| geneid | 8828 |
|---|---|
| ensemblid | ENSG00000118257.17 |
| hgncid | 8005 |
| symbol | NRP2 |
| name | neuropilin 2 |
| refseq_nuc | NM_003872.3 |
| refseq_prot | NP_003863.2 |
| ensembl_nuc | ENST00000357785.10 |
| ensembl_prot | ENSP00000350432.5 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 205682501 |
| end | 205798131 |
| strand | + |
| ver | v1.2 |
| region | chr2:205682501-205798131 |
| region5000 | chr2:205677501-205803131 |
| regionname0 | NRP2_chr2_205682501_205798131 |
| regionname5000 | NRP2_chr2_205677501_205803131 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 926 | 335 | 81 | 72 | 129 | 16 | 35 | 94 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| a0002 | 0/0 | 926 | 10 | 9 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| a0003 | 0/0 | 926 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| a0004 | 0/0 | 926 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| a0005 | 0/0 | 926 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| a0006 | 0/0 | 926 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| a0007 | 0/0 | 926 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| a0008 | 0/0 | 926 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/0 | 2781 | 100 | 2 | 28 | 48 | 8 | 14 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| c0002 | 0/1 | 2781 | 76 | 38 | 18 | 10 | 2 | 7 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| c0003 | 0/0 | 2781 | 59 | 10 | 7 | 35 | 1 | 6 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| c0004 | 0/0 | 2781 | 55 | 2 | 12 | 36 | 1 | 4 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| c0005 | 0/0 | 2781 | 9 | 3 | 3 | 0 | 2 | 1 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| c0006 | 0/0 | 2781 | 8 | 8 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| c0007 | 1/0 | 2781 | 5 | 4 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| c0008 | 0/0 | 2781 | 4 | 4 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| c0009 | 0/0 | 2781 | 4 | 1 | 3 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| c0010 | 0/0 | 2781 | 4 | 0 | 0 | 0 | 2 | 2 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| c0011 | 0/0 | 2781 | 2 | 2 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| c0012 | 0/0 | 2781 | 2 | 2 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| c0013 | 0/0 | 2781 | 2 | 2 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| c0014 | 0/0 | 2781 | 2 | 2 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| c0015 | 0/0 | 2781 | 2 | 2 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| c0016 | 0/0 | 2781 | 2 | 2 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| c0017 | 0/0 | 2781 | 2 | 2 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| c0018 | 0/0 | 2781 | 2 | 2 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| c0019 | 0/0 | 2781 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| c0020 | 0/0 | 2781 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| c0021 | 0/0 | 2781 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| c0022 | 0/0 | 2781 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| c0023 | 0/0 | 2781 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| c0024 | 0/0 | 2781 | 1 | 0 | 0 | 0 | 0 | 1 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| c0025 | 0/0 | 2781 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| c0026 | 0/0 | 2781 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| c0027 | 0/0 | 2781 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| c0028 | 0/0 | 2781 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| c0029 | 0/0 | 2781 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| c0030 | 0/0 | 2781 | 1 | 0 | 0 | 0 | 0 | 1 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 3867 | 43 | 4 | 11 | 23 | 1 | 4 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| t0002 | 0/0 | 3867 | 35 | 3 | 5 | 17 | 2 | 8 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| t0003 | 0/0 | 3861 | 28 | 0 | 5 | 23 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| t0004 | 0/0 | 3861 | 25 | 17 | 3 | 2 | 1 | 2 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| t0005 | 0/0 | 3873 | 22 | 0 | 2 | 18 | 1 | 1 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| t0006 | 0/0 | 3861 | 21 | 0 | 4 | 17 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| t0007 | 0/0 | 3867 | 19 | 8 | 9 | 0 | 1 | 1 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| t0008 | 0/0 | 3867 | 16 | 8 | 4 | 0 | 1 | 3 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| t0009 | 0/0 | 3870 | 13 | 3 | 2 | 1 | 3 | 4 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| t0010 | 0/0 | 3873 | 13 | 0 | 3 | 8 | 0 | 2 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| t0011 | 0/0 | 3861 | 12 | 9 | 1 | 1 | 0 | 1 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| t0012 | 0/0 | 3870 | 12 | 3 | 5 | 1 | 1 | 2 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| t0013 | 1/0 | 3864 | 9 | 5 | 1 | 0 | 1 | 1 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| t0014 | 0/0 | 3870 | 6 | 0 | 0 | 3 | 0 | 3 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| t0015 | 0/0 | 3870 | 5 | 0 | 1 | 3 | 0 | 1 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| t0016 | 0/0 | 3864 | 4 | 4 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| t0017 | 0/0 | 3864 | 3 | 3 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| t0018 | 0/0 | 3864 | 3 | 0 | 3 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| t0019 | 0/0 | 3867 | 3 | 0 | 3 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| t0020 | 0/0 | 3867 | 3 | 1 | 2 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| t0021 | 0/0 | 3873 | 3 | 1 | 0 | 2 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| t0022 | 0/0 | 3861 | 3 | 3 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| t0023 | 0/0 | 3867 | 3 | 0 | 1 | 0 | 2 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| t0024 | 0/0 | 3873 | 2 | 0 | 0 | 1 | 0 | 1 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| t0025 | 0/0 | 3876 | 2 | 0 | 1 | 0 | 0 | 1 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| t0026 | 0/0 | 3867 | 2 | 1 | 0 | 0 | 1 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| t0027 | 0/0 | 3876 | 2 | 0 | 1 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| t0028 | 0/0 | 3861 | 2 | 2 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| t0029 | 0/0 | 3861 | 2 | 1 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| t0030 | 0/0 | 3867 | 2 | 2 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| t0031 | 0/0 | 3867 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| t0032 | 0/1 | 3861 | 1 | 0 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| t0033 | 0/0 | 3870 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| t0034 | 0/0 | 3861 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| t0035 | 0/0 | 3861 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| t0036 | 0/0 | 3861 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| t0037 | 0/0 | 3861 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| t0038 | 0/0 | 3864 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| t0039 | 0/0 | 3864 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| t0040 | 0/0 | 3867 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| t0041 | 0/0 | 3870 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| t0042 | 0/0 | 3873 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| t0043 | 0/0 | 3861 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| t0044 | 0/0 | 3870 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| t0045 | 0/0 | 3861 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| t0046 | 0/0 | 3876 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| t0047 | 0/0 | 3867 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| t0048 | 0/0 | 3861 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| t0049 | 0/0 | 3861 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| t0050 | 0/0 | 3864 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| t0051 | 0/0 | 3864 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| t0052 | 0/0 | 3867 | 1 | 0 | 0 | 0 | 0 | 1 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| t0053 | 0/0 | 3867 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| t0054 | 0/0 | 3867 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| t0055 | 0/0 | 3870 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| t0056 | 0/0 | 3870 | 1 | 0 | 0 | 0 | 1 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| t0057 | 0/0 | 3870 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| t0058 | 0/0 | 3854 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| t0059 | 0/0 | 3873 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| t0060 | 0/0 | 3873 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| t0061 | 0/0 | 3861 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| t0062 | 0/0 | 3867 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| t0063 | 0/0 | 3864 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| t0064 | 0/0 | 3867 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0006 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0014 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0020 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0026 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0030 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0179 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0214 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0232 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0234 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0240 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0242 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0327 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0331 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0341 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0342 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 2781 | 100 | 2 | 28 | 48 | 8 | 14 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| a0001c0002 | 0/1 | 2781 | 76 | 38 | 18 | 10 | 2 | 7 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| a0001c0003 | 0/0 | 2781 | 59 | 10 | 7 | 35 | 1 | 6 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| a0001c0004 | 0/0 | 2781 | 55 | 2 | 12 | 36 | 1 | 4 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| a0001c0005 | 0/0 | 2781 | 9 | 3 | 3 | 0 | 2 | 1 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| a0001c0006 | 0/0 | 2781 | 8 | 8 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| a0001c0007 | 1/0 | 2781 | 5 | 4 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| a0001c0008 | 0/0 | 2781 | 4 | 4 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| a0001c0009 | 0/0 | 2781 | 4 | 1 | 3 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| a0001c0010 | 0/0 | 2781 | 4 | 0 | 0 | 0 | 2 | 2 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| a0001c0011 | 0/0 | 2781 | 2 | 2 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| a0001c0012 | 0/0 | 2781 | 2 | 2 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| a0001c0013 | 0/0 | 2781 | 2 | 2 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| a0001c0018 | 0/0 | 2781 | 2 | 2 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| a0001c0020 | 0/0 | 2781 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| a0001c0023 | 0/0 | 2781 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| a0001c0030 | 0/0 | 2781 | 1 | 0 | 0 | 0 | 0 | 1 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| a0002c0014 | 0/0 | 2781 | 2 | 2 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| a0002c0015 | 0/0 | 2781 | 2 | 2 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| a0002c0016 | 0/0 | 2781 | 2 | 2 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| a0002c0017 | 0/0 | 2781 | 2 | 2 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| a0002c0027 | 0/0 | 2781 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| a0002c0029 | 0/0 | 2781 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| a0003c0025 | 0/0 | 2781 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| a0003c0026 | 0/0 | 2781 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| a0004c0022 | 0/0 | 2781 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| a0005c0021 | 0/0 | 2781 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| a0006c0024 | 0/0 | 2781 | 1 | 0 | 0 | 0 | 0 | 1 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| a0007c0019 | 0/0 | 2781 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| a0008c0028 | 0/0 | 2781 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 6647 | 17 | 1 | 5 | 7 | 1 | 3 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| a0001c0001t0002 | 0/0 | 6647 | 10 | 0 | 2 | 5 | 1 | 2 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| a0001c0001t0003 | 0/0 | 6641 | 7 | 0 | 2 | 5 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| a0001c0001t0004 | 0/0 | 6641 | 7 | 0 | 2 | 2 | 1 | 2 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| a0001c0001t0005 | 0/0 | 6653 | 11 | 0 | 0 | 11 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| a0001c0001t0006 | 0/0 | 6641 | 7 | 0 | 2 | 5 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| a0001c0001t0007 | 0/0 | 6647 | 2 | 0 | 0 | 0 | 1 | 1 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| a0001c0001t0008 | 0/0 | 6647 | 3 | 0 | 1 | 0 | 1 | 1 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| a0001c0001t0009 | 0/0 | 6650 | 4 | 0 | 1 | 1 | 1 | 1 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| a0001c0001t0010 | 0/0 | 6653 | 9 | 0 | 2 | 7 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| a0001c0001t0011 | 0/0 | 6641 | 2 | 1 | 0 | 0 | 0 | 1 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| a0001c0001t0012 | 0/0 | 6650 | 6 | 0 | 3 | 0 | 1 | 2 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| a0001c0001t0013 | 0/0 | 6644 | 1 | 0 | 0 | 0 | 0 | 1 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| a0001c0001t0015 | 0/0 | 6650 | 3 | 0 | 0 | 3 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| a0001c0001t0018 | 0/0 | 6644 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| a0001c0001t0019 | 0/0 | 6647 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| a0001c0001t0020 | 0/0 | 6647 | 2 | 0 | 2 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| a0001c0001t0026 | 0/0 | 6647 | 1 | 0 | 0 | 0 | 1 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| a0001c0001t0027 | 0/0 | 6656 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| a0001c0001t0031 | 0/0 | 6647 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| a0001c0001t0037 | 0/0 | 6641 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| a0001c0001t0053 | 0/0 | 6647 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| a0001c0001t0057 | 0/0 | 6650 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| a0001c0001t0058 | 0/0 | 6634 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| a0001c0002t0001 | 0/0 | 6647 | 6 | 1 | 1 | 3 | 0 | 1 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| a0001c0002t0002 | 0/0 | 6647 | 5 | 3 | 1 | 0 | 0 | 1 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| a0001c0002t0003 | 0/0 | 6641 | 4 | 0 | 1 | 3 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| a0001c0002t0004 | 0/0 | 6641 | 6 | 5 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| a0001c0002t0005 | 0/0 | 6653 | 1 | 0 | 0 | 0 | 1 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| a0001c0002t0006 | 0/0 | 6641 | 3 | 0 | 0 | 3 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| a0001c0002t0007 | 0/0 | 6647 | 9 | 4 | 5 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| a0001c0002t0008 | 0/0 | 6647 | 7 | 4 | 2 | 0 | 0 | 1 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| a0001c0002t0009 | 0/0 | 6650 | 2 | 1 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| a0001c0002t0010 | 0/0 | 6653 | 3 | 0 | 1 | 0 | 0 | 2 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| a0001c0002t0011 | 0/0 | 6641 | 2 | 1 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| a0001c0002t0012 | 0/0 | 6650 | 2 | 1 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| a0001c0002t0013 | 0/0 | 6644 | 2 | 2 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| a0001c0002t0014 | 0/0 | 6650 | 1 | 0 | 0 | 0 | 0 | 1 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| a0001c0002t0015 | 0/0 | 6650 | 1 | 0 | 0 | 0 | 0 | 1 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| a0001c0002t0016 | 0/0 | 6644 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| a0001c0002t0017 | 0/0 | 6644 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| a0001c0002t0018 | 0/0 | 6644 | 2 | 0 | 2 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| a0001c0002t0020 | 0/0 | 6647 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| a0001c0002t0022 | 0/0 | 6641 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| a0001c0002t0025 | 0/0 | 6656 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| a0001c0002t0028 | 0/0 | 6641 | 2 | 2 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| a0001c0002t0029 | 0/0 | 6641 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| a0001c0002t0032 | 0/1 | 6641 | 1 | 0 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| a0001c0002t0033 | 0/0 | 6650 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| a0001c0002t0042 | 0/0 | 6653 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| a0001c0002t0043 | 0/0 | 6641 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| a0001c0002t0046 | 0/0 | 6656 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| a0001c0002t0048 | 0/0 | 6641 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| a0001c0002t0049 | 0/0 | 6641 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| a0001c0002t0051 | 0/0 | 6644 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| a0001c0002t0054 | 0/0 | 6647 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| a0001c0002t0056 | 0/0 | 6650 | 1 | 0 | 0 | 0 | 1 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| a0001c0002t0061 | 0/0 | 6641 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| a0001c0002t0063 | 0/0 | 6644 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| a0001c0003t0001 | 0/0 | 6647 | 10 | 0 | 0 | 10 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| a0001c0003t0002 | 0/0 | 6647 | 5 | 0 | 1 | 1 | 1 | 2 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| a0001c0003t0003 | 0/0 | 6641 | 8 | 0 | 0 | 8 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| a0001c0003t0004 | 0/0 | 6641 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| a0001c0003t0005 | 0/0 | 6653 | 3 | 0 | 0 | 3 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| a0001c0003t0006 | 0/0 | 6641 | 5 | 0 | 0 | 5 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| a0001c0003t0007 | 0/0 | 6647 | 3 | 1 | 2 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| a0001c0003t0008 | 0/0 | 6647 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| a0001c0003t0009 | 0/0 | 6650 | 2 | 1 | 0 | 0 | 0 | 1 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| a0001c0003t0011 | 0/0 | 6641 | 4 | 3 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| a0001c0003t0012 | 0/0 | 6650 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| a0001c0003t0014 | 0/0 | 6650 | 3 | 0 | 0 | 2 | 0 | 1 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| a0001c0003t0015 | 0/0 | 6650 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| a0001c0003t0021 | 0/0 | 6653 | 2 | 0 | 0 | 2 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| a0001c0003t0022 | 0/0 | 6641 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| a0001c0003t0024 | 0/0 | 6653 | 2 | 0 | 0 | 1 | 0 | 1 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| a0001c0003t0025 | 0/0 | 6656 | 1 | 0 | 0 | 0 | 0 | 1 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| a0001c0003t0034 | 0/0 | 6641 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| a0001c0003t0035 | 0/0 | 6641 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| a0001c0003t0040 | 0/0 | 6647 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| a0001c0003t0045 | 0/0 | 6641 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| a0001c0003t0047 | 0/0 | 6647 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| a0001c0003t0055 | 0/0 | 6650 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| a0001c0004t0001 | 0/0 | 6647 | 8 | 0 | 5 | 3 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| a0001c0004t0002 | 0/0 | 6647 | 13 | 0 | 1 | 10 | 0 | 2 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| a0001c0004t0003 | 0/0 | 6641 | 9 | 0 | 2 | 7 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| a0001c0004t0005 | 0/0 | 6653 | 5 | 0 | 0 | 4 | 0 | 1 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| a0001c0004t0006 | 0/0 | 6641 | 5 | 0 | 1 | 4 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| a0001c0004t0008 | 0/0 | 6647 | 1 | 0 | 0 | 0 | 0 | 1 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| a0001c0004t0010 | 0/0 | 6653 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| a0001c0004t0012 | 0/0 | 6650 | 2 | 0 | 1 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| a0001c0004t0013 | 0/0 | 6644 | 1 | 0 | 0 | 0 | 1 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| a0001c0004t0014 | 0/0 | 6650 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| a0001c0004t0019 | 0/0 | 6647 | 2 | 0 | 2 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| a0001c0004t0022 | 0/0 | 6641 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| a0001c0004t0026 | 0/0 | 6647 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| a0001c0004t0041 | 0/0 | 6650 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| a0001c0004t0044 | 0/0 | 6650 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| a0001c0004t0050 | 0/0 | 6644 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| a0001c0004t0059 | 0/0 | 6653 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| a0001c0004t0060 | 0/0 | 6653 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| a0001c0005t0004 | 0/0 | 6641 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| a0001c0005t0007 | 0/0 | 6647 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| a0001c0005t0008 | 0/0 | 6647 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| a0001c0005t0013 | 0/0 | 6644 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| a0001c0005t0014 | 0/0 | 6650 | 1 | 0 | 0 | 0 | 0 | 1 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| a0001c0005t0023 | 0/0 | 6647 | 3 | 0 | 1 | 0 | 2 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| a0001c0005t0029 | 0/0 | 6641 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| a0001c0006t0007 | 0/0 | 6647 | 2 | 2 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| a0001c0006t0009 | 0/0 | 6650 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| a0001c0006t0011 | 0/0 | 6641 | 3 | 3 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| a0001c0006t0036 | 0/0 | 6641 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| a0001c0006t0039 | 0/0 | 6644 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| a0001c0007t0008 | 0/0 | 6647 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| a0001c0007t0011 | 0/0 | 6641 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| a0001c0007t0013 | 1/0 | 6644 | 2 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| a0001c0007t0017 | 0/0 | 6644 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| a0001c0008t0004 | 0/0 | 6641 | 4 | 4 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| a0001c0009t0005 | 0/0 | 6653 | 2 | 0 | 2 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| a0001c0009t0021 | 0/0 | 6653 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| a0001c0009t0027 | 0/0 | 6656 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| a0001c0010t0009 | 0/0 | 6650 | 4 | 0 | 0 | 0 | 2 | 2 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| a0001c0011t0004 | 0/0 | 6641 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| a0001c0011t0008 | 0/0 | 6647 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| a0001c0012t0004 | 0/0 | 6641 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| a0001c0012t0017 | 0/0 | 6644 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| a0001c0013t0016 | 0/0 | 6644 | 2 | 2 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| a0001c0018t0007 | 0/0 | 6647 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| a0001c0018t0038 | 0/0 | 6644 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| a0001c0020t0012 | 0/0 | 6650 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| a0001c0023t0007 | 0/0 | 6647 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| a0001c0030t0052 | 0/0 | 6647 | 1 | 0 | 0 | 0 | 0 | 1 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| a0002c0014t0001 | 0/0 | 6647 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| a0002c0014t0008 | 0/0 | 6647 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| a0002c0015t0030 | 0/0 | 6647 | 2 | 2 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| a0002c0016t0001 | 0/0 | 6647 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| a0002c0016t0004 | 0/0 | 6641 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| a0002c0017t0004 | 0/0 | 6641 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| a0002c0017t0062 | 0/0 | 6647 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| a0002c0027t0064 | 0/0 | 6647 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| a0002c0029t0013 | 0/0 | 6644 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| a0003c0025t0013 | 0/0 | 6644 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| a0003c0026t0004 | 0/0 | 6641 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| a0004c0022t0006 | 0/0 | 6641 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| a0005c0021t0004 | 0/0 | 6641 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| a0006c0024t0002 | 0/0 | 6647 | 1 | 0 | 0 | 0 | 0 | 1 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| a0007c0019t0002 | 0/0 | 6647 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| a0008c0028t0016 | 0/0 | 6644 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | copy fasta | chr2 | 205677501 | 205803131 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0002g0006 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0002g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0002g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0003g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0003g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0003g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0003g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0003g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0003g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0003g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0004g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0004g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0004g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0004g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0004g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0004g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0004g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0005g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0005g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0005g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0005g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0005g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0005g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0005g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0005g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0005g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0005g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0005g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0006g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0006g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0006g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0006g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0006g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0006g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0006g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0007g0214 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0007g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0008g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0008g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0008g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0009g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0009g0240 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0009g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0009g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0010g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0010g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0010g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0010g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0010g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0010g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0010g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0010g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0010g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0011g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0011g0331 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0012g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0012g0020 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0012g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0012g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0012g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0012g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0013g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0015g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0015g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0015g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0018g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0019g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0020g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0020g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0026g0014 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0027g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0031g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0037g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0053g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0057g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0001t0058g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0002t0001g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0002t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0002t0002g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0002t0002g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0002t0002g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0002t0002g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0002t0002g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0002t0003g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0002t0003g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0002t0003g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0002t0003g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0002t0004g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0002t0004g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0002t0004g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0002t0004g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0002t0004g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0002t0004g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0002t0005g0030 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0002t0006g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0002t0006g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0002t0006g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0002t0007g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0002t0007g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0002t0007g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0002t0007g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0002t0007g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0002t0007g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0002t0007g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0002t0007g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0002t0007g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0002t0008g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0002t0008g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0002t0008g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0002t0008g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0002t0008g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0002t0008g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0002t0008g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0002t0009g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0002t0009g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0002t0010g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0002t0010g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0002t0010g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0002t0011g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0002t0011g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0002t0012g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0002t0012g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0002t0013g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0002t0013g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0002t0014g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0002t0015g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0002t0016g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0002t0017g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0002t0018g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0002t0018g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0002t0020g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0002t0022g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0002t0025g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0002t0028g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0002t0028g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0002t0029g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0002t0032g0179 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0002t0033g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0002t0042g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0002t0043g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0002t0046g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0002t0048g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0002t0049g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0002t0051g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0002t0054g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0002t0056g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0002t0061g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0002t0063g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0003t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0003t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0003t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0003t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0003t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0003t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0003t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0003t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0003t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0003t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0003t0002g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0003t0002g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0003t0002g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0003t0002g0327 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0003t0002g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0003t0003g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0003t0003g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0003t0003g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0003t0003g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0003t0003g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0003t0003g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0003t0003g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0003t0003g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0003t0004g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0003t0005g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0003t0005g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0003t0005g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0003t0006g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0003t0006g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0003t0006g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0003t0006g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0003t0006g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0003t0007g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0003t0007g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0003t0007g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0003t0008g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0003t0009g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0003t0009g0342 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0003t0011g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0003t0011g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0003t0011g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0003t0011g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0003t0012g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0003t0014g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0003t0014g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0003t0014g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0003t0015g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0003t0021g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0003t0021g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0003t0022g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0003t0024g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0003t0024g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0003t0025g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0003t0034g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0003t0035g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0003t0040g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0003t0045g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0003t0047g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0003t0055g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0004t0001g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0004t0001g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0004t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0004t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0004t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0004t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0004t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0004t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0004t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0004t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0004t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0004t0002g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0004t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0004t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0004t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0004t0002g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0004t0002g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0004t0002g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0004t0002g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0004t0003g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0004t0003g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0004t0003g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0004t0003g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0004t0003g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0004t0003g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0004t0003g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0004t0003g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0004t0003g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0004t0005g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0004t0005g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0004t0005g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0004t0005g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0004t0005g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0004t0006g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0004t0006g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0004t0006g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0004t0006g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0004t0006g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0004t0008g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0004t0010g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0004t0012g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0004t0012g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0004t0013g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0004t0014g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0004t0019g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0004t0019g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0004t0022g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0004t0026g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0004t0041g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0004t0044g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0004t0050g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0004t0059g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0004t0060g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0005t0004g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0005t0007g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0005t0008g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0005t0013g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0005t0014g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0005t0023g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0005t0023g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0005t0023g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0005t0029g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0006t0007g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0006t0007g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0006t0009g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0006t0011g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0006t0011g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0006t0011g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0006t0036g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0006t0039g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0007t0008g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0007t0011g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0007t0013g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0007t0013g0341 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0007t0017g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0008t0004g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0008t0004g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0008t0004g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0009t0005g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0009t0021g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0009t0027g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0010t0009g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0010t0009g0232 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0010t0009g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0010t0009g0234 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0011t0004g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0011t0008g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0012t0004g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0012t0017g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0013t0016g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0013t0016g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0018t0007g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0018t0038g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0020t0012g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0023t0007g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0001c0030t0052g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0002c0014t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0002c0014t0008g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0002c0015t0030g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0002c0016t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0002c0016t0004g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0002c0017t0004g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0002c0017t0062g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0002c0027t0064g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0002c0029t0013g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0003c0025t0013g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0003c0026t0004g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0004c0022t0006g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0005c0021t0004g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0006c0024t0002g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0007c0019t0002g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| a0008c0028t0016g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0026 | EUR | GBR | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0242 | EUR | GBR | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG00140 | hp1 | a0001 | c0002 | t0005 | g0030 | EUR | GBR | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG00140 | hp2 | a0001 | c0003 | t0002 | g0327 | EUR | GBR | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG00280 | hp1 | a0001 | c0001 | t0007 | g0214 | EUR | FIN | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG00280 | hp2 | a0001 | c0004 | t0013 | g0051 | EUR | FIN | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG00408 | hp1 | a0001 | c0004 | t0010 | g0237 | EAS | CHS | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG00408 | hp2 | a0001 | c0004 | t0006 | g0164 | EAS | CHS | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG00423 | hp1 | a0001 | c0001 | t0010 | g0313 | EAS | CHS | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG00423 | hp2 | a0001 | c0001 | t0006 | g0077 | EAS | CHS | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG00438 | hp1 | a0001 | c0001 | t0005 | g0040 | EAS | CHS | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0247 | EAS | CHS | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG00558 | hp1 | a0001 | c0004 | t0003 | g0315 | EAS | CHS | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG00558 | hp2 | a0001 | c0001 | t0005 | g0038 | EAS | CHS | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0224 | EAS | CHS | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG00621 | hp2 | a0001 | c0004 | t0002 | g0170 | EAS | CHS | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG00639 | hp1 | a0001 | c0001 | t0031 | g0328 | AMR | PUR | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG00639 | hp2 | a0001 | c0004 | t0012 | g0043 | AMR | PUR | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG00642 | hp1 | a0001 | c0001 | t0009 | g0239 | AMR | PUR | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG00642 | hp2 | a0001 | c0001 | t0003 | g0269 | AMR | PUR | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG00673 | hp1 | a0001 | c0004 | t0012 | g0146 | EAS | CHS | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG00673 | hp2 | a0001 | c0001 | t0006 | g0107 | EAS | CHS | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG00735 | hp1 | a0001 | c0009 | t0005 | g0001 | AMR | PUR | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG00735 | hp2 | a0001 | c0002 | t0008 | g0161 | AMR | PUR | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG00741 | hp1 | a0001 | c0001 | t0006 | g0115 | AMR | PUR | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG00741 | hp2 | a0001 | c0002 | t0018 | g0011 | AMR | PUR | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG01069 | hp1 | a0001 | c0004 | t0001 | g0003 | AMR | PUR | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG01069 | hp2 | a0001 | c0001 | t0020 | g0031 | AMR | PUR | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG01070 | hp1 | a0001 | c0002 | t0008 | g0013 | AMR | PUR | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG01070 | hp2 | a0001 | c0001 | t0012 | g0028 | AMR | PUR | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG01071 | hp1 | a0001 | c0001 | t0012 | g0027 | AMR | PUR | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG01071 | hp2 | a0001 | c0004 | t0001 | g0003 | AMR | PUR | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG01074 | hp1 | a0001 | c0002 | t0010 | g0277 | AMR | PUR | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG01074 | hp2 | a0001 | c0001 | t0008 | g0050 | AMR | PUR | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG01081 | hp1 | a0001 | c0003 | t0040 | g0256 | AMR | PUR | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG01081 | hp2 | a0001 | c0002 | t0018 | g0010 | AMR | PUR | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG01099 | hp1 | a0001 | c0002 | t0033 | g0294 | AMR | PUR | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG01099 | hp2 | a0001 | c0001 | t0037 | g0323 | AMR | PUR | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG01106 | hp1 | a0001 | c0001 | t0004 | g0117 | AMR | PUR | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG01106 | hp2 | a0001 | c0009 | t0005 | g0001 | AMR | PUR | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG01109 | hp1 | a0002 | c0029 | t0013 | g0276 | AMR | PUR | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0236 | AMR | PUR | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG01167 | hp1 | a0001 | c0003 | t0007 | g0332 | AMR | PUR | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG01167 | hp2 | a0001 | c0004 | t0001 | g0002 | AMR | PUR | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG01169 | hp1 | a0001 | c0005 | t0023 | g0119 | AMR | PUR | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG01169 | hp2 | a0001 | c0004 | t0001 | g0002 | AMR | PUR | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG01192 | hp1 | a0001 | c0003 | t0015 | g0260 | AMR | PUR | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG01192 | hp2 | a0001 | c0001 | t0010 | g0335 | AMR | PUR | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG01243 | hp1 | a0001 | c0003 | t0008 | g0172 | AMR | PUR | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG01243 | hp2 | a0001 | c0001 | t0057 | g0033 | AMR | PUR | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG01255 | hp1 | a0001 | c0001 | t0012 | g0009 | AMR | CLM | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG01255 | hp2 | a0001 | c0002 | t0009 | g0227 | AMR | CLM | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG01256 | hp1 | a0001 | c0002 | t0025 | g0253 | AMR | CLM | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG01256 | hp2 | a0001 | c0001 | t0018 | g0019 | AMR | CLM | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG01257 | hp1 | a0001 | c0002 | t0012 | g0109 | AMR | CLM | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG01257 | hp2 | a0001 | c0001 | t0003 | g0226 | AMR | CLM | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG01261 | hp1 | a0001 | c0001 | t0020 | g0072 | AMR | CLM | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG01261 | hp2 | a0001 | c0009 | t0027 | g0032 | AMR | CLM | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG01346 | hp1 | a0001 | c0002 | t0002 | g0295 | AMR | CLM | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0216 | AMR | CLM | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG01361 | hp1 | a0001 | c0002 | t0007 | g0286 | AMR | CLM | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG01361 | hp2 | a0001 | c0003 | t0002 | g0334 | AMR | CLM | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG01433 | hp1 | a0001 | c0005 | t0029 | g0118 | AMR | CLM | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG01433 | hp2 | a0001 | c0001 | t0058 | g0069 | AMR | CLM | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG01496 | hp1 | a0001 | c0002 | t0004 | g0012 | AMR | CLM | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG01496 | hp2 | a0001 | c0002 | t0001 | g0015 | AMR | CLM | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG01515 | hp1 | a0001 | c0001 | t0009 | g0240 | EUR | IBS | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG01515 | hp2 | a0001 | c0005 | t0023 | g0121 | EUR | IBS | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG01516 | hp1 | a0001 | c0001 | t0012 | g0020 | EUR | IBS | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG01516 | hp2 | a0001 | c0010 | t0009 | g0234 | EUR | IBS | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG01517 | hp1 | a0001 | c0010 | t0009 | g0232 | EUR | IBS | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG01517 | hp2 | a0001 | c0005 | t0023 | g0120 | EUR | IBS | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG01884 | hp1 | a0001 | c0002 | t0007 | g0127 | AFR | ACB | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG01884 | hp2 | a0001 | c0002 | t0046 | g0142 | AFR | ACB | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG01891 | hp1 | a0001 | c0002 | t0009 | g0254 | AFR | ACB | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG01891 | hp2 | a0001 | c0003 | t0004 | g0168 | AFR | ACB | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG01928 | hp1 | a0001 | c0004 | t0019 | g0089 | AMR | PEL | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG01928 | hp2 | a0001 | c0023 | t0007 | g0288 | AMR | PEL | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG01934 | hp1 | a0001 | c0004 | t0003 | g0225 | AMR | PEL | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0067 | AMR | PEL | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG01943 | hp1 | a0001 | c0001 | t0004 | g0080 | AMR | PEL | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0036 | AMR | PEL | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | PEL | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG01952 | hp2 | a0001 | c0001 | t0006 | g0114 | AMR | PEL | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG01975 | hp1 | a0001 | c0002 | t0007 | g0291 | AMR | PEL | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG01975 | hp2 | a0001 | c0004 | t0002 | g0228 | AMR | PEL | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG01978 | hp1 | a0001 | c0003 | t0007 | g0268 | AMR | PEL | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG01978 | hp2 | a0001 | c0002 | t0003 | g0287 | AMR | PEL | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG01981 | hp1 | a0001 | c0004 | t0006 | g0180 | AMR | PEL | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG01981 | hp2 | a0001 | c0002 | t0007 | g0290 | AMR | PEL | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG01993 | hp1 | a0004 | c0022 | t0006 | g0116 | AMR | PEL | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG01993 | hp2 | a0001 | c0004 | t0001 | g0087 | AMR | PEL | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG02004 | hp1 | a0001 | c0004 | t0019 | g0088 | AMR | PEL | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0064 | AMR | PEL | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG02015 | hp1 | a0001 | c0001 | t0010 | g0245 | EAS | KHV | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG02015 | hp2 | a0001 | c0002 | t0011 | g0257 | EAS | KHV | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG02040 | hp1 | a0001 | c0001 | t0006 | g0110 | EAS | KHV | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG02040 | hp2 | a0001 | c0004 | t0003 | g0330 | EAS | KHV | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG02055 | hp1 | a0001 | c0006 | t0011 | g0337 | AFR | ACB | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG02055 | hp2 | a0001 | c0020 | t0012 | g0016 | AFR | ACB | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG02056 | hp1 | a0001 | c0001 | t0010 | g0210 | EAS | KHV | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG02056 | hp2 | a0001 | c0003 | t0001 | g0099 | EAS | KHV | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG02071 | hp1 | a0001 | c0003 | t0006 | g0157 | EAS | KHV | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG02071 | hp2 | a0001 | c0001 | t0010 | g0076 | EAS | KHV | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG02080 | hp1 | a0001 | c0003 | t0005 | g0083 | EAS | KHV | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG02080 | hp2 | a0001 | c0003 | t0003 | g0218 | EAS | KHV | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG02083 | hp1 | a0001 | c0004 | t0006 | g0149 | EAS | KHV | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG02083 | hp2 | a0001 | c0003 | t0002 | g0298 | EAS | KHV | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG02129 | hp1 | a0007 | c0019 | t0002 | g0321 | EAS | KHV | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG02129 | hp2 | a0001 | c0001 | t0005 | g0034 | EAS | KHV | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG02132 | hp1 | a0001 | c0004 | t0050 | g0073 | EAS | KHV | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | KHV | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG02135 | hp1 | a0001 | c0001 | t0004 | g0061 | EAS | KHV | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG02135 | hp2 | a0001 | c0001 | t0003 | g0265 | EAS | KHV | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG02145 | hp1 | a0001 | c0002 | t0004 | g0192 | AFR | ACB | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG02145 | hp2 | a0001 | c0002 | t0042 | g0213 | AFR | ACB | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG02148 | hp1 | a0001 | c0001 | t0019 | g0090 | AMR | PEL | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG02148 | hp2 | a0001 | c0002 | t0007 | g0289 | AMR | PEL | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG02165 | hp1 | a0001 | c0001 | t0006 | g0066 | EAS | CDX | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG02165 | hp2 | a0001 | c0004 | t0001 | g0062 | EAS | CDX | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG02257 | hp1 | a0002 | c0017 | t0004 | g0340 | AFR | ACB | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG02257 | hp2 | a0001 | c0002 | t0004 | g0193 | AFR | ACB | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG02258 | hp1 | a0002 | c0016 | t0001 | g0274 | AFR | ACB | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG02258 | hp2 | a0001 | c0007 | t0017 | g0270 | AFR | ACB | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0037 | AMR | PEL | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG02273 | hp2 | a0001 | c0002 | t0007 | g0325 | AMR | PEL | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG02280 | hp1 | a0002 | c0014 | t0008 | g0195 | AFR | ACB | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG02280 | hp2 | a0001 | c0002 | t0061 | g0190 | AFR | ACB | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG02293 | hp1 | a0001 | c0001 | t0010 | g0229 | AMR | PEL | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG02293 | hp2 | a0001 | c0003 | t0011 | g0322 | AMR | PEL | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG02523 | hp1 | a0001 | c0004 | t0003 | g0297 | EAS | KHV | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG02523 | hp2 | a0001 | c0001 | t0005 | g0096 | EAS | KHV | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG02572 | hp1 | a0003 | c0025 | t0013 | g0167 | AFR | GWD | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG02572 | hp2 | a0001 | c0002 | t0007 | g0293 | AFR | GWD | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0104 | SAS | PJL | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG02602 | hp2 | a0001 | c0002 | t0002 | g0280 | SAS | PJL | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG02615 | hp1 | a0001 | c0002 | t0020 | g0186 | AFR | GWD | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG02615 | hp2 | a0001 | c0002 | t0001 | g0191 | AFR | GWD | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG02622 | hp1 | a0008 | c0028 | t0016 | g0143 | AFR | GWD | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG02622 | hp2 | a0001 | c0011 | t0004 | g0171 | AFR | GWD | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG02630 | hp1 | a0001 | c0008 | t0004 | g0005 | AFR | GWD | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG02630 | hp2 | a0001 | c0002 | t0002 | g0263 | AFR | GWD | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG02647 | hp1 | a0001 | c0004 | t0022 | g0184 | AFR | GWD | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG02647 | hp2 | a0001 | c0002 | t0008 | g0181 | AFR | GWD | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG02683 | hp1 | a0001 | c0003 | t0025 | g0301 | SAS | PJL | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG02683 | hp2 | a0001 | c0001 | t0012 | g0103 | SAS | PJL | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG02698 | hp1 | a0001 | c0003 | t0014 | g0017 | SAS | PJL | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG02698 | hp2 | a0001 | c0004 | t0002 | g0311 | SAS | PJL | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG02717 | hp1 | a0001 | c0013 | t0016 | g0132 | AFR | GWD | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG02717 | hp2 | a0001 | c0003 | t0009 | g0292 | AFR | GWD | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG02723 | hp1 | a0001 | c0008 | t0004 | g0129 | AFR | GWD | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG02723 | hp2 | a0001 | c0007 | t0008 | g0063 | AFR | GWD | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG02735 | hp1 | a0001 | c0003 | t0002 | g0320 | SAS | PJL | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG02735 | hp2 | a0001 | c0001 | t0011 | g0331 | SAS | PJL | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG02738 | hp1 | a0001 | c0001 | t0004 | g0018 | SAS | PJL | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG02738 | hp2 | a0001 | c0010 | t0009 | g0233 | SAS | PJL | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG02809 | hp1 | a0001 | c0002 | t0012 | g0131 | AFR | GWD | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG02809 | hp2 | a0001 | c0002 | t0048 | g0125 | AFR | GWD | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG02818 | hp1 | a0001 | c0006 | t0009 | g0303 | AFR | GWD | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG02818 | hp2 | a0001 | c0008 | t0004 | g0005 | AFR | GWD | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG02886 | hp1 | a0001 | c0002 | t0008 | g0200 | AFR | GWD | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | GWD | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG02895 | hp1 | a0001 | c0003 | t0011 | g0248 | AFR | GWD | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG02895 | hp2 | a0001 | c0006 | t0011 | g0338 | AFR | GWD | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG02896 | hp1 | a0001 | c0008 | t0004 | g0197 | AFR | GWD | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG02896 | hp2 | a0001 | c0002 | t0013 | g0199 | AFR | GWD | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG02897 | hp1 | a0001 | c0003 | t0011 | g0250 | AFR | GWD | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG02897 | hp2 | a0001 | c0002 | t0013 | g0198 | AFR | GWD | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG02922 | hp1 | a0001 | c0002 | t0063 | g0137 | AFR | ESN | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG02922 | hp2 | a0002 | c0015 | t0030 | g0004 | AFR | ESN | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG02965 | hp1 | a0001 | c0018 | t0007 | g0336 | AFR | ESN | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG02965 | hp2 | a0002 | c0027 | t0064 | g0177 | AFR | ESN | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG02970 | hp1 | a0002 | c0015 | t0030 | g0004 | AFR | ESN | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG02970 | hp2 | a0001 | c0007 | t0013 | g0189 | AFR | ESN | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG02976 | hp1 | a0001 | c0005 | t0013 | g0176 | AFR | ESN | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG02976 | hp2 | a0001 | c0003 | t0007 | g0249 | AFR | ESN | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG03041 | hp1 | a0001 | c0002 | t0054 | g0215 | AFR | GWD | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG03041 | hp2 | a0001 | c0002 | t0016 | g0134 | AFR | GWD | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG03098 | hp1 | a0001 | c0018 | t0038 | g0308 | AFR | MSL | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG03098 | hp2 | a0001 | c0002 | t0028 | g0187 | AFR | MSL | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG03130 | hp1 | a0001 | c0002 | t0028 | g0188 | AFR | ESN | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG03130 | hp2 | a0001 | c0003 | t0047 | g0126 | AFR | ESN | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG03139 | hp1 | a0001 | c0007 | t0011 | g0271 | AFR | ESN | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG03139 | hp2 | a0001 | c0002 | t0007 | g0284 | AFR | ESN | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG03195 | hp1 | a0001 | c0002 | t0002 | g0262 | AFR | ESN | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG03195 | hp2 | a0001 | c0012 | t0004 | g0138 | AFR | ESN | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG03209 | hp1 | a0001 | c0002 | t0004 | g0275 | AFR | MSL | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG03209 | hp2 | a0001 | c0012 | t0017 | g0273 | AFR | MSL | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG03225 | hp1 | a0001 | c0003 | t0011 | g0251 | AFR | MSL | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG03225 | hp2 | a0003 | c0026 | t0004 | g0166 | AFR | MSL | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG03453 | hp1 | a0001 | c0011 | t0008 | g0135 | AFR | MSL | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG03453 | hp2 | a0001 | c0006 | t0007 | g0329 | AFR | MSL | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG03490 | hp1 | a0001 | c0004 | t0008 | g0044 | SAS | PJL | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG03490 | hp2 | a0001 | c0002 | t0010 | g0278 | SAS | PJL | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0006 | SAS | PJL | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG03491 | hp2 | a0001 | c0003 | t0009 | g0342 | SAS | PJL | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0006 | SAS | PJL | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG03492 | hp2 | a0001 | c0002 | t0010 | g0279 | SAS | PJL | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG03516 | hp1 | a0001 | c0006 | t0036 | g0307 | AFR | ESN | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG03516 | hp2 | a0001 | c0002 | t0008 | g0201 | AFR | ESN | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG03540 | hp1 | a0002 | c0014 | t0001 | g0196 | AFR | GWD | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG03540 | hp2 | a0001 | c0002 | t0022 | g0185 | AFR | GWD | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG03579 | hp1 | a0001 | c0003 | t0035 | g0205 | AFR | MSL | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG03579 | hp2 | a0001 | c0013 | t0016 | g0133 | AFR | MSL | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG03654 | hp1 | a0001 | c0002 | t0015 | g0007 | SAS | PJL | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG03654 | hp2 | a0001 | c0001 | t0009 | g0310 | SAS | PJL | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG03669 | hp1 | a0001 | c0004 | t0002 | g0281 | SAS | PJL | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG03669 | hp2 | a0001 | c0001 | t0007 | g0243 | SAS | PJL | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG03704 | hp1 | a0001 | c0003 | t0024 | g0324 | SAS | PJL | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG03704 | hp2 | a0001 | c0001 | t0013 | g0042 | SAS | PJL | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG03710 | hp1 | a0001 | c0001 | t0004 | g0194 | SAS | PJL | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG03710 | hp2 | a0006 | c0024 | t0002 | g0261 | SAS | PJL | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG03927 | hp1 | a0001 | c0002 | t0008 | g0124 | SAS | BEB | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG03927 | hp2 | a0001 | c0002 | t0001 | g0169 | SAS | BEB | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG03942 | hp1 | a0001 | c0030 | t0052 | g0071 | SAS | BEB | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG03942 | hp2 | a0001 | c0005 | t0014 | g0128 | SAS | BEB | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG04184 | hp1 | a0001 | c0001 | t0012 | g0075 | SAS | BEB | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG04184 | hp2 | a0001 | c0001 | t0008 | g0079 | SAS | BEB | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG04199 | hp1 | a0001 | c0004 | t0005 | g0106 | SAS | STU | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0046 | SAS | STU | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG04228 | hp1 | a0001 | c0003 | t0002 | g0326 | SAS | STU | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG04228 | hp2 | a0001 | c0002 | t0014 | g0160 | SAS | STU | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA18747 | hp1 | a0001 | c0002 | t0006 | g0052 | EAS | CHB | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA18747 | hp2 | a0001 | c0003 | t0003 | g0108 | EAS | CHB | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA18906 | hp1 | a0001 | c0006 | t0039 | g0305 | AFR | YRI | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA18906 | hp2 | a0001 | c0003 | t0022 | g0174 | AFR | YRI | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA18950 | hp1 | a0001 | c0001 | t0005 | g0130 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA18950 | hp2 | a0001 | c0004 | t0001 | g0039 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA18951 | hp1 | a0001 | c0003 | t0003 | g0346 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA18951 | hp2 | a0001 | c0001 | t0003 | g0203 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA18953 | hp1 | a0001 | c0002 | t0003 | g0283 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA18954 | hp1 | a0001 | c0004 | t0002 | g0235 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA18954 | hp2 | a0001 | c0002 | t0006 | g0147 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA18957 | hp1 | a0001 | c0004 | t0003 | g0206 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA18957 | hp2 | a0001 | c0003 | t0005 | g0094 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA18961 | hp1 | a0001 | c0004 | t0005 | g0165 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA18961 | hp2 | a0001 | c0003 | t0003 | g0296 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA18964 | hp1 | a0001 | c0003 | t0003 | g0300 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA18964 | hp2 | a0001 | c0004 | t0006 | g0113 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA18965 | hp1 | a0001 | c0004 | t0003 | g0219 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA18965 | hp2 | a0001 | c0004 | t0002 | g0246 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA18966 | hp1 | a0001 | c0001 | t0005 | g0145 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA18966 | hp2 | a0001 | c0003 | t0001 | g0155 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA18967 | hp1 | a0001 | c0003 | t0001 | g0163 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA18967 | hp2 | a0001 | c0002 | t0003 | g0204 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0316 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA18969 | hp2 | a0001 | c0001 | t0004 | g0081 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA18972 | hp1 | a0001 | c0001 | t0005 | g0105 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA18972 | hp2 | a0001 | c0004 | t0041 | g0343 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA18973 | hp1 | a0001 | c0003 | t0045 | g0101 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA18973 | hp2 | a0001 | c0001 | t0010 | g0317 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA18975 | hp1 | a0001 | c0001 | t0005 | g0008 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA18975 | hp2 | a0001 | c0001 | t0002 | g0211 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA18978 | hp1 | a0001 | c0003 | t0001 | g0156 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA18978 | hp2 | a0001 | c0004 | t0005 | g0055 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA18982 | hp1 | a0001 | c0003 | t0003 | g0345 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA18982 | hp2 | a0001 | c0002 | t0001 | g0057 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA18983 | hp1 | a0001 | c0004 | t0003 | g0207 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA18983 | hp2 | a0001 | c0004 | t0002 | g0202 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA18984 | hp1 | a0001 | c0004 | t0005 | g0056 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA18984 | hp2 | a0001 | c0003 | t0055 | g0092 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA18986 | hp1 | a0001 | c0003 | t0003 | g0217 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA18986 | hp2 | a0001 | c0001 | t0006 | g0078 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA18992 | hp1 | a0001 | c0003 | t0001 | g0162 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA18992 | hp2 | a0001 | c0003 | t0034 | g0333 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA18993 | hp1 | a0001 | c0003 | t0014 | g0100 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA18993 | hp2 | a0001 | c0003 | t0003 | g0299 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA18994 | hp1 | a0001 | c0001 | t0003 | g0241 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA18994 | hp2 | a0001 | c0003 | t0001 | g0153 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA18995 | hp1 | a0001 | c0001 | t0003 | g0318 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA18995 | hp2 | a0001 | c0003 | t0006 | g0086 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA19001 | hp1 | a0001 | c0003 | t0006 | g0154 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA19001 | hp2 | a0001 | c0004 | t0002 | g0212 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA19002 | hp2 | a0001 | c0003 | t0006 | g0098 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA19004 | hp1 | a0001 | c0004 | t0002 | g0302 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA19004 | hp2 | a0001 | c0001 | t0015 | g0208 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA19005 | hp1 | a0001 | c0001 | t0003 | g0244 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA19005 | hp2 | a0001 | c0003 | t0006 | g0102 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA19009 | hp1 | a0001 | c0004 | t0002 | g0221 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA19009 | hp2 | a0001 | c0002 | t0006 | g0091 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA19010 | hp1 | a0001 | c0001 | t0053 | g0159 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA19030 | hp1 | a0001 | c0004 | t0026 | g0053 | AFR | LWK | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA19030 | hp2 | a0001 | c0002 | t0004 | g0140 | AFR | LWK | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA19043 | hp1 | a0001 | c0002 | t0051 | g0183 | AFR | LWK | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA19043 | hp2 | a0005 | c0021 | t0004 | g0139 | AFR | LWK | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA19054 | hp1 | a0001 | c0003 | t0001 | g0152 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA19054 | hp2 | a0001 | c0002 | t0001 | g0084 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA19056 | hp1 | a0001 | c0003 | t0001 | g0151 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA19056 | hp2 | a0001 | c0004 | t0014 | g0029 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA19057 | hp1 | a0001 | c0003 | t0024 | g0344 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA19057 | hp2 | a0001 | c0003 | t0005 | g0093 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA19058 | hp1 | a0001 | c0004 | t0005 | g0070 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA19058 | hp2 | a0001 | c0002 | t0001 | g0082 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA19060 | hp2 | a0001 | c0004 | t0003 | g0314 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA19063 | hp1 | a0001 | c0001 | t0010 | g0266 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA19063 | hp2 | a0001 | c0004 | t0002 | g0220 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA19066 | hp2 | a0001 | c0003 | t0001 | g0150 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA19068 | hp1 | a0001 | c0001 | t0009 | g0319 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA19070 | hp1 | a0001 | c0001 | t0005 | g0025 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA19070 | hp2 | a0001 | c0004 | t0044 | g0252 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA19074 | hp1 | a0001 | c0001 | t0005 | g0122 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA19074 | hp2 | a0001 | c0003 | t0001 | g0085 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA19080 | hp1 | a0001 | c0001 | t0005 | g0035 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA19080 | hp2 | a0001 | c0004 | t0002 | g0267 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA19081 | hp1 | a0001 | c0004 | t0006 | g0123 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA19081 | hp2 | a0001 | c0003 | t0014 | g0095 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA19082 | hp1 | a0001 | c0001 | t0010 | g0230 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA19082 | hp2 | a0001 | c0004 | t0060 | g0024 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0258 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA19084 | hp2 | a0001 | c0004 | t0059 | g0023 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA19085 | hp1 | a0001 | c0002 | t0003 | g0282 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA19085 | hp2 | a0001 | c0003 | t0021 | g0059 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA19088 | hp1 | a0001 | c0003 | t0021 | g0058 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA19088 | hp2 | a0001 | c0001 | t0027 | g0111 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA19090 | hp1 | a0001 | c0004 | t0001 | g0097 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA19090 | hp2 | a0001 | c0001 | t0015 | g0238 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA19240 | hp1 | a0001 | c0002 | t0017 | g0255 | AFR | YRI | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA19240 | hp2 | a0001 | c0006 | t0011 | g0304 | AFR | YRI | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA20129 | hp1 | a0001 | c0006 | t0007 | g0306 | AFR | ASW | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA20129 | hp2 | a0001 | c0002 | t0029 | g0136 | AFR | ASW | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA20752 | hp1 | a0001 | c0001 | t0004 | g0041 | EUR | TSI | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA20752 | hp2 | a0001 | c0001 | t0008 | g0047 | EUR | TSI | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA20805 | hp1 | a0001 | c0001 | t0026 | g0014 | EUR | TSI | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA20805 | hp2 | a0001 | c0002 | t0056 | g0148 | EUR | TSI | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA20905 | hp1 | a0001 | c0010 | t0009 | g0231 | SAS | GIH | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0060 | SAS | GIH | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG01123 | hp1 | a0001 | c0005 | t0007 | g0223 | AMR | CLM | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG01123 | hp2 | a0001 | c0004 | t0003 | g0309 | AMR | CLM | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG02109 | hp1 | a0001 | c0002 | t0007 | g0285 | AFR | ACB | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG02109 | hp2 | a0001 | c0002 | t0011 | g0272 | AFR | ACB | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG02486 | hp1 | a0001 | c0002 | t0008 | g0141 | AFR | ACB | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG02486 | hp2 | a0001 | c0002 | t0043 | g0259 | AFR | ACB | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG02559 | hp1 | a0001 | c0005 | t0004 | g0049 | AFR | ACB | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG02559 | hp2 | a0001 | c0001 | t0011 | g0222 | AFR | ACB | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG03471 | hp1 | a0002 | c0016 | t0004 | g0339 | AFR | MSL | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG03471 | hp2 | a0001 | c0002 | t0002 | g0264 | AFR | MSL | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG06807 | hp1 | a0001 | c0002 | t0049 | g0173 | AFR | USA | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| HG06807 | hp2 | a0001 | c0005 | t0008 | g0048 | AFR | USA | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA18955 | hp1 | a0001 | c0001 | t0015 | g0209 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA18955 | hp2 | a0001 | c0004 | t0002 | g0312 | EAS | JPT | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA20300 | hp1 | a0001 | c0009 | t0021 | g0045 | AFR | USA | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA20300 | hp2 | a0001 | c0002 | t0004 | g0182 | AFR | USA | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA21309 | hp1 | a0002 | c0017 | t0062 | g0178 | AFR | LWK | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| NA21309 | hp2 | a0001 | c0003 | t0012 | g0175 | AFR | LWK | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0002 | t0032 | g0179 | REF | REF | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| homoSapiens_grch38 | hp1 | a0001 | c0007 | t0013 | g0341 | REF | REF | NRP2_chr2_205677501_205803131 | NRP2 | chr2 | 205677501 | 205803131 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:205716309
|
A | G | 2 | a0002a0008 | 11 | HG01109.hp1 HG02257.hp1 HG02258.hp1 others(8): Show |
missense_variant | MODERATE | c.368A>G | p.Lys123Arg | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 3/17 | 1158/6644 | 368/2781 | 123/926 | chr2 | 205716309 | ||
| chr2:205722603
|
A | G | 1 | a0003 | 2 | HG02572.hp1 HG03225.hp2 |
missense_variant | MODERATE | c.559A>G | p.Ile187Val | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 4/17 | 1349/6644 | 559/2781 | 187/926 | chr2 | 205722603 | ||
| chr2:205723790
|
C | A | 1 | a0007 | 1 | HG02129.hp1 | missense_variant | MODERATE | c.670C>A | p.Pro224Thr | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 5/17 | 1460/6644 | 670/2781 | 224/926 | chr2 | 205723790 | ||
| chr2:205740654
|
C | T | 1 | a0006 | 1 | HG03710.hp2 | missense_variant | MODERATE | c.1282C>T | p.Arg428Trp | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 8/17 | 2072/6644 | 1282/2781 | 428/926 | chr2 | 205740654 | ||
| chr2:205749746
|
C | T | 1 | a0008 | 1 | HG02622.hp1 | missense_variant | MODERATE | c.1808C>T | p.Thr603Met | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 11/17 | 2598/6644 | 1808/2781 | 603/926 | chr2 | 205749746 | ||
| chr2:205749769
|
G | A | 1 | a0005 | 1 | NA19043.hp2 | missense_variant | MODERATE | c.1831G>A | p.Glu611Lys | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 11/17 | 2621/6644 | 1831/2781 | 611/926 | chr2 | 205749769 | ||
| chr2:205763908
|
T | C | 1 | a0004 | 1 | HG01993.hp1 | missense_variant | MODERATE | c.2279T>C | p.Ile760Thr | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 13/17 | 3069/6644 | 2279/2781 | 760/926 | chr2 | 205763908 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:205697593
|
C | T | 2 | a0001c0006a0001c0018 | 10 | HG02055.hp1 HG02818.hp1 HG02895.hp2 others(7): Show |
synonymous_variant | LOW | c.123C>T | p.Thr41Thr | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/17 | 913/6644 | 123/2781 | 41/926 | chr2 | 205697593 | ||
| chr2:205697635
|
C | T | 1 | a0001c0030 | 1 | HG03942.hp1 | synonymous_variant | LOW | c.165C>T | p.Cys55Cys | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/17 | 955/6644 | 165/2781 | 55/926 | chr2 | 205697635 | ||
| chr2:205716325
|
C | T | 1 | a0001c0010 | 4 | HG01516.hp2 HG01517.hp1 HG02738.hp2 others(1): Show |
synonymous_variant | LOW | c.384C>T | p.Tyr128Tyr | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 3/17 | 1174/6644 | 384/2781 | 128/926 | chr2 | 205716325 | ||
| chr2:205723846
|
G | A | 3 | a0001c0008a0001c0011a0001c0012 | 8 | HG02622.hp2 HG02630.hp1 HG02723.hp1 others(5): Show |
synonymous_variant | LOW | c.726G>A | p.Thr242Thr | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 5/17 | 1516/6644 | 726/2781 | 242/926 | chr2 | 205723846 | ||
| chr2:205725962
|
T | C | 3 | a0001c0005a0001c0020a0005c0021 | 11 | HG01123.hp1 HG01169.hp1 HG01433.hp1 others(8): Show |
synonymous_variant | LOW | c.870T>C | p.Asn290Asn | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 6/17 | 1660/6644 | 870/2781 | 290/926 | chr2 | 205725962 | ||
| chr2:205727971
|
T | C | 8 | a0001c0001a0001c0004a0001c0009others(5): Show | 168 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(165): Show |
synonymous_variant | LOW | c.1071T>C | p.Tyr357Tyr | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/17 | 1861/6644 | 1071/2781 | 357/926 | chr2 | 205727971 | ||
| chr2:205740521
|
A | G | 1 | a0001c0008 | 4 | HG02630.hp1 HG02723.hp1 HG02818.hp2 others(1): Show |
splice_region_variant&synonymous_variant | LOW | c.1149A>G | p.Val383Val | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 8/17 | 1939/6644 | 1149/2781 | 383/926 | chr2 | 205740521 | ||
| chr2:205743315
|
T | C | 25 | a0001c0001a0001c0002a0001c0003others(22): Show | 338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
synonymous_variant | LOW | c.1404T>C | p.Val468Val | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 9/17 | 2194/6644 | 1404/2781 | 468/926 | chr2 | 205743315 | ||
| chr2:205743327
|
G | A | 1 | a0001c0023 | 1 | HG01928.hp2 | synonymous_variant | LOW | c.1416G>A | p.Ser472Ser | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 9/17 | 2206/6644 | 1416/2781 | 472/926 | chr2 | 205743327 | ||
| chr2:205743360
|
C | T | 1 | a0001c0013 | 2 | HG02717.hp1 HG03579.hp2 |
synonymous_variant | LOW | c.1449C>T | p.Pro483Pro | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 9/17 | 2239/6644 | 1449/2781 | 483/926 | chr2 | 205743360 | ||
| chr2:205743366
|
G | A | 1 | a0002c0029 | 1 | HG01109.hp1 | synonymous_variant | LOW | c.1455G>A | p.Glu485Glu | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 9/17 | 2245/6644 | 1455/2781 | 485/926 | chr2 | 205743366 | ||
| chr2:205745778
|
T | G | 9 | a0001c0003a0001c0004a0001c0011others(6): Show | 124 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(121): Show |
synonymous_variant | LOW | c.1674T>G | p.Pro558Pro | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 10/17 | 2464/6644 | 1674/2781 | 558/926 | chr2 | 205745778 | ||
| chr2:205794956
|
C | T | 1 | a0002c0015 | 2 | HG02922.hp2 HG02970.hp1 |
synonymous_variant | LOW | c.2679C>T | p.Ser893Ser | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 17/17 | 3469/6644 | 2679/2781 | 893/926 | chr2 | 205794956 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:205682514
|
G | A | 1 | a0001c0001t0031 | 1 | HG00639.hp1 | 5_prime_UTR_variant | MODIFIER | c.-777G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/17 | 777 | chr2 | 205682514 | |||||
| chr2:205682787
|
A | G | 7 | a0001c0002t0029a0001c0002t0063a0001c0005t0023others(4): Show | 10 | HG01169.hp1 HG01433.hp1 HG01515.hp2 others(7): Show |
5_prime_UTR_variant | MODIFIER | c.-504A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/17 | 504 | chr2 | 205682787 | |||||
| chr2:205682821
|
T | C | 60 | a0001c0001t0002a0001c0001t0003a0001c0001t0007others(57): Show | 156 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(153): Show |
5_prime_UTR_variant | MODIFIER | c.-470T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/17 | 470 | chr2 | 205682821 | |||||
| chr2:205682875
|
A | G | 1 | a0001c0002t0028 | 2 | HG03098.hp2 HG03130.hp1 |
5_prime_UTR_variant | MODIFIER | c.-416A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/17 | 416 | chr2 | 205682875 | |||||
| chr2:205683023
|
T | C | 2 | a0001c0002t0032a0001c0002t0033 | 2 | HG01099.hp1 homoSapiens_chm13v2.hp1 |
5_prime_UTR_variant | MODIFIER | c.-268T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/17 | 268 | chr2 | 205683023 | |||||
| chr2:205683178
|
A | G | 1 | a0001c0004t0044 | 1 | NA19070.hp2 | 5_prime_UTR_variant | MODIFIER | c.-113A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/17 | 113 | chr2 | 205683178 | |||||
| chr2:205795119
|
C | A | 1 | a0001c0003t0045 | 1 | NA18973.hp1 | 3_prime_UTR_variant | MODIFIER | c.*61C>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 17/17 | 61 | chr2 | 205795119 | |||||
| chr2:205795203
|
C | A | 1 | a0001c0003t0034 | 1 | NA18992.hp2 | 3_prime_UTR_variant | MODIFIER | c.*145C>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 17/17 | 145 | chr2 | 205795203 | |||||
| chr2:205795240
|
G | T | 4 | a0001c0002t0022a0001c0002t0043a0001c0003t0022others(1): Show | 4 | HG02486.hp2 HG02647.hp1 HG03540.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*182G>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 17/17 | 182 | chr2 | 205795240 | |||||
| chr2:205795261
|
G | A | 2 | a0001c0002t0046a0001c0003t0047 | 2 | HG01884.hp2 HG03130.hp2 |
3_prime_UTR_variant | MODIFIER | c.*203G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 17/17 | 203 | chr2 | 205795261 | |||||
| chr2:205795286
|
G | A | 3 | a0001c0002t0016a0001c0013t0016a0008c0028t0016 | 4 | HG02622.hp1 HG02717.hp1 HG03041.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*228G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 17/17 | 228 | chr2 | 205795286 | |||||
| chr2:205795305
|
G | A | 1 | a0002c0017t0062 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*247G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 17/17 | 247 | chr2 | 205795305 | |||||
| chr2:205795313
|
C | T | 1 | a0001c0002t0061 | 1 | HG02280.hp2 | 3_prime_UTR_variant | MODIFIER | c.*255C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 17/17 | 255 | chr2 | 205795313 | |||||
| chr2:205795361
|
G | GTAT | 43 | a0001c0001t0001a0001c0001t0002a0001c0001t0007others(40): Show | 134 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(131): Show |
3_prime_UTR_variant | MODIFIER | c.*331_*333dupTAT | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 17/17 | 334 | INFO_REALIGN_3_PRIME | chr2 | 205795361 | ||||
| chr2:205795361
|
G | GTATTAT | 24 | a0001c0001t0009a0001c0001t0012a0001c0001t0015others(21): Show | 43 | HG00639.hp2 HG00642.hp1 HG00673.hp1 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*328_*333dupTATTAT | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 17/17 | 334 | INFO_REALIGN_3_PRIME | chr2 | 205795361 | ||||
| chr2:205795361
|
G | GTATTATT others(2): Show |
14 | a0001c0001t0005a0001c0001t0010a0001c0002t0005others(11): Show | 43 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*325_*333dupTATTAT others(3): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 17/17 | 334 | INFO_REALIGN_3_PRIME | chr2 | 205795361 | ||||
| chr2:205795361
|
G | GTATTATT others(5): Show |
4 | a0001c0001t0027a0001c0002t0025a0001c0003t0025others(1): Show | 4 | HG01256.hp1 HG01261.hp2 HG02683.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*322_*333dupTATTAT others(6): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 17/17 | 334 | INFO_REALIGN_3_PRIME | chr2 | 205795361 | ||||
| chr2:205795361
|
GTAT | G | 41 | a0001c0001t0003a0001c0001t0004a0001c0001t0006others(38): Show | 103 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(100): Show |
3_prime_UTR_variant | MODIFIER | c.*331_*333delTAT | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 17/17 | 331 | INFO_REALIGN_3_PRIME | chr2 | 205795361 | ||||
| chr2:205795418
|
C | A | 1 | a0001c0030t0052 | 1 | HG03942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*360C>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 17/17 | 360 | chr2 | 205795418 | |||||
| chr2:205795545
|
A | G | 1 | a0001c0002t0042 | 1 | HG02145.hp2 | 3_prime_UTR_variant | MODIFIER | c.*487A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 17/17 | 487 | chr2 | 205795545 | |||||
| chr2:205796191
|
T | C | 16 | a0001c0001t0003a0001c0001t0006a0001c0001t0053others(13): Show | 56 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(53): Show |
3_prime_UTR_variant | MODIFIER | c.*1133T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 17/17 | 1133 | chr2 | 205796191 | |||||
| chr2:205796244
|
G | A | 2 | a0001c0002t0048a0001c0003t0035 | 2 | HG02809.hp2 HG03579.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1186G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 17/17 | 1186 | chr2 | 205796244 | |||||
| chr2:205796332
|
G | A | 1 | a0001c0004t0059 | 1 | NA19084.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1274G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 17/17 | 1274 | chr2 | 205796332 | |||||
| chr2:205796335
|
A | C | 1 | a0001c0001t0037 | 1 | HG01099.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1277A>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 17/17 | 1277 | chr2 | 205796335 | |||||
