
|
G | C | 6 | a0003c0003t0001g0114a0003c0003t0001g0219a0005c0005t0001g0132others(3): Show | 6 | HG01884.hp2 HG02145.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.764-196G>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 7/11 | chr4 | 105942111 | ||||||
| chr4:105942113
|
G | A | 187 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0008others(184): Show | 191 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.764-194G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 7/11 | chr4 | 105942113 | ||||||
| chr4:105942115
|
G | A | 210 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0008others(207): Show | 215 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.764-192G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 7/11 | chr4 | 105942115 | ||||||
| chr4:105942115
|
G | GTA | 7 | a0003c0003t0004g0011a0003c0003t0004g0017a0003c0003t0004g0208others(4): Show | 7 | HG00099.hp2 HG00140.hp1 HG00642.hp2 others(4): Show |
intron_variant | MODIFIER | c.764-171_764-170dup others(2): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr4 | 105942115 | |||||
| chr4:105942117
|
A | G | 1 | a0003c0003t0015g0129 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.764-190A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 7/11 | chr4 | 105942117 | ||||||
| chr4:105942125
|
A | T | 1 | a0002c0002t0001g0161 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.764-182A>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 7/11 | chr4 | 105942125 | ||||||
| chr4:105942134
|
T | G | 156 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(153): Show | 159 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.764-173T>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 7/11 | chr4 | 105942134 | ||||||
| chr4:105942134
|
T | TAG | 6 | a0001c0001t0001g0059a0001c0001t0001g0090a0001c0001t0001g0103others(3): Show | 6 | HG01070.hp1 HG02004.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.764-172_764-171ins others(2): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr4 | 105942134 | |||||
| chr4:105942136
|
T | C | 167 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(164): Show | 171 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(168): Show |
intron_variant | MODIFIER | c.764-171T>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 7/11 | chr4 | 105942136 | ||||||
| chr4:105942136
|
T | TAGAC | 37 | a0001c0001t0001g0006a0001c0001t0001g0198a0001c0001t0001g0199others(34): Show | 39 | HG01069.hp1 HG01192.hp1 HG01192.hp2 others(36): Show |
intron_variant | MODIFIER | c.764-170_764-169ins others(4): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr4 | 105942136 | |||||
| chr4:105942136
|
T | TATAGAC | 5 | a0001c0001t0001g0094a0002c0002t0002g0151a0003c0003t0001g0120others(2): Show | 5 | HG01255.hp2 HG02965.hp2 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.764-170_764-169ins others(6): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr4 | 105942136 | |||||
| chr4:105942136
|
T | TATATATA others(9): Show |
1 | a0011c0011t0002g0130 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.764-170_764-169ins others(16): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr4 | 105942136 | |||||
| chr4:105942136
|
T | TATATATA others(9): Show |
4 | a0005c0005t0001g0132a0005c0005t0001g0134a0005c0005t0001g0135others(1): Show | 4 | HG01884.hp2 HG02559.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.764-170_764-169ins others(16): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr4 | 105942136 | |||||
| chr4:105942136
|
T | TATATATA others(13): Show |
1 | a0003c0003t0001g0219 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.764-170_764-169ins others(20): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr4 | 105942136 | |||||
| chr4:105942136
|
T | TATATATA others(15): Show |
1 | a0003c0003t0001g0114 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.764-170_764-169ins others(22): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr4 | 105942136 | |||||
| chr4:105942245
|
G | A | 1 | a0013c0010t0002g0191 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.764-62G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 7/11 | chr4 | 105942245 | ||||||
| chr4:105942252
|
T | C | 1 | a0001c0001t0001g0014 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.764-55T>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 7/11 | chr4 | 105942252 | ||||||
| chr4:105942771
|
C | T | 3 | a0002c0002t0001g0062a0002c0002t0003g0039a0002c0002t0003g0047 | 3 | HG01255.hp1 HG01261.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.1159+69C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105942771 | ||||||
| chr4:105942791
|
C | T | 1 | a0003c0003t0004g0200 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1159+89C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105942791 | ||||||
| chr4:105942949
|
G | A | 1 | a0001c0001t0002g0005 | 2 | HG02809.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1159+247G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105942949 | ||||||
| chr4:105942952
|
T | A | 1 | a0001c0001t0002g0099 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1159+250T>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105942952 | ||||||
| chr4:105942965
|
A | C | 1 | a0001c0001t0002g0213 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1159+263A>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105942965 | ||||||
| chr4:105943116
|
C | T | 204 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0008others(201): Show | 209 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(206): Show |
intron_variant | MODIFIER | c.1159+414C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105943116 | ||||||
| chr4:105943209
|
G | A | 1 | a0002c0002t0003g0181 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1159+507G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105943209 | ||||||
| chr4:105943640
|
A | G | 1 | a0001c0001t0002g0099 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1159+938A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105943640 | ||||||
| chr4:105943730
|
C | A | 7 | a0003c0003t0001g0120a0003c0003t0002g0190a0003c0003t0005g0113others(4): Show | 7 | HG02055.hp1 HG02630.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.1159+1028C>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105943730 | ||||||
| chr4:105943770
|
A | G | 1 | a0003c0014t0001g0131 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1159+1068A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105943770 | ||||||
| chr4:105944088
|
T | G | 195 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0008others(192): Show | 200 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.1159+1386T>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105944088 | ||||||
| chr4:105944234
|
C | T | 1 | a0003c0014t0001g0131 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1159+1532C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105944234 | ||||||
| chr4:105944272
|
A | G | 1 | a0001c0001t0011g0115 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1159+1570A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105944272 | ||||||
| chr4:105944405
|
A | G | 1 | a0011c0011t0002g0130 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1159+1703A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105944405 | ||||||
| chr4:105944428
|
T | C | 1 | a0011c0011t0002g0130 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1159+1726T>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105944428 | ||||||
| chr4:105944430
|
A | G | 2 | a0001c0001t0001g0138a0001c0001t0011g0115 | 2 | HG02280.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1159+1728A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105944430 | ||||||
| chr4:105944698
|
G | A | 2 | a0003c0003t0001g0210a0003c0003t0002g0209 | 2 | HG01884.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1159+1996G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105944698 | ||||||
| chr4:105944769
|
G | A | 1 | a0001c0001t0002g0213 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1159+2067G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105944769 | ||||||
| chr4:105944811
|