| chr2:205796437
|
TACACACA others(9): Show |
T | 1 | a0001c0001t0058 | 1 | HG01433.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1380_*1395delACAC others(12): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 17/17 | 1380 | chr2 | 205796437 | |||||
| chr2:205796556
|
A | C | 1 | a0001c0002t0049 | 1 | HG06807.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1498A>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 17/17 | 1498 | chr2 | 205796556 | |||||
| chr2:205796646
|
G | A | 1 | a0001c0002t0054 | 1 | HG03041.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1588G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 17/17 | 1588 | chr2 | 205796646 | |||||
| chr2:205796771
|
G | A | 3 | a0001c0002t0051a0001c0002t0063a0001c0018t0038 | 3 | HG02922.hp1 HG03098.hp1 NA19043.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1713G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 17/17 | 1713 | chr2 | 205796771 | |||||
| chr2:205796978
|
A | G | 1 | a0001c0001t0057 | 1 | HG01243.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1920A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 17/17 | 1920 | chr2 | 205796978 | |||||
| chr2:205797561
|
A | AAGCAGGG others(5): Show |
1 | a0001c0002t0046 | 1 | HG01884.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2506_*2517dupCAGG others(8): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 17/17 | 2518 | INFO_REALIGN_3_PRIME | chr2 | 205797561 | ||||
| chr2:205797573
|
C | G | 32 | a0001c0001t0001a0001c0001t0002a0001c0001t0015others(29): Show | 104 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(101): Show |
3_prime_UTR_variant | MODIFIER | c.*2515C>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 17/17 | 2515 | chr2 | 205797573 | |||||
| chr2:205797612
|
G | C | 31 | a0001c0001t0001a0001c0001t0002a0001c0001t0015others(28): Show | 104 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(101): Show |
3_prime_UTR_variant | MODIFIER | c.*2554G>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 17/17 | 2554 | chr2 | 205797612 | |||||
| chr2:205797619
|
A | G | 42 | a0001c0001t0001a0001c0001t0002a0001c0001t0015others(39): Show | 118 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(115): Show |
3_prime_UTR_variant | MODIFIER | c.*2561A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 17/17 | 2561 | chr2 | 205797619 | |||||
| chr2:205797836
|
G | T | 1 | a0001c0003t0055 | 1 | NA18984.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2778G>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 17/17 | 2778 | chr2 | 205797836 | |||||
| chr2:205797890
|
G | A | 1 | a0001c0004t0060 | 1 | NA19082.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2832G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 17/17 | 2832 | chr2 | 205797890 | |||||
| chr2:205798074
|
A | G | 1 | a0001c0002t0056 | 1 | NA20805.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3016A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 17/17 | 3016 | chr2 | 205798074 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:205683555
|
A | AGT | 5 | a0001c0003t0003g0345a0001c0003t0003g0346a0001c0003t0009g0342others(2): Show | 5 | HG03491.hp2 NA18951.hp1 NA18972.hp2 others(2): Show |
intron_variant | MODIFIER | c.73+222_73+223dupTG | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 205683555 | |||||
| chr2:205683555
|
AGT | A | 81 | a0001c0001t0002g0006a0001c0001t0002g0211a0001c0001t0002g0216others(78): Show | 82 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(79): Show |
intron_variant | MODIFIER | c.73+222_73+223delTG | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 205683555 | |||||
| chr2:205683555
|
AGTGT | A | 24 | a0001c0001t0004g0194a0001c0002t0001g0191a0001c0002t0004g0182others(21): Show | 25 | HG01981.hp1 HG02145.hp1 HG02257.hp2 others(22): Show |
intron_variant | MODIFIER | c.73+220_73+223delTG others(2): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 205683555 | |||||
| chr2:205683555
|
AGTGTGT | A | 16 | a0001c0002t0001g0169a0001c0002t0049g0173a0001c0003t0004g0168others(13): Show | 17 | HG00408.hp2 HG00621.hp2 HG01243.hp1 others(14): Show |
intron_variant | MODIFIER | c.73+218_73+223delTG others(4): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 205683555 | |||||
| chr2:205683555
|
AGTGTGTG others(1): Show |
A | 159 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0026others(156): Show | 162 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(159): Show |
intron_variant | MODIFIER | c.73+216_73+223delTG others(6): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 205683555 | |||||
| chr2:205683561
|
T | C | 1 | a0001c0002t0015g0007 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.73+198T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205683561 | ||||||
| chr2:205683620
|
T | C | 1 | a0001c0004t0002g0202 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.73+257T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205683620 | ||||||
| chr2:205683652
|
A | G | 1 | a0001c0002t0008g0201 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.73+289A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205683652 | ||||||
| chr2:205683719
|
T | C | 125 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0026others(122): Show | 127 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(124): Show |
intron_variant | MODIFIER | c.73+356T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205683719 | ||||||
| chr2:205683783
|
A | C | 1 | a0001c0002t0008g0124 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.73+420A>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205683783 | ||||||
| chr2:205683955
|
G | A | 1 | a0001c0002t0048g0125 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.73+592G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205683955 | ||||||
| chr2:205684192
|
C | T | 26 | a0001c0001t0001g0144a0001c0001t0001g0158a0001c0001t0005g0145others(23): Show | 27 | HG00673.hp1 HG00735.hp2 HG01069.hp1 others(24): Show |
intron_variant | MODIFIER | c.73+829C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205684192 | ||||||
| chr2:205684289
|
G | A | 1 | a0001c0002t0008g0181 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.73+926G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205684289 | ||||||
| chr2:205684315
|
A | G | 1 | a0001c0004t0006g0123 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.73+952A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205684315 | ||||||
| chr2:205684330
|
A | G | 1 | a0001c0001t0005g0122 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.73+967A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205684330 | ||||||
| chr2:205684583
|
C | G | 6 | a0001c0002t0004g0140a0001c0002t0008g0141a0001c0002t0046g0142others(3): Show | 6 | HG01884.hp2 HG02486.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.73+1220C>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205684583 | ||||||
| chr2:205684615
|
A | G | 4 | a0001c0005t0023g0119a0001c0005t0023g0120a0001c0005t0023g0121others(1): Show | 4 | HG01169.hp1 HG01433.hp1 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.73+1252A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205684615 | ||||||
| chr2:205684755
|
G | C | 317 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0026others(314): Show | 321 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(318): Show |
intron_variant | MODIFIER | c.73+1392G>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205684755 | ||||||
| chr2:205684859
|
C | CTG | 7 | a0001c0002t0049g0173a0001c0003t0008g0172a0001c0003t0012g0175others(4): Show | 7 | HG01243.hp1 HG02622.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.73+1507_73+1508dup others(2): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 205684859 | |||||
| chr2:205685073
|
T | C | 1 | a0001c0003t0035g0205 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.73+1710T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205685073 | ||||||
| chr2:205685138
|
C | T | 5 | a0001c0002t0004g0140a0001c0002t0008g0141a0001c0002t0046g0142others(2): Show | 5 | HG01884.hp2 HG02486.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.73+1775C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205685138 | ||||||
| chr2:205685158
|
G | C | 2 | a0001c0004t0003g0206a0001c0004t0003g0207 | 2 | NA18957.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.73+1795G>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205685158 | ||||||
| chr2:205685389
|
C | A | 2 | a0002c0016t0001g0274a0002c0016t0004g0339 | 2 | HG02258.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.73+2026C>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205685389 | ||||||
| chr2:205685413
|
C | T | 312 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0026others(309): Show | 316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.73+2050C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205685413 | ||||||
| chr2:205685415
|
CAT | C | 312 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0026others(309): Show | 316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.73+2054_73+2055del others(2): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 205685415 | |||||
| chr2:205685446
|
C | A | 1 | a0001c0004t0002g0212 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.73+2083C>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205685446 | ||||||
| chr2:205685554
|
C | A | 312 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0026others(309): Show | 316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.73+2191C>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205685554 | ||||||
| chr2:205685700
|
C | A | 1 | a0001c0001t0005g0008 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.73+2337C>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205685700 | ||||||
| chr2:205685728
|
G | C | 1 | a0001c0011t0004g0171 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.73+2365G>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205685728 | ||||||
| chr2:205685902
|
G | A | 1 | a0001c0003t0009g0342 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.73+2539G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205685902 | ||||||
| chr2:205685934
|
C | T | 1 | a0001c0012t0017g0273 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.73+2571C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205685934 | ||||||
| chr2:205685954
|
G | T | 1 | a0001c0002t0048g0125 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.73+2591G>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205685954 | ||||||
| chr2:205685974
|
C | G | 1 | a0004c0022t0006g0116 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.73+2611C>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205685974 | ||||||
| chr2:205685982
|
G | C | 1 | a0001c0011t0004g0171 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.73+2619G>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205685982 | ||||||
| chr2:205686123
|
T | A | 2 | a0001c0002t0003g0282a0001c0002t0003g0283 | 2 | NA18953.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.73+2760T>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205686123 | ||||||
| chr2:205686218
|
CCCT | C | 6 | a0001c0001t0004g0117a0001c0001t0004g0194a0001c0002t0001g0191others(3): Show | 6 | HG01106.hp1 HG02145.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.73+2874_73+2876del others(3): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 205686218 | |||||
| chr2:205686241
|
A | G | 1 | a0001c0006t0011g0338 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.73+2878A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205686241 | ||||||
| chr2:205686395
|
T | C | 1 | a0001c0001t0012g0009 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.73+3032T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205686395 | ||||||
| chr2:205686400
|
A | G | 1 | a0001c0005t0013g0176 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.73+3037A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205686400 | ||||||
| chr2:205686504
|
G | A | 1 | a0001c0002t0042g0213 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.73+3141G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205686504 | ||||||
| chr2:205686812
|
C | T | 1 | a0001c0003t0012g0175 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.73+3449C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205686812 | ||||||
| chr2:205686846
|
C | G | 15 | a0001c0001t0004g0117a0001c0001t0004g0194a0001c0002t0001g0191others(12): Show | 16 | HG01106.hp1 HG02145.hp1 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.73+3483C>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205686846 | ||||||
| chr2:205687254
|
C | T | 233 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0026others(230): Show | 236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.73+3891C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205687254 | ||||||
| chr2:205687371
|
C | T | 11 | a0001c0001t0002g0211a0001c0001t0003g0203a0001c0001t0004g0117others(8): Show | 11 | HG01106.hp1 HG02056.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.73+4008C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205687371 | ||||||
| chr2:205687438
|
ATT | A | 314 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0026others(311): Show | 318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.73+4079_73+4080del others(2): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 205687438 | |||||
| chr2:205687520
|
G | A | 68 | a0001c0001t0001g0144a0001c0001t0001g0158a0001c0001t0005g0145others(65): Show | 69 | HG00280.hp1 HG00673.hp1 HG00735.hp2 others(66): Show |
intron_variant | MODIFIER | c.73+4157G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205687520 | ||||||
| chr2:205687816
|
CA | C | 3 | a0001c0002t0011g0272a0001c0007t0011g0271a0001c0007t0017g0270 | 3 | HG02109.hp2 HG02258.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.73+4454delA | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205687816 | ||||||
| chr2:205687914
|
C | T | 4 | a0001c0001t0001g0112a0001c0001t0006g0114a0001c0001t0006g0115others(1): Show | 4 | HG00741.hp1 HG01952.hp2 NA18964.hp2 others(1): Show |
intron_variant | MODIFIER | c.73+4551C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205687914 | ||||||
| chr2:205688002
|
A | G | 314 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0026others(311): Show | 318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.73+4639A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205688002 | ||||||
| chr2:205688116
|
G | A | 1 | a0001c0001t0007g0214 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.73+4753G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205688116 | ||||||
| chr2:205688222
|
T | C | 11 | a0001c0001t0002g0211a0001c0001t0003g0203a0001c0001t0004g0117others(8): Show | 11 | HG01106.hp1 HG02056.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.73+4859T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205688222 | ||||||
| chr2:205688558
|
C | T | 1 | a0001c0001t0002g0216 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.73+5195C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205688558 | ||||||
| chr2:205688620
|
C | T | 2 | a0001c0002t0046g0142a0001c0012t0004g0138 | 2 | HG01884.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.73+5257C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205688620 | ||||||
| chr2:205688691
|
A | T | 1 | a0001c0011t0008g0135 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.73+5328A>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205688691 | ||||||
| chr2:205688803
|
G | A | 1 | a0001c0011t0004g0171 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.73+5440G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205688803 | ||||||
| chr2:205688804
|
G | A | 1 | a0001c0004t0001g0003 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.73+5441G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205688804 | ||||||
| chr2:205688826
|
T | G | 1 | a0001c0004t0006g0123 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.73+5463T>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205688826 | ||||||
| chr2:205688861
|
C | CA | 244 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0026others(241): Show | 248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
intron_variant | MODIFIER | c.73+5506dupA | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 205688861 | |||||
| chr2:205688861
|
C | CAA | 7 | a0001c0003t0002g0298a0001c0003t0003g0217a0001c0003t0003g0218others(4): Show | 7 | HG02080.hp2 HG02083.hp2 HG02523.hp1 others(4): Show |
intron_variant | MODIFIER | c.73+5505_73+5506dup others(2): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 205688861 | |||||
| chr2:205688870
|
C | A | 1 | a0001c0001t0004g0018 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.73+5507C>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205688870 | ||||||
| chr2:205688884
|
G | A | 3 | a0001c0001t0018g0019a0001c0003t0014g0017a0001c0020t0012g0016 | 3 | HG01256.hp2 HG02055.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.73+5521G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205688884 | ||||||
| chr2:205688984
|
A | G | 2 | a0001c0005t0023g0120a0001c0005t0023g0121 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.73+5621A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205688984 | ||||||
| chr2:205689035
|
T | C | 1 | a0001c0001t0012g0020 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.73+5672T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205689035 | ||||||
| chr2:205689116
|
A | G | 1 | a0001c0001t0002g0211 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.73+5753A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205689116 | ||||||
| chr2:205689280
|
T | G | 1 | a0001c0011t0004g0171 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.73+5917T>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205689280 | ||||||
| chr2:205689390
|
G | A | 107 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0026others(104): Show | 109 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(106): Show |
intron_variant | MODIFIER | c.73+6027G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205689390 | ||||||
| chr2:205689536
|
A | G | 10 | a0001c0002t0008g0200a0001c0002t0008g0201a0001c0002t0013g0198others(7): Show | 12 | HG02280.hp1 HG02630.hp1 HG02818.hp2 others(9): Show |
intron_variant | MODIFIER | c.73+6173A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205689536 | ||||||
| chr2:205689789
|
G | A | 6 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0005g0025others(3): Show | 6 | NA18953.hp2 NA19060.hp1 NA19070.hp1 others(3): Show |
intron_variant | MODIFIER | c.73+6426G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205689789 | ||||||
| chr2:205689798
|
T | C | 7 | a0001c0002t0049g0173a0001c0003t0008g0172a0001c0003t0012g0175others(4): Show | 7 | HG01243.hp1 HG02622.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.73+6435T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205689798 | ||||||
| chr2:205689820
|
G | A | 266 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0026others(263): Show | 270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.73+6457G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205689820 | ||||||
| chr2:205689981
|
G | A | 6 | a0001c0001t0004g0117a0001c0001t0004g0194a0001c0002t0001g0191others(3): Show | 6 | HG01106.hp1 HG02145.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.73+6618G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205689981 | ||||||
| chr2:205690025
|
G | A | 1 | a0001c0001t0001g0021 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.73+6662G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205690025 | ||||||
| chr2:205690033
|
C | G | 1 | a0002c0017t0062g0178 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.73+6670C>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205690033 | ||||||
| chr2:205690033
|
C | T | 1 | a0001c0002t0048g0125 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.73+6670C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205690033 | ||||||
| chr2:205690056
|
G | A | 1 | a0002c0017t0062g0178 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.73+6693G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205690056 | ||||||
| chr2:205690080
|
A | T | 1 | a0001c0001t0003g0269 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.73+6717A>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205690080 | ||||||
| chr2:205690112
|
G | A | 7 | a0001c0002t0049g0173a0001c0003t0008g0172a0001c0003t0012g0175others(4): Show | 7 | HG01243.hp1 HG02622.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.73+6749G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205690112 | ||||||
| chr2:205690447
|
A | T | 339 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0026others(336): Show | 345 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(342): Show |
intron_variant | MODIFIER | c.73+7084A>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205690447 | ||||||
| chr2:205690457
|
C | T | 66 | a0001c0001t0001g0158a0001c0001t0007g0214a0001c0001t0026g0014others(63): Show | 68 | HG00280.hp1 HG00735.hp2 HG00741.hp2 others(65): Show |
intron_variant | MODIFIER | c.74-7087C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205690457 | ||||||
| chr2:205690458
|
G | A | 270 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0026others(267): Show | 274 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(271): Show |
intron_variant | MODIFIER | c.74-7086G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205690458 | ||||||
| chr2:205690499
|
G | A | 271 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0026others(268): Show | 275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.74-7045G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205690499 | ||||||
| chr2:205690524
|
T | A | 2 | a0001c0001t0002g0224a0001c0001t0012g0103 | 2 | HG00621.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.74-7020T>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205690524 | ||||||
| chr2:205690579
|
T | TAC | 13 | a0001c0001t0001g0158a0001c0001t0007g0214a0001c0001t0053g0159others(10): Show | 14 | HG00280.hp1 HG01074.hp1 HG01099.hp1 others(11): Show |
intron_variant | MODIFIER | c.74-6915_74-6914dup others(2): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 205690579 | |||||
| chr2:205690579
|
T | TACAC | 8 | a0001c0002t0002g0280a0001c0002t0008g0161a0001c0002t0014g0160others(5): Show | 8 | HG00735.hp2 HG01891.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.74-6917_74-6914dup others(4): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 205690579 | |||||
| chr2:205690579
|
TAC | T | 21 | a0001c0001t0002g0216a0001c0001t0010g0210a0001c0001t0010g0335others(18): Show | 21 | HG01169.hp1 HG01192.hp2 HG01346.hp2 others(18): Show |
intron_variant | MODIFIER | c.74-6915_74-6914del others(2): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 205690579 | |||||
| chr2:205690579
|
TACAC | T | 39 | a0001c0001t0002g0258a0001c0001t0003g0203a0001c0001t0005g0096others(36): Show | 40 | HG01081.hp1 HG01167.hp1 HG01192.hp1 others(37): Show |
intron_variant | MODIFIER | c.74-6917_74-6914del others(4): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 205690579 | |||||
| chr2:205690579
|
TACACAC | T | 123 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0112others(120): Show | 125 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(122): Show |
intron_variant | MODIFIER | c.74-6919_74-6914del others(6): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 205690579 | |||||
| chr2:205690579
|
TACACACA others(1): Show |
T | 22 | a0001c0001t0001g0074a0001c0001t0001g0104a0001c0001t0004g0117others(19): Show | 22 | HG01106.hp1 HG01261.hp1 HG01975.hp2 others(19): Show |
intron_variant | MODIFIER | c.74-6921_74-6914del others(8): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 205690579 | |||||
| chr2:205690579
|
TACACACA others(3): Show |
T | 62 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0046others(59): Show | 64 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(61): Show |
intron_variant | MODIFIER | c.74-6923_74-6914del others(10): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 205690579 | |||||
| chr2:205690579
|
TACACACA others(5): Show |
T | 3 | a0001c0002t0005g0030a0001c0004t0006g0123a0001c0004t0014g0029 | 3 | HG00140.hp1 NA19056.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.74-6925_74-6914del others(12): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 205690579 | |||||
| chr2:205690579
|
TACACACA others(7): Show |
T | 4 | a0001c0001t0001g0026a0001c0001t0012g0027a0001c0001t0012g0028others(1): Show | 4 | HG00099.hp1 HG01070.hp2 HG01071.hp1 others(1): Show |
intron_variant | MODIFIER | c.74-6927_74-6914del others(14): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 205690579 | |||||
| chr2:205690579
|
TACACACA others(9): Show |
T | 1 | a0001c0002t0015g0007 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.74-6929_74-6914del others(16): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 205690579 | |||||
| chr2:205690579
|
TACACACA others(13): Show |
T | 1 | a0001c0003t0047g0126 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.74-6933_74-6914del others(20): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 205690579 | |||||
| chr2:205690579
|
TACACACA others(15): Show |
T | 16 | a0001c0002t0004g0182a0001c0002t0007g0284a0001c0002t0007g0285others(13): Show | 16 | HG01243.hp1 HG02109.hp1 HG02622.hp2 others(13): Show |
intron_variant | MODIFIER | c.74-6935_74-6914del others(22): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 205690579 | |||||
| chr2:205690579
|
TACACACA others(17): Show |
T | 4 | a0001c0002t0029g0136a0001c0002t0046g0142a0001c0002t0063g0137others(1): Show | 4 | HG01884.hp2 HG02922.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.74-6937_74-6914del others(24): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 205690579 | |||||
| chr2:205690579
|
TACACACA others(25): Show |
T | 1 | a0001c0012t0004g0138 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.74-6945_74-6914del others(32): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 205690579 | |||||
| chr2:205690651
|
G | A | 1 | a0002c0017t0062g0178 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.74-6893G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205690651 | ||||||
| chr2:205690781
|
A | AAAAAT | 3 | a0001c0010t0009g0231a0002c0014t0001g0196a0002c0014t0008g0195 | 3 | HG02280.hp1 HG03540.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.74-6742_74-6738dup others(5): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 205690781 | |||||
| chr2:205691080
|
C | A | 179 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0026others(176): Show | 183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.74-6464C>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205691080 | ||||||
| chr2:205691160
|
G | A | 1 | a0001c0012t0017g0273 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.74-6384G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205691160 | ||||||
| chr2:205691484
|
T | G | 344 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0026others(341): Show | 350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.74-6060T>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205691484 | ||||||
| chr2:205691934
|
T | C | 1 | a0001c0004t0002g0202 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.74-5610T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205691934 | ||||||
| chr2:205691977
|
C | T | 74 | a0001c0001t0001g0158a0001c0001t0007g0214a0001c0001t0012g0020others(71): Show | 75 | HG00280.hp1 HG00735.hp2 HG00741.hp2 others(72): Show |
intron_variant | MODIFIER | c.74-5567C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205691977 | ||||||
| chr2:205692209
|
T | C | 1 | a0001c0002t0004g0140 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.74-5335T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205692209 | ||||||
| chr2:205692428
|
G | A | 3 | a0001c0010t0009g0232a0001c0010t0009g0233a0001c0010t0009g0234 | 3 | HG01516.hp2 HG01517.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.74-5116G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205692428 | ||||||
| chr2:205692494
|
G | T | 2 | a0001c0002t0029g0136a0001c0002t0063g0137 | 2 | HG02922.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.74-5050G>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205692494 | ||||||
| chr2:205692606
|
A | T | 1 | a0001c0001t0010g0210 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.74-4938A>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205692606 | ||||||
| chr2:205692781
|
G | T | 1 | a0001c0002t0004g0140 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.74-4763G>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205692781 | ||||||
| chr2:205692802
|
C | T | 75 | a0001c0001t0001g0158a0001c0001t0004g0117a0001c0001t0004g0194others(72): Show | 77 | HG00280.hp1 HG00735.hp2 HG00741.hp2 others(74): Show |
intron_variant | MODIFIER | c.74-4742C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205692802 | ||||||
| chr2:205692815
|
G | A | 67 | a0001c0001t0001g0158a0001c0001t0007g0214a0001c0001t0012g0020others(64): Show | 69 | HG00280.hp1 HG00735.hp2 HG00741.hp2 others(66): Show |
intron_variant | MODIFIER | c.74-4729G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205692815 | ||||||
| chr2:205693008
|
C | A | 1 | a0001c0002t0020g0186 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.74-4536C>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205693008 | ||||||
| chr2:205693052
|
G | A | 1 | a0001c0004t0005g0106 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.74-4492G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205693052 | ||||||
| chr2:205693217
|
A | C | 3 | a0001c0002t0049g0173a0001c0003t0022g0174a0001c0011t0004g0171 | 3 | HG02622.hp2 HG06807.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.74-4327A>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205693217 | ||||||
| chr2:205693333
|
C | T | 10 | a0001c0002t0004g0182a0001c0002t0007g0284a0001c0002t0007g0285others(7): Show | 10 | HG02109.hp1 HG02647.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.74-4211C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205693333 | ||||||
| chr2:205693528
|
A | C | 2 | a0001c0005t0023g0119a0001c0005t0029g0118 | 2 | HG01169.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.74-4016A>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205693528 | ||||||
| chr2:205693550
|
G | A | 106 | a0001c0001t0001g0158a0001c0001t0004g0117a0001c0001t0004g0194others(103): Show | 108 | HG00280.hp1 HG00735.hp2 HG00741.hp2 others(105): Show |
intron_variant | MODIFIER | c.74-3994G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205693550 | ||||||
| chr2:205693716
|
C | A | 10 | a0001c0002t0004g0182a0001c0002t0007g0284a0001c0002t0007g0285others(7): Show | 10 | HG02109.hp1 HG02647.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.74-3828C>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205693716 | ||||||
| chr2:205693789
|
C | T | 105 | a0001c0001t0001g0158a0001c0001t0004g0117a0001c0001t0004g0194others(102): Show | 107 | HG00280.hp1 HG00735.hp2 HG00741.hp2 others(104): Show |
intron_variant | MODIFIER | c.74-3755C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205693789 | ||||||
| chr2:205693915
|
A | T | 7 | a0001c0002t0049g0173a0001c0003t0008g0172a0001c0003t0012g0175others(4): Show | 7 | HG01243.hp1 HG02622.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.74-3629A>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205693915 | ||||||
| chr2:205694044
|
G | A | 1 | a0001c0002t0004g0140 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.74-3500G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205694044 | ||||||
| chr2:205694085
|
A | C | 1 | a0001c0002t0004g0140 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.74-3459A>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205694085 | ||||||
| chr2:205694105
|
C | T | 3 | a0001c0002t0001g0191a0001c0002t0004g0192a0001c0002t0061g0190 | 3 | HG02145.hp1 HG02280.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.74-3439C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205694105 | ||||||
| chr2:205694146
|
A | G | 1 | a0001c0002t0008g0141 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.74-3398A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205694146 | ||||||
| chr2:205694371
|
G | A | 2 | a0001c0001t0020g0031a0001c0009t0027g0032 | 2 | HG01069.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.74-3173G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205694371 | ||||||
| chr2:205694458
|
T | C | 1 | a0001c0001t0057g0033 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.74-3086T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205694458 | ||||||
| chr2:205694501
|
A | G | 2 | a0002c0015t0030g0004a0002c0027t0064g0177 | 3 | HG02922.hp2 HG02965.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.74-3043A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205694501 | ||||||
| chr2:205694540
|
C | A | 1 | a0002c0027t0064g0177 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.74-3004C>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205694540 | ||||||
| chr2:205694914
|
A | G | 2 | a0001c0001t0058g0069a0001c0002t0005g0030 | 2 | HG00140.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.74-2630A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205694914 | ||||||
| chr2:205695509
|
G | C | 58 | a0001c0001t0001g0158a0001c0001t0007g0214a0001c0001t0012g0020others(55): Show | 58 | HG00280.hp1 HG00735.hp2 HG00741.hp2 others(55): Show |
intron_variant | MODIFIER | c.74-2035G>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205695509 | ||||||
| chr2:205695687
|
T | G | 1 | a0001c0001t0010g0335 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.74-1857T>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205695687 | ||||||
| chr2:205695717
|
T | C | 5 | a0001c0008t0004g0005a0001c0008t0004g0129a0001c0008t0004g0197others(2): Show | 6 | HG02280.hp1 HG02630.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.74-1827T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205695717 | ||||||
| chr2:205695816
|
G | A | 12 | a0001c0002t0004g0182a0001c0002t0007g0284a0001c0002t0007g0285others(9): Show | 12 | HG02109.hp1 HG02647.hp1 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.74-1728G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205695816 | ||||||
| chr2:205695824
|
T | C | 4 | a0001c0002t0012g0131a0001c0002t0016g0134a0001c0013t0016g0132others(1): Show | 4 | HG02717.hp1 HG02809.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.74-1720T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205695824 | ||||||
| chr2:205695875
|
T | C | 1 | a0001c0001t0018g0019 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.74-1669T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205695875 | ||||||
| chr2:205695889
|
G | A | 80 | a0001c0001t0001g0158a0001c0001t0007g0214a0001c0001t0012g0020others(77): Show | 82 | HG00280.hp1 HG00735.hp2 HG00741.hp2 others(79): Show |
intron_variant | MODIFIER | c.74-1655G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205695889 | ||||||
| chr2:205696014
|
C | T | 95 | a0001c0001t0001g0158a0001c0001t0007g0214a0001c0001t0012g0020others(92): Show | 97 | HG00280.hp1 HG00735.hp2 HG00741.hp2 others(94): Show |
intron_variant | MODIFIER | c.74-1530C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205696014 | ||||||
| chr2:205696113
|
C | T | 1 | a0001c0001t0031g0328 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.74-1431C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205696113 | ||||||
| chr2:205696123
|
A | G | 1 | a0001c0003t0047g0126 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.74-1421A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205696123 | ||||||
| chr2:205696160
|
C | T | 1 | a0001c0003t0003g0108 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.74-1384C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205696160 | ||||||
| chr2:205696174
|
A | G | 1 | a0001c0003t0047g0126 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.74-1370A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205696174 | ||||||
| chr2:205696189
|
G | A | 1 | a0001c0003t0002g0320 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.74-1355G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205696189 | ||||||
| chr2:205696346
|
G | A | 3 | a0001c0002t0007g0284a0001c0002t0007g0285a0001c0002t0008g0181 | 3 | HG02109.hp1 HG02647.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.74-1198G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205696346 | ||||||
| chr2:205696372
|
T | C | 12 | a0001c0002t0004g0182a0001c0002t0007g0284a0001c0002t0007g0285others(9): Show | 12 | HG02109.hp1 HG02647.hp1 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.74-1172T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205696372 | ||||||
| chr2:205696700
|
G | A | 6 | a0001c0001t0004g0117a0001c0001t0004g0194a0001c0002t0001g0191others(3): Show | 6 | HG01106.hp1 HG02145.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.74-844G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205696700 | ||||||
| chr2:205696703
|
C | T | 61 | a0001c0001t0001g0158a0001c0001t0007g0214a0001c0001t0012g0020others(58): Show | 61 | HG00280.hp1 HG00735.hp2 HG00741.hp2 others(58): Show |
intron_variant | MODIFIER | c.74-841C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205696703 | ||||||
| chr2:205697028
|
T | C | 4 | a0001c0003t0002g0298a0001c0003t0003g0296a0001c0003t0003g0299others(1): Show | 4 | HG02083.hp2 HG02523.hp1 NA18961.hp2 others(1): Show |
intron_variant | MODIFIER | c.74-516T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205697028 | ||||||
| chr2:205697183
|
G | A | 1 | a0001c0003t0014g0095 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.74-361G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205697183 | ||||||
| chr2:205697193
|
G | A | 1 | a0001c0011t0008g0135 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.74-351G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205697193 | ||||||
| chr2:205697309
|
C | T | 2 | a0001c0002t0029g0136a0001c0002t0063g0137 | 2 | HG02922.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.74-235C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205697309 | ||||||
| chr2:205697312
|
C | CTGTG | 3 | a0001c0002t0004g0182a0001c0002t0049g0173a0001c0003t0022g0174 | 3 | HG06807.hp1 NA18906.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.74-202_74-199dupGT others(2): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 205697312 | |||||
| chr2:205697312
|
C | CTGTGTGT others(1): Show |
5 | a0001c0002t0008g0200a0001c0002t0008g0201a0001c0002t0013g0198others(2): Show | 5 | HG02886.hp1 HG02896.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.74-206_74-199dupGT others(6): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 205697312 | |||||
| chr2:205697312
|
C | CTGTGTGT others(3): Show |
2 | a0002c0014t0001g0196a0002c0014t0008g0195 | 2 | HG02280.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.74-208_74-199dupGT others(8): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 205697312 | |||||
| chr2:205697312
|
C | CTGTGTGT others(9): Show |
4 | a0001c0002t0007g0284a0001c0002t0007g0285a0001c0002t0008g0181others(1): Show | 4 | HG02109.hp1 HG02647.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.74-214_74-199dupGT others(14): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 205697312 | |||||
| chr2:205697312
|
C | CTGTGTGT others(11): Show |
6 | a0001c0002t0022g0185a0001c0002t0051g0183a0001c0002t0054g0215others(3): Show | 6 | HG02647.hp1 HG02922.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.74-216_74-199dupGT others(16): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 205697312 | |||||
| chr2:205697312
|
C | CTGTGTGT others(15): Show |
1 | a0001c0003t0008g0172 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.74-220_74-199dupGT others(20): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 205697312 | |||||
| chr2:205697312
|
C | CTGTGTGT others(17): Show |
2 | a0001c0002t0004g0140a0001c0002t0046g0142 | 2 | HG01884.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.74-222_74-199dupGT others(22): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 205697312 | |||||
| chr2:205697312
|
C | CTGTGTGT others(19): Show |
3 | a0001c0011t0004g0171a0002c0015t0030g0004a0002c0027t0064g0177 | 4 | HG02622.hp2 HG02922.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.74-224_74-199dupGT others(24): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 205697312 | |||||
| chr2:205697312
|
C | CTGTGTGT others(21): Show |
3 | a0001c0003t0012g0175a0001c0005t0013g0176a0001c0012t0017g0273 | 3 | HG02976.hp1 HG03209.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.74-226_74-199dupGT others(26): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 205697312 | |||||
| chr2:205697312
|
C | CTGTGTGT others(25): Show |
1 | a0001c0012t0004g0138 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.74-230_74-199dupGT others(30): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 205697312 | |||||
| chr2:205697312
|
CTG | C | 234 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0026others(231): Show | 239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.74-200_74-199delGT | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 205697312 | |||||
| chr2:205697312
|
CTGTG | C | 49 | a0001c0001t0001g0158a0001c0001t0007g0214a0001c0001t0012g0020others(46): Show | 49 | HG00280.hp1 HG00639.hp1 HG00735.hp2 others(46): Show |
intron_variant | MODIFIER | c.74-202_74-199delGT others(2): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 205697312 | |||||
| chr2:205697499
|
T | C | 4 | a0001c0002t0004g0182a0001c0002t0049g0173a0001c0003t0022g0174others(1): Show | 4 | HG02723.hp2 HG06807.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.74-45T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205697499 | ||||||
| chr2:205697526
|
C | T | 303 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0026others(300): Show | 308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): Show |
intron_variant | MODIFIER | c.74-18C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 1/16 | chr2 | 205697526 | ||||||
| chr2:205697730
|
C | T | 1 | a0002c0029t0013g0276 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.251+9C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205697730 | ||||||
| chr2:205697842
|
A | G | 1 | a0001c0006t0011g0338 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.251+121A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205697842 | ||||||
| chr2:205697858
|
A | G | 6 | a0001c0001t0005g0008a0001c0003t0001g0099a0001c0003t0005g0093others(3): Show | 6 | HG02056.hp2 NA18957.hp2 NA18975.hp1 others(3): Show |
intron_variant | MODIFIER | c.251+137A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205697858 | ||||||
| chr2:205697887
|
G | T | 1 | a0001c0004t0001g0062 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.251+166G>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205697887 | ||||||
| chr2:205697958
|
C | A | 14 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0005g0034others(11): Show | 14 | HG00438.hp1 HG00558.hp2 HG01943.hp2 others(11): Show |
intron_variant | MODIFIER | c.251+237C>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205697958 | ||||||
| chr2:205698207
|
G | GA | 15 | a0001c0002t0007g0293a0001c0002t0008g0013a0001c0002t0028g0188others(12): Show | 15 | HG01070.hp1 HG01099.hp1 HG02071.hp1 others(12): Show |
intron_variant | MODIFIER | c.251+496dupA | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr2 | 205698207 | |||||
| chr2:205698218
|
G | A | 15 | a0001c0002t0004g0012a0001c0002t0006g0147a0001c0002t0008g0124others(12): Show | 15 | HG00741.hp2 HG01081.hp2 HG01496.hp1 others(12): Show |
intron_variant | MODIFIER | c.251+497G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205698218 | ||||||
| chr2:205698221
|
T | G | 15 | a0001c0002t0004g0012a0001c0002t0006g0147a0001c0002t0008g0124others(12): Show | 15 | HG00741.hp2 HG01081.hp2 HG01496.hp1 others(12): Show |
intron_variant | MODIFIER | c.251+500T>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205698221 | ||||||
| chr2:205698221
|
TA | T | 41 | a0001c0001t0007g0214a0001c0001t0009g0319a0001c0001t0012g0020others(38): Show | 41 | HG00280.hp1 HG00735.hp2 HG01070.hp1 others(38): Show |
intron_variant | MODIFIER | c.251+514delA | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr2 | 205698221 | |||||
| chr2:205698222
|
A | T | 15 | a0001c0002t0004g0012a0001c0002t0006g0147a0001c0002t0008g0124others(12): Show | 15 | HG00741.hp2 HG01081.hp2 HG01496.hp1 others(12): Show |
intron_variant | MODIFIER | c.251+501A>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205698222 | ||||||
| chr2:205698299
|
G | A | 232 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0026others(229): Show | 236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.251+578G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205698299 | ||||||
| chr2:205698460
|
G | C | 10 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0067others(7): Show | 10 | HG01106.hp1 HG01934.hp2 HG01943.hp1 others(7): Show |
intron_variant | MODIFIER | c.251+739G>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205698460 | ||||||
| chr2:205698515
|
A | G | 1 | a0001c0003t0047g0126 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.251+794A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205698515 | ||||||
| chr2:205698534
|
T | C | 245 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0026others(242): Show | 249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
intron_variant | MODIFIER | c.251+813T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205698534 | ||||||
| chr2:205698605
|
A | G | 5 | a0001c0003t0012g0175a0001c0005t0013g0176a0001c0011t0004g0171others(2): Show | 5 | HG02622.hp2 HG02976.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.251+884A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205698605 | ||||||
| chr2:205698738
|
T | C | 1 | a0005c0021t0004g0139 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.251+1017T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205698738 | ||||||
| chr2:205698981
|
T | A | 5 | a0001c0002t0029g0136a0001c0002t0063g0137a0002c0015t0030g0004others(2): Show | 6 | HG02922.hp1 HG02922.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.251+1260T>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205698981 | ||||||
| chr2:205699332
|
G | T | 5 | a0001c0002t0029g0136a0001c0002t0063g0137a0002c0015t0030g0004others(2): Show | 6 | HG02922.hp1 HG02922.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.251+1611G>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205699332 | ||||||
| chr2:205699417
|