A | G | 1 | a0001c0001t0001g0198 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1159+2109A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105944811 | ||||||
| chr4:105944898
|
G | A | 1 | a0001c0001t0002g0124 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1159+2196G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105944898 | ||||||
| chr4:105944920
|
T | G | 211 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0008others(208): Show | 216 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.1159+2218T>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105944920 | ||||||
| chr4:105945007
|
T | C | 195 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0008others(192): Show | 200 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.1159+2305T>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105945007 | ||||||
| chr4:105945171
|
G | C | 1 | a0002c0002t0002g0196 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1159+2469G>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105945171 | ||||||
| chr4:105945179
|
C | CTG | 195 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0008others(192): Show | 200 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.1159+2477_1159+247 others(6): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105945179 | ||||||
| chr4:105945216
|
G | A | 1 | a0012c0013t0010g0136 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1159+2514G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105945216 | ||||||
| chr4:105945257
|
C | T | 1 | a0013c0010t0002g0191 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1159+2555C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105945257 | ||||||
| chr4:105945416
|
G | A | 5 | a0001c0001t0002g0122a0001c0001t0002g0124a0001c0001t0002g0215others(2): Show | 5 | HG02451.hp1 HG02615.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.1159+2714G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105945416 | ||||||
| chr4:105945483
|
C | G | 1 | a0005c0005t0001g0132 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1159+2781C>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105945483 | ||||||
| chr4:105945705
|
T | C | 1 | a0002c0002t0001g0042 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1159+3003T>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105945705 | ||||||
| chr4:105945791
|
A | G | 185 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0008others(182): Show | 189 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(186): Show |
intron_variant | MODIFIER | c.1159+3089A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105945791 | ||||||
| chr4:105945823
|
A | G | 195 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0008others(192): Show | 200 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.1159+3121A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105945823 | ||||||
| chr4:105945910
|
G | A | 1 | a0001c0001t0002g0030 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1159+3208G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105945910 | ||||||
| chr4:105946057
|
A | G | 1 | a0001c0001t0002g0148 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1159+3355A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105946057 | ||||||
| chr4:105946065
|
A | G | 6 | a0003c0003t0001g0114a0003c0003t0001g0219a0005c0005t0001g0132others(3): Show | 6 | HG01884.hp2 HG02145.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.1159+3363A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105946065 | ||||||
| chr4:105946085
|
T | C | 1 | a0001c0001t0001g0022 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1159+3383T>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105946085 | ||||||
| chr4:105946115
|
G | A | 1 | a0012c0013t0010g0136 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1159+3413G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105946115 | ||||||
| chr4:105946185
|
A | G | 1 | a0011c0011t0002g0130 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1159+3483A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105946185 | ||||||
| chr4:105946501
|
C | G | 195 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0008others(192): Show | 200 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.1159+3799C>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105946501 | ||||||
| chr4:105946551
|
T | C | 2 | a0003c0014t0001g0131a0011c0011t0002g0130 | 2 | HG01070.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.1159+3849T>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105946551 | ||||||
| chr4:105946559
|
C | T | 2 | a0003c0014t0001g0131a0011c0011t0002g0130 | 2 | HG01070.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.1159+3857C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105946559 | ||||||
| chr4:105946683
|
G | T | 176 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(173): Show | 179 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(176): Show |
intron_variant | MODIFIER | c.1159+3981G>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105946683 | ||||||
| chr4:105946743
|
A | G | 1 | a0001c0001t0002g0005 | 2 | HG02809.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1159+4041A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105946743 | ||||||
| chr4:105946984
|
C | G | 1 | a0010c0012t0010g0123 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1159+4282C>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105946984 | ||||||
| chr4:105947272
|
G | A | 195 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0008others(192): Show | 200 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.1159+4570G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105947272 | ||||||
| chr4:105947351
|
C | G | 211 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0008others(208): Show | 216 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.1159+4649C>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105947351 | ||||||
| chr4:105947630
|
C | T | 1 | a0001c0001t0002g0207 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1159+4928C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105947630 | ||||||
| chr4:105947658
|
G | A | 7 | a0003c0003t0001g0120a0003c0003t0002g0190a0003c0003t0005g0113others(4): Show | 7 | HG02055.hp1 HG02630.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.1159+4956G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105947658 | ||||||
| chr4:105947673
|
G | C | 195 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0008others(192): Show | 200 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.1159+4971G>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105947673 | ||||||
| chr4:105947703
|
C | T | 1 | a0003c0014t0001g0131 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1159+5001C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105947703 | ||||||
| chr4:105947726
|
C | G | 1 | a0001c0001t0002g0124 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1159+5024C>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105947726 | ||||||
| chr4:105947770
|
T | C | 1 | a0013c0010t0002g0191 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1159+5068T>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105947770 | ||||||
| chr4:105947793
|
G | T | 1 | a0002c0002t0013g0107 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1159+5091G>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105947793 | ||||||
| chr4:105947932
|
G | A | 1 | a0001c0001t0002g0099 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1159+5230G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105947932 | ||||||
| chr4:105948113
|
A | G | 8 | a0003c0003t0001g0120a0003c0003t0002g0190a0003c0003t0005g0113others(5): Show | 8 | HG02055.hp1 HG02630.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.1159+5411A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105948113 | ||||||
| chr4:105948138
|
A | G | 1 | a0013c0010t0002g0191 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1159+5436A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105948138 | ||||||
| chr4:105948140
|
C | T | 6 | a0003c0003t0001g0114a0003c0003t0001g0219a0005c0005t0001g0132others(3): Show | 6 | HG01884.hp2 HG02145.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.1159+5438C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105948140 | ||||||
| chr4:105948614
|
C | T | 1 | a0011c0011t0002g0130 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1159+5912C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105948614 | ||||||
| chr4:105948620
|
A | T | 177 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(174): Show | 180 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(177): Show |
intron_variant | MODIFIER | c.1159+5918A>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105948620 | ||||||
| chr4:105948643
|
T | A | 205 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0008others(202): Show | 210 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.1159+5941T>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105948643 | ||||||
| chr4:105948700
|
A | G | 1 | a0011c0011t0002g0130 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1159+5998A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105948700 | ||||||
| chr4:105948725
|
A | G | 195 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0008others(192): Show | 200 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.1159+6023A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105948725 | ||||||
| chr4:105949020
|
T | C | 1 | a0001c0001t0001g0138 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1159+6318T>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105949020 | ||||||
| chr4:105949191
|
A | G | 1 | a0003c0014t0001g0131 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1159+6489A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105949191 | ||||||
| chr4:105949215
|
A | G | 2 | a0001c0001t0001g0073a0001c0001t0001g0090 | 2 | HG02129.hp2 NA18953.hp1 |
intron_variant | MODIFIER | c.1159+6513A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105949215 | ||||||
| chr4:105949252
|
G | A | 211 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0008others(208): Show | 216 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.1159+6550G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105949252 | ||||||
| chr4:105949330
|
A | T | 8 | a0001c0001t0001g0006a0001c0001t0001g0198a0001c0001t0001g0199others(5): Show | 9 | HG01069.hp1 HG01192.hp1 HG01975.hp2 others(6): Show |
intron_variant | MODIFIER | c.1159+6628A>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105949330 | ||||||
| chr4:105949408
|
T | A | 2 | a0001c0001t0001g0138a0001c0001t0011g0115 | 2 | HG02280.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1159+6706T>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105949408 | ||||||
| chr4:105949440
|
G | A | 188 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0008others(185): Show | 192 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.1159+6738G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105949440 | ||||||
| chr4:105949503
|
C | A | 5 | a0003c0003t0002g0001a0003c0003t0002g0216a0003c0003t0002g0217others(2): Show | 6 | HG00735.hp1 HG01243.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.1159+6801C>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105949503 | ||||||
| chr4:105949504
|
T | C | 211 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0008others(208): Show | 216 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.1159+6802T>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105949504 | ||||||
| chr4:105949699
|
T | C | 1 | a0013c0010t0002g0191 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1159+6997T>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105949699 | ||||||
| chr4:105949791
|
C | G | 176 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(173): Show | 179 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(176): Show |
intron_variant | MODIFIER | c.1159+7089C>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105949791 | ||||||
| chr4:105949818
|
A | G | 6 | a0003c0003t0001g0114a0003c0003t0001g0219a0005c0005t0001g0132others(3): Show | 6 | HG01884.hp2 HG02145.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.1159+7116A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105949818 | ||||||
| chr4:105949825
|
A | G | 1 | a0002c0002t0001g0061 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1159+7123A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105949825 | ||||||
| chr4:105949925
|
C | T | 1 | a0011c0011t0002g0130 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1159+7223C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105949925 | ||||||
| chr4:105949975
|
C | T | 1 | a0001c0001t0005g0112 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1159+7273C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105949975 | ||||||
| chr4:105949988
|
G | A | 1 | a0001c0001t0002g0099 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1159+7286G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105949988 | ||||||
| chr4:105949996
|
C | G | 2 | a0001c0001t0002g0124a0001c0001t0005g0112 | 2 | HG02451.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1159+7294C>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105949996 | ||||||
| chr4:105950004
|
C | A | 1 | a0011c0011t0002g0130 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1159+7302C>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105950004 | ||||||
| chr4:105950030
|
G | A | 202 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0008others(199): Show | 207 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.1159+7328G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105950030 | ||||||
| chr4:105950049
|
C | A | 2 | a0002c0002t0009g0227a0002c0002t0009g0228 | 2 | HG00099.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.1159+7347C>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105950049 | ||||||
| chr4:105950197
|
C | A | 203 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0008others(200): Show | 208 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(205): Show |
intron_variant | MODIFIER | c.1159+7495C>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105950197 | ||||||
| chr4:105950343
|
GTTATTT | G | 211 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0008others(208): Show | 216 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.1159+7643_1159+764 others(10): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr4 | 105950343 | |||||
| chr4:105950350
|
T | G | 211 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0008others(208): Show | 216 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.1159+7648T>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105950350 | ||||||
| chr4:105950354
|
C | A | 194 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0008others(191): Show | 199 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.1159+7652C>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105950354 | ||||||
| chr4:105950489
|
T | G | 206 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0008others(203): Show | 211 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.1159+7787T>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105950489 | ||||||
| chr4:105950498
|
A | G | 218 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0008others(215): Show | 224 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.1159+7796A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105950498 | ||||||
| chr4:105950964
|
C | T | 1 | a0001c0001t0002g0124 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1160-7507C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105950964 | ||||||
| chr4:105951072
|
G | T | 1 | a0002c0002t0002g0082 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1160-7399G>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105951072 | ||||||
| chr4:105951074
|
C | T | 1 | a0001c0001t0001g0022 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1160-7397C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105951074 | ||||||
| chr4:105951100
|
C | T | 7 | a0003c0003t0001g0120a0003c0003t0002g0190a0003c0003t0005g0113others(4): Show | 7 | HG02055.hp1 HG02630.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.1160-7371C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105951100 | ||||||
| chr4:105951160
|