G | A | 2 | a0001c0002t0013g0198a0001c0002t0013g0199 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.251+1696G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205699417 | ||||||
| chr2:205699429
|
T | C | 13 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0067others(10): Show | 13 | HG01106.hp1 HG01934.hp2 HG01943.hp1 others(10): Show |
intron_variant | MODIFIER | c.251+1708T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205699429 | ||||||
| chr2:205699574
|
A | G | 13 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0067others(10): Show | 13 | HG01106.hp1 HG01934.hp2 HG01943.hp1 others(10): Show |
intron_variant | MODIFIER | c.251+1853A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205699574 | ||||||
| chr2:205699993
|
A | G | 4 | a0001c0002t0003g0204a0001c0002t0003g0282a0001c0002t0003g0283others(1): Show | 4 | NA18953.hp1 NA18967.hp2 NA19009.hp2 others(1): Show |
intron_variant | MODIFIER | c.251+2272A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205699993 | ||||||
| chr2:205700065
|
C | T | 9 | a0001c0002t0004g0140a0001c0003t0012g0175a0001c0008t0004g0005others(6): Show | 10 | HG02280.hp1 HG02622.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.251+2344C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205700065 | ||||||
| chr2:205700211
|
C | T | 2 | a0001c0003t0009g0342a0001c0003t0025g0301 | 2 | HG02683.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.251+2490C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205700211 | ||||||
| chr2:205700247
|
C | G | 1 | a0001c0001t0005g0145 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.251+2526C>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205700247 | ||||||
| chr2:205700294
|
C | T | 1 | a0001c0002t0004g0182 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.251+2573C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205700294 | ||||||
| chr2:205700504
|
C | T | 4 | a0001c0002t0012g0131a0001c0002t0016g0134a0001c0013t0016g0132others(1): Show | 4 | HG02717.hp1 HG02809.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.251+2783C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205700504 | ||||||
| chr2:205700505
|
G | A | 1 | a0001c0001t0005g0034 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.251+2784G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205700505 | ||||||
| chr2:205700541
|
G | A | 1 | a0001c0004t0005g0106 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.251+2820G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205700541 | ||||||
| chr2:205700727
|
T | C | 4 | a0001c0002t0029g0136a0001c0002t0063g0137a0002c0015t0030g0004others(1): Show | 5 | HG02922.hp1 HG02922.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.251+3006T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205700727 | ||||||
| chr2:205700736
|
C | T | 1 | a0001c0002t0011g0272 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.251+3015C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205700736 | ||||||
| chr2:205700776
|
C | T | 46 | a0001c0001t0007g0214a0001c0002t0002g0280a0001c0002t0004g0012others(43): Show | 46 | HG00140.hp2 HG00280.hp1 HG00735.hp2 others(43): Show |
intron_variant | MODIFIER | c.251+3055C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205700776 | ||||||
| chr2:205700790
|
C | T | 1 | a0001c0002t0004g0140 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.251+3069C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205700790 | ||||||
| chr2:205700894
|
AC | A | 9 | a0001c0002t0004g0012a0001c0002t0007g0293a0001c0002t0008g0013others(6): Show | 9 | HG00741.hp2 HG01070.hp1 HG01081.hp2 others(6): Show |
intron_variant | MODIFIER | c.251+3174delC | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205700894 | ||||||
| chr2:205700896
|
T | G | 1 | a0001c0002t0018g0010 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.251+3175T>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205700896 | ||||||
| chr2:205700927
|
A | C | 13 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0067others(10): Show | 13 | HG01106.hp1 HG01934.hp2 HG01943.hp1 others(10): Show |
intron_variant | MODIFIER | c.251+3206A>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205700927 | ||||||
| chr2:205700950
|
G | A | 1 | a0001c0002t0042g0213 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.251+3229G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205700950 | ||||||
| chr2:205700953
|
T | C | 1 | a0001c0002t0020g0186 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.251+3232T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205700953 | ||||||
| chr2:205700988
|
G | A | 9 | a0001c0002t0004g0140a0001c0003t0012g0175a0001c0008t0004g0005others(6): Show | 10 | HG02280.hp1 HG02622.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.251+3267G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205700988 | ||||||
| chr2:205701018
|
G | A | 234 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0026others(231): Show | 238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.251+3297G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205701018 | ||||||
| chr2:205701130
|
T | C | 1 | a0001c0004t0002g0302 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.251+3409T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205701130 | ||||||
| chr2:205701247
|
G | A | 1 | a0001c0006t0009g0303 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.251+3526G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205701247 | ||||||
| chr2:205701538
|
C | CA | 295 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0026others(292): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.251+3833dupA | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr2 | 205701538 | |||||
| chr2:205701699
|
A | G | 301 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0026others(298): Show | 305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.251+3978A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205701699 | ||||||
| chr2:205701778
|
G | A | 1 | a0001c0001t0005g0145 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.251+4057G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205701778 | ||||||
| chr2:205701790
|
G | T | 11 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0067others(8): Show | 11 | HG01106.hp1 HG01934.hp2 HG01943.hp1 others(8): Show |
intron_variant | MODIFIER | c.251+4069G>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205701790 | ||||||
| chr2:205702053
|
T | G | 3 | a0001c0003t0004g0168a0003c0025t0013g0167a0003c0026t0004g0166 | 3 | HG01891.hp2 HG02572.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.251+4332T>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205702053 | ||||||
| chr2:205702070
|
C | T | 1 | a0004c0022t0006g0116 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.251+4349C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205702070 | ||||||
| chr2:205702149
|
G | GTTTGGGA others(363): Show |
1 | a0001c0001t0003g0318 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.251+4444_251+4445i others(372): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr2 | 205702149 | |||||
| chr2:205702149
|
G | GTTTGGGA others(371): Show |
1 | a0001c0001t0002g0211 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.251+4444_251+4445i others(380): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr2 | 205702149 | |||||
| chr2:205702149
|
G | GTTTGGGA others(386): Show |
1 | a0001c0004t0002g0302 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.251+4444_251+4445i others(395): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr2 | 205702149 | |||||
| chr2:205702149
|
G | GTTTGGGA others(399): Show |
1 | a0001c0004t0002g0246 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.251+4444_251+4445i others(408): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr2 | 205702149 | |||||
| chr2:205702153
|
G | A | 5 | a0001c0002t0029g0136a0001c0002t0063g0137a0002c0015t0030g0004others(2): Show | 6 | HG02922.hp1 HG02922.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.251+4432G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205702153 | ||||||
| chr2:205702164
|
C | A | 1 | a0001c0001t0005g0035 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.251+4443C>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205702164 | ||||||
| chr2:205702337
|
A | G | 2 | a0001c0001t0058g0069a0001c0002t0005g0030 | 2 | HG00140.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.251+4616A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205702337 | ||||||
| chr2:205702409
|
C | T | 1 | a0001c0001t0004g0061 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.251+4688C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205702409 | ||||||
| chr2:205702499
|
C | T | 4 | a0001c0002t0008g0200a0001c0002t0008g0201a0001c0002t0013g0198others(1): Show | 4 | HG02886.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.251+4778C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205702499 | ||||||
| chr2:205702538
|
C | G | 1 | a0005c0021t0004g0139 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.251+4817C>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205702538 | ||||||
| chr2:205702712
|
G | A | 1 | a0001c0001t0004g0041 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.251+4991G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205702712 | ||||||
| chr2:205703633
|
A | C | 1 | a0001c0001t0004g0061 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.251+5912A>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205703633 | ||||||
| chr2:205703683
|
T | C | 1 | a0001c0002t0020g0186 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.251+5962T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205703683 | ||||||
| chr2:205703686
|
G | T | 14 | a0001c0001t0002g0211a0001c0001t0002g0258a0001c0001t0002g0316others(11): Show | 14 | HG00423.hp1 HG00558.hp1 HG00673.hp2 others(11): Show |
intron_variant | MODIFIER | c.251+5965G>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205703686 | ||||||
| chr2:205703693
|
A | G | 6 | a0001c0003t0012g0175a0001c0005t0013g0176a0001c0011t0004g0171others(3): Show | 6 | HG02622.hp2 HG02976.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.251+5972A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205703693 | ||||||
| chr2:205703780
|
T | C | 15 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0067others(12): Show | 15 | HG01106.hp1 HG01934.hp2 HG01943.hp1 others(12): Show |
intron_variant | MODIFIER | c.251+6059T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205703780 | ||||||
| chr2:205703782
|
G | T | 1 | a0001c0002t0004g0275 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.251+6061G>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205703782 | ||||||
| chr2:205703902
|
G | A | 12 | a0001c0001t0015g0209a0001c0002t0004g0140a0001c0003t0012g0175others(9): Show | 13 | HG01169.hp1 HG01433.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.251+6181G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205703902 | ||||||
| chr2:205704100
|
G | A | 1 | a0001c0004t0002g0302 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.251+6379G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205704100 | ||||||
| chr2:205704513
|
G | A | 1 | a0001c0011t0004g0171 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.251+6792G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205704513 | ||||||
| chr2:205704604
|
T | C | 1 | a0001c0001t0001g0104 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.251+6883T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205704604 | ||||||
| chr2:205704609
|
C | T | 1 | a0001c0001t0053g0159 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.251+6888C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205704609 | ||||||
| chr2:205704610
|
A | G | 300 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0026others(297): Show | 304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.251+6889A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205704610 | ||||||
| chr2:205704731
|
T | C | 2 | a0001c0001t0013g0042a0001c0004t0012g0043 | 2 | HG00639.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.251+7010T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205704731 | ||||||
| chr2:205704803
|
A | C | 2 | a0002c0015t0030g0004a0002c0027t0064g0177 | 3 | HG02922.hp2 HG02965.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.251+7082A>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205704803 | ||||||
| chr2:205704809
|
C | T | 1 | a0001c0002t0002g0264 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.251+7088C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205704809 | ||||||
| chr2:205704810
|
C | T | 1 | a0001c0002t0002g0264 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.251+7089C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205704810 | ||||||
| chr2:205704812
|
C | T | 1 | a0001c0004t0005g0106 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.251+7091C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205704812 | ||||||
| chr2:205704899
|
C | A | 1 | a0001c0003t0055g0092 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.251+7178C>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205704899 | ||||||
| chr2:205705074
|
T | C | 1 | a0001c0001t0007g0214 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.251+7353T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205705074 | ||||||
| chr2:205705102
|
GGATTTAA others(24): Show |
G | 1 | a0001c0002t0001g0082 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.251+7382_251+7412d others(33): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205705102 | ||||||
| chr2:205705183
|
G | GA | 288 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0026others(285): Show | 292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): Show |
intron_variant | MODIFIER | c.251+7476dupA | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr2 | 205705183 | |||||
| chr2:205705183
|
G | GAA | 9 | a0001c0001t0001g0064a0001c0001t0005g0096a0001c0002t0006g0091others(6): Show | 9 | HG02004.hp2 HG02523.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.251+7475_251+7476d others(4): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr2 | 205705183 | |||||
| chr2:205705183
|
GA | G | 7 | a0001c0002t0008g0200a0001c0002t0008g0201a0001c0002t0013g0198others(4): Show | 7 | HG02622.hp2 HG02886.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.251+7476delA | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr2 | 205705183 | |||||
| chr2:205705230
|
A | T | 1 | a0001c0001t0001g0064 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.251+7509A>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205705230 | ||||||
| chr2:205705265
|
C | T | 1 | a0001c0002t0042g0213 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.251+7544C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205705265 | ||||||
| chr2:205705459
|
A | G | 6 | a0001c0001t0019g0090a0001c0002t0007g0291a0001c0004t0001g0087others(3): Show | 6 | HG01928.hp1 HG01975.hp1 HG01981.hp1 others(3): Show |
intron_variant | MODIFIER | c.251+7738A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205705459 | ||||||
| chr2:205705554
|
T | C | 15 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0067others(12): Show | 15 | HG01106.hp1 HG01934.hp2 HG01943.hp1 others(12): Show |
intron_variant | MODIFIER | c.251+7833T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205705554 | ||||||
| chr2:205705571
|
C | T | 54 | a0001c0001t0007g0214a0001c0002t0002g0280a0001c0002t0004g0012others(51): Show | 54 | HG00280.hp1 HG00735.hp2 HG00741.hp2 others(51): Show |
intron_variant | MODIFIER | c.251+7850C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205705571 | ||||||
| chr2:205705665
|
G | A | 1 | a0001c0001t0001g0026 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.251+7944G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205705665 | ||||||
| chr2:205705709
|
T | G | 328 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0026others(325): Show | 334 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(331): Show |
intron_variant | MODIFIER | c.251+7988T>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205705709 | ||||||
| chr2:205705895
|
C | T | 1 | a0001c0003t0002g0298 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.251+8174C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205705895 | ||||||
| chr2:205706081
|
C | T | 1 | a0001c0001t0001g0060 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.251+8360C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205706081 | ||||||
| chr2:205706266
|
T | G | 1 | a0001c0003t0009g0342 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.251+8545T>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205706266 | ||||||
| chr2:205706283
|
C | T | 4 | a0001c0002t0029g0136a0001c0002t0063g0137a0002c0015t0030g0004others(1): Show | 5 | HG02922.hp1 HG02922.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.251+8562C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205706283 | ||||||
| chr2:205706411
|
A | G | 75 | a0001c0001t0001g0021a0001c0001t0001g0054a0001c0001t0001g0064others(72): Show | 77 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(74): Show |
intron_variant | MODIFIER | c.251+8690A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205706411 | ||||||
| chr2:205706926
|
C | T | 10 | a0001c0001t0005g0035a0001c0001t0005g0038a0001c0001t0005g0040others(7): Show | 10 | HG00438.hp1 HG00558.hp2 HG02523.hp1 others(7): Show |
intron_variant | MODIFIER | c.251+9205C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205706926 | ||||||
| chr2:205707231
|
G | C | 10 | a0001c0006t0007g0306a0001c0006t0007g0329a0001c0006t0009g0303others(7): Show | 10 | HG02055.hp1 HG02818.hp1 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.252-8962G>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205707231 | ||||||
| chr2:205707247
|
G | A | 1 | a0001c0003t0011g0322 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.252-8946G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205707247 | ||||||
| chr2:205707415
|
A | G | 1 | a0001c0002t0017g0255 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.252-8778A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205707415 | ||||||
| chr2:205707728
|
G | T | 2 | a0001c0001t0008g0050a0001c0004t0013g0051 | 2 | HG00280.hp2 HG01074.hp2 |
intron_variant | MODIFIER | c.252-8465G>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205707728 | ||||||
| chr2:205707770
|
T | G | 1 | a0001c0003t0047g0126 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.252-8423T>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205707770 | ||||||
| chr2:205707810
|
C | G | 79 | a0001c0001t0005g0008a0001c0001t0031g0328a0001c0002t0001g0015others(76): Show | 79 | HG00639.hp1 HG01167.hp1 HG01192.hp1 others(76): Show |
intron_variant | MODIFIER | c.252-8383C>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205707810 | ||||||
| chr2:205707904
|
A | G | 175 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0026others(172): Show | 179 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(176): Show |
intron_variant | MODIFIER | c.252-8289A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205707904 | ||||||
| chr2:205708062
|
T | C | 1 | a0001c0002t0008g0141 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.252-8131T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205708062 | ||||||
| chr2:205708125
|
T | C | 2 | a0001c0005t0023g0120a0001c0005t0023g0121 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.252-8068T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205708125 | ||||||
| chr2:205708148
|
G | C | 5 | a0001c0002t0029g0136a0001c0002t0063g0137a0002c0015t0030g0004others(2): Show | 6 | HG02922.hp1 HG02922.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.252-8045G>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205708148 | ||||||
| chr2:205708224
|
C | G | 2 | a0001c0001t0005g0105a0001c0004t0002g0170 | 2 | HG00621.hp2 NA18972.hp1 |
intron_variant | MODIFIER | c.252-7969C>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205708224 | ||||||
| chr2:205708364
|
C | T | 1 | a0001c0003t0008g0172 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.252-7829C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205708364 | ||||||
| chr2:205708408
|
G | A | 1 | a0001c0001t0013g0042 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.252-7785G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205708408 | ||||||
| chr2:205708510
|
T | C | 325 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0026others(322): Show | 331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): Show |
intron_variant | MODIFIER | c.252-7683T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205708510 | ||||||
| chr2:205708547
|
G | A | 1 | a0001c0002t0049g0173 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.252-7646G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205708547 | ||||||
| chr2:205708673
|
T | TC | 167 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0026others(164): Show | 171 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(168): Show |
intron_variant | MODIFIER | c.252-7520_252-7519i others(3): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205708673 | ||||||
| chr2:205708808
|
A | G | 1 | a0007c0019t0002g0321 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.252-7385A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205708808 | ||||||
| chr2:205708912
|
C | A | 326 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0026others(323): Show | 332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.252-7281C>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205708912 | ||||||
| chr2:205709444
|
C | T | 1 | a0001c0001t0008g0047 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.252-6749C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205709444 | ||||||
| chr2:205709719
|
G | A | 2 | a0001c0002t0046g0142a0001c0003t0008g0172 | 2 | HG01243.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.252-6474G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205709719 | ||||||
| chr2:205709834
|
T | C | 1 | a0001c0002t0011g0257 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.252-6359T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205709834 | ||||||
| chr2:205709906
|
A | G | 2 | a0001c0002t0029g0136a0001c0002t0063g0137 | 2 | HG02922.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.252-6287A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205709906 | ||||||
| chr2:205709963
|
G | A | 1 | a0001c0001t0002g0236 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.252-6230G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205709963 | ||||||
| chr2:205709994
|
G | T | 1 | a0001c0001t0001g0060 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.252-6199G>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205709994 | ||||||
| chr2:205709995
|
C | A | 1 | a0001c0001t0001g0060 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.252-6198C>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205709995 | ||||||
| chr2:205710531
|
G | A | 4 | a0001c0005t0023g0119a0001c0005t0023g0120a0001c0005t0023g0121others(1): Show | 4 | HG01169.hp1 HG01433.hp1 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.252-5662G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205710531 | ||||||
| chr2:205710541
|
T | G | 1 | a0001c0001t0010g0313 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.252-5652T>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205710541 | ||||||
| chr2:205710643
|
C | G | 1 | a0001c0002t0018g0011 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.252-5550C>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205710643 | ||||||
| chr2:205710644
|
G | A | 6 | a0001c0001t0002g0216a0001c0005t0014g0128a0001c0005t0023g0119others(3): Show | 6 | HG01169.hp1 HG01346.hp2 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.252-5549G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205710644 | ||||||
| chr2:205710644
|
G | C | 2 | a0001c0001t0013g0042a0001c0004t0012g0043 | 2 | HG00639.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.252-5549G>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205710644 | ||||||
| chr2:205710680
|
A | G | 148 | a0001c0001t0002g0216a0001c0001t0005g0008a0001c0001t0005g0096others(145): Show | 148 | HG00140.hp2 HG00280.hp1 HG00639.hp1 others(145): Show |
intron_variant | MODIFIER | c.252-5513A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205710680 | ||||||
| chr2:205710695
|
C | T | 3 | a0001c0003t0003g0217a0001c0003t0003g0218a0001c0003t0003g0300 | 3 | HG02080.hp2 NA18964.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.252-5498C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205710695 | ||||||
| chr2:205711003
|
G | T | 5 | a0001c0001t0019g0090a0001c0004t0001g0087a0001c0004t0006g0180others(2): Show | 5 | HG01928.hp1 HG01981.hp1 HG01993.hp2 others(2): Show |
intron_variant | MODIFIER | c.252-5190G>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205711003 | ||||||
| chr2:205711024
|
T | A | 153 | a0001c0001t0002g0216a0001c0001t0005g0008a0001c0001t0007g0214others(150): Show | 153 | HG00140.hp2 HG00280.hp1 HG00639.hp1 others(150): Show |
intron_variant | MODIFIER | c.252-5169T>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205711024 | ||||||
| chr2:205711140
|
C | T | 1 | a0001c0002t0007g0127 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.252-5053C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205711140 | ||||||
| chr2:205711365
|
A | T | 1 | a0001c0004t0012g0043 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.252-4828A>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205711365 | ||||||
| chr2:205711459
|
C | A | 160 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0026others(157): Show | 164 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(161): Show |
intron_variant | MODIFIER | c.252-4734C>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205711459 | ||||||
| chr2:205711513
|
G | A | 11 | a0001c0002t0008g0200a0001c0002t0008g0201a0001c0002t0013g0198others(8): Show | 12 | HG01243.hp1 HG01884.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.252-4680G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205711513 | ||||||
| chr2:205711585
|
A | T | 1 | a0001c0001t0001g0068 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.252-4608A>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205711585 | ||||||
| chr2:205711724
|
C | T | 10 | a0001c0002t0004g0275a0001c0002t0007g0127a0001c0003t0004g0168others(7): Show | 10 | HG01169.hp1 HG01433.hp1 HG01515.hp2 others(7): Show |
intron_variant | MODIFIER | c.252-4469C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205711724 | ||||||
| chr2:205711747
|
C | T | 1 | a0002c0029t0013g0276 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.252-4446C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205711747 | ||||||
| chr2:205711773
|
T | A | 1 | a0001c0001t0004g0117 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.252-4420T>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205711773 | ||||||
| chr2:205711795
|
T | G | 58 | a0001c0001t0007g0214a0001c0002t0002g0280a0001c0002t0004g0012others(55): Show | 58 | HG00140.hp2 HG00280.hp1 HG00735.hp2 others(55): Show |
intron_variant | MODIFIER | c.252-4398T>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205711795 | ||||||
| chr2:205711873
|
G | A | 1 | a0001c0004t0002g0212 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.252-4320G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205711873 | ||||||
| chr2:205712101
|
G | C | 6 | a0001c0002t0004g0140a0001c0005t0013g0176a0001c0011t0004g0171others(3): Show | 6 | HG02622.hp2 HG02976.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.252-4092G>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205712101 | ||||||
| chr2:205712250
|
T | G | 2 | a0001c0002t0029g0136a0001c0002t0063g0137 | 2 | HG02922.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.252-3943T>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205712250 | ||||||
| chr2:205712390
|
G | A | 145 | a0001c0001t0005g0008a0001c0001t0007g0214a0001c0001t0031g0328others(142): Show | 145 | HG00140.hp2 HG00280.hp1 HG00639.hp1 others(142): Show |
intron_variant | MODIFIER | c.252-3803G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205712390 | ||||||
| chr2:205712430
|
A | G | 5 | a0001c0002t0004g0140a0001c0003t0012g0175a0001c0008t0004g0005others(2): Show | 6 | HG02630.hp1 HG02723.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.252-3763A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205712430 | ||||||
| chr2:205712687
|
A | G | 96 | a0001c0001t0001g0026a0001c0001t0005g0008a0001c0001t0005g0096others(93): Show | 96 | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(93): Show |
intron_variant | MODIFIER | c.252-3506A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205712687 | ||||||
| chr2:205712719
|
G | C | 1 | a0001c0003t0008g0172 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.252-3474G>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205712719 | ||||||
| chr2:205712804
|
G | C | 168 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0026others(165): Show | 173 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(170): Show |
intron_variant | MODIFIER | c.252-3389G>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205712804 | ||||||
| chr2:205712854
|
T | C | 15 | a0001c0001t0002g0211a0001c0001t0002g0258a0001c0001t0002g0316others(12): Show | 15 | HG00423.hp1 HG00558.hp1 HG00673.hp2 others(12): Show |
intron_variant | MODIFIER | c.252-3339T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205712854 | ||||||
| chr2:205713079
|
C | T | 6 | a0001c0002t0002g0295a0001c0002t0003g0287a0001c0002t0007g0286others(3): Show | 6 | HG01346.hp1 HG01361.hp1 HG01928.hp2 others(3): Show |
intron_variant | MODIFIER | c.252-3114C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205713079 | ||||||
| chr2:205713195
|
C | T | 1 | a0001c0002t0046g0142 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.252-2998C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205713195 | ||||||
| chr2:205713450
|
C | T | 1 | a0001c0004t0001g0097 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.252-2743C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205713450 | ||||||
| chr2:205713572
|
A | G | 3 | a0001c0001t0008g0050a0001c0001t0012g0075a0001c0004t0013g0051 | 3 | HG00280.hp2 HG01074.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.252-2621A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205713572 | ||||||
| chr2:205713573
|
T | G | 1 | a0001c0004t0010g0237 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.252-2620T>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205713573 | ||||||
| chr2:205713699
|
G | T | 2 | a0001c0002t0046g0142a0001c0003t0008g0172 | 2 | HG01243.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.252-2494G>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205713699 | ||||||
| chr2:205713752
|
C | A | 4 | a0001c0001t0010g0313a0001c0004t0003g0314a0001c0004t0003g0315others(1): Show | 4 | HG00423.hp1 HG00558.hp1 HG02040.hp2 others(1): Show |
intron_variant | MODIFIER | c.252-2441C>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205713752 | ||||||
| chr2:205714312
|
T | G | 3 | a0001c0001t0001g0026a0001c0001t0012g0027a0001c0001t0012g0028 | 3 | HG00099.hp1 HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.252-1881T>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205714312 | ||||||
| chr2:205714541
|
G | A | 1 | a0005c0021t0004g0139 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.252-1652G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205714541 | ||||||
| chr2:205714610
|
C | T | 6 | a0001c0001t0004g0061a0001c0001t0019g0090a0001c0004t0001g0087others(3): Show | 6 | HG01928.hp1 HG01981.hp1 HG01993.hp2 others(3): Show |
intron_variant | MODIFIER | c.252-1583C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205714610 | ||||||
| chr2:205714643
|
T | C | 329 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0026others(326): Show | 335 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(332): Show |
intron_variant | MODIFIER | c.252-1550T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205714643 | ||||||
| chr2:205714678
|
T | TGG | 12 | a0001c0002t0002g0262a0001c0002t0002g0263a0001c0002t0002g0264others(9): Show | 12 | HG02258.hp2 HG02486.hp2 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.252-1511_252-1510d others(4): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr2 | 205714678 | |||||
| chr2:205714764
|
G | A | 1 | a0001c0002t0010g0277 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.252-1429G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205714764 | ||||||
| chr2:205714928
|
T | C | 1 | a0001c0002t0022g0185 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.252-1265T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205714928 | ||||||
| chr2:205715013
|
A | G | 7 | a0001c0006t0007g0306a0001c0006t0011g0337a0001c0006t0011g0338others(4): Show | 7 | HG02055.hp1 HG02895.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.252-1180A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205715013 | ||||||
| chr2:205715099
|
G | A | 5 | a0001c0002t0029g0136a0001c0002t0063g0137a0002c0015t0030g0004others(2): Show | 6 | HG02922.hp1 HG02922.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.252-1094G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205715099 | ||||||
| chr2:205715101
|
G | A | 136 | a0001c0001t0005g0008a0001c0001t0007g0214a0001c0001t0031g0328others(133): Show | 136 | HG00140.hp2 HG00280.hp1 HG00639.hp1 others(133): Show |
intron_variant | MODIFIER | c.252-1092G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205715101 | ||||||
| chr2:205715369
|
C | T | 3 | a0001c0002t0049g0173a0001c0003t0022g0174a0001c0007t0008g0063 | 3 | HG02723.hp2 HG06807.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.252-824C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205715369 | ||||||
| chr2:205715421
|
C | T | 1 | a0001c0002t0011g0257 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.252-772C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205715421 | ||||||
| chr2:205715428
|
A | G | 191 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0026others(188): Show | 195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.252-765A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205715428 | ||||||
| chr2:205715431
|
G | A | 1 | a0001c0002t0006g0052 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.252-762G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205715431 | ||||||
| chr2:205715467
|
G | A | 1 | a0001c0002t0017g0255 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.252-726G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205715467 | ||||||
| chr2:205715990
|
T | G | 190 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0026others(187): Show | 194 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(191): Show |
intron_variant | MODIFIER | c.252-203T>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205715990 | ||||||
| chr2:205716156
|
C | G | 2 | a0001c0002t0046g0142a0001c0003t0008g0172 | 2 | HG01243.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.252-37C>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 2/16 | chr2 | 205716156 | ||||||
| chr2:205716577
|
C | CG | 21 | a0001c0001t0001g0022a0001c0001t0001g0112a0001c0001t0003g0203others(18): Show | 21 | HG00423.hp1 HG00423.hp2 HG02895.hp1 others(18): Show |
intron_variant | MODIFIER | c.433+210dupG | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 205716577 | |||||
| chr2:205716585
|
T | G | 1 | a0001c0001t0015g0238 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.433+211T>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 3/16 | chr2 | 205716585 | ||||||
| chr2:205716999
|
T | C | 5 | a0001c0001t0009g0239a0001c0010t0009g0231a0001c0010t0009g0232others(2): Show | 5 | HG00642.hp1 HG01516.hp2 HG01517.hp1 others(2): Show |
intron_variant | MODIFIER | c.433+625T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 3/16 | chr2 | 205716999 | ||||||
| chr2:205717119
|
C | T | 1 | a0001c0002t0004g0140 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.433+745C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 3/16 | chr2 | 205717119 | ||||||
| chr2:205717138
|
A | AGTGT | 71 | a0001c0001t0002g0216a0001c0002t0001g0015a0001c0002t0002g0280others(68): Show | 71 | HG00140.hp1 HG00735.hp2 HG00741.hp2 others(68): Show |
intron_variant | MODIFIER | c.433+764_433+765ins others(4): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 3/16 | chr2 | 205717138 | ||||||
| chr2:205717139
|
A | G | 1 | a0001c0003t0008g0172 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.433+765A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 3/16 | chr2 | 205717139 | ||||||
| chr2:205717206
|
T | G | 1 | a0002c0017t0062g0178 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.433+832T>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 3/16 | chr2 | 205717206 | ||||||
| chr2:205717206
|
T | TG | 186 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0026others(183): Show | 192 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(189): Show |
intron_variant | MODIFIER | c.433+833dupG | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 205717206 | |||||
| chr2:205717313
|
G | A | 1 | a0001c0001t0015g0209 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.433+939G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 3/16 | chr2 | 205717313 | ||||||
| chr2:205717331
|
G | A | 1 | a0001c0004t0002g0281 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.433+957G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 3/16 | chr2 | 205717331 | ||||||
| chr2:205717512
|
G | A | 1 | a0001c0002t0017g0255 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.433+1138G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 3/16 | chr2 | 205717512 | ||||||
| chr2:205717625
|
G | A | 3 | a0001c0002t0001g0191a0001c0002t0004g0192a0001c0002t0061g0190 | 3 | HG02145.hp1 HG02280.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.433+1251G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 3/16 | chr2 | 205717625 | ||||||
| chr2:205717738
|
G | A | 154 | a0001c0001t0002g0216a0001c0002t0001g0015a0001c0002t0001g0057others(151): Show | 155 | HG00140.hp1 HG00140.hp2 HG00735.hp2 others(152): Show |
intron_variant | MODIFIER | c.433+1364G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 3/16 | chr2 | 205717738 | ||||||
| chr2:205717913
|
T | C | 1 | a0001c0002t0007g0127 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.433+1539T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 3/16 | chr2 | 205717913 | ||||||
| chr2:205718030
|
C | T | 4 | a0001c0002t0008g0200a0001c0002t0008g0201a0001c0002t0013g0198others(1): Show | 4 | HG02886.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.433+1656C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 3/16 | chr2 | 205718030 | ||||||
| chr2:205718271
|
A | G | 4 | a0001c0001t0003g0265a0001c0001t0005g0008a0001c0001t0010g0266others(1): Show | 4 | HG02135.hp2 NA18975.hp1 NA19063.hp1 others(1): Show |
intron_variant | MODIFIER | c.433+1897A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 3/16 | chr2 | 205718271 | ||||||
| chr2:205718410
|
G | A | 1 | a0001c0002t0017g0255 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.433+2036G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 3/16 | chr2 | 205718410 | ||||||
| chr2:205718452
|
A | C | 1 | a0001c0001t0004g0061 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.433+2078A>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 3/16 | chr2 | 205718452 | ||||||
| chr2:205718603
|
G | A | 1 | a0001c0003t0008g0172 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.433+2229G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 3/16 | chr2 | 205718603 | ||||||
| chr2:205718701
|
G | A | 4 | a0001c0002t0001g0191a0001c0002t0004g0140a0001c0002t0004g0192others(1): Show | 4 | HG02145.hp1 HG02280.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.433+2327G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 3/16 | chr2 | 205718701 | ||||||
| chr2:205718920
|
C | T | 3 | a0001c0005t0007g0223a0001c0005t0023g0120a0001c0005t0023g0121 | 3 | HG01123.hp1 HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.433+2546C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 3/16 | chr2 | 205718920 | ||||||
| chr2:205718929
|
C | T | 3 | a0001c0008t0004g0005a0001c0008t0004g0129a0001c0008t0004g0197 | 4 | HG02630.hp1 HG02723.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.433+2555C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 3/16 | chr2 | 205718929 | ||||||
| chr2:205718942
|
C | CA | 171 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0026others(168): Show | 176 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(173): Show |
intron_variant | MODIFIER | c.433+2582dupA | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 205718942 | |||||
| chr2:205718942
|
C | CAA | 148 | a0001c0001t0002g0216a0001c0001t0005g0096a0001c0002t0001g0015others(145): Show | 148 | HG00140.hp1 HG00140.hp2 HG00735.hp2 others(145): Show |
intron_variant | MODIFIER | c.433+2581_433+2582d others(4): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 205718942 | |||||
| chr2:205718968
|
A | G | 1 | a0001c0003t0008g0172 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.433+2594A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 3/16 | chr2 | 205718968 | ||||||
| chr2:205719037
|
A | G | 1 | a0001c0003t0008g0172 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.433+2663A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 3/16 | chr2 | 205719037 | ||||||
| chr2:205719226
|
A | G | 78 | a0001c0001t0002g0216a0001c0002t0001g0015a0001c0002t0002g0280others(75): Show | 78 | HG00140.hp1 HG00140.hp2 HG00735.hp2 others(75): Show |
intron_variant | MODIFIER | c.433+2852A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 3/16 | chr2 | 205719226 | ||||||
| chr2:205719473
|
C | CA | 19 | a0001c0001t0003g0265a0001c0001t0005g0008a0001c0001t0010g0266others(16): Show | 19 | HG02055.hp1 HG02135.hp2 HG02717.hp1 others(16): Show |
intron_variant | MODIFIER | c.434-2991dupA | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 205719473 | |||||
| chr2:205719473
|
CA | C | 10 | a0001c0001t0002g0247a0001c0001t0003g0244a0001c0001t0005g0040others(7): Show | 10 | HG00438.hp1 HG00438.hp2 HG00621.hp2 others(7): Show |
intron_variant | MODIFIER | c.434-2991delA | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 205719473 | |||||
| chr2:205719536
|
A | ATG | 3 | a0001c0002t0049g0173a0001c0003t0022g0174a0001c0007t0008g0063 | 3 | HG02723.hp2 HG06807.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.434-2926_434-2925d others(4): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 205719536 | |||||
| chr2:205719672
|
C | T | 11 | a0001c0001t0001g0021a0001c0001t0005g0145a0001c0001t0010g0210others(8): Show | 12 | HG00673.hp1 HG01069.hp1 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.434-2806C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 3/16 | chr2 | 205719672 | ||||||
| chr2:205719783
|
A | G | 2 | a0002c0015t0030g0004a0002c0027t0064g0177 | 3 | HG02922.hp2 HG02965.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.434-2695A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 3/16 | chr2 | 205719783 | ||||||
| chr2:205719811
|
TA | T | 7 | a0001c0002t0007g0127a0001c0002t0051g0183a0001c0002t0054g0215others(4): Show | 7 | HG01884.hp1 HG01891.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.434-2663delA | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 205719811 | |||||
| chr2:205720238
|
T | C | 1 | a0001c0001t0001g0060 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.434-2240T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 3/16 | chr2 | 205720238 | ||||||
| chr2:205720262
|
CT | C | 24 | a0001c0001t0001g0144a0001c0001t0009g0240a0001c0001t0018g0019others(21): Show | 25 | HG00735.hp1 HG01106.hp2 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.434-2195delT | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 205720262 | |||||
| chr2:205720262
|
CTTTTTTT | C | 87 | a0001c0002t0001g0015a0001c0002t0002g0262a0001c0002t0002g0263others(84): Show | 87 | HG00140.hp1 HG00140.hp2 HG00735.hp2 others(84): Show |
intron_variant | MODIFIER | c.434-2201_434-2195d others(9): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 205720262 | |||||
| chr2:205720262
|
CTTTTTTT others(1): Show |
C | 68 | a0001c0002t0001g0057a0001c0002t0001g0082a0001c0002t0001g0084others(65): Show | 69 | HG01081.hp1 HG01123.hp1 HG01167.hp1 others(66): Show |
intron_variant | MODIFIER | c.434-2202_434-2195d others(10): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 205720262 | |||||
| chr2:205720268
|
T | C | 3 | a0002c0015t0030g0004a0002c0017t0062g0178a0002c0027t0064g0177 | 4 | HG02922.hp2 HG02965.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.434-2210T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 3/16 | chr2 | 205720268 | ||||||
| chr2:205720447
|
A | C | 4 | a0001c0011t0004g0171a0001c0011t0008g0135a0001c0012t0004g0138others(1): Show | 4 | HG02622.hp2 HG03195.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.434-2031A>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 3/16 | chr2 | 205720447 | ||||||
| chr2:205720479
|
G | T | 2 | a0003c0025t0013g0167a0003c0026t0004g0166 | 2 | HG02572.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.434-1999G>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 3/16 | chr2 | 205720479 | ||||||
| chr2:205720726
|
G | A | 1 | a0001c0007t0013g0189 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.434-1752G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 3/16 | chr2 | 205720726 | ||||||
| chr2:205720763
|
C | T | 159 | a0001c0002t0001g0015a0001c0002t0001g0057a0001c0002t0001g0082others(156): Show | 160 | HG00140.hp1 HG00140.hp2 HG00735.hp2 others(157): Show |
intron_variant | MODIFIER | c.434-1715C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 3/16 | chr2 | 205720763 | ||||||
| chr2:205720772
|
A | G | 1 | a0001c0002t0016g0134 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.434-1706A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 3/16 | chr2 | 205720772 | ||||||
| chr2:205720896
|
C | T | 1 | a0001c0003t0008g0172 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.434-1582C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 3/16 | chr2 | 205720896 | ||||||
| chr2:205721068
|
A | G | 4 | a0001c0002t0001g0191a0001c0002t0004g0140a0001c0002t0004g0192others(1): Show | 4 | HG02145.hp1 HG02280.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.434-1410A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 3/16 | chr2 | 205721068 | ||||||
| chr2:205721125
|
T | A | 1 | a0001c0003t0008g0172 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.434-1353T>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 3/16 | chr2 | 205721125 | ||||||