A | T | 2 | a0001c0001t0002g0207a0012c0013t0010g0136 | 2 | HG02280.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1160-7311A>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105951160 | ||||||
| chr4:105951219
|
C | T | 8 | a0001c0001t0001g0006a0001c0001t0001g0198a0001c0001t0001g0199others(5): Show | 9 | HG01069.hp1 HG01192.hp1 HG01975.hp2 others(6): Show |
intron_variant | MODIFIER | c.1160-7252C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105951219 | ||||||
| chr4:105951220
|
G | A | 1 | a0001c0001t0002g0005 | 2 | HG02809.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1160-7251G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105951220 | ||||||
| chr4:105951275
|
T | G | 1 | a0003c0014t0001g0131 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1160-7196T>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105951275 | ||||||
| chr4:105951396
|
G | A | 204 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0008others(201): Show | 209 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(206): Show |
intron_variant | MODIFIER | c.1160-7075G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105951396 | ||||||
| chr4:105951417
|
C | T | 2 | a0001c0001t0001g0064a0001c0001t0001g0095 | 2 | HG00408.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.1160-7054C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105951417 | ||||||
| chr4:105951704
|
T | C | 25 | a0002c0002t0001g0042a0002c0002t0001g0061a0002c0002t0001g0070others(22): Show | 26 | HG01361.hp1 HG01516.hp2 HG01517.hp2 others(23): Show |
intron_variant | MODIFIER | c.1160-6767T>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105951704 | ||||||
| chr4:105952005
|
G | A | 11 | a0001c0001t0001g0006a0001c0001t0001g0198a0001c0001t0001g0199others(8): Show | 12 | HG01069.hp1 HG01070.hp2 HG01192.hp1 others(9): Show |
intron_variant | MODIFIER | c.1160-6466G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105952005 | ||||||
| chr4:105952092
|
G | A | 1 | a0001c0001t0002g0204 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1160-6379G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105952092 | ||||||
| chr4:105952274
|
T | C | 1 | a0002c0002t0002g0223 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1160-6197T>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105952274 | ||||||
| chr4:105952312
|
G | T | 3 | a0001c0001t0002g0207a0011c0011t0002g0130a0012c0013t0010g0136 | 3 | HG01070.hp2 HG02280.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1160-6159G>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105952312 | ||||||
| chr4:105952369
|
T | G | 3 | a0001c0001t0002g0207a0011c0011t0002g0130a0012c0013t0010g0136 | 3 | HG01070.hp2 HG02280.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1160-6102T>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105952369 | ||||||
| chr4:105952421
|
C | T | 1 | a0001c0001t0001g0077 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1160-6050C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105952421 | ||||||
| chr4:105952765
|
A | G | 1 | a0002c0002t0002g0211 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1160-5706A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105952765 | ||||||
| chr4:105952855
|
C | G | 5 | a0001c0001t0002g0122a0001c0001t0002g0124a0001c0001t0002g0215others(2): Show | 5 | HG02451.hp1 HG02615.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.1160-5616C>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105952855 | ||||||
| chr4:105952861
|
C | T | 1 | a0013c0010t0002g0191 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1160-5610C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105952861 | ||||||
| chr4:105952922
|
G | A | 8 | a0001c0001t0001g0006a0001c0001t0001g0198a0001c0001t0001g0199others(5): Show | 9 | HG01069.hp1 HG01192.hp1 HG01975.hp2 others(6): Show |
intron_variant | MODIFIER | c.1160-5549G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105952922 | ||||||
| chr4:105953044
|
G | T | 1 | a0013c0010t0002g0191 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1160-5427G>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105953044 | ||||||
| chr4:105953117
|
G | A | 8 | a0003c0003t0001g0120a0003c0003t0002g0190a0003c0003t0005g0113others(5): Show | 8 | HG02055.hp1 HG02630.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.1160-5354G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105953117 | ||||||
| chr4:105953130
|
C | T | 2 | a0001c0001t0001g0138a0003c0014t0001g0131 | 2 | HG01192.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1160-5341C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105953130 | ||||||
| chr4:105953248
|
G | A | 199 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0008others(196): Show | 204 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(201): Show |
intron_variant | MODIFIER | c.1160-5223G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105953248 | ||||||
| chr4:105953410
|
G | C | 3 | a0001c0001t0002g0207a0011c0011t0002g0130a0012c0013t0010g0136 | 3 | HG01070.hp2 HG02280.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1160-5061G>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105953410 | ||||||
| chr4:105953843
|
G | A | 1 | a0011c0011t0002g0130 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1160-4628G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105953843 | ||||||
| chr4:105954608
|
C | T | 199 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0008others(196): Show | 204 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(201): Show |
intron_variant | MODIFIER | c.1160-3863C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105954608 | ||||||
| chr4:105955192
|
A | G | 1 | a0001c0001t0001g0031 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1160-3279A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105955192 | ||||||
| chr4:105955459
|
A | G | 3 | a0001c0001t0001g0138a0001c0001t0011g0115a0003c0014t0001g0131 | 3 | HG01192.hp2 HG02280.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1160-3012A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105955459 | ||||||
| chr4:105955468
|
C | T | 2 | a0002c0002t0002g0066a0002c0002t0002g0085 | 2 | NA18979.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.1160-3003C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105955468 | ||||||
| chr4:105955690
|
CT | C | 26 | a0001c0001t0002g0207a0003c0003t0001g0114a0003c0003t0001g0210others(23): Show | 27 | HG00099.hp2 HG00140.hp1 HG00642.hp2 others(24): Show |
intron_variant | MODIFIER | c.1160-2772delT | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr4 | 105955690 | |||||
| chr4:105955724
|
G | T | 9 | a0003c0003t0001g0210a0003c0003t0002g0209a0003c0003t0004g0011others(6): Show | 9 | HG00099.hp2 HG00140.hp1 HG00642.hp2 others(6): Show |
intron_variant | MODIFIER | c.1160-2747G>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105955724 | ||||||
| chr4:105955742
|
T | C | 25 | a0002c0002t0001g0042a0002c0002t0001g0061a0002c0002t0001g0070others(22): Show | 26 | HG01361.hp1 HG01516.hp2 HG01517.hp2 others(23): Show |
intron_variant | MODIFIER | c.1160-2729T>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105955742 | ||||||
| chr4:105955758
|
T | A | 3 | a0001c0001t0001g0138a0001c0001t0011g0115a0003c0014t0001g0131 | 3 | HG01192.hp2 HG02280.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1160-2713T>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105955758 | ||||||
| chr4:105955806
|
C | CA | 27 | a0001c0001t0001g0138a0001c0001t0002g0207a0001c0001t0011g0115others(24): Show | 28 | HG00099.hp2 HG00140.hp1 HG00642.hp2 others(25): Show |
intron_variant | MODIFIER | c.1160-2665_1160-266 others(5): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105955806 | ||||||
| chr4:105955820
|
T | G | 52 | a0001c0001t0001g0006a0001c0001t0001g0138a0001c0001t0001g0198others(49): Show | 55 | HG00099.hp2 HG00140.hp1 HG00642.hp2 others(52): Show |
intron_variant | MODIFIER | c.1160-2651T>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105955820 | ||||||
| chr4:105956086
|
A | G | 3 | a0001c0001t0001g0174a0001c0001t0001g0187a0001c0001t0001g0189 | 3 | HG01109.hp1 HG01175.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.1160-2385A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105956086 | ||||||
| chr4:105956152
|