| chr2:205721196
|
T | A | 1 | a0005c0021t0004g0139 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.434-1282T>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 3/16 | chr2 | 205721196 | ||||||
| chr2:205721220
|
T | C | 157 | a0001c0001t0005g0096a0001c0002t0001g0015a0001c0002t0001g0057others(154): Show | 158 | HG00140.hp1 HG00140.hp2 HG00735.hp2 others(155): Show |
intron_variant | MODIFIER | c.434-1258T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 3/16 | chr2 | 205721220 | ||||||
| chr2:205721249
|
A | G | 74 | a0001c0002t0001g0015a0001c0002t0002g0280a0001c0002t0002g0295others(71): Show | 74 | HG00140.hp1 HG00735.hp2 HG00741.hp2 others(71): Show |
intron_variant | MODIFIER | c.434-1229A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 3/16 | chr2 | 205721249 | ||||||
| chr2:205721273
|
G | C | 1 | a0005c0021t0004g0139 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.434-1205G>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 3/16 | chr2 | 205721273 | ||||||
| chr2:205721314
|
G | C | 72 | a0001c0001t0005g0096a0001c0001t0019g0090a0001c0002t0001g0057others(69): Show | 72 | HG00140.hp2 HG01081.hp1 HG01167.hp1 others(69): Show |
intron_variant | MODIFIER | c.434-1164G>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 3/16 | chr2 | 205721314 | ||||||
| chr2:205721379
|
G | A | 1 | a0001c0003t0008g0172 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.434-1099G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 3/16 | chr2 | 205721379 | ||||||
| chr2:205721458
|
C | T | 1 | a0001c0012t0017g0273 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.434-1020C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 3/16 | chr2 | 205721458 | ||||||
| chr2:205721688
|
G | A | 60 | a0001c0002t0001g0057a0001c0002t0001g0082a0001c0002t0001g0084others(57): Show | 60 | HG00140.hp2 HG01081.hp1 HG01167.hp1 others(57): Show |
intron_variant | MODIFIER | c.434-790G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 3/16 | chr2 | 205721688 | ||||||
| chr2:205721743
|
C | A | 158 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0026others(155): Show | 162 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(159): Show |
intron_variant | MODIFIER | c.434-735C>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 3/16 | chr2 | 205721743 | ||||||
| chr2:205722012
|
C | T | 17 | a0001c0002t0002g0262a0001c0002t0002g0263a0001c0002t0002g0264others(14): Show | 17 | HG01243.hp1 HG02258.hp2 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.434-466C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 3/16 | chr2 | 205722012 | ||||||
| chr2:205722145
|
C | CCT | 32 | a0001c0001t0003g0269a0001c0001t0004g0018a0001c0001t0004g0061others(29): Show | 32 | HG00408.hp1 HG00642.hp1 HG00642.hp2 others(29): Show |
intron_variant | MODIFIER | c.434-309_434-308dup others(2): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 205722145 | |||||
| chr2:205722145
|
C | CCTCT | 10 | a0001c0001t0019g0090a0001c0002t0004g0182a0001c0002t0004g0275others(7): Show | 10 | HG01928.hp1 HG01981.hp1 HG02004.hp1 others(7): Show |
intron_variant | MODIFIER | c.434-311_434-308dup others(4): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 205722145 | |||||
| chr2:205722145
|
CCTCT | C | 2 | a0001c0002t0008g0124a0001c0008t0004g0005 | 3 | HG02630.hp1 HG02818.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.434-311_434-308del others(4): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 205722145 | |||||
| chr2:205722152
|
C | CTT | 12 | a0001c0002t0002g0262a0001c0002t0002g0263a0001c0002t0002g0264others(9): Show | 12 | HG02258.hp2 HG02486.hp2 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.434-325_434-324ins others(2): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 205722152 | |||||
| chr2:205722162
|
CTCTCTCT others(3): Show |
C | 1 | a0001c0001t0002g0006 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.434-315_434-306del others(10): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 3/16 | chr2 | 205722162 | ||||||
| chr2:205722165
|
T | A | 2 | a0002c0015t0030g0004a0002c0027t0064g0177 | 3 | HG02922.hp2 HG02965.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.434-313T>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 3/16 | chr2 | 205722165 | ||||||
| chr2:205722165
|
TCTCTCAT others(3): Show |
T | 1 | a0001c0008t0004g0129 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.434-311_434-302del others(10): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 205722165 | |||||
| chr2:205722167
|
T | A | 2 | a0002c0015t0030g0004a0002c0027t0064g0177 | 3 | HG02922.hp2 HG02965.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.434-311T>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 3/16 | chr2 | 205722167 | ||||||
| chr2:205722169
|
T | A | 3 | a0001c0008t0004g0005a0002c0015t0030g0004a0002c0027t0064g0177 | 5 | HG02630.hp1 HG02818.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.434-309T>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 3/16 | chr2 | 205722169 | ||||||
| chr2:205722169
|
T | TCTCATAC others(3): Show |
1 | a0001c0002t0009g0254 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.434-308_434-307ins others(10): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 205722169 | |||||
| chr2:205722169
|
T | TCTCTCTC others(5): Show |
1 | a0001c0003t0022g0174 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.434-308_434-307ins others(12): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 205722169 | |||||
| chr2:205722169
|
TCATA | T | 14 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0067others(11): Show | 14 | HG01243.hp2 HG01884.hp1 HG01934.hp2 others(11): Show |
intron_variant | MODIFIER | c.434-306_434-303del others(4): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 205722169 | |||||
| chr2:205722169
|
TCATACAC others(1): Show |
T | 3 | a0001c0002t0001g0191a0001c0002t0004g0192a0001c0002t0061g0190 | 3 | HG02145.hp1 HG02280.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.434-306_434-299del others(8): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 205722169 | |||||
| chr2:205722170
|
C | CTCAT | 6 | a0001c0001t0011g0331a0001c0001t0012g0020a0001c0002t0014g0160others(3): Show | 6 | HG01081.hp2 HG01516.hp1 HG01884.hp2 others(3): Show |
intron_variant | MODIFIER | c.434-308_434-307ins others(4): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 3/16 | chr2 | 205722170 | ||||||
| chr2:205722170
|
CAT | C | 14 | a0001c0001t0001g0037a0001c0001t0001g0144a0001c0001t0004g0080others(11): Show | 14 | HG01106.hp1 HG01943.hp1 HG01952.hp1 others(11): Show |
intron_variant | MODIFIER | c.434-306_434-305del others(2): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 205722170 | |||||
| chr2:205722171
|
A | T | 161 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0026others(158): Show | 164 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(161): Show |
intron_variant | MODIFIER | c.434-307A>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 3/16 | chr2 | 205722171 | ||||||
| chr2:205722172
|
T | C | 177 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0026others(174): Show | 182 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(179): Show |
intron_variant | MODIFIER | c.434-306T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 3/16 | chr2 | 205722172 | ||||||
| chr2:205722172
|
T | TAC | 6 | a0001c0002t0017g0255a0001c0003t0003g0296a0001c0003t0007g0249others(3): Show | 6 | HG02698.hp1 HG02976.hp2 NA18961.hp2 others(3): Show |
intron_variant | MODIFIER | c.434-267_434-266dup others(2): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 205722172 | |||||
| chr2:205722172
|
T | TACAC | 10 | a0001c0002t0001g0057a0001c0002t0006g0052a0001c0002t0012g0131others(7): Show | 10 | HG01167.hp1 HG01192.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.434-269_434-266dup others(4): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 205722172 | |||||
| chr2:205722172
|
TAC | T | 15 | a0001c0002t0013g0198a0001c0002t0013g0199a0001c0003t0014g0100others(12): Show | 15 | HG00639.hp2 HG02055.hp1 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.434-267_434-266del others(2): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 205722172 | |||||
| chr2:205722172
|
TACAC | T | 4 | a0001c0003t0003g0299a0001c0003t0006g0086a0001c0003t0014g0095others(1): Show | 4 | NA18973.hp1 NA18993.hp2 NA18995.hp2 others(1): Show |
intron_variant | MODIFIER | c.434-269_434-266del others(4): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 205722172 | |||||
| chr2:205722173
|
A | T | 16 | a0001c0001t0001g0037a0001c0001t0001g0144a0001c0001t0004g0080others(13): Show | 16 | HG01106.hp1 HG01943.hp1 HG01952.hp1 others(13): Show |
intron_variant | MODIFIER | c.434-305A>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 3/16 | chr2 | 205722173 | ||||||
| chr2:205722174
|
C | T | 162 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0026others(159): Show | 166 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(163): Show |
intron_variant | MODIFIER | c.434-304C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 3/16 | chr2 | 205722174 | ||||||
| chr2:205722175
|
A | T | 15 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0067others(12): Show | 15 | HG01243.hp2 HG01884.hp1 HG01934.hp2 others(12): Show |
intron_variant | MODIFIER | c.434-303A>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 3/16 | chr2 | 205722175 | ||||||
| chr2:205722176
|
C | T | 15 | a0001c0001t0001g0037a0001c0001t0001g0144a0001c0001t0004g0080others(12): Show | 15 | HG01106.hp1 HG01943.hp1 HG01952.hp1 others(12): Show |
intron_variant | MODIFIER | c.434-302C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 3/16 | chr2 | 205722176 | ||||||
| chr2:205722177
|
A | T | 2 | a0001c0001t0003g0265a0001c0003t0047g0126 | 2 | HG02135.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.434-301A>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 3/16 | chr2 | 205722177 | ||||||
| chr2:205722178
|
C | T | 14 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0067others(11): Show | 14 | HG01243.hp2 HG01884.hp1 HG01934.hp2 others(11): Show |
intron_variant | MODIFIER | c.434-300C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 3/16 | chr2 | 205722178 | ||||||
| chr2:205722179
|
A | T | 3 | a0001c0002t0001g0191a0001c0002t0004g0192a0001c0002t0061g0190 | 3 | HG02145.hp1 HG02280.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.434-299A>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 3/16 | chr2 | 205722179 | ||||||
| chr2:205722180
|
C | T | 2 | a0001c0001t0003g0265a0001c0003t0047g0126 | 2 | HG02135.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.434-298C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 3/16 | chr2 | 205722180 | ||||||
| chr2:205722182
|
C | T | 3 | a0001c0002t0001g0191a0001c0002t0004g0192a0001c0002t0061g0190 | 3 | HG02145.hp1 HG02280.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.434-296C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 3/16 | chr2 | 205722182 | ||||||
| chr2:205722725
|
G | A | 1 | a0002c0017t0062g0178 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.664+17G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 4/16 | chr2 | 205722725 | ||||||
| chr2:205722874
|
T | C | 1 | a0001c0002t0020g0186 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.664+166T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 4/16 | chr2 | 205722874 | ||||||
| chr2:205722895
|
C | T | 2 | a0001c0002t0007g0289a0001c0002t0007g0290 | 2 | HG01981.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.664+187C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 4/16 | chr2 | 205722895 | ||||||
| chr2:205722947
|
G | A | 62 | a0001c0002t0001g0057a0001c0002t0001g0082a0001c0002t0001g0084others(59): Show | 62 | HG00140.hp2 HG01081.hp1 HG01167.hp1 others(59): Show |
intron_variant | MODIFIER | c.664+239G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 4/16 | chr2 | 205722947 | ||||||
| chr2:205723099
|
A | T | 1 | a0001c0003t0006g0102 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.664+391A>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 4/16 | chr2 | 205723099 | ||||||
| chr2:205723183
|
C | T | 300 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0026others(297): Show | 305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.664+475C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 4/16 | chr2 | 205723183 | ||||||
| chr2:205723246
|
G | A | 1 | a0002c0015t0030g0004 | 2 | HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.664+538G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 4/16 | chr2 | 205723246 | ||||||
| chr2:205723252
|
G | A | 156 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0026others(153): Show | 160 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.665-533G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 4/16 | chr2 | 205723252 | ||||||
| chr2:205723389
|
A | G | 1 | a0001c0003t0002g0334 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.665-396A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 4/16 | chr2 | 205723389 | ||||||
| chr2:205723390
|
T | G | 325 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0026others(322): Show | 330 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(327): Show |
intron_variant | MODIFIER | c.665-395T>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 4/16 | chr2 | 205723390 | ||||||
| chr2:205723751
|
T | C | 2 | a0001c0002t0013g0198a0001c0002t0013g0199 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.665-34T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 4/16 | chr2 | 205723751 | ||||||
| chr2:205723996
|
G | A | 3 | a0001c0002t0001g0191a0001c0002t0004g0192a0001c0002t0061g0190 | 3 | HG02145.hp1 HG02280.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.820+56G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 5/16 | chr2 | 205723996 | ||||||
| chr2:205724047
|
C | T | 1 | a0001c0001t0009g0319 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.820+107C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 5/16 | chr2 | 205724047 | ||||||
| chr2:205724153
|
AAT | A | 128 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0026others(125): Show | 131 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(128): Show |
intron_variant | MODIFIER | c.820+222_820+223del others(2): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr2 | 205724153 | |||||
| chr2:205724160
|
A | G | 1 | a0008c0028t0016g0143 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.820+220A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 5/16 | chr2 | 205724160 | ||||||
| chr2:205724341
|
G | A | 1 | a0001c0004t0005g0106 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.820+401G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 5/16 | chr2 | 205724341 | ||||||
| chr2:205724363
|
A | T | 4 | a0001c0002t0001g0191a0001c0002t0004g0140a0001c0002t0004g0192others(1): Show | 4 | HG02145.hp1 HG02280.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.820+423A>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 5/16 | chr2 | 205724363 | ||||||
| chr2:205724386
|
T | C | 1 | a0001c0001t0004g0117 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.820+446T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 5/16 | chr2 | 205724386 | ||||||
| chr2:205724397
|
A | G | 149 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0026others(146): Show | 152 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(149): Show |
intron_variant | MODIFIER | c.820+457A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 5/16 | chr2 | 205724397 | ||||||
| chr2:205724534
|
C | G | 1 | a0001c0004t0006g0123 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.820+594C>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 5/16 | chr2 | 205724534 | ||||||
| chr2:205724654
|
C | CT | 149 | a0001c0001t0001g0046a0001c0001t0001g0104a0001c0001t0001g0158others(146): Show | 149 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(146): Show |
intron_variant | MODIFIER | c.820+740dupT | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr2 | 205724654 | |||||
| chr2:205724654
|
C | CTT | 33 | a0001c0001t0019g0090a0001c0002t0002g0263a0001c0002t0003g0204others(30): Show | 33 | HG00735.hp2 HG01361.hp2 HG01515.hp2 others(30): Show |
intron_variant | MODIFIER | c.820+739_820+740dup others(2): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr2 | 205724654 | |||||
| chr2:205724654
|
CT | C | 12 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0067others(9): Show | 12 | HG00408.hp1 HG00408.hp2 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.820+740delT | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr2 | 205724654 | |||||
| chr2:205724749
|
C | G | 1 | a0001c0001t0001g0104 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.820+809C>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 5/16 | chr2 | 205724749 | ||||||
| chr2:205724896
|
C | G | 334 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0026others(331): Show | 340 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(337): Show |
intron_variant | MODIFIER | c.820+956C>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 5/16 | chr2 | 205724896 | ||||||
| chr2:205725153
|
C | G | 1 | a0001c0002t0022g0185 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.821-760C>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 5/16 | chr2 | 205725153 | ||||||
| chr2:205725240
|
C | T | 3 | a0001c0002t0002g0262a0001c0002t0002g0263a0001c0002t0002g0264 | 3 | HG02630.hp2 HG03195.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.821-673C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 5/16 | chr2 | 205725240 | ||||||
| chr2:205725369
|
G | A | 2 | a0001c0003t0021g0058a0001c0003t0021g0059 | 2 | NA19085.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.821-544G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 5/16 | chr2 | 205725369 | ||||||
| chr2:205725509
|
G | T | 1 | a0001c0006t0036g0307 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.821-404G>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 5/16 | chr2 | 205725509 | ||||||
| chr2:205725511
|
G | A | 2 | a0001c0003t0011g0248a0001c0003t0011g0250 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.821-402G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 5/16 | chr2 | 205725511 | ||||||
| chr2:205725559
|
G | A | 4 | a0001c0011t0004g0171a0001c0011t0008g0135a0001c0012t0004g0138others(1): Show | 4 | HG02622.hp2 HG03195.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.821-354G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 5/16 | chr2 | 205725559 | ||||||
| chr2:205725865
|
G | A | 1 | a0001c0003t0009g0292 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.821-48G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 5/16 | chr2 | 205725865 | ||||||
| chr2:205725898
|
G | A | 1 | a0001c0002t0008g0141 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.821-15G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 5/16 | chr2 | 205725898 | ||||||
| chr2:205726155
|
C | T | 59 | a0001c0002t0001g0057a0001c0002t0001g0082a0001c0002t0001g0084others(56): Show | 59 | HG01081.hp1 HG01167.hp1 HG01192.hp1 others(56): Show |
intron_variant | MODIFIER | c.990+73C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 6/16 | chr2 | 205726155 | ||||||
| chr2:205726550
|
C | T | 3 | a0001c0008t0004g0005a0001c0008t0004g0129a0001c0008t0004g0197 | 4 | HG02630.hp1 HG02723.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.990+468C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 6/16 | chr2 | 205726550 | ||||||
| chr2:205726690
|
A | G | 1 | a0001c0001t0053g0159 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.990+608A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 6/16 | chr2 | 205726690 | ||||||
| chr2:205726883
|
C | G | 178 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0026others(175): Show | 184 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(181): Show |
intron_variant | MODIFIER | c.990+801C>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 6/16 | chr2 | 205726883 | ||||||
| chr2:205727027
|
C | A | 1 | a0001c0001t0003g0244 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.991-864C>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 6/16 | chr2 | 205727027 | ||||||
| chr2:205727344
|
C | T | 9 | a0001c0002t0004g0182a0001c0002t0007g0284a0001c0002t0007g0285others(6): Show | 9 | HG02109.hp1 HG02647.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.991-547C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 6/16 | chr2 | 205727344 | ||||||
| chr2:205727419
|
C | A | 1 | a0001c0002t0007g0284 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.991-472C>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 6/16 | chr2 | 205727419 | ||||||
| chr2:205727532
|
A | C | 1 | a0001c0003t0001g0163 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.991-359A>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 6/16 | chr2 | 205727532 | ||||||
| chr2:205727677
|
A | C | 3 | a0001c0009t0005g0001a0001c0009t0021g0045a0001c0009t0027g0032 | 4 | HG00735.hp1 HG01106.hp2 HG01261.hp2 others(1): Show |
intron_variant | MODIFIER | c.991-214A>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 6/16 | chr2 | 205727677 | ||||||
| chr2:205727801
|
A | G | 163 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0026others(160): Show | 167 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.991-90A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 6/16 | chr2 | 205727801 | ||||||
| chr2:205727810
|
T | C | 76 | a0001c0001t0001g0104a0001c0001t0005g0096a0001c0002t0001g0057others(73): Show | 76 | HG00140.hp2 HG01081.hp1 HG01167.hp1 others(73): Show |
intron_variant | MODIFIER | c.991-81T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 6/16 | chr2 | 205727810 | ||||||
| chr2:205727825
|
G | GA | 3 | a0001c0009t0005g0001a0001c0009t0021g0045a0001c0009t0027g0032 | 4 | HG00735.hp1 HG01106.hp2 HG01261.hp2 others(1): Show |
intron_variant | MODIFIER | c.991-59dupA | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr2 | 205727825 | |||||
| chr2:205728183
|
G | A | 1 | a0001c0002t0005g0030 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1146+137G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205728183 | ||||||
| chr2:205728195
|
A | C | 1 | a0001c0001t0010g0313 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1146+149A>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205728195 | ||||||
| chr2:205728234
|
G | A | 13 | a0001c0002t0004g0182a0001c0002t0007g0284a0001c0002t0007g0285others(10): Show | 14 | HG02109.hp1 HG02647.hp2 HG02723.hp2 others(11): Show |
intron_variant | MODIFIER | c.1146+188G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205728234 | ||||||
| chr2:205728517
|
T | C | 164 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0026others(161): Show | 168 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.1146+471T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205728517 | ||||||
| chr2:205728593
|
T | C | 1 | a0001c0001t0010g0076 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1146+547T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205728593 | ||||||
| chr2:205728825
|
T | C | 1 | a0001c0002t0043g0259 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1146+779T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205728825 | ||||||
| chr2:205728854
|
C | G | 1 | a0001c0012t0004g0138 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1146+808C>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205728854 | ||||||
| chr2:205728906
|
T | C | 336 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0026others(333): Show | 342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.1146+860T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205728906 | ||||||
| chr2:205728971
|
C | T | 1 | a0001c0001t0058g0069 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1146+925C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205728971 | ||||||
| chr2:205728979
|
G | A | 13 | a0001c0002t0004g0182a0001c0002t0007g0284a0001c0002t0007g0285others(10): Show | 14 | HG02109.hp1 HG02647.hp2 HG02723.hp2 others(11): Show |
intron_variant | MODIFIER | c.1146+933G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205728979 | ||||||
| chr2:205728996
|
A | G | 54 | a0001c0001t0012g0020a0001c0002t0001g0015a0001c0002t0002g0280others(51): Show | 54 | HG00140.hp1 HG00140.hp2 HG00735.hp2 others(51): Show |
intron_variant | MODIFIER | c.1146+950A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205728996 | ||||||
| chr2:205729224
|
T | C | 3 | a0002c0015t0030g0004a0002c0017t0062g0178a0002c0027t0064g0177 | 4 | HG02922.hp2 HG02965.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1146+1178T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205729224 | ||||||
| chr2:205729230
|
T | C | 8 | a0001c0002t0016g0134a0001c0006t0007g0306a0001c0006t0011g0337others(5): Show | 8 | HG02055.hp1 HG02895.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.1146+1184T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205729230 | ||||||
| chr2:205729252
|
T | C | 1 | a0001c0002t0004g0140 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1146+1206T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205729252 | ||||||
| chr2:205729319
|
G | A | 2 | a0002c0015t0030g0004a0002c0027t0064g0177 | 3 | HG02922.hp2 HG02965.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1146+1273G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205729319 | ||||||
| chr2:205729324
|
G | A | 1 | a0001c0001t0001g0068 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1146+1278G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205729324 | ||||||
| chr2:205729347
|
G | C | 2 | a0001c0002t0049g0173a0001c0007t0008g0063 | 2 | HG02723.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1146+1301G>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205729347 | ||||||
| chr2:205729417
|
G | T | 147 | a0001c0002t0001g0015a0001c0002t0001g0082a0001c0002t0001g0084others(144): Show | 147 | HG00140.hp1 HG00140.hp2 HG00735.hp2 others(144): Show |
intron_variant | MODIFIER | c.1146+1371G>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205729417 | ||||||
| chr2:205729444
|
G | A | 3 | a0001c0002t0012g0131a0001c0013t0016g0132a0001c0013t0016g0133 | 3 | HG02717.hp1 HG02809.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1146+1398G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205729444 | ||||||
| chr2:205729512
|
G | A | 1 | a0005c0021t0004g0139 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1146+1466G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205729512 | ||||||
| chr2:205729640
|
G | T | 3 | a0001c0002t0004g0012a0001c0002t0018g0010a0001c0002t0018g0011 | 3 | HG00741.hp2 HG01081.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.1146+1594G>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205729640 | ||||||
| chr2:205729855
|
A | G | 5 | a0001c0002t0051g0183a0001c0002t0054g0215a0001c0003t0004g0168others(2): Show | 5 | HG01891.hp2 HG02572.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1146+1809A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205729855 | ||||||
| chr2:205730111
|
C | A | 7 | a0001c0002t0004g0182a0001c0002t0007g0127a0001c0002t0007g0285others(4): Show | 7 | HG01884.hp1 HG01891.hp2 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.1146+2065C>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205730111 | ||||||
| chr2:205730200
|
A | T | 1 | a0001c0002t0008g0141 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1146+2154A>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205730200 | ||||||
| chr2:205730219
|
T | C | 2 | a0001c0003t0002g0327a0001c0003t0014g0017 | 2 | HG00140.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.1146+2173T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205730219 | ||||||
| chr2:205730448
|
G | A | 2 | a0001c0003t0003g0296a0001c0003t0005g0083 | 2 | HG02080.hp1 NA18961.hp2 |
intron_variant | MODIFIER | c.1146+2402G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205730448 | ||||||
| chr2:205730488
|
T | G | 6 | a0001c0002t0001g0191a0001c0002t0004g0192a0001c0002t0007g0127others(3): Show | 6 | HG01884.hp1 HG02015.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.1146+2442T>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205730488 | ||||||
| chr2:205730614
|
T | C | 206 | a0001c0001t0001g0022a0001c0001t0001g0026a0001c0001t0001g0036others(203): Show | 211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.1146+2568T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205730614 | ||||||
| chr2:205730708
|
A | T | 1 | a0001c0003t0034g0333 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1146+2662A>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205730708 | ||||||
| chr2:205730812
|
T | C | 1 | a0001c0001t0009g0240 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1146+2766T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205730812 | ||||||
| chr2:205730824
|
C | T | 1 | a0001c0002t0032g0179 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1146+2778C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205730824 | ||||||
| chr2:205730974
|
C | T | 1 | a0001c0003t0022g0174 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1146+2928C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205730974 | ||||||
| chr2:205731086
|
C | T | 90 | a0001c0001t0001g0022a0001c0001t0001g0026a0001c0001t0001g0036others(87): Show | 90 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(87): Show |
intron_variant | MODIFIER | c.1146+3040C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205731086 | ||||||
| chr2:205731212
|
G | A | 140 | a0001c0001t0001g0021a0001c0001t0001g0074a0001c0001t0001g0104others(137): Show | 144 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.1146+3166G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205731212 | ||||||
| chr2:205731338
|
C | A | 59 | a0001c0001t0009g0240a0001c0001t0011g0222a0001c0001t0026g0014others(56): Show | 59 | HG00140.hp2 HG00735.hp2 HG00741.hp2 others(56): Show |
intron_variant | MODIFIER | c.1146+3292C>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205731338 | ||||||
| chr2:205731395
|
T | C | 65 | a0001c0001t0009g0240a0001c0001t0011g0222a0001c0001t0026g0014others(62): Show | 65 | HG00140.hp2 HG00735.hp2 HG00741.hp2 others(62): Show |
intron_variant | MODIFIER | c.1146+3349T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205731395 | ||||||
| chr2:205731410
|
A | G | 6 | a0001c0001t0001g0054a0001c0002t0008g0181a0001c0011t0004g0171others(3): Show | 6 | HG02622.hp2 HG02647.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1146+3364A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205731410 | ||||||
| chr2:205731420
|
A | C | 1 | a0001c0004t0041g0343 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1146+3374A>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205731420 | ||||||
| chr2:205731566
|
T | C | 5 | a0001c0001t0010g0313a0001c0004t0003g0314a0001c0004t0003g0315others(2): Show | 5 | HG00423.hp1 HG00558.hp1 HG02040.hp2 others(2): Show |
intron_variant | MODIFIER | c.1146+3520T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205731566 | ||||||
| chr2:205731732
|
C | T | 1 | a0007c0019t0002g0321 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1146+3686C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205731732 | ||||||
| chr2:205731939
|
T | C | 97 | a0001c0001t0009g0240a0001c0001t0011g0222a0001c0001t0020g0031others(94): Show | 99 | HG00735.hp1 HG00735.hp2 HG00741.hp2 others(96): Show |
intron_variant | MODIFIER | c.1146+3893T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205731939 | ||||||
| chr2:205732083
|
T | G | 4 | a0001c0001t0001g0054a0001c0002t0008g0181a0001c0012t0004g0138others(1): Show | 4 | HG02647.hp2 HG02886.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1146+4037T>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205732083 | ||||||
| chr2:205732107
|
A | G | 3 | a0001c0008t0004g0005a0001c0008t0004g0129a0001c0008t0004g0197 | 4 | HG02630.hp1 HG02723.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.1146+4061A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205732107 | ||||||
| chr2:205732371
|
A | G | 2 | a0001c0003t0002g0327a0001c0003t0014g0017 | 2 | HG00140.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.1146+4325A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205732371 | ||||||
| chr2:205732455
|
T | C | 3 | a0001c0002t0012g0131a0001c0013t0016g0132a0001c0013t0016g0133 | 3 | HG02717.hp1 HG02809.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1146+4409T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205732455 | ||||||
| chr2:205732685
|
G | A | 1 | a0001c0001t0004g0018 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1146+4639G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205732685 | ||||||
| chr2:205732846
|
T | C | 1 | a0001c0002t0028g0188 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1146+4800T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205732846 | ||||||
| chr2:205732877
|
T | C | 2 | a0002c0015t0030g0004a0002c0027t0064g0177 | 3 | HG02922.hp2 HG02965.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1146+4831T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205732877 | ||||||
| chr2:205732881
|
T | TA | 8 | a0001c0001t0001g0054a0001c0002t0008g0181a0001c0002t0012g0131others(5): Show | 8 | HG02647.hp2 HG02717.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.1146+4842dupA | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr2 | 205732881 | |||||
| chr2:205732931
|
A | G | 1 | a0001c0003t0007g0268 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1146+4885A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205732931 | ||||||
| chr2:205733000
|
G | C | 2 | a0001c0002t0029g0136a0001c0002t0063g0137 | 2 | HG02922.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1146+4954G>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205733000 | ||||||
| chr2:205733009
|
C | T | 248 | a0001c0001t0001g0021a0001c0001t0001g0054a0001c0001t0001g0074others(245): Show | 254 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(251): Show |
intron_variant | MODIFIER | c.1146+4963C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205733009 | ||||||
| chr2:205733145
|
C | G | 143 | a0001c0001t0001g0021a0001c0001t0001g0074a0001c0001t0001g0104others(140): Show | 147 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(144): Show |
intron_variant | MODIFIER | c.1146+5099C>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205733145 | ||||||
| chr2:205733303
|
T | G | 4 | a0001c0002t0001g0169a0001c0009t0005g0001a0001c0009t0021g0045others(1): Show | 5 | HG00735.hp1 HG01106.hp2 HG01261.hp2 others(2): Show |
intron_variant | MODIFIER | c.1146+5257T>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205733303 | ||||||
| chr2:205733344
|
G | A | 4 | a0001c0001t0001g0054a0001c0002t0008g0181a0001c0012t0004g0138others(1): Show | 4 | HG02647.hp2 HG02886.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1146+5298G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205733344 | ||||||
| chr2:205733434
|
C | A | 3 | a0001c0002t0012g0131a0001c0013t0016g0132a0001c0013t0016g0133 | 3 | HG02717.hp1 HG02809.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1146+5388C>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205733434 | ||||||
| chr2:205733566
|
C | T | 2 | a0001c0001t0005g0040a0001c0001t0010g0245 | 2 | HG00438.hp1 HG02015.hp1 |
intron_variant | MODIFIER | c.1146+5520C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205733566 | ||||||
| chr2:205733569
|
A | G | 2 | a0001c0002t0010g0278a0001c0002t0010g0279 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1146+5523A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205733569 | ||||||
| chr2:205733634
|
A | G | 24 | a0001c0001t0020g0031a0001c0001t0020g0072a0001c0002t0002g0262others(21): Show | 24 | HG01069.hp2 HG01109.hp1 HG01261.hp1 others(21): Show |
intron_variant | MODIFIER | c.1146+5588A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205733634 | ||||||
| chr2:205733718
|
T | C | 11 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0067others(8): Show | 11 | HG01106.hp1 HG01934.hp2 HG01943.hp1 others(8): Show |
intron_variant | MODIFIER | c.1146+5672T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205733718 | ||||||
| chr2:205733829
|
T | C | 3 | a0001c0008t0004g0005a0001c0008t0004g0129a0001c0008t0004g0197 | 4 | HG02630.hp1 HG02723.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.1146+5783T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205733829 | ||||||
| chr2:205733927
|
G | A | 1 | a0001c0004t0005g0165 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1146+5881G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205733927 | ||||||
| chr2:205733944
|
C | T | 1 | a0001c0001t0058g0069 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1146+5898C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205733944 | ||||||
| chr2:205734067
|
G | C | 3 | a0001c0002t0012g0131a0001c0013t0016g0132a0001c0013t0016g0133 | 3 | HG02717.hp1 HG02809.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1146+6021G>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205734067 | ||||||
| chr2:205734170
|
T | TTA | 11 | a0001c0001t0001g0074a0001c0001t0002g0236a0001c0001t0015g0238others(8): Show | 12 | HG00673.hp1 HG01069.hp1 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.1146+6141_1146+614 others(6): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr2 | 205734170 | |||||
| chr2:205734170
|
T | TTATATA | 2 | a0001c0008t0004g0005a0001c0008t0004g0197 | 3 | HG02630.hp1 HG02818.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.1146+6137_1146+614 others(10): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr2 | 205734170 | |||||
| chr2:205734170
|
TTA | T | 63 | a0001c0001t0001g0054a0001c0001t0009g0240a0001c0001t0026g0014others(60): Show | 64 | HG00735.hp2 HG00741.hp2 HG01070.hp1 others(61): Show |
intron_variant | MODIFIER | c.1146+6141_1146+614 others(6): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr2 | 205734170 | |||||
| chr2:205734215
|
G | GCACACAC others(1): Show |
4 | a0001c0001t0001g0054a0001c0002t0008g0181a0001c0012t0004g0138others(1): Show | 4 | HG02647.hp2 HG02886.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1146+6180_1146+618 others(12): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr2 | 205734215 | |||||
| chr2:205734339
|
A | G | 1 | a0001c0001t0011g0331 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1147-6180A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205734339 | ||||||
| chr2:205734375
|
A | T | 1 | a0001c0003t0006g0157 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1147-6144A>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205734375 | ||||||
| chr2:205734399
|
G | GC | 47 | a0001c0001t0001g0068a0001c0001t0002g0236a0001c0001t0003g0244others(44): Show | 48 | HG00741.hp2 HG01070.hp1 HG01099.hp1 others(45): Show |
intron_variant | MODIFIER | c.1147-6111dupC | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr2 | 205734399 | |||||
| chr2:205734403
|
C | CA | 20 | a0001c0002t0001g0015a0001c0002t0002g0295a0001c0002t0003g0204others(17): Show | 20 | HG00735.hp2 HG01255.hp2 HG01257.hp1 others(17): Show |
intron_variant | MODIFIER | c.1147-6116_1147-611 others(5): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205734403 | ||||||
| chr2:205734406
|
C | A | 1 | a0001c0002t0017g0255 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1147-6113C>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205734406 | ||||||
| chr2:205734406
|
C | CG | 2 | a0002c0015t0030g0004a0002c0027t0064g0177 | 3 | HG02922.hp2 HG02965.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1147-6113_1147-611 others(5): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205734406 | ||||||
| chr2:205734416
|
A | G | 2 | a0002c0015t0030g0004a0002c0027t0064g0177 | 3 | HG02922.hp2 HG02965.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1147-6103A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205734416 | ||||||
| chr2:205734442
|
G | C | 2 | a0001c0002t0029g0136a0001c0002t0063g0137 | 2 | HG02922.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1147-6077G>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205734442 | ||||||
| chr2:205734477
|
G | C | 11 | a0001c0001t0020g0031a0001c0001t0020g0072a0001c0002t0002g0262others(8): Show | 11 | HG01069.hp2 HG01261.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.1147-6042G>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205734477 | ||||||
| chr2:205734539
|
C | T | 1 | a0001c0001t0001g0158 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1147-5980C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205734539 | ||||||
| chr2:205734548
|
G | T | 3 | a0001c0004t0002g0235a0001c0004t0005g0056a0001c0004t0008g0044 | 3 | HG03490.hp1 NA18954.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.1147-5971G>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205734548 | ||||||
| chr2:205734704
|
C | T | 242 | a0001c0001t0001g0021a0001c0001t0001g0054a0001c0001t0001g0074others(239): Show | 247 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(244): Show |
intron_variant | MODIFIER | c.1147-5815C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205734704 | ||||||
| chr2:205734769
|
T | C | 2 | a0001c0002t0008g0013a0001c0002t0025g0253 | 2 | HG01070.hp1 HG01256.hp1 |
intron_variant | MODIFIER | c.1147-5750T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205734769 | ||||||
| chr2:205734987
|
C | T | 3 | a0001c0002t0007g0127a0001c0002t0048g0125a0001c0006t0007g0306 | 3 | HG01884.hp1 HG02809.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1147-5532C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205734987 | ||||||
| chr2:205735043
|
G | A | 63 | a0001c0001t0009g0240a0001c0001t0011g0222a0001c0001t0026g0014others(60): Show | 64 | HG00735.hp2 HG00741.hp2 HG01070.hp1 others(61): Show |
intron_variant | MODIFIER | c.1147-5476G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205735043 | ||||||
| chr2:205735047
|
C | T | 3 | a0001c0008t0004g0005a0001c0008t0004g0129a0001c0008t0004g0197 | 4 | HG02630.hp1 HG02723.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.1147-5472C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205735047 | ||||||
| chr2:205735077
|
C | T | 7 | a0001c0002t0001g0191a0001c0002t0004g0192a0001c0002t0011g0257others(4): Show | 7 | HG02015.hp2 HG02109.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.1147-5442C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205735077 | ||||||
| chr2:205735234
|
GA | G | 64 | a0001c0001t0009g0240a0001c0001t0011g0222a0001c0001t0026g0014others(61): Show | 65 | HG00735.hp2 HG01070.hp1 HG01099.hp1 others(62): Show |
intron_variant | MODIFIER | c.1147-5280delA | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr2 | 205735234 | |||||
| chr2:205735365
|
T | C | 7 | a0001c0002t0001g0191a0001c0002t0004g0192a0001c0002t0011g0257others(4): Show | 7 | HG02015.hp2 HG02109.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.1147-5154T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205735365 | ||||||
| chr2:205735440
|
G | GCTT | 17 | a0001c0002t0001g0169a0001c0002t0001g0191a0001c0002t0004g0140others(14): Show | 19 | HG00735.hp1 HG01106.hp2 HG01261.hp2 others(16): Show |
intron_variant | MODIFIER | c.1147-5075_1147-507 others(7): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr2 | 205735440 | |||||
| chr2:205735517
|
GAATGAAT others(9): Show |
G | 17 | a0001c0002t0001g0169a0001c0002t0001g0191a0001c0002t0004g0140others(14): Show | 19 | HG00735.hp1 HG01106.hp2 HG01261.hp2 others(16): Show |
intron_variant | MODIFIER | c.1147-4998_1147-498 others(20): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr2 | 205735517 | |||||
| chr2:205735570
|
G | A | 1 | a0001c0003t0006g0098 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1147-4949G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205735570 | ||||||
| chr2:205735817
|
A | G | 29 | a0001c0002t0001g0169a0001c0002t0001g0191a0001c0002t0004g0140others(26): Show | 31 | HG00735.hp1 HG01106.hp2 HG01261.hp2 others(28): Show |
intron_variant | MODIFIER | c.1147-4702A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205735817 | ||||||
| chr2:205735940
|
A | C | 3 | a0001c0004t0001g0003a0001c0004t0003g0309a0001c0004t0012g0146 | 4 | HG00673.hp1 HG01069.hp1 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.1147-4579A>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205735940 | ||||||
| chr2:205736199
|
A | G | 16 | a0001c0001t0020g0031a0001c0001t0020g0072a0001c0002t0002g0262others(13): Show | 16 | HG01069.hp2 HG01261.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.1147-4320A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205736199 | ||||||
| chr2:205736210
|
C | T | 7 | a0001c0001t0001g0021a0001c0001t0001g0036a0001c0001t0001g0037others(4): Show | 7 | HG01943.hp2 HG02056.hp1 HG02129.hp2 others(4): Show |
intron_variant | MODIFIER | c.1147-4309C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205736210 | ||||||
| chr2:205736274
|
A | G | 1 | a0001c0003t0040g0256 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1147-4245A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205736274 | ||||||
| chr2:205736517
|
C | T | 2 | a0001c0004t0002g0312a0001c0004t0003g0219 | 2 | NA18955.hp2 NA18965.hp1 |
intron_variant | MODIFIER | c.1147-4002C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205736517 | ||||||
| chr2:205736685
|
A | G | 1 | a0001c0020t0012g0016 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1147-3834A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205736685 | ||||||
| chr2:205736785
|
G | A | 3 | a0001c0004t0002g0220a0001c0004t0002g0221a0001c0004t0002g0246 | 3 | NA18965.hp2 NA19009.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.1147-3734G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205736785 | ||||||
| chr2:205736828
|
C | T | 4 | a0001c0002t0003g0204a0001c0002t0003g0282a0001c0002t0003g0283others(1): Show | 4 | NA18953.hp1 NA18967.hp2 NA19009.hp2 others(1): Show |
intron_variant | MODIFIER | c.1147-3691C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205736828 | ||||||
| chr2:205736992
|
A | C | 249 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0067others(246): Show | 254 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(251): Show |
intron_variant | MODIFIER | c.1147-3527A>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205736992 | ||||||
| chr2:205737034
|
A | T | 3 | a0001c0002t0012g0131a0001c0013t0016g0132a0001c0013t0016g0133 | 3 | HG02717.hp1 HG02809.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1147-3485A>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205737034 | ||||||
| chr2:205737039
|
T | A | 4 | a0001c0002t0012g0131a0001c0013t0016g0132a0001c0013t0016g0133others(1): Show | 4 | HG01109.hp1 HG02717.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.1147-3480T>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205737039 | ||||||
| chr2:205737043
|
T | C | 2 | a0002c0015t0030g0004a0002c0027t0064g0177 | 3 | HG02922.hp2 HG02965.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1147-3476T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205737043 | ||||||
| chr2:205737066
|
T | A | 1 | a0001c0004t0001g0003 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1147-3453T>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205737066 | ||||||
| chr2:205737492
|
T | C | 1 | a0001c0004t0026g0053 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1147-3027T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205737492 | ||||||
| chr2:205737518
|
G | A | 99 | a0001c0001t0002g0224a0001c0001t0008g0050a0001c0001t0008g0079others(96): Show | 101 | HG00280.hp2 HG00408.hp1 HG00558.hp1 others(98): Show |
intron_variant | MODIFIER | c.1147-3001G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205737518 | ||||||
| chr2:205737792
|
G | A | 32 | a0001c0001t0001g0054a0001c0002t0001g0191a0001c0002t0004g0192others(29): Show | 32 | HG01884.hp1 HG01884.hp2 HG02015.hp2 others(29): Show |
intron_variant | MODIFIER | c.1147-2727G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205737792 | ||||||
| chr2:205737805
|
C | A | 26 | a0001c0002t0001g0191a0001c0002t0004g0192a0001c0002t0007g0127others(23): Show | 26 | HG01884.hp1 HG02015.hp2 HG02055.hp1 others(23): Show |
intron_variant | MODIFIER | c.1147-2714C>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205737805 | ||||||
| chr2:205737827
|
T | C | 2 | a0001c0002t0049g0173a0002c0016t0004g0339 | 2 | HG03471.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1147-2692T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205737827 | ||||||
| chr2:205737843
|
T | C | 2 | a0001c0003t0021g0058a0001c0003t0021g0059 | 2 | NA19085.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.1147-2676T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205737843 | ||||||
| chr2:205737986
|
A | C | 105 | a0001c0001t0002g0224a0001c0001t0008g0079a0001c0001t0011g0331others(102): Show | 107 | HG00280.hp2 HG00408.hp1 HG00558.hp1 others(104): Show |
intron_variant | MODIFIER | c.1147-2533A>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205737986 | ||||||
| chr2:205738041
|
C | T | 100 | a0001c0001t0001g0054a0001c0001t0002g0224a0001c0001t0008g0079others(97): Show | 102 | HG00280.hp2 HG00408.hp1 HG00558.hp1 others(99): Show |
intron_variant | MODIFIER | c.1147-2478C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205738041 | ||||||
| chr2:205738073
|
C | T | 1 | a0001c0001t0005g0096 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1147-2446C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205738073 | ||||||
| chr2:205738159
|
G | A | 2 | a0001c0001t0020g0031a0001c0001t0020g0072 | 2 | HG01069.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.1147-2360G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205738159 | ||||||
| chr2:205738236
|
T | C | 1 | a0001c0001t0004g0018 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1147-2283T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205738236 | ||||||
| chr2:205738331
|
C | T | 2 | a0001c0001t0006g0114a0001c0001t0006g0115 | 2 | HG00741.hp1 HG01952.hp2 |
intron_variant | MODIFIER | c.1147-2188C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205738331 | ||||||
| chr2:205738516
|
T | A | 340 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0026others(337): Show | 346 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(343): Show |
intron_variant | MODIFIER | c.1147-2003T>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205738516 | ||||||
| chr2:205738585
|
T | C | 122 | a0001c0001t0002g0224a0001c0001t0005g0096a0001c0001t0008g0079others(119): Show | 124 | HG00280.hp2 HG00408.hp1 HG00558.hp1 others(121): Show |
intron_variant | MODIFIER | c.1147-1934T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205738585 | ||||||
| chr2:205738718
|
C | T | 1 | a0001c0001t0010g0210 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1147-1801C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205738718 | ||||||
| chr2:205738774
|
G | T | 2 | a0001c0002t0008g0200a0001c0002t0008g0201 | 2 | HG02886.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1147-1745G>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205738774 | ||||||
| chr2:205738798
|
G | T | 94 | a0001c0001t0002g0224a0001c0001t0008g0079a0001c0001t0012g0103others(91): Show | 96 | HG00280.hp2 HG00408.hp1 HG00558.hp1 others(93): Show |
intron_variant | MODIFIER | c.1147-1721G>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205738798 | ||||||
| chr2:205738841
|
T | G | 1 | a0001c0002t0042g0213 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1147-1678T>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205738841 | ||||||
| chr2:205738859
|
G | A | 3 | a0002c0014t0001g0196a0002c0014t0008g0195a0002c0029t0013g0276 | 3 | HG01109.hp1 HG02280.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1147-1660G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205738859 | ||||||
| chr2:205738868
|
C | T | 1 | a0001c0008t0004g0129 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1147-1651C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205738868 | ||||||
| chr2:205739105
|
G | A | 4 | a0001c0001t0020g0031a0001c0001t0020g0072a0001c0002t0002g0264others(1): Show | 4 | HG01069.hp2 HG01261.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1147-1414G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205739105 | ||||||
| chr2:205739148
|
T | C | 1 | a0001c0030t0052g0071 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1147-1371T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205739148 | ||||||
| chr2:205739265
|
G | A | 1 | a0001c0004t0002g0202 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1147-1254G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205739265 | ||||||
| chr2:205739367
|
A | G | 68 | a0001c0001t0001g0074a0001c0001t0001g0158a0001c0001t0002g0006others(65): Show | 69 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(66): Show |
intron_variant | MODIFIER | c.1147-1152A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205739367 | ||||||
| chr2:205739506
|
C | T | 1 | a0001c0002t0004g0182 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1147-1013C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205739506 | ||||||
| chr2:205739607
|
G | C | 89 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0026others(86): Show | 90 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(87): Show |
intron_variant | MODIFIER | c.1147-912G>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205739607 | ||||||
| chr2:205739665
|
A | G | 5 | a0001c0002t0004g0140a0001c0002t0017g0255a0001c0002t0049g0173others(2): Show | 5 | HG02976.hp1 HG03471.hp1 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.1147-854A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205739665 | ||||||
| chr2:205739682
|
C | CT | 81 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0026others(78): Show | 82 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(79): Show |
intron_variant | MODIFIER | c.1147-817dupT | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr2 | 205739682 | |||||
| chr2:205739682
|
C | CTT | 6 | a0001c0001t0008g0079a0001c0001t0010g0317a0001c0002t0001g0169others(3): Show | 6 | HG01934.hp1 HG03927.hp2 HG04184.hp2 others(3): Show |
intron_variant | MODIFIER | c.1147-818_1147-817d others(4): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr2 | 205739682 | |||||
| chr2:205739682
|
CT | C | 24 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0067others(21): Show | 25 | HG01070.hp1 HG01106.hp1 HG01169.hp1 others(22): Show |
intron_variant | MODIFIER | c.1147-817delT | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr2 | 205739682 | |||||
| chr2:205739682
|
CTT | C | 75 | a0001c0001t0002g0224a0001c0001t0012g0103a0001c0002t0008g0200others(72): Show | 77 | HG00280.hp2 HG00408.hp1 HG00558.hp1 others(74): Show |
intron_variant | MODIFIER | c.1147-818_1147-817d others(4): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr2 | 205739682 | |||||
| chr2:205739682
|
CTTT | C | 17 | a0001c0003t0001g0099a0001c0003t0001g0162a0001c0003t0003g0108others(14): Show | 17 | HG02056.hp2 NA18747.hp2 NA18950.hp2 others(14): Show |
intron_variant | MODIFIER | c.1147-819_1147-817d others(5): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr2 | 205739682 | |||||
| chr2:205739696
|
T | G | 1 | a0001c0001t0005g0034 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1147-823T>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205739696 | ||||||
| chr2:205739705
|
G | A | 92 | a0001c0001t0002g0224a0001c0001t0012g0103a0001c0002t0008g0200others(89): Show | 94 | HG00280.hp2 HG00408.hp1 HG00558.hp1 others(91): Show |
intron_variant | MODIFIER | c.1147-814G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205739705 | ||||||
| chr2:205739874
|
C | T | 1 | a0001c0002t0006g0147 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1147-645C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205739874 | ||||||
| chr2:205739875
|
A | G | 337 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0026others(334): Show | 343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.1147-644A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205739875 | ||||||
| chr2:205740089
|
C | G | 1 | a0001c0030t0052g0071 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1147-430C>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205740089 | ||||||
| chr2:205740281
|
T | C | 1 | a0001c0003t0003g0108 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1147-238T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205740281 | ||||||
| chr2:205740347
|
AT | A | 4 | a0001c0001t0001g0021a0001c0001t0020g0031a0001c0001t0020g0072others(1): Show | 4 | HG01069.hp2 HG01261.hp1 HG02129.hp1 others(1): Show |
intron_variant | MODIFIER | c.1147-164delT | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr2 | 205740347 | |||||
| chr2:205740456
|
T | G | 120 | a0001c0001t0002g0224a0001c0001t0008g0079a0001c0001t0011g0331others(117): Show | 122 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(119): Show |
intron_variant | MODIFIER | c.1147-63T>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205740456 | ||||||
| chr2:205740499
|
T | C | 4 | a0001c0003t0002g0327a0001c0003t0014g0017a0001c0004t0002g0228others(1): Show | 4 | HG00140.hp2 HG01975.hp2 HG02698.hp1 others(1): Show |
intron_variant | MODIFIER | c.1147-20T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 7/16 | chr2 | 205740499 | ||||||
| chr2:205740879
|
T | C | 3 | a0001c0008t0004g0005a0001c0008t0004g0129a0001c0008t0004g0197 | 4 | HG02630.hp1 HG02723.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.1291+216T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 8/16 | chr2 | 205740879 | ||||||
| chr2:205740994
|
T | TA | 102 | a0001c0001t0002g0224a0001c0001t0008g0079a0001c0001t0011g0331others(99): Show | 104 | HG00280.hp2 HG00408.hp1 HG00558.hp1 others(101): Show |
intron_variant | MODIFIER | c.1291+334dupA | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr2 | 205740994 | |||||
| chr2:205741034
|
G | A | 102 | a0001c0001t0002g0224a0001c0001t0008g0079a0001c0001t0011g0331others(99): Show | 104 | HG00280.hp2 HG00408.hp1 HG00558.hp1 others(101): Show |
intron_variant | MODIFIER | c.1291+371G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 8/16 | chr2 | 205741034 | ||||||
| chr2:205741099
|
C | T | 93 | a0001c0001t0002g0224a0001c0001t0008g0079a0001c0001t0012g0103others(90): Show | 95 | HG00280.hp2 HG00408.hp1 HG00558.hp1 others(92): Show |
intron_variant | MODIFIER | c.1291+436C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 8/16 | chr2 | 205741099 | ||||||
| chr2:205741138
|
G | A | 17 | a0001c0002t0001g0191a0001c0002t0004g0192a0001c0002t0007g0284others(14): Show | 17 | HG01884.hp2 HG02015.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.1291+475G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 8/16 | chr2 | 205741138 | ||||||
| chr2:205741142
|
G | A | 106 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0067others(103): Show | 107 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(104): Show |
intron_variant | MODIFIER | c.1291+479G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 8/16 | chr2 | 205741142 | ||||||
| chr2:205741168
|
T | C | 123 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0026others(120): Show | 125 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(122): Show |
intron_variant | MODIFIER | c.1291+505T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 8/16 | chr2 | 205741168 | ||||||
| chr2:205741272
|
C | T | 1 | a0002c0027t0064g0177 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1291+609C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 8/16 | chr2 | 205741272 | ||||||
| chr2:205741317
|
G | A | 93 | a0001c0001t0002g0224a0001c0001t0008g0079a0001c0001t0012g0103others(90): Show | 95 | HG00280.hp2 HG00408.hp1 HG00558.hp1 others(92): Show |
intron_variant | MODIFIER | c.1291+654G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 8/16 | chr2 | 205741317 | ||||||
| chr2:205741329
|
A | G | 1 | a0001c0001t0001g0074 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1291+666A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 8/16 | chr2 | 205741329 | ||||||
| chr2:205741459
|
A | G | 3 | a0001c0008t0004g0005a0001c0008t0004g0129a0001c0008t0004g0197 | 4 | HG02630.hp1 HG02723.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.1291+796A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 8/16 | chr2 | 205741459 | ||||||
| chr2:205741687
|
C | T | 1 | a0001c0002t0009g0254 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1291+1024C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 8/16 | chr2 | 205741687 | ||||||
| chr2:205742072
|
T | A | 11 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0067others(8): Show | 11 | HG01106.hp1 HG01934.hp2 HG01943.hp1 others(8): Show |
intron_variant | MODIFIER | c.1292-1131T>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 8/16 | chr2 | 205742072 | ||||||
| chr2:205742152
|
A | C | 1 | a0001c0002t0001g0191 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1292-1051A>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 8/16 | chr2 | 205742152 | ||||||
| chr2:205742163
|
G | C | 135 | a0001c0001t0002g0224a0001c0001t0008g0079a0001c0001t0012g0103others(132): Show | 139 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.1292-1040G>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 8/16 | chr2 | 205742163 | ||||||
| chr2:205742174
|
T | C | 135 | a0001c0001t0002g0224a0001c0001t0005g0096a0001c0001t0008g0079others(132): Show | 138 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(135): Show |
intron_variant | MODIFIER | c.1292-1029T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 8/16 | chr2 | 205742174 | ||||||
| chr2:205742194
|
T | A | 55 | a0001c0001t0001g0074a0001c0001t0001g0158a0001c0001t0002g0006others(52): Show | 56 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(53): Show |
intron_variant | MODIFIER | c.1292-1009T>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 8/16 | chr2 | 205742194 | ||||||
| chr2:205742219
|
A | G | 3 | a0001c0008t0004g0005a0001c0008t0004g0129a0001c0008t0004g0197 | 4 | HG02630.hp1 HG02723.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.1292-984A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 8/16 | chr2 | 205742219 | ||||||
| chr2:205742335
|
T | C | 8 | a0001c0003t0004g0168a0001c0003t0007g0249a0001c0003t0011g0248others(5): Show | 8 | HG01891.hp2 HG02647.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.1292-868T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 8/16 | chr2 | 205742335 | ||||||
| chr2:205742339
|
T | C | 1 | a0001c0003t0021g0058 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1292-864T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 8/16 | chr2 | 205742339 | ||||||
| chr2:205742352
|
A | G | 2 | a0002c0014t0001g0196a0002c0014t0008g0195 | 2 | HG02280.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1292-851A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 8/16 | chr2 | 205742352 | ||||||
| chr2:205742433
|
G | A | 1 | a0001c0002t0011g0257 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1292-770G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 8/16 | chr2 | 205742433 | ||||||
| chr2:205742460
|
C | A | 1 | a0001c0001t0004g0041 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1292-743C>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 8/16 | chr2 | 205742460 | ||||||
| chr2:205742506
|
A | T | 130 | a0001c0001t0002g0224a0001c0001t0008g0079a0001c0001t0011g0331others(127): Show | 132 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(129): Show |
intron_variant | MODIFIER | c.1292-697A>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 8/16 | chr2 | 205742506 | ||||||
| chr2:205742512
|
C | G | 1 | a0001c0001t0004g0194 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1292-691C>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 8/16 | chr2 | 205742512 | ||||||
| chr2:205742604
|
G | A | 3 | a0001c0018t0038g0308a0002c0015t0030g0004a0002c0027t0064g0177 | 4 | HG02922.hp2 HG02965.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1292-599G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 8/16 | chr2 | 205742604 | ||||||
| chr2:205742700
|
T | C | 1 | a0001c0001t0007g0243 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1292-503T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 8/16 | chr2 | 205742700 | ||||||
| chr2:205742832
|
T | C | 4 | a0001c0001t0003g0265a0001c0001t0005g0008a0001c0001t0005g0035others(1): Show | 4 | HG02135.hp2 NA18975.hp1 NA19063.hp1 others(1): Show |
intron_variant | MODIFIER | c.1292-371T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 8/16 | chr2 | 205742832 | ||||||
| chr2:205742976
|
C | T | 53 | a0001c0001t0001g0074a0001c0001t0001g0158a0001c0001t0002g0006others(50): Show | 54 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(51): Show |
intron_variant | MODIFIER | c.1292-227C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 8/16 | chr2 | 205742976 | ||||||
| chr2:205743170
|
A | G | 2 | a0001c0002t0028g0187a0001c0002t0028g0188 | 2 | HG03098.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1292-33A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 8/16 | chr2 | 205743170 | ||||||
| chr2:205743580
|
C | T | 2 | a0002c0017t0062g0178a0002c0029t0013g0276 | 2 | HG01109.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1641+28C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 9/16 | chr2 | 205743580 | ||||||
| chr2:205743658
|
A | G | 1 | a0001c0002t0004g0193 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1641+106A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 9/16 | chr2 | 205743658 | ||||||
| chr2:205743672
|
A | G | 3 | a0001c0001t0001g0054a0001c0002t0007g0285a0001c0002t0020g0186 | 3 | HG02109.hp1 HG02615.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1641+120A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 9/16 | chr2 | 205743672 | ||||||
| chr2:205743740
|
T | TTTTG | 120 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0067others(117): Show | 121 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(118): Show |
intron_variant | MODIFIER | c.1641+208_1641+211d others(6): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr2 | 205743740 | |||||
| chr2:205743837
|
G | A | 1 | a0001c0001t0003g0241 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1641+285G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 9/16 | chr2 | 205743837 | ||||||
| chr2:205743897
|
C | G | 1 | a0001c0001t0027g0111 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1641+345C>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 9/16 | chr2 | 205743897 | ||||||
| chr2:205743975
|
C | T | 3 | a0001c0001t0001g0054a0001c0002t0007g0285a0001c0002t0020g0186 | 3 | HG02109.hp1 HG02615.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1641+423C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 9/16 | chr2 | 205743975 | ||||||
| chr2:205744043
|
C | G | 1 | a0001c0001t0001g0067 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1641+491C>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 9/16 | chr2 | 205744043 | ||||||
| chr2:205744086
|
C | T | 2 | a0001c0002t0014g0160a0001c0005t0014g0128 | 2 | HG03942.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.1641+534C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 9/16 | chr2 | 205744086 | ||||||
| chr2:205744105
|
T | C | 6 | a0001c0002t0004g0140a0001c0002t0017g0255a0001c0002t0049g0173others(3): Show | 6 | HG02976.hp1 HG03225.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.1641+553T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 9/16 | chr2 | 205744105 | ||||||
| chr2:205744198
|
G | A | 1 | a0001c0004t0019g0088 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1641+646G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 9/16 | chr2 | 205744198 | ||||||
| chr2:205744250
|
C | T | 1 | a0001c0010t0009g0234 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1641+698C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 9/16 | chr2 | 205744250 | ||||||
| chr2:205744360
|
C | T | 1 | a0001c0001t0005g0145 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1641+808C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 9/16 | chr2 | 205744360 | ||||||
| chr2:205744470
|
C | T | 1 | a0001c0004t0006g0149 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1641+918C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 9/16 | chr2 | 205744470 | ||||||
| chr2:205744540
|
C | T | 86 | a0001c0003t0001g0085a0001c0003t0001g0099a0001c0003t0001g0150others(83): Show | 88 | HG00280.hp2 HG00408.hp1 HG00558.hp1 others(85): Show |
intron_variant | MODIFIER | c.1641+988C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 9/16 | chr2 | 205744540 | ||||||
| chr2:205744567
|
C | T | 1 | a0001c0002t0028g0188 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1641+1015C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 9/16 | chr2 | 205744567 | ||||||
| chr2:205744702
|
C | T | 4 | a0001c0002t0008g0200a0001c0002t0008g0201a0001c0002t0013g0198others(1): Show | 4 | HG02886.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1642-1044C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 9/16 | chr2 | 205744702 | ||||||
| chr2:205744796
|
G | A | 1 | a0001c0006t0007g0306 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1642-950G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 9/16 | chr2 | 205744796 | ||||||
| chr2:205744859
|
C | T | 1 | a0001c0003t0001g0163 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1642-887C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 9/16 | chr2 | 205744859 | ||||||
| chr2:205744860
|
G | A | 1 | a0001c0003t0003g0217 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1642-886G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 9/16 | chr2 | 205744860 | ||||||
| chr2:205745150
|
A | G | 338 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0026others(335): Show | 344 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(341): Show |
intron_variant | MODIFIER | c.1642-596A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 9/16 | chr2 | 205745150 | ||||||
| chr2:205745233
|
A | G | 1 | a0001c0002t0056g0148 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1642-513A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 9/16 | chr2 | 205745233 | ||||||
| chr2:205745264
|
G | A | 97 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0067others(94): Show | 98 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.1642-482G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 9/16 | chr2 | 205745264 | ||||||
| chr2:205745327
|
A | G | 170 | a0001c0001t0001g0022a0001c0001t0001g0054a0001c0001t0002g0216others(167): Show | 174 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(171): Show |
intron_variant | MODIFIER | c.1642-419A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 9/16 | chr2 | 205745327 | ||||||
| chr2:205745346
|
T | C | 320 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0026others(317): Show | 326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
intron_variant | MODIFIER | c.1642-400T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 9/16 | chr2 | 205745346 | ||||||
| chr2:205745405
|
C | G | 13 | a0001c0001t0002g0216a0001c0002t0007g0127a0001c0002t0008g0181others(10): Show | 13 | HG00140.hp2 HG01346.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.1642-341C>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 9/16 | chr2 | 205745405 | ||||||
| chr2:205745501
|
T | C | 15 | a0001c0001t0001g0054a0001c0002t0007g0285a0001c0002t0008g0200others(12): Show | 16 | HG02109.hp1 HG02258.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.1642-245T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 9/16 | chr2 | 205745501 | ||||||
| chr2:205745610
|
A | T | 3 | a0001c0009t0005g0001a0001c0009t0021g0045a0001c0009t0027g0032 | 4 | HG00735.hp1 HG01106.hp2 HG01261.hp2 others(1): Show |
intron_variant | MODIFIER | c.1642-136A>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 9/16 | chr2 | 205745610 | ||||||
| chr2:205745953
|
C | T | 3 | a0001c0009t0005g0001a0001c0009t0021g0045a0001c0009t0027g0032 | 4 | HG00735.hp1 HG01106.hp2 HG01261.hp2 others(1): Show |
intron_variant | MODIFIER | c.1786+63C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 10/16 | chr2 | 205745953 | ||||||
| chr2:205745974
|
G | A | 1 | a0002c0029t0013g0276 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1786+84G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 10/16 | chr2 | 205745974 | ||||||
| chr2:205746045
|
T | C | 1 | a0001c0002t0054g0215 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1786+155T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 10/16 | chr2 | 205746045 | ||||||
| chr2:205746626
|
T | C | 329 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0026others(326): Show | 335 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(332): Show |
intron_variant | MODIFIER | c.1786+736T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 10/16 | chr2 | 205746626 | ||||||
| chr2:205746639
|
G | C | 2 | a0002c0014t0001g0196a0002c0014t0008g0195 | 2 | HG02280.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1786+749G>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 10/16 | chr2 | 205746639 | ||||||
| chr2:205746692
|
T | C | 2 | a0002c0014t0001g0196a0002c0014t0008g0195 | 2 | HG02280.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1786+802T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 10/16 | chr2 | 205746692 | ||||||
| chr2:205746734
|
T | C | 1 | a0002c0017t0062g0178 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1786+844T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 10/16 | chr2 | 205746734 | ||||||
| chr2:205746754
|
C | T | 3 | a0001c0001t0001g0054a0001c0002t0007g0285a0001c0002t0020g0186 | 3 | HG02109.hp1 HG02615.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1786+864C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 10/16 | chr2 | 205746754 | ||||||
| chr2:205747030
|
G | A | 7 | a0001c0001t0001g0054a0001c0002t0007g0285a0001c0002t0020g0186others(4): Show | 7 | HG02109.hp1 HG02280.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.1786+1140G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 10/16 | chr2 | 205747030 | ||||||
| chr2:205747107
|
G | A | 1 | a0001c0001t0011g0331 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1786+1217G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 10/16 | chr2 | 205747107 | ||||||
| chr2:205747109
|
T | C | 2 | a0001c0003t0004g0168a0001c0004t0022g0184 | 2 | HG01891.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.1786+1219T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 10/16 | chr2 | 205747109 | ||||||
| chr2:205747167
|
A | C | 5 | a0001c0002t0004g0140a0001c0002t0049g0173a0001c0005t0004g0049others(2): Show | 5 | HG02559.hp1 HG03225.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.1786+1277A>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 10/16 | chr2 | 205747167 | ||||||
| chr2:205747197
|
G | T | 3 | a0001c0002t0042g0213a0001c0002t0051g0183a0001c0002t0054g0215 | 3 | HG02145.hp2 HG03041.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1786+1307G>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 10/16 | chr2 | 205747197 | ||||||
| chr2:205747306
|
G | T | 4 | a0001c0002t0016g0134a0001c0012t0017g0273a0001c0013t0016g0132others(1): Show | 4 | HG02717.hp1 HG03041.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1786+1416G>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 10/16 | chr2 | 205747306 | ||||||
| chr2:205747454
|
G | C | 2 | a0001c0002t0017g0255a0001c0005t0013g0176 | 2 | HG02976.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1786+1564G>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 10/16 | chr2 | 205747454 | ||||||
| chr2:205747588
|
C | T | 6 | a0001c0001t0020g0031a0001c0001t0020g0072a0001c0002t0002g0262others(3): Show | 6 | HG01069.hp2 HG01261.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1786+1698C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 10/16 | chr2 | 205747588 | ||||||
| chr2:205747597
|
C | G | 1 | a0001c0001t0002g0247 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1786+1707C>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 10/16 | chr2 | 205747597 | ||||||
| chr2:205747861
|
T | C | 103 | a0001c0001t0001g0074a0001c0001t0001g0104a0001c0001t0001g0158others(100): Show | 103 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(100): Show |
intron_variant | MODIFIER | c.1787-1864T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 10/16 | chr2 | 205747861 | ||||||
| chr2:205747990
|
G | A | 45 | a0001c0001t0001g0026a0001c0001t0001g0046a0001c0001t0001g0064others(42): Show | 46 | HG00099.hp1 HG00438.hp2 HG00639.hp1 others(43): Show |
intron_variant | MODIFIER | c.1787-1735G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 10/16 | chr2 | 205747990 | ||||||
| chr2:205747996
|
G | A | 1 | a0001c0005t0004g0049 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1787-1729G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 10/16 | chr2 | 205747996 | ||||||
| chr2:205748071
|
G | C | 117 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0036others(114): Show | 120 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(117): Show |
intron_variant | MODIFIER | c.1787-1654G>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 10/16 | chr2 | 205748071 | ||||||
| chr2:205748076
|
C | T | 5 | a0001c0002t0007g0284a0001c0006t0007g0329a0001c0018t0038g0308others(2): Show | 6 | HG02922.hp2 HG02965.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.1787-1649C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 10/16 | chr2 | 205748076 | ||||||
| chr2:205748083
|
T | A | 4 | a0001c0001t0004g0041a0001c0001t0012g0020a0001c0001t0031g0328others(1): Show | 4 | HG00639.hp1 HG01243.hp2 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1787-1642T>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 10/16 | chr2 | 205748083 | ||||||
| chr2:205748211
|
G | A | 4 | a0001c0002t0008g0200a0001c0002t0008g0201a0001c0002t0013g0198others(1): Show | 4 | HG02886.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1787-1514G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 10/16 | chr2 | 205748211 | ||||||
| chr2:205748228
|
T | C | 9 | a0001c0003t0001g0150a0001c0003t0001g0151a0001c0003t0001g0152others(6): Show | 9 | NA18966.hp2 NA18967.hp1 NA18978.hp1 others(6): Show |
intron_variant | MODIFIER | c.1787-1497T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 10/16 | chr2 | 205748228 | ||||||
| chr2:205748256
|
T | C | 1 | a0001c0001t0002g0236 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1787-1469T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 10/16 | chr2 | 205748256 | ||||||
| chr2:205748262
|
G | C | 1 | a0001c0001t0002g0211 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1787-1463G>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 10/16 | chr2 | 205748262 | ||||||
| chr2:205748557
|
G | A | 1 | a0001c0008t0004g0129 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1787-1168G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 10/16 | chr2 | 205748557 | ||||||
| chr2:205748709
|
G | C | 1 | a0001c0001t0002g0211 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1787-1016G>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 10/16 | chr2 | 205748709 | ||||||
| chr2:205748940
|
C | G | 1 | a0001c0001t0015g0209 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1787-785C>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 10/16 | chr2 | 205748940 | ||||||
| chr2:205749095
|
A | C | 6 | a0001c0002t0051g0183a0001c0002t0054g0215a0001c0007t0008g0063others(3): Show | 6 | HG02257.hp1 HG02723.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.1787-630A>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 10/16 | chr2 | 205749095 | ||||||
| chr2:205749123
|
T | A | 2 | a0001c0004t0002g0312a0001c0004t0003g0219 | 2 | NA18955.hp2 NA18965.hp1 |
intron_variant | MODIFIER | c.1787-602T>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 10/16 | chr2 | 205749123 | ||||||
| chr2:205749337
|
T | G | 4 | a0001c0001t0008g0047a0001c0002t0007g0127a0001c0002t0011g0257others(1): Show | 4 | HG01884.hp1 HG02015.hp2 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.1787-388T>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 10/16 | chr2 | 205749337 | ||||||
| chr2:205749367
|
T | G | 174 | a0001c0001t0001g0054a0001c0001t0001g0068a0001c0001t0001g0074others(171): Show | 177 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.1787-358T>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 10/16 | chr2 | 205749367 | ||||||
| chr2:205749420
|
G | A | 1 | a0001c0003t0001g0151 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1787-305G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 10/16 | chr2 | 205749420 | ||||||
| chr2:205749426
|
A | G | 141 | a0001c0001t0001g0054a0001c0001t0001g0074a0001c0001t0001g0158others(138): Show | 142 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(139): Show |
intron_variant | MODIFIER | c.1787-299A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 10/16 | chr2 | 205749426 | ||||||
| chr2:205749436
|
A | G | 214 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0026others(211): Show | 215 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(212): Show |
intron_variant | MODIFIER | c.1787-289A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 10/16 | chr2 | 205749436 | ||||||
| chr2:205749922
|
T | G | 190 | a0001c0001t0001g0054a0001c0001t0001g0068a0001c0001t0001g0074others(187): Show | 193 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(190): Show |
intron_variant | MODIFIER | c.1903+81T>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 11/16 | chr2 | 205749922 | ||||||
| chr2:205749924
|
G | T | 4 | a0001c0002t0008g0200a0001c0002t0008g0201a0001c0002t0013g0198others(1): Show | 4 | HG02886.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1903+83G>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 11/16 | chr2 | 205749924 | ||||||
| chr2:205750224
|
G | A | 2 | a0001c0002t0017g0255a0001c0005t0013g0176 | 2 | HG02976.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1903+383G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 11/16 | chr2 | 205750224 | ||||||
| chr2:205750240
|
G | C | 201 | a0001c0001t0001g0054a0001c0001t0001g0068a0001c0001t0001g0074others(198): Show | 204 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(201): Show |
intron_variant | MODIFIER | c.1903+399G>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 11/16 | chr2 | 205750240 | ||||||
| chr2:205750342
|
A | G | 178 | a0001c0001t0001g0054a0001c0001t0001g0068a0001c0001t0001g0074others(175): Show | 181 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.1903+501A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 11/16 | chr2 | 205750342 | ||||||
| chr2:205750413
|
G | C | 4 | a0001c0001t0008g0050a0001c0005t0007g0223a0001c0005t0023g0120others(1): Show | 4 | HG01074.hp2 HG01123.hp1 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.1903+572G>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 11/16 | chr2 | 205750413 | ||||||
| chr2:205750454
|
C | T | 1 | a0001c0002t0008g0124 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1903+613C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 11/16 | chr2 | 205750454 | ||||||
| chr2:205750537
|
T | G | 6 | a0001c0002t0002g0280a0001c0002t0005g0030a0001c0002t0010g0277others(3): Show | 6 | HG00140.hp1 HG01074.hp1 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.1903+696T>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 11/16 | chr2 | 205750537 | ||||||
| chr2:205750786
|
T | C | 1 | a0001c0001t0009g0240 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1903+945T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 11/16 | chr2 | 205750786 | ||||||
| chr2:205750815
|
T | C | 187 | a0001c0001t0001g0054a0001c0001t0001g0068a0001c0001t0001g0074others(184): Show | 190 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(187): Show |
intron_variant | MODIFIER | c.1903+974T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 11/16 | chr2 | 205750815 | ||||||
| chr2:205750953
|
C | T | 16 | a0001c0001t0001g0068a0001c0001t0002g0006a0001c0001t0003g0226others(13): Show | 17 | HG00423.hp2 HG00741.hp1 HG01257.hp2 others(14): Show |
intron_variant | MODIFIER | c.1903+1112C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 11/16 | chr2 | 205750953 | ||||||
| chr2:205751189
|
C | A | 11 | a0001c0001t0002g0247a0001c0001t0003g0241a0001c0003t0001g0085others(8): Show | 11 | HG00438.hp2 HG00621.hp2 HG01081.hp1 others(8): Show |
intron_variant | MODIFIER | c.1903+1348C>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 11/16 | chr2 | 205751189 | ||||||
| chr2:205751245
|
C | A | 1 | a0001c0001t0001g0068 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1903+1404C>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 11/16 | chr2 | 205751245 | ||||||
| chr2:205751287
|
T | C | 4 | a0001c0001t0008g0047a0001c0002t0007g0127a0001c0002t0011g0257others(1): Show | 4 | HG01884.hp1 HG02015.hp2 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.1903+1446T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 11/16 | chr2 | 205751287 | ||||||
| chr2:205751350
|
T | C | 5 | a0001c0002t0051g0183a0001c0002t0054g0215a0001c0007t0008g0063others(2): Show | 5 | HG02257.hp1 HG02723.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1904-1485T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 11/16 | chr2 | 205751350 | ||||||
| chr2:205751381
|
T | C | 1 | a0001c0001t0006g0066 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1904-1454T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 11/16 | chr2 | 205751381 | ||||||
| chr2:205751425
|
C | T | 2 | a0001c0001t0007g0214a0001c0001t0010g0229 | 2 | HG00280.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.1904-1410C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 11/16 | chr2 | 205751425 | ||||||
| chr2:205751426
|
G | A | 15 | a0001c0002t0008g0181a0001c0002t0022g0185a0001c0002t0029g0136others(12): Show | 15 | HG02257.hp1 HG02258.hp2 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.1904-1409G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 11/16 | chr2 | 205751426 | ||||||
| chr2:205751485
|
T | TA | 5 | a0001c0002t0051g0183a0001c0002t0054g0215a0001c0007t0008g0063others(2): Show | 5 | HG02257.hp1 HG02723.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1904-1348dupA | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 11/16 | INFO_REALIGN_3_PRIME | chr2 | 205751485 | |||||
| chr2:205751651
|
A | G | 6 | a0001c0002t0029g0136a0001c0002t0063g0137a0001c0007t0013g0189others(3): Show | 6 | HG02258.hp2 HG02922.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.1904-1184A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 11/16 | chr2 | 205751651 | ||||||
| chr2:205752057
|
A | G | 1 | a0001c0002t0004g0275 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1904-778A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 11/16 | chr2 | 205752057 | ||||||
| chr2:205753126
|
C | A | 1 | a0001c0002t0028g0187 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2044+151C>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205753126 | ||||||
| chr2:205753350
|
G | A | 1 | a0003c0026t0004g0166 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2044+375G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205753350 | ||||||
| chr2:205753568
|
A | G | 5 | a0001c0001t0008g0047a0001c0002t0007g0127a0001c0002t0011g0257others(2): Show | 5 | HG01884.hp1 HG01884.hp2 HG02015.hp2 others(2): Show |
intron_variant | MODIFIER | c.2044+593A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205753568 | ||||||
| chr2:205753672
|
C | T | 4 | a0001c0001t0003g0269a0001c0001t0006g0114a0001c0001t0010g0230others(1): Show | 4 | HG00642.hp2 HG01952.hp2 HG01978.hp2 others(1): Show |
intron_variant | MODIFIER | c.2044+697C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205753672 | ||||||
| chr2:205753719
|
G | A | 1 | a0001c0009t0005g0001 | 2 | HG00735.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.2044+744G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205753719 | ||||||
| chr2:205754083
|
C | T | 1 | a0001c0004t0006g0149 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.2044+1108C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205754083 | ||||||
| chr2:205754126
|
C | T | 1 | a0001c0003t0001g0153 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.2044+1151C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205754126 | ||||||
| chr2:205754199
|
G | C | 7 | a0001c0001t0008g0047a0001c0002t0007g0127a0001c0002t0011g0257others(4): Show | 7 | HG01884.hp1 HG01884.hp2 HG02015.hp2 others(4): Show |
intron_variant | MODIFIER | c.2044+1224G>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205754199 | ||||||
| chr2:205754224
|
G | T | 18 | a0001c0001t0001g0054a0001c0001t0004g0041a0001c0001t0018g0019others(15): Show | 18 | HG01069.hp2 HG01256.hp2 HG01261.hp1 others(15): Show |
intron_variant | MODIFIER | c.2044+1249G>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205754224 | ||||||
| chr2:205754599
|
G | C | 1 | a0001c0002t0043g0259 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2044+1624G>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205754599 | ||||||
| chr2:205754805
|
G | GGT | 151 | a0001c0001t0001g0054a0001c0001t0001g0074a0001c0001t0001g0158others(148): Show | 152 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(149): Show |
intron_variant | MODIFIER | c.2044+1843_2044+184 others(6): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr2 | 205754805 | |||||
| chr2:205754847
|
G | T | 3 | a0001c0001t0008g0047a0001c0002t0011g0257a0001c0006t0007g0306 | 3 | HG02015.hp2 NA20129.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.2044+1872G>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205754847 | ||||||
| chr2:205754869
|
C | T | 2 | a0001c0008t0004g0129a0002c0029t0013g0276 | 2 | HG01109.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.2044+1894C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205754869 | ||||||
| chr2:205755044
|
G | A | 1 | a0001c0006t0009g0303 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2044+2069G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205755044 | ||||||
| chr2:205755151
|
A | G | 1 | a0001c0003t0001g0163 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.2044+2176A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205755151 | ||||||
| chr2:205755164
|
G | A | 1 | a0001c0002t0042g0213 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2044+2189G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205755164 | ||||||
| chr2:205755256
|
G | A | 1 | a0001c0002t0002g0264 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2044+2281G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205755256 | ||||||
| chr2:205755263
|
G | A | 3 | a0001c0002t0007g0284a0001c0006t0007g0329a0002c0015t0030g0004 | 4 | HG02922.hp2 HG02970.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.2044+2288G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205755263 | ||||||
| chr2:205755308
|
C | G | 304 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0026others(301): Show | 310 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(307): Show |
intron_variant | MODIFIER | c.2044+2333C>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205755308 | ||||||
| chr2:205755513
|
A | C | 1 | a0001c0004t0002g0311 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.2044+2538A>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205755513 | ||||||
| chr2:205755596
|
T | C | 2 | a0001c0001t0004g0117a0001c0005t0023g0119 | 2 | HG01106.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.2044+2621T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205755596 | ||||||
| chr2:205755609
|
G | GA | 162 | a0001c0001t0001g0068a0001c0001t0001g0074a0001c0001t0001g0158others(159): Show | 165 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(162): Show |
intron_variant | MODIFIER | c.2044+2634_2044+263 others(5): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205755609 | ||||||
| chr2:205755610
|
G | A | 235 | a0001c0001t0001g0054a0001c0001t0001g0068a0001c0001t0001g0074others(232): Show | 240 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(237): Show |
intron_variant | MODIFIER | c.2044+2635G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205755610 | ||||||
| chr2:205755704
|
A | T | 2 | a0001c0002t0008g0181a0001c0002t0022g0185 | 2 | HG02647.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.2044+2729A>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205755704 | ||||||
| chr2:205755727
|
G | A | 5 | a0001c0002t0051g0183a0001c0002t0054g0215a0001c0007t0008g0063others(2): Show | 5 | HG02257.hp1 HG02723.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.2044+2752G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205755727 | ||||||
| chr2:205755941
|
G | C | 1 | a0002c0014t0001g0196 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2044+2966G>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205755941 | ||||||
| chr2:205756045
|
C | G | 18 | a0001c0001t0001g0068a0001c0001t0002g0006a0001c0001t0003g0226others(15): Show | 19 | HG00423.hp2 HG00741.hp1 HG01123.hp2 others(16): Show |
intron_variant | MODIFIER | c.2044+3070C>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205756045 | ||||||
| chr2:205756544
|
G | C | 1 | a0001c0007t0017g0270 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2044+3569G>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205756544 | ||||||
| chr2:205756679
|
T | C | 224 | a0001c0001t0001g0054a0001c0001t0001g0068a0001c0001t0001g0074others(221): Show | 229 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(226): Show |