CTG | C | 81 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0013others(78): Show | 82 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(79): Show |
intron_variant | MODIFIER | c.1160-2317_1160-231 others(6): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr4 | 105956152 | |||||
| chr4:105956186
|
T | G | 3 | a0001c0001t0002g0207a0011c0011t0002g0130a0012c0013t0010g0136 | 3 | HG01070.hp2 HG02280.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1160-2285T>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105956186 | ||||||
| chr4:105956271
|
G | C | 6 | a0003c0003t0001g0114a0003c0003t0001g0219a0005c0005t0001g0132others(3): Show | 6 | HG01884.hp2 HG02145.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.1160-2200G>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105956271 | ||||||
| chr4:105956308
|
A | G | 1 | a0001c0001t0001g0056 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1160-2163A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105956308 | ||||||
| chr4:105956441
|
G | A | 1 | a0001c0001t0006g0010 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1160-2030G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105956441 | ||||||
| chr4:105956474
|
A | G | 23 | a0003c0003t0001g0114a0003c0003t0001g0210a0003c0003t0001g0219others(20): Show | 24 | HG00099.hp2 HG00140.hp1 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.1160-1997A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105956474 | ||||||
| chr4:105956485
|
C | T | 1 | a0001c0001t0001g0198 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1160-1986C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105956485 | ||||||
| chr4:105956486
|
G | A | 1 | a0001c0001t0002g0215 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1160-1985G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105956486 | ||||||
| chr4:105956582
|
A | G | 3 | a0001c0001t0002g0207a0011c0011t0002g0130a0012c0013t0010g0136 | 3 | HG01070.hp2 HG02280.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1160-1889A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105956582 | ||||||
| chr4:105956684
|
A | G | 2 | a0001c0001t0002g0185a0001c0001t0002g0222 | 2 | HG03017.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.1160-1787A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105956684 | ||||||
| chr4:105956714
|
A | G | 4 | a0001c0001t0002g0207a0002c0002t0002g0160a0011c0011t0002g0130others(1): Show | 4 | HG01070.hp2 HG02145.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.1160-1757A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105956714 | ||||||
| chr4:105956886
|
G | A | 23 | a0003c0003t0001g0114a0003c0003t0001g0210a0003c0003t0001g0219others(20): Show | 24 | HG00099.hp2 HG00140.hp1 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.1160-1585G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105956886 | ||||||
| chr4:105956888
|
C | A | 6 | a0002c0002t0002g0158a0002c0002t0002g0159a0002c0002t0002g0167others(3): Show | 6 | HG00280.hp2 HG00639.hp2 HG00741.hp1 others(3): Show |
intron_variant | MODIFIER | c.1160-1583C>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105956888 | ||||||
| chr4:105956979
|
A | G | 1 | a0003c0014t0001g0131 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1160-1492A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105956979 | ||||||
| chr4:105957254
|
G | A | 1 | a0001c0001t0002g0213 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1160-1217G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105957254 | ||||||
| chr4:105957371
|
G | A | 2 | a0001c0001t0001g0138a0003c0014t0001g0131 | 2 | HG01192.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1160-1100G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105957371 | ||||||
| chr4:105957398
|
C | CTGAT | 23 | a0003c0003t0001g0114a0003c0003t0001g0210a0003c0003t0001g0219others(20): Show | 24 | HG00099.hp2 HG00140.hp1 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.1160-1069_1160-106 others(8): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr4 | 105957398 | |||||
| chr4:105957450
|
T | G | 1 | a0001c0001t0001g0138 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1160-1021T>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105957450 | ||||||
| chr4:105957496
|
G | T | 1 | a0001c0001t0001g0055 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1160-975G>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105957496 | ||||||
| chr4:105957582
|
A | G | 3 | a0002c0002t0002g0108a0002c0002t0002g0109a0002c0002t0002g0110 | 3 | HG02647.hp1 HG02922.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1160-889A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105957582 | ||||||
| chr4:105957769
|
C | T | 1 | a0001c0001t0002g0005 | 2 | HG02809.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1160-702C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105957769 | ||||||
| chr4:105957831
|
G | A | 2 | a0011c0011t0002g0130a0012c0013t0010g0136 | 2 | HG01070.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.1160-640G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105957831 | ||||||
| chr4:105957866
|
A | G | 1 | a0002c0002t0001g0070 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1160-605A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105957866 | ||||||
| chr4:105957914
|
G | T | 1 | a0012c0013t0010g0136 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1160-557G>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105957914 | ||||||
| chr4:105958315
|
C | T | 1 | a0002c0002t0001g0061 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1160-156C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105958315 | ||||||
| chr4:105958422
|
A | G | 23 | a0003c0003t0001g0114a0003c0003t0001g0210a0003c0003t0001g0219others(20): Show | 24 | HG00099.hp2 HG00140.hp1 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.1160-49A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105958422 | ||||||
| chr4:105958427
|
T | TCA | 9 | a0001c0001t0001g0006a0001c0001t0001g0198a0001c0001t0001g0199others(6): Show | 10 | HG01069.hp1 HG01192.hp1 HG01975.hp2 others(7): Show |
intron_variant | MODIFIER | c.1160-27_1160-26dup others(2): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr4 | 105958427 | |||||
| chr4:105958435
|
A | G | 3 | a0001c0001t0001g0138a0001c0001t0011g0115a0003c0014t0001g0131 | 3 | HG01192.hp2 HG02280.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1160-36A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 8/11 | chr4 | 105958435 | ||||||
| chr4:105958618
|
A | G | 2 | a0001c0001t0002g0122a0001c0001t0002g0215 | 2 | HG02615.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1246+61A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 9/11 | chr4 | 105958618 | ||||||
| chr4:105958812
|
A | G | 1 | a0001c0001t0002g0221 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1247-216A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 9/11 | chr4 | 105958812 | ||||||
| chr4:105958899
|
A | G | 41 | a0002c0002t0001g0062a0002c0002t0001g0164a0002c0002t0002g0007others(38): Show | 42 | HG00099.hp2 HG00140.hp1 HG00642.hp2 others(39): Show |
intron_variant | MODIFIER | c.1247-129A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 9/11 | chr4 | 105958899 | ||||||
| chr4:105958900
|
T | C | 1 | a0002c0002t0003g0178 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.1247-128T>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 9/11 | chr4 | 105958900 | ||||||
| chr4:105959288
|
A | G | 23 | a0003c0003t0001g0114a0003c0003t0001g0210a0003c0003t0001g0219others(20): Show | 24 | HG00099.hp2 HG00140.hp1 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.1345+162A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | chr4 | 105959288 | ||||||
| chr4:105959356
|
A | G | 23 | a0003c0003t0001g0114a0003c0003t0001g0210a0003c0003t0001g0219others(20): Show | 24 | HG00099.hp2 HG00140.hp1 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.1345+230A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | chr4 | 105959356 | ||||||
| chr4:105959523
|
C | CT | 27 | a0001c0001t0001g0095a0001c0001t0002g0122a0001c0001t0002g0207others(24): Show | 28 | HG00099.hp2 HG00140.hp1 HG00642.hp2 others(25): Show |
intron_variant | MODIFIER | c.1345+413dupT | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr4 | 105959523 | |||||
| chr4:105959523
|
C | T | 1 | a0001c0001t0002g0213 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1345+397C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | chr4 | 105959523 | ||||||
| chr4:105959523
|
CT | C | 25 | a0001c0001t0001g0041a0001c0001t0001g0138a0001c0001t0002g0124others(22): Show | 25 | HG01192.hp2 HG01255.hp1 HG01261.hp1 others(22): Show |
intron_variant | MODIFIER | c.1345+413delT | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr4 | 105959523 | |||||
| chr4:105959592
|
T | C | 2 | a0001c0001t0002g0203a0001c0001t0002g0204 | 2 | HG02965.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1345+466T>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | chr4 | 105959592 | ||||||
| chr4:105959644
|
G | A | 23 | a0003c0003t0001g0114a0003c0003t0001g0210a0003c0003t0001g0219others(20): Show | 24 | HG00099.hp2 HG00140.hp1 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.1345+518G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | chr4 | 105959644 | ||||||
| chr4:105959809
|
C | CT | 29 | a0001c0001t0001g0006a0001c0001t0001g0031a0001c0001t0001g0198others(26): Show | 30 | HG01069.hp1 HG01192.hp1 HG01192.hp2 others(27): Show |
intron_variant | MODIFIER | c.1345+701dupT | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr4 | 105959809 | |||||
| chr4:105959809
|
CT | C | 6 | a0001c0001t0001g0059a0001c0001t0001g0084a0001c0001t0001g0138others(3): Show | 6 | HG01070.hp1 HG01258.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.1345+701delT | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr4 | 105959809 | |||||
| chr4:105959809
|
CTT | C | 18 | a0001c0001t0002g0207a0003c0003t0001g0210a0003c0003t0002g0001others(15): Show | 19 | HG00099.hp2 HG00140.hp1 HG00642.hp2 others(16): Show |
intron_variant | MODIFIER | c.1345+700_1345+701d others(4): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr4 | 105959809 | |||||
| chr4:105959809
|
CTTT | C | 6 | a0003c0003t0001g0114a0003c0003t0001g0219a0005c0005t0001g0132others(3): Show | 6 | HG01884.hp2 HG02145.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.1345+699_1345+701d others(5): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr4 | 105959809 | |||||
| chr4:105959836
|
G | A | 1 | a0001c0001t0002g0124 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1345+710G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | chr4 | 105959836 | ||||||
| chr4:105959863
|
G | A | 1 | a0003c0014t0001g0131 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1345+737G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | chr4 | 105959863 | ||||||
| chr4:105959966
|
T | C | 5 | a0001c0001t0001g0137a0001c0001t0001g0229a0001c0001t0006g0010others(2): Show | 5 | HG00735.hp2 HG01258.hp1 HG01496.hp2 others(2): Show |
intron_variant | MODIFIER | c.1345+840T>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | chr4 | 105959966 | ||||||
| chr4:105960012
|
C | G | 6 | a0002c0002t0001g0088a0002c0002t0003g0166a0002c0002t0003g0171others(3): Show | 6 | HG00140.hp1 HG00741.hp2 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.1345+886C>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | chr4 | 105960012 | ||||||
| chr4:105960027
|
G | T | 179 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(176): Show | 183 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.1345+901G>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | chr4 | 105960027 | ||||||
| chr4:105960100
|
G | A | 1 | a0001c0001t0002g0068 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.1345+974G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | chr4 | 105960100 | ||||||
| chr4:105960200
|
G | A | 28 | a0001c0001t0002g0122a0001c0001t0002g0124a0001c0001t0002g0215others(25): Show | 29 | HG00099.hp2 HG00140.hp1 HG00642.hp2 others(26): Show |
intron_variant | MODIFIER | c.1345+1074G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | chr4 | 105960200 | ||||||
| chr4:105960279
|
T | C | 42 | a0001c0001t0001g0006a0001c0001t0001g0198a0001c0001t0001g0199others(39): Show | 44 | HG00099.hp2 HG00140.hp1 HG00642.hp2 others(41): Show |
intron_variant | MODIFIER | c.1345+1153T>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | chr4 | 105960279 | ||||||
| chr4:105960284
|
A | G | 1 | a0002c0002t0001g0119 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1345+1158A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | chr4 | 105960284 | ||||||
| chr4:105960498
|
A | G | 1 | a0001c0001t0002g0122 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1345+1372A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | chr4 | 105960498 | ||||||
| chr4:105960594
|
C | T | 2 | a0002c0002t0009g0227a0002c0002t0009g0228 | 2 | HG00099.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.1345+1468C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | chr4 | 105960594 | ||||||
| chr4:105960622
|
A | G | 1 | a0001c0001t0002g0005 | 2 | HG02809.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1345+1496A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | chr4 | 105960622 | ||||||
| chr4:105960761
|
C | CGT | 14 | a0001c0001t0001g0008a0001c0001t0001g0201a0001c0001t0002g0005others(11): Show | 15 | HG01070.hp2 HG01192.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.1345+1656_1345+165 others(6): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr4 | 105960761 | |||||
| chr4:105960761
|
C | CGTGT | 8 | a0001c0001t0001g0006a0001c0001t0001g0198a0001c0001t0001g0199others(5): Show | 9 | HG01069.hp1 HG01192.hp1 HG01975.hp2 others(6): Show |
intron_variant | MODIFIER | c.1345+1654_1345+165 others(8): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr4 | 105960761 | |||||
| chr4:105960761
|
CGTGT | C | 28 | a0001c0001t0002g0122a0001c0001t0002g0124a0001c0001t0002g0215others(25): Show | 29 | HG00099.hp2 HG00140.hp1 HG00642.hp2 others(26): Show |
intron_variant | MODIFIER | c.1345+1654_1345+165 others(8): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr4 | 105960761 | |||||
| chr4:105960921
|
A | G | 28 | a0001c0001t0002g0122a0001c0001t0002g0124a0001c0001t0002g0215others(25): Show | 29 | HG00099.hp2 HG00140.hp1 HG00642.hp2 others(26): Show |
intron_variant | MODIFIER | c.1345+1795A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | chr4 | 105960921 | ||||||
| chr4:105960960
|
C | G | 1 | a0001c0001t0002g0053 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1345+1834C>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | chr4 | 105960960 | ||||||
| chr4:105961059
|
C | A | 1 | a0001c0001t0002g0220 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1345+1933C>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | chr4 | 105961059 | ||||||
| chr4:105961239
|
A | C | 1 | a0012c0013t0010g0136 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1345+2113A>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | chr4 | 105961239 | ||||||
| chr4:105961241
|
C | A | 1 | a0012c0013t0010g0136 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1345+2115C>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | chr4 | 105961241 | ||||||
| chr4:105961377
|
A | G | 1 | a0011c0011t0002g0130 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1345+2251A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | chr4 | 105961377 | ||||||
| chr4:105961401
|
A | G | 6 | a0003c0003t0001g0114a0003c0003t0001g0219a0005c0005t0001g0132others(3): Show | 6 | HG01884.hp2 HG02145.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.1345+2275A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | chr4 | 105961401 | ||||||
| chr4:105961437
|
C | T | 32 | a0001c0001t0001g0138a0001c0001t0002g0122a0001c0001t0002g0124others(29): Show | 33 | HG00099.hp2 HG00140.hp1 HG00642.hp2 others(30): Show |
intron_variant | MODIFIER | c.1345+2311C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | chr4 | 105961437 | ||||||
| chr4:105961699
|
C | T | 28 | a0001c0001t0002g0122a0001c0001t0002g0124a0001c0001t0002g0215others(25): Show | 29 | HG00099.hp2 HG00140.hp1 HG00642.hp2 others(26): Show |
intron_variant | MODIFIER | c.1345+2573C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | chr4 | 105961699 | ||||||
| chr4:105961735
|