intron_variant | MODIFIER | c.2044+3704T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205756679 | ||||||
| chr2:205756682
|
G | C | 3 | a0001c0002t0017g0255a0001c0005t0013g0176a0001c0012t0017g0273 | 3 | HG02976.hp1 HG03209.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2044+3707G>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205756682 | ||||||
| chr2:205756873
|
T | C | 5 | a0001c0005t0004g0049a0001c0012t0004g0138a0002c0014t0001g0196others(2): Show | 5 | HG02280.hp1 HG02559.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.2044+3898T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205756873 | ||||||
| chr2:205756904
|
G | T | 1 | a0001c0002t0042g0213 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2044+3929G>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205756904 | ||||||
| chr2:205756968
|
T | C | 6 | a0001c0001t0002g0216a0001c0001t0008g0047a0001c0002t0011g0257others(3): Show | 6 | HG01346.hp2 HG01975.hp2 HG02015.hp2 others(3): Show |
intron_variant | MODIFIER | c.2044+3993T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205756968 | ||||||
| chr2:205756981
|
C | T | 2 | a0001c0002t0029g0136a0001c0002t0063g0137 | 2 | HG02922.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2044+4006C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205756981 | ||||||
| chr2:205757007
|
A | G | 1 | a0001c0011t0008g0135 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2044+4032A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205757007 | ||||||
| chr2:205757264
|
G | A | 30 | a0001c0001t0002g0006a0001c0001t0003g0226a0001c0001t0006g0066others(27): Show | 32 | HG00423.hp2 HG00741.hp1 HG01257.hp2 others(29): Show |
intron_variant | MODIFIER | c.2044+4289G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205757264 | ||||||
| chr2:205757435
|
G | A | 1 | a0001c0004t0006g0180 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.2044+4460G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205757435 | ||||||
| chr2:205757647
|
A | G | 5 | a0001c0005t0004g0049a0001c0012t0004g0138a0002c0014t0001g0196others(2): Show | 5 | HG02280.hp1 HG02559.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.2044+4672A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205757647 | ||||||
| chr2:205757852
|
A | G | 81 | a0001c0001t0001g0054a0001c0001t0001g0068a0001c0001t0002g0211others(78): Show | 83 | HG00408.hp1 HG00621.hp1 HG00673.hp1 others(80): Show |
intron_variant | MODIFIER | c.2044+4877A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205757852 | ||||||
| chr2:205757877
|
A | G | 5 | a0001c0001t0009g0240a0001c0001t0012g0027a0001c0001t0012g0028others(2): Show | 5 | HG01070.hp1 HG01070.hp2 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.2044+4902A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205757877 | ||||||
| chr2:205757886
|
C | T | 1 | a0001c0001t0015g0238 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.2044+4911C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205757886 | ||||||
| chr2:205757897
|
CT | C | 19 | a0001c0001t0002g0216a0001c0001t0008g0047a0001c0001t0037g0323others(16): Show | 19 | HG01099.hp2 HG01346.hp2 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.2044+4935delT | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr2 | 205757897 | |||||
| chr2:205757897
|
CTT | C | 173 | a0001c0001t0001g0054a0001c0001t0001g0068a0001c0001t0001g0074others(170): Show | 175 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(172): Show |
intron_variant | MODIFIER | c.2044+4934_2044+493 others(6): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr2 | 205757897 | |||||
| chr2:205757897
|
CTTT | C | 29 | a0001c0001t0002g0006a0001c0001t0003g0226a0001c0001t0006g0066others(26): Show | 31 | HG00423.hp2 HG00741.hp1 HG01257.hp2 others(28): Show |
intron_variant | MODIFIER | c.2044+4933_2044+493 others(7): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr2 | 205757897 | |||||
| chr2:205757898
|
T | C | 1 | a0001c0001t0003g0203 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.2044+4923T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205757898 | ||||||
| chr2:205757921
|
A | T | 1 | a0001c0013t0016g0133 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2044+4946A>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205757921 | ||||||
| chr2:205758088
|
A | G | 1 | a0001c0001t0001g0026 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.2044+5113A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205758088 | ||||||
| chr2:205758185
|
T | C | 2 | a0001c0001t0004g0117a0001c0005t0023g0119 | 2 | HG01106.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.2044+5210T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205758185 | ||||||
| chr2:205758194
|
C | A | 3 | a0001c0002t0004g0275a0001c0002t0028g0187a0001c0002t0028g0188 | 3 | HG03098.hp2 HG03130.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.2044+5219C>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205758194 | ||||||
| chr2:205758195
|
A | G | 3 | a0001c0002t0004g0275a0001c0002t0028g0187a0001c0002t0028g0188 | 3 | HG03098.hp2 HG03130.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.2044+5220A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205758195 | ||||||
| chr2:205758222
|
A | G | 47 | a0001c0001t0001g0068a0001c0001t0002g0211a0001c0001t0002g0224others(44): Show | 49 | HG00408.hp1 HG00621.hp1 HG00673.hp1 others(46): Show |
intron_variant | MODIFIER | c.2044+5247A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205758222 | ||||||
| chr2:205758263
|
A | G | 1 | a0001c0003t0001g0150 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.2044+5288A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205758263 | ||||||
| chr2:205758518
|
G | C | 18 | a0001c0001t0004g0041a0001c0001t0018g0019a0001c0002t0002g0262others(15): Show | 18 | HG00741.hp2 HG01081.hp2 HG01256.hp2 others(15): Show |
intron_variant | MODIFIER | c.2045-5156G>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205758518 | ||||||
| chr2:205758547
|
G | A | 1 | a0001c0001t0003g0265 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.2045-5127G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205758547 | ||||||
| chr2:205758603
|
G | A | 30 | a0001c0001t0002g0006a0001c0001t0003g0226a0001c0001t0006g0066others(27): Show | 32 | HG00423.hp2 HG00741.hp1 HG01257.hp2 others(29): Show |
intron_variant | MODIFIER | c.2045-5071G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205758603 | ||||||
| chr2:205758605
|
G | A | 30 | a0001c0001t0002g0006a0001c0001t0003g0226a0001c0001t0006g0066others(27): Show | 32 | HG00423.hp2 HG00741.hp1 HG01257.hp2 others(29): Show |
intron_variant | MODIFIER | c.2045-5069G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205758605 | ||||||
| chr2:205758659
|
C | T | 5 | a0001c0003t0001g0150a0001c0003t0001g0155a0001c0003t0001g0156others(2): Show | 5 | NA18966.hp2 NA18978.hp1 NA19001.hp1 others(2): Show |
intron_variant | MODIFIER | c.2045-5015C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205758659 | ||||||
| chr2:205758870
|
C | G | 106 | a0001c0001t0001g0074a0001c0001t0001g0158a0001c0001t0002g0258others(103): Show | 107 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.2045-4804C>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205758870 | ||||||
| chr2:205759054
|
G | T | 13 | a0001c0002t0008g0181a0001c0002t0022g0185a0001c0002t0051g0183others(10): Show | 13 | HG01891.hp2 HG02257.hp1 HG02647.hp2 others(10): Show |
intron_variant | MODIFIER | c.2045-4620G>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205759054 | ||||||
| chr2:205759202
|
G | A | 1 | a0001c0004t0003g0297 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.2045-4472G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205759202 | ||||||
| chr2:205759208
|
G | C | 4 | a0001c0002t0004g0140a0001c0002t0007g0285a0001c0002t0008g0141others(1): Show | 4 | HG02109.hp1 HG02486.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.2045-4466G>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205759208 | ||||||
| chr2:205759302
|
G | T | 1 | a0001c0004t0008g0044 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.2045-4372G>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205759302 | ||||||
| chr2:205759303
|
T | A | 1 | a0001c0004t0008g0044 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.2045-4371T>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205759303 | ||||||
| chr2:205759641
|
G | T | 1 | a0001c0002t0007g0291 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.2045-4033G>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205759641 | ||||||
| chr2:205759678
|
C | T | 1 | a0001c0002t0010g0277 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.2045-3996C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205759678 | ||||||
| chr2:205759821
|
C | T | 1 | a0001c0003t0025g0301 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2045-3853C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205759821 | ||||||
| chr2:205759899
|
T | A | 13 | a0001c0001t0004g0041a0001c0001t0018g0019a0001c0002t0004g0140others(10): Show | 13 | HG00741.hp2 HG01081.hp2 HG01256.hp2 others(10): Show |
intron_variant | MODIFIER | c.2045-3775T>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205759899 | ||||||
| chr2:205759902
|
A | G | 1 | a0001c0003t0035g0205 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2045-3772A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205759902 | ||||||
| chr2:205760161
|
G | A | 1 | a0001c0002t0008g0200 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2045-3513G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205760161 | ||||||
| chr2:205760171
|
G | A | 1 | a0001c0011t0008g0135 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2045-3503G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205760171 | ||||||
| chr2:205760542
|
C | G | 59 | a0001c0001t0001g0054a0001c0001t0002g0211a0001c0001t0002g0224others(56): Show | 61 | HG00408.hp1 HG00621.hp1 HG00673.hp1 others(58): Show |
intron_variant | MODIFIER | c.2045-3132C>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205760542 | ||||||
| chr2:205760653
|
T | C | 237 | a0001c0001t0001g0054a0001c0001t0001g0068a0001c0001t0001g0074others(234): Show | 241 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(238): Show |
intron_variant | MODIFIER | c.2045-3021T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205760653 | ||||||
| chr2:205760654
|
G | A | 2 | a0001c0001t0005g0040a0001c0001t0010g0245 | 2 | HG00438.hp1 HG02015.hp1 |
intron_variant | MODIFIER | c.2045-3020G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205760654 | ||||||
| chr2:205761000
|
G | T | 1 | a0001c0001t0004g0041 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.2045-2674G>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205761000 | ||||||
| chr2:205761039
|
C | T | 1 | a0001c0003t0022g0174 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2045-2635C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205761039 | ||||||
| chr2:205761061
|
A | G | 1 | a0001c0030t0052g0071 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.2045-2613A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205761061 | ||||||
| chr2:205761115
|
G | A | 1 | a0001c0001t0002g0216 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.2045-2559G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205761115 | ||||||
| chr2:205761177
|
C | T | 1 | a0001c0004t0003g0207 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.2045-2497C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205761177 | ||||||
| chr2:205761288
|
T | C | 1 | a0001c0001t0008g0079 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.2045-2386T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205761288 | ||||||
| chr2:205761346
|
C | T | 28 | a0001c0001t0002g0006a0001c0001t0003g0226a0001c0001t0006g0066others(25): Show | 30 | HG00423.hp2 HG00741.hp1 HG01123.hp2 others(27): Show |
intron_variant | MODIFIER | c.2045-2328C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205761346 | ||||||
| chr2:205761841
|
T | C | 1 | a0001c0004t0001g0002 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.2045-1833T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205761841 | ||||||
| chr2:205761861
|
G | A | 58 | a0001c0001t0001g0054a0001c0001t0001g0068a0001c0001t0002g0211others(55): Show | 60 | HG00408.hp1 HG00621.hp1 HG00673.hp1 others(57): Show |
intron_variant | MODIFIER | c.2045-1813G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205761861 | ||||||
| chr2:205761960
|
T | C | 68 | a0001c0001t0001g0054a0001c0001t0001g0068a0001c0001t0002g0211others(65): Show | 70 | HG00408.hp1 HG00621.hp1 HG00673.hp1 others(67): Show |
intron_variant | MODIFIER | c.2045-1714T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205761960 | ||||||
| chr2:205762133
|
T | G | 1 | a0001c0002t0016g0134 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2045-1541T>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205762133 | ||||||
| chr2:205762205
|
C | T | 2 | a0001c0002t0029g0136a0001c0002t0063g0137 | 2 | HG02922.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2045-1469C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205762205 | ||||||
| chr2:205762222
|
T | A | 1 | a0001c0001t0058g0069 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2045-1452T>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205762222 | ||||||
| chr2:205762284
|
G | A | 3 | a0001c0001t0012g0020a0001c0001t0031g0328a0001c0001t0057g0033 | 3 | HG00639.hp1 HG01243.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.2045-1390G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205762284 | ||||||
| chr2:205762285
|
A | G | 235 | a0001c0001t0001g0054a0001c0001t0001g0068a0001c0001t0001g0074others(232): Show | 240 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(237): Show |
intron_variant | MODIFIER | c.2045-1389A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205762285 | ||||||
| chr2:205762297
|
C | T | 5 | a0001c0002t0051g0183a0001c0002t0054g0215a0001c0007t0008g0063others(2): Show | 5 | HG02257.hp1 HG02723.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.2045-1377C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205762297 | ||||||
| chr2:205762587
|
G | A | 187 | a0001c0001t0001g0054a0001c0001t0001g0074a0001c0001t0001g0158others(184): Show | 189 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(186): Show |
intron_variant | MODIFIER | c.2045-1087G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205762587 | ||||||
| chr2:205762659
|
C | T | 3 | a0001c0001t0004g0041a0001c0001t0018g0019a0001c0002t0020g0186 | 3 | HG01256.hp2 HG02615.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.2045-1015C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205762659 | ||||||
| chr2:205762686
|
G | A | 17 | a0001c0001t0002g0006a0001c0001t0003g0226a0001c0001t0006g0066others(14): Show | 19 | HG00423.hp2 HG00741.hp1 HG01257.hp2 others(16): Show |
intron_variant | MODIFIER | c.2045-988G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205762686 | ||||||
| chr2:205762691
|
T | C | 188 | a0001c0001t0001g0054a0001c0001t0001g0068a0001c0001t0001g0074others(185): Show | 191 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(188): Show |
intron_variant | MODIFIER | c.2045-983T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205762691 | ||||||
| chr2:205762749
|
T | C | 70 | a0001c0001t0001g0054a0001c0001t0001g0068a0001c0001t0002g0211others(67): Show | 72 | HG00408.hp1 HG00621.hp1 HG00673.hp1 others(69): Show |
intron_variant | MODIFIER | c.2045-925T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205762749 | ||||||
| chr2:205762966
|
C | A | 4 | a0001c0001t0003g0226a0001c0001t0006g0115a0001c0004t0003g0309others(1): Show | 4 | HG00741.hp1 HG01123.hp2 HG01257.hp2 others(1): Show |
intron_variant | MODIFIER | c.2045-708C>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205762966 | ||||||
| chr2:205763087
|
C | G | 1 | a0001c0003t0004g0168 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2045-587C>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205763087 | ||||||
| chr2:205763244
|
A | C | 7 | a0001c0002t0022g0185a0001c0003t0004g0168a0001c0003t0007g0249others(4): Show | 7 | HG01891.hp2 HG02895.hp1 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.2045-430A>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205763244 | ||||||
| chr2:205763289
|
C | G | 1 | a0001c0001t0026g0014 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.2045-385C>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205763289 | ||||||
| chr2:205763333
|
C | A | 2 | a0001c0001t0002g0316a0001c0001t0009g0319 | 2 | NA18969.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.2045-341C>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205763333 | ||||||
| chr2:205763348
|
A | C | 1 | a0001c0003t0002g0327 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.2045-326A>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205763348 | ||||||
| chr2:205763403
|
T | C | 8 | a0001c0002t0008g0181a0001c0002t0022g0185a0001c0003t0004g0168others(5): Show | 8 | HG01891.hp2 HG02647.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.2045-271T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205763403 | ||||||
| chr2:205763445
|
T | C | 14 | a0001c0001t0001g0054a0001c0001t0020g0031a0001c0001t0020g0072others(11): Show | 14 | HG01069.hp2 HG01261.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.2045-229T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205763445 | ||||||
| chr2:205763476
|
T | G | 3 | a0001c0001t0012g0020a0001c0001t0031g0328a0001c0001t0057g0033 | 3 | HG00639.hp1 HG01243.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.2045-198T>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 12/16 | chr2 | 205763476 | ||||||
| chr2:205764006
|
T | C | 1 | a0001c0004t0013g0051 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.2307+70T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 13/16 | chr2 | 205764006 | ||||||
| chr2:205764199
|
T | A | 1 | a0001c0002t0002g0262 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2307+263T>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 13/16 | chr2 | 205764199 | ||||||
| chr2:205764390
|
A | T | 31 | a0001c0001t0002g0006a0001c0001t0003g0203a0001c0001t0003g0226others(28): Show | 32 | HG00423.hp2 HG00642.hp2 HG00741.hp1 others(29): Show |
intron_variant | MODIFIER | c.2307+454A>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 13/16 | chr2 | 205764390 | ||||||
| chr2:205764505
|
C | T | 2 | a0001c0001t0004g0117a0001c0002t0004g0193 | 2 | HG01106.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.2307+569C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 13/16 | chr2 | 205764505 | ||||||
| chr2:205764517
|
T | G | 1 | a0001c0002t0002g0280 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.2307+581T>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 13/16 | chr2 | 205764517 | ||||||
| chr2:205764537
|
T | C | 6 | a0001c0002t0002g0262a0001c0002t0002g0263a0001c0002t0002g0264others(3): Show | 6 | HG02109.hp2 HG02145.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.2307+601T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 13/16 | chr2 | 205764537 | ||||||
| chr2:205764617
|
A | G | 330 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0026others(327): Show | 335 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(332): Show |
intron_variant | MODIFIER | c.2307+681A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 13/16 | chr2 | 205764617 | ||||||
| chr2:205764652
|
T | A | 1 | a0001c0003t0047g0126 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2307+716T>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 13/16 | chr2 | 205764652 | ||||||
| chr2:205765349
|
A | AAC | 201 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0026others(198): Show | 205 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(202): Show |
intron_variant | MODIFIER | c.2308-107_2308-106d others(4): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr2 | 205765349 | |||||
| chr2:205765369
|
T | C | 2 | a0001c0002t0007g0285a0001c0002t0008g0141 | 2 | HG02109.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.2308-105T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 13/16 | chr2 | 205765369 | ||||||
| chr2:205765637
|
G | A | 2 | a0001c0002t0022g0185a0001c0002t0043g0259 | 2 | HG02486.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.2404+67G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 14/16 | chr2 | 205765637 | ||||||
| chr2:205765759
|
G | A | 5 | a0001c0002t0013g0198a0001c0002t0013g0199a0001c0002t0017g0255others(2): Show | 5 | HG02896.hp2 HG02897.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.2404+189G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 14/16 | chr2 | 205765759 | ||||||
| chr2:205765783
|
G | A | 11 | a0001c0002t0001g0191a0001c0002t0004g0192a0001c0002t0004g0275others(8): Show | 12 | HG02145.hp1 HG02280.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.2404+213G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 14/16 | chr2 | 205765783 | ||||||
| chr2:205765827
|
G | A | 1 | a0001c0006t0036g0307 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2404+257G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 14/16 | chr2 | 205765827 | ||||||
| chr2:205766163
|
C | T | 97 | a0001c0001t0002g0258a0001c0001t0003g0203a0001c0001t0003g0244others(94): Show | 97 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(94): Show |
intron_variant | MODIFIER | c.2404+593C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 14/16 | chr2 | 205766163 | ||||||
| chr2:205766175
|
C | G | 1 | a0001c0002t0004g0182 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2404+605C>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 14/16 | chr2 | 205766175 | ||||||
| chr2:205766530
|
A | G | 192 | a0001c0001t0001g0068a0001c0001t0001g0074a0001c0001t0001g0158others(189): Show | 196 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.2405-253A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 14/16 | chr2 | 205766530 | ||||||
| chr2:205766676
|
C | G | 1 | a0001c0001t0008g0079 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.2405-107C>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 14/16 | chr2 | 205766676 | ||||||
| chr2:205766830
|
T | A | 2 | a0001c0002t0020g0186a0001c0002t0042g0213 | 2 | HG02145.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.2425+27T>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205766830 | ||||||
| chr2:205766877
|
TG | T | 6 | a0001c0001t0012g0020a0001c0001t0018g0019a0001c0001t0031g0328others(3): Show | 6 | HG00639.hp1 HG00741.hp2 HG01081.hp2 others(3): Show |
intron_variant | MODIFIER | c.2425+80delG | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr2 | 205766877 | |||||
| chr2:205766897
|
A | G | 1 | a0001c0002t0046g0142 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2425+94A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205766897 | ||||||
| chr2:205766926
|
C | T | 3 | a0001c0011t0004g0171a0001c0011t0008g0135a0008c0028t0016g0143 | 3 | HG02622.hp1 HG02622.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.2425+123C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205766926 | ||||||
| chr2:205766945
|
T | C | 6 | a0001c0001t0002g0216a0001c0001t0004g0018a0001c0001t0004g0194others(3): Show | 6 | HG01081.hp1 HG01099.hp2 HG01346.hp2 others(3): Show |
intron_variant | MODIFIER | c.2425+142T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205766945 | ||||||
| chr2:205767041
|
A | G | 2 | a0001c0001t0019g0090a0001c0004t0003g0225 | 2 | HG01934.hp1 HG02148.hp1 |
intron_variant | MODIFIER | c.2425+238A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205767041 | ||||||
| chr2:205767145
|
C | CA | 82 | a0001c0001t0002g0224a0001c0001t0002g0258a0001c0001t0002g0316others(79): Show | 83 | HG00140.hp1 HG00280.hp1 HG00558.hp2 others(80): Show |
intron_variant | MODIFIER | c.2425+357dupA | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr2 | 205767145 | |||||
| chr2:205767145
|
CA | C | 7 | a0001c0002t0013g0198a0001c0002t0013g0199a0001c0002t0017g0255others(4): Show | 8 | HG02630.hp1 HG02818.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.2425+357delA | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr2 | 205767145 | |||||
| chr2:205767543
|
GAGA | G | 5 | a0001c0002t0013g0198a0001c0002t0013g0199a0001c0002t0017g0255others(2): Show | 5 | HG02896.hp2 HG02897.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.2425+745_2425+747d others(5): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr2 | 205767543 | |||||
| chr2:205767578
|
T | TA | 25 | a0001c0001t0004g0061a0001c0001t0008g0079a0001c0002t0013g0198others(22): Show | 25 | HG01109.hp1 HG01891.hp2 HG02135.hp1 others(22): Show |
intron_variant | MODIFIER | c.2425+788dupA | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr2 | 205767578 | |||||
| chr2:205767927
|
G | A | 3 | a0001c0001t0020g0031a0001c0001t0020g0072a0001c0002t0020g0186 | 3 | HG01069.hp2 HG01261.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.2425+1124G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205767927 | ||||||
| chr2:205767954
|
T | C | 1 | a0001c0003t0001g0156 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.2425+1151T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205767954 | ||||||
| chr2:205768108
|
C | T | 2 | a0001c0003t0021g0058a0001c0003t0021g0059 | 2 | NA19085.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.2425+1305C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205768108 | ||||||
| chr2:205768121
|
A | G | 1 | a0001c0002t0046g0142 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2425+1318A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205768121 | ||||||
| chr2:205768142
|
C | T | 1 | a0001c0002t0007g0285 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2425+1339C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205768142 | ||||||
| chr2:205768285
|
T | C | 1 | a0001c0001t0010g0335 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.2425+1482T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205768285 | ||||||
| chr2:205768778
|
G | C | 8 | a0001c0002t0004g0192a0001c0002t0004g0275a0001c0002t0028g0187others(5): Show | 8 | HG02145.hp1 HG02145.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.2425+1975G>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205768778 | ||||||
| chr2:205768783
|
C | T | 7 | a0001c0002t0051g0183a0001c0003t0007g0249a0001c0003t0011g0248others(4): Show | 7 | HG02257.hp1 HG02895.hp1 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.2425+1980C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205768783 | ||||||
| chr2:205768784
|
G | A | 1 | a0001c0013t0016g0132 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2425+1981G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205768784 | ||||||
| chr2:205768955
|
A | G | 2 | a0001c0002t0008g0141a0001c0002t0046g0142 | 2 | HG01884.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.2425+2152A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205768955 | ||||||
| chr2:205769119
|
C | A | 147 | a0001c0001t0002g0006a0001c0001t0002g0216a0001c0001t0002g0224others(144): Show | 150 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(147): Show |
intron_variant | MODIFIER | c.2425+2316C>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205769119 | ||||||
| chr2:205769484
|
G | C | 1 | a0001c0003t0002g0298 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.2425+2681G>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205769484 | ||||||
| chr2:205769492
|
G | A | 1 | a0001c0001t0001g0104 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.2425+2689G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205769492 | ||||||
| chr2:205769505
|
T | C | 2 | a0001c0001t0001g0104a0001c0002t0010g0277 | 2 | HG01074.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.2425+2702T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205769505 | ||||||
| chr2:205769505
|
T | TAC | 14 | a0001c0001t0001g0054a0001c0001t0008g0047a0001c0002t0008g0124others(11): Show | 15 | HG00408.hp2 HG01169.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.2425+2736_2425+273 others(6): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr2 | 205769505 | |||||
| chr2:205769505
|
T | TACAC | 18 | a0001c0001t0001g0064a0001c0001t0002g0006a0001c0002t0002g0262others(15): Show | 20 | HG00140.hp1 HG00735.hp1 HG01106.hp2 others(17): Show |
intron_variant | MODIFIER | c.2425+2734_2425+273 others(8): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr2 | 205769505 | |||||
| chr2:205769505
|
T | TACACAC | 117 | a0001c0001t0001g0022a0001c0001t0001g0026a0001c0001t0001g0046others(114): Show | 119 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(116): Show |
intron_variant | MODIFIER | c.2425+2732_2425+273 others(10): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr2 | 205769505 | |||||
| chr2:205769505
|
T | TACACACA others(1): Show |
76 | a0001c0001t0001g0021a0001c0001t0001g0036a0001c0001t0001g0037others(73): Show | 76 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(73): Show |
intron_variant | MODIFIER | c.2425+2730_2425+273 others(12): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr2 | 205769505 | |||||
| chr2:205769505
|
T | TACACACA others(3): Show |
48 | a0001c0001t0002g0224a0001c0001t0002g0258a0001c0001t0002g0316others(45): Show | 48 | HG00621.hp1 HG00639.hp2 HG00642.hp1 others(45): Show |
intron_variant | MODIFIER | c.2425+2728_2425+273 others(14): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr2 | 205769505 | |||||
| chr2:205769505
|
T | TACACACA others(5): Show |
9 | a0001c0001t0001g0060a0001c0001t0002g0216a0001c0001t0005g0008others(6): Show | 9 | HG01346.hp2 HG02004.hp1 HG02015.hp2 others(6): Show |
intron_variant | MODIFIER | c.2425+2726_2425+273 others(16): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr2 | 205769505 | |||||
| chr2:205769505
|
T | TACACACA others(7): Show |
6 | a0001c0001t0003g0265a0001c0001t0010g0266a0001c0003t0024g0344others(3): Show | 6 | HG02135.hp2 HG03195.hp2 NA19004.hp1 others(3): Show |
intron_variant | MODIFIER | c.2425+2724_2425+273 others(18): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr2 | 205769505 | |||||
| chr2:205769505
|
T | TACACACA others(9): Show |
1 | a0002c0027t0064g0177 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2425+2722_2425+273 others(20): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr2 | 205769505 | |||||
| chr2:205769505
|
T | TACACACA others(17): Show |
1 | a0001c0001t0005g0035 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.2425+2714_2425+273 others(28): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr2 | 205769505 | |||||
| chr2:205769505
|
TAC | T | 10 | a0001c0002t0013g0198a0001c0002t0013g0199a0001c0002t0017g0255others(7): Show | 10 | HG01243.hp1 HG02717.hp1 HG02896.hp2 others(7): Show |
intron_variant | MODIFIER | c.2425+2736_2425+273 others(6): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr2 | 205769505 | |||||
| chr2:205769505
|
TACAC | T | 13 | a0001c0002t0008g0141a0001c0002t0016g0134a0001c0002t0022g0185others(10): Show | 14 | HG02055.hp1 HG02258.hp1 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.2425+2734_2425+273 others(8): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr2 | 205769505 | |||||
| chr2:205769541
|
G | C | 1 | a0001c0004t0002g0281 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2425+2738G>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205769541 | ||||||
| chr2:205769864
|
G | T | 1 | a0001c0004t0001g0002 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.2425+3061G>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205769864 | ||||||
| chr2:205769885
|
C | T | 1 | a0001c0003t0025g0301 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2425+3082C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205769885 | ||||||
| chr2:205770145
|
G | A | 126 | a0001c0001t0002g0006a0001c0001t0002g0216a0001c0001t0002g0258others(123): Show | 128 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(125): Show |
intron_variant | MODIFIER | c.2425+3342G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205770145 | ||||||
| chr2:205770169
|
C | T | 1 | a0001c0030t0052g0071 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.2425+3366C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205770169 | ||||||
| chr2:205770467
|
ATC | A | 99 | a0001c0001t0001g0022a0001c0001t0001g0046a0001c0001t0001g0054others(96): Show | 99 | HG00280.hp2 HG00423.hp1 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.2425+3668_2425+366 others(6): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr2 | 205770467 | |||||
| chr2:205770573
|
G | C | 1 | a0001c0001t0008g0079 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.2425+3770G>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205770573 | ||||||
| chr2:205770974
|
A | G | 3 | a0001c0002t0004g0193a0001c0003t0008g0172a0001c0005t0004g0049 | 3 | HG01243.hp1 HG02257.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.2425+4171A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205770974 | ||||||
| chr2:205770975
|
T | C | 4 | a0001c0001t0004g0018a0001c0002t0004g0012a0001c0002t0032g0179others(1): Show | 4 | HG01099.hp1 HG01496.hp1 HG02738.hp1 others(1): Show |
intron_variant | MODIFIER | c.2425+4172T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205770975 | ||||||
| chr2:205770988
|
C | T | 1 | a0001c0005t0013g0176 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2425+4185C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205770988 | ||||||
| chr2:205771107
|
G | A | 8 | a0001c0002t0051g0183a0001c0002t0063g0137a0001c0003t0007g0249others(5): Show | 8 | HG02895.hp1 HG02897.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.2425+4304G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205771107 | ||||||
| chr2:205771190
|
T | A | 1 | a0001c0001t0002g0216 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.2425+4387T>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205771190 | ||||||
| chr2:205771209
|
TC | T | 3 | a0001c0002t0008g0181a0001c0002t0042g0213a0003c0025t0013g0167 | 3 | HG02145.hp2 HG02572.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.2425+4409delC | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr2 | 205771209 | |||||
| chr2:205771287
|
G | A | 5 | a0001c0003t0047g0126a0001c0013t0016g0132a0001c0013t0016g0133others(2): Show | 5 | HG02622.hp1 HG02717.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.2425+4484G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205771287 | ||||||
| chr2:205771399
|
C | A | 104 | a0001c0001t0003g0241a0001c0001t0004g0061a0001c0001t0005g0008others(101): Show | 106 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(103): Show |
intron_variant | MODIFIER | c.2425+4596C>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205771399 | ||||||
| chr2:205771419
|
C | T | 321 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0026others(318): Show | 327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
intron_variant | MODIFIER | c.2425+4616C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205771419 | ||||||
| chr2:205771664
|
C | G | 1 | a0001c0001t0011g0222 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2425+4861C>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205771664 | ||||||
| chr2:205771948
|
A | C | 345 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0026others(342): Show | 351 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(348): Show |
intron_variant | MODIFIER | c.2425+5145A>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205771948 | ||||||
| chr2:205771970
|
C | A | 1 | a0001c0001t0010g0317 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.2425+5167C>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205771970 | ||||||
| chr2:205772039
|
T | G | 336 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0026others(333): Show | 342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.2425+5236T>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205772039 | ||||||
| chr2:205772327
|
C | T | 1 | a0001c0006t0039g0305 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2425+5524C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205772327 | ||||||
| chr2:205772595
|
T | C | 9 | a0001c0002t0013g0198a0001c0002t0013g0199a0001c0002t0017g0255others(6): Show | 9 | HG01109.hp1 HG02896.hp2 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.2425+5792T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205772595 | ||||||
| chr2:205773102
|
T | C | 1 | a0002c0029t0013g0276 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2425+6299T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205773102 | ||||||
| chr2:205773169
|
C | T | 3 | a0001c0002t0008g0181a0001c0002t0056g0148a0003c0025t0013g0167 | 3 | HG02572.hp1 HG02647.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.2425+6366C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205773169 | ||||||
| chr2:205773438
|
G | T | 1 | a0001c0008t0004g0129 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2425+6635G>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205773438 | ||||||
| chr2:205773584
|
T | C | 4 | a0001c0002t0008g0141a0001c0003t0007g0249a0001c0018t0007g0336others(1): Show | 4 | HG02280.hp1 HG02486.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.2425+6781T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205773584 | ||||||
| chr2:205773608
|
T | C | 1 | a0001c0002t0028g0188 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2425+6805T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205773608 | ||||||
| chr2:205773806
|
C | A | 1 | a0001c0004t0050g0073 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.2425+7003C>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205773806 | ||||||
| chr2:205774177
|
C | A | 1 | a0001c0003t0040g0256 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2425+7374C>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205774177 | ||||||
| chr2:205774179
|
T | G | 1 | a0001c0003t0040g0256 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2425+7376T>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205774179 | ||||||
| chr2:205774218
|
C | G | 1 | a0001c0004t0003g0309 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.2425+7415C>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205774218 | ||||||
| chr2:205774383
|
C | T | 11 | a0001c0002t0008g0181a0001c0002t0013g0198a0001c0002t0013g0199others(8): Show | 11 | HG02572.hp1 HG02647.hp2 HG02896.hp2 others(8): Show |
intron_variant | MODIFIER | c.2425+7580C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205774383 | ||||||
| chr2:205774571
|
C | T | 1 | a0001c0002t0046g0142 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2425+7768C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205774571 | ||||||
| chr2:205774693
|
CATT | C | 3 | a0001c0002t0008g0181a0001c0002t0056g0148a0003c0025t0013g0167 | 3 | HG02572.hp1 HG02647.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.2425+7892_2425+789 others(7): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr2 | 205774693 | |||||
| chr2:205775062
|
C | T | 4 | a0001c0001t0018g0019a0001c0001t0020g0031a0001c0001t0020g0072others(1): Show | 4 | HG01069.hp2 HG01256.hp2 HG01261.hp1 others(1): Show |
intron_variant | MODIFIER | c.2425+8259C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205775062 | ||||||
| chr2:205775068
|
T | G | 3 | a0001c0002t0008g0181a0001c0002t0056g0148a0003c0025t0013g0167 | 3 | HG02572.hp1 HG02647.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.2425+8265T>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205775068 | ||||||
| chr2:205775107
|
G | A | 87 | a0001c0001t0003g0226a0001c0001t0003g0244a0001c0001t0003g0265others(84): Show | 88 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(85): Show |
intron_variant | MODIFIER | c.2425+8304G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205775107 | ||||||
| chr2:205775354
|
C | T | 1 | a0001c0013t0016g0132 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2425+8551C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205775354 | ||||||
| chr2:205775445
|
T | C | 5 | a0001c0001t0001g0054a0001c0002t0002g0262a0001c0002t0002g0263others(2): Show | 5 | HG02257.hp1 HG02630.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.2425+8642T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205775445 | ||||||
| chr2:205775450
|
C | T | 5 | a0001c0002t0042g0213a0001c0003t0047g0126a0001c0013t0016g0132others(2): Show | 5 | HG02145.hp2 HG02622.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.2425+8647C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205775450 | ||||||
| chr2:205775472
|
C | G | 5 | a0001c0002t0004g0192a0001c0002t0028g0187a0001c0002t0061g0190others(2): Show | 5 | HG02145.hp1 HG02280.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.2425+8669C>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205775472 | ||||||
| chr2:205775522
|
C | A | 1 | a0001c0001t0003g0244 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.2425+8719C>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205775522 | ||||||
| chr2:205775609
|
G | A | 1 | a0001c0002t0002g0295 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.2425+8806G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205775609 | ||||||
| chr2:205775635
|
A | G | 1 | a0001c0001t0004g0194 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.2425+8832A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205775635 | ||||||
| chr2:205775771
|
T | C | 1 | a0002c0029t0013g0276 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2425+8968T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205775771 | ||||||
| chr2:205775778
|
C | T | 3 | a0001c0002t0008g0181a0001c0002t0056g0148a0003c0025t0013g0167 | 3 | HG02572.hp1 HG02647.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.2425+8975C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205775778 | ||||||
| chr2:205775916
|
G | A | 102 | a0001c0001t0003g0226a0001c0001t0003g0244a0001c0001t0003g0265others(99): Show | 103 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(100): Show |
intron_variant | MODIFIER | c.2425+9113G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205775916 | ||||||
| chr2:205775979
|
A | G | 4 | a0001c0001t0018g0019a0001c0002t0004g0193a0001c0002t0018g0010others(1): Show | 4 | HG00741.hp2 HG01081.hp2 HG01256.hp2 others(1): Show |
intron_variant | MODIFIER | c.2425+9176A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205775979 | ||||||
| chr2:205776051
|
A | C | 1 | a0001c0008t0004g0129 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2425+9248A>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205776051 | ||||||
| chr2:205776516
|
CGCA | C | 9 | a0001c0001t0004g0041a0001c0001t0004g0117a0001c0001t0011g0222others(6): Show | 10 | HG01106.hp1 HG01433.hp1 HG02015.hp2 others(7): Show |
intron_variant | MODIFIER | c.2425+9714_2425+971 others(7): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205776516 | ||||||
| chr2:205776520
|
C | T | 9 | a0001c0001t0004g0041a0001c0001t0004g0117a0001c0001t0011g0222others(6): Show | 10 | HG01106.hp1 HG01433.hp1 HG02015.hp2 others(7): Show |
intron_variant | MODIFIER | c.2425+9717C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205776520 | ||||||
| chr2:205776521
|
T | A | 9 | a0001c0001t0004g0041a0001c0001t0004g0117a0001c0001t0011g0222others(6): Show | 10 | HG01106.hp1 HG01433.hp1 HG02015.hp2 others(7): Show |
intron_variant | MODIFIER | c.2425+9718T>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205776521 | ||||||
| chr2:205776903
|
A | C | 2 | a0001c0001t0006g0115a0001c0004t0003g0309 | 2 | HG00741.hp1 HG01123.hp2 |
intron_variant | MODIFIER | c.2425+10100A>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205776903 | ||||||
| chr2:205777021
|
C | T | 1 | a0001c0001t0011g0222 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2425+10218C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205777021 | ||||||
| chr2:205777060
|
T | C | 1 | a0001c0001t0003g0269 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.2425+10257T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205777060 | ||||||
| chr2:205777260
|
C | T | 112 | a0001c0001t0004g0061a0001c0001t0005g0008a0001c0001t0005g0025others(109): Show | 113 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(110): Show |
intron_variant | MODIFIER | c.2425+10457C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205777260 | ||||||
| chr2:205777277
|
A | C | 1 | a0001c0002t0025g0253 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.2425+10474A>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205777277 | ||||||
| chr2:205777385
|
A | C | 8 | a0001c0001t0018g0019a0001c0001t0020g0031a0001c0001t0020g0072others(5): Show | 8 | HG00741.hp2 HG01069.hp2 HG01081.hp2 others(5): Show |
intron_variant | MODIFIER | c.2425+10582A>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205777385 | ||||||
| chr2:205777496
|
C | T | 33 | a0001c0001t0007g0214a0001c0001t0007g0243a0001c0001t0008g0047others(30): Show | 33 | HG00280.hp1 HG00639.hp1 HG00735.hp2 others(30): Show |
intron_variant | MODIFIER | c.2425+10693C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205777496 | ||||||
| chr2:205777613
|
G | A | 113 | a0001c0001t0004g0061a0001c0001t0005g0008a0001c0001t0005g0025others(110): Show | 114 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(111): Show |
intron_variant | MODIFIER | c.2425+10810G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205777613 | ||||||
| chr2:205777728
|
T | G | 10 | a0001c0002t0007g0127a0001c0002t0011g0272a0001c0002t0016g0134others(7): Show | 10 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.2425+10925T>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205777728 | ||||||
| chr2:205778149
|
T | A | 1 | a0001c0001t0010g0076 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.2425+11346T>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205778149 | ||||||
| chr2:205778220
|
A | AT | 15 | a0001c0001t0002g0258a0001c0003t0001g0163a0001c0003t0014g0095others(12): Show | 16 | HG01261.hp2 HG02055.hp2 HG02818.hp1 others(13): Show |
intron_variant | MODIFIER | c.2425+11433dupT | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr2 | 205778220 | |||||
| chr2:205778220
|
AT | A | 119 | a0001c0001t0003g0226a0001c0001t0003g0244a0001c0001t0003g0265others(116): Show | 119 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(116): Show |
intron_variant | MODIFIER | c.2425+11433delT | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr2 | 205778220 | |||||
| chr2:205778249
|
G | C | 2 | a0001c0001t0004g0080a0001c0003t0011g0322 | 2 | HG01943.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.2425+11446G>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205778249 | ||||||
| chr2:205778343
|
C | T | 1 | a0001c0002t0056g0148 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.2425+11540C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205778343 | ||||||
| chr2:205778379
|