C | T | 1 | a0001c0001t0008g0058 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1345+2609C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | chr4 | 105961735 | ||||||
| chr4:105961987
|
G | T | 28 | a0001c0001t0002g0122a0001c0001t0002g0124a0001c0001t0002g0215others(25): Show | 29 | HG00099.hp2 HG00140.hp1 HG00642.hp2 others(26): Show |
intron_variant | MODIFIER | c.1345+2861G>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | chr4 | 105961987 | ||||||
| chr4:105962059
|
G | A | 3 | a0001c0001t0001g0138a0001c0001t0011g0115a0003c0014t0001g0131 | 3 | HG01192.hp2 HG02280.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1345+2933G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | chr4 | 105962059 | ||||||
| chr4:105962345
|
A | G | 2 | a0001c0001t0001g0008a0001c0001t0001g0201 | 2 | HG03098.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1345+3219A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | chr4 | 105962345 | ||||||
| chr4:105962460
|
T | C | 28 | a0001c0001t0002g0122a0001c0001t0002g0124a0001c0001t0002g0215others(25): Show | 29 | HG00099.hp2 HG00140.hp1 HG00642.hp2 others(26): Show |
intron_variant | MODIFIER | c.1345+3334T>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | chr4 | 105962460 | ||||||
| chr4:105962803
|
T | C | 1 | a0003c0014t0001g0131 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1345+3677T>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | chr4 | 105962803 | ||||||
| chr4:105962816
|
T | C | 28 | a0001c0001t0002g0122a0001c0001t0002g0124a0001c0001t0002g0215others(25): Show | 29 | HG00099.hp2 HG00140.hp1 HG00642.hp2 others(26): Show |
intron_variant | MODIFIER | c.1345+3690T>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | chr4 | 105962816 | ||||||
| chr4:105962851
|
A | ATG | 7 | a0001c0001t0001g0067a0001c0001t0001g0071a0001c0001t0001g0077others(4): Show | 7 | HG00099.hp1 HG00438.hp2 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.1345+3743_1345+374 others(6): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr4 | 105962851 | |||||
| chr4:105962851
|
ATG | A | 12 | a0001c0001t0001g0138a0003c0003t0001g0120a0003c0003t0002g0190others(9): Show | 12 | HG01070.hp2 HG01192.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.1345+3743_1345+374 others(6): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr4 | 105962851 | |||||
| chr4:105962851
|
ATGTG | A | 12 | a0001c0001t0002g0122a0001c0001t0002g0124a0001c0001t0002g0215others(9): Show | 12 | HG01884.hp2 HG02145.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.1345+3741_1345+374 others(8): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr4 | 105962851 | |||||
| chr4:105962865
|
GTGTGTA | G | 16 | a0003c0003t0001g0210a0003c0003t0002g0001a0003c0003t0002g0209others(13): Show | 17 | HG00099.hp2 HG00140.hp1 HG00642.hp2 others(14): Show |
intron_variant | MODIFIER | c.1345+3745_1345+375 others(10): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr4 | 105962865 | |||||
| chr4:105962873
|
G | A | 16 | a0003c0003t0001g0210a0003c0003t0002g0001a0003c0003t0002g0209others(13): Show | 17 | HG00099.hp2 HG00140.hp1 HG00642.hp2 others(14): Show |
intron_variant | MODIFIER | c.1345+3747G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | chr4 | 105962873 | ||||||
| chr4:105962885
|
A | G | 1 | a0011c0011t0002g0130 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1345+3759A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | chr4 | 105962885 | ||||||
| chr4:105963019
|
G | A | 5 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0002g0202others(2): Show | 5 | HG01975.hp2 HG02965.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1345+3893G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | chr4 | 105963019 | ||||||
| chr4:105963086
|
G | A | 3 | a0001c0001t0001g0138a0001c0001t0011g0115a0003c0014t0001g0131 | 3 | HG01192.hp2 HG02280.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1345+3960G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | chr4 | 105963086 | ||||||
| chr4:105963097
|
C | A | 28 | a0001c0001t0002g0122a0001c0001t0002g0124a0001c0001t0002g0215others(25): Show | 29 | HG00099.hp2 HG00140.hp1 HG00642.hp2 others(26): Show |
intron_variant | MODIFIER | c.1345+3971C>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | chr4 | 105963097 | ||||||
| chr4:105963133
|
G | A | 3 | a0002c0002t0002g0192a0006c0006t0002g0193a0006c0006t0002g0195 | 3 | HG02896.hp1 HG02897.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1345+4007G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | chr4 | 105963133 | ||||||
| chr4:105963145
|
A | G | 8 | a0003c0003t0001g0120a0003c0003t0002g0190a0003c0003t0005g0113others(5): Show | 8 | HG02055.hp1 HG02630.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.1345+4019A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | chr4 | 105963145 | ||||||
| chr4:105963200
|
A | G | 31 | a0001c0001t0002g0005a0001c0001t0002g0122a0001c0001t0002g0124others(28): Show | 33 | HG00099.hp2 HG00140.hp1 HG00642.hp2 others(30): Show |
intron_variant | MODIFIER | c.1346-3988A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | chr4 | 105963200 | ||||||
| chr4:105963229
|
A | AT | 28 | a0001c0001t0002g0122a0001c0001t0002g0124a0001c0001t0002g0215others(25): Show | 29 | HG00099.hp2 HG00140.hp1 HG00642.hp2 others(26): Show |
intron_variant | MODIFIER | c.1346-3959_1346-395 others(5): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | chr4 | 105963229 | ||||||
| chr4:105963582
|
G | A | 28 | a0001c0001t0002g0122a0001c0001t0002g0124a0001c0001t0002g0215others(25): Show | 29 | HG00099.hp2 HG00140.hp1 HG00642.hp2 others(26): Show |
intron_variant | MODIFIER | c.1346-3606G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | chr4 | 105963582 | ||||||
| chr4:105963639
|
A | C | 28 | a0001c0001t0002g0122a0001c0001t0002g0124a0001c0001t0002g0215others(25): Show | 29 | HG00099.hp2 HG00140.hp1 HG00642.hp2 others(26): Show |
intron_variant | MODIFIER | c.1346-3549A>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | chr4 | 105963639 | ||||||
| chr4:105963660
|
C | A | 28 | a0001c0001t0002g0122a0001c0001t0002g0124a0001c0001t0002g0215others(25): Show | 29 | HG00099.hp2 HG00140.hp1 HG00642.hp2 others(26): Show |
intron_variant | MODIFIER | c.1346-3528C>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | chr4 | 105963660 | ||||||
| chr4:105963806
|
A | G | 1 | a0001c0001t0001g0052 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1346-3382A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | chr4 | 105963806 | ||||||
| chr4:105963873
|
G | A | 1 | a0002c0002t0002g0026 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1346-3315G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | chr4 | 105963873 | ||||||
| chr4:105963877
|
C | G | 1 | a0001c0001t0011g0115 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1346-3311C>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | chr4 | 105963877 | ||||||
| chr4:105963988
|
C | A | 1 | a0001c0001t0002g0207 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1346-3200C>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | chr4 | 105963988 | ||||||
| chr4:105964199
|
C | T | 1 | a0002c0002t0003g0184 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1346-2989C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | chr4 | 105964199 | ||||||
| chr4:105964341
|
G | A | 28 | a0001c0001t0002g0122a0001c0001t0002g0124a0001c0001t0002g0215others(25): Show | 29 | HG00099.hp2 HG00140.hp1 HG00642.hp2 others(26): Show |
intron_variant | MODIFIER | c.1346-2847G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | chr4 | 105964341 | ||||||
| chr4:105964429
|
G | A | 28 | a0001c0001t0002g0122a0001c0001t0002g0124a0001c0001t0002g0215others(25): Show | 29 | HG00099.hp2 HG00140.hp1 HG00642.hp2 others(26): Show |
intron_variant | MODIFIER | c.1346-2759G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | chr4 | 105964429 | ||||||
| chr4:105964695
|
T | C | 1 | a0001c0001t0001g0138 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1346-2493T>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | chr4 | 105964695 | ||||||
| chr4:105964861
|
T | G | 1 | a0001c0001t0002g0124 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1346-2327T>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | chr4 | 105964861 | ||||||