A | G | 1 | a0002c0029t0013g0276 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2425+11576A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205778379 | ||||||
| chr2:205778478
|
A | G | 5 | a0001c0002t0016g0134a0001c0003t0047g0126a0001c0013t0016g0132others(2): Show | 5 | HG02622.hp1 HG02717.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.2425+11675A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205778478 | ||||||
| chr2:205778479
|
G | A | 1 | a0001c0004t0060g0024 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.2425+11676G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205778479 | ||||||
| chr2:205778489
|
C | T | 1 | a0002c0016t0001g0274 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2425+11686C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205778489 | ||||||
| chr2:205778706
|
T | C | 1 | a0001c0001t0005g0038 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.2425+11903T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205778706 | ||||||
| chr2:205778708
|
C | G | 225 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0026others(222): Show | 229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.2425+11905C>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205778708 | ||||||
| chr2:205778756
|
C | A | 1 | a0001c0001t0005g0122 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.2425+11953C>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205778756 | ||||||
| chr2:205778762
|
A | G | 1 | a0002c0015t0030g0004 | 2 | HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.2425+11959A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205778762 | ||||||
| chr2:205778792
|
A | T | 225 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0026others(222): Show | 229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.2425+11989A>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205778792 | ||||||
| chr2:205778875
|
C | T | 1 | a0001c0003t0003g0108 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.2425+12072C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205778875 | ||||||
| chr2:205778956
|
TG | T | 3 | a0001c0002t0051g0183a0001c0002t0063g0137a0001c0018t0038g0308 | 3 | HG02922.hp1 HG03098.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.2425+12154delG | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205778956 | ||||||
| chr2:205778970
|
C | G | 1 | a0001c0003t0003g0296 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.2425+12167C>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205778970 | ||||||
| chr2:205778994
|
G | A | 1 | a0001c0002t0004g0182 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2425+12191G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205778994 | ||||||
| chr2:205779029
|
G | A | 1 | a0001c0004t0001g0003 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.2425+12226G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205779029 | ||||||
| chr2:205779032
|
A | G | 1 | a0001c0002t0006g0147 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.2425+12229A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205779032 | ||||||
| chr2:205779201
|
C | T | 1 | a0001c0002t0004g0193 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2425+12398C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205779201 | ||||||
| chr2:205779651
|
C | T | 1 | a0001c0002t0006g0052 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.2426-12584C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205779651 | ||||||
| chr2:205779901
|
T | C | 4 | a0001c0002t0008g0141a0001c0003t0007g0249a0001c0018t0007g0336others(1): Show | 4 | HG02280.hp1 HG02486.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.2426-12334T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205779901 | ||||||
| chr2:205779996
|
C | A | 1 | a0001c0001t0003g0241 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.2426-12239C>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205779996 | ||||||
| chr2:205780050
|
G | C | 51 | a0001c0001t0003g0226a0001c0001t0003g0241a0001c0001t0003g0244others(48): Show | 51 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(48): Show |
intron_variant | MODIFIER | c.2426-12185G>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205780050 | ||||||
| chr2:205780055
|
C | T | 1 | a0001c0001t0001g0158 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.2426-12180C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205780055 | ||||||
| chr2:205780256
|
C | T | 1 | a0001c0006t0011g0304 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2426-11979C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205780256 | ||||||
| chr2:205780325
|
A | G | 3 | a0001c0002t0051g0183a0001c0002t0063g0137a0001c0018t0038g0308 | 3 | HG02922.hp1 HG03098.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.2426-11910A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205780325 | ||||||
| chr2:205780409
|
T | A | 1 | a0001c0003t0005g0094 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.2426-11826T>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205780409 | ||||||
| chr2:205780442
|
C | T | 61 | a0001c0001t0001g0026a0001c0001t0001g0054a0001c0001t0001g0060others(58): Show | 63 | HG00099.hp1 HG00438.hp2 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.2426-11793C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205780442 | ||||||
| chr2:205780523
|
G | C | 57 | a0001c0001t0001g0021a0001c0001t0001g0036a0001c0001t0001g0037others(54): Show | 59 | HG00099.hp2 HG00140.hp2 HG01069.hp1 others(56): Show |
intron_variant | MODIFIER | c.2426-11712G>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205780523 | ||||||
| chr2:205780823
|
T | C | 1 | a0001c0004t0012g0043 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.2426-11412T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205780823 | ||||||
| chr2:205780923
|
TG | T | 3 | a0001c0002t0051g0183a0001c0002t0063g0137a0001c0018t0038g0308 | 3 | HG02922.hp1 HG03098.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.2426-11311delG | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205780923 | ||||||
| chr2:205781186
|
A | T | 13 | a0001c0001t0003g0226a0001c0001t0003g0265a0001c0001t0003g0269others(10): Show | 13 | HG00423.hp2 HG00642.hp2 HG00741.hp1 others(10): Show |
intron_variant | MODIFIER | c.2426-11049A>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205781186 | ||||||
| chr2:205781263
|
A | G | 1 | a0001c0002t0012g0131 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2426-10972A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205781263 | ||||||
| chr2:205781878
|
T | A | 1 | a0001c0002t0008g0124 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.2426-10357T>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205781878 | ||||||
| chr2:205781912
|
A | G | 1 | a0001c0006t0036g0307 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2426-10323A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205781912 | ||||||
| chr2:205782030
|
T | G | 7 | a0001c0001t0018g0019a0001c0001t0020g0031a0001c0001t0020g0072others(4): Show | 7 | HG01069.hp2 HG01109.hp1 HG01256.hp2 others(4): Show |
intron_variant | MODIFIER | c.2426-10205T>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205782030 | ||||||
| chr2:205782056
|
G | A | 1 | a0001c0004t0050g0073 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.2426-10179G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205782056 | ||||||
| chr2:205782069
|
C | A | 1 | a0001c0001t0010g0335 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.2426-10166C>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205782069 | ||||||
| chr2:205782073
|
A | ATT | 111 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0026others(108): Show | 114 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(111): Show |
intron_variant | MODIFIER | c.2426-10160_2426-10 others(8): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr2 | 205782073 | |||||
| chr2:205782387
|
G | T | 5 | a0001c0002t0013g0198a0001c0002t0013g0199a0001c0002t0017g0255others(2): Show | 5 | HG02896.hp2 HG02897.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.2426-9848G>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205782387 | ||||||
| chr2:205782646
|
T | C | 3 | a0001c0001t0018g0019a0001c0002t0004g0193a0001c0006t0039g0305 | 3 | HG01256.hp2 HG02257.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2426-9589T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205782646 | ||||||
| chr2:205782763
|
C | T | 2 | a0001c0002t0002g0262a0001c0002t0002g0263 | 2 | HG02630.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.2426-9472C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205782763 | ||||||
| chr2:205782812
|
G | A | 1 | a0001c0002t0056g0148 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.2426-9423G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205782812 | ||||||
| chr2:205782827
|
C | T | 1 | a0001c0001t0037g0323 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.2426-9408C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205782827 | ||||||
| chr2:205782855
|
GT | G | 19 | a0001c0001t0018g0019a0001c0002t0004g0182a0001c0002t0008g0181others(16): Show | 19 | HG01256.hp2 HG02257.hp1 HG02572.hp1 others(16): Show |
intron_variant | MODIFIER | c.2426-9366delT | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr2 | 205782855 | |||||
| chr2:205782861
|
T | C | 4 | a0001c0002t0016g0134a0001c0013t0016g0132a0001c0013t0016g0133others(1): Show | 4 | HG02622.hp1 HG02717.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.2426-9374T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205782861 | ||||||
| chr2:205783209
|
C | T | 2 | a0001c0001t0003g0318a0001c0003t0006g0098 | 2 | NA18995.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.2426-9026C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205783209 | ||||||
| chr2:205783353
|
T | A | 1 | a0001c0002t0056g0148 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.2426-8882T>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205783353 | ||||||
| chr2:205783429
|
T | C | 1 | a0001c0001t0002g0211 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.2426-8806T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205783429 | ||||||
| chr2:205783721
|
C | T | 1 | a0001c0002t0049g0173 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2426-8514C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205783721 | ||||||
| chr2:205784001
|
G | GAC | 268 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0036others(265): Show | 272 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(269): Show |
intron_variant | MODIFIER | c.2426-8214_2426-821 others(6): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr2 | 205784001 | |||||
| chr2:205784001
|
G | GACAC | 7 | a0001c0001t0007g0214a0001c0001t0026g0014a0001c0003t0014g0017others(4): Show | 7 | HG00280.hp1 HG00280.hp2 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.2426-8216_2426-821 others(8): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr2 | 205784001 | |||||
| chr2:205784001
|
G | GACACACA others(3): Show |
1 | a0001c0002t0056g0148 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.2426-8222_2426-821 others(14): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr2 | 205784001 | |||||
| chr2:205784001
|
G | GACACACA others(9): Show |
7 | a0001c0002t0007g0284a0001c0002t0016g0134a0001c0002t0046g0142others(4): Show | 7 | HG01884.hp2 HG02622.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.2426-8228_2426-821 others(20): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr2 | 205784001 | |||||
| chr2:205784001
|
G | GACACACA others(11): Show |
6 | a0001c0001t0002g0216a0001c0001t0018g0019a0001c0002t0002g0262others(3): Show | 6 | HG01256.hp2 HG01346.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.2426-8230_2426-821 others(22): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr2 | 205784001 | |||||
| chr2:205784001
|
G | GACACACA others(13): Show |
2 | a0002c0016t0001g0274a0002c0027t0064g0177 | 2 | HG02258.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.2426-8232_2426-821 others(24): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr2 | 205784001 | |||||
| chr2:205784001
|
G | GACACACA others(15): Show |
1 | a0001c0001t0001g0054 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2426-8213_2426-821 others(26): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr2 | 205784001 | |||||
| chr2:205784001
|
G | GACACACA others(17): Show |
3 | a0001c0002t0001g0191a0001c0006t0039g0305a0002c0014t0001g0196 | 3 | HG02615.hp2 HG03540.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2426-8213_2426-821 others(28): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr2 | 205784001 | |||||
| chr2:205784001
|
G | GACACACA others(19): Show |
7 | a0001c0001t0002g0224a0001c0002t0015g0007a0001c0003t0002g0326others(4): Show | 7 | HG00621.hp1 HG00621.hp2 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.2426-8213_2426-821 others(30): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr2 | 205784001 | |||||
| chr2:205784001
|
G | GACACACA others(21): Show |
13 | a0001c0001t0001g0060a0001c0002t0001g0169a0001c0002t0008g0181others(10): Show | 13 | HG02056.hp2 HG02083.hp2 HG02129.hp1 others(10): Show |
intron_variant | MODIFIER | c.2426-8213_2426-821 others(32): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr2 | 205784001 | |||||
| chr2:205784001
|
G | GACACACA others(23): Show |
18 | a0001c0001t0001g0026a0001c0001t0001g0104a0001c0001t0002g0006others(15): Show | 20 | HG00099.hp1 HG00438.hp2 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.2426-8213_2426-821 others(34): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr2 | 205784001 | |||||
| chr2:205784001
|
G | GACACACA others(25): Show |
1 | a0001c0003t0001g0085 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.2426-8213_2426-821 others(36): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr2 | 205784001 | |||||
| chr2:205784001
|
G | GACACACA others(27): Show |
1 | a0001c0003t0015g0260 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.2426-8213_2426-821 others(38): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr2 | 205784001 | |||||
| chr2:205784351
|
C | G | 1 | a0001c0002t0001g0082 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.2426-7884C>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205784351 | ||||||
| chr2:205784383
|
T | C | 1 | a0001c0001t0001g0158 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.2426-7852T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205784383 | ||||||
| chr2:205784386
|
G | A | 1 | a0001c0002t0056g0148 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.2426-7849G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205784386 | ||||||
| chr2:205784407
|
A | C | 1 | a0001c0004t0060g0024 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.2426-7828A>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205784407 | ||||||
| chr2:205784502
|
A | T | 8 | a0001c0002t0007g0127a0001c0002t0011g0272a0001c0006t0007g0306others(5): Show | 8 | HG01884.hp1 HG02055.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.2426-7733A>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205784502 | ||||||
| chr2:205784614
|
T | C | 109 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0026others(106): Show | 112 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(109): Show |
intron_variant | MODIFIER | c.2426-7621T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205784614 | ||||||
| chr2:205784867
|
G | A | 1 | a0001c0001t0003g0244 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.2426-7368G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205784867 | ||||||
| chr2:205784893
|
A | G | 1 | a0001c0001t0031g0328 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.2426-7342A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205784893 | ||||||
| chr2:205784910
|
C | A | 2 | a0001c0002t0004g0275a0001c0002t0028g0188 | 2 | HG03130.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.2426-7325C>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205784910 | ||||||
| chr2:205784961
|
A | G | 17 | a0001c0001t0018g0019a0001c0001t0020g0031a0001c0001t0020g0072others(14): Show | 18 | HG00741.hp2 HG01069.hp2 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.2426-7274A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205784961 | ||||||
| chr2:205784963
|
T | C | 1 | a0001c0011t0008g0135 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2426-7272T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205784963 | ||||||
| chr2:205785019
|
A | G | 112 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0026others(109): Show | 115 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(112): Show |
intron_variant | MODIFIER | c.2426-7216A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205785019 | ||||||
| chr2:205785227
|
G | C | 2 | a0001c0002t0004g0275a0001c0002t0028g0188 | 2 | HG03130.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.2426-7008G>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205785227 | ||||||
| chr2:205785417
|
A | G | 1 | a0001c0009t0005g0001 | 2 | HG00735.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.2426-6818A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205785417 | ||||||
| chr2:205785580
|
T | C | 1 | a0001c0001t0007g0214 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.2426-6655T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205785580 | ||||||
| chr2:205785690
|
C | A | 1 | a0001c0001t0026g0014 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.2426-6545C>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205785690 | ||||||
| chr2:205785915
|
G | A | 1 | a0001c0003t0001g0151 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.2426-6320G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205785915 | ||||||
| chr2:205785984
|
C | T | 1 | a0002c0015t0030g0004 | 2 | HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.2426-6251C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205785984 | ||||||
| chr2:205786076
|
C | T | 2 | a0001c0002t0010g0278a0001c0002t0010g0279 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.2426-6159C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205786076 | ||||||
| chr2:205786100
|
G | T | 1 | a0001c0002t0002g0280 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.2426-6135G>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205786100 | ||||||
| chr2:205786383
|
C | T | 8 | a0001c0002t0007g0286a0001c0002t0007g0289a0001c0002t0007g0290others(5): Show | 8 | HG00735.hp2 HG01361.hp1 HG01928.hp2 others(5): Show |
intron_variant | MODIFIER | c.2426-5852C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205786383 | ||||||
| chr2:205786519
|
C | T | 1 | a0001c0001t0002g0006 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.2426-5716C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205786519 | ||||||
| chr2:205786591
|
C | T | 6 | a0001c0001t0009g0240a0001c0001t0012g0009a0001c0002t0018g0010others(3): Show | 6 | HG00741.hp2 HG01081.hp2 HG01255.hp1 others(3): Show |
intron_variant | MODIFIER | c.2426-5644C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205786591 | ||||||
| chr2:205786898
|
C | T | 1 | a0001c0002t0046g0142 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2426-5337C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205786898 | ||||||
| chr2:205787159
|
G | C | 3 | a0001c0013t0016g0132a0001c0013t0016g0133a0008c0028t0016g0143 | 3 | HG02622.hp1 HG02717.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2426-5076G>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205787159 | ||||||
| chr2:205787190
|
C | G | 1 | a0001c0001t0001g0046 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.2426-5045C>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205787190 | ||||||
| chr2:205787202
|
C | A | 1 | a0001c0001t0020g0031 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.2426-5033C>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205787202 | ||||||
| chr2:205787529
|
T | C | 1 | a0001c0003t0004g0168 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2426-4706T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205787529 | ||||||
| chr2:205787576
|
C | G | 125 | a0001c0001t0003g0203a0001c0001t0004g0061a0001c0001t0005g0008others(122): Show | 126 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(123): Show |
intron_variant | MODIFIER | c.2426-4659C>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205787576 | ||||||
| chr2:205787705
|
T | TA | 23 | a0001c0001t0002g0224a0001c0001t0018g0019a0001c0001t0020g0031others(20): Show | 24 | HG00621.hp1 HG00621.hp2 HG00741.hp2 others(21): Show |
intron_variant | MODIFIER | c.2426-4522dupA | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr2 | 205787705 | |||||
| chr2:205787713
|
AGTGTC | A | 43 | a0001c0001t0001g0026a0001c0001t0001g0054a0001c0001t0001g0060others(40): Show | 44 | HG00099.hp1 HG00438.hp2 HG01099.hp1 others(41): Show |
intron_variant | MODIFIER | c.2426-4521_2426-451 others(9): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205787713 | ||||||
| chr2:205787718
|
C | CTG | 14 | a0001c0001t0004g0041a0001c0001t0004g0117a0001c0001t0011g0222others(11): Show | 15 | HG01106.hp1 HG01256.hp2 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.2426-4481_2426-448 others(6): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr2 | 205787718 | |||||
| chr2:205787718
|
C | CTGTG | 8 | a0001c0002t0004g0182a0001c0002t0051g0183a0001c0002t0063g0137others(5): Show | 8 | HG02257.hp1 HG02922.hp1 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.2426-4483_2426-448 others(8): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr2 | 205787718 | |||||
| chr2:205787718
|
C | CTGTGTG | 4 | a0001c0002t0029g0136a0001c0003t0011g0248a0001c0003t0011g0250others(1): Show | 4 | HG02723.hp2 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.2426-4485_2426-448 others(10): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr2 | 205787718 | |||||
| chr2:205787718
|
C | CTGTGTGT others(3): Show |
1 | a0001c0002t0042g0213 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2426-4489_2426-448 others(14): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr2 | 205787718 | |||||
| chr2:205787718
|
CTG | C | 179 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0036others(176): Show | 182 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.2426-4481_2426-448 others(6): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr2 | 205787718 | |||||
| chr2:205787718
|
CTGTG | C | 60 | a0001c0001t0002g0224a0001c0001t0003g0226a0001c0001t0003g0241others(57): Show | 60 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(57): Show |
intron_variant | MODIFIER | c.2426-4483_2426-448 others(8): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr2 | 205787718 | |||||
| chr2:205787718
|
CTGTGTGT others(3): Show |
C | 1 | a0004c0022t0006g0116 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.2426-4489_2426-448 others(14): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr2 | 205787718 | |||||
| chr2:205787719
|
T | A | 43 | a0001c0001t0001g0026a0001c0001t0001g0054a0001c0001t0001g0060others(40): Show | 44 | HG00099.hp1 HG00438.hp2 HG01099.hp1 others(41): Show |
intron_variant | MODIFIER | c.2426-4516T>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205787719 | ||||||
| chr2:205787721
|
T | A | 1 | a0001c0002t0046g0142 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2426-4514T>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205787721 | ||||||
| chr2:205787724
|
G | C | 43 | a0001c0001t0001g0026a0001c0001t0001g0054a0001c0001t0001g0060others(40): Show | 44 | HG00099.hp1 HG00438.hp2 HG01099.hp1 others(41): Show |
intron_variant | MODIFIER | c.2426-4511G>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205787724 | ||||||
| chr2:205787726
|
G | C | 1 | a0001c0002t0046g0142 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2426-4509G>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205787726 | ||||||
| chr2:205787809
|
T | G | 1 | a0002c0027t0064g0177 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2426-4426T>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205787809 | ||||||
| chr2:205787825
|
C | A | 2 | a0001c0003t0003g0218a0001c0004t0006g0113 | 2 | HG02080.hp2 NA18964.hp2 |
intron_variant | MODIFIER | c.2426-4410C>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205787825 | ||||||
| chr2:205787882
|
G | A | 2 | a0001c0002t0008g0181a0003c0025t0013g0167 | 2 | HG02572.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.2426-4353G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205787882 | ||||||
| chr2:205787988
|
G | A | 1 | a0001c0002t0008g0200 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2426-4247G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205787988 | ||||||
| chr2:205788000
|
T | C | 2 | a0001c0001t0010g0076a0001c0004t0010g0237 | 2 | HG00408.hp1 HG02071.hp2 |
intron_variant | MODIFIER | c.2426-4235T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205788000 | ||||||
| chr2:205788239
|
T | C | 69 | a0001c0001t0001g0026a0001c0001t0001g0054a0001c0001t0001g0060others(66): Show | 71 | HG00099.hp1 HG00438.hp2 HG00621.hp1 others(68): Show |
intron_variant | MODIFIER | c.2426-3996T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205788239 | ||||||
| chr2:205788370
|
C | A | 1 | a0002c0029t0013g0276 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2426-3865C>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205788370 | ||||||
| chr2:205788424
|
A | G | 345 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0026others(342): Show | 351 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(348): Show |
intron_variant | MODIFIER | c.2426-3811A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205788424 | ||||||
| chr2:205788491
|
C | T | 1 | a0001c0002t0001g0169 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.2426-3744C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205788491 | ||||||
| chr2:205788554
|
C | T | 1 | a0001c0002t0042g0213 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2426-3681C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205788554 | ||||||
| chr2:205788557
|
GT | G | 85 | a0001c0001t0003g0226a0001c0001t0003g0241a0001c0001t0003g0244others(82): Show | 86 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(83): Show |
intron_variant | MODIFIER | c.2426-3675delT | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr2 | 205788557 | |||||
| chr2:205788696
|
C | G | 1 | a0001c0001t0009g0310 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2426-3539C>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205788696 | ||||||
| chr2:205788741
|
G | A | 1 | a0001c0002t0028g0187 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2426-3494G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205788741 | ||||||
| chr2:205788756
|
C | G | 1 | a0001c0002t0054g0215 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2426-3479C>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205788756 | ||||||
| chr2:205788883
|
G | A | 1 | a0001c0011t0008g0135 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2426-3352G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205788883 | ||||||
| chr2:205788914
|
T | C | 2 | a0001c0001t0004g0194a0001c0001t0037g0323 | 2 | HG01099.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.2426-3321T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205788914 | ||||||
| chr2:205788915
|
A | T | 2 | a0001c0001t0004g0194a0001c0001t0037g0323 | 2 | HG01099.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.2426-3320A>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205788915 | ||||||
| chr2:205788982
|
T | C | 1 | a0001c0001t0009g0239 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.2426-3253T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205788982 | ||||||
| chr2:205789191
|
C | T | 7 | a0001c0001t0004g0018a0001c0001t0004g0080a0001c0001t0004g0194others(4): Show | 7 | HG01099.hp2 HG01496.hp1 HG01943.hp1 others(4): Show |
intron_variant | MODIFIER | c.2426-3044C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205789191 | ||||||
| chr2:205789235
|
C | T | 7 | a0001c0002t0011g0272a0001c0003t0004g0168a0001c0006t0011g0304others(4): Show | 7 | HG01891.hp2 HG02055.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.2426-3000C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205789235 | ||||||
| chr2:205789277
|
C | A | 3 | a0001c0001t0011g0222a0001c0008t0004g0005a0001c0008t0004g0197 | 4 | HG02559.hp2 HG02630.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.2426-2958C>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205789277 | ||||||
| chr2:205789319
|
C | T | 1 | a0001c0002t0054g0215 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2426-2916C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205789319 | ||||||
| chr2:205789399
|
C | A | 92 | a0001c0001t0003g0226a0001c0001t0003g0241a0001c0001t0003g0244others(89): Show | 93 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(90): Show |
intron_variant | MODIFIER | c.2426-2836C>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205789399 | ||||||
| chr2:205789512
|
C | G | 1 | a0001c0001t0057g0033 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2426-2723C>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205789512 | ||||||
| chr2:205789521
|
T | G | 4 | a0001c0002t0003g0204a0001c0002t0003g0282a0001c0002t0003g0283others(1): Show | 4 | NA18953.hp1 NA18965.hp1 NA18967.hp2 others(1): Show |
intron_variant | MODIFIER | c.2426-2714T>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205789521 | ||||||
| chr2:205789536
|
C | T | 1 | a0001c0004t0005g0165 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.2426-2699C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205789536 | ||||||
| chr2:205789537
|
T | A | 2 | a0001c0001t0015g0209a0001c0001t0015g0238 | 2 | NA18955.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.2426-2698T>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205789537 | ||||||
| chr2:205789626
|
T | C | 1 | a0002c0017t0062g0178 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2426-2609T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205789626 | ||||||
| chr2:205789682
|
C | T | 1 | a0001c0011t0008g0135 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2426-2553C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205789682 | ||||||
| chr2:205789716
|
C | G | 15 | a0001c0001t0018g0019a0001c0002t0004g0193a0001c0002t0008g0181others(12): Show | 16 | HG00741.hp2 HG01081.hp2 HG01109.hp1 others(13): Show |
intron_variant | MODIFIER | c.2426-2519C>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205789716 | ||||||
| chr2:205789742
|
A | G | 2 | a0001c0007t0013g0189a0001c0007t0017g0270 | 2 | HG02258.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.2426-2493A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205789742 | ||||||
| chr2:205789750
|
A | G | 251 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0026others(248): Show | 256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.2426-2485A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205789750 | ||||||
| chr2:205789752
|
T | A | 2 | a0001c0003t0007g0249a0001c0018t0007g0336 | 2 | HG02965.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.2426-2483T>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205789752 | ||||||
| chr2:205789950
|
T | C | 1 | a0001c0001t0009g0240 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.2426-2285T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205789950 | ||||||
| chr2:205790290
|
A | G | 1 | a0002c0015t0030g0004 | 2 | HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.2426-1945A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205790290 | ||||||
| chr2:205790452
|
T | G | 1 | a0001c0002t0056g0148 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.2426-1783T>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205790452 | ||||||
| chr2:205790457
|
G | A | 1 | a0001c0002t0006g0147 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.2426-1778G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205790457 | ||||||
| chr2:205790520
|
G | A | 1 | a0001c0003t0055g0092 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.2426-1715G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205790520 | ||||||
| chr2:205790524
|
T | A | 1 | a0001c0003t0055g0092 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.2426-1711T>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205790524 | ||||||
| chr2:205790527
|
T | TATTCACA others(6): Show |
1 | a0001c0003t0055g0092 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.2426-1708_2426-170 others(17): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205790527 | ||||||
| chr2:205790529
|
C | A | 1 | a0001c0003t0055g0092 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.2426-1706C>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205790529 | ||||||
| chr2:205790634
|
C | T | 45 | a0001c0001t0001g0054a0001c0001t0001g0060a0001c0001t0001g0104others(42): Show | 46 | HG00438.hp2 HG00621.hp1 HG00621.hp2 others(43): Show |
intron_variant | MODIFIER | c.2426-1601C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205790634 | ||||||
| chr2:205790648
|
G | GT | 173 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0036others(170): Show | 176 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(173): Show |
intron_variant | MODIFIER | c.2426-1573dupT | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr2 | 205790648 | |||||
| chr2:205790648
|
G | GTT | 16 | a0001c0001t0001g0065a0001c0001t0006g0110a0001c0001t0007g0214others(13): Show | 16 | HG00280.hp1 HG00639.hp1 HG01123.hp1 others(13): Show |
intron_variant | MODIFIER | c.2426-1574_2426-157 others(6): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr2 | 205790648 | |||||
| chr2:205790648
|
GTT | G | 9 | a0001c0002t0008g0181a0001c0002t0016g0134a0001c0002t0046g0142others(6): Show | 9 | HG01109.hp1 HG01884.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.2426-1574_2426-157 others(6): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr2 | 205790648 | |||||
| chr2:205790831
|
C | T | 1 | a0001c0004t0012g0043 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.2426-1404C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205790831 | ||||||
| chr2:205790835
|
C | T | 1 | a0001c0004t0001g0062 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.2426-1400C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205790835 | ||||||
| chr2:205790844
|
C | T | 1 | a0001c0002t0002g0280 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.2426-1391C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205790844 | ||||||
| chr2:205790963
|
C | G | 1 | a0001c0003t0002g0326 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.2426-1272C>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205790963 | ||||||
| chr2:205790967
|
G | C | 257 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0026others(254): Show | 262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
intron_variant | MODIFIER | c.2426-1268G>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205790967 | ||||||
| chr2:205790970
|
C | A | 3 | a0001c0001t0001g0104a0001c0003t0002g0334a0001c0009t0021g0045 | 3 | HG01361.hp2 HG02602.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.2426-1265C>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205790970 | ||||||
| chr2:205790983
|
G | C | 1 | a0001c0003t0001g0162 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.2426-1252G>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205790983 | ||||||
| chr2:205791015
|
A | G | 258 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0026others(255): Show | 263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.2426-1220A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205791015 | ||||||
| chr2:205791071
|
G | A | 1 | a0001c0003t0047g0126 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2426-1164G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205791071 | ||||||
| chr2:205791099
|
A | G | 1 | a0001c0002t0056g0148 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.2426-1136A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205791099 | ||||||
| chr2:205791154
|
G | A | 1 | a0001c0003t0025g0301 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2426-1081G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205791154 | ||||||
| chr2:205791159
|
G | A | 1 | a0001c0008t0004g0129 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2426-1076G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205791159 | ||||||
| chr2:205791200
|
C | T | 2 | a0001c0001t0008g0050a0001c0002t0007g0325 | 2 | HG01074.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.2426-1035C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205791200 | ||||||
| chr2:205791229
|
T | G | 17 | a0001c0001t0018g0019a0001c0001t0020g0031a0001c0001t0020g0072others(14): Show | 18 | HG00741.hp2 HG01069.hp2 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.2426-1006T>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205791229 | ||||||
| chr2:205791246
|
A | G | 1 | a0001c0003t0009g0292 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2426-989A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205791246 | ||||||
| chr2:205791418
|
C | T | 10 | a0001c0001t0007g0243a0001c0002t0007g0286a0001c0002t0007g0289others(7): Show | 10 | HG00735.hp2 HG01070.hp1 HG01361.hp1 others(7): Show |
intron_variant | MODIFIER | c.2426-817C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205791418 | ||||||
| chr2:205791461
|
C | G | 105 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0026others(102): Show | 108 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(105): Show |
intron_variant | MODIFIER | c.2426-774C>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205791461 | ||||||
| chr2:205791572
|
T | C | 3 | a0001c0005t0007g0223a0001c0005t0023g0120a0001c0005t0023g0121 | 3 | HG01123.hp1 HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.2426-663T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205791572 | ||||||
| chr2:205791667
|
A | G | 2 | a0001c0002t0007g0127a0001c0006t0007g0306 | 2 | HG01884.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.2426-568A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205791667 | ||||||
| chr2:205791696
|
A | G | 1 | a0002c0015t0030g0004 | 2 | HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.2426-539A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205791696 | ||||||
| chr2:205791744
|
A | AAAC | 17 | a0001c0001t0018g0019a0001c0001t0020g0031a0001c0001t0020g0072others(14): Show | 18 | HG00741.hp2 HG01069.hp2 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.2426-489_2426-487d others(5): Show |
NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr2 | 205791744 | |||||
| chr2:205791936
|
T | A | 1 | a0001c0002t0042g0213 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2426-299T>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205791936 | ||||||
| chr2:205791940
|
A | T | 38 | a0001c0001t0007g0214a0001c0001t0007g0243a0001c0001t0008g0047others(35): Show | 38 | HG00280.hp1 HG00639.hp1 HG00735.hp2 others(35): Show |
intron_variant | MODIFIER | c.2426-295A>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205791940 | ||||||
| chr2:205792070
|
A | G | 1 | a0002c0015t0030g0004 | 2 | HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.2426-165A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205792070 | ||||||
| chr2:205792192
|
T | C | 10 | a0001c0002t0008g0181a0001c0002t0016g0134a0001c0002t0046g0142others(7): Show | 11 | HG01109.hp1 HG01884.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.2426-43T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205792192 | ||||||
| chr2:205792195
|
A | T | 10 | a0001c0002t0008g0181a0001c0002t0016g0134a0001c0002t0046g0142others(7): Show | 11 | HG01109.hp1 HG01884.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.2426-40A>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 15/16 | chr2 | 205792195 | ||||||
| chr2:205792579
|
A | T | 7 | a0001c0001t0018g0019a0001c0001t0020g0031a0001c0001t0020g0072others(4): Show | 7 | HG00741.hp2 HG01069.hp2 HG01081.hp2 others(4): Show |
intron_variant | MODIFIER | c.2476+294A>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 16/16 | chr2 | 205792579 | ||||||
| chr2:205792927
|
G | A | 1 | a0001c0004t0001g0002 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.2476+642G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 16/16 | chr2 | 205792927 | ||||||
| chr2:205792960
|
A | C | 3 | a0001c0001t0008g0050a0001c0002t0007g0325a0001c0002t0008g0124 | 3 | HG01074.hp2 HG02273.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.2476+675A>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 16/16 | chr2 | 205792960 | ||||||
| chr2:205793192
|
C | T | 8 | a0001c0002t0008g0181a0001c0002t0016g0134a0001c0002t0046g0142others(5): Show | 8 | HG01884.hp2 HG02572.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.2476+907C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 16/16 | chr2 | 205793192 | ||||||
| chr2:205793193
|
G | T | 1 | a0002c0015t0030g0004 | 2 | HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.2476+908G>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 16/16 | chr2 | 205793193 | ||||||
| chr2:205793384
|
C | A | 5 | a0001c0002t0013g0198a0001c0002t0013g0199a0001c0002t0017g0255others(2): Show | 5 | HG02896.hp2 HG02897.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.2476+1099C>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 16/16 | chr2 | 205793384 | ||||||
| chr2:205793425
|
T | C | 12 | a0001c0001t0001g0022a0001c0001t0001g0064a0001c0001t0001g0065others(9): Show | 13 | HG01069.hp1 HG01071.hp2 HG01346.hp1 others(10): Show |
intron_variant | MODIFIER | c.2476+1140T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 16/16 | chr2 | 205793425 | ||||||
| chr2:205793604
|
G | T | 3 | a0001c0002t0002g0262a0001c0002t0002g0263a0001c0002t0002g0264 | 3 | HG02630.hp2 HG03195.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.2477-1150G>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 16/16 | chr2 | 205793604 | ||||||
| chr2:205793659
|
G | A | 1 | a0001c0001t0027g0111 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.2477-1095G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 16/16 | chr2 | 205793659 | ||||||
| chr2:205793668
|
T | C | 1 | a0002c0027t0064g0177 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2477-1086T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 16/16 | chr2 | 205793668 | ||||||
| chr2:205793705
|
A | T | 8 | a0001c0002t0008g0181a0001c0002t0016g0134a0001c0002t0046g0142others(5): Show | 8 | HG01884.hp2 HG02572.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.2477-1049A>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 16/16 | chr2 | 205793705 | ||||||
| chr2:205793719
|
G | A | 6 | a0001c0002t0016g0134a0001c0002t0046g0142a0001c0003t0047g0126others(3): Show | 6 | HG01884.hp2 HG02622.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.2477-1035G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 16/16 | chr2 | 205793719 | ||||||
| chr2:205793810
|
A | G | 1 | a0001c0002t0042g0213 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2477-944A>G | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 16/16 | chr2 | 205793810 | ||||||
| chr2:205793921
|
G | A | 2 | a0001c0002t0046g0142a0001c0003t0047g0126 | 2 | HG01884.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.2477-833G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 16/16 | chr2 | 205793921 | ||||||
| chr2:205793979
|
A | C | 5 | a0001c0002t0015g0007a0001c0002t0033g0294a0001c0003t0014g0017others(2): Show | 5 | HG01099.hp1 HG01192.hp1 HG01975.hp2 others(2): Show |
intron_variant | MODIFIER | c.2477-775A>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 16/16 | chr2 | 205793979 | ||||||
| chr2:205794120
|
A | T | 5 | a0001c0001t0003g0318a0001c0003t0006g0098a0001c0003t0024g0324others(2): Show | 6 | HG01167.hp2 HG01169.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.2477-634A>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 16/16 | chr2 | 205794120 | ||||||
| chr2:205794124
|
T | A | 4 | a0001c0002t0022g0185a0001c0002t0043g0259a0001c0003t0022g0174others(1): Show | 4 | HG02486.hp2 HG02647.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.2477-630T>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 16/16 | chr2 | 205794124 | ||||||
| chr2:205794155
|
G | C | 1 | a0001c0001t0010g0076 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.2477-599G>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 16/16 | chr2 | 205794155 | ||||||
| chr2:205794179
|
C | T | 1 | a0002c0027t0064g0177 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2477-575C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 16/16 | chr2 | 205794179 | ||||||
| chr2:205794244
|
G | A | 1 | a0001c0001t0001g0112 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.2477-510G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 16/16 | chr2 | 205794244 | ||||||
| chr2:205794301
|
G | A | 1 | a0001c0001t0004g0081 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.2477-453G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 16/16 | chr2 | 205794301 | ||||||
| chr2:205794389
|
C | T | 7 | a0001c0002t0004g0192a0001c0002t0004g0275a0001c0002t0028g0187others(4): Show | 7 | HG02145.hp1 HG02280.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.2477-365C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 16/16 | chr2 | 205794389 | ||||||
| chr2:205794394
|
G | C | 1 | a0001c0009t0027g0032 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.2477-360G>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 16/16 | chr2 | 205794394 | ||||||
| chr2:205794401
|
C | T | 11 | a0001c0001t0007g0243a0001c0002t0007g0286a0001c0002t0007g0289others(8): Show | 11 | HG00735.hp2 HG01070.hp1 HG01361.hp1 others(8): Show |
intron_variant | MODIFIER | c.2477-353C>T | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 16/16 | chr2 | 205794401 | ||||||
| chr2:205794597
|
G | A | 1 | a0001c0001t0001g0104 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.2477-157G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 16/16 | chr2 | 205794597 | ||||||
| chr2:205794602
|
G | A | 2 | a0001c0001t0001g0074a0001c0003t0001g0156 | 2 | NA18978.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.2477-152G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 16/16 | chr2 | 205794602 | ||||||
| chr2:205794739
|
T | C | 4 | a0001c0002t0004g0192a0001c0002t0061g0190a0001c0005t0004g0049others(1): Show | 4 | HG02145.hp1 HG02280.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.2477-15T>C | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 16/16 | chr2 | 205794739 | ||||||
| chr2:205794750
|
G | A | 1 | a0001c0002t0056g0148 | 1 | NA20805.hp2 | splice_region_variant&intron_variant | LOW | c.2477-4G>A | NRP2 | ENSG00000118257.17 | transcript | ENST00000357785.10 | protein_coding | 16/16 | chr2 | 205794750 |