| chr4:105964912
|
A | G | 1 | a0001c0001t0002g0124 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1346-2276A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | chr4 | 105964912 | ||||||
| chr4:105965182
|
T | C | 6 | a0001c0001t0002g0050a0003c0003t0001g0114a0003c0003t0001g0219others(3): Show | 6 | HG01884.hp2 HG02145.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.1346-2006T>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | chr4 | 105965182 | ||||||
| chr4:105965302
|
G | C | 1 | a0001c0001t0001g0194 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1346-1886G>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | chr4 | 105965302 | ||||||
| chr4:105965360
|
C | CA | 21 | a0001c0001t0001g0083a0001c0001t0002g0065a0001c0001t0002g0099others(18): Show | 21 | HG00642.hp1 HG02055.hp1 HG02630.hp2 others(18): Show |
intron_variant | MODIFIER | c.1346-1811dupA | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr4 | 105965360 | |||||
| chr4:105965360
|
C | CAAA | 14 | a0001c0001t0002g0078a0001c0001t0002g0122a0001c0001t0002g0215others(11): Show | 15 | HG01884.hp2 HG02145.hp2 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.1346-1813_1346-181 others(7): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr4 | 105965360 | |||||
| chr4:105965360
|
CA | C | 24 | a0001c0001t0001g0059a0001c0001t0001g0174a0001c0001t0001g0187others(21): Show | 24 | HG00408.hp1 HG00438.hp1 HG00597.hp2 others(21): Show |
intron_variant | MODIFIER | c.1346-1811delA | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr4 | 105965360 | |||||
| chr4:105965399
|
C | T | 12 | a0001c0001t0002g0005a0001c0001t0002g0207a0003c0003t0001g0120others(9): Show | 13 | HG01070.hp2 HG02055.hp1 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.1346-1789C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | chr4 | 105965399 | ||||||
| chr4:105965733
|
A | G | 1 | a0001c0001t0001g0018 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1346-1455A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | chr4 | 105965733 | ||||||
| chr4:105965836
|
G | T | 2 | a0010c0012t0010g0123a0012c0013t0010g0136 | 2 | HG02280.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1346-1352G>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | chr4 | 105965836 | ||||||
| chr4:105965862
|
G | A | 9 | a0001c0001t0005g0112a0003c0003t0005g0113a0003c0003t0005g0121others(6): Show | 9 | HG02055.hp1 HG02451.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.1346-1326G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | chr4 | 105965862 | ||||||
| chr4:105966006
|
G | A | 83 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0013others(80): Show | 84 | HG00408.hp2 HG00438.hp2 HG00597.hp1 others(81): Show |
intron_variant | MODIFIER | c.1346-1182G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | chr4 | 105966006 | ||||||
| chr4:105966017
|
G | GAGA | 135 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0008others(132): Show | 139 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.1346-1167_1346-116 others(7): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr4 | 105966017 | |||||
| chr4:105966148
|
T | C | 1 | a0002c0002t0001g0042 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1346-1040T>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | chr4 | 105966148 | ||||||
| chr4:105966285
|
T | C | 8 | a0001c0001t0005g0112a0003c0003t0005g0113a0003c0003t0005g0121others(5): Show | 8 | HG02055.hp1 HG02451.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1346-903T>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | chr4 | 105966285 | ||||||
| chr4:105966331
|
A | AT | 5 | a0001c0001t0001g0055a0001c0001t0001g0100a0001c0001t0001g0101others(2): Show | 5 | HG01069.hp2 HG01081.hp2 HG01346.hp1 others(2): Show |
intron_variant | MODIFIER | c.1346-849dupT | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr4 | 105966331 | |||||
| chr4:105966341
|
T | G | 6 | a0003c0003t0005g0113a0003c0003t0005g0121a0003c0003t0005g0126others(3): Show | 6 | HG02055.hp1 HG02630.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1346-847T>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | chr4 | 105966341 | ||||||
| chr4:105966478
|
A | G | 2 | a0010c0012t0010g0123a0012c0013t0010g0136 | 2 | HG02280.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1346-710A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | chr4 | 105966478 | ||||||
| chr4:105966626
|
C | CT | 4 | a0001c0001t0002g0122a0001c0001t0002g0215a0003c0003t0002g0209others(1): Show | 4 | HG02615.hp1 HG03209.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1346-561dupT | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr4 | 105966626 | |||||
| chr4:105966661
|
C | T | 1 | a0010c0012t0010g0123 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1346-527C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | chr4 | 105966661 | ||||||
| chr4:105966670
|
ATTT | A | 8 | a0001c0001t0005g0112a0003c0003t0005g0113a0003c0003t0005g0121others(5): Show | 8 | HG02055.hp1 HG02451.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1346-508_1346-506d others(5): Show |
NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr4 | 105966670 | |||||
| chr4:105966889
|
T | C | 123 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0008others(120): Show | 125 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(122): Show |
intron_variant | MODIFIER | c.1346-299T>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | chr4 | 105966889 | ||||||
| chr4:105966918
|
C | T | 121 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0008others(118): Show | 123 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(120): Show |
intron_variant | MODIFIER | c.1346-270C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | chr4 | 105966918 | ||||||
| chr4:105966951
|
T | C | 1 | a0013c0010t0002g0191 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1346-237T>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | chr4 | 105966951 | ||||||
| chr4:105967052
|
A | G | 1 | a0003c0003t0002g0217 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1346-136A>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | chr4 | 105967052 | ||||||
| chr4:105967106
|
A | C | 97 | a0001c0001t0001g0008a0001c0001t0001g0201a0001c0001t0002g0025others(94): Show | 99 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.1346-82A>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 10/11 | chr4 | 105967106 | ||||||
| chr4:105967479
|
C | T | 1 | a0001c0001t0001g0074 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1602+35C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 11/11 | chr4 | 105967479 | ||||||
| chr4:105967524
|
C | G | 1 | a0003c0003t0002g0217 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1602+80C>G | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 11/11 | chr4 | 105967524 | ||||||
| chr4:105967585
|
C | T | 1 | a0013c0010t0002g0191 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1602+141C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 11/11 | chr4 | 105967585 | ||||||
| chr4:105967728
|
G | T | 1 | a0001c0001t0001g0052 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1602+284G>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 11/11 | chr4 | 105967728 | ||||||
| chr4:105967931
|
G | A | 1 | a0001c0001t0005g0112 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1602+487G>A | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 11/11 | chr4 | 105967931 | ||||||
| chr4:105968333
|
G | C | 104 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0008others(101): Show | 106 | HG00408.hp2 HG00438.hp2 HG00597.hp1 others(103): Show |
intron_variant | MODIFIER | c.1603-562G>C | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 11/11 | chr4 | 105968333 | ||||||
| chr4:105968423
|
C | T | 2 | a0001c0001t0002g0207a0011c0011t0002g0130 | 2 | HG01070.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1603-472C>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 11/11 | chr4 | 105968423 | ||||||
| chr4:105968560
|
G | T | 1 | a0009c0009t0001g0156 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1603-335G>T | NPNT | ENSG00000168743.13 | transcript | ENST00000379987.7 | protein_coding | 11/11 | chr4 | 105968560 |